William S. Sly - Concepedia

Author

William S. Sly

Saint Louis University

Also Known As

Larry Shapiro, W S Sly, W Sly, W. S. Sly, W. Sly, W.S. Sly, WILLIAM S. SLY, William S Sly, William S. Sly, William SLY

389

Publications

29.7K

Citations

H-Index

270

Concepts

All Affiliations

Saint Louis University Washington University in St. Louis University of Oulu Tampere University Hospital

About

William S. Sly is an author at Saint Louis University specializing in medicine, biochemistry, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	63	141	13.8K
2	Natural Sciences	38	55	5.9K
3	Health Sciences	14	15	2.1K
4	Engineering	7	7	218
5	Public Health	1	1	29

William S. Sly

277

Publications

26K

Citations

H-Index

Page 1

	Year	Citations
Chloroquine inhibits lysosomal enzyme pinocytosis and enhances lysosomal enzyme secretion by impairing receptor recycling. Alfonso González‐Noriega, Jeffrey H. Grubb, Venugopal D. Talkad, The Journal of Cell Biology Bioorganic ChemistryMolecular BiologyEnzymatic ModificationBioanalysisEndocytic Pathway	1980	741
Expression of Hypoxia-Inducible Cell-Surface Transmembrane Carbonic Anhydrases in Human Cancer Sergey V. Ivanov, Shu‐Yuan Liao, Alla Ivanova, American Journal Of Pathology Tumor BiologyTumor MicroenvironmentBiochemistryNatural SciencesRedox Regulator	2001	675
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification. William S. Sly, David Hewett‐Emmett, Michael P. Whyte, Proceedings of the National Academy of Sciences Electrolyte DisorderCarbonic Anhydrase IiPathologyCerebral CalcificationOsteoporosis	1983	618
Phosphohexosyl components of a lysosomal enzyme are recognized by pinocytosis receptors on human fibroblasts. A Kaplan, Daniel T. Achord, William S. Sly Proceedings of the National Academy of Sciences GlycobiologyPhosphohexosyl ComponentsCharge HeterogeneityCulture MediumCellular Physiology	1977	576
HFE gene knockout produces mouse model of hereditary hemochromatosis Xiao Zhou, Shunji Tomatsu, Robert E. Fleming, Proceedings of the National Academy of Sciences	1998	527
Beta glucuronidase deficiency: Report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosis William S. Sly, Barbara A. Quinton, William H. McAlister, The Journal of Pediatrics MedicineGlycobiologyPathologyNew MucopolysaccharidosisBeta Glucuronidase Deficiency	1973	508
The Hemochromatosis Founder Mutation in HLA-H Disrupts β2-Microglobulin Interaction and Cell Surface Expression John N. Feder, Zenta Tsuchihashi, Alivelu Irrinki, Journal of Biological Chemistry	1997	479
Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with β <sub>2</sub> -microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells Abdül Waheed, Seppo Parkkila, Xiao Zhou, Proceedings of the National Academy of Sciences	1997	387
The Taste of Carbonation Jayaram Chandrashekar, David A. Yarmolinsky, Lars von Buchholtz, Science Chemical BiologySensory ScienceSensory SystemsFood ChemistrySensometrics	2009	361
Human carbonic anhydrase XII: cDNA cloning, expression, and chromosomal localization of a carbonic anhydrase gene that is overexpressed in some renal cell cancers Özlem Türeci, Uğur Şahin, Evi Vollmar, Proceedings of the National Academy of Sciences	1998	357

Page 1