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American Journal of Human Genetics|May 26, 2009
Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndromeJoy Armistead, Sunita Khatkar, Britta Meyer, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|September 18, 2023
Enzymatic Resolution and Decarboxylative Functionalization of α-Sulfinyl EstersSuraksha Gahalawat, Yesu Addepalli, Stephen P Fink, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 1, 2019
SPAM1/HYAL5 double deficiency in male mice leads to severe male subfertility caused by a cumulus-oocyte complex penetration defectSoojin Park, Young-Hyun Kim, Pil-Soo Jeong, et al.
Biology Open|September 8, 2025
Generation of mice with combined Hexa Gly269Ser KI or KO and Neu3 KO alleles to create new models of GM2 gangliosidosesEmily N Barker, Mehrafarin Ashiri, Jennifer T Saville, et al.
Oncogene|December 8, 2004
Colon cancer secreted protein-2 (CCSP-2), a novel candidate serological marker of colon neoplasiaBaozhong Xin, Petra Platzer, Stephen P Fink, et al.
Cancer Research|August 5, 2008
Ugene, a newly identified protein that is commonly overexpressed in cancer and binds uracil DNA glycosylaseChunguang Guo, Xiaodong Zhang, Stephen P Fink, et al.
Plos One|May 30, 2013
Genetic variation in 15-hydroxyprostaglandin dehydrogenase and colon cancer susceptibilityCheryl L Thompson, Stephen P Fink, James D Lutterbaugh, et al.
American Journal of Human Genetics|May 15, 2012
GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndromeDan Doherty, Albert E Chudley, Gail Coghlan, et al.
Nature Communications|February 11, 2023
Small molecule inhibitors of 15-PGDH exploit a physiologic induced-fit closing systemWei Huang, Hongyun Li, Janna Kiselar, et al.
Digestive Diseases and Sciences|April 30, 2013
Colonic 15-PGDH levels are stable across distance and time and are not perturbed by aspirin interventionStephen P Fink, Dong-Hoon Yang, Jill S Barnholtz-Sloan, et al.
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