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

Molecular Cloning, Expression Pattern and Polymorphisms of NADPH-Cytochrome P450 Reductase in the Bird Cherry-Oat Aphid Rhopalosiphum padi (L.)

Kang Wang, Xiong Peng, [ ... ], Maohua Chen

Diverse Basis of β-Catenin Activation in Human Hepatocellular Carcinoma: Implications in Biology and Prognosis

Hirohisa Okabe, Hiroki Kinoshita, [ ... ], Yoshihiko Maehara

Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia)

Alexander Y. Сhurbanov, Tatiana M. Karafet, [ ... ], Olga L. Posukh

Involvement of Endoplasmic Reticulum Stress in TULP1 Induced Retinal Degeneration

Glenn P. Lobo, Adrian Au, Philip D. Kiser, Stephanie A. Hagstrom

Missense Mutations Allow a Sequence-Blind Mutant of SpoIIIE to Successfully Translocate Chromosomes during Sporulation

Baundauna Bose, Sydney E. Reed, Marina Besprozvannaya, Briana M. Burton

High Frequency of Pulmonary Hypertension-Causing Gene Mutation in Chinese Patients with Chronic Thromboembolic Pulmonary Hypertension

Qunying Xi, Zhihong Liu, [ ... ], Zhiwei Huang

FANCA Gene Mutations with 8 Novel Molecular Changes in Indian Fanconi Anemia Patients

Avani Solanki, Purvi Mohanty, [ ... ], Babu Rao Vundinti

Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing

Nicole Weisschuh, Anja K. Mayer, [ ... ], Bernd Wissinger

Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association

Slađana Andrejević, Peter Korošec, [ ... ], Matija Rijavec

A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia

Haochen Liu, Tingting Ding, Yuan Zhan, Hailan Feng

Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts

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

Functional Impact of 14 Single Nucleotide Polymorphisms Causing Missense Mutations of Human α7 Nicotinic Receptor

Qinhui Zhang, Yingjie Du, [ ... ], Yongchang Chang

Overexpression of Both ERG11 and ABC2 Genes Might Be Responsible for Itraconazole Resistance in Clinical Isolates of Candida krusei

Xiaoyuan He, Mingfeng Zhao, [ ... ], Tao Sui

Advertisement

Create a weekly email alert for: Missense mutation

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