A common haplotype at the CD36 locus is associated with high free fatty acid levels and increased cardiovascular risk in Caucasians (English)
- New search for: Ma, Xiaowei
- New search for: Bacci, Simonetta
- New search for: Mlynarski, Wojciech
- New search for: Gottardo, Lucia
- New search for: Soccio, Teresa
- New search for: Menzaghi, Claudia
- New search for: Iori, Elisabetta
- New search for: Lager, Robert A.
- New search for: Shroff, Adhir R.
- New search for: Gervino, Ernest V.
- New search for: Nesto, Richard W.
- New search for: Johnstone, Michael T.
- New search for: Abumrad, Nada A.
- New search for: Avogaro, Angelo
- New search for: Trischitta, Vincenzo
- New search for: Doria, Alessandro
- New search for: Ma, Xiaowei
- New search for: Bacci, Simonetta
- New search for: Mlynarski, Wojciech
- New search for: Gottardo, Lucia
- New search for: Soccio, Teresa
- New search for: Menzaghi, Claudia
- New search for: Iori, Elisabetta
- New search for: Lager, Robert A.
- New search for: Shroff, Adhir R.
- New search for: Gervino, Ernest V.
- New search for: Nesto, Richard W.
- New search for: Johnstone, Michael T.
- New search for: Abumrad, Nada A.
- New search for: Avogaro, Angelo
- New search for: Trischitta, Vincenzo
- New search for: Doria, Alessandro
In:
Human molecular genetics
;
14
, 24
;
3973-
;
2005
- Article (Journal) / Electronic Resource
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Title:A common haplotype at the CD36 locus is associated with high free fatty acid levels and increased cardiovascular risk in Caucasians
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Contributors:Ma, Xiaowei ( author ) / Bacci, Simonetta ( author ) / Mlynarski, Wojciech ( author ) / Gottardo, Lucia ( author ) / Soccio, Teresa ( author ) / Menzaghi, Claudia ( author ) / Iori, Elisabetta ( author ) / Lager, Robert A. ( author ) / Shroff, Adhir R. ( author ) / Gervino, Ernest V. ( author )
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Published in:Human molecular genetics ; 14, 24 ; 3973-
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Publisher:
- New search for: Oxford University Press
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Publication date:2005-12-15
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 14, Issue 24
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 3775
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CDKL5/Stk9 kinase inactivation is associated with neuronal developmental disordersLin, Clark / Franco, Brunella / Rosner, Marsha Rich et al. | 2005
- 3787
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Frataxin deficiency alters heme pathway transcripts and decreases mitochondrial heme metabolites in mammalian cellsSchoenfeld, Robert A. / Napoli, Eleonora / Wong, Alice / Zhan, Shan / Reutenauer, Laurence / Morin, Dexter / Buckpitt, Alan R. / Taroni, Franco / Lonnerdal, Bo / Ristow, Michael et al. | 2005
- 3801
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Endoplasmic reticulum stress and mitochondrial cell death pathways mediate A53T mutant alpha-synuclein-induced toxicitySmith, Wanli W. / Jiang, Haibing / Pei, Zhong / Tanaka, Yuji / Morita, Hokuto / Sawa, Akira / Dawson, Valina L. / Dawson, Ted M. / Ross, Christopher A. et al. | 2005
- 3813
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Physiological identification of human transcripts translationally regulated by a specific microRNANakamoto, Mika / Jin, Peng / O'Donnell, William T. / Warren, Stephen T. et al. | 2005
- 3823
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Selective degeneration and nuclear localization of mutant huntingtin in the YAC128 mouse model of Huntington diseaseVan Raamsdonk, Jeremy M. / Murphy, Zoe / Slow, Elizabeth J. / Leavitt, Blair R. / Hayden, Michael R. et al. | 2005
- 3837
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Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancerGrice, Elizabeth A. / Rochelle, Erin S. / Green, Eric D. / Chakravarti, Aravinda / McCallion, Andrew S. et al. | 2005
- 3847
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Molecular complementation of IL-12R{beta}1 deficiency reveals functional differences between IL-12R{beta}1 alleles including partial IL-12R{beta}1 deficiencyvan de Vosse, Esther / de Paus, Roelof A. / van Dissel, Jaap T. / Ottenhoff, Tom H.M. et al. | 2005
- 3847
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Molecular complementation of IL-12Rb1 deficiency reveals functional differences between IL-12Rb1 alleles including partial IL-12Rb1 deficiencyvan de Vosse, E. / de Paus, R. A. / van Dissel, J. T. / Ottenhoff, T. H. et al. | 2005
- 3857
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Targeted disruption of hepatic frataxin expression causes impaired mitochondrial function, decreased life span and tumor growth in miceThierbach, René / Schulz, Tim J. / Isken, Frank / Voigt, Anja / Mietzner, Brun / Drewes, Gunnar / von Kleist-Retzow, Jürgen-Christoph / Wiesner, Rudolf J. / Magnuson, Mark A. / Puccio, Hélène et al. | 2005
- 3865
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Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycleThompson, Debra A. / Janecke, Andreas R. / Lange, Jessica / Feathers, Kecia L. / Hübner, Christian A. / McHenry, Christina L. / Stockton, David W. / Rammesmayer, Gabriele / Lupski, James R. / Antinolo, Guillermo et al. | 2005
- 3877
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A loss of genome buffering capacity of Dahl salt-sensitive model to modulate blood pressure as a cause of hypertensionCharron, Sophie / Lambert, Raphaëlle / Eliopoulos, Vasiliki / Duong, Chenda / Ménard, Annie / Roy, Julie / Deng, Alan Y. et al. | 2005
- 3885
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Stress-induced alterations in parkin solubility promote parkin aggregation and compromise parkin's protective functionWang, Cheng / Ko, Han Seok / Thomas, Bobby / Tsang, Fai / Chew, Katherine C.M. / Tay, Shiam-Peng / Ho, Michelle W.L. / Lim, Tit-Meng / Soong, Tuck-Wah / Pletnikova, Olga et al. | 2005
- 3899
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Dazl binds in vivo to specific transcripts and can regulate the pre-meiotic translation of Mvh in germ cellsReynolds, Nicola / Collier, Brian / Maratou, Klio / Bingham, Victoria / Speed, Robert M. / Taggart, Mary / Semple, Colin A. / Gray, Nicola K. / Cooke, Howard J. et al. | 2005
- 3911
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Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsyLerer, Israela / Sagi, Michal / Meiner, Vardiella / Cohen, Tirza / Zlotogora, Joel / Abeliovich, Dvorah et al. | 2005
- 3921
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Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cellsAdato, Avital / Lefèvre, Gaëlle / Delprat, Benjamin / Michel, Vincent / Michalski, Nicolas / Chardenoux, Sébastien / Weil, Dominique / El-Amraoui, Aziz / Petit, Christine et al. | 2005
- 3933
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Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2Reiners, Jan / van Wijk, Erwin / Märker, Tina / Zimmermann, Ulrike / Jürgens, Karin / te Brinke, Heleen / Overlack, Nora / Roepman, Ronald / Knipper, Marlies / Kremer, Hannie et al. | 2005
- 3945
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T-13910 DNA variant associated with lactase persistence interacts with Oct-1 and stimulates lactase promoter activity in vitroLewinsky, Rikke H. / Jensen, Tine G.K. / Møller, Jette / Stensballe, Allan / Olsen, Jørgen / Troelsen, Jesper T. et al. | 2005
- 3955
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Meta-analysis of genome-wide linkage studies for quantitative lipid traits in African AmericansMalhotra, Alka / Coon, Hilary / Feitosa, Mary F. / Li, Wei-Dong / North, Kari E. / Price, R. Arlen / Bouchard, Claude / Hunt, Steven C. / Wolford, Johanna K. / The American Diabetes Association GENNID Study Group, et al. | 2005
- 3963
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Mapping common regulatory variants to human haplotypesPastinen, Tomi / Ge, Bing / Gurd, Scott / Gaudin, Tiffany / Dore, Carole / Lemire, Mathieu / Lepage, Pierre / Harmsen, Eef / Hudson, Thomas J. et al. | 2005
- 3973
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A common haplotype at the CD36 locus is associated with high free fatty acid levels and increased cardiovascular risk in CaucasiansMa, Xiaowei / Bacci, Simonetta / Mlynarski, Wojciech / Gottardo, Lucia / Soccio, Teresa / Menzaghi, Claudia / Iori, Elisabetta / Lager, Robert A. / Shroff, Adhir R. / Gervino, Ernest V. et al. | 2005