„Mutations“
Suchergebnisse
10.000+ Treffer
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Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women
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Hirschsprung Disease – Clinical Relevance of RET Mutations
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Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria
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Adhesion of Escherichia coli under flow conditions reveals potential novel effects of FimH mutations
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RETRACTED ARTICLE: Prevalence of the C282Y and H63D mutations of the HFE hemochromatosis gene in Azerian major β-thalassemia and iron overload
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FasL −844T/C and Fas −1377G/A: mutations of pulmonary adenocarcinoma in South China and their clinical significances
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Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VI
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Epidemiological study of HER-2 mutations among EGFR wild-type lung adenocarcinoma patients in China
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Reproductive Decision-Making in Women with BRCA1/2 Mutations
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Comparison between two amplicon-based sequencing panels of different scales in the detection of somatic mutations associated with gastric cancer
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Investigating the effects of point mutations on the affinity between the cyanobacterial lectin microvirin and high mannose-type glycans present on the HIV envelope glycoprotein
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Decreased urinary excretion of the ectodomain form of megalin (A-megalin) in children with OCRL gene mutations
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JAK2V617F and calreticulin mutations in recurrent venous thromboembolism: results from the EDITH prospective cohort
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Timing of renal replacement therapy does not influence survival and growth in children with congenital nephrotic syndrome caused by mutations in NPHS1: data from the ESPN/ERA-EDTA Registry
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Recurrent KIF2A mutations are responsible for classic lissencephaly
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Functional characterization of missense mutations in severe methylenetetrahydrofolate reductase deficiency using a human expression system
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The effect of losartan therapy on ventricular function in Marfan patients with haploinsufficient or dominant negative FBN1 mutations
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The potential of a multiplex high-throughput molecular assay for early detection of first and second line tuberculosis drug resistance mutations to improve infection control and reduce costs: a decision analytical modeling study
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Direct stacking of sequence-specific nuclease-induced mutations to produce high oleic and low linolenic soybean oil
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Genome-wide association study for hereditary ataxia in the Parson Russell Terrier and DNA-testing for ataxia-associated mutations in the Parson and Jack Russell Terrier