A two-microRNA signature as a diagnostic and prognostic marker of pancreatic adenocarcinoma
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Assay May Help Avoid Needless Prostate Biopsies.
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Assay May Help Avoid Needless Prostate Biopsies.
Interferon λ cures persistent murine norovirus infection in the absence of adaptive immunity.
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Disruption of the PRKCD–FBXO25–HAX-1 axis attenuates the apoptotic response and drives lymphomagenesis.
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A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death.
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Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy.
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Variation at HLA-DRB1 is associated with resistance to enteric fever.
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Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease.
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Rescue of Hippo coactivator YAP1 triggers DNA damage–induced apoptosis in hematological cancers
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Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine
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Recurrent gain-of-function mutations of RHOA in diffuse-type gastric carcinoma
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Recurrent PAX3-MAML3 fusion in biphenotypic sinonasal sarcoma
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CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation
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Activating Hotspot L205R Mutation in PRKACA and Adrenal Cushing's Syndrome
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The ryanodine receptor store-sensing gate controls Ca2+ waves and Ca2+-triggered arrhythmias.
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RIPK3 as a potential therapeutic target for Gaucher's disease.
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Fas ligand–mediated immune surveillance by T cells is essential for the control of spontaneous B cell lymphomas.
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Evolution and transmission of drug-resistant tuberculosis in a Russian population.
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RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia.
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Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes.
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