„Mutations“
Suchergebnisse
10.000+ Treffer
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Histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six H3F3A mutated cases
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The dual combination therapy panobinostat-lorlatinib is effective against neuroblastomas harboring genomic TERT rearrangements and ALK mutations
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Author Correction: Loss-of-function mutations in PLD4 lead to systemic lupus erythematosus
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Validierung eines etablierten IGHV-Mutationsstatus-Test und die klinische Bedeutung des IGHV-Mutationsstatus bei Patienten mit chronisch lymphatischer Leukämie
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La Genèse de Raoul de Presles. Éditée par Martine Pagan, suivi de Une Babel indécise. Mutations de la Genèse en langue d’oïl (XII e -XIV e siècle). Paris: Honoré Champion, 2021 (« Classiques français du Moyen, 196 »), 543 pp.
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Generation of two hiPSCs lines of two patients carrying truncating mutations in the dimerization domain of filamin C
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Clinical, Immunological, and Genetic Features in Patients with NFKB1 and NFKB2 Mutations: a Systematic Review
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Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling
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Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer
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Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4
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Downregulation of SFRP1 is a protumorigenic event in hepatoblastoma and correlates with beta-catenin mutations
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Crybb2 Mutations Consistently Affect Schizophrenia Endophenotypes in Mice
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Mediation analysis reveals common mechanisms of RUNX1 point mutations and RUNX1/RUNX1T1 fusions influencing survival of patients with acute myeloid leukemia
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A specific screen for oligosaccharyltransferase mutations identifies the 9 kDa OST5 protein required for optimal activity in vivo and in vitro
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Mammalian Raf‐1 is activated by mutations that restore Raf signaling in Drosophila
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Two nuclear mutations disrupt distinct pathways for targeting proteins to the chloroplast thylakoid.
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Mutagen sensitivity and suppression of position‐effect variegation result from mutations in mus209, the Drosophila gene encoding PCNA.
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The embryonic expression of the Notch locus of Drosophila melanogaster and the implications of point mutations in the extracellular EGF‐like domain of the predicted protein.
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Molecular cloning, DNA structure, and RNA analysis of the arginase gene in Saccharomyces cerevisiae. A study of cis‐dominant regulatory mutations.
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In-depth assessment of BRAF, NRAS, KRAS, EGFR, and PIK3CA mutations on cell-free DNA in the blood of melanoma patients receiving immune checkpoint inhibition