Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Plos Genetics|January 13, 2017
Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and MiceMartina M A Muggenthaler, Biswajit Chowdhury, S Naimul Hasan, et al.
JCI Insight|March 22, 2024
Characterization of HMGA2 variants expands the spectrum of Silver-Russell syndromeAvinaash V Maharaj, Emily Cottrell, Thatchawan Thanasupawat, et al.
Science Translational Medicine|April 25, 2014
Aspirin and the risk of colorectal cancer in relation to the expression of 15-hydroxyprostaglandin dehydrogenase (HPGD)Stephen P Fink, Mai Yamauchi, Reiko Nishihara, et al.
Carcinogenesis|December 16, 2014
Sulindac reversal of 15-PGDH-mediated resistance to colon tumor chemoprevention with NSAIDsStephen P Fink, Dawn M Dawson, Yongyou Zhang, et al.
Cancer Prevention Research (Philadelphia, Pa.)|May 20, 2014
Inactivating mutation in the prostaglandin transporter gene, SLCO2A1, associated with familial digital clubbing, colon neoplasia, and NSAID resistanceKishore Guda, Stephen P Fink, Ginger L Milne, et al.
Cancer Investigation|April 8, 2011
15-hydroxyprostaglandin dehydrogenase is downregulated and exhibits tumor suppressor activity in gastric cancerHo June Song, Seung-Jae Myung, In-Wha Kim, et al.
Oncotarget|October 6, 2015
Induction of KIAA1199/CEMIP is associated with colon cancer phenotype and poor patient survivalStephen P Fink, Lois L Myeroff, Revital Kariv, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 28, 2009
15-Hydroxyprostaglandin dehydrogenase inactivation as a mechanism of resistance to celecoxib chemoprevention of colon tumorsMin Yan, Seung-Jae Myung, Stephen P Fink, et al.
Plos One|September 19, 2017
A nonrandomized trial of vitamin D supplementation for Barrett's esophagusLinda C Cummings, Prashanthi N Thota, Joseph E Willis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Elucidating the clinical spectrum and molecular basis of HYAL2 deficiencyJames Fasham, Siying Lin, Promita Ghosh, et al.
Pageof 6