Search Results - "Gos, A"

Gene Ontology annotations and resources by Blake, J A, Dolan, M, Drabkin, H, Hill, D P, Li, Ni, Sitnikov, D, Bridges, S, Burgess, S, Buza, T, McCarthy, F, Peddinti, D, Pillai, L, Carbon, S, Dietze, H, Ireland, A, Lewis, S E, Mungall, C J, Gaudet, P, Chrisholm, R L, Fey, P, Kibbe, W A, Basu, S, Siegele, D A, McIntosh, B K, Renfro, D P, Zweifel, A E, Hu, J C, Brown, N H, Tweedie, S, Alam-Faruque, Y, Apweiler, R, Auchinchloss, A, Axelsen, K, Bely, B, Blatter, M -C, Bonilla, C, Bouguerleret, L, Boutet, E, Breuza, L, Bridge, A, Chan, W M, Chavali, G, Coudert, E, Dimmer, E, Estreicher, A, Famiglietti, L, Feuermann, M, Gos, A, Gruaz-Gumowski, N, Hieta, R, Hinz, C, Hulo, C, Huntley, R, James, J, Jungo, F, Keller, G, Laiho, K, Legge, D, Lemercier, P, Lieberherr, D, Magrane, M, Martin, M J, Masson, P, Mutowo-Muellenet, P, O'Donovan, C, Pedruzzi, I, Pichler, K, Poggioli, D, Porras Millán, P, Poux, S, Rivoire, C, Roechert, B, Sawford, T, Schneider, M, Stutz, A, Sundaram, S, Tognolli, M, Xenarios, I, Foulgar, R, Lomax, J, Roncaglia, P, Khodiyar, V K, Lovering, R C, Talmud, P J, Chibucos, M, Giglio, M Gwinn, Chang, H -Y, Hunter, S, McAnulla, C, Mitchell, A, Sangrador, A, Stephan, R, Harris, M A, Oliver, S G, Rutherford, K, Wood, V, Bahler, J, Lock, A, Kersey, P J, McDowall, D M

“…The Gene Ontology (GO) Consortium (GOC, http://www.geneontology.org) is a community-based bioinformatics resource that classifies gene product function through…”
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Combined spatial and temporal imaging of brain activity during visual selective attention in humans by Heinze, H. J, Mangun, G. R, Burchert, W, Hinrichs, H, Scholz, M, Münte, T. F, Gös, A, Scherg, M, Johannes, S, Hundeshagen, H, Gazzaniga, M. S, Hillyard, S. A

“…Visual-spatial attention is an essential brain function that enables us to select and preferentially process high priority information in the visual fields…”
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3313 The next generation sequencing (NGS) analysis of selected genes and pathways in clinical stage III cutaneous melanoma by Lugowska, I, Mierzejewska, E, Kowalik, A, Gos, A, Zięba, S, Siedlecki, J, Kosea-Paterczyk, H, Szumera-Ciéckiewicz, A, Jurkowska, M, Rutkowski, P

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3348 Cell-free DNA V600E measurements during vemurafenib therapy of metastatic melanoma patients by Kozak, K, Lugowska, I, Kowalik, A, Gos, A, Jurkowska, M, Stępniak, J, Switaj, T, Paterczyk, H. Kosela, Klimczak, A, Falkowski, S, Jagielska, B, Siedlecki, J, Chlopek, M, Kalisz, J, Rutkowski, P

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Schizophrenia Susceptibility Associated with Interstitial Deletions of Chromosome 22q11 by Karayiorgou, Maria, Morris, Michael A., Morrow, Bernice, Shprintzen, Robert J., Goldberg, Rosalie, Borrow, Julian, Gos, Arnaud, Nestadt, Gerald, Wolyniec, Paula S., Lasseter, Virginia K., Eisen, Harvey, Childs, Barton, Kazazian, Haig H., Kucherlapati, Raju, Antonarakis, Stylianos E., Pulver, Ann E., Housman, David E.

“…We report the results of two studies examining the genetic overlap between schizophrenia and velocardiofacial syndrome. In study A, we characterize two…”
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591P The utility of next generation sequencing for KRAS gene variants prevalence in cytological and tissue samples in real-world NSCLC patients: A large single institution real-world study by Pluzanski, A., Tysarowski, A., Seliga, K., Gos, A., Zub, R., Krzakowski, M.J.

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A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y by HAIMING CHEN, ROSSIER, C, MORRIS, M. A, SCOTT, H. S, GOS, A, BAIROCH, A, ANTONARAKIS, S. E

“…To contribute to the creation of a transcription map of human chromosome 21 (HC21) and to the identification of genes that may be involved in the pathogenesis…”
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Surface morphology during anisotropic wet chemical etching of crystalline silicon by Gosálvez, M A, Nieminen, R M

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Ongoing and future developments at the Universal Protein Resource by Morgat, Anne, Apweiler, Rolf, Martin, Maria-Jesus, O'Donovan, C., Magrane, M., Alam-Faruque, Y., Antunes, R., Barrell, D., Bely, B., Bingley, M., Binns, D., Bower, L., Browne, P., Wm, Chan, Dimmer, E., Eberhardt, R., Fazzini, Pier-Francesco, Fedotov, A., Foulger, R., Garavelli, J., Lg, Castro, Huntley, R., Jacobsen, J., Kleen, M., Laiho, K., Legge, D., Lin, Q., Liu, W., Luo, J., Orchard, S., Patient, S., Pichler, K., Poggioli, D., Pontikos, N., Pruess, M., Rosanoff, S., Sawford, T., Sehra, H., Turner, E., Corbett, M., Donnelly, M., Rensburg P, Van, Xenarios, I., Bougueleret, L., Auchincloss, A., Argoud-Puy, G., Axelsen, K., Bairoch, A., Baratin, D., Mc, Blatter, Boeckmann, B., Bolleman, J., Bollondi, L., Boutet, E., Sb, Quintaje, Breuza, L., Bridge, A., Decastro, E., Coudert, E., Cusin, I., Doche, M., Dornevil, D., Duvaud, S., Estreicher, A., Famiglietti, L., Feuermann, M., Gehant, S., Ferro, S., Gasteiger, E., Gateau, A., Gerritsen, V., Gos, A., Gruaz-Gumowski, N., Hinz, U., Hulo, C., Hulo, N., James, J., Jimenez, S., Jungo, F., Kappler, T., Keller, G., Lara, V., Lemercier, P., Lieberherr, D., Martin, X., Masson, P., Moinat, M., Paesano, S., Pedruzzi, I., Pilbout, S., Poux, S., Pozzato, M., Redaschi, N., Rivoire, C., Roechert, B., Schneider, M., Sigrist, C., Sonesson, K., Staehli, S., Stanley, E.

“…The primary mission of Universal Protein Resource (UniProt) is to support biological research by maintaining a stable, comprehensive, fully classified, richly…”
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Gene structure and chromosomal localization of the human P2X7 receptor by Buell, G N, Talabot, F, Gos, A, Lorenz, J, Lai, E, Morris, M A, Antonarakis, S E

“…The genomic organization for the human P2X7 receptor gene was determined to comprise 13 exons. Alignment of the exon-intron junctions with those for the rat…”
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The Gene Ontology: enhancements for 2011

“…The Gene Ontology (GO) (http://www.geneontology.org) is a community bioinformatics resource that represents gene product function through the use of…”
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Schizophrenia and chromosomal deletions within 22q11.2 by Lindsay, E A, Morris, M A, Gos, A, Nestadt, G, Wolyniec, P S, Lasseter, V K, Shprintzen, R, Antonarakis, S E, Baldini, A, Pulver, A E

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Fortuitous detection of uniparental isodisomy of chromosome 6 by Bittencourt, M C, Morris, M A, Chabod, J, Gos, A, Lamy, B, Fellmann, F, Antonarakis, S E, Plouvier, E, Herve, P, Tiberghien, P

“…Uniparental isodisomy is defined as the inheritance of two copies of the same parental chromosome and can result in defects when it produces homozygosity for a…”
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Programmed Death Ligand-1 (Pd-L1) Expression and Prognostic Value in Synovial Sarcoma by Kozak, K., Szumera-Cieckiewicz, A., Rembiszewska, A., Podgorska, A., Paterczyk, H.M. Kosela, Przybyl, J., Gos, A., Switaj, T., Prochorec-Sobieszek, M., Rutkowski, P.

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1441PPROGRAMMED DEATH LIGAND-1 (PD-L1) EXPRESSION AND PROGNOSTIC VALUE IN SYNOVIAL SARCOMA by Kozak, K., Szumera-Cieckiewicz, A., Rembiszewska, A., Podgorska, A., Paterczyk, H.M. Kosela, Przybyl, J., Gos, A., Switaj, T., Prochorec-Sobieszek, M., Rutkowski, P.

“…Abstract Aim: The interaction between PD-L1 expressed by neoplastic cells and its receptor PD-1 on activated T cells results in T cell suppression and…”
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Mapping of the Gene for the p60 Subunit of the Human Chromatin Assembly Factor (CAF1A) to the Down Syndrome Region of Chromosome 21 by Blouin, Jean-Louis, Duriaux-Sail, Geneviève, Chen, Haiming, Gos, Arnaud, Morris, Michael A., Rossier, Colette, Antonarakis, Stylianos E.

“…Exon trapping was used to clone portions of genes from the Down syndrome critical region (DSCR) of human chromosome 21. One trapped sequence showed complete…”
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Localization of a Human Homolog of the Mouse Pericentrin Gene (PCNT) to Chromosome 21qter by Chen, Haiming, Gos, Arnaud, Morris, Michael A., Antonarakis, Stylianos E.

“…Exon trapping was used to identify portions of genes from cosmid DNA of a human chromosome 21-specific library LL21NC02-Q. More than 650 potential exons have…”
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Attention to adjacent and separate positions in space: an electrophysiological analysis by Heinze, H J, Luck, S J, Münte, T F, Gös, A, Mangun, G R, Hillyard, S A

“…Some theories of visuospatial attention propose that attention can be divided between separated zones of space that exclude the intervening region, whereas…”
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Isolation and characterization of the mouse Aire gene by Mittaz, L, Rossier, C, Heino, M, Peterson, P, Krohn, K J, Gos, A, Morris, M A, Kudoh, J, Shimizu, N, Antonarakis, S E, Scott, H S

“…Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a rare autosomal recessive disorder characterized by Addison's disease and/or…”
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The mTOR kinase directly regulates FBP1 gene expression via interaction with SWI/SNF chromatin remodeling complex in clear cell renal cell carcinoma (ccRCC) by Sarnowska, E., Cwiek, P., Szarkowska, J., Leszczynski, M., Rusetska, N., Szymanski, M., Jancewicz, I., Stachowiak, M., Kubala, S., Chrzan, A., Gos, A., Balcerak, A., Demkow, T., Siedlecki, J.A., Sarnowski, T.J.

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