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

por Asgharian, Alimohammad, Banan, Mehdi, Najmabadi, Hossein
Publicado 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 2014

The First Case of BENTA Disease (B Cell Expansion with NF-κB and T Cell Anergy) from Iran

por Neishabury, Maryam, Azarkeivan, Azita, Mehri, Maghsood, Najmabadi, Hossein, Cheraghi, Taher
Publicado 2021

The Effect of Xmn -1 Polymorphism and Coinheritance of Alpha Mutations on Age at First Blood Transfusion in Iranian Patients with Homozygote IVSI-5 Mutation

por Hashemieh, Mozhgan, Saadatmandi, Zahra Al Sadat, Azarkeivan, Azita, Najmabadi, Hossein
Publicado 2022

The liver-derived exosomes stimulate insulin gene expression in pancreatic beta cells under condition of insulin resistance

por Mahmoudi-Aznaveh, Azam, Tavoosidana, Gholamreza, Najmabadi, Hossein, Azizi, Zahra, Ardestani, Amin
Publicado 2023

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 2012

Clinical and Genetic Characteristics of Splicing Variant in CYP27A1 in an Iranian Family with Cerebrotendinous xanthomatosis

por Rashvand, Zahra, Kahrizi, Kimia, Najmabadi, Hossein, Najafipour, Reza, Omrani, Mir Davood
Publicado 2021

Understanding the Molecular Basis of Fragile X Syndrome Using Differentiated Mesenchymal Stem Cells

por FAZELI, Zahra, GHADERIAN, Sayyed Mohammad Hossein, NAJMABADI, Hossein, OMRANI, Mir Davood
Publicado 2022

Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery

por Saghi, Mostafa, InanlooRahatloo, Kolsoum, Alavi, Afagh, Kahrizi, Kimia, Najmabadi, Hossein
Publicado 2022

Identification of a homozygous frameshift mutation in the FGF3 gene in a consanguineous Iranian family: First report of labyrinthine aplasia, microtia, and microdontia syndrome in...

por Jamshidi, Fereshteh, Shokouhian, Ebrahim, Mohseni, Marzieh, Kahrizi, Kimia, Najmabadi, Hossein, Babanejad, Mojgan
Publicado 2023

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 2016

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 2013

Phenotype and genotype spectrum of variants in guanine nucleotide exchange factor genes in a broad cohort of Iranian patients

por Mosallaei, Meysam, Ehtesham, Naeim, Beheshtian, Maryam, Khoshbakht, Shahrouz, Davarnia, Behzad, Kahrizi, Kimia, Najmabadi, Hossein
Publicado 2022

DNA Banking to Assess Genetic Influences on Schizophrenia

por Sadighi, Gita, Nazeri Astaneh, Ali, Najmabadi, Hossein, Khodaei Ardakani, Mohammad Reza, Latifi-Navid, Saeid
Publicado 2022

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 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 2013

Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities

por Najafi, Kimia, Mehrjoo, Zohreh, Ardalani, Fariba, Ghaderi-Sohi, Siavash, Kariminejad, Ariana, Kariminejad, Roxana, Najmabadi, Hossein
Publicado 2021

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 2015

Bi‐allelic loss of function variant in the NRCAM gene is associated with motor‐predominant axonal polyneuropathy; the second report

por Elahi, Zohreh, Soveyzi, Mohamad, Nafissi, Shahriar, Nilipour, Yalda, Goleyjani Moghadam, Masoumeh, Keshavarz, Elham, Kariminejad, Ariana, Najmabadi, Hossein, Fattahi, Zohreh
Publicado 2023

Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization

por Behjati, Farkhondeh, Firouzabadi, Saghar Ghasemi, Kariminejad, Roxana, Vameghi, Roshanak, Sajedi, Firouzeh, Shafaghati, Yousef, Ghasemlou, Behruz Ebrahimizade, Shojaei, Azadeh, Jamali, Peyman, Bahman, Ideh, Najmabadi, Hossein
Publicado 2013