CURRICULUM VITAE
……………………………………………………………………………………
MOHAMMAD H. SANATI
B.Sc.,Chem.;M.Sc.,Biochem.(I.R.I);
Ph.D.,Medical Biotechnology (
……………………………………………………………………………………….
Date and Place of Birth:
Address for Correspondence:
National Institute for Genetic
Engineering and Biotechnology (NIGEB)
P.O.Box : 14155-6343,
Telephone Numbers:
+
98 21 44580346 (work), +98 21 88905500 (home)
+98 912 275 5392 (cell phone)
Facsimile Number:
+98
21 44580346
E-mail:
mhsanati@yahoo.com
………………………………………………………………………………………
CURRENT SITUATION:
- Researcher, Medical Genetics Department, NIGEB, (Since March 1997).
………………………………………………………………………………………….
EDUCATIONAL QUALIFICATIONS:
1991-1996
Ph.D. (Biotechnology) at Biotechnology Research Group,
1985-1988:
M.Sc. (Biochemistry), Biochemistry Department, School of
Medical Sciences,
1977-1984:
B.Sc. (Chemistry), Chemistry Department,
Ferdousi Uneversity,
Topics of Thesis:
PhD:
Cloning and characterization of a novel mitochondrial
autoantigen involved in multiple sclerosis
MSc:
Production of antibody against the Small Molecules
BSc:
Isolation and purification of color pigments from plant leaves.
WORK EXPERIENCES:
2006- Until now: Researcher at the Medical Genetic Department, National
Institute for Genetic Engineering and Biotechnology,
1997 – 2005: President of the National Institute for Genetic Engineering
and Biotechnology,
1995: Part time research assistant (work on multiple sclerosis
diseases),
1996: Full time researcher in
1994: Demonstrator (practical molecular biology for undergraduate
students),
a) Papers published in Scientific Journals:
105.
Zahra Lashgary,Ahmad Khodadadi,Yoginder Singh,Seyed Massoud Houshmand,
Frouzandeh
Mahjoubi,Prithviraj Sharma,Shweta Singh,Mahtab Seyedin, Amit
Srivastava,Mirtra Ataee,Zeinab Sadat Mohammadi,Nima Rezaei, Rameshwar
N.K.Bamezai & Mohammad Hossein Sanati,
Y chromosome diversity among the Iranian religious groups: a reservoir
of genetic variation, Annals of human Biology, In Press.
104. Fazeli AS, Nasrabadi D,
Sanati MH, Pouya A, Ibrahim SM, Baharvand H, Salekdeh GH.
Proteome analysis of brain in murine experimental autoimmune
encephalomyelitis.
Proteomics,
2010 Aug;10(15):2822-32.
103.
Alasti F, Peeters N, Wuyts W, Sanati MH, Van
Camp G.
Novel human pathological mutations. Gene symbol: SLC26A4. Disease:
Deafness, non-syndromic, autosomal recessive.
Hum Genet. 2010 Jan;127(1):116.
102.
Sareh Asadi, Mohammad Javan, Abolhassan Ahmadiani,
Mohammad Hossein
Sanati, Alternative splicing in
the synaptic protein interaction site of rat Cav2.2
(α1B)
calcium channels: Changes induced by chronic inflammatory pain,
J Mol Neurosci. 2009 Sep; 39(1-2):40-8. Epub 2009 Jan 6.
99.
Abolhassan Shahzadeh Fazeli , Mohammad Hossein
Sanati, Davood Nasrabadi, Alireza Pouya, Hossein Baharvand,
Ghasem Hosseini Salekdeh, Central Nervous System Proteomics in Animal
Model of Multiple Sclerosis Revealed Down-Regulation of Mithochondrial
Proteins,
Yakhteh Medical Journal,Vol 11,
No 2, Summer 2009, Pages:236-243.
98.
Abdorrahim
Sadeghi, Mohammad Hossein Sanati, Fatemeh Alasti, Morteza
Hashemzadeh Chaleshtori, Saeid Mahmoudian, Mitra Ataei,
Contribution of GJB2 mutations
and Four common DFNB loci in autosomal
recessive non-syndromic hearing impairment in Markazi and Qom provinces
of Iran,
Iranian Journal of
Biotechnology (IJB), Vol 7, No 2 (2009), 108-111.
97.
Mojdeh Ghabaee, Asghar Bayati, Shahla Amri
Saroukolaei, Mohamad Ali Sahraian, Mohammad Hosein Sanaati,
Parisa Karimi, Massoud Houshmand, Homa Sadeghian, Leila Hashemi Chelavi,
Analysis of HLA DR2&DQ6 (DRB1*1501, DQA1*0102, DQB1*0602) Haplotypes in
Iranian Patients with Multiple Sclerosis,
Cell Mol Neurobiol DOI
10.1007/s10571-008-9302-1.
96. M.
Jahanshahi, M.H.Sanati, S. Hajizadeh and Z. Babaei,
Gelatin nanoparticle fabrication
and optimization of the particle
size, phys.stat.sol.(a)205,No.12,2898 –2902 (2008)/DOI
10.1002/pssa.200824329
94.
Mit Ghabaee M, Omranisikaroudi M, Amrisaroukolaei S, Meysamie A,
Sahraian MA, Bayati A, Sanati
MH, Houshman M, Sadeghian H, Vajihazaman
K. Mitochondrial Mutation in Iranian Patients with Multiple Sclerosis,
Correlation Between Haplogroups H, A and Clinical Manifestations.
Cell Mol Neurobiol. 2008 Nov 14.
PMID:
19009343
Glucose sensors with increased sensitivity
based on composite gels containing immobilized boronic acid,
Reactive & Functional Polymers 68 (2008)1625
–1635.
92.
Jadali Z and Sanati MH
The autoimmune diseases manifested by production of
autoantibodies: the autoantigens identified by random peptide library.
PMID: 18780947
91.
Allameh A,
Maleklou N, Zargari M, Sanati MH. The influence of
uric acid treatments on liver glutathione system prevent oxidative
damages in experimental autoimmune encephalomyelitis mice. Neurosci
Lett. 2008 Jul 4;439(1):111-5.
Epub 2008 Apr 20.
PMID: 18501514
90.
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11.
Clin Genet. 2008 Jun 26. [Epub ahead of print]
PMID: 18616530
89.
Variation of DAT1 VNTR alleles and genotypes among old ethnic groups in
Mesopotamia to the
Hum Biol. 2008 Feb;80(1):73-81.
PMID: 18505046
88.
Alasti F, A. sadeghi, N.H. Sanati, M.
farhadi,
A Mutation in HOXA2 is responsible for autosomal recessive
microtia in an Iranian family.
American Journal of Human Genetic, 2008, accepted for
publication.
87.
Bayat B., S. Yazdian, A. Alavi, M. Chiani, F. Chitsazian,
B. Khoramian, F. Suri, M. Narooie-Nejad, M. H. Sanati, and
E. Elahi.
Contribution of MYCO and CYP1B1 mutations to JOAG, EJP,
2008, accepted for publication.
86.
Alasti F, Sanati MH,
Behrouzifard AH, Sadeghi A, de Brouwer AP, Kremer H, Smith RJ, Van Camp
G.
A novel TECTA mutation confirms the recognizable phenotype among
autosomal recessive hearing impairment families.
Int J Pediatr Otorhinolaryngol. 2008 Feb;72(2):249-55.
PMID: 18022253
85.
Mehrizi AA, Zakeri S, Salmanian AH,
Sanati MH, Djadid ND.
Plasmodium falciparum: Sequence analysis of the gene encoding the
C-terminus region of the merozoite surface protein-1, a potential
malaria vaccine antigen, in Iranian clinical isolates.
Exp Parasitol. 2008 Mar;118(3):378-85.
PMID: 18053992
84.
Bayat B, Houshmand M, Sanati MH,
Moin M, Panahi MS, Aleyasin SA, Isaian A, Farhoodi A.
Use of D11S2179 and D11S1343 as markers for prenatal diagnosis of ataxia
telangiectasia in Iranian patients.
Arch Med Res. 2007 Oct;38(7):803-5.
Epub 2007 Jul 5.
PMID: 17845903 [PubMed - indexed for MEDLINE]
83.
Diversity and relationship between Iranian ethnic groups: human dopamine
transporter gene (DAT1) VNTR genotyping.
Am J Hum Biol. 2007 Nov-Dec;19(6):821-6.
PMID: 17712789 [PubMed - indexed for MEDLINE]
82.
CYP1B1 mutation profile of Iranian primary congenital glaucoma patients
and associated haplotypes.
J Mol Diagn. 2007 Jul;9(3):382-93.
PMID: 17591938 [PubMed - indexed for MEDLINE]
81.
Golalipour M, Mahjoubi F, Sanati
MH, Kamran A.
Gene dosage is not responsible for the upregulation of MRP1 gene
expression in adult leukemia patients.
Arch Med Res. 2007 Apr;38(3):297-304.
Erratum in: Arch Med Res. 2007 Nov;38(8):909.
PMID: 17350479 [PubMed - indexed for MEDLINE]
80.
A comprehensive study on the major mutations in glucose-6-phosphate
dehydrogenase-deficient polymorphic variants identified in the coastal
provinces of Caspian Sea in the north of
Clin Biochem. 2007 Jun;40(9-10):699-704.
Epub 2007 Apr 6.
PMID: 17499234 [PubMed - indexed for MEDLINE]
79.
Sabouri A.A.,
H. Ghourchaei, M.H. Sanati, M.S. Atri, M. Rezaei-Tawiriani
and G.H. Hakimelahi.
Binding properties and structural changes of human growth hormone upon
interaction with cobalt ion, Journal of Thermal analysis and
Calorimetry, Vol. 89 (2007) 3, 921-927.
78.
Zargari M, Allameh A, Sanati MH, Tiraihi T, Lavasani S, Emadyan
O.
Relationship between the clinical scoring and demyelination in central
nervous system with total antioxidant capacity of plasma during
experimental autoimmune encephalomyelitis development in mice.
Neurosci Lett. 2007 Jan 22;412(1):24-8.
Epub 2006 Dec 8.
PMID: 17157437 [PubMed - indexed for MEDLINE]
77.
Bairamijamal F., M.H. Sanati, M.M.
Banoei, B. Bayat,
Genetic Polymorphism Analysis
of NAD(P)H: quinine Oxidoreductase 1 in Different Iranian Ethnic Groups,
Arjmand and D. Farhud, Current Science, Vol. 91, No. 8, 2006.
Houshmand M, M.H. Sanati,
B Hooshiar Kashani, M Shafa Shariat Panahi, Y Eisaian, M.
Moien, M Farhoudi.
Role of mitochondria in Iranian
Ataxia-Telangiectasia: Investigation of mitochondrial deletions and
Haplogroups, Iranian Journal of Biotechnology (IJB), Vol.4, No. 1, 2006,
64-68.
76.
A haplotype framework for cystic fibrosis mutations in
J Mol Diagn. 2006 Feb;8(1):119-27.
PMID: 16436643 [PubMed - indexed for MEDLINE]
75.
Hassani-Kumleh H, Houshmand M,
Panahi MS, Riazi GH, Sanati MH, Gharagozli K, Ghabaee M.
Mitochondrial D-loop variation in Persian multiple sclerosis patients: K
and A haplogroups as a risk factor!!
Cell Mol Neurobiol. 2006 Mar;26(2):119-25.
Epub 2006 May 6.
PMID: 16763779 [PubMed - indexed for MEDLINE]
74.
Kumleh HH, Riazi GH, Houshmand M,
Sanati MH, Gharagozli K, Shafa M.
Complex I deficiency in Persian multiple sclerosis patients.
J Neurol Sci. 2006 Apr 15;243(1-2):65-9.
Epub 2006 Jan 18.
PMID: 16413582 [PubMed - indexed for MEDLINE]
73.
Mosayebi G., Moazzeni S.M., Sanati M.H.
Effect of Sex on Susceptibility to Experimental Autoimmune
Encephalomyelities Induced with MOG35-55 Peptide in C57BL/6 Mice,
Medical Journal of
72.
Mosayebi G, S.M. Moazzeni and M.H. Sanati,
Prevalence of Malignant Lesions in Single Cold
Thyroid Nodules and Determination Accuracy of FNAB in These Single Cold
Nodules, Medical Journal of Tabriz University of Medical Science, Vol.
28, No. 4, 2006, 95-100.
71.
Montazeri M, M. Houshmand, M. Shafa Shariat Panahi,
F. Noohi, G. Nozar, M.H. Sanati, E.V. Zaklyazminskaya,
Investigation of Polymorphisms In non-coding Region
of human Mitochondrial DNA in 31 Iranian Hypertrophic Cardiomyopathy
(HCM) Patients. Iranian Journal of Biotechnology, 2006 July; Vol. 3, No.
3, 157-162.
70.
Lack of association between interferon-gamma receptor-1 polymorphism and pulmonary TB in Iranian population sample.
J Infect. 2006 May;52(5):374-7. Epub 2005 Oct 17.
PMID: 16233916 [PubMed - indexed for MEDLINE]
69.
Noori-Dalooii M.R., Hejazi S.H., Yousefi A., Mohammad gangi S., Soltani
S., Javadi K.R. and Sanati M.H.
Identification of Mutations in
Glucose-6-Posphate Dehydrogenase (G6PD)
Gene in Patients in Hormozgan
Province of Iran, Journal of Science (I.R. of iran), 17(4):313-316,
2006.
68.
Noori-Daloii M.R., S. Soltanian, S. H. Mohammad
Gangi, A. Yousefi, S. Hejazi, A. Bani-hashemi, S. Hitratfar, and
M. Sanati,
Molecular Identification of the Most Prevalent
Mutations of Glucose-6-Posphate Dehydrogenase (G6PD) Gene in Deficient
Patients in
67.
Saboury AA, Atri MS, Sanati MH,
Moosavi-Movahedi AA, Hakimelahi GH, Sadeghi M.
A thermodynamic study on the interaction between magnesium ion and human
growth hormone.
Biopolymers. 2006 Feb 5;81(2):120-6.
PMID: 16208769 [PubMed - indexed for MEDLINE]
66. Saboury A.A., M.S. Atri, M.H. Sanati, M. Sadeghi
Application of a Simple Calorimetric Data Analysis on the Binding Study
of Calcium Ions by Human Growth Hormone, Journal of Thermal Analysis and
Calorimetry, Vol. 83 (2006) 1, 175-179.
65.
Atri M.S, A.A Saboury, M. Rezaei-Tavirani, M.H. Sanati,
A.A. Moosavi Movahedi, M. Sadeghi, H. Mansuri-Torshizi, K. Haghbeen,
Binding Properties and Conformational Change of Human Growth Hormone Upon
Interaction with Fe+3, Thermochimica Acta, 438, 2005,
178-183.
64.
Esteghamat F, Noorinayer B,
Sanati MH, Hekmatdoost A, Zafarghandi M, Shalmani HM, Agah M, Zali
MR.
C77G mutation in protein tyrosine phosphatase CD45 gene and autoimmune
hepatitis.
Hepatol Res. 2005 Jul;32(3):154-7.
Epub 2005 Jun 15.
PMID: 15963758 [PubMed - in process]
63.
Hadavi V, D. Farhoud, M.H. Sanati, M. Houshmand, S.M.
Navabi, M. Seyedian, M. Younesian
An Investigation of Human Apolipoprotein E Polymorphism in Multiple
Sclerosis Patients of
62.
Population screening for association of mitochondrial haplogroups BM, J,
K and M with multiple sclerosis: interrelation between haplogroup J and
MS in Persian patients.
Mult Scler. 2005 Dec;11(6):728-30.
PMID: 16320736 [PubMed - indexed for MEDLINE]
61.
Jadali
Z, Esfahanian F, Eslami MB, Sanati MH.
Serum Antibodies against Hepatitis C Virus in Iranian Patients with
Graves' Disease
Iran J Allergy Asthma Immunol. 2005 Jun;4(2):91-4.
PMID: 17301428 [PubMed - in process]
60.
Jadali Z, Eslami MB, Sanati MH, Mansouri P, Mahmoudi M, Maghsoudi
N, Esfahanian F.
Identification of peptides specific for antibodies in vitiligo using a
phage library.
Clin Exp Dermatol. 2005 Nov;30(6):694-701.
PMID: 16197391 [PubMed - indexed for MEDLINE]
59.
Jadali Z, M.B. Eslami, M.H. Sanati, P.
Mansouri, M. Mahmoudi, F.
Hepatitis C Virus Antibodies and Vitiligo Disease,
Esfahanian, Iranian J Public Health, 2005, Vol. 34, No 1, pp.23-26.
58.
Moosavi MA, Yazdanparast R,
Sanati MH, Nejad AS.
3-Hydrogenkwadaphnin targets inosine 5'-monophosphate dehydrogenase and
triggers post-G1 arrest apoptosis in human leukemia cell lines.
Int J Biochem Cell Biol. 2005 Nov;37(11):2366-79.
PMID: 16084123 [PubMed - indexed for MEDLINE]
57.
Manatunga V, H. Sanati,
P. Tan and P.A. O’Brian
Maceration of Plant Tissue by Fungi is inhibited by
Recombinant Antipectinase Antibodies, European Journal of Plant
Pathology, (2005) 112: 211-220.
56.
Mosayebi G, S.M. Moazzeni and M.H. Sanati,
The Role of Spleen and Liver Dendritic Cells in
Induction of TH1 and TH2 Response, Journal of Iran University of Medical
Sciences, Vol. 12, No. 47, 2005, 135-143.
55.
Moosavi MA, Yazdanparast R, Sanati MH.
The cytotoxic and anti-proliferative effects of 3-hydrogenkwadaphnin in
K562 and jurkat cells is reduced by guanosine.
J Biochem Mol Biol. 2005 Jul 31;38(4):391-8.
PMID: 16053705 [PubMed - indexed for MEDLINE]
54.
Moosavi MA, Yazdanparast R, Sanati MH,
Nejad AS.
3-Hydrogenkwadaphnin targets inosine
5'-monophosphate dehydrogenase and triggers post-G1 arrest apoptosis in
human leukemia cell lines.
Int J Biochem Cell Biol. 2005 Nov;37(11):2366-79.
PMID: 16084123 [PubMed - indexed for
MEDLINE]
53.
Noori-Daloii M.R, A. Yousefi,
S. Mohammad Ganji, S.H.
Hejazi,
Molecular Identification of the Most Prevalent Mutation of
Glucose-6-phosphate Dehydrogenase Gene in Deficient Patients in Sistan
and Balochestan Province of Iran, Journal of Sceinces, Islamic Republic
of Iran, 16(4):321-325, 2005.
52.
Saboury AA, Atri MS, Sanati MH,
Moosavi-Movahedi AA, Haghbeen K.
Effects of calcium binding on the structure and stability of human
growth hormone.
Int J Biol Macromol. 2005 Sep 28;36(5):305-9.
PMID: 16102809 [PubMed - indexed for MEDLINE]
51.
Saboury A.A, M. Kordbacheh, M.H. Sanati,
F. Mizani, M. Shamsipur, M.B. Yakhchali, A.A. Moosavi Movahedi,
Thermodynamics of Binding Copper(II) Ion by Human Growth Hormone, Asian
Journal of Chemistry, Vol. 17, No. 4, 2005, 2773-2782
50.
Sadeghi A, M.H. Sanati, F. Alasti, M. Hashemzadeh
Chaleshtari,
Accesing Genetic and Environmental Factors of Hearin
Loss in 354 Familis in Qom and Central Provices of Iran, Journal of
Rehabilitation (English abstract), Vol. 6, No. 2, 2005, 7-10.
49.
Sadeghi A, M.H. Sanati,
F. Alasti, M. Hashemzadeh Chleshtari, M. Ataei,
Mutation Analysis of Connexin 26 gene and
del(GJB6-D13S1830) in Patients with Hereditary Deafness from two
Provinces in Iran, Iranian journal of Biotechnology, Vol. 3, No. 4,
255-258, 2005.
48.
Tabandeh F, S.A. Shojaosadati, M. Khodabandeh and
M.H. Sanati,
Optimization of Heat
Induction Strategy in production of Human Growh Hormone During High Cell
Density Culture of Escherichia coli, Vol. 3, No. 1, 24-30, 2005.
47.
Manatunga V, H. Sanati, P. Tan and
P.A. O'Brien,
Macceration of Plant Tissue by Fungi is inhibited by
Recombinant Antipectinase Antibody, European Journal of Plant Pathology,
(2005) 112:211-220
46.
Yazdanparast R, Moosavi MA, Mahdavi M, Sanati MH.
3-Hydrogenkwadaphnin from Dendrostellera lessertii induces
differentiation and apoptosis in HL-60 cells.
Planta Med. 2005 Dec;71(12):1112-7.
PMID: 16395646 [PubMed - indexed for MEDLINE]
45.
Ahangari G, Ostadali MR, Rabani A,
Rashidian J, Sanati MH, Zarindast MR.
Growth hormone antibodies formation in patients treated with recombinant
human growth hormone.
Int J Immunopathol Pharmacol. 2004 Jan-Apr;17(1):33-8.
PMID: 15000864 [PubMed - indexed for MEDLINE]
44.
Ahangari
G., Hassan Akrami, M.H. Sanati, and Ali Rabbani
Antibody production against
E-coli polypeptide (ECP) by Dot blotting and ELIZA methods for ECP assay
in recombinant drug and patients sera. Iranian Journal of Pediatrics.
Vol. 13. 1, 2004.
43.
Biramijamal F.,
M.H. Sanati, G. Iravanloo, K. Shamimi and D. Farhud,
Detection of NAD(P): Quinone
Oxidoreductase 609 C > T Polymorphisem in Blood and Archival
Human Tissues Using a Simple PCR Method, Iranian journal of
Biotechnology Vol. 2.No.3.July 2004, 203-206
42.
Ghasemi F, A. Zomorodipour, S. Shojai, F. Ataei, M. Khodabandeh, M.H.
Sanati
Using L-arabinose for Production of Human Growth
Hormone in Escherichia coli, studying the Processing of gIII::hGH
Precursor, Iranian Journal of Biotechnology, Vol. 2, No. 4, October
2004.
41.
Hadavi V, M.H. Sanati, D. Farhud, M.
Houshmand, M. Hashemzadeh Chaleshtori, S.M. Nabavi, M. Younesian, M.
Seyedian.
Association of Apolipoprotein E Polymorphism with Susceptibility to
Multiple Sclerosis. Iranian Journal of Biotechnology, Vol. 2, No. 1,
January 2004, 49-54.
40.
Houshmand M, Sharifpanah F, Tabasi
A, Sanati MH, Vakilian M, Lavasani SH, Joughehdoust S.
Leber's hereditary optic neuropathy: the spectrum of mitochondrial DNA
mutations in Iranian patients.
Ann N Y Acad Sci. 2004 Apr;1011:345-9.
PMID: 15126312 [PubMed - indexed for MEDLINE]
39.
Houshmand M, M.H. Sanati, M.
Vakilian, M. Akuchekian, F. Babrzadeh, M. Teimori, D. Farhud.
Investigation of the mitochondrial haplogroups M, BM, N, J, K and their
frequencies in five regions in
38.
Houshmand M, Sanati MH,
Rashedi I, Sharifpanah F, Asghari E, Lotfi J.
Lack of association between Leber's hereditary optic neuropathy primary
point mutations and multiple sclerosis in
Eur Neurol. 2004;51(2):68-71.
Epub 2003 Dec 10.
PMID: 14671420 [PubMed - indexed for MEDLINE]
37.
Alemohammad SA, DD Farhud, M Hooshmand, M Sanati, P
Derakhshandeh-Peykar, SJ Imam, M Rahmani
Distribution of Mitochondrial DNA Intergenic COII/tRNALYS
9 bp
Deletion in Iranian Populations
Iranian J Publ Health, Vol.32, No.2, pp.1-5, 2003.
36.
Hormozian F, M. H.sanati, R.Ghiasvand, M.M Banoie.
Moulecular analysis of the (CAG)n repeat causing huntigton’s disease in
34 Iranian families,.Indian Journal of Human Genetic 2004 July-December,
No.10.
35.
Manatunga V, M.H. Sanati, P. Tan and Philip A. O’ Brien.
Maceration of Plant Tissue by Fungi is
inhibited by Recombinant Antipectinase Antibodies. European Journal of
Plant Pathology.
34.
Mosayyebi G., M.H.
Sanati, Mohammad Moazzeni, and Mahnaz Aghayipour
Seperation, Phonotype determination and studying the
performance of dandritic cells in of mice spleen using the flocytometer
method, , Kosar Medical Journal, 9 (1), 11-19, 2004.
33.
Noori-Daloii MR, Najafi L, Mohammad
Ganji S, Hajebrahimi Z, Sanati MH.
Molecular identification of mutations in G6PD gene in patients with
favism in
J Physiol Biochem. 2004 Dec;60(4):273-7.
PMID: 15957246 [PubMed - indexed for MEDLINE]
32.
Sanati MH, Bayat B, Aleyasin A,
Atashi Shirazi H, Isaian A, Farhoudi A, Moin M.
ATM Gene Mutations Detection in Iranian
Ataxia-Telangiectasia Patients.
PMID: 17301393 [PubMed - in process]
31. Sanati M. H., F. Alasti, H. Aleyasin,
H. Mostafavi and P. Carnegie,
Expression and purification of recombinant Outer
Surface Protein D (OspD) of Borrelia Burgdorferi, Archives of Razi J,
58, 2004, 19-27.
30.
Tabandeh F.,
S.A. Shojaosadat, A. Zomorodipour, M. Khodabandeh, M.H. Sanati
and B. Yakhchali
Heat-Induced
production of human growth hormone by high cell density cultivation
of recombinant Escherichia coli.
Biotechnol Lett. 2004 Feb;26(3):245-50.
PMID: 15049371 [PubMed - indexed for MEDLINE].
29.
Tabandeh, F., Yakhchali, B.,
28.
Zomorrodipour A, B. Yakhchali, M. Khodabandeh, A. Deezagi, S.M. Hosseini
Mazinani, S. Valian Borujeni, M. Ahmadzadeh Raji, M. Rahimi, H. Ahmadi
Daneshmand, M.H. Sanati,
The Over-Expression of Biologically Active
Human growth Hormone in a T5-based System in Escherichia Coli, Studying
Temperature Effect, Journal of Sciences (I.R. of Iran), 15(1): 27-32,
2004.
27.
Alasti F and M.H. Sanati,
Making an Experimental Animal Model for Multiple Sclerosis disease,
Medical Journal of I.R. of Iran, 17(3): 245- 249, 2003.
26.
Arbabi M., F. Alasti, M.H. Sanati,
S. Hosseini, A. Deldar, N. Maghsoodi
Cloning and Expression of Human Gamma-interferon cDNA in E.coli, Iranian
Journal of Biotechnology, 1(2): 87-94, 2003.
25.
Dinparast Jadid N, M.H. Sanati, M.
Zare and A. Hassanzehi,
rDNA-ITS2 Identification of Anopheles Pulcherrimus (Diphtera: Culicidae):
Genetic Differences and Phylogenetic Relation with Other Iranian Vector
and Its Implications for Malaria Control, Iranian Biomedical Journal,
7(1):1-6, 2003.
24.
Jadali1 Z, Eslami MB, Sanati MH,
Mansoori P, Mahmoudi M, Maghsoodi N, Arbabi Ghahroudi M.
Identification of Hitherto Undefined B-Cell Epitopes by Antibodies in
the Sera of Vitiligo Patients Using Phage-Display Peptide Library.
Iran J Allergy Asthma Immunol.
2003 Dec;2(4):197-201.
PMID: 17301381 [PubMed - as supplied by publisher]
23.
Khodabandeh M, B.
Yakhchali, M.Rahimi, Z. Moghaddasi Jahromi, A. Zomorrodipour, A.
deezagi, M.H. Sanati,
Purification of Large Quantities of Biologically
Active Recombinant Human Growth Hormone, Iranian Journal of
Biotechnology, 1(4):207-212,2003.
22.
Kiany J, A. Zomorodipour,
M. Ahmadzadeh Raji, and M.H. Sanati,
Construction of Recombinant Plasmids for the
Periplasmic Expression of Human Growth Hormone in Escherichia Coli under T7
and Lac Promoters, Journal of Sciences (I.R. of
21.
Noori-Daloii M.R., Z. Hajebrahimi, L. Najafi, S.
Mohammad Ganji, M. Sadeghizadeh, and M.H. Sanati,
Molecular Identification of the Most Prevalent Mutations of Glucose-6-
phosphate Dehydrogenase (G6PD) Gene in Deficient Patients in Gilan
Province, Journal of Sciences (I.R. of Iran), 14(4): 327-331, 2003.
20.
Distinctive audiometric profile associated with DFNB21 alleles of TECTA.
J Med Genet. 2003 May;40(5):360-3.
No abstract available.
PMID: 12746400 [PubMed - indexed for MEDLINE]
19.
Rasti A., M. Moazeni and M.H. Sanati
Study of Humoral Immunity Borrelia in Sera and CSF of Multiple Sclerosis
patients against Borellia antigens, Iranian Medical Journal of Yakhteh,
Vol. 17, 35-41, 2003.
18.
Manijeh Rahmani, Seyed Mohammad Moazzeni and
M.H. Sanati,
Studying lymphocyte Reaction in Multiple Sclerosis
patients, Shahed University Journal of Daneshwar, 2003.
17. Sanati M.H., C. Stanyon, D. Mehmet,
F. Alasti and P. R. Carnegie,
Improved procedure for Screening Expression Libraries for Novel
Autoantigens, Iranian Journal of Biotechnology, 1(1): 31-35, 2003.
16.
Tafreshi A.P., and M.H. Sanati
An In vivo Assay for Biological Activity of Synthesized Recombinant Human
Growth Hormone, Arch. Razi Ins., 56, 2003, 103-108.
15.
Tabandeh F, S.A.
Shojaosadati, B. Yakhchali, M. Khodabandeh and M.H. Sanati,
Evaluation of Heat Induction Strategy for
Recombinant Human Growth Hormone Expression in Fed-Batch Fermentation,
Iranian Journal of Biotechnology, Vol. 3, No. 1,
2003, 24-30.
14.
Hossein Ale-Yasin, Ali Sarai, Farshid
Alaeddini, Elaheh Ansarian, Jamshid Lotfi, Mohammad Hossein Sanati
Multiple Sclerosis: A study of 318 Cases, Archives of Iranian Medicine, Vol.5, No.1, 24-27, 2002.
13.
Mesbah-Namin SA, Sanati MH,
Mowjoodi A, Mason PJ, Vulliamy TJ, Noori-Daloii MR.
Three major glucose-6-phosphate dehydrogenase-deficient polymorphic
variants identified in Mazandaran state of
Br J Haematol. 2002 Jun;117(3):763-4.
PMID: 12028056 [PubMed - indexed for MEDLINE]
12.
Nouraei M. and M.H. Sanati,
Guideline Planning for Biotechnology Research,
Journal for Research Programing in Higher Education, Vol. 3, 211-221,
2002.
11.
Sanati M.H., P.R. Carnegie
Antibody to Mitochondrial complex-I in some patients with Multiple
Sclerosis., Medical Journal of I. R. of IRAN, 15(4): 203-207, 2002.
10. Sabouri A.A.,
Thermodinamic Studies of Myelin Basic Protein upon Interaction with zinc,
Journal of the Chineese chemical Society, 48, 827-831, 2001.
9. Alasti F. and M.H. Sanati,
The importance of transgenic living creatures in
biotechnology, J of Sharif University, Paper in Farsi with English
Abstract, Vol. 18, 23-29, 2000.
8. Mesbah Namin
Spread of the Glucose-6-Phosphate Dehydrogenase variant
(G6PD-Mediteranian) in one of the coastal Provinces of Caspian Sea in
7.
Sanati M.H. and P.R. Carnegie
Cloning and Sequencing of a Mitochondrial Autoantigen with Immunoglobulin
G from Patients with Multiple Sclerosis. Journal of Sciences (I.R. Of
6.
M.H. Sanati,
Hossein Ale Yassin,
Interoduction of the International Biosafety
Protocol, Journal of the Iranian Biotechnology Commision, Vol. 2,
105-110, 1999.
5.
M.H. Sanati
Recombinant Human Growth Hormone , Journal of the
Iranian Biotechnology Commision, Vol. 2, 58-63, 1999.
4.
Hossein Ale Yassin, M.H. Sanati
Human Genome Project (hopes and fears), Journal of
the Iranian Biotechnology Commision, Vol. 1(2), 1998.
3.
Hossein Ale Yassin, M.H. Sanati
Human Genome Project (concepts and basics), Hossein
Ale Yassin, M.H. 77. Human Genome Project (concepts and
basics), Journal of the Iranian Biotechnology Commision, 1(3), 25-30,
1988.
2.
M.H.
Sanati,
Introduction of the "International Biotechnology and
Genetic
1. M.H.
Sanati, Bagher Yakhchali
Introduction of the
Patent:
1. M.H. Sanati
and P.R. Carnegie,
A novel autoantigen in multiple Sclerosis, Patent, March 1995,
PCT/AU96/00166, Murdoch university,
2.
M.H. Sanati, M.
Jahanshahi and Z. Babaei.
Production of
gelatin nanoparticles for drug delivery to the target tissues, 43062,
2.
M.H. Sanati
Haplotype markers for diagnosis of Ataxia Telangictasia,
29656, May 2004, Organization for submitting the official documents of the
Intelectual Property Right,
Islamic Republic of Iran.
Projects:
a. As Principal investigator:
1-
Preparation of the National Strategy for Biotechnology Development.
In this 3 year project, I had the leadership of more than 200
specialists in 8 research groups. The result of this project was the
finalization of the National Strategic Plan for Biotechnology
development in
2-
Research project titled: Study of the presence of antibodies against
Borrelia proteins in Sera and CSF of Multiple Sclerosis patients and
determinig the immunological activity of these proteins in animal
models.
3-
Cloning auto-antigenes in Multiple Sclerosis.
4-
Production of Recombinant Human Growth Hormone (phase 2 and 3).
5-
Studying the Mutation of Ataxia
Telangictasia in Iranian patients.
6-
Studying the genetic factors of Multiple Sclerosis.
7-
Preparation of Encyclopaedia in Biotechnology and Genetics.
8-
Determinig the normal level of biochemical factors in infants’ sera.
9-
Genetic study of hearing impairments in Iranian patients.
10-
Cloning and Expression of Human Gamma Interferon in Bacteria.
11-
Genetic study of Visual Impairment (Congenital Glaucoma). This is a
collaboration research project granted by WHO-COMSTECH.
b. As Collaborating
Investigator:
1-
The National project for
2-
Studying the mutations of the G6PD gene in patients
with favism in the Northern Provinces of Iran.
3-
Production of Recombinant Gama Interferon. A
Research Project Granted by NIGEB.
4-
Production of Novel Hormone (GnRH) for Induction of
Spawning in Carp, Trout, and Sturgeons, a Research Project Granted by
NIGEB.
Various Executive and Scientific Activities:
1-
Chairman and Editor-in-Chief of the Iranian Journal of Biotechnology
(IJB) since 2003 to 2007.
2-
Member of the Khwarazmi Scientific Award judgment committee,
since 2001 till now.
3-
Member of the evaluation committee of the field of Genetics in the
Iranian Ministry of Health since 2000 to 2003.
4-
Secretary of the National Biotechnology Committee (Iranian Ministry of
Science, Research and Technology) since 2000 to 2005.
5-
Secretary of the National Biosafety Committee (Iranian Ministry of
Science, Research and Technology) from 1999 to 2005.
6-
Secretary of the first International Bioethics Congress held from 26th
to
7-
Secretary of the 1st National Biotechnology Congress,
8-
Member of the Genetic Committee, National welfare Organization,
9-
Chairman of the Iranian Biotechnology Society, 2000
– 2006.
10-
Member of the
Editorial Board of the Scientific Journal named: Archive of Razi, since
2000 until now.
11-
Member of the Editorial Board, Iranian Journal of
Immunology, Asthma and Allergy, year 2003 until now.
12-
Member of the
“Federation of European Biotechnology (FEB)”, since year 2002 until now.
13-
Member of the Iranian Genetic Society, year 2000 until now.
14-
Member of the "Iranian Ethics Society for Science and Technology" as
well as the member of Founder and management Committee, since year 2005.
15-
Governor for
16-
Member of the Biotechnologi Information of Asia (BINASIA), as a national
representative for
17-
Member of the Iranian Delegation Team at the Negotiation Meetinge for
International Biosafety Protocol, UNEP/CBD:
-
14
-19 and 22-23 Feb. 1999, Sixth Ordinary Meeting of the Ope-Ended Ad Hoc
working Group on Biosafety Protocol, and the Extraordinary Meeting of
the Conference of the Parties to the Convesion on Biologicad Diversity,
Cartagena, Colombia.
-
-
11-15 Dec. 2000, first
Meeting of the Intergovenmental Committee for the Cartagena Protocol on
biosafety,
-
22-26 Apr. 2002, Third Meeting of the Intergovernmental Committee for
the Cartagena Protocol on biosafety,
-
23-27 Feb. 2004, First Meeting of the Conference of the Parties Serving
as the Meeting of the Parties for
Awards:
1.
Selected manager according the criteria identified by Ministry of Science,
Research and Technology in 2001 and receiving the award from Iranian
President Seyed Mohammad Khatami.
2.
Award for top research project in biotechnology "Production of Recombinant
Human Growth Hormone", 2000,
3.
Award for best oral paper presentation in the general biological science
conference in 1994 in
4.
Award for top paper presented in the 47th meeting of the heads of
universities and research centers of
5.
Award from Iranian President Seyed Mohammad Khatami for Organizing the first
International Bioethics Congress in
6.
Award received from Iranian Minister of Science, Research and Technology,
for Carrying out the "National Strategic Plan for Development of
Biotechnology across the Country" Project and Success in Preparation of
the Documents which was ratified by the Government.
Thesis: As Supervisor
1. Study of association between MRP1 gene and multidrug resistance in
leukemic patients. Theisi by Masoud Golalipour for Phd degree in
molecular genetic,
2. Linkage analysis of some autosomal recessive deafness loci and detection
of new mutation in some population of
3. Investigation of relationship between NDUFS1 gene with Multiple
Sclerosis. Theisi for MsC degree in molecular genetic by Zohre Baratieh,
4. Isolation and Characterization of Reacting
Peptides with antibody Isolated from Vitiligo Patients Sera, Thesis by
Z. Jadali for PhD Degree in Medical immunology, Tehran University of
Medical Sciences,
5. Linkage analysis of DNFB3 and DNFB21 Loci in Non
Syndromic Autosomal Recessive Hearing Loss in Iranian Population, Thesis
By M.H. Behroozi-fard for MS.c Degree in Cell and molecular Biology,
Khatam University, Tehran, Iran, 2005.
6. Investigation of Four SNP Markers as well as a
YAP Marker of Y Chromosome in Three Iranian Ethnic group (
7. Screening of 12-mer Random Peptide Phage Display
Library on Leprosy Patient Sera,
8. Mutation and Chromosomal Haplotype Analysis in
ATM Gene in Iranian Ataxia Telagictasia Patients, Thesis By S.
Lotfipanah for MS.c Degree in Cell and molecular Biology, Khatam
University, Tehran, Iran, 2004.
9. Study of C77G Mutation in Protein Tyrosin
Phosphatase Gene CD45 in Hepatitis Autoimmune Patients, Thesis By F.
Sadat Esteghmat Hanzaei for MS.c Degree in Cell and Molecular Biology,
Khatam University, Tehran, Iran, 2004.
10. Mutation Analysis in Iranian Ataxia Telangictasia Patients, Thesis By H.
Atashi Shirazi for MS.c Degree in Cell and Molecular Biology, Khatam
University, Tehran, Iran, 2002.
11. Analysis of Tri-Nucleotide Repeats (CAG) in Iranian Families Suffering
from Huntington Disease, Thesis By F. Hormozian for MS.c Degree in Human
Genetics, Azad University, Tehran, Iran, 2000.
12.
Study of the Relationship between Mitochondrial
Haplogroup M and Multiple Sclerosis diseases, Thesis by M. Timouri for
MS.c Degree in Cell and Molecular Biology, Research and Science Unit,
13. Detection of Polymorphism In the Apo-E Region and the Association with
Progression of Multiple Sclerosis,
Thesis By V. Hadavi for MS.c Degree in Human
Genetic, Faculty of Health, Tehran Medical Science University, Tehran,
Iran, 2003.
14.
Investigation of mutation in Exon 3 of Gene CYP1B1 in 60 Iranian Family
Suffering from Glaucoma. Thesis By F. Chitsazan for
MS.c Degree in Cell and Molecular Biology, Faculty of Science, Tehran
University, Tehran, Iran, 2005.
15.
Proteomics Profiling of the Central Nervous
System in Murine Exprimental Autoimmune Encephalomylities befor
and after treatment with Neural
precursor Cells Drived from Mouse Emberionic Stem Cell, Thesis by
S.A. Shahzadeh Fazeli for PhD Degree in Molecular Genetic, National
Institute for Genetic Engineering and Biotechnology, Teharn, Iran, 2010.
16. The
role of BAX, BAK and BIK gene mutations in ataxia telangictasia, and AT
with lymphoma or leukemia, and in the ATM carrier and reaction of these
genes in cancers of lymphoma and leukemia, Thesis by Anna Isaian for PhD
Degree in Molecular Genetic, National Institute for Genetic Engineering
and Biotechnology, Teharn, Iran, 2010.
17.
Investigation of the molecular techniques for the diagnosis of
thalasemia and identifying the method of choice, Thesis by Fatemeh
Kashani Motlagh for M.Sc
Degree in Biology/Biochemistry, Payam Noor University, Teharn, Iran,
2010.
18.
Investigation of the role of maternal KIR and paternal HLA-C genotype in
recurrent miscarriage, Thesis by
Mona Khosravi, Azarbaijan University of Tarbiat Moalem, for M.Sc
Degree in Cell and Molecular Biology, Azarbaijan, Iran, 2010.
19.
Study of relationship between endothelial nitric oxide synthase
polymorphism & recurrent miscarriage, Thesis by Fatemeh Abbasi,
Azrbaijan University of Tarbiat Moalem, for M.Sc
Degree in Cell and Molecular Biology,
20.
Study of association between multiple sclerosis and the
polymorphisem in ILII alpha receptor gene, Thesis by Mostafa Ali for
M.Sc Degree in Cell and
Molecular Biology, Azad University, Tehran, Iran, 2009.
21.
Study of association between multiple sclerosis and the polymorphisem in
mitochondrial polymerase gama gene, Thesis by Hossein Soltanzadeh for
M.Sc Degree in Cell and
Molecular Biology, Azad University, Tehran, Iran, 2008.
22.
Study of the expression patern of splice variants of N-type
voltage-dependent calcium channel alpha 1 subunit in rat hyppocampas and
lumber spinal cord, Thesis by Sareh Asadi for M.Sc
Degree in Cell and Molecular Biology,
Tarbiat Modarres University,
Tehran, Iran, 2008.
23.
Study of hot spot mutations in Iranian patients suffered from cystic
fibrosis, Thesis by Mahnaz Amiri for M.Sc Degree in Cell and Molecular
Biology,
Thesis: as Co- Supervisor
1. Point Mutations Analysis in LHON Patients with
Nerve degeneration. Thesis By F Sharifpanah for MS.c Degree in Human
Genetic, Research and Science Unit, Azad university, Tehran, Iran, 2001.
2. Isolation and identification of Sulfide/Sulfoxide
Monooxygenase Gene from Rhodococcus FMF,
Thesis by M. Kazemi for MS.c Degree in Genetic, Research and
Science Unit,
3. Biochemical Diagnosis and Determination of Q188R,
K285N, L195P, X380R and Q169K Mutations in Galactosemic Patients, Thesis
By N. Naghibzadeh for MS.c Degree in Human Genetic, Research and Science
Unit, Azad university, Tehran, Iran, 2003.
4. Study of Interaction between Myelin Basic Protein
(MBP) and Zn and Cu Ions, Thesis By S Saeidi for MS.c Degree in
Biochemistry, Institute for Biophysics and Biochemistry, Tehran
University, Tehran, Iran, 2000.
5. Study of Y Chromosome Microdeletions in Iranian
Infertile Men, Thesis By S Ghavam-Poor for MS.c Degree in Cell and
molecular Biology, Faculty of sciences, Tehran University, Tehran, Iran,
2003.
6. An Investigation of Chromosomal Abnormalities and
physiological Deficiencies in Mentally Retard Boys, Thesis By B. Bayat
for MS.c Degree in Biology, Faculty of sciences, Shahid Baheshti
University, Tehran, Iran, 1998.
7. Study of G6PD Gene Mutations in Patients from
Golestan Province of Iran, Thesis By L. Najafi for MS.c Degree in
Genetic, Faculty of Basic Sciences, Tarbiat Modarres University, Tehran,
Iran, 2003.
8. Study of Mitochondrial Haplogroup J, M, BM and N
in Iranian Families and its relation to LHON Disease, Thesis by M.
Vakilian for MS.c Degree in Human Genetic, Faculty of Health, Tehran
Medical Science University, Tehran, Iran, 2003.
9. Identification of Molecular Mutations of G6PD
Gene in Deficient Patients in State of Mazandaran, Thesis by A.
Mesbah-Namin for PhD Degree in Clinical Biochemistry, Faculty of Basic
Medical sciences, Tehran, Iran, 2001.
9. Study of G6PD Gene Mutations in Patients from
Gilan Province of Iran, Thesis By Z. Haj-Ebrahimi for MS.c Degree in
Genetic, Faculty of Basic Sciences, Tarbiat Modarres University, Tehran,
Iran, 2003.
10. Analysis of Four Locus (DaT1, D1S80, D17S5 and
ApoB) Markers In three Ethnic Group Azeri Fars and Kord. Thesis by N.
Jahangir Soltani for MS.c Degree in
Cell and Molecular Biology, Research and Science Unit, Azad
University, Tehran, Iran, 2005.
11. Study of Four Microstelite Markers (DYS19,
DYS388, DYS390 and DYS391) in three
12.
Study of Four Markers (D19S20, ApoB, D17S5 and D1S80) in two
13.
Study of Four Y-STR Markers (DYS392, DYS393, DYS391 and DYS389II) In
three Ethnic Group in Iran, Azari, Fars and Kord,
Thesis By M. Marvi for MS.c Degree in Cell and Molecular Biology,
Research and Science Unit, Azad University, Tehran, Iran, 2005.
14.
Study of Four Polymorphic Allele in Y-Chromosome In three Ethnic Group
in
15.
Study of Four Mutations W1282X, G551D, G542X, DeltaF508 and N1303K in
Iranian Patients affected to Cystic Fibrosis, Thesis by M. JalaliRad for
MS.c Degree in Cell and Molecular Biology, Faculty of Science,
16. Production and optimization of gelatin
nanoparticle for drug delivery, thesis By Zahra Babaei for MS.c Degree
in chemical engineering, Noshirvani university, Babol,
17. Linkage
analysis of three loci in non syndromic autosomal recessive deafness
patients from Qom and Markazi provinces of Iran, thesis By M.
Sadat Taghavi for MS.c Degree in Cell and Molecular Biology, Azad
university, Tehran, Iran, 2008.
18. Cloning, expression and evaluation of plasmodium
vivax and P. Falciparum region of Merozoite Surface Protein 1 in animal
model, thesis By Akram Abouie Mehrizi for PhD Degree in Molecular
Genetics, National Institute for Genetic Engineering and Biotechnology,
Tehran, Iran, 2010.
19. Determination of frequency mutations in the
first half of exon 2 of CYP1B1 gene among 60 iranian patients afflicted
with Primary Congenital Glaucoma, thesis By Btsabeh Khoramian Tusi for
M.Sc Degree in Cell and Molecular Biology,
Publications
a.
Published books written in Farsi language Except for No. 7 which is in
both Farsi and English and No. 8 which is in English.
1Genetic and You, General Information in Genetic,
M.H. Sanati, Ali Reza Mowjoodi and Sakineh Abbasi, 1998.
2.
Genetic Engineering, Technology for manipulation of Living Organisems,
M.H. Sanati, M. Khazab, C. Azeempoor, In Farsi, 2000.
3.
International Biosafety Protocol, Translation of
4.
Biotecnology, a solution to solve mankind problems during the 21th
century, M.H. Snati and N. Ismailzadeh, 2001.
5.
Biosafety Guidlines, In Farsi, M.H. Sanati and Colleagues,
2001.
6.
Bioethics and Biotechnology, M.H. Sanati and Colleagues,
2002.
7.
The
Tehran Statement and the Final Report of the International Congress of
Bioethics in
8.
Understanding Bioethics, M.H. Sanati and Colleagues, 2005.
9.
Editor in Cief and co-authors for the "Encyclopedia of Biotechnology and
Genetics, 2009.
b. Selected
Abstract presented in different scientific congress:
1.
Haplotype Analysis of Related ATM Markers Facilitate Prenatal Diagnosis
in Iranian Ataxia Telangictasia Patients.
Bayat B, Sanati M, Alyasin A, Moein M,
Farhoodi, Eesaian A, Human Genome Diversity in Islamic Countries
Seminar, 7-8 May 2002
2. Investigation of mtDNA
Haplogroups and Disease (Report from
Houshmand M., Sharifpanah
F, Alemohamad A, Rahmani M, Joughehdost S,Babrzadeh F., Vakilian M,
Sanati MH, Human Genome Diversity in Islamic Countries, 7-8 May, 2002,
Tehran, IRAN
3.
Some Molecular Genetic Aspects of Hearing Loss in Iranian Population.
F.
Alasti, M. H. Sanati, Ed.
Wicox, Salehi Tabar, A. Mojoodi and T.B.
Friedman, Human Genome Diversity In Islamic Countries, Seminar 7-8 May
2002, Tehran,Iran.
4.
Absence of Mitochondrial DNA
Intergenic COII/ t RNA Lys 9 bp Deletion within a sample of Iranian
Populatons, Alemohamad S., Rahmani M, Houshmand M., Farhoud D, S.,
Sanati M.H, Human Genome Diversity In Islamic Countries Seminar, 7-8 May
2002, Tehran, Iran.
5.
Introduction of Patients Cell Bank in National Research Center for
Genetic Engineering and Biotechnology, M. M. Banoei, F. Hormozian, F.
Mirzajaani, M. Houshmand, M.H. Sanati, Human Genome Diversity In Islamic
Countries, 7-8 May 2002, Tehran, Iran.
6..Relation
Between LHON primary Point Mutations and MS, Sanati M.H., Sharifpanah
F., Houshmand M., Rashedi F, Asghari R.E., Lotfi J, Human Genome
Diversity In Islamic Countries Seminar, 7-8 May 2002, Tehran, Iran.
7.
Molecular Analysis of Iranian Patients with Huntington's Disease,
F. Hormozian , M. Houshmand, R. Ghiasvand, M.H Sanati, Human Genome
Diversity in Islamic Countries, 7-8 May 2002, Tehran, Iran.
8.
Genetic Counseling Report (one Year Experiences( , Joughedoust S.,
Shafeghati Y., Molavi M., Sobouti S., Babamohamadi G.H.R.
,Zolfaghari N., Houshmand M. and Sanati M.H., Human Genome Diversity In
Islamic Countries, 7-8 May 2002,
9.
Detection of Mitochondrial Mutation in Iranian Deaf Families., Salehi Tabar R., Sanati M.H., Mowjoodi A., Elahi E. and Houshmand M.,
Human Genome Diversity In Islamic Countries, 7-8 May 2002, Tehran, Iran.
10.
Distribution of 9bp Deletion between the Lys tRNA and COII region of
mtDNA in Iranian populations.,
Allemohammad SA, Rahmani M., Houshmand S.M., Sanati M.H., Farhud
D.,Euromit 5,
Venice, Italy, 19-23 sep. 2001.,
Mitochondrion (The official Journal of the Mitochondrial Research
Society), Vol.1, Suppl.1 sep. 2001, ISN 1567-7249
11.
Detection of Mitochondrial Mutation in Iranian Deaf Family., Salehi Tabar R., Sanati
M.H., Mowjoodi A, Sokhansanj A., Elahi E., HoushmandM., Euromit 5,
Venice , Italy, 19-23 Sep. 2001.,Mitochondrion (the official Journal of the Mitochondrial Research
Society), Vol. 1, Suppl. 1, Sep.2001, ISSN 1567-7249.
12.
Relationship between LHON primary point Mutations and MS ., Sanati M.H.,
Sharifpanah F., Houshmand M. Euromit 5, Venice, Italy, 19-23 sep.2001.
Mitochondrion (The official Journal of The Mitochondrial Research
Society), vol.1,SUPPL.1, Sep. 2001, ISSN 1567-7249.
13.
Investigations
of Proliferation Response of Multiple Sclerosis patients' Lymphocytes
against Borrelia Antigens.,
Rahmani M., Moazzeni S.M., Sanati M.H, Euromit 5, Venice, Italy, 19-23
sep.2001. Mitochondrion (the official Journal of the Mitochondrial
Research Society),Vol. 1, SUPPL. 1,
Sep. 2001, ISSN 1567-7249.
14.
Three Major G6PD-Deficient Polymorphic Variants Identified in the
Mazandaran State of Iran., S.A. Mesbah Namin, M.H.
Sanati, A. Mowjoodi, T.J. Voliamy and M.R.Noori-Daloii, 9th APCCB, 28th
Annual Conferece of ACBI, 9-14 March 2002, NewDelhi, India
15.
Haplotype Analysis of related ATM Markers Facilite prenatal Diagnosis in
Iranian Ataxia Telangiectasia Patients., B. Bayat, M.H. Sanati, A. Aleyasin, A. Farhoudi, M. Moin, A. Isaian.,
EuropeanHuman Genetics Conferece , 25-28
May 2002,
16- Introducing of Iranian Patients Cell Bank in the National
Research center
for Genetic Engineering and Biotechnology (NRCGEB(,
M.M. Banoei,
F.Hourmozian, M. Houshmand, M.H. Sanati, European
Human Genetics
Conferece, 25-28 May 2002
Genetics, Vol.10, Suppl.1, May 2002,
17. Investigation of LHON Primary point Mutations in Iranian MS Patients.
H.
Houshmand, E.
Sharifpanah, M. Sanati, A. Tabasi, Y. shafeghati.
European Journal of Human Genetics, Vol. 10, Suppl. 1, May 2002.
25-29 May 2002 ,
18.
Molecular
Analysis of Iranian Patients with Huntington's Disease.
F. Hormozian, M. Houshmand, R. Ghiasvand, M. Sanati, 10th
InternationalCongress of Human Genetics,
European Journal of Human Genetics vol. 9, Suppl. 1, May 2001.
19.
First Report on Molecular
Identification of Anopheles Pulcherrimus by using rDNA -
ITS2 Region , Navid Dinparast jadid, S. Zeinali, M.H. Sanati, M. Zare, A.
Hassan zehi
20.
Identification of p53 genotype among Iranian Ataxiatelangiectasia (A-T)
Patients, Behnaz Bayat, Firouzeh Biramijamal, Mohammad Hossein Sanati,
Mohammad mehdi Banoei
21.
Studying the Production of Human Growth Hormone
under
T7/LacRegulatory System in Escherichia Coli., Alireza Zomorodipour , Abdolkhalegh Deezaji, & Mohammad Hossein Sanati
,
Medical Biotechnology Congress, 20-25 Oct. 2002,
24- Progress in Multiple Sclerosis Research, 16-19 Sep 1995
25. Combined Biological Science Meeting,
26.
International Symposia on Myelin and Myelin Forming Cells, 1995,
27. Progress in Multiple Sclerosis Research, 1994,
28. Second Asian Pacific Society for Neurochemistry (APSN) Meeting,
29. Combined Biological Science Meeting,
30. Gordon Conference on Myelin, 13-18 Mar 1994,
31. "Determination of normal level of biochemical factors in infants sera
in south of
32.
"Producation of antibody againstthe organophosphorous compounds", M. H.
Sanati, Z. M. Hassan and M.Taghikhani, 9th Iranian Congress of
Physiology and Pharmacology,
33. "Hapten-Protein Conjugation", Sanati M.H. and Hassan Z. M., First
Iranian congress of immunology and allergy in Tehran University, Tehran,
Iran, 1988.
34. Detection the most Prevalent mutations in G6PD gene in Gilan and
Golestan Provinees of Iran, Noori Dalooii M.R., Najafi L., Hajebrahimi
Z., Mohammad Ganji and Sanati M.H.,2nd Iranian congress of Genetic Disorders & Disabilities, December
2002,Tehran,
Iran
35.
Investigation of mtDNA haplogroups and disease (Report from
Houshmand M., sharifpanah F., Alemohamad A., Rahmani M., Joughedost
S.,Babrzadeh F., Vakilian M., Sanati M.H.,2nd
Iranian Congress of Genetic Disorders &C Disabilities, December
2002,Tehran, Iran.
36.
Detection of mutation In
Iranian deaf families.,Salehi
tabar R., Sanati M.H., Elahi E., Houshmand M.,
2nd Iranian Congress of Genetic Disorders &C Disabi Lities, December
2002,Tehran, Iran
37. Biochemical and
Molecular Diagnosis of Galactosemia,
Naghibzadeh Tabatabaee N., Houshmand M., Zare sh., Talachian Z., Majd
I.,Sanati M.H., Mirzajani F.,
2nd
Iranian congress of Genetic Disorders and Disabilives December
2002,Tehran, Iran
38- Cloning
and expression of human gamma- interferon cDNA in Ecoli.,
Fatemeh Alasti and M.H. Sanati
(2003) third national congress of biotechnology, Mashhad, Iran.
39- The
molecular biology aspects of recessive hearing loss in Iranian
population, Fatemeh Alasti and M.H. Sanati, (2003) 8th
Iranian Genetics Congress,
40-
Polymorphisms of Apolipoprotein E: Association with Susceptibility and
Severity of Multiple Sclerosis., V.Hadavi, D.D.Farhud, M.H. sanati,
M.Hushmand,S.M.Nabavi, M.Seyedian, M.Younesian (2004) The American
Society of Human Genetics 54th Annual Meeting
41-P53
Polymorphism in Iranian Population with Four Different Ethnicity and
incidence Pattern of Esophageal Cancer. S.Tanhaei, F.Biramijamal,
M. H. Sanati, M. Sheidai. The 3rd Regional
Conference of Asian Pacific Organization for Cancer Prevention (APOCP)
GI Cancer Control.April 2005.Zibakenar,
42-Is Genetic Polymorphism at GST-P1 Locus Associate With Type of P53
Gene Mutation in Esophageal Squamous Cell Carcinoma from
F.Biramijamal,
M.H.Sanati, G.Iravanloo, N. Saligheh Araghi,
S.Tanhaei, R.Sharifi,
A.Allameh, The 3rd Regional Conference of Asian Pacific
Organization for Cancer Prevention (APOCP) GI Cancer Control.April
2005.Zibakenar,
43-Investigation of P53 Polymorphisms among Iranian Esophageal Squamous
Cell Carcinoma from to find its role in Developing cancer.
N. Saligheh Araghi, F.Biramijamal, M.H.Sanati, G.Iravanloo, S.Tanhaei, B.
Bayat, M.M Banoei. The 3rd
Regional Conference of Asian Pacific Organization for Cancer Prevention
(APOCP) GI Cancer Control.April 2005.Zibakenar,
44-Structure Study of human growth hormone: A thermodynamic and
spectroscopic Approch”,
M.S. Atri, M. Rezaei- tavirani, M.
H. Sanati, A.A. Saboury and A. A. Moosavi- Movahed, 49th
Annual Meeting of Biophysical Socity, Long Beach, California, USA ( 12-
16 Feb.2005).
45- Thermodynamics of binding some metal ions on
human growth hormone
A.A. Saboury, M.S. Atri, M. Kordbacheh, H. Ghourchaei and M.H. Sanati, 30th
FEBS Conference & 9th IUBMB Conference, Budapest, Hungary(2-7
July 2005)
46- “Spectroscopy, calorimetry and potentiometry study on the interaction
of human growth hormone with copper ion”, M.Kordbacheh, S. Safarian,
F.Mizani, M.H.Sanati, M. Shamsipur,
B. Yakhchali and A.A.
Moosavi- Movahedi, Sixth Iranian Biophysical Chemistry Conferencer,
Damghan University of Basic Science, Damghan ( sept. 7-9, 2004).
47- Is P53 gene polymorphism associated with multiple sclerosis in
M. Sanati, F. Biramijamal, B. Bayat, M. Banoei. ESHG,
48. Genetic polymorphism analysis of p53 in Iranian population with three
different ethnicity and incidence pattern of Esophageal cancer. S.
Tanhaei. F. Biramijamal. M. Sanati. ESHG,
49. Strategic Planning for Prevention and Management of Genetic Disorders
in Developing Countries, Mohemmed Hossein Sanati, Oral presentation as
an invited speaker, The Thirteenth International Biotechnology Symposium
and Exhibition, IBS-2008, 12-17 Oct. 2008, Dalian, China.
50. Controlled Fabrication of Gelatin Nanoparticla as Drug Carriers, M.
Jahanshahi, M.H. Sanati, Z. Minuchehr, S. Hajizadeh and Babaei,
Nanotechnology and Its Applications, First Sharjah International
Conference on Nanotechnology and Its Application,
51. Genetic of Multiple Sclerosis, Mohammad Hossein Sanati, 7th
International Congress of Multiple Sclerosis, 4-5 Nov., 2010, Imam
Khomaini Hospital, Tehran, Iran.
52. Genetics of Hearing Impairement, Mohammah Hossein Sanati, 4th
Annual Iranian Neurogenetic Congress Advances in Neurogenetics, 24-26
Nov. 2010, Tehran, Iran.
53.
Recombinant human coagulation factor IX transgenic goats produced by
transfer of nuclei from transfected fetal fibroblast, Goorabi H., Sanati
M.H. et all, 11th Iranian Genetic Congress, 22-24 May 2010,
Tehran, Iran.