Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Anna Marie Frischauf"'
Autor:
Kevin Clark, Blanche P. Alter, Douglas R. Higgs, Jonathan Flint, John F. Peden, R. J. Daniels, Jonathan Frampton, Kian Tan-Un, Cristina Tufarelli, Ross C. Hardison, Webb Miller, Tara McMorrow, Sjaak Philipsen, Anna Marie Frischauf
Publikováno v:
Human Molecular Genetics, 10(4), 1-12. Oxford University Press
We have cloned, sequenced and annotated segments of DNA spanning the mouse, chicken and pufferfish alpha globin gene clusters and compared them with the corresponding region in man. This has defined a small segment ( approximately 135-155 kb) of synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfddfacee37da840cd89b557a6409c7c
https://pubmed.ncbi.nlm.nih.gov/11157800
https://pubmed.ncbi.nlm.nih.gov/11157800
Autor:
Thomas Theil, Brian P. Chadwick, Anna-Marie Frischauf, Stephanie Kate Heath, Kerstin Hasenpusch-Theil, David G. Wilkinson
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 10(3)
We have isolated and characterized a novel PHD finger gene, PHF2, which maps to human Chromosome (Chr) 9q22 close to D9S196. Its mouse homolog was also characterized and mapped to the syntenic region on mouse Chr 13. The predicted human and mouse pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7538afec97c011f57daca7d5ae8a390b
https://pubmed.ncbi.nlm.nih.gov/10051327
https://pubmed.ncbi.nlm.nih.gov/10051327
Autor:
D. Timothy Bishop, Julia A. Newton Bishop, Gordon Peters, Elizabeth Pinney, Anna-Marie Frischauf, Mark Harland, Nelleke A. Gruis, Peter Selby, Rolando Meloni, Veronique Bataille, Nigel K. Spurr, Sharon Brookes, Jack Cuzick
Publikováno v:
Human molecular genetics. 6(12)
Germline mutations in CDKN2 on chromosome 9p21, which codes for the cyclin D kinase inhibitor p16, and more rarely, mutations in the gene coding for CDK4, the protein to which p16 binds, underlie susceptibility in some melanoma families. We have sequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c3a82886b658957888dac6366d8f929
https://pubmed.ncbi.nlm.nih.gov/9328469
https://pubmed.ncbi.nlm.nih.gov/9328469
Autor:
Anna Marie Frischauf, Reinhard Becher, Felix Mitelman, Curt I. Civin, Julian Borrow, Vincent P. Stanton, J. Michael Andresen, Stefano Volinia, Doug Horsman, David E. Housman, Frederick G. Behm, Ann E. Watmore, Christine M. Disteche, Raju S.K. Chaganti, Ian D. Dubé
Publikováno v:
Nature genetics. 14(1)
The recurrent translocation t(8;16)(p11;p13) is a cytogenetic hallmark for the M4/M5 subtype of acute myeloid leukaemia. Here we identify the breakpoint-associated genes. Positional cloning on chromosome 16 implicates the CREB-binding protein (CBP),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5767395310844c4a172601b86c0fd18
https://pubmed.ncbi.nlm.nih.gov/8782807
https://pubmed.ncbi.nlm.nih.gov/8782807
Autor:
Huw Thomas, Liliana Varesco, Anna-Marie Frischauf, Paul A. Lawson, S Cottrell, Günther Zehetner, Walter F. Bodmer, Ellen Solomon, Denise Sheer, Sarah V. Williams, Tristan Ward, Tania A. Jones
Publikováno v:
Genes, chromosomescancer. 3(5)
The gene for adenomatous polyposis coli has been localized to 5q21–22. We have mapped six probes from this region using isotopic or nonisotopic in situ hybridization. Using tritium-labeled probes we localized 11227 (D5S37) to 5q 14–15 and ECB27 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b44d95ff28effa2d4dad9c720e805797
https://pubmed.ncbi.nlm.nih.gov/1665706
https://pubmed.ncbi.nlm.nih.gov/1665706
Autor:
Huw Thomas, Liliana Varesco, Walter F. Bodmer, Tania A. Jones, Ellen Solomon, I.B. Kerr, Anna-Marie Frischauf, S Cottrell, V.A. Murday, M.E.F. Smith, Sarah V. Williams
Publikováno v:
Molecular Mechanisms and their Clinical Application in Malignancies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::457a04ed82625d0242f644df2b5073d1
https://doi.org/10.1016/b978-0-12-091075-5.50016-0
https://doi.org/10.1016/b978-0-12-091075-5.50016-0
Autor:
Michael Zimmer, Annemarie Poustka, W. Lance Whaley, Jonathan L. Haines, Marcy E. MacDonald, Hans Lehrach, John J. Wasmuth, Maja Bucan, Barbara Smith, Nancy S. Wexler, Julie Leavitt, Bernice A. Allitto, James F. Gusella, Anna Marie Frischauf, Shirley V. Cheng, S. Youngman, Peter S. Harper
Publikováno v:
Neuron. 3:183-190
The Huntington's disease gene ( HD ) maps distal to the D4S10 marker in the terminal 4p16.3 subband of chromosome 4. Directed cloning has provided several DNA segments that have been grouped into three clusters on a physical map of approximately 5 ×
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ed70542d6f6c84e4fa37760cbf91e4e
https://doi.org/10.1016/0896-6273(89)90031-7
https://doi.org/10.1016/0896-6273(89)90031-7