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International Journal of Molecular and Cellular Medicine
|
December 13, 2016
MAP3K1 May be a Promising Susceptibility Gene for Type 2 Diabetes Mellitus in an Iranian Population
Shahram Torkamandi, Milad Bastami, Hamid Ghaedi, et al.
International Journal of Molecular and Cellular Medicine
|
August 2, 2016
A Bioinformatics Approach to Prioritize Single Nucleotide Polymorphisms in TLRs Signaling Pathway Genes
Behnam Alipoor, Hamid Ghaedi, Mir Davood Omrani, et al.
Archives of Physiology and Biochemistry
|
May 26, 2020
Variation in the expression level of MALAT1, MIAT and XIST lncRNAs in coronary artery disease patients with and without type 2 diabetes mellitus
Nasim Sohrabifar, Sayyed Mohammad Hossein Ghaderian, Saeed Alipour Parsa, et al.
Iranian Red Crescent Medical Journal
|
September 20, 2014
Single-Nucleotide Polymorphisms Within MicroRNAs Sequences and Their 3' UTR Target Sites May Regulate Gene Expression in Gastrointestinal Tract Cancers
Zahra Saadatian, Andrea Masotti, Ziba Nariman Saleh Fam, et al.
International Journal of Molecular and Cellular Medicine
|
April 24, 2018
Association of MiR-146a Expression and Type 2 Diabetes Mellitus: A Meta-Analysis
Behnam Alipoor, Hamid Ghaedi, Reza Meshkani, et al.
Heliyon
|
October 27, 2021
Up-regulation of <i>FOXN3-AS1</i> in invasive ductal carcinoma of breast cancer patients
Samira Molaei Ramshe, Hamid Ghaedi, Mir Davood Omrani, et al.
Proteins
|
June 23, 2019
The effects of somatic mutations on EGFR interaction with anti-EGFR monoclonal antibodies: Implication for acquired resistance
Maryam Tabasinezhad, Eskanadr Omidinia, Yeganeh Talebkhan, et al.
Molecular Biology Reports
|
May 16, 2019
Expression analysis and genotyping of DGKZ: a GWAS-derived risk gene for schizophrenia
Somayeh Alinaghi, Elham Alehabib, Amir Hossein Johari, et al.
Molecular Biology Reports
|
November 24, 2020
SUCLG1 mutations and mitochondrial encephalomyopathy: a case study and review of the literature
Samira Molaei Ramsheh, Maryam Erfanian Omidvar, Maryam Tabasinezhad, et al.
Gene
|
July 22, 2018
Premutations of FMR1 CGG repeats are not related to idiopathic premature ovarian failure in Iranian patients: A case control study
Rezvaneh Asadi, Mir Davood Omrani, Hamid Ghaedi, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 65) with videos related to
Sort By:
Page
of 7
International Journal of Molecular and Cellular Medicine
|
December 13, 2016
MAP3K1 May be a Promising Susceptibility Gene for Type 2 Diabetes Mellitus in an Iranian Population
Shahram Torkamandi, Milad Bastami, Hamid Ghaedi, et al.
International Journal of Molecular and Cellular Medicine
|
August 2, 2016
A Bioinformatics Approach to Prioritize Single Nucleotide Polymorphisms in TLRs Signaling Pathway Genes
Behnam Alipoor, Hamid Ghaedi, Mir Davood Omrani, et al.
Archives of Physiology and Biochemistry
|
May 26, 2020
Variation in the expression level of MALAT1, MIAT and XIST lncRNAs in coronary artery disease patients with and without type 2 diabetes mellitus
Nasim Sohrabifar, Sayyed Mohammad Hossein Ghaderian, Saeed Alipour Parsa, et al.
Iranian Red Crescent Medical Journal
|
September 20, 2014
Single-Nucleotide Polymorphisms Within MicroRNAs Sequences and Their 3' UTR Target Sites May Regulate Gene Expression in Gastrointestinal Tract Cancers
Zahra Saadatian, Andrea Masotti, Ziba Nariman Saleh Fam, et al.
International Journal of Molecular and Cellular Medicine
|
April 24, 2018
Association of MiR-146a Expression and Type 2 Diabetes Mellitus: A Meta-Analysis
Behnam Alipoor, Hamid Ghaedi, Reza Meshkani, et al.
Heliyon
|
October 27, 2021
Up-regulation of <i>FOXN3-AS1</i> in invasive ductal carcinoma of breast cancer patients
Samira Molaei Ramshe, Hamid Ghaedi, Mir Davood Omrani, et al.
Proteins
|
June 23, 2019
The effects of somatic mutations on EGFR interaction with anti-EGFR monoclonal antibodies: Implication for acquired resistance
Maryam Tabasinezhad, Eskanadr Omidinia, Yeganeh Talebkhan, et al.
Molecular Biology Reports
|
May 16, 2019
Expression analysis and genotyping of DGKZ: a GWAS-derived risk gene for schizophrenia
Somayeh Alinaghi, Elham Alehabib, Amir Hossein Johari, et al.
Molecular Biology Reports
|
November 24, 2020
SUCLG1 mutations and mitochondrial encephalomyopathy: a case study and review of the literature
Samira Molaei Ramsheh, Maryam Erfanian Omidvar, Maryam Tabasinezhad, et al.
Gene
|
July 22, 2018
Premutations of FMR1 CGG repeats are not related to idiopathic premature ovarian failure in Iranian patients: A case control study
Rezvaneh Asadi, Mir Davood Omrani, Hamid Ghaedi, et al.
Page
of 7