Search Result "missense mutation"
Computational Approaches for Predicting Causal Missense Mutations in Cancer Genome Projects
Journal: Current Bioinformatics
Volume: 3 Issue: 1 Year: 2008 Page: 46-55
Author(s): Zemin Zhang, Lawrence S. Hon, Joshua S. Kaminker
Effect of Disease Causing Missense Mutations on Intrinsically DisorderedRegions in Proteins
Journal: Protein & Peptide Letters
Volume: 29 Issue: 3 Year: 2022 Page: 254-267
Author(s): Hampapathalu A. Nagarajaram,Suryanarayana Seera
Disease Risk of Missense Mutations Using Structural Inference from Predicted Function
Journal: Current Protein & Peptide Science
Volume: 11 Issue: 7 Year: 2010 Page: 573-588
Author(s): Jeremy A. Horst, Kai Wang, Orapin V. Horst, Michael L. Cunningham, Ram Samudrala
In Silico Identification and Analysis of Drug Resistant Mutants of ABL Tyrosine Kinase Based on Detrimental Missense Mutations
Journal: Current Signal Transduction Therapy
Volume: 6 Issue: 3 Year: 2011 Page: 396-404
Author(s): R. Rajasekaran, C. George Priya Doss, G. Arun Prasad, Rao Sethumadhavan
TargetMM: Accurate Missense Mutation Prediction by Utilizing Local and Global Sequence Information with Classifier Ensemble
Journal: Combinatorial Chemistry & High Throughput Screening
Volume: 25 Issue: 1 Year: 2022 Page: 38-52
Author(s): Fang Ge,Jun Hu,Yi-Heng Zhu,Muhammad Arif,Dong-Jun Yu
Identification of a Missense Mutation in the α-galactosidase A Gene in a Chinese Family with Fabry Disease
Journal: Current Genomics
Volume: 19 Issue: 1 Year: 2018 Page: 70-75
Author(s): Yuan Wu,Hong Xia,Jinzhong Yuan,Hongbo Xu,Xiong Deng,Jun Liu,Hao Zhang,Hao Deng
In Silico Criterion for Prediction of Effects of p53 Gene Missense Mutations on p53-Mdm2 Feedback Loop
Journal: Protein & Peptide Letters
Volume: 13 Issue: 8 Year: 2006 Page: 807-814
Author(s): Nevena Veljkovic, Vladimir Perovic
Abdomen Malignant Myxoid Leiomyosarcoma with PDGFRA and TP53Missense Mutation: A Case Report
Journal: Current Cancer Therapy Reviews
Volume: 20 Issue: 5 Year: 2024 Page: 517-521
Author(s):
Frontotemporal Dementia Caused by CHMP2B Mutations
Journal: Current Alzheimer Research
Volume: 8 Issue: 3 Year: 2011 Page: 246-251
Author(s): A. M. Isaacs, P. Johannsen, I. Holm, J. E. Nielsen, FReJA Consortium
Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T)#
Journal: Cardiovascular & Hematological Disorders-Drug Targets
Volume: 17 Issue: 2 Year: 2017 Page: 136-141
Author(s): Antonio Girolami,Salvador Minoldo,Silvia Ferrari,Diego Colussi,Anna Maria Lombardi,Hugo Guglielmone