Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells. Nature https://doi.org/10.1038/s41586-020-2786-7 (2020). Zhou, W. et al. Mosaic loss of chromosome Y is associated with common variation near TCL1A. Nat. Genet. 48, 563–568 (2016). Article CAS PubMed PubMed ...
Convergent phenotypic evolution often results from similar genetic changes in independent species by a process known as parallel evolution. Sometimes, convergent evolution results from the evolution of a genetic change that is inherited from an ancestral population or from hybridization between species, whi...
In the group designated hereditary feeble-mindedness there are 164 family histories in which either there are so many feeble-minded individuals or the feeble-mindedness occurs in such relation to the case that there can be no doubt that the condition is inherited. The group designated probably ...
Here we look for evidence of such factors using a genetic cross between two natural inbred lines: one with high, and one with low gbM. We confirm that methylation states are stably inherited, but also see large somatic deviations from the inherited state, in particular a...
Language therapy, physical therapy, and educational intervention can be used to help improve the quality of life of affected individuals. The minority of cri-du-chat cases are inherited; the parent who carries the genetic abnormality typically is unaffected by the disorder, owing to a phenomenon ...
University of British Columbia, Canada.SILVA, G.A. 2007. Causes ... GDS Anders. 被引量: 0发表: 2007年 Colonization with long-distance seed dispersal and genetic structure of maternally inherited genes in forest trees : simulation study Since the last glacial period forest trees have expanded ...
harknessii CMS is controlled by two pairs of independently inherited genes: a dominant gene and a recessive gene. Weaver et al. (1977) and Sheetz et al. (1980) have reported that the fertility recovery was controlled by a partially dominant gene (Rf). Dasilva et al. (1981) have ...
Hermansky-Pudlak syndrome (HPS) types 1 and 4 are caused by defective vesicle trafficking. The mechanism for Crohn’s disease-like inflammation, lung fibrosis, and macrophage lipid accumulation in these patients remains enigmatic. The aim of this study i
Genetics of inherited colour vision deficiencies. In: Foster DH, editor. Inherited and acquired colour vision deficiencies, vision and visual dysfunction, volume 7. Boca Raton FL: CRC Press; 1991. p. 98–9. Google Scholar Regan BC, Juliot C, Simmen B, Viénot F, Charles-Dominique PC, ...
Genetic variation can be defined as the genetic makeup of organisms within a population change.Genesare inherited segments ofDNAthat contain codes for the production of proteins. Genes exist in alternate versions, oralleles, that determine distinct traits that can be passed on from parents to offsp...