Zobrazeno 1 - 10
of 24
pro vyhledávání: '"F, Maggouta"'
The proximal region of chromosome 15q is predisposed to a wide range of structural rearrangements. Deletions of this region, spanning approximately 4 Mb, can be paternally or maternally derived and result in Prader-Willi syndrome and Angelman syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2621df78ed9e32248e93a894002e722
https://europepmc.org/articles/PMC1735529/
https://europepmc.org/articles/PMC1735529/
Autor:
C, Voelkel-Johnson, D J, Voeks, N M, Greenberg, R, Barrios, F, Maggouta, D T, Kurtz, D A, Schwartz, G M, Keller, T, Papenbrock, G A, Clawson, J S, Norris
Publikováno v:
Carcinogenesis. 21(8)
To develop animal models that represent the broad spectrum of human prostate cancer, we created transgenic mice with targeted prostate-specific expression of two genes (ECO:RI and c-fos) implicated in the induction of genomic instability. Expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eff46894a25d1f70fd54ca2f94e8fb96
https://pubmed.ncbi.nlm.nih.gov/10910968
https://pubmed.ncbi.nlm.nih.gov/10910968
Publikováno v:
Advances in experimental medicine and biology. 465
This chapter describes procedural aspects for development of ribozymes in general, and specifically, that cleave mRNA to an essential cellular gene, the AC40 subunit of RNA pol I. Ribozyme design includes functional selection of binding sites followe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c370c7717eaa1ff8723cdc450cbe2cb6
https://pubmed.ncbi.nlm.nih.gov/10810634
https://pubmed.ncbi.nlm.nih.gov/10810634
Publikováno v:
Cancer research. 59(10)
An estrogen receptor-driven, multistep process for estrogen carcinogenesis in the Syrian hamster kidney is proposed. Because in this species the reproductive and urogenital tracts arise from the same embryonic germinal ridge, it is evident that the k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bbe9a1d58fe3557d1beaaeb9f15e056e
https://pubmed.ncbi.nlm.nih.gov/10344741
https://pubmed.ncbi.nlm.nih.gov/10344741
Publikováno v:
Mammalian Genome. 7:469-470
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b6fd8f2e23fe23f9d76b902fc963133
https://doi.org/10.1007/s003359900139
https://doi.org/10.1007/s003359900139
Publikováno v:
Journal of Medical Genetics. 39:9e-9
The chromosome 15 region q11-q13 is imprinted and contains a number of genes that are expressed only from the paternally or the maternally inherited chromosome. This region is also prone to structural rearrangements including interstitial duplication
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fa8cf6f865e0f8fa5b4f7fa45a1e4ed
https://doi.org/10.1136/jmg.39.2.e9
https://doi.org/10.1136/jmg.39.2.e9
Publikováno v:
The American Journal of Human Genetics. (5):1061-1072
Supernumerary marker chromosomes (SMCs) of chromosome 15, designated “SMC(15)s,” are the most common SMC in humans, accounting for as much as 60% of all those observed. We report the characterization of 46 large SMC(15)s, using both fluorescence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::116971b176488566cdb137c09de1c886
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