Concepedia

S Hubl

SH

Statistics

Publications

8

Citations

686

H-Index

8

Active since

1989

Affiliations

Gladstone Institutes(Current)

University of California, Berkeley

University of California, San Francisco

Johnson & Johnson (United States)

S Hubl is an author at Gladstone Institutes specializing in life sciences, genetics, and human genetics.

Publications per year

1989–2001

8

Publications

8

Phenotypes of apolipoprotein B and apolipoprotein E after liver transplantation.

MacRae F. Linton, Robert G. Gish, S Hubl et al. · Journal of Clinical Investigation · 1991 · 368 citations · Full text

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Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins.

Stephen G. Young, S Hubl, R. Stephen Smith et al. · Journal of Clinical Investigation · 1990 · 76 citations · Full text

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Familial Hypobetalipoproteinemia Associated with a Mutant Species of Apolipoprotein B (B-46)

Stephen G. Young, S Hubl, David Chappell et al. · New England Journal of Medicine · 1989 · 74 citations

, , +16

A truncated species of apolipoprotein B (B67) in a kindred with familial hypobetalipoproteinemia.

Francine K. Welty, S Hubl, Vincenzo Pierotti et al. · Journal of Clinical Investigation · 1991 · 44 citations · Full text

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An ApaLI restriction site polymorphism is associated with the MB19 polymorphism in apolipoprotein B.

Stephen G. Young, S Hubl · Journal of Lipid Research · 1989 · 43 citations · Full text

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