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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.
Review
2012
Review
2012
Influence of species differences on the neuropathology of transgenic Huntington's disease animal models.
Xiao-Jiang Li
,
Shihua Li
Journal of genetics and genomics = Yi chuan xue…
2012
Corpus ID: 5950077
2007
2007
BH3‐only proteins Bid and BimEL are differentially involved in neuronal dysfunction in mouse models of Huntington's disease
J. M. García-Martínez
,
E. Pérez-Navarro
,
+6 authors
J. Alberch
Journal of Neuroscience Research
2007
Corpus ID: 22601324
Apoptosis, a cell death mechanism regulated by Bcl‐2 family members, has been proposed as one of the mechanisms leading to…
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2006
2006
Genetic analysis of candidate genes modifying the age-at-onset in Huntington’s disease
S. Metzger
,
P. Bauer
,
+28 authors
O. Riess
Human Genetics
2006
Corpus ID: 36942282
The expansion of a polymorphic CAG repeat in the HD gene encoding huntingtin has been identified as the major cause of Huntington…
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Highly Cited
2005
Highly Cited
2005
Progressive and selective striatal degeneration in primary neuronal cultures using lentiviral vector coding for a mutant huntingtin fragment
D. Zala
,
A. Benchoua
,
+5 authors
N. Déglon
Neurobiology of Disease
2005
Corpus ID: 2460925
Highly Cited
2005
Highly Cited
2005
Modulation of age at onset of Huntington disease patients by variations in TP53 and human caspase activated DNase (hCAD) genes
B. Chattopadhyay
,
Kanad Baksi
,
Saikat Mukhopadhyay
,
N. Bhattacharyya
Neuroscience Letters
2005
Corpus ID: 23987689
Highly Cited
2003
Highly Cited
2003
Expression of Mutant Huntingtin Blocks Exocytosis in PC12 Cells by Depletion of Complexin II*
J. Edwardson
,
Chih-Tien Wang
,
+6 authors
A. Morton
Journal of Biological Chemistry
2003
Corpus ID: 30515323
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder caused by an expanded CAG repeat in the HD gene. We…
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Highly Cited
2002
Highly Cited
2002
Maintenance of Susceptibility to Neurodegeneration Following Intrastriatal Injections of Quinolinic Acid in a New Transgenic Mouse Model of Huntington's Disease
Å. Petersén
,
K. Chase
,
Z. Puschban
,
M. Difiglia
,
P. Brundin
,
N. Aronin
Experimental Neurology
2002
Corpus ID: 23188244
A transgenic mouse model of Huntington's disease (R6/1 and R6/2 lines) expressing exon 1 of the HD gene with 115-150 CAG repeats…
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Highly Cited
1999
Highly Cited
1999
Corrigendum: Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin (Human Molecular Genetics (1999) 8 (397-407))
G. Schilling
,
M. Becher
,
+11 authors
D. Borchelt
1999
Corpus ID: 90516433
Review
1999
Review
1999
Recent Insights into the Molecular Pathogenesis of Huntington Disease
B. Leavitt
,
C. Wellington
,
Michael Hayden
Seminars in neurology
1999
Corpus ID: 19488607
in vitro
Review
1998
Review
1998
Molecular aspects of Huntington's disease
H. Walling
,
J. Baldassare
,
T. Westfall
Journal of Neuroscience Research
1998
Corpus ID: 42784339
Huntington's disease (HD) is a progressive neurodegenerative disease striking principally medium spiny GABAergic neurons of the…
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