Zobrazeno 1 - 9
of 9
pro vyhledávání: '"K L, Chambliss"'
Publikováno v:
Journal of Lipid Research, Vol 38, Iss 11, Pp 2216-2223 (1997)
To assess the potential for feedback inhibition by isoprene intermediates in the cholesterol and nonsterol isoprene biosynthetic pathway, we expressed human cDNAs encoding mevalonate kinase (MKase), phosphomevalonate kinase (PMKase), and mevalonate d
Externí odkaz:
https://doaj.org/article/c674d29318464d23b3a550fff97f1c0d
Autor:
K. L. Chambliss
Publikováno v:
Molecular Endocrinology. 16:938-946
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff6c91f373da4222ee8a8746a5d86173
https://doi.org/10.1210/me.16.5.938
https://doi.org/10.1210/me.16.5.938
Publikováno v:
Journal of Inherited Metabolic Disease. 23:497-504
Three patients have been reported with (putative) methylmalonic semialdehyde dehydrogenase (MMSDH) deficiency. The urine metabolic pattern was strikingly different in all, including beta-alanine, 3-hydroxypropionic acid, both isomers of 3-amino- and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::578de16d7bb09c2964800b0dad0e85a6
https://doi.org/10.1023/a:1005616315087
https://doi.org/10.1023/a:1005616315087
Publikováno v:
Journal of lipid research. 40(4)
Phosphomevalonate kinase catalyzes the conversion of mevalonate-5-phosphate to mevalonate-5-diphosphate and was originally believed to be a cytosolic enzyme. In this study we have localized the phosphomevalonate kinase gene to chromosome 1p13-1q22-23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0c75c087f408f81c0a6bece1fb2b78f6
https://pubmed.ncbi.nlm.nih.gov/10191291
https://pubmed.ncbi.nlm.nih.gov/10191291
Publikováno v:
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology. 5(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::daffa952f431635360063af1ee4d075a
https://pubmed.ncbi.nlm.nih.gov/9146921
https://pubmed.ncbi.nlm.nih.gov/9146921
Autor:
F, Trettel, P, Malaspina, C, Jodice, A, Novelletto, C A, Slaughter, D L, Caudle, D D, Hinson, K L, Chambliss, K M, Gibson
Publikováno v:
Advances in experimental medicine and biology. 414
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a60ce410c682b84b3978e56d7a43e160
https://pubmed.ncbi.nlm.nih.gov/9059628
https://pubmed.ncbi.nlm.nih.gov/9059628
Autor:
K L, Chambliss, D L, Caudle, D D, Hinson, C R, Moomaw, C A, Slaughter, C, Jakobs, K M, Gibson
Publikováno v:
The Journal of biological chemistry. 270(1)
Three rat brain cDNA clones approximately 3500, 1465, and 1135 base pairs in length encoding succinic semialdehyde dehydrogenase (SSADH; EC 1.2.1.24) were isolated from two cDNA libraries using a polymerase chain reaction derived probe. Restriction m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5836f22f14190b7f31a0ec62a9d5563d
https://pubmed.ncbi.nlm.nih.gov/7814412
https://pubmed.ncbi.nlm.nih.gov/7814412
Publikováno v:
Journal of inherited metabolic disease. 16(3)
Succinic semialdehyde dehydrogenase (SSADH; EC 1.2. 1.24) deficiency (McKusick 271980) is an inborn error of 4-aminobutyric acid (GABA) metabolism. The enzymatic defect blocks the oxidation of succinic semialdehyde (SSA) to succinic acid, resulting i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1baa4709a22b9deaeda8675dc476bd18
https://pubmed.ncbi.nlm.nih.gov/7609442
https://pubmed.ncbi.nlm.nih.gov/7609442
Autor:
Jaak Jaeken, B. Francois, K. L. Chambliss, Kenneth M. Gibson, V. Kamali, C. F. Lee, C.A.J.M. Jakobs
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 196(2-3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcb940aa82893dcd98ab06e5f6494ffd
https://pubmed.ncbi.nlm.nih.gov/2029787
https://pubmed.ncbi.nlm.nih.gov/2029787