PubTator4TogoVar  

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source DB source ID text size updated at # proj. # Ann. updated_at
PubMed 34907358 Distal mutation V486M disrupts the catalytic activity of DPP4 by affecting the flap of the propeller domain. Dipeptidyl peptidase-4 (DPP4) plays a crucial role in regulating the bioactivity of glucago 1.44 KB 2024-01-10 1 0
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PMC 3875916 Dietary Magnesium and Genetic Interactions in Diabetes and Related Risk Factors: A Brief Overview of Current Knowledge Abstract Nutritional genomics has exploded in the last decade, yielding insights 43.3 KB 2025-10-02 5 9
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PubMed 12352684 Functional study of GJB2 in hereditary hearing loss. OBJECTIVES/HYPOTHESIS: The gene of the gap junction protein connexin 26 (Cx26) was found to be the main causative gene of autosomal recessive nonsy 1.82 KB 2015-11-17 2 0
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PMC 10713754 Causal relationship between psychiatric traits and temporomandibular disorders: a bidirectional two-sample Mendelian randomization study Abstract Objectives This study was to investigate the causal r 24.4 KB 2025-10-02 3 0
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PubMed 25127677 Nicotine promotes initiation and progression of KRAS-induced pancreatic cancer via Gata6-dependent dedifferentiation of acinar cells in mice. BACKGROUND & AIMS: Although smoking is a leading risk fact 2.31 KB 2015-11-27 7 0
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PubMed 17964839 Beta-ureidopropionase deficiency presenting with congenital anomalies of the urogenital and colorectal systems. Beta-ureidopropionase deficiency (McKusick 606673) is an autosomal recessive condition c 1.14 KB 2015-11-23 10 0
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PubMed 21362127 Common large partial VWF gene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population. BACKGROUND: Type 3 von Willebrand disease (VWD) is an autosomal 1.79 KB 2015-11-26 5 0
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PMC 6393335 Association Between ERCC1 rs3212986 and ERCC2/XPD rs1799793 and OS in Patients With Advanced Esophageal Cancer Abstract Esophageal cancer (EC) is a very aggressive tumor, and no reliable prognostic m 25.2 KB 2025-10-02 5 79
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PubMed 26537299 SERPINE1 rs1799768 polymorphism contributes to sepsis risk and mortality. INTRODUCTION: The present meta-analysis aimed to investigate whether there is an association between SERPINE1 rs1799768 polymo 1.43 KB 2025-10-02 6 7
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PubMed 12574942 Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH). Hereditary cystathioninuria (MIM 219500) is presumed to be caused by deficiency of the 1.35 KB 2015-11-18 3 0
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