D R Webster|J C Armour - JoVE Visualize

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Journal of Inherited Metabolic Disease|January 1, 1981

Pyrimidine and purine metabolites in ornithine carbamoyl transferase deficiencyD R Webster, H A Simmonds, D M Barry, et al.

Journal of Inherited Metabolic Disease|January 1, 1984

Failure of protein loading tests to identify heterozygosity for ornithine carbamoyltransferase deficiencyD M Becroft, D M Barry, D R Webster, et al.

Proceedings of the National Academy of Sciences of the United States of America|December 1, 1987

Differential turnover of tyrosinated and detyrosinated microtubulesD R Webster, G G Gundersen, J C Bulinski, et al.

Journal of Paediatrics and Child Health|October 8, 2004

Use of the newborn screening card to define cause of death in a 12-year-old diagnosed with epilepsyJ R Skinner, B Chong, M Fawkner, et al.

Naunyn-Schmiedeberg'S Archives of Pharmacology|June 1, 1986

Relationship of metabolism of 2'-, 3'- and 5'-adenine nucleotides to presynaptic inhibition of transmitter release in rat vas deferensD R Webster, G D Boston, N H Holford, et al.

Cell Death and Differentiation|January 30, 2010

Cyclin-C-dependent cell-cycle entry is required for activation of non-homologous end joining DNA repair in postmitotic neuronsA Tomashevski, D R Webster, P Grammas, et al.

The Journal of Cell Biology|July 1, 1987

Assembly and turnover of detyrosinated tubulin in vivoD R Webster, G G Gundersen, J C Bulinski, et al.

Bioscience Reports|May 1, 1982

Formation and degradation of deoxyadenosine nucleotides in inherited adenosine deaminase deficiencyH A Simmonds, D R Webster, D Perrett, et al.

Biochemical Pharmacology|March 15, 1982

GTP depletion and other erythrocyte abnormalities in inherited PNP deficiencyH A Simmonds, A R Watson, D R Webster, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1988

Altered erythrocyte nucleotide patterns are characteristic of inherited disorders of purine or pyrimidine metabolismH A Simmonds, L D Fairbanks, G S Morris, et al.

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Showing results (31-40 of 45) with videos related to

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Pageof 5

Journal of Inherited Metabolic Disease|January 1, 1981

Pyrimidine and purine metabolites in ornithine carbamoyl transferase deficiencyD R Webster, H A Simmonds, D M Barry, et al.

Journal of Inherited Metabolic Disease|January 1, 1984

Failure of protein loading tests to identify heterozygosity for ornithine carbamoyltransferase deficiencyD M Becroft, D M Barry, D R Webster, et al.

Proceedings of the National Academy of Sciences of the United States of America|December 1, 1987

Differential turnover of tyrosinated and detyrosinated microtubulesD R Webster, G G Gundersen, J C Bulinski, et al.

Journal of Paediatrics and Child Health|October 8, 2004

Use of the newborn screening card to define cause of death in a 12-year-old diagnosed with epilepsyJ R Skinner, B Chong, M Fawkner, et al.

Naunyn-Schmiedeberg'S Archives of Pharmacology|June 1, 1986

Relationship of metabolism of 2'-, 3'- and 5'-adenine nucleotides to presynaptic inhibition of transmitter release in rat vas deferensD R Webster, G D Boston, N H Holford, et al.

Cell Death and Differentiation|January 30, 2010

Cyclin-C-dependent cell-cycle entry is required for activation of non-homologous end joining DNA repair in postmitotic neuronsA Tomashevski, D R Webster, P Grammas, et al.

The Journal of Cell Biology|July 1, 1987

Assembly and turnover of detyrosinated tubulin in vivoD R Webster, G G Gundersen, J C Bulinski, et al.

Bioscience Reports|May 1, 1982

Formation and degradation of deoxyadenosine nucleotides in inherited adenosine deaminase deficiencyH A Simmonds, D R Webster, D Perrett, et al.

Biochemical Pharmacology|March 15, 1982

GTP depletion and other erythrocyte abnormalities in inherited PNP deficiencyH A Simmonds, A R Watson, D R Webster, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1988

Altered erythrocyte nucleotide patterns are characteristic of inherited disorders of purine or pyrimidine metabolismH A Simmonds, L D Fairbanks, G S Morris, et al.

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