Zobrazeno 1 - 10
of 55
pro vyhledávání: '"G. A. P. Bruns"'
Autor:
Tara C. Matise, Nicholas C. Dracopoli, G. A P Bruns, G. M. Landes, Jeffery M. Vance, A. Weith, Garrett M. Brodeur, Michael F. Seldin
Publikováno v:
Cytogenetic and Genome Research. 67:143-174
Autor:
G. A. P. Bruns, Steven J. Qualman, Anja König, Manfred Gessler, Jay W. Moore, Webster K. Cavenee, Karen C. Arden
Publikováno v:
Genes, Chromosomes and Cancer. 7:131-136
Wilms' tumor is a childhood nephroblastoma that is postulated to arise through the inactivation of a tumor suppressor gene by a two-hit mechanism. A candidate II p 13 Wilms' tumor gene, WT I, has been cloned and shown to encode a z:inc finger protein
Autor:
G. A. P. Bruns, Louis M. Kunkel, T. J. Byers, Joan H.M. Knoll, Alan H. Beggs, Frederick M. Boyce
Publikováno v:
Journal of Biological Chemistry. 267:9281-9288
Conserved sequences of dystrophin, beta-spectrin, and alpha-actinin were used to plan a set of degenerate oligonucleotide primers with which we amplified a portion of a human alpha-actinin gene transcript. Using this short clone as a probe, we isolat
Publikováno v:
Journal of Biological Chemistry. 267:1279-1285
Previously, we showed that the promoter of the gene encoding preproendothelin-1 (PPET-1) contains a GATA motif that is essential for activity and interacts with a nuclear factor similar in size and binding specificity to the erythroid transcription f
Autor:
G. Benson, Deborah E. Schuback, Christo Shalish, Ian W. Craig, Xandra O. Breakefield, Zheng-Yi Chen, R.V. Lebo, G. A. P. Bruns, Katherine B. Sims, M.S. Golbus
Publikováno v:
Human Molecular Genetics. 1:83-89
Norrie disease is a human X-linked recessive disorder of unknown etiology characterized by congenital blindness, sensory neural deafness and mental retardation. This disease gene was previously linked to the DXS7 (L1.28) locus and the MAO genes in ba
Publikováno v:
Japanese journal of human genetics. 35:145-150
Human vascular smooth muscle actin gene (ACTSA) was cloned and its unique sequence was used as the hybridization probe for Southern blot analysis of DNAs from 18 rodent-human somatic cell hybrids; the gene was assigned to human chromosome 10. Regiona
Publikováno v:
Human Genetics. 94
Developmental delay or mental retardation is a frequent component of multi-system anomaly syndromes associated with chromosomal deletions. Isolation of genes involved in the mental dysfunction in these disorders should define loci important in brain
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 5(4)
Autor:
Fabienne Prieur, Anne Puech, Marie-Françoise Berthéas, Manfred Gessler, F. Barichard, Claudine Junien, G. A. P. Bruns, Isabelle Henry, Marcel M.A.M. Mannens, Jan M.N. Hoovers
Publikováno v:
Genes, chromosomes & cancer, 7(1), 57-62. Wiley-Liss Inc.
Scopus-Elsevier
Scopus-Elsevier
The combined use of qualitative and quantitative analysis of I I p I 3 polymorphic markers tagether with chromosomal in situ suppression hybridization (CISS) with biotin labeled probes mapping to I I p allowed us to characterize a complex rearrangeme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c5ff2c6e8356846ebb21e170bfbd642
https://pure.amc.nl/en/publications/pericentric-intrachromosomal-insertion-responsible-for-recurrence-of-del11p13p14-in-a-family(d5defb2d-d015-41c8-a9d7-1dbd321f9a8b).html
https://pure.amc.nl/en/publications/pericentric-intrachromosomal-insertion-responsible-for-recurrence-of-del11p13p14-in-a-family(d5defb2d-d015-41c8-a9d7-1dbd321f9a8b).html
Publikováno v:
Experimental eye research. 53(5)
We have cloned cDNAs corresponding to the human gamma subunit of retinal cyclic GMP phosphodiesterase (gamma-cGMP-PDE). The coding region of these cDNAs was identical to that reported previously by Tuteja et al. (Gene 1990, 88, 227-32). We also confi