„Mutations“
Suchergebnisse
10.000+ Treffer
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A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype
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Comprehensive analyses of mutations and hepatitis B virus integration in hepatocellular carcinoma with clinicopathological features
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Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57
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Dominant Splice Site Mutations in PIK3R1 Cause Hyper IgM Syndrome, Lymphadenopathy and Short Stature
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Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes
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Searching for potential microRNA-binding site mutations amongst known disease-associated 3′ UTR variants
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Loss of nonsense mediated decay suppresses mutations in Saccharomyces cerevisiae TRA1
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High resolution mapping and positional cloning of ENU-induced mutations in the Rw region of mouse chromosome 5
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Sex enhances adaptation by unlinking beneficial from detrimental mutations in experimental yeast populations
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Standing variation and new mutations both contribute to a fast response to selection for flowering time in maize inbreds
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Phenotypic effect of mutations in evolving populations of RNA molecules
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Loss-of-function mutations affecting a specific Glycine max R2R3 MYB transcription factor result in brown hilum and brown seed coats
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High resolution melting analysis for the detection of EMS induced mutations in wheat Sbella genes
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Translation reinitiation and development are compromised in similar ways by mutations in translation initiation factor eIF3h and the ribosomal protein RPL24
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Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation
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Effects of missense mutations in sortase A gene on enzyme activity in Streptococcus mutans
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Novel COL2A1 mutations causing spondyloepiphyseal dysplasia congenita in three unrelated Chinese families
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Identical TP53 mutations in pelvic carcinosarcomas and associated serous tubal intraepithelial carcinomas provide evidence of their clonal relationship
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Deciphering intra-tumor heterogeneity of lung adenocarcinoma confirms that dominant, branching, and private gene mutations occur within individual tumor nodules
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Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits