Hakutulokset - Mohammad KERAMATIPOUR

Identification of a Novel Mutation in CNNM4 Gene in an Iranian Family with Jalili Syndrome Tekijä Mohammad Ghofrani, Mohammad Keramatipour

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Effect of Embryonic Cerebrospinal Fluid on Proliferation and Differentiation of Neuroprogenitor Cells Tekijä Mohammad Keramatipour, Mohammad Nabiuni, Kazem Parivar, Siamak Yari

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Lack of Association between Single Nucleotide Polymorphism rs10818488 in TRAF1/C5 Region and Rheumatoid Arthritis in Iranian Population Tekijä Somayeh Ahmadlou, Mohsen Akhiani, Ahmad Salimzadeh, Mohammad Keramatipour

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SPOAN syndrome: a novel mutation and new ocular findings; a case report Tekijä Fatemeh Bazvand, Mohammad Keramatipour, Hamid Riazi-Esfahani, Alireza Mahmoudi

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Comparison of Two Different PCR-based Methods for Detection of GAA Expansions in Frataxin Gene Tekijä Mona ENTEZA­M, Akbar AMIRFIROOZI, Mansoureh TOGHA, Mohammad KERAMATIPOUR

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Functional Analysis of A Novel Splicing Mutation in The Mutase Gene of Two Unrelated Pedigrees Tekijä Somayeh Ahmadloo, Saeed Talebi, Mohammad Miryounesi, Parvin Pasalar, Mohammad Keramatipour

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Single Nucleotide Polymorphism rs 2476601 of PTPN22 Gene and Susceptibility to Rheumatoid Arthritis in Iranian Population Tekijä Somayeh Ahmadloo, Mohsen Taghizadeh, Mohsen Akhiani, Ahmad Salimzadeh, Mohammad Keramatipour

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Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation Tekijä Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Mohammad Keramatipour, Saeid Morovvati

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Investigating the Effect of rs3783605 Single-nucleotide Polymorphism on the Activity of VCAM-1 Promoter in Human Umbilical Vein Endohelial Cells Tekijä Fatemeh Dadgar Pakdel, Mohammad Keramatipour, Farshid Noorbakhsh, Saeed Talebi, Mohammad Vodjgani

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Once in a Blue Moon, a Very Rare Coexistence of Glutaric Acidemia Type I and Mucopolysaccharidosis Type IIIB in a Patient Tekijä Mohammad Reza Alaei, Meghdad Kheirkhahan, Saeed Talebi, Elham Davoudi-Dehaghani, Mohammad Keramatipour

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X-linked SCID with a rare mutation Tekijä Fatemeh Sadat Mahdavi, Mohammad Keramatipour, Sarina Ansari, Samin Sharafian, Arezou Karamzade, Marzieh Tavakol

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PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data Tekijä Mona Entezam, Mohammad Reza Khatami, Fereshteh Saddadi, Mohsen Ayati, Jamshid Roozbeh, Mohammad Keramatipour

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Investigation of the association of G-7A and T-138C single nucleotide polymorphisms on the promoter of MGP gene with renal stone Tekijä Mohammad Keramatipour, Babak Ahadi, Mohsen Taghizadeh, Ali Tabibi, Farshad Zohrabi, Babak Javanmard, Behzad Narouie

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Three Novel Variants identified in FBN1 and TGFBR2 in seven Iranian families with suspected Marfan syndrome Tekijä Fatemeh Bitarafan, Ehsan Razmara, Mehrnoosh Khodaeian, Mohammad Keramatipour, Alireza Kalhor, Ehsan Jafarinia, Masoud Garshasbi

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A comprehensive report of the clinical and mutational profiles of 30 Iranian malignant infantile osteopetrosis patients Tekijä Akbar Amirfiroozy, Maryam Naghinejad, Azim Rezamand, Hamid Farhangi, Zahra Golchehre, Hossein Jalali, Mohammad Taheri, Mohammad Keramatipour

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Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report Tekijä Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Aliagha Alishiri, Mohammad Keramatipour, Zeynab Javanfekr Shahri, Saeid Morovvati

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Identification of a Novel Mutation in the PAH Gene in an Iranian Phenylketonuria Family: A Case Report Tekijä Masoumeh RAZIPOUR, Daniz KOOSHAVAR, Elaheh ALAVINEJAD, Seyede Zahra SAJEDI, Neda MOHAJER, Aria SETOODEH, Saeed TALEBI, Mohammad KERAMATIPOUR

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Analysis of CFTR Gene Mutations in Children with Cystic Fibrosis, First Report from North-East of Iran Tekijä Atieh Mehdizadeh Hakkak, Mohammad Keramatipour, Saeid Talebi, Azam Brook, Jalil Tavakol Afshari, Amin Raazi, Hamid Reza Kianifar

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An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria Tekijä Saeed Talebi, Mona Entezam, Neda Mohajer, Golnaz-Ensieh Kazemi-sefat, Masoumeh Razipour, Somayeh Ahmadloo, Aria Setoodeh, Mohammad Keramatipour

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The importance of CDC27 in cancer: molecular pathology and clinical aspects Tekijä Golnaz Ensieh Kazemi-Sefat, Mohammad Keramatipour, Saeed Talebi, Kaveh Kavousi, Roya Sajed, Nazanin Atieh Kazemi-Sefat, Kazem Mousavizadeh

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