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Archives of Biochemistry and Biophysics
|
March 24, 1999
Functional characterization of the carnitine transporter defective in primary carnitine deficiency
F Scaglia, Y Wang, N Longo
American Journal of Physiology. Cell Physiology
|
March 14, 2001
Insulin increases the turnover rate of Na+-K+-ATPase in human fibroblasts
N Longo, F Scaglia, Y Wang
Journal of Inherited Metabolic Disease
|
January 5, 2002
Decreased half-life of insulin-like growth factor I in Rabson-Mendenhall syndrome
N Longo, R Singh, L J Elsas
The Journal of Biological Chemistry
|
April 28, 2000
Abnormal sodium stimulation of carnitine transport in primary carnitine deficiency
Y Wang, T A Meadows, N Longo
Minerva Medica
|
December 29, 1977
[Prognostic and therapeutic considerations on intraventricular block during a course of acute myocardial infarct]
F N Longo, G Trovato, A Oddo
American Journal of Medical Genetics
|
January 1, 1987
Progressive form of multiple pterygium syndrome in association with nemalin-myopathy: report of a female followed for twelve years
F Papadia, N Longo, L Serlenga, et al.
Human Mutation
|
November 3, 2000
Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: lack of genotype-phenotype correlation
Y Wang, F Taroni, B Garavaglia, et al.
The American Journal of Physiology
|
June 1, 1991
A simple method for evaluation of Rb+ transport and Na(+)-K+ pump stoichiometry in adherent cells
N Longo, L D Griffin, L J Elsas
The American Journal of Physiology
|
May 1, 1988
Influx and efflux of 3-O-methyl-D-glucose by cultured human fibroblasts
N Longo, L D Griffin, L J Elsas
Proceedings of the National Academy of Sciences of the United States of America
|
March 3, 1999
Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency
Y Wang, J Ye, V Ganapathy, et al.
Page
of 12
Search research articles
Search
Showing results (11-20 of 119) with videos related to
Sort By:
Page
of 12
Archives of Biochemistry and Biophysics
|
March 24, 1999
Functional characterization of the carnitine transporter defective in primary carnitine deficiency
F Scaglia, Y Wang, N Longo
American Journal of Physiology. Cell Physiology
|
March 14, 2001
Insulin increases the turnover rate of Na+-K+-ATPase in human fibroblasts
N Longo, F Scaglia, Y Wang
Journal of Inherited Metabolic Disease
|
January 5, 2002
Decreased half-life of insulin-like growth factor I in Rabson-Mendenhall syndrome
N Longo, R Singh, L J Elsas
The Journal of Biological Chemistry
|
April 28, 2000
Abnormal sodium stimulation of carnitine transport in primary carnitine deficiency
Y Wang, T A Meadows, N Longo
Minerva Medica
|
December 29, 1977
[Prognostic and therapeutic considerations on intraventricular block during a course of acute myocardial infarct]
F N Longo, G Trovato, A Oddo
American Journal of Medical Genetics
|
January 1, 1987
Progressive form of multiple pterygium syndrome in association with nemalin-myopathy: report of a female followed for twelve years
F Papadia, N Longo, L Serlenga, et al.
Human Mutation
|
November 3, 2000
Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: lack of genotype-phenotype correlation
Y Wang, F Taroni, B Garavaglia, et al.
The American Journal of Physiology
|
June 1, 1991
A simple method for evaluation of Rb+ transport and Na(+)-K+ pump stoichiometry in adherent cells
N Longo, L D Griffin, L J Elsas
The American Journal of Physiology
|
May 1, 1988
Influx and efflux of 3-O-methyl-D-glucose by cultured human fibroblasts
N Longo, L D Griffin, L J Elsas
Proceedings of the National Academy of Sciences of the United States of America
|
March 3, 1999
Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency
Y Wang, J Ye, V Ganapathy, et al.
Page
of 12