C. Ronald Scott - Concepedia

Author

C. Ronald Scott

University of Washington

Also Known As

C R Scott, C Ronald Scott, C. RONALD SCOTT, C. Ronald Scott, C.Ronald Scott, CS Scott

Publications

524

Citations

H-Index

Concepts

All Affiliations

University of Washington

About

C. Ronald Scott is an author at University of Washington specializing in medicine, genetics, and autoimmunity.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	253
2	Cell Biology	3	3	69
3	Natural Sciences	2	2	32
4	Biochemistry	2	2	32
5	Chemical Biology	1	1	18

C. Ronald Scott

Publications

486

Citations

H-Index

Page 1

	Year	Citations
Purine Nucleoside Phosphorylase Deficiency William Osborne, Shi-Han Chen, Eloise R. Giblett, Journal of Clinical Investigation	1977	74
Variable Severity of Pulmonary Disease in Adults with Identical Cystic Fibrosis Mutations Wylie Burke, Moira L. Aitken, Shi-Han Chen, CHEST Journal Variable SeverityAdvanced Lung DiseaseGenetic EpidemiologyPathologyPulmonary Fibrosis	1992	63
Bryostatin 1 induces differentiation of B-chronic lymphocytic leukemia cells H. Drexler, SM Gignac, RA Jones, Blood	1989	51
Inborn errors of specific immunity C. Ronald Scott Europe PMC (PubMed Central) Primary ImmunodeficiencyMaternal ImmunizationInborn ErrorsAutoimmune DiseasePathogenesis	1980	50
Purine Nucleoside Phosphorylase Deficiency: A Molecular Model for Selective Loss of T Cell Function Ute H. Ochs, Shi-Han Chen, Hans D. Ochs, The Journal of Immunology Lymphocyte DevelopmentImmunodeficienciesT-regulatory CellImmunologyImmune Regulation	1979	37
Electrophoretic and cytochemical characterization of alpha-naphthyl acetate esterases in acute myeloid leukemia: relationships with membrane receptor and monocyte-specific antigen expression C. Ronald Scott, DC Linch, A. G. Bynoe, Blood	1984	35
Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients Birthe Gericke, Mahdi Amiri, C. Ronald Scott, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease Developmental AnomalyNovel Sucrase-isomaltase MutationsMendelian DisorderGenetic DisorderGenetics	2017	34
Low-dose agalsidase beta treatment in male pediatric patients with Fabry disease: A 5-year randomized controlled trial Uma Ramaswami, Daniel G. Bichet, L. Clarke, Molecular Genetics and Metabolism	2019	32
Characterization of unusual hexosaminidase A (HEX A) deficient human mutants. J S O′Brien, Linda Tennant, M. Lois Veath, PubMed	1978	31
Human erythrocyte pyrimidine nucleoside monophosphate kinase. Partial purification and properties of two allelic gene products. Yanting Teng, S H Chen, C. Ronald Scott Journal of Biological Chemistry Molecular BiologyMolecular GeneticsPolymorphic EnzymeChemical BiologyRedox Biology	1976	18

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