Computational insights of K1444N substitution in GAP-related domain of NF1 gene associated with neurofibromatosis type 1 disease: a molecular modeling and dynamics approach
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical),Biochemistry
Link
http://link.springer.com/article/10.1007/s11011-018-0251-1/fulltext.html
Reference97 articles.
1. Abdel-Azeim S, Oliva R, Chermak E et al (2014) Molecular dynamics characterization of five pathogenic factor X mutants associated with decreased catalytic activity. Biochemistry 53:6992–7001. https://doi.org/10.1021/bi500770p
2. Acharya V, Nagarajaram HA (2012) Hansa: an automated method for discriminating disease and neutral human nsSNPs. Hum Mutat 33:332–337. https://doi.org/10.1002/humu.21642
3. Adjei AA (2001) Blocking oncogenic Ras signaling for cancer therapy. J Natl Cancer Inst 93:1062–1074. https://doi.org/10.1016/S0378-4274(02)00422-8
4. Adzhubei IA, Schmidt S, Peshkin L et al (2010) A method and server for predicting damaging missense mutations. Nat Methods 7:248–249
5. Agrahari A, George Priya Doss C (2015) Impact of I30T and I30M substitution in MPZ gene associated with Dejerine-Sottas syndrome type B (DSSB): a molecular modeling and dynamics. J Theor Biol 382:23–33. https://doi.org/10.1016/j.jtbi.2015.06.019
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