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Mutation

Genetic and Phenotypic Comparison of Facultative Methylotrophy between Methylobacterium extorquens Strains PA1 and AM1

Dipti D. Nayak, Christopher J. Marx

Genetic Features of Late Onset Primary Hemophagocytic Lymphohistiocytosis in Adolescence or Adulthood

Yini Wang, Zhao Wang, [ ... ], Ling Ye

First Report of a Deletion Encompassing an Entire Exon in the Homogentisate 1,2-Dioxygenase Gene Causing Alkaptonuria

Mohammad Zouheir Habbal, Tarek Bou-Assi, [ ... ], Farid F. Chehab

Replicative Bypass of Abasic Site in Escherichia coli and Human Cells: Similarities and Differences

Savithri Weerasooriya, Vijay P. Jasti, Ashis K. Basu

New Insights into FAK Phosphorylation Based on a FAT Domain-Defective Mutation

Xuqian Fang, Xiangfan Liu, [ ... ], Qishi Fan

Patients with Exon 19 Deletion Were Associated with Longer Progression-Free Survival Compared to Those with L858R Mutation after First-Line EGFR-TKIs for Advanced Non-Small Cell Lung Cancer: A Meta-Analysis

Yaxiong Zhang, Jin Sheng, [ ... ], Li Zhang

XLOS-Observed Mutations of MID1 Bbox1 Domain Cause Domain Unfolding

Katharine M. Wright, Kuanlin Wu, [ ... ], Michael A. Massiah

Impact of EGFR Mutation Detection Methods on the Efficacy of Erlotinib in Patients with Advanced EGFR-Wild Type Lung Adenocarcinoma

Jeng-Sen Tseng, Chih-Liang Wang, [ ... ], Gee-Chen Chang

Two Novel Tyrosinase (TYR) Gene Mutations with Pathogenic Impact on Oculocutaneous Albinism Type 1 (OCA1)

Vadieh Ghodsinejad Kalahroudi, Behnam Kamalidehghan, [ ... ], Massoud Houshmand

Molecular Genetics of the Usher Syndrome in Lebanon: Identification of 11 Novel Protein Truncating Mutations by Whole Exome Sequencing

Ramesh Reddy, Somayyeh Fahiminiya, [ ... ], Rima Slim

Orthogonal Relations and Color Constancy in Dichromatic Colorblindness

Ralph W. Pridmore

Wolfram Syndrome in the Japanese Population; Molecular Analysis of WFS1 Gene and Characterization of Clinical Features

Kimie Matsunaga, Katsuya Tanabe, [ ... ], Yukio Tanizawa

Mutation of a Salmonella Serogroup-C1-Specific Gene Abrogates O₇-Antigen Biosynthesis and Triggers NaCl-Dependent Motility Deficiency

Xiujuan Zhou, Bin Liu, Chunlei Shi, Xianming Shi

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