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Mortaza Bonyadi, Mortaza Jabbarpour Bonyadi, Morteza Bonyadi
Mortaza Bonyadi, Mortaza Jabbarpour Bonyadi, Morteza Bonyadi
Verified email at tabrizu.ac.ir
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Year
Mesenchymal progenitor self-renewal deficiency leads to age-dependent osteoporosis in Sca-1/Ly-6A null mice
M Bonyadi, SD Waldman, D Liu, JE Aubin, MD Grynpas, WL Stanford
Proceedings of the National Academy of Sciences 100 (10), 5840-5845, 2003
3012003
Mapping of a major genetic modifier of embryonic lethality in TGFβ1 knockout mice
M Bonyadi, SAB Rusholme, FM Cousins, HC Su, CA Biron, M Farrall, ...
Nature genetics 15 (2), 207-211, 1997
2201997
Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss
O Diaz-Horta, D Duman, J Foster, A Sırmacı, M Gonzalez, N Mahdieh, ...
PloS one 7 (11), e50628, 2012
1702012
Colorectal cancer in Iran: molecular epidemiology and screening strategies
R Dolatkhah, MH Somi, MJ Bonyadi, I Asvadi Kermani, F Farassati, ...
Journal of cancer epidemiology 2015, 2015
1632015
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort
G Bademci, J Foster, N Mahdieh, M Bonyadi, D Duman, FB Cengiz, ...
Genetics in Medicine 18 (4), 364-371, 2016
1502016
Regulation of Chk2 phosphorylation by interaction with protein phosphatase 2A via its B'regulatory subunit
C Dozier, M Bonyadi, L Baricault, L Tonasso, JM Darbon
Biology of the Cell 96 (7), 509-517, 2004
772004
Mutation Analysis of Familial GJB2-Related Deafness in Iranian Azeri Turkish Patients
M Bonyadi, M Esmaeili, M Abhari, A Lotfi
Genetic testing and molecular biomarkers 13 (5), 689-692, 2009
682009
TNF-α gene polymorphisms in Iranian Azeri Turkish patients with Behcet’s Disease
M Bonyadi, Z Jahanafrooz, M Esmaeili, S Kolahi, A Khabazi, AA Ebrahimi, ...
Rheumatology international 30, 285-289, 2009
572009
Helicobacter pylori vacA d1 genotype predicts risk of gastric adenocarcinoma and peptic ulcers in northwestern Iran
Z Basiri, R Safaralizadeh, MJ Bonyadi, MH Somi, M Mahdavi, ...
Asian Pacific Journal of Cancer Prevention 15 (4), 1575-1579, 2014
552014
Effects of bovine prolactin gene polymorphism within exon 4 on milk related traits and genetic trends in Iranian Holstein bulls
Y Mehmannavaz, C Amirinia, M Bonyadi, RV Torshizi
African Journal of Biotechnology 8 (19), 2009
522009
Common MEFV mutation analysis in Iranian Azeri Turkish patients with familial Mediterranean fever
M Esmaeili, M Bonyadi, M Rafeey, K Sakha, MH Somi
Seminars in arthritis and rheumatism 37 (5), 334-338, 2008
502008
MEFV mutations in Iranian Azeri Turkish patients with familial Mediterranean fever
M Bonyadi, M Esmaeili, H Jalali, MH Somi, A Ghaffari, M Rafeey, K Sakha, ...
Clinical genetics 76 (5), 477-480, 2009
462009
HPV typing in women with cervical precancerous and cancerous lesions in northwestern Iran
M Esmaeili, M Bonyadi, A Dastranj, M Alizadeh, MS Melli, MJ Shobeiri
Gynecologic and obstetric investigation 66 (1), 68-72, 2008
462008
Mutations of the phenylalanine hydroxylase gene in Iranian Azeri Turkish patients with phenylketonuria
M Bonyadi, O Omrani, SM Moghanjoghi, S Shiva
Genetic testing and molecular biomarkers 14 (2), 233-235, 2010
452010
Variations in multiple syndromic deafness genes mimic non-syndromic hearing loss
G Bademci, FB Cengiz, J Foster Ii, D Duman, L Sennaroglu, O Diaz-Horta, ...
Scientific reports 6 (1), 31622, 2016
442016
Common MEFV mutations in Iranian Azeri Turkish patients with Behçet's disease
M Esmaeili, M Bonyadi, A Khabbazi, AA Ebrahimi, SK Sharif, M Hajialilo, ...
Scandinavian journal of rheumatology 40 (5), 383-386, 2011
422011
Spectrum of CFTR gene mutations in Iranian Azeri Turkish patients with cystic fibrosis
M Bonyadi, O Omrani, M Rafeey, N Bilan
Genetic testing and molecular biomarkers 15 (1-2), 89-92, 2011
372011
Association of IGF-1 gene polymorphism with milk production traits and paternal genetic trends in Iranian Holstein bulls
Y Mehmannavaz, C Amirinia, M Bonyadi, RV Torshizi
African Journal of Microbiology Research 4 (1), 110-114, 2010
372010
Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: simultaneous detection of two common …
M Esmaeili, M Bonyadi, M Nejadkazem
International journal of pediatric otorhinolaryngology 71 (6), 869-873, 2007
362007
Associations of the ANKK1 and DRD2 gene polymorphisms with overweight, obesity and hedonic hunger among women from the Northwest of Iran
F Aliasghari, SA Nazm, S Yasari, R Mahdavi, M Bonyadi
Eating and Weight Disorders-Studies on Anorexia, Bulimia and Obesity 26, 305-312, 2021
352021
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Articles 1–20