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A M Lamhonwah

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Biochemical and Biophysical Research Communications|November 25, 1998
Carnitine uptake defect: frameshift mutations in the human plasmalemmal carnitine transporter geneA M Lamhonwah, I Tein
Biochemical and Biophysical Research Communications|November 2, 1999
GFP-Human high-affinity carnitine transporter OCTN2 protein: subcellular localization and functional restoration of carnitine uptake in mutant cell lines with the carnitine transporter defectA M Lamhonwah, I Tein
American Journal of Human Genetics|December 1, 1987
Propionicacidemia: absence of alpha-chain mRNA in fibroblasts from patients of the pccA complementation groupA M Lamhonwah, R A Gravel
Archives of Biochemistry and Biophysics|May 1, 1987
Sequence homology around the biotin-binding site of human propionyl-CoA carboxylase and pyruvate carboxylaseA M Lamhonwah, F Quan, R A Gravel
Biochemical and Biophysical Research Communications|June 28, 1991
Isolation and expression of a full-length cDNA encoding the human GM2 activator proteinB Xie, B McInnes, K Neote, et al.
Genomics|October 1, 1990
Two distinct mutations at the same site in the PCCB gene in propionic acidemiaA M Lamhonwah, C E Troxel, S Schuster, et al.
Journal of Inherited Metabolic Disease|August 11, 2004
OCTN2 mutation (R254X) found in Saudi Arabian kindred: recurrent mutation or ancient founder mutation?A-M Lamhonwah, R Onizuka, S E Olpin, et al.
Genomics|February 1, 1994
Correction of the metabolic defect in propionic acidemia fibroblasts by microinjection of a full-length cDNA or RNA transcript encoding the propionyl-CoA carboxylase beta subunitA M Lamhonwah, D Leclerc, M Loyer, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1986
Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genesA M Lamhonwah, T J Barankiewicz, H F Willard, et al.
American Journal of Human Genetics|July 1, 1994
Mutations participating in interallelic complementation in propionic acidemiaR A Gravel, B R Akerman, A M Lamhonwah, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Biochemical and Biophysical Research Communications|November 25, 1998
Carnitine uptake defect: frameshift mutations in the human plasmalemmal carnitine transporter geneA M Lamhonwah, I Tein
Biochemical and Biophysical Research Communications|November 2, 1999
GFP-Human high-affinity carnitine transporter OCTN2 protein: subcellular localization and functional restoration of carnitine uptake in mutant cell lines with the carnitine transporter defectA M Lamhonwah, I Tein
American Journal of Human Genetics|December 1, 1987
Propionicacidemia: absence of alpha-chain mRNA in fibroblasts from patients of the pccA complementation groupA M Lamhonwah, R A Gravel
Archives of Biochemistry and Biophysics|May 1, 1987
Sequence homology around the biotin-binding site of human propionyl-CoA carboxylase and pyruvate carboxylaseA M Lamhonwah, F Quan, R A Gravel
Biochemical and Biophysical Research Communications|June 28, 1991
Isolation and expression of a full-length cDNA encoding the human GM2 activator proteinB Xie, B McInnes, K Neote, et al.
Genomics|October 1, 1990
Two distinct mutations at the same site in the PCCB gene in propionic acidemiaA M Lamhonwah, C E Troxel, S Schuster, et al.
Journal of Inherited Metabolic Disease|August 11, 2004
OCTN2 mutation (R254X) found in Saudi Arabian kindred: recurrent mutation or ancient founder mutation?A-M Lamhonwah, R Onizuka, S E Olpin, et al.
Genomics|February 1, 1994
Correction of the metabolic defect in propionic acidemia fibroblasts by microinjection of a full-length cDNA or RNA transcript encoding the propionyl-CoA carboxylase beta subunitA M Lamhonwah, D Leclerc, M Loyer, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1986
Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genesA M Lamhonwah, T J Barankiewicz, H F Willard, et al.
American Journal of Human Genetics|July 1, 1994
Mutations participating in interallelic complementation in propionic acidemiaR A Gravel, B R Akerman, A M Lamhonwah, et al.
Pageof 2