Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
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Seite 36
... enzyme - specific . Segregation at the chromosome 5 site is without effect on the development of other measured enzymes . Similar timing control genes mapping in close proximity to enzyme structural genes have been reported for maize ...
... enzyme - specific . Segregation at the chromosome 5 site is without effect on the development of other measured enzymes . Similar timing control genes mapping in close proximity to enzyme structural genes have been reported for maize ...
Seite 37
... enzyme synthesis to respond to homeostatic signals , such as the induction of enzymes by hormones . Because an inducible enzyme is not really inducible in all cells , even though the necessary receptor proteins may be present , we ...
... enzyme synthesis to respond to homeostatic signals , such as the induction of enzymes by hormones . Because an inducible enzyme is not really inducible in all cells , even though the necessary receptor proteins may be present , we ...
Seite 38
... enzyme level ( synthesis ) , must the signal persist for the change to persist , or can a signal induce a change in the functional capacity of DNA that will continue after the signal is exhausted ? 5. How is programmatic information ...
... enzyme level ( synthesis ) , must the signal persist for the change to persist , or can a signal induce a change in the functional capacity of DNA that will continue after the signal is exhausted ? 5. How is programmatic information ...
Inhalt
The legal aspects of genetic screening and counseling | 3 |
Some trends in the study of spontaneous and induced mutation in | 19 |
Temporal genes and developmental programs | 33 |
Urheberrecht | |
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aberrations Acad activity alleles Amer amniocentesis amniotic fluid amniotic fluid cells analysis antenatal antigens assay autosomal banding biochemical blood group Bodmer cancer cell hybridization chromatid chromosome abnormalities clinical clones congenital correlation culture cytogenetic deficiency detected determined differentiation disease disorders donor Down's syndrome Editors environmental enzyme errors of metabolism extinction factors fetal fetus fibroblasts frequency functions Galjaard gene genetic distance genome H-2 complex hemoglobin HLA-D Human Genetics inborn errors individuals inheritance involved karyotype lactose Lancet linkage disequilibrium loci locus lymphocytes malformations marker maternal methods microcell Milunsky mouse mutagens mutation rates Nature Lond neural tube defects newborns normal observed parents patients phenotype phenylketonuria polymorphism population genetics possible pregnancies prenatal diagnosis Press Proc protein recent risk Ruddle samples selection somatic cell specific structural studies suggested Table techniques tissue translocation tumors variants X chromosome Zinkernagel