Molecular mechanisms of autosomal recessive hypercholesterolemia (English)
- New search for: Wilund, Kenneth R.
- New search for: Yi, Ming
- New search for: Campagna, Filomena
- New search for: Arca, Marcello
- New search for: Zuliani, Giovanni
- New search for: Fellin, Renato
- New search for: Ho, Yiu-Kee
- New search for: Garcia, J. Victor
- New search for: Hobbs, Helen H.
- New search for: Cohen, Jonathan C.
- New search for: Wilund, Kenneth R.
- New search for: Yi, Ming
- New search for: Campagna, Filomena
- New search for: Arca, Marcello
- New search for: Zuliani, Giovanni
- New search for: Fellin, Renato
- New search for: Ho, Yiu-Kee
- New search for: Garcia, J. Victor
- New search for: Hobbs, Helen H.
- New search for: Cohen, Jonathan C.
In:
Human molecular genetics
;
11
, 24
;
3019-
;
2002
- Article (Journal) / Electronic Resource
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Title:Molecular mechanisms of autosomal recessive hypercholesterolemia
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Contributors:Wilund, Kenneth R. ( author ) / Yi, Ming ( author ) / Campagna, Filomena ( author ) / Arca, Marcello ( author ) / Zuliani, Giovanni ( author ) / Fellin, Renato ( author ) / Ho, Yiu-Kee ( author ) / Garcia, J. Victor ( author ) / Hobbs, Helen H. ( author ) / Cohen, Jonathan C. ( author )
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Published in:Human molecular genetics ; 11, 24 ; 3019-
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Publisher:
- New search for: Oxford University Press
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Publication date:2002-11-15
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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 11, 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.
- 2997
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Identification of the coding sequences responsible for Tsc2-mediated tumor suppression using a transgenic rat systemMomose, Shuji / Kobayashi, Toshiyuki / Mitani, Hiroaki / Hirabayashi, Masumi / Ito, Kazumi / Ueda, Masatsugu / Nabeshima, Yo-ichi / Hino, Okio et al. | 2002
- 3007
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Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repressionMazroui, Rachid / Huot, Marc-Etienne / Tremblay, Sandra / Filion, Christine / Labelle, Yves / Khandjian, Edouard W. et al. | 2002
- 3019
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Molecular mechanisms of autosomal recessive hypercholesterolemiaWilund, Kenneth R. / Yi, Ming / Campagna, Filomena / Arca, Marcello / Zuliani, Giovanni / Fellin, Renato / Ho, Yiu-Kee / Garcia, J. Victor / Hobbs, Helen H. / Cohen, Jonathan C. et al. | 2002
- 3031
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Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levelsPennacchio, Len A. / Olivier, Michael / Hubacek, Jaroslav A. / Krauss, Ronald M. / Rubin, Edward M. / Cohen, Jonathan C. et al. | 2002
- 3039
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Relative contribution of variation within the APOC3/A4/A5 gene cluster in determining plasma triglyceridesTalmud, Philippa J. / Hawe, Emma / Martin, Steve / Olivier, Michael / Miller, George J. / Rubin, Edward M. / Pennacchio, Len A. / Humphries, Steve E. et al. | 2002
- 3047
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A novel gene, Pog, is necessary for primordial germ cell proliferation in the mouse and underlies the germ cell deficient mutation, gcdAgoulnik, Alexander I. / Lu, Baisong / Zhu, Qichao / Truong, Cavatina / Ty, Maria T. / Arango, Nelson / Chada, Kiran K. / Bishop, Colin E. et al. | 2002
- 3055
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A cellular model for Friedreich Ataxia reveals small-molecule glutathione peroxidase mimetics as novel treatment strategyJauslin, Matthias L. / Wirth, Thomas / Meier, Thomas / Schoumacher, Fabrice et al. | 2002
- 3065
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Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3Grayson, Celene / Bartolini, Francesca / Chapple, J. Paul / Willison, Keith R. / Bhamidipati, Arunashree / Lewis, Sally A. / Luthert, Philip J. / Hardcastle, Alison J. / Cowan, Nicholas J. / Cheetham, Michael E. et al. | 2002
- 3075
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Sox10 haploinsufficiency affects maintenance of progenitor cells in a mouse model of Hirschsprung diseaseParatore, Christian / Eichenberger, Christof / Suter, Ueli / Sommer, Lukas et al. | 2002
- 3087
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Mutations in congenital myasthenic syndromes reveal an {varepsilon} subunit C-terminal cysteine, C470, crucial for maturation and surface expression of adult AChREaling, John / Webster, Richard / Brownlow, Sharon / Abdelgany, Amr / Oosterhuis, Hans / Muntoni, Francesco / Vaux, David J. / Vincent, Angela / Beeson, David et al. | 2002
- 3097
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Intracellular retention of mutant retinoschisin is the pathological mechanism underlying X-linked retinoschisisWang, Tao / Waters, Caroline T. / Rothman, Alex M.K. / Jakins, Tracy J. / Römisch, Karin / Trump, Dorothy et al. | 2002
- 3107
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Rescue of neurodegeneration in Niemann-Pick C mice by a prion-promoter-driven Npc1 cDNA transgeneLoftus, Stacie K. / Erickson, Robert P. / Walkley, Steven U. / Bryant, Mark A. / Incao, Arturo / Heidenreich, Randall A. / Pavan, William J. et al. | 2002