Zobrazeno 1 - 10 of 27 pro vyhledávání: '"Jane W. Fountain"'
1
Markers and Tissue Resources for Melanoma: Meeting Report
Autor: Magdalena Thurin, Vernon K. Sondak, Dorothea Becker, Martin C. Mihm, Stephen M. Hewitt, Jane W. Fountain
Publikováno v: Cancer Research. 66:10652-10657
The Markers and Tissue Resources for Melanoma meeting convened by the Cancer Diagnosis Program, Division of Cancer Treatment and Diagnosis, Specialized Programs of Research Excellence at the Organ Systems Branch of the National Cancer Institute (NCI)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2856cfdcce2d2b8f71e3bebca3524990
https://doi.org/10.1158/0008-5472.can-06-0921
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2
PTEN inactivation is rare in melanoma tumours but occurs frequently in melanoma cell lines
Autor: T Que Noy, Graeme J. Walker, N C Bloch, J M Glendening, Pamela M. Pollock, Jane W. Fountain, Nicholas K. Hayward
Publikováno v: Melanoma Research. 12:565-575
Deletions detected in cytogenetic and loss of heterozygosity (LOH) studies indicate that at least one tumour suppressor gene maps to the long arm of chromosome 10. Previous deletion mapping studies have observed LOH on 10q in about 30% of melanomas a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dd6db650cd48a0504626f8c4b3cfb67
https://doi.org/10.1097/00008390-200212000-00006
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3
In vitro loss of heterozygosity targets the PTEN/MMAC1 gene in melanoma
Autor: Gavin P. Robertson, H.-J. Su Huang, Jane W. Fountain, Frank B. Furnari, Tracy G. Lugo, Webster K. Cavenee, Danny R. Welch, Mary E. Miele, Michael J. Glendening
Publikováno v: Proceedings of the National Academy of Sciences. 95:9418-9423
Gross genetic lesions of chromosome 10 occur in 30–50% of sporadic human melanomas. To test the functional significance of this observation, we have developed an in vitro loss of heterozygosity approach in which a wild-type chromosome 10 was transf
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::145dcf82ad8eb6ee119588dada18970d
https://doi.org/10.1073/pnas.95.16.9418
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4
Virtually 100% of melanoma cell lines harbor alterations at the DNA level withinCDKN2A, CDKN2B, or one of their downstream targets
Autor: Walker Gj, Isabel D.C. Markl, Flores Jf, J. Michael Glendening, Amy H. Lin, Jane W. Fountain
Publikováno v: Genes, Chromosomes and Cancer. 22:157-163
The cyclin-dependent kinase inhibitor 2A (CDKN2A), or p16INK4a, gene on 9p21 is important in the genesis of both familial and sporadic melanoma. Homozygous deletions and intragenic mutations of this gene have been identified in both melanoma cell lin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::187e5e3cf75cfa946a739aae99506f7f
https://doi.org/10.1002/(sici)1098-2264(199806)22:2<157::aid-gcc11>3.0.co
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5
Haplotype analysis of two recurrentCDKN2A mutations in 10 melanoma families: Evidence for common founders and independent mutations
Autor: Jane W. Fountain, Margaret A. Tucker, Tim Bishop, Ray Barnhill, Nigel K. Spurr, Julia Newton-Bishop, Alisa M. Goldstein, William D. Foulkes, Nicholas K. Hayward, Pamela M. Pollock, Nelleke A. Gruis, Daniel A. Haber, Pieter A. van der Velden
Publikováno v: Human Mutation. 11:424-431
Germ-line mutations in CDKN2A have been shown to predispose to cutaneous malignant melanoma. We have identified 2 new melanoma kindreds which carry a duplication of a 24bp repeat present in the 5' region of CDKN2A previously identified in melanoma fa
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b09049e102311cf47987f00fd4152eb4
https://doi.org/10.1002/(sici)1098-1004(1998)11:6<424::aid-humu2>3.0.co
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7
Linkage mapping of the Aldo-2, Pax-5, Ambp , and D4H9S3E loci on mouse chromosome 4 in the region of homology with human chromosome 9
Autor: Catherine M. Abbott, Jo Peters, Jane W. Fountain, Alison Pilz
Publikováno v: Genomics. 18:705-708
The genes for aldolase-B (ALDOB), the alpha 1-microglobulin/bikunin precursor (AMBP), the paired box gene PAX5, and the anonymous DNA marker D9S3 map to human chromosome 9 (HSA9). We have set out to map the mouse homologues of each of these genes. Th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc7885e0c01d4a4129d99a0370040545
https://doi.org/10.1016/s0888-7543(05)80379-9
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8
Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines
Autor: Nicholas C. Dracopoli, Thomas W. Glover, Francis S. Collins, Susan A. Tarlé, Lone B. Andersen, David H. Gutmann, Jane W. Fountain, David E. Housman
Publikováno v: Nature Genetics. 3:118-121
Neurofibromatosis type 1 (NF1) is a common autosomal dominant disorder characterized by progressive and variable involvement of tissues predominantly derived from the neural crest and a predisposition toward malignancies. The NF1 gene encodes neurofi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b228dc837ea1bf258258db6a160b5cdd
https://doi.org/10.1038/ng0293-118
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9
Report of the Second International Workshop on Human Chromosome 9 Mapping 1993
Autor: David J. Kwiatkowski, John A.L. Armour, Margaret A. Knowles, D.R. Goudie, Alison Pilz, Susan A. Slaugenhaupt, Jonathan L. Haines, Allen E. Bale, Sue Povey, Jane W. Fountain
Publikováno v: Cytogenetic and Genome Research. 64:93-121
The Second International Workshop on Human Chromosome 9 was held in Chatham, Massachusetts on April 18--20, 1993. Fifty-three abstracts were received and the data presented on posters. The purpose of the meeting was to bring together all interested i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::afe38c66048c3017464a61eab1a33092
https://doi.org/10.1159/000133566
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10
REPORT on the First International Workshop on Chromosome 9 held at Girton College Cambridge, UK, 22?24 March, 1992
Autor: Dominic P. Kwiatkowski, Ian J. Jackson, Jane W. Fountain, Jonathan L. Haines, M Hultén, M Lawrie, Susan Povey, Catherine M. Abbott, Maureen E. Smith, Allen E. Bale
Publikováno v: POVEY, S; SMITH, M; HAINES, J; KWIATKOWSKI, D; FOUNTAIN, J; BALE, A; et al.(1992). REPORT on the First International Workshop on Chromosome 9 held at Girton College Cambridge, UK, 22?24 March, 1992. Annals of Human Genetics, 56(3), 167-182. doi: 10.1111/j.1469-1809.1992.tb01145.x. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/5k97g95t
Ann. Hum. Genet. (1992), 56, 167-221 Printd in &eat Britain REPORT on the First International Workshop on Chromosome 9 held at Girton College Cambridge, UK, 22-24 March, 1992 Prepared by: S. POVEY, M. SMITH, J. HAINES, D. KWIATKOWSKI, J . FOUNTAIN, A
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b6d564a6a734d5b6acf03affa53216c
https://doi.org/10.1111/j.1469-1809.1992.tb01145.x
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