Zobrazeno 1 - 10 of 56 pro vyhledávání: '"Won G. Ng"'
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[Untitled]
Autor: Wendy Cozen, Juan C. Felix, Ruth K. Peters, Peggy Wan, Juergen K. V. Reichardt, Malcolm C. Pike, Won G. Ng
Publikováno v: Cancer Causes and Control. 13:113-120
Objective: Previous studies have suggested that high levels of galactose consumption and/or low levels of galactose-1-phosphate uridyl transferase (GALT) activity may result in an increased risk of epithelial ovarian cancer. Similarly, some have repo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3fcff5dde427dc8e1ed70ed899b715ac
https://doi.org/10.1023/a:1014384027523
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2
Molecular and Biochemical Basis of Galactosemia
Autor: Lee-Jun C. Wong, Yan-Kang Xu, Won G. Ng, Boris B.T. Wang
Publikováno v: Molecular Genetics and Metabolism. 63:263-269
Galactosemia is a clinically heterogeneous autosomal recessive inborn error of metabolism caused by deficiency of galactose-1-phosphate uridylyltransferase (GALT). Despite the numerous point mutations identified in the GALT gene, the prevalence of th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8536618f6c1797e34e3fd9a753b5a3c8
https://doi.org/10.1006/mgme.1998.2678
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3
Characteristics of Women with a family history of ovarian cancer. I. Galactose consumption and metabolism
Autor: William R. Welch, Won G. Ng, Huijuan Xu, Betsy Valles, Juergen K. V. Reichardt, Daniel W. Cramer, Michael G. Muto
Publikováno v: Cancer. 74:1309-1317
BACKGROUND Galactose metabolism may be a risk factor for ovarian cancer based upon evidence that galactose causes ovarian failure and that ovarian cancer arises from premature ovarian failure. This study examines galactose-1-phosphate uridyl transfer
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::eddd242bd71c3b9172ddf9230b760ebe
https://doi.org/10.1002/1097-0142(19940815)74:4<1309::aid-cncr2820740421>3.0.co
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4
Erythrocyte uridine diphosphate galactose-4-epimerase deficiency identified by newborn screening for galactosemia in the United States
Autor: Tina M. Cowan, Harvey L. Levy, Yan-Kang Xu, Walter C. Kruckeberg, Richard J. Allen, Won G. Ng, Hans-Georg O. Bock, Miriam G. Blitzer
Publikováno v: Screening. 2:179-186
Eight infants (two whites and six blacks) with erythrocyte uridine diphosphate galactose-4epimerase (epimerase) deficiency were identified in four newborn screening programs for galactosemia in the United States. The initial biochemical findings in a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7b5e49a362619f19f8d444b675e03f9b
https://doi.org/10.1016/0925-6164(93)90001-y
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5
Neurologic complications in galactosemia
Autor: Joseph E. Wagstaff, Thomas K. Koch, Kathleen Schmidt, Seymour Packman, Won G. Ng
Publikováno v: Pediatric Neurology. 8:217-220
Two siblings, a 27-year-old man and his 24-year-old sister were diagnosed with classic transferase deficiency galactosemia at birth and were treated with strict lactose restriction. Despite well-documented dietary management, both siblings are mental
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f57f9a54b3809cdea0a4d221321253b
https://doi.org/10.1016/0887-8994(92)90072-7
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7
Association of galactose-1-phosphate uridyltransferase activity and N314D genotype with the risk of ovarian cancer
Autor: Won G. Ng, Marc T. Goodman, Anna H. Wu, Lynne R. Wilkens, Ko-Hui Tung, Katharine McDuffie, Juergen K. V. Reichardt, Keith Terada, Daniel W. Cramer
Publikováno v: American journal of epidemiology. 156(8)
Deficiency in the galactose-1-phosphate uridyltransferase (GALT) enzyme results in accumulation of galactose and its metabolites in the ovary (Am J Epidemiol 1989;130:904-10). Galactose may raise gonadotropin levels, resulting in proliferation of ova
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::021fa1749776bbae4c5c0d4ddf36d34c
https://pubmed.ncbi.nlm.nih.gov/12370157
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10
Endometriosis associated with the N314D mutation of galactose-1-phosphate uridyl transferase (GALT)
Autor: Won G. Ng, Daniel W. Cramer, Mark D. Hornstein, Robert L. Barbieri
Publikováno v: Molecular human reproduction. 2(3)
To explore a possible connection between endometriosis, Mullerian anomalies, and possession of the N314D allele of the gene for galactose-1-phosphate uridyl transferase (GALT), we studied 33 women with endometriosis attending a fertility clinic. Pati
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35144d1f63ec2261c8948fee81e2a18a
https://pubmed.ncbi.nlm.nih.gov/9238674
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