Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countries-Reference-Cited by-同舟云学术

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Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countries

Published:2014-02 Issue:2 Volume:535 Page:250-254
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Nouri Narges,Fazel-Najafabadi Esmat,Behnam Mahdieh,Nouri Nayereh,Aryani Omid,Ghasemi Majid,Nasiri Jafar,Sedghi Maryam

Funder

Isfahan University of Medical Sciences, Isfahan, Iran

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference29 articles.

1. Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule;Aartsma-Rus;Muscle Nerve,2006

2. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010

3. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs;Altschul;Nucleic Acids Res.,1997

4. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction;Beggs;Hum. Genet.,1990

5. Function and genetics of dystrophin and dystrophin-related proteins in muscle;Blake;Physiol. Rev.,2002

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1. A novel mutation (c.121-13T>A) in the polypyrimidine tract of the splice acceptor site of intron 2 causes exon 3 skipping in mitochondrial acetoacetyl-CoA thiolase gene;Molecular Medicine Reports;2017-04-04

2. Human MTHFR-G1793A transition may be a protective mutation against male infertility: a genetic association study and in silico analysis;Human Fertility;2017-03-07

3. Investigating polymorphisms by bioinformatics is a potential cost-effective method to screen for germline mutations in Chinese familial adenomatous polyposis patients;Oncology Letters;2016-05-30

4. Structural and functional impact of missense mutations in TPMT: An integrated computational approach;Computational Biology and Chemistry;2015-12

5. Analyses of the presence of mutations in Dystrophin protein to predict their relative influences in the onset of Duchenne Muscular Dystrophy;Cellular Signalling;2014-12

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