Zobrazeno 1 - 10
of 10
pro vyhledávání: '"R B, Wadey"'
Publikováno v:
Oncogene. 6(4)
We have analysed 55 Wilms' tumour DNAs using the cDNA from the candidate Wilms' predisposition gene, WT1. One tumour, GOS 129, shows a partial homozygous deletion involving only the 3'-most exon of the gene. An adjacent 3' DNA sequence, J7-18, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a8b58c263a4c4a0b2fbecea0f8ad95d
https://pubmed.ncbi.nlm.nih.gov/1851548
https://pubmed.ncbi.nlm.nih.gov/1851548
Publikováno v:
Human genetics. 86(5)
The association of nephropathy, Wilms' tumour and genital abnormalities is known as Drash syndrome. Two of these features are also seen in the WAGR (Wilms' tumour, aniridia, genito-urinary abnormalities, mental retardation) complex, known to be assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c130e2a97d72c4102eb6826c663742b7
https://pubmed.ncbi.nlm.nih.gov/1849870
https://pubmed.ncbi.nlm.nih.gov/1849870
Publikováno v:
Oncogene. 5(11)
Loss of heterozygosity at loci on the short arm of chromosome 11 has been reported in 31% (11/38) of Wilms' tumours in our series. Lymphoblastoid cell lines were prepared from the parents of 10/11 of the patients showing allele loss in their tumours.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7fdb692c6e498d70a7a9942b0509d6cc
https://pubmed.ncbi.nlm.nih.gov/1980007
https://pubmed.ncbi.nlm.nih.gov/1980007
Publikováno v:
Oncogene. 5(6)
Pairs of tumour and normal DNA samples from 38 Wilms' tumour patients have been investigated for loss of heterozygosity using 12 probes from chromosome 11. Allele loss was detected in only 11 cases (31%). Densitometric analysis showed that allele los
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8c0fb46498877d3bb38a9c200c64cd40
https://pubmed.ncbi.nlm.nih.gov/2163053
https://pubmed.ncbi.nlm.nih.gov/2163053
Publikováno v:
Human Genetics. 84
A cosmid library has been prepared in the lorist-B vector from a mouse/human somatic cell hybrid containing region 11q23-11pter as the only human component. This chromosome region is stably maintained in the hybrid as a result of translocation onto o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da039c0c1c1a17f2b6f5f3684b45e234
https://doi.org/10.1007/bf00195812
https://doi.org/10.1007/bf00195812
Autor:
T, Boehm, I, Lavenir, A, Forster, R B, Wadey, J K, Cowell, J, Harbott, F, Lampert, J, Waters, P, Sherrington, P, Couillin
Publikováno v:
Oncogene. 3(6)
A breakpoint cluster region (T-ALLbcr) has been previously described on 11p13 for T-ALL carrying t(11;14)(p13;q11). One further T-ALL breakpoint is described bringing to 5 out of 6 such translocations which are found to break within a maximum of 6.7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c4ce97e4d931df901a5ac6e4168bf743
https://pubmed.ncbi.nlm.nih.gov/2577871
https://pubmed.ncbi.nlm.nih.gov/2577871
Publikováno v:
Advances in Nitrogen Fixation Research ISBN: 9789400969254
Tolerance of Rhizobium isolates to heavy metals was screened by multi-point inoculation of defined medium agar plates each with a metal ion at a particular concentration.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59f10fbbeecfd03e6055ecc85be05177
https://doi.org/10.1007/978-94-009-6923-0_112
https://doi.org/10.1007/978-94-009-6923-0_112
Publikováno v:
Human genetics. 82(2)
We have analysed karyotypes and DNA from three patients with aniridia (congenital absence of irises) and Wilms' tumour. All three had constitutional deletions from the short arm of chromosome 11. The minimum region of overlap of the deletion involves
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47c16549267bbeb559fe0178f5baf53e
https://pubmed.ncbi.nlm.nih.gov/2542153
https://pubmed.ncbi.nlm.nih.gov/2542153
Autor:
Leslie B. Rall, Jon Pritchard, R. B. Wadey, C. F. Graham, L.M. Priestley, James F. Scott, B. Hopkins, Graeme I. Bell, M.E. Robertson, Timothy J. Knott, John K. Cowell
Publikováno v:
Nature. 317(6034)
Wilms' tumour (nephroblastoma) is an embryonal neoplasm occurring in hereditary and spontaneous forms. Both types show rearrangements of the short arm of chromosome 11. The germ line of children with the rare inherited triad of aniridia, genitourinar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbd7013933cee8f611c37c128dfbe56d
https://pubmed.ncbi.nlm.nih.gov/2995818
https://pubmed.ncbi.nlm.nih.gov/2995818
Autor:
R. B. Wadey, John K. Cowell
Publikováno v:
Nucleic Acids Research. 17:3332-3332
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16bae451f26e9105339236341c5eb23a
https://doi.org/10.1093/nar/17.8.3332
https://doi.org/10.1093/nar/17.8.3332