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1.
mHTT Seeding Activity: A Marker of Disease Progression and Neurotoxicity in Models of Huntington's Disease.
Mol Cell
; 71(5): 675-688.e6, 2018 09 06.
Article
in English
| MEDLINE | ID: mdl-30193095
2.
Effects of mutant huntingtin in oxytocin neurons on non-motor features of Huntington's disease.
Neuropathol Appl Neurobiol
; 49(2): e12891, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36776123
3.
Effects of mutant huntingtin inactivation on Huntington disease-related behaviours in the BACHD mouse model.
Neuropathol Appl Neurobiol
; 47(4): 564-578, 2021 06.
Article
in English
| MEDLINE | ID: mdl-33330988
4.
Loss of the metabolism and sleep regulating neuronal populations expressing orexin and oxytocin in the hypothalamus in amyotrophic lateral sclerosis.
Neuropathol Appl Neurobiol
; 47(7): 979-989, 2021 12.
Article
in English
| MEDLINE | ID: mdl-33755993
5.
Brain white matter lesions are associated with reduced hypothalamic volume and cranial radiotherapy in childhood-onset craniopharyngioma.
Clin Endocrinol (Oxf)
; 94(1): 48-57, 2021 01.
Article
in English
| MEDLINE | ID: mdl-32762072
6.
Early white matter pathology in the fornix of the limbic system in Huntington disease.
Acta Neuropathol
; 142(5): 791-806, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34448021
7.
Early postnatal behavioral, cellular, and molecular changes in models of Huntington disease are reversible by HDAC inhibition.
Proc Natl Acad Sci U S A
; 115(37): E8765-E8774, 2018 09 11.
Article
in English
| MEDLINE | ID: mdl-30150378
8.
Gene therapy for Parkinson's disease: Disease modification by GDNF family of ligands.
Neurobiol Dis
; 97(Pt B): 179-188, 2017 01.
Article
in English
| MEDLINE | ID: mdl-27616425
9.
Low dietary protein content alleviates motor symptoms in mice with mutant dynactin/dynein-mediated neurodegeneration.
Hum Mol Genet
; 24(8): 2228-40, 2015 Apr 15.
Article
in English
| MEDLINE | ID: mdl-25552654
10.
Microstructure alterations in the hypothalamus in cranially radiated childhood leukaemia survivors but not in craniopharyngioma patients unaffected by hypothalamic damage.
Clin Endocrinol (Oxf)
; 87(4): 359-366, 2017 Oct.
Article
in English
| MEDLINE | ID: mdl-28502079
11.
Hypothalamic atrophy is related to body mass index and age at onset in amyotrophic lateral sclerosis.
J Neurol Neurosurg Psychiatry
; 88(12): 1033-1041, 2017 12.
Article
in English
| MEDLINE | ID: mdl-28596251
12.
Neuropeptide Y (NPY) in cerebrospinal fluid from patients with Huntington's Disease: increased NPY levels and differential degradation of the NPY1-30 fragment.
J Neurochem
; 137(5): 820-37, 2016 06.
Article
in English
| MEDLINE | ID: mdl-27016395
13.
Ubiquitin-specific protease-14 reduces cellular aggregates and protects against mutant huntingtin-induced cell degeneration: involvement of the proteasome and ER stress-activated kinase IRE1α.
Hum Mol Genet
; 23(22): 5928-39, 2014 Nov 15.
Article
in English
| MEDLINE | ID: mdl-24951540
14.
Ethical aspects of a predictive test for Huntington's Disease: A long term perspective.
Nurs Ethics
; 23(5): 565-75, 2016 Aug.
Article
in English
| MEDLINE | ID: mdl-25899725
15.
Proteolytic degradation of neuropeptide Y (NPY) from head to toe: Identification of novel NPY-cleaving peptidases and potential drug interactions in CNS and Periphery.
J Neurochem
; 135(5): 1019-37, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-26442809
16.
Hypothalamic expression of mutant huntingtin contributes to the development of depressive-like behavior in the BAC transgenic mouse model of Huntington's disease.
Hum Mol Genet
; 22(17): 3485-97, 2013 Sep 01.
Article
in English
| MEDLINE | ID: mdl-23697793
17.
Attenuated huntingtin gene CAG nucleotide repeat size in individuals with Lynch syndrome.
Sci Rep
; 14(1): 4300, 2024 02 21.
Article
in English
| MEDLINE | ID: mdl-38383663
18.
Ethical aspects of undergoing a predictive genetic testing for Huntington's disease.
Nurs Ethics
; 20(2): 189-99, 2013 Mar.
Article
in English
| MEDLINE | ID: mdl-22918057
19.
Comorbidities and clinical outcomes in adult- and juvenile-onset Huntington's disease: a study of linked Swedish National Registries (2002-2019).
J Neurol
; 270(2): 864-876, 2023 Feb.
Article
in English
| MEDLINE | ID: mdl-36253622
20.
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons.
Hum Mol Genet
; 19(22): 4385-98, 2010 Nov 15.
Article
in English
| MEDLINE | ID: mdl-20807776