Human Genetics. Proceedings of the 6th International Congress..., Sept. 13-18, 1981, Jerusalem: Medical aspects. II, Teil 2Batsheva Bonné-Tamir Liss, 1982 - 619 Seiten |
Im Buch
Ergebnisse 1-3 von 90
Seite 120
... ACTIVITY IN HEALTHY PEOPLE The problem of possible genetic control of LDL cell membrane receptor activity in the general population is difficult to approach because of the considerable experimental variation in LDL receptor activity ...
... ACTIVITY IN HEALTHY PEOPLE The problem of possible genetic control of LDL cell membrane receptor activity in the general population is difficult to approach because of the considerable experimental variation in LDL receptor activity ...
Seite 121
... activity levels in offspring of hypercholesterolemia heterozygotes ( who can pass on only one gene for normal receptor activity to offspring ) . The limited studies conducted thus far have supported the hypothesis . It is possible that ...
... activity levels in offspring of hypercholesterolemia heterozygotes ( who can pass on only one gene for normal receptor activity to offspring ) . The limited studies conducted thus far have supported the hypothesis . It is possible that ...
Seite 198
... activity showed no response to supplementation , whereas those with some residual activity demonstrated increased propionate fixation . In essence , then , it appears that “ leaky " mutants do respond to Cul supplementation in culture ...
... activity showed no response to supplementation , whereas those with some residual activity demonstrated increased propionate fixation . In essence , then , it appears that “ leaky " mutants do respond to Cul supplementation in culture ...
Inhalt
Carrier Detection | 15 |
HLA and Infectious Diseases | 37 |
HLA and Diabetes | 55 |
Urheberrecht | |
49 weitere Abschnitte werden nicht angezeigt.
Andere Ausgaben - Alle anzeigen
Häufige Begriffe und Wortgruppen
abnormalities activity addition affected allele analysis antigens appears association binding biochemical blood carrier cells changes chromosome clinical common complex cultured defect deficiency Department determined diabetes diabetes mellitus diagnosis disease disorders distribution dominant environmental enzyme estimated et al evidence expression factors fibroblasts findings frequency gene glucose haplotypes heterogeneity heterozygotes Hum Genet human hypertension IDDM immune important increased indicated individuals inheritance internalization involved Italy levels linkage linked locus lysosomal major marker measured Medical method mode of inheritance multiple mutant neural tube normal observed occur origin pairs parents patients phenotype population possible pregnancy prenatal present problems protein recently receptor recessive relative reported Research response risk screening showed shown significant specific structure studies suggested syndrome Table tissue trait translocation tumor twin ulcer University values York