Search Results - "Kastury, K"

Cloning and characterization of two members of the vertebrate Dlx gene family by Simeone, A, Acampora, D, Pannese, M, D'Esposito, M, Stornaiuolo, A, Gulisano, M, Mallamaci, A, Kastury, K, Druck, T, Huebner, K

“…A number of vertebrate genes of the Dlx gene family have been cloned in mouse, frog, and zebrafish. These genes contain a homeobox related to that of…”
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Structure of the Human Receptor Tyrosine Phosphatase Gamma Gene (PTPRG) and Relation to the Familial RCC t(3;8) Chromosome Translocation by Kastury, K., Ohta, M., Lasota, J., Moir, D., Dorman, T., LaForgia, S., Druck, T., Huebner, K.

“…The receptor protein tyrosine phosphatase γ gene, PTPγ (locus namePTPRG), was previously mapped to chromosome region 3p14.2, within a 2- to 4-Mb region…”
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Chromosome locations of human EMX and OTX genes by Kastury, K, Druck, T, Huebner, K, Barletta, C, Acampora, D, Simeone, A, Faiella, A, Boncinelli, E

“…We have determined the chromosomal localization of four human homeobox-containing genes, EMX1, EMX2, OTX1, and OTX2, related to Drosophila genes expressed in…”
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Complementary deoxyribonucleic acid cloning and characterization of a putative human axonemal dynein light chain gene by KASTURY, K, TAYLOR, W. E, SHEN, R, ARVER, S, GUTIERREZ, M, FISHER, C. E, COUCKE, P. J, VAN HAUWE, P, VAN CAMP, G, BHASIN, S

“…Immotile Cilia Syndrome (ICS) is characterized by recurrent sinus and lung infections, bronchiectasis, and sperm immotility. Nasal cilia and sperm tails in…”
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The Human Homologue of the Retroviral Oncogene qin Maps to Chromosome 14q13 by Kastury, Kumar, Li, Jian, Druck, Teresa, Su, Heyun, Vogt, Peter K., Croce, Carlo M., Huebner, Kay

“…Chromosomal mapping of the human QIN gene (renamed FKH2 by the Human Genome Organization Nomenclature Committee) was initially accomplished by correlation of…”
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Chromosome locations of genes encoding human signal transduction adapter proteins, Nck (NCK), Shc (SHC1), and Grb2 (GRB2) by Huebner, K, Kastury, K, Druck, T, Salcini, A E, Lanfrancone, L, Pelicci, G, Lowenstein, E, Li, W, Park, S H, Cannizzaro, L

“…Abnormalities due to chromosomal aberration or point mutation in gene products of growth factor receptors or in ras gene products, which lie on the same…”
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The FHIT Gene, Spanning the Chromosome 3p14.2 Fragile Site and Renal Carcinoma–Associated t(3;8) Breakpoint, Is Abnormal in Digestive Tract Cancers by Ohta, Masataka, Inoue, Hiroshi, Cotticelli, Maria Grazia, Kastury, Kumar, Baffa, Raffaele, Palazzo, Juan, Siprashvili, Zurab, Mori, Masaki, McCue, Peter, Druck, Teresa, Croce, Carlo M, Huebner, Kay

“…A 200–300 kb region of chromosome 3p14.2, including the fragile site locus FRA3B, is homozygously deleted in multiple tumor-derived cell lines. Exon…”
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Analysis of genomic DNA alterations and mRNA expression patterns in a panel of human pancreatic cancer cell lines by Gysin, Stephan, Rickert, Paula, Kastury, Kumar, McMahon, Martin

“…Genomic alterations influencing the expression and/or activity of tumor suppressors or oncogenes such as KRAS2, CDKN2A, TP53, and DPC4 have been directly…”
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Characterization of the Mammalian YAP (Yes-associated Protein) Gene and Its Role in Defining a Novel Protein Module, the WW Domain by Sudol, Marius, Bork, Peer, Einbond, Aaron, Kastury, Kumar, Druck, Teresa, Negrini, Massimo, Huebner, Kay, Lehman, David

“…We report cDNA cloning and characterization of the human and mouse orthologs of the chicken YAP (Yes-associated protein) gene which encodes a novel protein…”
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Structure and expression of the human FHIT gene in normal and tumor cells by DRUCK, T, HADACZEK, P, ROTHSTEIN, J, MCCUE, P, COTTICELLI, M. G, INOUE, H, CROCE, C. M, HUEBNER, K, FU, T.-B, OHTA, M, SIPRASHVILI, Z, BAFFA, R, NEGRINI, M, KASTURY, K, VERONESE, M. L, ROSEN, D

“…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)…”
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Mutations in the KCNQ4 Gene Are Responsible for Autosomal Dominant Deafness in Four DFNA2 Families by Coucke, Paul J., Van Hauwe, Peter, Kelley, Philip M., Kunst, Henricus, Schatteman, Isabelle, Van Velzen, Désirée, Meyers, Johan, Ensink, Robbert J., Verstreken, Margriet, Declau, Frank, Marres, Henri, Kastury, Kumar, Bhasin, Shalender, McGuirt, Wyman T., Smith, Richard J. H., Cremers, Cor W.R.J., Van de Heyning, Paul, Willems, Patrick J., Smith, Shelley D., Van Camp, Guy

“…We have previously found linkage to chromosome 1p34 in five large families with autosomal dominant non-syndromic hearing impairment (DFNA2). In all five…”
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Positions of chromosome 3p14.2 fragile sites (FRA3B) within the FHIT gene by ZIMONJIC, D. B, DRUCK, T, OHTA, M, KASTURY, K, CROCE, C. M, POPESCU, N. C, HUEBNER, K

“…The FHIT gene spans approximately 1 Mb of DNA at chromosome band 3p14.2, which includes the familial renal cell carcinoma chromosome translocation breakpoint…”
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Potential gastrointestinal tumor suppressor locus at the 3p14.2 FRA3B site identified by homozygous deletions in tumor cell lines by KASTURY, K, BAFFA, R, PALAZZO, J, HUEBNER, K, DRUCK, T, OHTA, M, COTTICELLI, M, INOUE, H, NEGRINI, M, RUGGE, M, HUANG, D, CROCE, C. M

“…A number of DNA fragments, identified by representational difference analysis, which were homozygously deleted in various cancer cell lines were previously…”
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Loss of heterozygosity at the familial RCC t(3;8) locus in most clear cell renal carcinomas by DRUCK, T, KASTURY, K, LUBINSKI, J, HUEBNER, K, HADACZEK, P, PODOLSKI, J, TOLOCZKO, A, SIKORSKI, A, OHTA, M, LAFORGIA, S, LASOTA, J, MCCUE, P

“…Previously, we had observed that more than 80% of clear cell renal carcinomas (RCCs) exhibited loss of heterozygosity (LOH) between the microsatellite markers…”
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Gene structure, promoter activity, and chromosomal location of the DR-nm23 gene, a related member of the nm23 gene family by MARTINEZ, R, VENTURELLI, D, PERROTTI, D, VERONESE, M. L, KASTURY, K, DRUCK, T, HUEBNER, K, CALABRETTA, B

“…DR-nm23 cDNA was cloned recently by differential screening of a cDNA library derived from chronic myelogenous leukemia-blast crisis primary cells. It is highly…”
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Assignment of DAP1 and DAPK—Genes That Positively Mediate Programmed Cell Death Triggered by IFN-γ—to Chromosome Regions 5p12.2 and 9q34.1, Respectively by Feinstein, Elena, Druck, Teresa, Kastury, Kumar, Berissi, Hanna, Goodart, Sheryl A., Overhauser, Joan, Kimchi, Adi, Huebner, Kay

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Detailed genetic and physical map of the 3p chromosome region surrounding the familial renal cell carcinoma chromosome translocation, t(3;8)(p14.2;q24.1) by LAFORGIA, S, LASOTA, J, SCHLESSINGER, J, MODI, W, KUZMIN, I, TORY, K, ZBAR, B, CROCE, C. M, LERMAN, M, HUEBNER, K, LATIF, F, BOGHOSIAN-SELL, L, KASTURY, K, OHTA, M, DRUCK, T, ATCHISON, L, CANNIZZARO, L. A, BARNEA, G

“…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…”
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Complementary deoxyribonucleic acid cloning and characterization of a putative human axonemal dynein light chain gene by Kastury, K, Taylor, WE, Shen, RQ, Arver, S, Gutierrez, M, Fisher, CE, Coucke, PJ, VanHauwe, P, VanCamp, G, Bhasin, S

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Chromosomal Mapping of Two Members of the Human Dynein Gene Family to Chromosome Regions 7p15 and 11q13 near the Deafness Loci DFNA 5 and DFNA 11 by Kastury, Kumar, Taylor, Wayne E., Gutierrez, Matthew, Ramirez, Luz, Coucke, Paul J., Van Hauwe, Peter, Van Camp, Guy, Bhasin, Shalender

“…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…”
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FLT4 receptor tyrosine kinase gene mapping to chromosome band 5q35 in relation to the t(2;5), t(5;6), and t(3;5) translocations by Armstrong, E, Kastury, K, Aprelikova, O, Bullrich, F, Nezelof, C, Gogusev, J, Wasmuth, J J, Alitalo, K, Morris, S, Huebner, K

“…FLT4 is a recently cloned receptor tyrosine kinase cDNA, which is characterized by seven immunoglobulin-like loops in its extracellular domain. We have…”
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