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Deficient transcription of XIST from tiny ring X chromosomes in females with severe phenotypes

Autor: Teresa L. Yang-Feng, B. A. Stasiowski, P. A. Jacobs, D. L. Van Dyke, J. E. Wiley, Shengyuan Luo, Joyce Axelman, Barbara R. Migeon, Mihir M. Jani, Lester Weiss

Publikováno v: Proceedings of the National Academy of Sciences. 90:12025-12029

The severe phenotype of human females whose karyotype includes tiny ring X chromosomes has been attributed to the inability of the small ring X chromosome to inactivate. The XIST locus is expressed only from the inactive X chromosome, resides at the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5afb2d2f12cef6bdcb0545955bd3f739
https://doi.org/10.1073/pnas.90.24.12025

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Replication banding and FISH analysis reveal the origin of the Hyla femoralis karyotype and XY/XX sex chromosomes

Autor: J E, Wiley

Publikováno v: Cytogenetic and genome research. 101(1)

The pine woods treefrog, Hyla femoralis, is unique among North American hylid frogs in having a metacentric chromosome 6 and heteromorphic sex chromosomes of the XY/XX type. The X chromosome is distinguished by having a nucleolar organizing region (N

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f329b34b1634969fa499202137fce824
https://pubmed.ncbi.nlm.nih.gov/14571141

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Cloning of the 18S rDNA gene, an internal transcribed spacer, and the 5' region of the 28S rDNA gene of Cope's gray treefrog, Hyla chrysoscelis

Autor: G, Owens, J E, Wiley

Publikováno v: Cytogenetics and cell genetics. 92(1-2)

The location of rDNA genes on the chromosomes of most species is identical within that species, usually occurring on the same chromosome or chromosomes. This is not the case in Cope's gray treefrog, Hyla chrysoscelis, where the rDNA genes are polymor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b69776f7e3bcad8407809be8063c3506
https://pubmed.ncbi.nlm.nih.gov/11306807

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Assignment of the mitochondrial translation elongation factor Ts gene (TSFM) to human chromosome 12 bands q13--q14 by in situ hybridization and with somatic cell hybrids

Autor: J L, Vernon, P C, Burr, J E, Wiley, M A, Farwell

Publikováno v: Cytogenetics and cell genetics. 89(3-4)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::df36209b6389a5583bc573d643ff2591
https://pubmed.ncbi.nlm.nih.gov/10965106

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Replication banding patterns of the diploid-tetraploid treefrogs Hyla chrysoscelis and H. versicolor

Autor: J E, Wiley, M L, Little

Publikováno v: Cytogenetics and cell genetics. 88(1-2)

Populations of the diploid-tetraploid treefrogs Hyla chrysoscelis and H. versicolor can be defined by the polymorphic positions of the nucleolar organizing regions (NORs) on their chromosomes. Evidence from NOR positions and interstitial telomere seq

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::41bb1679b8845397720719f51f6e3d26
https://pubmed.ncbi.nlm.nih.gov/10773656

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Assignment1 of the mitochondrial translational initiation factor 2 gene (MTIF2) to human chromosome 2 bands p16--p14 by in situ hybridization and with somatic cell hybrids

Autor: D S, Bonner, J E, Wiley, M A, Farwell

Publikováno v: Cytogenetics and cell genetics. 83(1-2)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::74531752586abbdbbf1af8ffd5b991d1
https://pubmed.ncbi.nlm.nih.gov/9925935

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Familial cryptic translocation resulting in Angelman syndrome:implications for imprinting or location of the Angelman gene?

Autor: L W, Burke, J E, Wiley, C C, Glenn, D J, Driscoll, K M, Loud, A J, Smith, T, Kushnick

Publikováno v: American journal of human genetics. 58(4)

Angelman syndrome (AS) is associated with a loss of maternal genetic information, which typically occurs as a result of a deletion at 15q11-q13 or paternal uniparental disomy of chromosome 15. We report a patient with AS as a result of an unbalanced

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4ce75d5586512147a01a6b830eeac141
https://pubmed.ncbi.nlm.nih.gov/8644742

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Tamoxifen induces hepatic aneuploidy and mitotic spindle disruption after a single in vivo administration to female Sprague-Dawley rats

Autor: L M, Sargent, Y P, Dragan, N, Bahnub, J E, Wiley, C A, Sattler, P, Schroeder, G L, Sattler, V C, Jordan, H C, Pitot

Publikováno v: Cancer research. 54(13)

Tamoxifen has found extensive use in the treatment of all stages of human breast cancer. The efficacy of tamoxifen treatment for the prevention of second primary tumors and its chemosuppressive action in animal models have led to initiation of clinic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2e00e630c30766a7921a401128f77f24
https://pubmed.ncbi.nlm.nih.gov/8012949

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Interstitial hybridization sites of the (TTAGGG)n telomeric sequence on the chromosomes of some North American hylid frogs

Autor: J E, Wiley, J, Meyne, M L, Little, J C, Stout

Publikováno v: Cytogenetics and cell genetics. 61(1)

Interstitial hybridization sites for the (TTAGGG)n telomeric repeat sequence were present in all seven species of hylid frogs examined and in a triploid hybrid between two of the species. Intra- and interspecific differences and similarities in hybri

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bb6b047a65e83bc35da3e852b8d33f7c
https://pubmed.ncbi.nlm.nih.gov/1505232

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Ribosomal RNA gene site polymorphism in Bufo terrestris

Autor: D L, Foote, J E, Wiley, M L, Little, J, Meyne

Publikováno v: Cytogenetics and cell genetics. 57(4)

Individual specimens of Bufo terrestris were discovered that possessed ribosomal gene locations in addition to those normally found. Every specimen from an island population that was examined had extra sites, whereas fewer individuals from coastal ma

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1d75931c27128ab3979a729ae93c3f41
https://pubmed.ncbi.nlm.nih.gov/1743073

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