Producing a Mammalian GFP Expression Vector Containing Neomycin Resistance Gene

Por Izadi, Manizheh, Abiri, Maryam, Keramatipour, Mohammad
Publicado em 2009

Effect of Embryonic Cerebrospinal Fluid on Proliferation and Differentiation of Neuroprogenitor Cells

Por Yari, Siamak, Parivar, Kazem, Nabiuni, Mohammad, Keramatipour, Mohammad
Publicado em 2013

Comparison of Two Different PCR-based Methods for Detection of GAA Expansions in Frataxin Gene

Por ENTEZAM, Mona, AMIRFIROOZI, Akbar, TOGHA, Mansoureh, KERAMATIPOUR, Mohammad
Publicado no Iran J Public Health (2017)

A Case Series: Congenital Hyperinsulinism

Por Alaei, Mohammad Reza, Akbaroghli, Susan, Keramatipour, Mohammad, Alaei, Ali
Publicado no Int J Endocrinol Metab (2016)

Functional Analysis of A Novel Splicing Mutation in The Mutase Gene of Two Unrelated Pedigrees

Por Ahmadloo, Somayeh, Talebi, Saeed, Miryounesi, Mohammad, Pasalar, Parvin, Keramatipour, Mohammad
Publicado no Cell J (2016)

Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient

Por Alaei, Mohammad Reza, Talebi, Saeed, Ghofrani, Mohammad, Taghizadeh, Mohsen, Keramatipour, Mohammad
Publicado no Iran Biomed J (2016)

PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data()

Por Entezam, Mona, Khatami, Mohammad Reza, Saddadi, Fereshteh, Ayati, Mohsen, Roozbeh, Jamshid, Keramatipour, Mohammad
Publicado no Kidney Res Clin Pract (2016)

Analysis of CFTR Gene Mutations in Children with Cystic Fibrosis, First Report from North-East of Iran

Por Mehdizadeh Hakkak, Atieh, Keramatipour, Mohammad, Talebi, Saeid, Brook, Azam, Tavakol Afshari, Jalil, Raazi, Amin, Kianifar, Hamid Reza
Publicado em 2013

An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria

Por Talebi, Saeed, Entezam, Mona, Mohajer, Neda, Kazemi-sefat, Golnaz-Ensieh, Razipour, Masoumeh, Ahmadloo, Somayeh, Setoodeh, Aria, Keramatipour, Mohammad
Publicado no Cell J (2016)

Setting up Multiplex Panels for Genetic Testing of Familial Hypertrophic Cardiomyopathy Based on Linkage Analysis

Por SAGHAFI, Hoorieh, HAGHJOO, Majid, SABBAGH, Sima, SAMIEE, Niloofar, VAKILIAN, Farve, SALEHI OMRAN, Mohammad Taghi, DADASHI, Masoomeh, AMIN, Ahmad, KERAMATIPOUR, Mohammad
Publicado no Iran J Public Health (2016)

Replication of TCF7L2 rs7903146 association with type 2 diabetes in an Iranian population

Por Amoli, Mahsa M., Amiri, Parvin, Tavakkoly-Bazzaz, Javad, Charmchi, Elham, Hafeziyeh, Jila, Keramatipour, Mohammad, Abiri, Maryam, Ranjbar, Shirin Hasani, Larijani, Bagher
Publicado em 2010

The Relationship Between Coronary Artery Disease and Genetic Polymorphisms of Melanoma Inhibitory Activity 3

Por Zaimkohan, Hooshang, Keramatipour, Mohammad, Mirhafez, Seyed Reza, Tavakkoly-Bazzaz, Javad, Tahooni, Azadeh, Piryaei, Mohammad, Ghayour-Mobarhan, Majid, Ghaderian, Seyed Mohammad Hossein
Publicado no Iran Red Crescent Med J (2016)