Advertisement

Browse Subject Areas

?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

Missense mutation

Sperm parameters and mitochondrial DNA sequence variants among patients at a fertility clinic in Ghana

Bartholomew Dzudzor, Bismarck Bimah, Vincent Amarh, Augustine Ocloo

Loss-of-function of Fbxo10, encoding a post-translational regulator of BCL2 in lymphomas, has no discernible effect on BCL2 or B lymphocyte accumulation in mice

Etienne Masle-Farquhar, Amanda Russell, [ ... ], Christopher C. Goodnow

Lack of collagen α6(IV) chain in mice does not cause severe-to-profound hearing loss or cochlear malformation, a distinct phenotype from nonsyndromic hearing loss with COL4A6 missense mutation

Shaoying Tang, Tomoko Yonezawa, [ ... ], Toshitaka Oohashi

Whole-genome sequencing of SARS-CoV-2 reveals the detection of G614 variant in Pakistan

Massab Umair, Aamer Ikram, [ ... ], John Klena

Correlation of genetic alterations by whole-exome sequencing with clinical outcomes of glioblastoma patients from the Lebanese population

Fadi S. Saadeh, Rami Z. Morsi, [ ... ], Hazem I. Assi

Algorithmic assessment of missense mutation severity in the Von-Hippel Lindau protein

Francisco R. Fields, Niraja Suresh, [ ... ], Shaun W. Lee

Conserved mammalian modularity of quantitative trait loci revealed human functional orthologs in blood pressure control

Alan Y. Deng, Annie Ménard

Characterisation of ACP5 missense mutations encoding tartrate-resistant acid phosphatase associated with spondyloenchondrodysplasia

Janani Ramesh, Latha K. Parthasarathy, [ ... ], Bhuvarahamurthy Venugopal

HLA class I restricted epitopes prediction of common tumor antigens in white and East Asian populations: Implication on antigen selection for cancer vaccine design

Wei Hu, Meifang He, Liangping Li

Novel EGFR ectodomain mutations associated with ligand-independent activation and cetuximab resistance in head and neck cancer

Sindhu Nair, Hoa Q. Trummell, [ ... ], Markus Bredel

Two novel mutations in MSX1 causing oligodontia

Le Yang, Jia Liang, Haitang Yue, Zhuan Bian

Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family

Xiaodong Jiao, Shahid Y. Khan, [ ... ], S. Amer Riazuddin

Disease-associated mutations in human TUBB3 disturb netrin repulsive signaling

Qiangqiang Shao, Tao Yang, [ ... ], Guofa Liu

Advertisement

Create a weekly email alert for: Missense mutation

You can change these options by clicking profile then "Alerts and Notifications"