Literature DB >> 16263095

Normal hypocretin-1 (orexin-A) levels in the cerebrospinal fluid of patients with Huntington's disease.

Andreas Meier1, Brit Mollenhauer, Stefan Cohrs, Andrea Rodenbeck, Wolfgang Jordan, Johannes Meller, Markus Otto.   

Abstract

A significant atrophy and loss of hypocretin neurons in the brains of human patients with Huntington's disease (HD) and in R6/2 mice have been reported. We included 10 patients with HD and 12 patients with chorea-like hyperkinetic movement disorders (non-HD). All patients of the HD group and eleven patients of the non-HD group showed normal hypocretin-1 levels. Thus, hypocretin-1 may not serve as an additional diagnostic marker for HD.

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Year:  2005        PMID: 16263095     DOI: 10.1016/j.brainres.2005.09.028

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  5 in total

1.  Paradoxical function of orexin/hypocretin circuits in a mouse model of Huntington's disease.

Authors:  Rhîannan H Williams; A Jennifer Morton; Denis Burdakov
Journal:  Neurobiol Dis       Date:  2011-02-13       Impact factor: 5.996

2.  Neurophysiological and Behavioral Effects of Anti-Orexinergic Treatments in a Mouse Model of Huntington's Disease.

Authors:  Magali Cabanas; Cristiana Pistono; Laura Puygrenier; Divyangana Rakesh; Yannick Jeantet; Maurice Garret; Yoon H Cho
Journal:  Neurotherapeutics       Date:  2019-07       Impact factor: 7.620

Review 3.  G proteins, p60TRP, and neurodegenerative diseases.

Authors:  Klaus Heese
Journal:  Mol Neurobiol       Date:  2013-01-24       Impact factor: 5.590

Review 4.  Chronic sleep disturbance and neural injury: links to neurodegenerative disease.

Authors:  Sabra M Abbott; Aleksandar Videnovic
Journal:  Nat Sci Sleep       Date:  2016-01-25

5.  The Role of Hypothalamic Pathology for Non-Motor Features of Huntington's Disease.

Authors:  Rachel Y Cheong; Sanaz Gabery; Åsa Petersén
Journal:  J Huntingtons Dis       Date:  2019
  5 in total

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