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Gene Mutations and Polymorphisms of TP53 and FHIT in Chronic Esophagitis and Esophageal Carcinoma
(Int Inst Anticancer Research, 2011-05-01)
Aim: The aim of this study was to investigate genetic changes of the TP53 (tumor protein p53) and FHIT (fragile histidine triad) genes in precursor lesion such as chronic esophagitis (CE) and in esophageal squamous cell ...
Gene mutations and polymorphisms of TP53 and FHIT in chronic esophagitis and esophageal carcinoma
(2011-05-01)
Aim: The aim of this study was to investigate genetic changes of the TP53 (tumor protein p53) and FHIT (fragile histidine triad) genes in precursor lesion such as chronic esophagitis (CE) and in esophageal squamous cell ...
Complete XY gonadal dysgenesis due to p.D293N homozygous mutation in the NR5A1 gene: a case study
(Polish Acad Sciences, Inst Plant GeneticsPoznanPolónia, 2010)
Mutación del gen p53 en el cáncer de colon y recto
(Sociedad Médica de Santiago, 2000)
Genomic Strategy Identifies a Missense Mutation in WD-Repeat Domain 65 (WDR65) in an Individual With Van der Woude Syndrome
(Wiley-Blackwell, 2011-06-01)
Genetic variation in the transcription factor interferon regulatory factor 6 (IRF6) causes and contributes risk for oral clefting disorders. We hypothesized that genes regulated by IRF6 are also involved in oral clefting ...
PIK3CA exon 20 mutations are associated with poor prognosis in breast cancer patients
(HOSPITAL CLINICAS, UNIV SAO PAULOSAO PAULO, 2012)
OBJECTIVES: The phosphatidylinositol 3-kinase/AKT axis is an important cell-signaling pathway that mediates cell proliferation and survival, two biological processes that regulate malignant cell growth. The phosphatidylinositol ...
APC germline mutations in families with familial adenomatous polyposis
(Spandidos Publ LtdAthensGrécia, 2013)
Molecular study in Brazilian cochlear implant recipients
(Wiley-lissHobokenEUA, 2007)