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Massoud Houshmand

Showing results (121-130 of 161) with videos related to

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Biomedical Reports|June 23, 2018
Mitochondrial G8292A and C8794T mutations in patients with Niemann-Pick disease type CShahin Maserrat, Fatemeh Sharifpanah, Leila Akbari, et al.
Cellular and Molecular Neurobiology|April 4, 2008
Investigation of tRNA(Leu/Lys) and ATPase 6 genes mutations in Huntington's diseaseSadaf Kasraie, Massoud Houshmand, Mohammad Mehdi Banoei, et al.
Iranian Journal of Allergy, Asthma, and Immunology|December 25, 2012
Molecular analysis of four cases of chronic granulomatous disease caused by defects in NCF-2: the gene encoding the p67-phoxMohsen Badalzadeh, Fatemeh Fattahi, Mohammad Reza Fazlollahi, et al.
Diabetes, Metabolic Syndrome and Obesity : Targets and Therapy|April 11, 2020
<i>SLC30A8, CDKAL1, TCF7L2, KCNQ1</i> and <i>IGF2BP2</i> are Associated with Type 2 Diabetes Mellitus in Iranian PatientsKazem Vatankhah Yazdi, Seyed Mehdi Kalantar, Massoud Houshmand, et al.
Molecular Vision|November 10, 2009
Genotyping results of Iranian PCG families suggests one or more PCG locus other than GCL3A, GCL3B, and GCL3C existMehrnaz Narooie-Nejad, Fereshteh Chitsazian, Betsabeh Khoramian Tusi, et al.
Scandinavian Journal of Urology and Nephrology|July 7, 2010
Association between calcium-sensing receptor gene polymorphisms and recurrent calcium kidney stone disease: a comprehensive gene analysisNasser Shakhssalim, Bahram Kazemi, Abbas Basiri, et al.
The Journal of Investigative Dermatology|May 13, 2006
Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotypeElahe Elahi, Reza Kalhor, Setareh S Banihosseini, et al.
Cellular and Molecular Neurobiology|August 30, 2008
Analysis of HLA DR2&DQ6 (DRB1*1501, DQA1*0102, DQB1*0602) haplotypes in Iranian patients with multiple sclerosisMojdeh Ghabaee, Asghar Bayati, Shahla Amri Saroukolaei, et al.
Drug Design, Development and Therapy|May 23, 2015
Prevalence of the CYP2D6*10 (C100T), *4 (G1846A), and *14 (G1758A) alleles among Iranians of different ethnicitiesAli Bagheri, Behnam Kamalidehghan, Maryam Haghshenas, et al.
International Journal of Molecular Sciences|March 27, 2015
Four novel p.N385K, p.V36A, c.1033-1034insT and c.1417-1418delCT mutations in the sphingomyelin Phosphodiesterase 1 (SMPD1) gene in patients with types A and B Niemann-Pick disease (NPD)Masoumeh Dehghan Manshadi, Behnam Kamalidehghan, Fatemeh Keshavarzi, et al.
Pageof 17

Showing results (121-130 of 161) with videos related to

Sort By:
Pageof 17
Biomedical Reports|June 23, 2018
Mitochondrial G8292A and C8794T mutations in patients with Niemann-Pick disease type CShahin Maserrat, Fatemeh Sharifpanah, Leila Akbari, et al.
Cellular and Molecular Neurobiology|April 4, 2008
Investigation of tRNA(Leu/Lys) and ATPase 6 genes mutations in Huntington's diseaseSadaf Kasraie, Massoud Houshmand, Mohammad Mehdi Banoei, et al.
Iranian Journal of Allergy, Asthma, and Immunology|December 25, 2012
Molecular analysis of four cases of chronic granulomatous disease caused by defects in NCF-2: the gene encoding the p67-phoxMohsen Badalzadeh, Fatemeh Fattahi, Mohammad Reza Fazlollahi, et al.
Diabetes, Metabolic Syndrome and Obesity : Targets and Therapy|April 11, 2020
<i>SLC30A8, CDKAL1, TCF7L2, KCNQ1</i> and <i>IGF2BP2</i> are Associated with Type 2 Diabetes Mellitus in Iranian PatientsKazem Vatankhah Yazdi, Seyed Mehdi Kalantar, Massoud Houshmand, et al.
Molecular Vision|November 10, 2009
Genotyping results of Iranian PCG families suggests one or more PCG locus other than GCL3A, GCL3B, and GCL3C existMehrnaz Narooie-Nejad, Fereshteh Chitsazian, Betsabeh Khoramian Tusi, et al.
Scandinavian Journal of Urology and Nephrology|July 7, 2010
Association between calcium-sensing receptor gene polymorphisms and recurrent calcium kidney stone disease: a comprehensive gene analysisNasser Shakhssalim, Bahram Kazemi, Abbas Basiri, et al.
The Journal of Investigative Dermatology|May 13, 2006
Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotypeElahe Elahi, Reza Kalhor, Setareh S Banihosseini, et al.
Cellular and Molecular Neurobiology|August 30, 2008
Analysis of HLA DR2&DQ6 (DRB1*1501, DQA1*0102, DQB1*0602) haplotypes in Iranian patients with multiple sclerosisMojdeh Ghabaee, Asghar Bayati, Shahla Amri Saroukolaei, et al.
Drug Design, Development and Therapy|May 23, 2015
Prevalence of the CYP2D6*10 (C100T), *4 (G1846A), and *14 (G1758A) alleles among Iranians of different ethnicitiesAli Bagheri, Behnam Kamalidehghan, Maryam Haghshenas, et al.
International Journal of Molecular Sciences|March 27, 2015
Four novel p.N385K, p.V36A, c.1033-1034insT and c.1417-1418delCT mutations in the sphingomyelin Phosphodiesterase 1 (SMPD1) gene in patients with types A and B Niemann-Pick disease (NPD)Masoumeh Dehghan Manshadi, Behnam Kamalidehghan, Fatemeh Keshavarzi, et al.
Pageof 17