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Massoud Houshmand

Showing results (111-120 of 161) with videos related to

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Drug Design, Development and Therapy|November 26, 2015
Prevalence of the rs7903146C>T polymorphism in TCF7L2 gene for prediction of type 2 diabetes risk among Iranians of different ethnicitiesMojgan Allahdini, Behnam Kamalidehghan, Leila Akbari, et al.
Cellular and Molecular Neurobiology|June 10, 2006
Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!!Hassan Hassani-Kumleh, Massoud Houshmand, Mehdi Shafa Shariat Panahi, et al.
Plos One|September 13, 2014
Two novel tyrosinase (TYR) gene mutations with pathogenic impact on oculocutaneous albinism type 1 (OCA1)Vadieh Ghodsinejad Kalahroudi, Behnam Kamalidehghan, Ahoura Arasteh Kani, et al.
Neuro-Degenerative Diseases|December 11, 2008
Mitochondrial tRNALeu/Lys and ATPase 6/8 gene variations in spinocerebellar ataxiasSepideh Safaei, Massoud Houshmand, Mohammad Mehdi Banoei, et al.
Hereditas|January 28, 2022
Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutationsRezvan Abtahi, Parvaneh Karimzadeh, Omid Aryani, et al.
Therapeutics and Clinical Risk Management|July 4, 2017
Four novel <i>ARSA</i> gene mutations with pathogenic impacts on metachromatic leukodystrophy: a bioinformatics approach to predict pathogenic mutationsMasoumeh Dehghan Manshadi, Behnam Kamalidehghan, Omid Aryani, et al.
Biomedical Reports|December 15, 2018
Erratum: Mitochondrial G8292A and C8794T mutations in patients with Niemann-Pick disease type CShahin Maserrat, Fatemeh Sharifpanah, Leila Akbari, et al.
Archives of Medical Research|September 12, 2007
Use of D11S2179 and D11S1343 as markers for prenatal diagnosis of ataxia telangiectasia in Iranian patientsBehnaz Bayat, Massoud Houshmand, Mohammad Hossein Sanati, et al.
Molecular Medicine Reports|January 13, 2018
Prevalence of the CYP2C19*2 (681 G>A), *3 (636 G>A) and *17 (‑806 C>T) alleles among an Iranian population of different ethnicitiesMahshid Dehbozorgi, Behnam Kamalidehghan, Iman Hosseini, et al.
Human Biology|May 29, 2008
Variation of DAT1 VNTR alleles and genotypes among old ethnic groups in Mesopotamia to the Oxus regionMohammad Mehdi Banoei, Morteza Hashemzadeh Chaleshtori, Mohammad Hossein Sanati, et al.
Pageof 17

Showing results (111-120 of 161) with videos related to

Sort By:
Pageof 17
Drug Design, Development and Therapy|November 26, 2015
Prevalence of the rs7903146C>T polymorphism in TCF7L2 gene for prediction of type 2 diabetes risk among Iranians of different ethnicitiesMojgan Allahdini, Behnam Kamalidehghan, Leila Akbari, et al.
Cellular and Molecular Neurobiology|June 10, 2006
Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!!Hassan Hassani-Kumleh, Massoud Houshmand, Mehdi Shafa Shariat Panahi, et al.
Plos One|September 13, 2014
Two novel tyrosinase (TYR) gene mutations with pathogenic impact on oculocutaneous albinism type 1 (OCA1)Vadieh Ghodsinejad Kalahroudi, Behnam Kamalidehghan, Ahoura Arasteh Kani, et al.
Neuro-Degenerative Diseases|December 11, 2008
Mitochondrial tRNALeu/Lys and ATPase 6/8 gene variations in spinocerebellar ataxiasSepideh Safaei, Massoud Houshmand, Mohammad Mehdi Banoei, et al.
Hereditas|January 28, 2022
Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutationsRezvan Abtahi, Parvaneh Karimzadeh, Omid Aryani, et al.
Therapeutics and Clinical Risk Management|July 4, 2017
Four novel <i>ARSA</i> gene mutations with pathogenic impacts on metachromatic leukodystrophy: a bioinformatics approach to predict pathogenic mutationsMasoumeh Dehghan Manshadi, Behnam Kamalidehghan, Omid Aryani, et al.
Biomedical Reports|December 15, 2018
Erratum: Mitochondrial G8292A and C8794T mutations in patients with Niemann-Pick disease type CShahin Maserrat, Fatemeh Sharifpanah, Leila Akbari, et al.
Archives of Medical Research|September 12, 2007
Use of D11S2179 and D11S1343 as markers for prenatal diagnosis of ataxia telangiectasia in Iranian patientsBehnaz Bayat, Massoud Houshmand, Mohammad Hossein Sanati, et al.
Molecular Medicine Reports|January 13, 2018
Prevalence of the CYP2C19*2 (681 G>A), *3 (636 G>A) and *17 (‑806 C>T) alleles among an Iranian population of different ethnicitiesMahshid Dehbozorgi, Behnam Kamalidehghan, Iman Hosseini, et al.
Human Biology|May 29, 2008
Variation of DAT1 VNTR alleles and genotypes among old ethnic groups in Mesopotamia to the Oxus regionMohammad Mehdi Banoei, Morteza Hashemzadeh Chaleshtori, Mohammad Hossein Sanati, et al.
Pageof 17