The Human Phenome Project (Englisch)
Nationallizenz
- Neue Suche nach: Freimer, Nelson
- Neue Suche nach: Sabatti, Chiara
- Neue Suche nach: Freimer, Nelson
- Neue Suche nach: Sabatti, Chiara
In:
Nature Genetics
;
34
, 1
;
15-21
;
2003
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ISSN:
- Aufsatz (Zeitschrift) / Elektronische Ressource
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Titel:The Human Phenome Project
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Beteiligte:Freimer, Nelson ( Autor:in ) / Sabatti, Chiara ( Autor:in )
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Erschienen in:Nature Genetics ; 34, 1 ; 15-21
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Verlag:
- Neue Suche nach: Nature Publishing Group
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Erscheinungsdatum:01.05.2003
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Format / Umfang:7 pages
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ISSN:
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DOI:
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Medientyp:Aufsatz (Zeitschrift)
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Format:Elektronische Ressource
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Sprache:Englisch
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Datenquelle:
Inhaltsverzeichnis – Band 34, Ausgabe 1
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- 1
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From the ground up| 2003
- 3
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Conjugal rites of mycobacteriaBhatt, Apoorva / Jacobs, William R. et al. | 2003
- 4
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A nuclear address with influenceShannon, M. Frances et al. | 2003
- 6
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Centrosomes as DNA damage regulatorsSibon, Ody C. M. et al. | 2003
- 8
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ORFeomics: correcting the wiggle in worm genesBoone, Charles / Andrews, Brenda et al. | 2003
- 11
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Touching base| 2003
- 13
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How to book for microarraysCarroll, Adam et al. | 2003
- 15
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The Human Phenome ProjectFreimer, Nelson / Sabatti, Chiara et al. | 2003
- 23
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Genetic background is an important determinant of metastatic potentialHunter, Kent / Welch, Danny R. / Liu, Edison T. et al. | 2003
- 23
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Genomic analysis of primary tumors does not address the prevalence of metastatic cells in the populationFidler, Isaiah J. / Kripke, Margaret L. et al. | 2003
- 25
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Reply to "Genomic analysis of primary tumors does not address the prevalence of metastatic cells in the population" and "Genetic background is an important determinant of metastatic potential"Ramaswamy, Sridhar / Ross, Ken N. / Lander, Eric S. / Golub, Todd R. et al. | 2003
- 27
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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autismJamain, Stéphane / Quach, Hélène / Betancur, Catalina / Råstam, Maria / Colineaux, Catherine / Gillberg, I. Carina / Soderstrom, Henrik / Giros, Bruno / Leboyer, Marion / Gillberg, Christopher et al. | 2003
- 29
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Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disordersJones, Bethan / Jones, Emma L. / Bonney, Stephanie A. / Patel, Hetal N. / Mensenkamp, Arjen R. / Eichenbaum-Voline, Sophie / Rudling, Mats / Myrdal, Urban / Annesi, Grazia / Naik, Sandhia et al. | 2003
- 32
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Dax1 is required for testis determinationMeeks, Joshua J. / Weiss, Jeffrey / Jameson, J. Larry et al. | 2003
- 35
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C. elegans ORFeome version 1.1: experimental verification of the genome annotation and resource for proteome-scale protein expressionReboul, Jérôme / Vaglio, Philippe / Rual, Jean-François / Lamesch, Philippe / Martinez, Monica / Armstrong, Christopher M. / Li, Siming / Jacotot, Laurent / Bertin, Nicolas / Janky, Rekin's et al. | 2003
- 42
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Tissue-specific nuclear architecture and gene expession regulated by SATB1Cai, Shutao / Han, Hye-Jung / Kohwi-Shigematsu, Terumi et al. | 2003
- 53
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Prox1 function controls progenitor cell proliferation and horizontal cell genesis in the mammalian retinaDyer, Michael A. / Livesey, Frederick J. / Cepko, Constance L. / Oliver, Guillermo et al. | 2003
- 59
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Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiencyPaw, Barry H. / Davidson, Alan J. / Zhou, Yi / Li, Rong / Pratt, Stephen J. / Lee, Charles / Trede, Nikolaus S. / Brownlie, Alison / Donovan, Adriana / Liao, Eric C. et al. | 2003
- 65
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Maintenance of CpG methylation is essential for epigenetic inheritance during plant gametogenesisSaze, Hidetoshi / Scheid, Ortrun Mittelsten / Paszkowski, Jerzy et al. | 2003
- 70
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Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency diseaseHernandez, Paolo A. / Gorlin, Robert J. / Lukens, John N. / Taniuchi, Shoichiro / Bohinjec, Jože / Francois, Fleur / Klotman, Mary E. / Diaz, George A. et al. | 2003
- 75
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Trimethylated lysine 9 of histone H3 is a mark for DNA methylation in Neurospora crassaTamaru, Hisashi / Zhang, Xing / McMillen, Debra / Singh, Prim B. / Nakayama, Jun-ichi / Grewal, Shiv I. / Allis, C. David / Cheng, Xiaodong / Selker, Eric U. et al. | 2003
- 80
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Unconventional conjugal DNA transfer in mycobacteriaWang, Jun / Parsons, Linda M. / Derbyshire, Keith M. et al. | 2003
- 85
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Treatment-specific changes in gene expression discriminate in vivo drug response in human leukemia cellsCheok, Meyling H. / Yang, Wenjian / Pui, Ching-Hon / Downing, James R. / Cheng, Cheng / Naeve, Clayton W. / Relling, Mary V. / Evans, William E. et al. | 2003
- 91
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Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAATCarlton, Victoria E. H. / Harris, Baruch Z. / Puffenberger, Erik G. / Batta, A. K. / Knisely, A. S. / Robinson, Donna L. / Strauss, Kevin A. / Shneider, Benjamin L. / Lim, Wendell A. / Salen, Gerald et al. | 2003
- 97
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Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosisNicolas, Gaël / Viatte, Lydie / Lou, Dan-Qing / Bennoun, Myriam / Beaumont, Carole / Kahn, Axel / Andrews, Nancy C. / Vaulont, Sophie et al. | 2003
- 102
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Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosisMuckenthaler, Martina / Roy, Cindy N. / Custodio, Ángel O. / Miñana, Belén / deGraaf, Jos / Montross, Lynne K. / Andrews, Nancy C. / Hentze, Matthias W. et al. | 2003
- 108
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Melanoma mouse model implicates metabotropic glutamate signaling in melanocytic neoplasiaPollock, Pamela M. / Cohen-Solal, Karine / Sood, Raman / Namkoong, Jin / Martino, Jeffrey J. / Koganti, Aruna / Zhu, Hua / Robbins, Christiane / Makalowska, Izabela / Shin, Seung-Shick et al. | 2003
- 113
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A defective response to Hedgehog signaling in disorders of cholesterol biosynthesisCooper, M K / Wassif, C A / Krakowiak, P A / Taipale, J / Gong, R / Kelley, R I / Porter, F D / Beachy, P A et al. | 2003
- 113
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Sir3p phosphorylation by the Slt2p pathway effects redistribution of silencing function and shortened lifespanRay, A / Hector, R E / Roy, N / Song, J-H / Berkner, K L / Runge, K W et al. | 2003