Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Vibha Dave"'
Publikováno v:
Archives of biochemistry and biophysics
The molecular abnormality of a phosphoglycerate kinase variant which was associated with severe tissue enzyme deficiency and episodes of muscle contractions and myoglobinuria was examined. Analysis of the patient's DNA showed the existence of a nucle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04df3e94e8e6a94c43d63b104e96ac88
https://hdl.handle.net/10067/132790151162165141
https://hdl.handle.net/10067/132790151162165141
Publikováno v:
Blood cells, moleculesdiseases. 21(3)
The molecular abnormality of a phosphoglycerate kinase variant associated with severe red cell enzyme deficiency ( about 4% of normal) and episodes of hemolysis with jaundice was examined. The Michaelis constants for the substrates and co-enzymes (1.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::583ee175c3922c159a2cf39a9285bf71
https://pubmed.ncbi.nlm.nih.gov/8673469
https://pubmed.ncbi.nlm.nih.gov/8673469
Diverse polymorphism within a short coding region of the human aldehyde dehydrogenase-5 (ALDH5) gene
Publikováno v:
Human genetics. 92(5)
Human aldehyde dehydrogenase-5 gene (originally named as ALDHX) is expressed in liver and testis. The ALDH5 does not contain introns in the coding sequence for 517 amino acid residues. Within a short nucleotide region of the gene, the following three
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bd7202100cb2d0f8508ac0fca707759
https://pubmed.ncbi.nlm.nih.gov/8244338
https://pubmed.ncbi.nlm.nih.gov/8244338
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9781461362593
Cyclophosphamide, an important cancer chemotherapeutic agent, has been shown to be effective against some types of cancer (Hilton, 1984a; Manthey and Sladek, 1989). However, both natural and acquired resistance to cyclophosphamide limits its utility
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10c740cb88eb9a0239d78a246d851f76
https://doi.org/10.1007/978-1-4615-2904-0_8
https://doi.org/10.1007/978-1-4615-2904-0_8
Publikováno v:
Enzyme. 46(4-5)
The major cytosolic aldehyde dehydrogenase isozyme (ALDH1) exhibits strong activity for oxidation of retinal to retinoic acid, while the major mitochondrial ALDH2 and the stomach cytosolic ALDH3 have no such activity. The Km of ALDH1 for retinal is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::094c4b7d2665b50c25aab7a069fd8dd0
https://pubmed.ncbi.nlm.nih.gov/1292933
https://pubmed.ncbi.nlm.nih.gov/1292933
Autor:
A Macpherson, Roberta J. Ward, Margaret Warren-Perry, Tim J Peters, Lily C. Hsu, Vibha Dave, Akira Yoshida
Publikováno v:
Alcoholism ISBN: 9781468459487
At least nine isoenzymes of aldehyde dehydrogenase (E.C.1.2.1.3.) have been identified in man based on their enzymatic characteristics and physiochemical properties (Yoshida et al., 1990). Liver mitochondrial aldehyde dehydrogenase (ALDH2) probably p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f199d1fc58b1c89182d317c0d3eda0d3
https://doi.org/10.1007/978-1-4684-5946-3_15
https://doi.org/10.1007/978-1-4684-5946-3_15
Autor:
Graeme Semple, Beatriz Fioravanti, Guillherme Pereira, Imelda Calderon, Jane Uy, Karoline Choi, Yifeng Xiong, Albert Ren, Michael Morgan, Vibha Dave, William Thomsen, David J. Unett, Charles Xing, Stuart Bossie, Chris Carroll, Zhi-Liang Chu, Andrew J. Grottick, Erin K. Hauser, James Leonard, Robert M. Jones
Publikováno v:
Journal of Medicinal Chemistry; Jul2008, Vol. 51 Issue 17, p5172-5175, 4p
Publikováno v:
Annals of Human Genetics. 53:1-7
Although mitochondrial aldehyde dehydrogenase (ALDH2) has been thought to play a major role in acetaldehyde detoxification, and the high incidence of 'alcohol flushing' among Orientals is attributed to the inherited deficiency of ALDH2, the role of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52f7e65af732b4f9acef0542f0645f7c
https://doi.org/10.1111/j.1469-1809.1989.tb01116.x
https://doi.org/10.1111/j.1469-1809.1989.tb01116.x
Autor:
Ira A. Shulman, David A. Wheeler, Mitsuko Okamoto, Akira Yoshida, Vibha Dave, Janice M. Nelson
Publikováno v:
Blood. 63:711-713
The designation B4 is proposed for a weak variant of type B blood found in a Salvadorian woman and her two daughters. The red cells were weakly agglutinated by anti-B and anti-A,B; the serum contained anti-B; and the saliva contained H but not B subs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0688f56e7723f236fb6d306d345d65c6
https://doi.org/10.1182/blood.v63.3.711.711
https://doi.org/10.1182/blood.v63.3.711.711
Publikováno v:
Blood. 66:990-992
The B antigen activity was severely diminished in a patient's RBCs at the preleukemic stage prior to chemo- or radiotherapy. The amount of H sites of the patient's RBC membranes was found to be comparable to that of O RBC membranes. The activity of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee82306a23a04f4e2cff54f428e2332a
https://doi.org/10.1182/blood.v66.4.990.990
https://doi.org/10.1182/blood.v66.4.990.990