Optimizing A Lipocomplex-Based Gene Transfer Method into HeLa Cell Line

Por Asgharian, Alimohammad, Banan, Mehdi, Najmabadi, Hossein
Publicado em 2014

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...

Por Taghizadeh, Sara, Najmabadi, Hossein, Kamali, Koorosh, Behjati, Farkhondeh
Publicado no J Environ Health Sci Eng (2014)

Hemoglobin Q-Iran detected in family members from Northern Iran: a case report

Por Khorshidi, Mohammad, Roshan, Payam, Bayat, Nooshin, Mahdavi, Mohammad Reza, Najmabadi, Hossein
Publicado em 2012

Old gene, new phenotype: Splicing altering variants in CEACAM16 cause recessive non-syndromic hearing impairment

Por Booth, Kevin T, Kahrizi, Kimia, Najmabadi, Hossein, Azaiez, Hela, Smith, Richard J
Publicado no J Med Genet (2018)

Novel CFTR Mutations in Two Iranian Families with Severe Cystic Fibrosis

Por Mohseni, Marzieh, Razzaghmanesh, Mohammad, Mehr, Elham Parsi, Zare, Hanieh, Beheshtian, Maryam, Najmabadi, Hossein
Publicado no Iran Biomed J (2016)

A novel mutation adjacent to the Bth mouse mutation in the TMC1 gene makes this mouse an excellent model of human deafness at the DFNA36 locus

Por Yang, Tao, Kahrizi, Kimia, Bazazzadeghan, Niloofar, Meyer, Nicole, Najmabadi, Hossein, Smith, Richard J.H.
Publicado em 2010

Serotonin Transporter Polymorphism (5-HTTLPR) and Citalopram Effectiveness in Iranian Patients with Major Depressive Disorder

Por Sahraian, Shima, Babashams, Mohammad, Reza-Soltani, Pouria, Najmabadi, Hossein, Kahrizi, Kimia, Gorgani, Sahel Hemmati
Publicado em 2013

Iranian hereditary hemochromatosis patients: Baseline characteristics, laboratory data and gene mutations

Por Zamani, Farhad, Bagheri, Zohreh, Bayat, Maryam, Fereshtehnejad, Seyed-Mohammad, Basi, Ali, Najmabadi, Hossein, Ajdarkosh, Hossein
Publicado em 2012

A Novel Deletion Mutation in ASPM Gene in an Iranian Family with Autosomal Recessive Primary Microcephaly

Por AKBARIAZAR, Elinaz, EBRAHIMPOUR, Mohammad, AKBARI, Saeedeh, ARZHANGHI, Sanaz, ABEDINI, Seydeh Sedigheh, NAJMABADI, Hossein, KAHRIZI, Kimia
Publicado em 2013

A large deletion in GPR98 causes type IIC Usher syndrome in male and female patients of an Iranian family

Por Hilgert, Nele, Kahrizi, Kimia, Najmabadi, Hossein, Dieltjens, Nele, Bazazzadegan, Niloofar, Smith, Richard JH, Van Camp, Guy
Publicado no J Med Genet (2009)

Association Study of the TREM2 Gene and Identification of a Novel Variant in Exon 2 in Iranian Patients with Late-Onset Alzheimer's Disease

Por Mehrjoo, Zohreh, Najmabadi, Amin, Abedini, Seyedeh Sedigheh, Mohseni, Marzieh, Kamali, Koorosh, Najmabadi, Hossein, Khorram Khorshid, Hamid Reza
Publicado no Med Princ Pract (2015)

Ethnic Specific Distribution of Mutations in 716 Patients with Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency

Por Wilson, Robert C., Nimkarn, Saroj, Dumic, Miro, Obeid, Jihad, Razzaghy Azar, Maryam, Najmabadi, Hossein, Saffari, Fatemeh, New, Maria I.
Publicado em 2007

miRNA Mutations are Not a Common Cause of Deafness

Por Hildebrand, Michael S., Witmer, P. Dane, Xu, Shunbin, Newton, Stephen S., Kahrizi, Kimia, Najmabadi, Hossein, Valle, David, Smith, Richard J.H.
Publicado em 2010

Exonic mutations and exon skipping: lessons learned from DFNA5

Por Booth, Kevin T, Azaiez, Hela, Kahrizi, Kimia, Wang, Donghong, Zhang, Yuzhou, Frees, Kathy, Nishimura, Carla, Najmabadi, Hossein, Smith, Richard J
Publicado no Hum Mutat (2018)

An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4

Por Kahrizi, Kimia, Najmabadi, Hossein, Kariminejad, Roxana, Jamali, Payman, Malekpour, Mahdi, Garshasbi, Masoud, Ropers, Hans Hilger, Kuss, Andreas Walter, Tzschach, Andreas
Publicado em 2009

A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation

Por Garshasbi, Masoud, Hadavi, Valeh, Habibi, Haleh, Kahrizi, Kimia, Kariminejad, Roxana, Behjati, Farkhondeh, Tzschach, Andreas, Najmabadi, Hossein, Ropers, Hans Hilger, Kuss, Andreas Walter
Publicado em 2008

Human Male Infertility Caused by Mutations in the CATSPER1 Channel Protein

Por Avenarius, Matthew R., Hildebrand, Michael S., Zhang, Yuzhou, Meyer, Nicole C., Smith, Luke L.H., Kahrizi, Kimia, Najmabadi, Hossein, Smith, Richard J.H.
Publicado em 2009

Sensorineural deafness and male infertility: a contiguous gene deletion syndrome

Por Zhang, Yuzhou, Malekpour, Mahdi, Al‐Madani, Navid, Kahrizi, Kimia, Zanganeh, Marvam, Mohseni, Marzieh, Mojahedi, Faezeh, Daneshi, Ahmad, Najmabadi, Hossein, Smith, Richard J H
Publicado em 2007

Sensorineural deafness and male infertility: a contiguous gene deletion syndrome

Por Zhang, Yuzhou, Malekpour, Mahdi, Al-Madani, Navid, Kahrizi, Kimia, Zanganeh, Marvam, Mohseni, Marzieh, Mojahedi, Faezeh, Daneshi, Ahmad, Najmabadi, Hossein, Smith, Richard J H
Publicado em 2009

Hydroxyurea responsiveness in β-thalassemic patients is determined by the stress response adaptation of erythroid progenitors and their differentiation propensity

Por Pourfarzad, Farzin, von Lindern, Marieke, Azarkeivan, Azita, Hou, Jun, Kia, Sima Kheradmand, Esteghamat, Fatemehsadat, van IJcken, Wilfred, Philipsen, Sjaak, Najmabadi, Hossein, Grosveld, Frank
Publicado em 2013