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Year | Number of Results |
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2002 | 1 |
2003 | 1 |
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Targeted disruption of Huntingtin-associated protein-1 (Hap1) results in postnatal death due to depressed feeding behavior.
Hum Mol Genet. 2002 Apr 15;11(8):945-59. doi: 10.1093/hmg/11.8.945.
Hum Mol Genet. 2002.
PMID: 11971876
Lack of huntingtin-associated protein-1 causes neuronal death resembling hypothalamic degeneration in Huntington's disease.
Li SH, Yu ZX, Li CL, Nguyen HP, Zhou YX, Deng C, Li XJ.
Li SH, et al.
J Neurosci. 2003 Jul 30;23(17):6956-64. doi: 10.1523/JNEUROSCI.23-17-06956.2003.
J Neurosci. 2003.
PMID: 12890790
Free PMC article.
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Huntingtin-associated protein 1 (Hap1) mutant mice bypassing the early postnatal lethality are neuroanatomically normal and fertile but display growth retardation.
Dragatsis I, Zeitlin S, Dietrich P.
Dragatsis I, et al.
Hum Mol Genet. 2004 Dec 15;13(24):3115-25. doi: 10.1093/hmg/ddh328. Epub 2004 Oct 20.
Hum Mol Genet. 2004.
PMID: 15496430
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Huntingtin-associated protein-1 deficiency in orexin-producing neurons impairs neuronal process extension and leads to abnormal behavior in mice.
Lin YF, Xu X, Cape A, Li S, Li XJ.
Lin YF, et al.
J Biol Chem. 2010 May 21;285(21):15941-9. doi: 10.1074/jbc.M110.107318. Epub 2010 Mar 19.
J Biol Chem. 2010.
PMID: 20304926
Free PMC article.
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