Identification of a Novel Mutation in CNNM4 Gene in an Iranian Family with Jalili Syndrome

by Mohammad Ghofrani, Mohammad Keramatipour
Published 2019-10-01

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

by Mohammad Keramatipour, Mohammad Nabiuni, Kazem Parivar, Siamak Yari
Published 2013-01-01

Lack of Association between Single Nucleotide Polymorphism rs10818488 in TRAF1/C5 Region and Rheumatoid Arthritis in Iranian Population

by Somayeh Ahmadlou, Mohsen Akhiani, Ahmad Salimzadeh, Mohammad Keramatipour
Published 2014-02-01

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

by Mona ENTEZA­M, Akbar AMIRFIROOZI, Mansoureh TOGHA, Mohammad KERAMATIPOUR
Published 2017-02-01

SPOAN syndrome: a novel mutation and new ocular findings; a case report

by Fatemeh Bazvand, Mohammad Keramatipour, Hamid Riazi-Esfahani, Alireza Mahmoudi
Published 2021-01-01

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

by Somayeh Ahmadloo, Saeed Talebi, Mohammad Miryounesi, Parvin Pasalar, Mohammad Keramatipour
Published 2016-09-01

Single Nucleotide Polymorphism rs 2476601 of PTPN22 Gene and Susceptibility to Rheumatoid Arthritis in Iranian Population

by Somayeh Ahmadloo, Mohsen Taghizadeh, Mohsen Akhiani, Ahmad Salimzadeh, Mohammad Keramatipour
Published 2015-10-01

Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation

by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Mohammad Keramatipour, Saeid Morovvati
Published 2021-09-01

Investigating the Effect of rs3783605 Single-nucleotide Polymorphism on the Activity of VCAM-1 Promoter in Human Umbilical Vein Endohelial Cells

by Fatemeh Dadgar Pakdel, Mohammad Keramatipour, Farshid Noorbakhsh, Saeed Talebi, Mohammad Vodjgani
Published 2015-04-01

Once in a Blue Moon, a Very Rare Coexistence of Glutaric Acidemia Type I and Mucopolysaccharidosis Type IIIB in a Patient

by Mohammad Reza Alaei, Meghdad Kheirkhahan, Saeed Talebi, Elham Davoudi-Dehaghani, Mohammad Keramatipour
Published 2020-05-01

X-linked SCID with a rare mutation

by Fatemeh Sadat Mahdavi, Mohammad Keramatipour, Sarina Ansari, Samin Sharafian, Arezou Karamzade, Marzieh Tavakol
Published 2021-10-01

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

by Mona Entezam, Mohammad Reza Khatami, Fereshteh Saddadi, Mohsen Ayati, Jamshid Roozbeh, Mohammad Keramatipour
Published 2016-06-01

Investigation of the association of G-7A and T-138C single nucleotide polymorphisms on the promoter of MGP gene with renal stone

by Mohammad Keramatipour, Babak Ahadi, Mohsen Taghizadeh, Ali Tabibi, Farshad Zohrabi, Babak Javanmard, Behzad Narouie
Published 2018-05-01

Three Novel Variants identified in FBN1 and TGFBR2 in seven Iranian families with suspected Marfan syndrome

by Fatemeh Bitarafan, Ehsan Razmara, Mehrnoosh Khodaeian, Mohammad Keramatipour, Alireza Kalhor, Ehsan Jafarinia, Masoud Garshasbi
Published 2020-08-01

Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report

by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Aliagha Alishiri, Mohammad Keramatipour, Zeynab Javanfekr Shahri, Saeid Morovvati
Published 2021-02-01

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

by Atieh Mehdizadeh Hakkak, Mohammad Keramatipour, Saeid Talebi, Azam Brook, Jalil Tavakol Afshari, Amin Raazi, Hamid Reza Kianifar
Published 2013-08-01

Identification of a Novel Mutation in the PAH Gene in an Iranian Phenylketonuria Family: A Case Report

by Masoumeh RAZIPOUR, Daniz KOOSHAVAR, Elaheh ALAVINEJAD, Seyede Zahra SAJEDI, Neda MOHAJER, Aria SETOODEH, Saeed TALEBI, Mohammad KERAMATIPOUR
Published 2017-04-01

The importance of CDC27 in cancer: molecular pathology and clinical aspects

by Golnaz Ensieh Kazemi-Sefat, Mohammad Keramatipour, Saeed Talebi, Kaveh Kavousi, Roya Sajed, Nazanin Atieh Kazemi-Sefat, Kazem Mousavizadeh
Published 2021-03-01

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

by Saeed Talebi, Mona Entezam, Neda Mohajer, Golnaz-Ensieh Kazemi-sefat, Masoumeh Razipour, Somayeh Ahmadloo, Aria Setoodeh, Mohammad Keramatipour
Published 2016-07-01

CTLA-4 Gene Polymorphisms (-318C/T, +49A/G, +6230A/G) in Iranian Patients with Multiple Sclerosis

by Abolfazl Heidari, Mohammad Keramatipour, Ali Akbar Amirzargar, Ali Rashidinezhad, Ahmad Ali Sahmani, Hossein Mozhdehipanah, Mohammad Reza Noori Daloii
Published 2010-12-01