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HTT gene
Known as:
HD GENE
, HUNTINGTIN
, IT15
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This gene may be involved in vesicle transport.
National Institutes of Health
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Related topics
Related topics
6 relations
HD protein, human
Homo sapiens
Huntington Disease
Ligand Binding
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HTT wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
ETHICAL AND GENETIC ASPECTS REGARDING PRESYMPTOMATIC TESTING FOR NEURODEGENERATIVE DISEASES.
G. Cozaru
,
M. Așchie
,
A. Mitroi
,
I. Poinăreanu
,
E. Gorduza
Revista medico-chirurgicala a Societatii de…
2016
Corpus ID: 2223483
Neurodegenerative diseases, such as Alzheimer's dementia, Huntington's chorea, Parkinson's disease or spinocerebellar ataxia…
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2013
2013
Family history in juvenile Huntington disease
Rebecca K. Lehman
,
M. Nance
Neurology
2013
Corpus ID: 207122758
Juvenile Huntington disease (JHD)—Huntington disease (HD) with an onset ≤20 years—accounts for approximately 10% of all HD cases…
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2011
2011
Preparation of antibodies against amino terminal and carboxyl terminal poly peptide of huntingtin-associated protein 1
Li He
2011
Corpus ID: 88129481
Objective To prepare polyclonal antibodies against N-terminal and C-terminal polypeptide of two isoforms of huntingtin-associated…
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2010
2010
TRACKING MUTANT HUNTINGTIN AGGREGATION KINETICS IN CELLS REVEALS THREE MAJOR POPULATIONS INCLUDING AN INVARIANT OLIGOMER POOL *
Maya A. Olshina
,
L. Angley
,
+4 authors
D. Hatters
2010
Corpus ID: 42811229
Huntington’s disease is caused by expanded polyglutamine (polyQ) sequences in huntingtin, which procures its aggregation into…
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Review
2009
Review
2009
Review article Symptoms, pathogenesis and current pharmacological treatment of Huntington’s disease. European Huntington’s Disease Network
D. Zielonka
2009
Corpus ID: 79410312
Huntington's disease (HD) is an autosomal-dominant, progressive neurodegenerative disorder with a characteristic phenotype, with…
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2008
2008
Serum glial fibrillary acidic protein—a diagnostic biomarker for glioblastoma multiforme
Nature Clinical Practice Neurology
2008
Corpus ID: 2079311
A promising treatment approach to Huntington’s disease is promotion of autophagy to dispose of aggregate-prone proteins such as…
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2008
2008
Effects of long-term and global huntingtin silencing
Valérie Drouet
,
V. Perrin
,
+7 authors
N. Déglon
2008
Corpus ID: 86026716
Reference EPFL-CONF-160374View record in Web of Science Record created on 2010-11-30, modified on 2016-08-09
2001
2001
The Caenorhabditis elegans homologue of huntingtin interacting protein 1 has multiple roles in development
J. A. Parker
2001
Corpus ID: 87927743
1998
1998
HAP 1-huntingtin interactions do not contribute to the molecular pathology in Huntington ' s disease transgenic mice
F. Bertaux
,
A. Sharp
,
C. Ross
,
H. Lehrach
,
G. Bates
,
E. Wanker
1998
Corpus ID: 109935367
HAP1 (huntingtin associated protein) has previously been found to interact with huntingtin (htt) in a glutamine length dependent…
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1997
1997
[Molecular analysis of the IT15 gene in 79 Spanish families with Huntington's disease: diagnostic confirmation and presymptomatic diagnosis].
A. Sánchez
,
Montserrat Milà
,
+4 authors
X. Estivill
Medicina clínica (Ed. impresa)
1997
Corpus ID: 25794209
BACKGROUND Huntington's disease (HD) is a neurodegenerative disorder with late age of onset, caused by (CAG), expansion in the…
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