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Deletion mutation

Development of an immuno-wall device for the rapid and sensitive detection of EGFR mutations in tumor tissues resected from lung cancer patients

Naoyuki Yogo, Tetsunari Hase, [ ... ], Yoshinori Hasegawa

The Ribosomal Biogenesis Protein Utp21 Interacts with Hsp90 and Has Differing Requirements for Hsp90-Associated Proteins

Victoria R. Tenge, Jared Knowles, Jill L. Johnson

The PitA protein contributes to colistin susceptibility in Pseudomonas aeruginosa

Mareike B. Erdmann, Paul P. Gardner, Iain L. Lamont

Improved transformation efficiency of group A Streptococcus by inactivation of a type I restriction modification system

Meredith B. Finn, Kathryn M. Ramsey, [ ... ], Michael R. Wessels

Identification of a Novel Mutation in the COL2A1 Gene in a Chinese Family with Spondyloepiphyseal Dysplasia Congenita

Xiangjun Huang, Xiong Deng, [ ... ], Hao Deng

Arrhythmogenic Biophysical Phenotype for SCN5A Mutation S1787N Depends upon Splice Variant Background and Intracellular Acidosis

Rou-Mu Hu, Bi-Hua Tan, [ ... ], Jonathan C. Makielski

Elovl4 5-bp deletion does not accelerate cone photoreceptor degeneration in an all-cone mouse

Christian Schori, Martin-Paul Agbaga, [ ... ], Marijana Samardzija

Alterations in the mir-15a/16-1 Loci Impairs Its Processing and Augments B-1 Expansion in De Novo Mouse Model of Chronic Lymphocytic Leukemia (CLL)

Siddha Kasar, Chingiz Underbayev, [ ... ], Mona Batish

No Evidence for Pathogenic Role of UBQLN2 Mutations in Sporadic Amyotrophic Lateral Sclerosis in the Mainland Chinese Population

Xiao Huang, Shen Shen, Dongsheng Fan

A RT-qPCR system using a degenerate probe for specific identification and differentiation of SARS-CoV-2 Omicron (B.1.1.529) variants of concern

Randi Jessen, Line Nielsen, [ ... ], Katja Spiess

Comparison of Epidermal Growth Factor Receptor Mutations between Metastatic Lymph Node Diagnosed by EBUS-TBNA and Primary Tumor in Non-Small Cell Lung Cancer

Hyo Jae Kang, Bin Hwangbo, [ ... ], Geon-Kook Lee

Discovery of a Novel Mutation (X8Del) Resulting in an 8-bp Deletion in the Hepatitis B Virus X Gene Associated with Occult Infection in Korean Vaccinated Individuals

Hong Kim, Jeong-Ryeol Gong, Seoung-Ae Lee, Bum-Joon Kim

Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents

Nidaa A. Ababneh, Dema Ali, [ ... ], Abdalla Awidi

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