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1Academic Journal
المؤلفون: Lee, H., Greer, S.U., Pavlichin, D.S., Zhou, B., Urban, A.E., Weissman, T., Ji, H.P.
مصطلحات موضوعية: Cancer Research, Topic 1: Genes, Cells and Cell-Based Medicine
وصف الملف: application/pdf; other
Relation: http://edoc.mdc-berlin.de/23724/1/23724oa.pdf; http://edoc.mdc-berlin.de/23724/2/23724suppl.zip; Pan-conserved segment tags identify ultra-conserved sequences across assemblies in the human pangenome. Lee, H. and Greer, S.U. and Pavlichin, D.S. and Zhou, B. and Urban, A.E. and Weissman, T. and Ji, H.P. Cell Reports Methods 3 (8): 100543. 28 August 2023
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2Academic Journal
المؤلفون: Yang, E.-W., Bahn, J.H., Hsiao, E.Y.-H., Tan, B.X., Sun, Y., Fu, T., Zhou, B., Van Nostrand, E.L., Pratt, G.A., Freese, P., Wei, X., Quinones-Valdez, G., Urban, A.E., Graveley, B.R., Burge, C.B., Yeo, G.W., Xiao, X.
المساهمون: PHYSIOLOGY
المصدر: Scopus OA2019
Relation: Yang, E.-W., Bahn, J.H., Hsiao, E.Y.-H., Tan, B.X., Sun, Y., Fu, T., Zhou, B., Van Nostrand, E.L., Pratt, G.A., Freese, P., Wei, X., Quinones-Valdez, G., Urban, A.E., Graveley, B.R., Burge, C.B., Yeo, G.W., Xiao, X. (2019). Allele-specific binding of RNA-binding proteins reveals functional genetic variants in the RNA. Nature Communications 10 (1) : 1338. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-019-09292-w; https://scholarbank.nus.edu.sg/handle/10635/212197
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3Academic Journal
المؤلفون: Kalinowski, A., Liliental, J., Anker, L., Linkovski, O., Culbertson, C., Hall, J., Pattni, R., Sabatti, C., Noordsy, D., Hallmayer, J.F., Mellins, E., Ballon, J.S., O'Hara, R., Levinson, D.F., Urban, A.E.
المصدر: Brain, Behavior, and Immunity ; volume 98, page 23 ; ISSN 0889-1591
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4Academic Journal
المؤلفون: Pozzi, M., Remig, J., Fimmers, R., Urban, A.E.
المصدر: The Journal of Thoracic and Cardiovascular Surgery ; volume 101, issue 1, page 138-142 ; ISSN 0022-5223
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5Academic Journal
المؤلفون: Winkelmann J., Lin L., Schormair B., Kornum B.R., Faraco J., Plazzi G., Melberg A., Cornelio F., Urban A.E., Pizza F., Poli F., Grubert F., Wieland T., Graf E., Hallmayer J., Strom T.M., Mignot E.
المساهمون: Winkelmann, J., Lin, L., Schormair, B., Kornum, B. R., Faraco, J., Plazzi, G., Melberg, A., Cornelio, F., Urban, A. E., Pizza, F., Poli, F., Grubert, F., Wieland, T., Graf, E., Hallmayer, J., Strom, T. M., Mignot, E.
مصطلحات موضوعية: narcolepsy genetic, phenotype
Relation: info:eu-repo/semantics/altIdentifier/pmid/22328086; info:eu-repo/semantics/altIdentifier/wos/WOS:000303333700006; volume:21; issue:10; firstpage:2205; lastpage:2210; numberofpages:6; journal:HUMAN MOLECULAR GENETICS; http://hdl.handle.net/11380/1205988; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84860491605
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6Academic Journal
المؤلفون: Birney, E., Stamatoyannopoulos, J.A., Dutta, A., Guigó, R., Gingeras, T.R., Margulies, E.H., Weng, Z., Snyder, M., Dermitzakis, E.T., Thurman, R.E., Kuehn, M.S., Taylor, C.M., Neph, S., Koch, C.M., Asthana, S., Malhotra, A., Adzhubei, I., Greenbaum, J.A., Andrews, R.M., Flicek, P., Boyle, P.J., Cao, H., Carter, N.P., Clelland, G.K., Davis, S., Day, N., Dhami, P., Dillon, S.C., Dorschner, M.O., Fiegler, H., Giresi, P.G., Goldy, J., Hawrylycz, M., Haydock, A., Humbert, R., James, K.D., Johnson, B.E., Johnson, E.M., Frum, T.T., Rosenzweig, E.R., Karnani, N., Lee, K., Lefebvre, G.C., Navas, P.A., Neri, F., Parker, S.C., Sabo, P.J., Sandstrom, R., Shafer, A., Vetrie, D., Weaver, M., Wilcox, S., Yu, M., Collins, F.S., Dekker, J., Lieb, J.D., Tullius, T.D., Crawford, G.E., Sunyaev, S., Noble, W.S., Dunham, I., Denoeud, F., Reymond, A., Kapranov, P., Rozowsky, J., Zheng, D., Castelo, R., Frankish, A., Harrow, J., Ghosh, S., Sandelin, A., Hofacker, I.L., Baertsch, R., Keefe, D., Dike, S., Cheng, J., Hirsch, H.A., Sekinger, E.A., Lagarde, J., Abril, J.F., Shahab, A., Flamm, C., Fried, C., Hackermüller, J., Hertel, J., Lindemeyer, M., Missal, K., Tanzer, A., Washietl, S., Korbel, J., Emanuelsson, O., Pedersen, J.S., Holroyd, N., Taylor, R., Swarbreck, D., Matthews, N., Dickson, M.C., Thomas, D.J., Weirauch, M.T., Gilbert, J., Drenkow, J., Bell, I., Zhao, X., Srinivasan, K.G., Sung, W.K., Ooi, H.S., Chiu, K.P., Foissac, S., Alioto, T., Brent, M., Pachter, L., Tress, M.L., Valencia, A., Choo, S.W., Choo, C.Y., Ucla, C., Manzano, C., Wyss, C., Cheung, E., Clark, T.G., Brown, J.B., Ganesh, M., Patel, S., Tammana, H., Chrast, J., Henrichsen, C.N., Kai, C., Kawai, J., Nagalakshmi, U., Wu, J., Lian, Z., Lian, J., Newburger, P., Zhang, X., Bickel, P., Mattick, J.S., Carninci, P., Hayashizaki, Y., Weissman, S., Hubbard, T., Myers, R.M., Rogers, J., Stadler, P.F., Lowe, T.M., Wei, C.L., Ruan, Y., Struhl, K., Gerstein, M., Antonarakis, S.E., Fu, Y., Green, E.D., Karaöz, U., Siepel, A., Taylor, J., Liefer, L.A., Wetterstrand, K.A., Good, P.J., Feingold, E.A., Guyer, M.S., Cooper, G.M., Asimenos, G., Dewey, C.N., Hou, M., Nikolaev, S., Montoya-Burgos, J.I., Löytynoja, A., Whelan, S., Pardi, F., Massingham, T., Huang, H., Zhang, N.R., Holmes, I., Mullikin, J.C., Ureta-Vidal, A., Paten, B., Seringhaus, M., Church, D., Rosenbloom, K., Kent, W.J., Stone, E.A., Batzoglou, S., Goldman, N., Hardison, R.C., Haussler, D., Miller, W., Sidow, A., Trinklein, N.D., Zhang, Z.D., Barrera, L., Stuart, R., King, D.C., Ameur, A., Enroth, S., Bieda, M.C., Kim, J., Bhinge, A.A., Jiang, N., Liu, J., Yao, F., Vega, V.B., Lee, C.W., Ng, P., Yang, A., Moqtaderi, Z., Zhu, Z., Xu, X., Squazzo, S., Oberley, M.J., Inman, D., Singer, M.A., Richmond, T.A., Munn, K.J., Rada-Iglesias, A., Wallerman, O., Komorowski, J., Fowler, J.C., Couttet, P., Bruce, A.W., Dovey, O.M., Ellis, P.D., Langford, C.F., Nix, D.A., Euskirchen, G., Hartman, S., Urban, A.E., Kraus, P., Van Calcar, S., Heintzman, N., Kim, T.H., Wang, K., Qu, C., Hon, G., Luna, R., Glass, C.K., Rosenfeld, M.G., Aldred, S.F., Cooper, S.J., Halees, A., Lin, J.M., Shulha, H.P., Xu, M., Haidar, J.N., Yu, Y., Iyer, V.R., Green, R.D., Wadelius, C., Farnham, P.J., Ren, B., Harte, R.A., Hinrichs, A.S., Trumbower, H., Clawson, H., Hillman-Jackson, J., Zweig, A.S., Smith, K., Thakkapallayil, A., Barber, G., Kuhn, R.M., Karolchik, D., Armengol, L., Bird, C.P., de Bakker, P.I., Kern, A.D., Lopez-Bigas, N., Martin, J.D., Stranger, B.E., Woodroffe, A., Davydov, E., Dimas, A., Eyras, E., Hallgrímsdóttir, I.B., Huppert, J., Zody, M.C., Abecasis, G.R., Estivill, X., Bouffard, G.G., Guan, X., Hansen, N.F., Idol, J.R., Maduro, V.V., Maskeri, B., McDowell, J.C., Park, M., Thomas, P.J., Young, A.C., Blakesley, R.W., Muzny, D.M., Sodergren, E., Wheeler, D.A., Worley, K.C., Jiang, H., Weinstock, G.M., Gibbs, R.A., Graves, T., Fulton, R., Mardis, E.R., Wilson, R.K., Clamp, M., Cuff, J., Gnerre, S., Jaffe, D.B., Chang, J.L., Lindblad-Toh, K., Lander, E.S., Koriabine, M., Nefedov, M., Osoegawa, K., Yoshinaga, Y., Zhu, B., de Jong, P.J.
المصدر: Nature, vol. 447, no. 7146, pp. 799-816
مصطلحات موضوعية: Chromatin/genetics, Chromatin/metabolism, Chromatin Immunoprecipitation, Conserved Sequence/genetics, DNA Replication, Evolution, Molecular, Exons/genetics, Genetic Variation/genetics, Genome, Human/genetics, Genomics, Heterozygote, Histones/metabolism, Humans, Pilot Projects, Protein Binding, RNA, Messenger/genetics, Untranslated/genetics, Regulatory Sequences, Nucleic Acid/genetics, Transcription Factors/metabolism, Transcription Initiation Site, Transcription, Genetic/genetics
Relation: info:eu-repo/semantics/altIdentifier/pmid/17571346; info:eu-repo/semantics/altIdentifier/pissn/1476-4687[electronic]; https://serval.unil.ch/notice/serval:BIB_1573FA50DE7C
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7Conference
المؤلفون: Sayward, F.G., Yang, J., Nelson, F.K., Euskirchen, G., Urban, A.E., Bertone, P., Rinn, J., Weissman, S., Gerstein, M., Snyder, M., Miller, P.L.
المصدر: 2006 40th Annual Conference on Information Sciences & Systems; 2006, p1578-1598, 21p
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8Periodical
المؤلفون: Sinzobahamvya, N., Arenz, C., Brecher, A.M., Urban, A.E.
المصدر: Cardiovascular Surgery; 1999, Vol. 7 Issue: 4 p436-442, 7p
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9Academic Journal
المؤلفون: Urban, A.E., Stark, J., Waterston, D.J.
المصدر: The Annals of Thoracic Surgery ; volume 21, issue 4, page 304-310 ; ISSN 0003-4975
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10Academic Journal
المؤلفون: Urban, A.E., Anderson, R.H., Stark, J.
المصدر: American Heart Journal ; volume 94, issue 1, page 91-95 ; ISSN 0002-8703
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11Academic Journal
المؤلفون: Davis K. N., Qu P. -P., Ma S., Lin L., Plastini M., Dahl N., Plazzi G., Pizza F., O'Hara R., Wong W. H., Hallmayer J., Mignot E., Zhang X., Urban A. E.
المساهمون: Davis K.N., Qu P.-P., Ma S., Lin L., Plastini M., Dahl N., Plazzi G., Pizza F., O'Hara R., Wong W.H., Hallmayer J., Mignot E., Zhang X., Urban A.E.
مصطلحات موضوعية: methyltransferase, DNMT, epigenomic, transcriptomic, neurodevelopment
وصف الملف: STAMPA
Relation: info:eu-repo/semantics/altIdentifier/pmid/37584462; info:eu-repo/semantics/altIdentifier/wos/WOS:001102978600007; volume:32; issue:21; firstpage:3105; lastpage:3120; numberofpages:16; journal:HUMAN MOLECULAR GENETICS; https://hdl.handle.net/11585/958372; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85174641050
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12
المؤلفون: Birgitte Rahbek Kornum, Tim M. Strom, Fabian Grubert, Elisabeth Graf, Fabio Pizza, Ling Lin, Juliette Faraco, Atle Melberg, Alexander E. Urban, Juliane Winkelmann, Giuseppe Plazzi, Barbara Schormair, Francesca Poli, Thomas Wieland, Emmanuel Mignot, Ferdinando Cornelio, Joachim Hallmayer
المساهمون: Winkelmann J., Lin L., Schormair B., Kornum B.R., Faraco J., Plazzi G., Melberg A., Cornelio F., Urban A.E., Pizza F., Poli F., Grubert F., Wieland T., Graf E., Hallmayer J., Strom T.M., Mignot E.
المصدر: Hum. Mol. Genet. 21, 2205-2210 (2012)
Human Molecular Genetics
Human Molecular Genetics; Vol 21مصطلحات موضوعية: DNA (Cytosine-5-)-Methyltransferase 1, Ataxia, Cerebellar Ataxia, phenotype, Molecular Sequence Data, Biology, Deafness, medicine.disease_cause, 03 medical and health sciences, Exon, symbols.namesake, 0302 clinical medicine, Autosomal dominant cerebellar ataxia, Genetics, medicine, Humans, Exome, Amino Acid Sequence, DNA (Cytosine-5-)-Methyltransferases, Molecular Biology, Genetics (clinical), Exome sequencing, 030304 developmental biology, Genes, Dominant, Narcolepsy, Sanger sequencing, 0303 health sciences, Mutation, Cerebellar ataxia, General Medicine, Articles, Exons, medicine.disease, narcolepsy genetics, Pedigree, Phenotype, narcolepsy genetic, symbols, medicine.symptom, 030217 neurology & neurosurgery
وصف الملف: application/pdf; ELETTRONICO