Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Renata M.J. Hamvas"'
Publikováno v:
Mammalian Genome. 8:S320-S342
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11340dad763666d1d8c2c34dec7fc3c4
https://doi.org/10.1007/s003359900662
https://doi.org/10.1007/s003359900662
Publikováno v:
Genomics. 44:1-7
The TATA-binding protein (TBP) is a factor required for the transcription of all classes of eukaryotic genes. Here, we demonstrate that in the mouse the TBP-encoding gene (Tbp) resides next to the proteasomal subunit C5-encoding gene (Psmb1). The gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e965fbbf0afa6c62243332153732efbe
https://doi.org/10.1006/geno.1997.4839
https://doi.org/10.1006/geno.1997.4839
Autor:
Sona Gregorova, Werner E. Mayer, Renata M.J. Hamvas, Vladimir Vincek, Zdenek Trachtulec, Hans Lehrach, Monika Mňuková-Fajdelová, Jiří Forejt, Jan Klein
Publikováno v:
Mammalian Genome. 8:312-316
The Hybrid sterility 1 (Hst1) gene causes male infertility in crosses between certain inbred strains of the laboratory and wild mouse, Mus musculus. To identify the causative gene, we have searched YAC clones encompassing the Hstl region for testis-e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa723c470fc54163a370424a53bfbad8
https://doi.org/10.1007/s003359900430
https://doi.org/10.1007/s003359900430
Publikováno v:
Genomics. 23:132-137
Hybrid sterility 1 (Hst1) is the major gene responsible for sterility of male hybrids between Mus musculus and certain laboratory strains. Thus, Hst1 is of importance in studying both postreproductive isolation of closely related species and male fer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7205c4e9586d0446347d6a8e17d2325
https://doi.org/10.1006/geno.1994.1468
https://doi.org/10.1006/geno.1994.1468
Publikováno v:
Mammalian Genome. 2:72-75
Modifiers of position-effect-variegation in Drosophila are thought to encode proteins that are either structural components of heterochromatin or enzymes that modify these components. We have recently shown that a sequence motif found in one Drosophi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06970f78c7eb2566fe0475820da0cb08
https://doi.org/10.1007/bf00570443
https://doi.org/10.1007/bf00570443
Autor:
Neil Brockdorff, Renata M.J. Hamvas, J. T. Keer, Stephen D.M. Brown, David C. Page, Sohaila Rastan
Publikováno v:
Genomics. 7:566-572
The mouse X-inactivation center lies just distal to the T16H breakpoint. Utilizing pedigree analysis of backcross progeny from a Mus domesticus/Mus spretus interspecific cross, we have mapped a number of genetic loci, gene probes, microclones, and Ea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79c558746b7095f6e314b0d72200a9b8
https://doi.org/10.1016/0888-7543(90)90200-e
https://doi.org/10.1016/0888-7543(90)90200-e
Autor:
M. Loudová, Vladimir Vincek, Gregorová S, J. Čapková, M. Mňuková-Fajdelová, Jiri Forejt, Hans Lehrach, M. Hoglund, Zdenek Trachtulec, Jan Klein, Renata M.J. Hamvas
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 7(2)
We have generated a high-resolution genetic map, 0.071 cM per backcross animal, of the 13 cM T-H2 region of the mouse Chromosome (Chr) 17. The map contains two phenotypic loci, T and Hst1, 12 RFLP markers, and 24 microsatellite loci. The Hst1 gene wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f02cc4e74345106e6c8439fba4f080e3
https://pubmed.ncbi.nlm.nih.gov/8835526
https://pubmed.ncbi.nlm.nih.gov/8835526
Autor:
Hans Lehrach, Renata M.J. Hamvas
Publikováno v:
Electrophoresis. 16(9)
This review presents some properties of interspersed repeats, particularly human and mouse repeats, and shows how these have been utilized in long-range genome mapping. The link between the distribution of such repeats and their relationship with gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f440443fbcf6a806b62e439b6bc15d7
https://pubmed.ncbi.nlm.nih.gov/8582341
https://pubmed.ncbi.nlm.nih.gov/8582341
Autor:
Renata M.J. Hamvas, Chee Gee See, Marc K. Drezner, J. L. H. O'Riordan, Peter S. N. Rowe, Fiona Francis, Frances Benham, Hans Lehrach, Michael J. Econs
Publikováno v:
Genomics. 21(1)
Dominant X-linked hypophosphatemic rickets (HYP) is the most common form of familial rickets. Linkage studies have localized the gene for this disorder to Xp22.1 between the markers DXS365 and DXS274, a region estimated to be approximately 3.5 cM. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4642d2ffc0359aa64fea0113682938e
https://pubmed.ncbi.nlm.nih.gov/8088792
https://pubmed.ncbi.nlm.nih.gov/8088792
Autor:
Annie Dutriaux, Renata M.J. Hamvas, Richard Mott, Lisa Gellen, Günther Zehetner, Andrei Grigorlev, Carmela Lopes, Hans Lehrach, Marie-Laure Yaspo, Christine Van Broeckhoven, Radost Vatcheva, Dean Nižetić, Marie-Claude Potler, Jean-M. Delabar
Publikováno v:
Human molecular genetics
We describe here the construction of an ordered clone map of human chromosome 21, based on the identification of ordered sets of YAC clones covering > 90% of the chromosome, and their use to identify groups of cosmid clones (cosmid pockets) localised
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3433fb64fd4f074734b80cb0966cba4
http://ora.ox.ac.uk/objects/uuid:b81f768c-3afa-419a-9d80-d9f9c382a6c1
http://ora.ox.ac.uk/objects/uuid:b81f768c-3afa-419a-9d80-d9f9c382a6c1