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Hossein Najmabadi

Showing results (1-10 of 305) with videos related to

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Blood Cells, Molecules & Diseases|October 14, 2015
Diagnostic pitfalls of less well recognized HbH diseaseSamaneh Farashi, Hossein Najmabadi
International Journal of Pediatric Otorhinolaryngology|October 5, 2014
Genetics of non-syndromic hearing loss in the Middle EastHossein Najmabadi, Kimia Kahrizi
Archives of Iranian Medicine|May 15, 2016
Genetic Studies in Intellectual Disability and Behavioral ImpairmentHoda Mehregan, Hossein Najmabadi, Kimia Kahrizi
Archives of Iranian Medicine|April 26, 2018
Calpains: Diverse Functions but EnigmaticMasoumeh Hosseini, Hossein Najmabadi, Kimia Kahrizi
Blood Cells, Molecules & Diseases|November 7, 2009
Frequency of positive XmnIGgamma polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutationMaryam Neishabury, Azita Azarkeivan, Hossein Najmabadi
Archives of Iranian Medicine|April 18, 2018
Intellectual Disability and Ataxia: Genetic CollisionsSomayeh Kazeminasab, Hossein Najmabadi, Kimia Kahrizi
Cell Journal|January 2, 2014
Optimizing A Lipocomplex-Based Gene Transfer Method into HeLa Cell LineAlimohammad Asgharian, Mehdi Banan, Hossein Najmabadi
Archives of Iranian Medicine|October 2, 2007
Molecular analysis of the neuronal apoptosis inhibitory protein gene in families with spinal muscular atrophyIman Salahshourifar, Yousef Shafeghati, Zahra Golkar, et al.
Journal of Environmental Health Science & Engineering|January 22, 2015
Evaluation of chromosomal aberrations caused by air pollutants in some taxi drivers from two polluted districts of urban Tehran and its comparison with drivers from rural areas of Lahijan: a pilot studySara Taghizadeh, Hossein Najmabadi, Koorosh Kamali, et al.
Journal of Genetics|October 7, 2015
Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian familiesZohreh Mehrjoo, Mojgan Babanejad, Kimia Kahrizi, et al.
Pageof 31

Showing results (1-10 of 305) with videos related to

Sort By:
Pageof 31
Blood Cells, Molecules & Diseases|October 14, 2015
Diagnostic pitfalls of less well recognized HbH diseaseSamaneh Farashi, Hossein Najmabadi
International Journal of Pediatric Otorhinolaryngology|October 5, 2014
Genetics of non-syndromic hearing loss in the Middle EastHossein Najmabadi, Kimia Kahrizi
Archives of Iranian Medicine|May 15, 2016
Genetic Studies in Intellectual Disability and Behavioral ImpairmentHoda Mehregan, Hossein Najmabadi, Kimia Kahrizi
Archives of Iranian Medicine|April 26, 2018
Calpains: Diverse Functions but EnigmaticMasoumeh Hosseini, Hossein Najmabadi, Kimia Kahrizi
Blood Cells, Molecules & Diseases|November 7, 2009
Frequency of positive XmnIGgamma polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutationMaryam Neishabury, Azita Azarkeivan, Hossein Najmabadi
Archives of Iranian Medicine|April 18, 2018
Intellectual Disability and Ataxia: Genetic CollisionsSomayeh Kazeminasab, Hossein Najmabadi, Kimia Kahrizi
Cell Journal|January 2, 2014
Optimizing A Lipocomplex-Based Gene Transfer Method into HeLa Cell LineAlimohammad Asgharian, Mehdi Banan, Hossein Najmabadi
Archives of Iranian Medicine|October 2, 2007
Molecular analysis of the neuronal apoptosis inhibitory protein gene in families with spinal muscular atrophyIman Salahshourifar, Yousef Shafeghati, Zahra Golkar, et al.
Journal of Environmental Health Science & Engineering|January 22, 2015
Evaluation of chromosomal aberrations caused by air pollutants in some taxi drivers from two polluted districts of urban Tehran and its comparison with drivers from rural areas of Lahijan: a pilot studySara Taghizadeh, Hossein Najmabadi, Koorosh Kamali, et al.
Journal of Genetics|October 7, 2015
Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian familiesZohreh Mehrjoo, Mojgan Babanejad, Kimia Kahrizi, et al.
Pageof 31