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Journal of Inherited Metabolic Disease
|
January 5, 2002
A case of PDH-E1 alpha mosaicism in a male patient with severe metabolic lactic acidosis
A Seyda, K Chun, S Packman, et al.
American Journal of Human Genetics
|
September 1, 1985
Defective intramitochondrial NADH oxidation in skin fibroblasts from an infant with fatal neonatal lacticacidemia
B H Robinson, N McKay, P Goodyer, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1981
Lactic acidosis due to pyruvate carboxylase deficiency
J C Haworth, B H Robinson, T L Perry
Human Molecular Genetics
|
April 18, 2000
Sequential deletion of C-terminal amino acids of the E(1)alpha component of the pyruvate dehydrogenase (PDH) complex leads to reduced steady-state levels of functional E(1)alpha(2)beta(2) tetramers: implications for patients with PDH deficiency
A Seyda, G McEachern, R Haas, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 13, 1997
The role of London forces in defining noncentrosymmetric order of high dipole moment-high hyperpolarizability chromophores in electrically poled polymeric thin films
L R Dalton, A W Harper, B H Robinson
Biochimica Et Biophysica Acta
|
August 3, 1995
Macrocyclic lactone synthesis by lipases in water-in-oil microemulsions
G D Rees, B H Robinson, G R Stephenson
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 31, 1985
Immunoextraction of lipoamide dehydrogenase from cultured skin fibroblasts in patients with combined alpha-ketoacid dehydrogenase deficiency
G Otulakowski, W Nyhan, L Sweetman, et al.
American Journal of Human Genetics
|
September 1, 1994
Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene
F Merante, I Tein, L Benson, et al.
Biochimica Et Biophysica Acta
|
October 26, 1995
Preparative-scale kinetic resolutions catalysed by microbial lipases immobilised in AOT-stabilised microemulsion-based organogels: cryoenzymology as a tool for improving enantioselectivity
G D Rees, B H Robinson, G R Stephenson
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 1, 1971
A study of calcium absorption using an automated fluorimetric assay procedure
M L Rushton, H G Sammons, B H Robinson
Page
of 26
Search research articles
Search
Showing results (91-100 of 257) with videos related to
Sort By:
Page
of 26
Journal of Inherited Metabolic Disease
|
January 5, 2002
A case of PDH-E1 alpha mosaicism in a male patient with severe metabolic lactic acidosis
A Seyda, K Chun, S Packman, et al.
American Journal of Human Genetics
|
September 1, 1985
Defective intramitochondrial NADH oxidation in skin fibroblasts from an infant with fatal neonatal lacticacidemia
B H Robinson, N McKay, P Goodyer, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1981
Lactic acidosis due to pyruvate carboxylase deficiency
J C Haworth, B H Robinson, T L Perry
Human Molecular Genetics
|
April 18, 2000
Sequential deletion of C-terminal amino acids of the E(1)alpha component of the pyruvate dehydrogenase (PDH) complex leads to reduced steady-state levels of functional E(1)alpha(2)beta(2) tetramers: implications for patients with PDH deficiency
A Seyda, G McEachern, R Haas, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 13, 1997
The role of London forces in defining noncentrosymmetric order of high dipole moment-high hyperpolarizability chromophores in electrically poled polymeric thin films
L R Dalton, A W Harper, B H Robinson
Biochimica Et Biophysica Acta
|
August 3, 1995
Macrocyclic lactone synthesis by lipases in water-in-oil microemulsions
G D Rees, B H Robinson, G R Stephenson
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 31, 1985
Immunoextraction of lipoamide dehydrogenase from cultured skin fibroblasts in patients with combined alpha-ketoacid dehydrogenase deficiency
G Otulakowski, W Nyhan, L Sweetman, et al.
American Journal of Human Genetics
|
September 1, 1994
Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene
F Merante, I Tein, L Benson, et al.
Biochimica Et Biophysica Acta
|
October 26, 1995
Preparative-scale kinetic resolutions catalysed by microbial lipases immobilised in AOT-stabilised microemulsion-based organogels: cryoenzymology as a tool for improving enantioselectivity
G D Rees, B H Robinson, G R Stephenson
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 1, 1971
A study of calcium absorption using an automated fluorimetric assay procedure
M L Rushton, H G Sammons, B H Robinson
Page
of 26