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Urologia Internationalis
|
December 4, 2013
Genetic polymorphisms in calcitonin receptor gene and risk for recurrent kidney calcium stone disease
Nasser Shakhssalim, Abbas Basiri, Massoud Houshmand, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
January 8, 2018
Four novel mutations of the BCKDHA, BCKDHB and DBT genes in Iranian patients with maple syrup urine disease
Monica Zeynalzadeh, Alireza Tafazoli, Azadeh Aarabi, et al.
Journal of Molecular Neuroscience : MN
|
September 23, 2021
Analysis of the HEXA, HEXB, ARSA, and SMPD1 Genes in 68 Iranian Patients
Rezvan Abtahi, Parvaneh Karimzadeh, Alireza Rezayi, et al.
Hepatitis Monthly
|
January 27, 2017
Liver Mitochondrial DNA Copy Number and Deletion Levels May Contribute to Nonalcoholic Fatty Liver Disease Susceptibility
Sharareh Kamfar, Seyed Moayed Alavian, Massoud Houshmand, et al.
Genetics Research
|
February 23, 2023
Allelic and Genotype Frequencies of CYP2B6<sup>∗</sup>2 (64C > T) and CYP2B6<sup>∗</sup>3 (777C > A) in Three Dominant Ethnicities of the Iranian Population
Armin Khavandegar, Bahareh Tavakoli-Far, Sarina Ansari, et al.
Journal of Andrology
|
December 4, 2010
A novel mutation in the transactivation-regulating domain of the androgen receptor in a patient with azoospermia
Reza Mirfakhraie, Sayed-Mahdi Kalantar, Farzaneh Mirzajani, et al.
Cellular and Molecular Neurobiology
|
October 24, 2007
Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion?!
Mohammad Mehdi Banoei, Massoud Houshmand, Mehdi Shafa Shariat Panahi, et al.
Urological Research
|
August 5, 2011
Coding region analysis of vitamin D receptor gene and its association with active calcium stone disease
Abbas Basiri, Nasser Shakhssalim, Massoud Houshmand, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology
|
April 17, 2009
Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?
Mehri Khatami, Massoud Houshmand, Majid Sadeghizadeh, et al.
Cancer Cell International
|
December 7, 2013
The mitochondrial C16069T polymorphism, not mitochondrial D310 (D-loop) mononucleotide sequence variations, is associated with bladder cancer
Nasser Shakhssalim, Massoud Houshmand, Behnam Kamalidehghan, et al.
Page
of 17
Search research articles
Search
Showing results (101-110 of 161) with videos related to
Sort By:
Page
of 17
Urologia Internationalis
|
December 4, 2013
Genetic polymorphisms in calcitonin receptor gene and risk for recurrent kidney calcium stone disease
Nasser Shakhssalim, Abbas Basiri, Massoud Houshmand, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
January 8, 2018
Four novel mutations of the BCKDHA, BCKDHB and DBT genes in Iranian patients with maple syrup urine disease
Monica Zeynalzadeh, Alireza Tafazoli, Azadeh Aarabi, et al.
Journal of Molecular Neuroscience : MN
|
September 23, 2021
Analysis of the HEXA, HEXB, ARSA, and SMPD1 Genes in 68 Iranian Patients
Rezvan Abtahi, Parvaneh Karimzadeh, Alireza Rezayi, et al.
Hepatitis Monthly
|
January 27, 2017
Liver Mitochondrial DNA Copy Number and Deletion Levels May Contribute to Nonalcoholic Fatty Liver Disease Susceptibility
Sharareh Kamfar, Seyed Moayed Alavian, Massoud Houshmand, et al.
Genetics Research
|
February 23, 2023
Allelic and Genotype Frequencies of CYP2B6<sup>∗</sup>2 (64C > T) and CYP2B6<sup>∗</sup>3 (777C > A) in Three Dominant Ethnicities of the Iranian Population
Armin Khavandegar, Bahareh Tavakoli-Far, Sarina Ansari, et al.
Journal of Andrology
|
December 4, 2010
A novel mutation in the transactivation-regulating domain of the androgen receptor in a patient with azoospermia
Reza Mirfakhraie, Sayed-Mahdi Kalantar, Farzaneh Mirzajani, et al.
Cellular and Molecular Neurobiology
|
October 24, 2007
Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion?!
Mohammad Mehdi Banoei, Massoud Houshmand, Mehdi Shafa Shariat Panahi, et al.
Urological Research
|
August 5, 2011
Coding region analysis of vitamin D receptor gene and its association with active calcium stone disease
Abbas Basiri, Nasser Shakhssalim, Massoud Houshmand, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology
|
April 17, 2009
Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?
Mehri Khatami, Massoud Houshmand, Majid Sadeghizadeh, et al.
Cancer Cell International
|
December 7, 2013
The mitochondrial C16069T polymorphism, not mitochondrial D310 (D-loop) mononucleotide sequence variations, is associated with bladder cancer
Nasser Shakhssalim, Massoud Houshmand, Behnam Kamalidehghan, et al.
Page
of 17