„Mutations“
Suchergebnisse
10.000+ Treffer
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SDHA loss of function mutations in a subset of young adult wild-type gastrointestinal stromal tumors
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Impact of complex NOTCH1 mutations on survival in paediatric T-cell leukaemia
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Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countries
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Somatic mitochondrial DNA mutations in cancer escape purifying selection and high pathogenicity mutations lead to the oncocytic phenotype: pathogenicity analysis of reported somatic mtDNA mutations in tumors
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Frequency of CDH1 germline mutations in gastric carcinoma coming from high- and low-risk areas: metanalysis and systematic review of the literature
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Hepatitis B virus core promoter mutations G1613A and C1653T are significantly associated with hepatocellular carcinoma in genotype C HBV-infected patients
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Germ-line mutations in epidermal growth factor receptor (EGFR) are rare but may contribute to oncogenesis: A novel germ-line mutation in EGFR detected in a patient with lung adenocarcinoma
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FLT3 mutations in canine acute lymphocytic leukemia
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Limited importance of the dominant-negative effect of TP53missense mutations
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Mutational profiling reveals PIK3CA mutations in gallbladder carcinoma
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Simplifying the detection of MUTYH mutations by high resolution melting analysis
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Colorectal carcinomas with microsatellite instability display a different pattern of target gene mutations according to large bowel site of origin
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Combined mutations of ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in myelodysplastic syndromes and acute myeloid leukemias
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Comparing the frequency of common genetic variants and haplotypes between carriers and non-carriers of BRCA1 and BRCA2deleterious mutations in Australian women diagnosed with breast cancer before 40 years of age
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Mutations in the WTX- gene are found in some high-grade microsatellite instable (MSI-H) colorectal cancers
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Dietary, lifestyle and clinicopathological factors associated with BRAF and K-ras mutations arising in distinct subsets of colorectal cancers in the EPIC Norfolk study
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BRCA1-mutated and basal-like breast cancers have similar aCGH profiles and a high incidence of protein truncating TP53 mutations
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Potential pitfalls in MitoChip detected tumor-specific somatic mutations: a call for caution when interpreting patient data
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Canine and human gastrointestinal stromal tumors display similar mutations in c-KIT exon 11
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Target enzyme mutations are the molecular basis for resistance towards pharmacological inhibition of nicotinamide phosphoribosyltransferase