„Mutations“
Suchergebnisse
10.000+ Treffer
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KIT and BRAF heterogeneous mutations in gastrointestinal stromal tumors after secondary imatinib resistance
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Identification of potential mutations and genomic alterations in the epithelial and spindle cell components of biphasic synovial sarcomas using a human exome SNP chip
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BRCA1, BRCA2 and PALB2 mutations and CHEK2 c.1100delC in different South African ethnic groups diagnosed with premenopausal and/or triple negative breast cancer
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Next-generation sequencing of tyrosine kinase inhibitor-resistant non-small-cell lung cancers in patients harboring epidermal growth factor-activating mutations
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A kinome siRNA screen identifies HGS as a potential target for liver cancers with oncogenic mutations in CTNNB1
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Clinical detection and categorization of uncommon and concomitant mutations involving BRAF
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Whole exome sequencing of microdissected splenic marginal zone lymphoma: a study to discover novel tumor-specific mutations
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Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes
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ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases
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Targeted exome sequencing reveals novel USH2A mutations in Chinese patients with simplex Usher syndrome
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Biochemical effects of mutations in the gene encoding the alpha subunit of eukaryotic initiation factor (eIF) 2B associated with Vanishing White Matter disease
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NPHS2 mutations account for only 15 % of nephrotic syndrome cases
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Next-generation-sequencing-based identification of familial hypercholesterolemia-related mutations in subjects with increased LDL–C levels in a latvian population
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Novel FOXL2 mutations in two Chinese families with blepharophimosis-ptosis-epicanthus inversus syndrome
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Genetic mutations in SPINK1, CFTR, CTRC genes in acute pancreatitis
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Production of infectious HCV genotype 1b virus in cell culture using a novel Set of adaptive mutations
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High prevalence of TERT promoter mutations in micropapillary urothelial carcinoma
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Identification of novel senataxin mutations in Chinese patients with autosomal recessive cerebellar ataxias by targeted next-generation sequencing
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Novel mutations in quinolone resistance-determining regions of gyrA, gyrB, parC and parE in Shigella flexneri clinical isolates from eastern Chinese populations between 2001 and 2011
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Genetic causes of Parkinson’s disease in the Maltese: a study of selected mutations in LRRK2, MTHFR, QDPR and SPR