Associated Papers
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Elife, 2024
38277211 (PubMed )
Supplement: elife-89762-supp1.xlsx › Variants
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Biorxiv : the Preprint Server for Biology, 2023
37292598 (PubMed )
Supplement: media-1.xlsx › Variants
A synergetic effect of BARD1 mutations on tumorigenesis.
Li W et al.
Nature Communications, 2021
33623049 (PubMed )
Supplement: 41467_2021_21519_MOESM6_ESM.xlsx › Sheet1
Meta-analysis and field synopsis of genetic variants associated with the risk and severity of acute pancreatitis.
van den Berg FF et al.
Bjs Open, 2020
32011822 (PubMed )
Supplement: BJS5-4-3-s002.xlsx › OUD_Table_3
Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL.
Schrader A et al.
Nature Communications, 2018
29449575 (PubMed )
Supplement: 41467_2017_2688_MOESM20_ESM.xlsx › d__Freq_TP093
Co-existence of BRAF and NRAS driver mutations in the same melanoma cells results in heterogeneity of targeted therapy resistance.
Raaijmakers MI et al.
Oncotarget, 2016
27791198 (PubMed )
Supplement: oncotarget-07-77163-s002.xlsx › M121224
Hereditary pancreatitis: dilemmas in differential diagnosis and therapeutic approach.
Mastoraki A et al.
Journal of Gastrointestinal Cancer, 2014
Genetic background is different between sentinel and recurrent acute pancreatitis.
Masamune A et al.
Journal of Gastroenterology and Hepatology, 2011
Complete analysis of the human mesotrypsinogen gene (PRSS3) in patients with chronic pancreatitis.
Rosendahl J et al.
Pancreatology : Official Journal of the International Association of Pancreatology (iap) ... [et Al.], 2010
Trypsinogen mutations in pancreatic disorders.
Vitone LJ et al.
Endocrinology and Metabolism Clinics of North America, 2006
Genetic and biochemical characterization of the E32del polymorphism in human mesotrypsinogen.
Nemoda Z et al.
Pancreatology : Official Journal of the International Association of Pancreatology (iap) ... [et Al.], 2005
Exclusion of anionic trypsinogen and mesotrypsinogen involvement in hereditary pancreatitis without cationic trypsinogen gene mutations.
Chen JM et al.
Scandinavian Journal of Gastroenterology, 1999
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