نتایج جستجو برای: dna mutational analysis

تعداد نتایج: 3221390  

Journal: :Bioinformatics 2017
Xiaoqing Huang Damian Wójtowicz Teresa M. Przytycka

Motivation Cancers arise as the result of somatically acquired changes in the DNA of cancer cells. However, in addition to the mutations that confer a growth advantage, cancer genomes accumulate a large number of somatic mutations resulting from normal DNA damage and repair processes as well as carcinogenic exposures or cancer related aberrations of DNA maintenance machinery. These mutagenic pr...

2011
Nicola Normanno Carmine Pinto Francesca Castiglione Alberto Bardelli Marcello Gambacorta Gerardo Botti Oscar Nappi Salvatore Siena Fortunato Ciardiello GianLuigi Taddei Antonio Marchetti

BACKGROUND Monoclonal antibodies directed against the epidermal growth factor receptor (EGFR) have been approved for the treatment of patients with metastatic colorectal carcinoma (mCRC) that do not carry KRAS mutations. Therefore, KRAS testing has become mandatory to chose the most appropriate therapy for these patients. METHODOLOGY/PRINCIPAL FINDINGS In order to guarantee the possibility fo...

Journal: :Molecular and Cellular Biology 1993

Journal: :Journal of Biological Chemistry 1995

Journal: :Molecular Microbiology 2010

Journal: :The Journal of clinical investigation 1997
A J Manheimer-Lory G Zandman-Goddard A Davidson C Aranow B Diamond

The F4 idiotype is a heavy chain determinant expressed almost exclusively on IgG immunoglobulins and is highly associated with specificity for double-stranded DNA. Since high-titered F4 expression is present predominantly in sera of patients with systemic lupus erythematosus (SLE), we thought F4+ IgG antibodies might constitute a useful subset of immunoglobulins in which to investigate lupus-sp...

2009
Sang-Chan Lee Hyang-Sook Kim Yeong-Eun Park Young-Chul Choi Kyu-Hyun Park Dae-Seong Kim

BACKGROUND AND PURPOSE Mutations of the skeletal muscle sodium channel gene SCN4A, which is located on chromosome 17q23-25, are associated with various neuromuscular disorders that are labeled collectively as skeletal muscle sodium channelopathy. These disorders include hyperkalemic periodic paralysis (HYPP), hypokalemic periodic paralysis, paramyotonia congenita (PMC), potassium-aggravated myo...

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