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Mohammad Hossein Sanati
Mohammad Hossein Sanati
Professor of medical genetic, National Institute for Genetic Engineering and Biotechnology: Tehran, Tehran, Iran
在 nigeb.ac.ir 的电子邮件经过验证
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引用次数
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Mitochondrial DNA signals of late glacial recolonization of Europe from near eastern refugia
M Pala, A Olivieri, A Achilli, M Accetturo, E Metspalu, M Reidla, E Tamm, ...
The American journal of human genetics 90 (5), 915-924, 2012
2512012
Ancient migratory events in the Middle East: new clues from the Y-chromosome variation of modern Iranians
V Grugni, V Battaglia, B Hooshiar Kashani, S Parolo, N Al-Zahery, ...
PloS one 7 (7), e41252, 2012
1402012
Distinguishing the co-ancestries of haplogroup G Y-chromosomes in the populations of Europe and the Caucasus
S Rootsi, NM Myres, AA Lin, M Järve, RJ King, I Kutuev, VM Cabrera, ...
European journal of human genetics 20 (12), 1275-1282, 2012
1362012
Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations
A Amiri-Yekta, C Coutton, ZE Kherraf, T Karaouzène, P Le Tanno, ...
Human Reproduction, 1-9, 2016
1282016
A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family
F Alasti, A Sadeghi, MH Sanati, M Farhadi, E Stollar, T Somers, ...
The American Journal of Human Genetics 82 (4), 982-991, 2008
1282008
MiRNA-375 promotes beta pancreatic differentiation in human induced pluripotent stem (hiPS) cells
R Lahmy, M Soleimani, MH Sanati, M Behmanesh, F Kouhkan, N Mobarra
Molecular biology reports 41, 2055-2066, 2014
1082014
CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes
F Chitsazian, BK Tusi, E Elahi, HA Saroei, MH Sanati, S Yazdani, ...
The Journal of Molecular Diagnostics 9 (3), 382-393, 2007
922007
Granisetron adjunct to fluvoxamine for moderate to severe obsessive-compulsive disorder: a randomized, double-blind, placebo-controlled trial
N Askari, M Moin, M Sanati, M Tajdini, SMR Hosseini, A Modabbernia, ...
CNS drugs 26, 883-892, 2012
792012
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11
N Hilgert, F Alasti, N Dieltjens, B Pawlik, B Wollnik, O Uyguner, ...
Clinical genetics 74 (3), 223-232, 2008
752008
Contributions of MYOC and CYP1B1 mutations to JOAG
B Bayat, S Yazdani, A Alavi, M Chiani, F Chitsazian, BK Tusi, F Suri, ...
Molecular vision 14, 508, 2008
752008
Heat-Induced Production of Human Growth Hormone by High Cell Density Cultivation of Recombinant Escherichia Coli
F Tabandeh, SA Shojaosadati, A Zomorodipour, M Khodabandeh, ...
Biotechnology letters 26, 245-250, 2004
722004
Distinctive audiometric profile associated with DFNB21 alleles of TECTA
S Naz, F Alasti, A Mowjoodi, S Riazuddin, MH Sanati, TB Friedman, ...
Journal of medical genetics 40 (5), 360-363, 2003
712003
Expression and prognostic significance of bcl-2 and bax in the progression and clinical outcome of transitional bladder cell carcinoma
BG Eimani, MH Sanati, M Houshmand, M Ataei, F Akbarian, ...
Cell Journal (Yakhteh) 15 (4), 356, 2014
672014
Three major glucose‐6‐phosphate dehydrogenase‐deficient polymorphic variants identified in Mazandaran state of Iran
SA Mesbah‐Namin, MH Sanati, A Mowjoodi, PJ Mason, TJ Vulliamy, ...
British journal of haematology 117 (3), 763-764, 2002
662002
Optimization of parameters for the fabrication of gelatin nanoparticles by the Taguchi robust design method
M Jahanshahi, MH Sanati, Z Babaei
Journal of Applied Statistics 35 (12), 1345-1353, 2008
632008
Gelatin nanoparticle fabrication and optimization of the particle size
M Jahanshahi, MH Sanati, S Hajizadeh, Z Babaei
physica status solidi (a) 205 (12), 2898-2902, 2008
602008
Effect of flavonoids rich extract of Capparis spinosa on inflammatory involved genes in amyloid-beta peptide injected rat model of Alzheimer's disease
N Mohebali, SA Shahzadeh Fazeli, H Ghafoori, Z Farahmand, ...
Nutritional neuroscience 21 (2), 143-150, 2018
572018
A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families
F Alasti, MH Sanati, AH Behrouzifard, A Sadeghi, APM De Brouwer, ...
International journal of pediatric otorhinolaryngology 72 (2), 249-255, 2008
562008
Effects of calcium binding on the structure and stability of human growth hormone
AA Saboury, MS Atri, MH Sanati, AA Moosavi-Movahedi, K Haghbeen
International journal of biological macromolecules 36 (5), 305-309, 2005
562005
The analysis of correlation between IL-1B gene expression and genotyping in multiple sclerosis patients
M Heidary, N Rakhshi, MP Kakhki, M Behmanesh, MH Sanati, ...
Journal of the neurological sciences 343 (1-2), 41-45, 2014
522014
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