Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Vaira P. Wellner"'
Publikováno v:
Proceedings of the National Academy of Sciences. 71:2505-2509
Enzyme studies on placenta, cultured skin fibroblasts, and erythrocytes from two sisters with the inborn error 5-oxoprolinuria (pyroglutamic aciduria) indicate that the metabolic lesion in this disease is at the glutathione synthetase (EC 6.3.2.3) st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a881da6d67f5a5ec39e07155997d913e
https://doi.org/10.1073/pnas.71.6.2505
https://doi.org/10.1073/pnas.71.6.2505
Autor:
Vaira P. Wellner, Alton Meister
Publikováno v:
Biochemistry. 5:872-879
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ced3177a66d74e7153ea3bde8b0385b4
https://doi.org/10.1021/bi00867a010
https://doi.org/10.1021/bi00867a010
Publikováno v:
Biochemistry. 12:2061-2066
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3920c772c905977b7a40499cbfee9881
https://doi.org/10.1021/bi00735a006
https://doi.org/10.1021/bi00735a006
Publikováno v:
Proceedings of the National Academy of Sciences. 70:2717-2721
Glutamine-dependent carbamylphosphate synthetase ( Escherichia coli ) is composed of a heavy subunit (molecular weight about 130,000) and a light subunit (molecular weight about 42,000), which can be separated with retention of catalytic activities.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a36446c89604623575cfceec68baaae
https://doi.org/10.1073/pnas.70.10.2717
https://doi.org/10.1073/pnas.70.10.2717
Publikováno v:
Biochemistry. 3:824-828
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbdc1419f63ba33210997a2ccfd9860f
https://doi.org/10.1021/bi00894a017
https://doi.org/10.1021/bi00894a017
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 81(15)
Glutathione is not effectively transported into human lymphoid cells, normal human skin fibroblasts, and fibroblasts from patients with genetic deficiencies of gamma-glutamylcysteine synthetase or glutathione synthetase. On the other hand, the monoet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04b1cccfffe80499ce61e06783449b8d
https://pubmed.ncbi.nlm.nih.gov/6146978
https://pubmed.ncbi.nlm.nih.gov/6146978
Autor:
Lenore S. Levine, Maria I. New, Daniel Wellner, Vaira P. Wellner, Peter G. Steinherz, Alton Meister, Shigeru Sassa, Elizabeth Stoner, Arleen B. Rifkind, A. Grenier, H Starkman
Publikováno v:
Pediatric research. 18(12)
Metabolic and enzymatic studies in a patient with hereditary tyrosinemia demonstrated for the first time a deficiency of erythrocyte and hepatic glutathione. Markedly decreased hepatic fumarylacetoacetate hydrolase activity was demonstrated in this p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76e0249acfe6276bc9dd633f445d7904
https://pubmed.ncbi.nlm.nih.gov/6522148
https://pubmed.ncbi.nlm.nih.gov/6522148
Publisher Summary This chapter discusses the assay, purification, and properties of glutamine synthetase from sheep brain. The activity of glutamine synthetase may be determined by measuring the rate of formation of inorganic phosphate, adenosine dip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8323edb99156882598ebb2ef4fec632e
https://doi.org/10.1016/0076-6879(71)17304-1
https://doi.org/10.1016/0076-6879(71)17304-1
Publikováno v:
Biochemistry. 5(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1087819c0b4b805a826486799ce4d3f0
https://pubmed.ncbi.nlm.nih.gov/5972332
https://pubmed.ncbi.nlm.nih.gov/5972332
Publikováno v:
Biochemistry. 7(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4b700de1c06ea1b14acd5fe78d1188a
https://pubmed.ncbi.nlm.nih.gov/4875281
https://pubmed.ncbi.nlm.nih.gov/4875281