Zobrazeno 1 - 10
of 48
pro vyhledávání: '"M Chiano"'
Autor:
D. Goudie, M. Chiano, A. J. Jeffreys, Denis C. Shields, M. Lathrop, Susan Povey, J. Weissenbach, J. Weber, John A.L. Armour, J. Attwood, N. Dracopoli, A. Retief, Pericak-Vance Margareta A, H. Donis-Keller, Andrew Collins, C. Falk, John R.W. Yates, Jonathan L. Haines, J. Fountain, R. White, Susan A. Slaugenhaupt, Tara C. Matise, G. Vergnaud, J. Phillips, Hope Northrup, J. Gusella, David J. Kwiatkowski, Elizabeth B. Robson
Publikováno v:
Genomics. 19:203-214
This paper describes the Centre d'Etude du Polymorphisme Humain (CEPH) consortium linkage map of chromosome 9. A total of 124 markers were typed in the CEPH family DNAs by 14 contributing laboratories; of these, 42 loci are ordered on the map with li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f02b3255ae70b29d995bd6599fd448e3
https://doi.org/10.1006/geno.1994.1049
https://doi.org/10.1006/geno.1994.1049
Autor:
S. J. Payne, E. Bentley, Eamonn R. Maher, Frances M. Richards, M Chiano, Farida Latif, John R.W. Yates, David E. Barton, Marston Linehan, S Hosoe
Publikováno v:
Journal of Medical Genetics. 29:902-905
Von Hippel-Lindau (VHL) disease is a dominantly inherited cancer syndrome characterised by the development of retinal, cerebellar, and spinal haemangioblastomas, renal cell carcinoma, and phaeochromocytoma. The gene for VHL disease has been mapped to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9feae4c7ab0c328235f01c1966a74722
https://doi.org/10.1136/jmg.29.12.902
https://doi.org/10.1136/jmg.29.12.902
Autor:
M Chiano, H J Wong, Tim D. Spector, A Line, E Lank, M Galley, Jerry S. Lanchbury, David B. Thompson, David P. Strachan, P.W. Reed, Kourosh R. Ahmadi
Publikováno v:
Genes and immunity. 4(4)
Asthma is a common, heterogeneous, complex disease accompanied by raised total and specific immunoglobulin-E (IgE) antibody levels. Despite numerous previous reports of linkage and association of asthma, atopy and serum IgE levels to genes within the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::604762848019fb9fdb9fe055208f0a31
https://pubmed.ncbi.nlm.nih.gov/12761566
https://pubmed.ncbi.nlm.nih.gov/12761566
Autor:
Alex J. MacGregor, P Smith, Harold Snieder, R W Keen, H Molloy, T D Spector, M Chiano, J Daniels, F Gibson, D Gewert, L Fairbairn
Publikováno v:
Rheumatology (Oxford, England). 40(1)
OBJECTIVE: Bone mineral density (BMD) in later life is a major determinant of osteoporotic fracture risk and has been shown to be under strong genetic influence. Transforming growth factor beta 1 (TGF- beta 1) is an important regulatory cytokine, is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a114ef40ad619046020a8c67db2fbec
https://pubmed.ncbi.nlm.nih.gov/11157141
https://pubmed.ncbi.nlm.nih.gov/11157141
Akademický článek
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Autor:
Elisabeth Rosser, A Dodge, M. Chiano, David Craufurd, Jayne Leggo, Gail Norbury, S. Korn, David C. Rubinsztein
Publikováno v:
Neurology. 49(3)
The CAG repeat number on Huntington's disease (HD) chromosomes accounts for about 60% of the variance in the age at onset of HD. However, distinct familial factors may also influence the age at onset. HD is associated with loss of medium-sized GABA-e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cfb3a51dfbd3e3d521180531f52baf6
https://pubmed.ncbi.nlm.nih.gov/9305364
https://pubmed.ncbi.nlm.nih.gov/9305364
Publikováno v:
Clinical Science. 103:11P-12P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2dd9b322a1100c2101734a82a71978a
https://doi.org/10.1042/cs103011pb
https://doi.org/10.1042/cs103011pb
Autor:
L. P. Briley, M. Casey, Vincent Mooser, Colin F. Spraggs, Karen S. King, F. Sapunar, A. Preston, Lon R. Cardon, M. Chiano
Publikováno v:
Journal of Clinical Oncology. 29:552-552
552 Background: Diarrhea is common during lapatinib treatment. Most events are mild to moderate, self-limiting and managed proactively to prevent serious complications, however diarrhea may lead to non-compliance and possibly poor treatment outcomes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73715e9563d21bc6322113ec444eed6b
https://doi.org/10.1200/jco.2011.29.15_suppl.552
https://doi.org/10.1200/jco.2011.29.15_suppl.552
Akademický článek
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Autor:
Michael Doherty, Roland W. Moskowitz, S. Brady, Jordan B. Renner, Marc C. Hochberg, U. Atif, Virginia B. Kraus, E.M. Woldu, J. Aponte, Anthony G. Wilson, M. Chiano, Anie Philip, Richard F. Loeser, Joanne M. Jordan
Publikováno v:
Osteoarthritis and Cartilage. (10):1174-1177
Summary Objective An association between osteoarthritis (OA) and functional polymorphisms in the aspartic acid (d) repeat of the asporin ( ASPN ) gene was reported in Japanese and Han Chinese populations. The aim of this study was to assess the assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40f217426de80e7266ec94f68295c27f