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pro vyhledávání: '"R. Wevrick"'
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Publikováno v:
Cytogenetic and Genome Research. 92:149-152
Identification of imprinted genes in the Prader-Willi/Angelman syndrome deletion region is complicated by the presence of large flanking repeats. While inactive copies of DEXI are located within the repeats, we have now localized the active DEXI gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a9b07104a121dff104f3d5ba602bc36
https://doi.org/10.1159/000056887
https://doi.org/10.1159/000056887
Autor:
C.C. Morton, S.L. Christian, T.A. Donlon, D.J. Driscoll, J.K. Fink, J.M. Gabriel, G. Gotway, J.M. Greally, M.P. Hitchins, H.C. Howard, Y. Ji, S. Leonard, T. Lerner, E. Magenis, S. Malcolm, T. Ohta, S. Rainier, M. Rees, B. Riley, W.P. Robinson, S. Saitoh, R. Schultz, S. Sell, J.D. Sharp, C. Talbot, R. Trent, R. Wevrick, R.D. Nicholls
Publikováno v:
Cytogenetic and Genome Research. 84:11-21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ec4a8244df4e5ea222a475e3ba1b1c2
https://doi.org/10.1159/000015203
https://doi.org/10.1159/000015203
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 12
Complex genomes are characterized by large amounts of tandemly repeated DNA that can comprise up to several percent of the genome in some organisms (1,2). The analysis of the organization of this type of DNA presents certain challenges owing to its r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f08a7cba1411024a8e745fd0ed2fe9f9
https://pubmed.ncbi.nlm.nih.gov/21409641
https://pubmed.ncbi.nlm.nih.gov/21409641
Publikováno v:
BMC Genetics
Background Proximal chromosome 15q is implicated in neurodevelopmental disorders including Prader-Willi and Angelman syndromes, autistic disorder and developmental abnormalities resulting from chromosomal deletions or duplications. A subset of genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3f716e1f8e26c92e7c9dff33545fbbfe
https://pubmed.ncbi.nlm.nih.gov/11782285
https://pubmed.ncbi.nlm.nih.gov/11782285
Publikováno v:
Cytogenetics and cell genetics. 92(1-2)
Identification of imprinted genes in the Prader-Willi/Angelman syndrome deletion region is complicated by the presence of large flanking repeats. While inactive copies of DEXI are located within the repeats, we have now localized the active DEXI gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4857768d7ea3c18288b672969808d0f4
https://pubmed.ncbi.nlm.nih.gov/11306815
https://pubmed.ncbi.nlm.nih.gov/11306815
Autor:
M L, Hanel, R, Wevrick
Publikováno v:
Clinical genetics. 59(3)
Normal human development involves a delicate interplay of gene expression in specific tissues at narrow windows of time. Temporally and spatially regulated gene expression is controlled both by gene-specific factors and chromatin-specific factors. Ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b16925114a6b7782cf51da1a83ba878
https://pubmed.ncbi.nlm.nih.gov/11260224
https://pubmed.ncbi.nlm.nih.gov/11260224
Publikováno v:
Clinical and investigative medicine. Medecine clinique et experimentale. 23(3)
As knowledge of the mechanisms of genetic action expands, this new information must be incorporated into the whole. The result is that old concepts are modified or deleted or new paradigms are created. The authors review advances in the understanding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c0e9660ff5a0035e04816070d750d4c
https://pubmed.ncbi.nlm.nih.gov/10911549
https://pubmed.ncbi.nlm.nih.gov/10911549
Akademický článek
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Akademický článek
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