Zobrazeno 1 - 10
of 53
pro vyhledávání: '"K, Kastury"'
Autor:
P. van Hauwe, C.W.R.J. Cremers, P.H.G.M. Willems, M. Verstreken, Paul Coucke, P.M. Kelley, K. Kastury, P. Van de Heyning, G. Van Camp, Isabelle Schatteman, Frank Declau, Richard J.H. Smith, Wyman T. McGuirt, R.J.H. Ensink, D. van Velzen, Henri A. M. Marres, Shalender Bhasin, Henricus P. M. Kunst, J. Meyers, Shelley D. Smith
Publikováno v:
Human molecular genetics
Human Molecular Genetics, 8, 1321-1328
Human Molecular Genetics, 8, 7, pp. 1321-1328
Human Molecular Genetics, 8, 1321-1328
Human Molecular Genetics, 8, 7, pp. 1321-1328
We have previously found linkage to chromosome 1p34 in five large families with autosomal dominant non-syndromic hearing impairment (DFNA2). In all five families, the connexin31 gene ( GJB3 ), located at 1p34 and responsible for non-syndromic autosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b28aae8f4876312aa1aeb28222de0157
https://hdl.handle.net/10067/274180151162165141
https://hdl.handle.net/10067/274180151162165141
Autor:
K, Kastury, W E, Taylor, R, Shen, S, Arver, M, Gutierrez, C E, Fisher, P J, Coucke, P, Van Hauwe, G, Van Camp, S, Bhasin
Publikováno v:
The Journal of clinical endocrinology and metabolism. 82(9)
Immotile Cilia Syndrome (ICS) is characterized by recurrent sinus and lung infections, bronchiectasis, and sperm immotility. Nasal cilia and sperm tails in patients with ICS exhibit a variety of ultrastructural defects, often including shortening or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::57cea4b841de58cec5c3f5cce43147e7
https://pubmed.ncbi.nlm.nih.gov/9284741
https://pubmed.ncbi.nlm.nih.gov/9284741
Publikováno v:
Cancer research. 57(6)
The FHIT gene spans approximately 1 Mb of DNA at chromosome band 3p14.2, which includes the familial renal cell carcinoma chromosome translocation breakpoint (between FHIT exons 3 and 4), the most frequently expressed human constitutive chromosomal f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3f44e4125b82a3aeac7f2e6490d9c325
https://pubmed.ncbi.nlm.nih.gov/9067288
https://pubmed.ncbi.nlm.nih.gov/9067288
Autor:
T, Druck, P, Hadaczek, T B, Fu, M, Ohta, Z, Siprashvili, R, Baffa, M, Negrini, K, Kastury, M L, Veronese, D, Rosen, J, Rothstein, P, McCue, M G, Cotticelli, H, Inoue, C M, Croce, K, Huebner
Publikováno v:
Cancer research. 57(3)
The FHIT gene, encoded by 10 exons in a 1.1-kb transcript, encompasses approximately 1 Mb of genomic DNA, which includes the hereditary RCC t(3;8) translocation break at 3p14.2, the FRA3B common fragile region, and homozygous deletions in various can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0c5acea4c9e4f1b645874af556116f3d
https://pubmed.ncbi.nlm.nih.gov/9012482
https://pubmed.ncbi.nlm.nih.gov/9012482
Autor:
P. van Hauwe, Paul Coucke, K. Kastury, Wayne E. Taylor, G. Van Camp, Shalender Bhasin, L. Ramirez, M. Gutierrez
Publikováno v:
Genomics: international journal of gene mapping and nucleotide sequencing
We mapped expressed tagged sequences (ESTs) corresponding to two human dynein heavy chain genes: β heavy chain of the outer dynein arm and heavy chain isotype 1B (DYH1B), by using somatic cell hybrids and radiation hybrid panels. The EST for the β
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fc2654b4db7dd891df0930918e59188
https://hdl.handle.net/10067/213700151162165141
https://hdl.handle.net/10067/213700151162165141
Autor:
T, Druck, K, Kastury, P, Hadaczek, J, Podolski, A, Toloczko, A, Sikorski, M, Ohta, S, LaForgia, J, Lasota, P, McCue
Publikováno v:
Cancer research. 55(22)
Previously, we had observed that more than 80% of clear cell renal carcinomas (RCCs) exhibited loss of heterozygosity (LOH) between the microsatellite markers D3S1285 (in 3p14.1) and D3S1295 (in 3p21.1), a region which includes the protein tyrosine p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c5040705d20b0c8e0c684b562107bf5c
https://pubmed.ncbi.nlm.nih.gov/7585599
https://pubmed.ncbi.nlm.nih.gov/7585599
Autor:
S, LaForgia, J, Lasota, F, Latif, L, Boghosian-Sell, K, Kastury, M, Ohta, T, Druck, L, Atchison, L A, Cannizzaro, G, Barnea
Publikováno v:
Cancer research. 53(13)
Extensive studies of loss of heterozygosity of 3p markers in renal cell carcinomas (RCCs) have established that there are at least three regions critical in kidney tumorigenesis, one most likely coincident with the von Hippel-Lindau gene at 3p25.3, o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d03795c7dd551dcc2af7269deba8b730
https://pubmed.ncbi.nlm.nih.gov/8319219
https://pubmed.ncbi.nlm.nih.gov/8319219
Publikováno v:
Indian journal of ophthalmology. 29(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9b00b655fc2f75d5a293570e9a3c6e70
https://pubmed.ncbi.nlm.nih.gov/7346439
https://pubmed.ncbi.nlm.nih.gov/7346439
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Akademický článek
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