X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (3353) 3353
Publication (357) 357
Book Chapter (58) 58
Book Review (32) 32
Dissertation (13) 13
Conference Proceeding (9) 9
Data Set (1) 1
Journal / eJournal (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (2362) 2362
cag repeat (1589) 1589
male (1296) 1296
index medicus (1130) 1130
female (1017) 1017
neurosciences (838) 838
animals (795) 795
adult (775) 775
middle aged (753) 753
genetics & heredity (689) 689
trinucleotide repeats (658) 658
clinical neurology (614) 614
huntington disease - genetics (552) 552
biochemistry & molecular biology (549) 549
gene (537) 537
mutation (535) 535
expansion (529) 529
nerve tissue proteins - genetics (518) 518
mice (515) 515
aged (506) 506
cag repeats (488) 488
trinucleotide repeat (483) 483
receptors, androgen - genetics (437) 437
huntington's disease (416) 416
alleles (358) 358
genetic aspects (349) 349
androgen receptor (345) 345
spinocerebellar ataxia (335) 335
phenotype (334) 334
disease (305) 305
polyglutamine (305) 305
huntingtons-disease (302) 302
nuclear proteins - genetics (302) 302
analysis (300) 300
disease models, animal (291) 291
huntingtin protein (290) 290
genotype (287) 287
trinucleotide repeats - genetics (279) 279
trinucleotide repeat expansion (264) 264
transgenic mice (263) 263
adolescent (261) 261
cag repeat length (260) 260
polymorphism, genetic (255) 255
androgen receptor gene (253) 253
genetics (252) 252
huntington disease - pathology (248) 248
mice, transgenic (246) 246
research (245) 245
trinucleotide repeat expansion - genetics (242) 242
mutant huntingtin (236) 236
huntington's chorea (235) 235
neurodegeneration (231) 231
spinocerebellar ataxias - genetics (230) 230
age of onset (229) 229
neuronal intranuclear inclusions (224) 224
nerve tissue proteins - metabolism (216) 216
pedigree (216) 216
genes (214) 214
cag repeat polymorphism (213) 213
risk factors (212) 212
polymerase chain reaction (211) 211
brain (209) 209
expression (209) 209
nervous system diseases (209) 209
machado-joseph disease (207) 207
neurodegenerative diseases (204) 204
base sequence (201) 201
machado-joseph-disease (201) 201
neurology (200) 200
testosterone (198) 198
dentatorubral-pallidoluysian atrophy (197) 197
cell biology (195) 195
ataxia (194) 194
endocrinology & metabolism (187) 187
length (187) 187
psychiatry (187) 187
instability (186) 186
molecular sequence data (184) 184
proteins (183) 183
huntington disease - metabolism (181) 181
polymorphism (178) 178
dna (172) 172
association (170) 170
brain - pathology (170) 170
huntington disease (170) 170
huntingtin (169) 169
age (166) 166
article (166) 166
child (162) 162
peptides - genetics (159) 159
dominant cerebellar-ataxia (158) 158
aged, 80 and over (157) 157
case-control studies (157) 157
protein (156) 156
bulbar muscular-atrophy (153) 153
cag repeat expansion (153) 153
gene expression (152) 152
genetic research (149) 149
oncology (149) 149
nuclear proteins - metabolism (147) 147
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3285) 3285
Spanish (22) 22
French (20) 20
German (19) 19
Japanese (16) 16
Chinese (10) 10
Russian (9) 9
Czech (5) 5
Polish (5) 5
Portuguese (4) 4
Korean (3) 3
Lithuanian (1) 1
Persian (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Movement disorders : official journal of the Movement Disorder Society, ISSN 0885-3185, 3/2018, Volume 33, Issue 3, pp. 472 - 478
Journal Article
LANCET NEUROLOGY, ISSN 1474-4422, 10/2013, Volume 12, Issue 10, pp. 978 - 988
Background Hexanucleotide repeat expansions in chromosome 9 open reading frame 72 (C9ORF72) are the most common known genetic cause of frontotemporal dementia... 
CAG REPEAT | SPINOCEREBELLAR ATAXIA TYPE-1 | MYOTONIC-DYSTROPHY TYPE-1 | INSTABILITY | MACHADO-JOSEPH-DISEASE | CTG REPEATS | DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY | SOMATIC MOSAICISM | HEXANUCLEOTIDE REPEAT | C9ORF72 | CLINICAL NEUROLOGY
Journal Article
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, ISSN 0027-8424, 03/2004, Volume 101, Issue 10, pp. 3498 - 3503
Huntington's disease (HID) is an autosomal dominant neurodegenerative disease caused by a triplet (CAG) expansion mutation. The length of the triplet repeat is... 
CAG REPEAT | MULTIDISCIPLINARY SCIENCES | EXPANSION | LENGTH | ASSOCIATION | TRINUCLEOTIDE REPEAT | FEATURES
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 11/2018, Volume 24, Issue 21, pp. 5313 - 5320
Purpose: Taxane-induced peripheral neuropathy is a common side effect induced by anticancer agents, and no drug capable of preventing its occurrence or... 
CAG REPEAT | NEUROPATHIC PAIN | INHIBITION | HSKCA3 | RAT | ONCOLOGY | CA2+-ACTIVATED K+ CHANNELS | SCHIZOPHRENIA
Journal Article
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, p. 1307
We have previously shown that exon 1 of the huntingtin gene does not always splice to exon 2 resulting in the production of a small polyadenylated mRNA... 
CAG REPEAT | R6/2 | INSTABILITY | MULTIDISCIPLINARY SCIENCES | MUTANT HUNTINGTIN | LENGTH | GENE-EXPRESSION | IN MOUSE MODEL | ANTISENSE OLIGONUCLEOTIDES | BRAIN | TRANSGENIC MICE
Journal Article
Neurology, ISSN 0028-3878, 02/2019, Volume 92, Issue 6, pp. e548 - e559
OBJECTIVETo investigate the phenotypic features, with emphasis on muscle, in 40 patients with spinobulbar muscular atrophy (SBMA) using quantitative MRI,... 
FATIGUE SEVERITY SCALE | DYSTROPHY | INVOLVEMENT | VALIDATION | MUSCLE MRI | BULBAR | CAG-REPEAT | ANDROGEN RECEPTOR GENE | CLINICAL NEUROLOGY | FEATURES | INFILTRATION
Journal Article
by Zhou, X and Wang, C and Ding, D and Chen, Z and Peng, Y and Peng, H and Hou, X and Wang, P and Ye, W and Li, T and Yang, H and Qiu, R and Xia, K and Sequeiros, J and Tang, B and Jiang, H
SCIENTIFIC REPORTS, ISSN 2045-2322, 03/2018, Volume 8
Multiple system atrophy (MSA) is a complex and multifactorial neurodegenerative disease, and its pathogenesis remains uncertain. Patients with MSA or... 
SPINOCEREBELLAR ATAXIA TYPE-2 | CAG REPEAT | GENETICS | MULTIDISCIPLINARY SCIENCES | ALPHA-SYNUCLEIN | CLINICAL-FEATURES
Journal Article
PLOS ONE, ISSN 1932-6203, 07/2017, Volume 12, Issue 7
Molecular diagnosis of Huntington disease (HD) is currently performed by fluorescent repeat-flanking or triplet-primed PCR (TP-PCR) with capillary... 
CAG REPEAT | ACCURATE DETERMINATION | INSTABILITY | GENE | MULTIDISCIPLINARY SCIENCES | EXPANSION | FLUORESCENT PCR | ADJACENT | IT15
Journal Article
Neurology, ISSN 0028-3878, 06/2018, Volume 90, Issue 24, pp. e2099 - e2106
OBJECTIVEA fundamental but still unresolved issue regarding Huntington disease (HD) pathogenesis is whether the factors that determine age at onset are the... 
PATHOGENESIS | DISRUPTION | OF-ONSET | MODELS | GENE | MUTANT HUNTINGTIN | EXPANSION | CAG-REPEAT LENGTH | WEIGHT | CLINICAL PROGRESSION | CLINICAL NEUROLOGY | 164
Journal Article
SCIENCE TRANSLATIONAL MEDICINE, ISSN 1946-6234, 10/2019, Volume 11, Issue 514
Astrocytes are implicated in neurodegenerative disorders and may contribute to striatal neuron loss or dysfunction in Huntington's disease (HD). Here, we... 
CAG REPEAT | MEDICINE, RESEARCH & EXPERIMENTAL | GENE | LENGTH | NEURONS | SYMPTOMS | CLINICAL-FEATURES | GLIA | RECEPTORS | EXPRESSION | CELL BIOLOGY
Journal Article