„Mutations“
Suchergebnisse
1.000+ Treffer
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Molecular Profile of Subungual Melanoma: A MelaNostrum Consortium Study of 68 Cases Reporting BRAF, NRAS, KIT, and TERT Promoter Status
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Clinical, biological, electrophysiological and therapeutic profile of patients with anti-MAG neuropathy according to MYD88L265P and CXCR4 mutations and underlying haemopathy
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Longitudinal analyses of CLL in mice identify leukemia-related clonal changes including a Myc gain predicting poor outcome in patients
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Cutaneous epithelioid haemangiomas show somatic mutations in the mitogen-activated protein kinase pathway
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Somatic BRCA1 mutations in clinically sporadic breast cancer with medullary histological features
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Gaining insight into crizotinib resistance mechanisms caused by L2026M and G2032R mutations in ROS1 via molecular dynamics simulations and free-energy calculations
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Focal segmental glomerulosclerosis and medullary nephrocalcinosis in children with ADCK4 mutations
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Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes disease
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Emerging role of mutations in epigenetic regulators including MLL2 derived from The Cancer Genome Atlas for cervical cancer
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An association study between CHEK2 gene mutations and susceptibility to breast cancer
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Targeted next-generation sequencing identified novel mutations in triple-negative myeloproliferative neoplasms
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Central nervous system progression in advanced non–small cell lung cancer patients with EGFR mutations in response to first-line treatment with two EGFR-TKIs, gefitinib and erlotinib: a comparative study
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Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment
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Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder
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A Psychological Perspective on Factors Predicting Prophylactic Salpingo-Oophorectomy in a Sample of Italian Women from the General Population. Results from a Hypothetical Study in the Context of BRCA Mutations
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Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations
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Mitochondrial mutations in maternally inherited hearing loss
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Clinically proven mtDNA mutations are not common in those with chronic fatigue syndrome
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Mutations in catalase-peroxidase KatG from isoniazid resistant Mycobacterium tuberculosis clinical isolates: insights from molecular dynamics simulations
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Identification of two novel mutations in the SLC45A2 gene in a Hungarian pedigree affected by unusual OCA type 4