X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2885) 2885
Book Review (511) 511
Publication (339) 339
Book Chapter (40) 40
Dissertation (13) 13
Book / eBook (6) 6
Conference Proceeding (5) 5
Web Resource (3) 3
Data Set (1) 1
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (2554) 2554
humans (2205) 2205
trinucleotide repeats (1169) 1169
male (1010) 1010
genetics & heredity (980) 980
female (944) 944
mutation (787) 787
trinucleotide repeat (672) 672
biochemistry & molecular biology (641) 641
animals (626) 626
instability (578) 578
trinucleotide repeat expansion (564) 564
adult (555) 555
trinucleotide repeat expansion - genetics (531) 531
alleles (521) 521
expansion (516) 516
middle aged (483) 483
nerve tissue proteins - genetics (472) 472
gene (465) 465
neurosciences (451) 451
trinucleotide repeats - genetics (433) 433
huntington disease - genetics (409) 409
fragile x syndrome - genetics (408) 408
dna (396) 396
genetic aspects (373) 373
mice (364) 364
genetics (363) 363
clinical neurology (359) 359
base sequence (343) 343
cag repeat (328) 328
aged (321) 321
research (301) 301
disease (290) 290
phenotype (284) 284
congenital, hereditary, and neonatal diseases and abnormalities (270) 270
cell biology (267) 267
pedigree (267) 267
analysis (264) 264
polyglutamine (257) 257
genes (252) 252
huntington's disease (252) 252
polymerase chain reaction (249) 249
molecular sequence data (239) 239
proteins (236) 236
myotonic dystrophy - genetics (231) 231
ataxia (230) 230
adolescent (229) 229
spinocerebellar ataxia (228) 228
huntingtons-disease (227) 227
fragile-x-syndrome (225) 225
fragile x syndrome (216) 216
nervous system diseases (216) 216
myotonic-dystrophy (212) 212
article (205) 205
child (204) 204
age of onset (202) 202
nuclear proteins - genetics (202) 202
dna repair (199) 199
neurology (199) 199
fragile x mental retardation protein - genetics (196) 196
cgg repeat (192) 192
trinucleotide repeat diseases (191) 191
myotonic dystrophy (190) 190
gene expression (188) 188
transgenic mice (185) 185
spinocerebellar ataxias - genetics (184) 184
dna - genetics (182) 182
mice, transgenic (179) 179
disease models, animal (178) 178
research article (178) 178
length (176) 176
neurodegenerative diseases (176) 176
fragile x mental retardation protein (175) 175
huntingtin protein (169) 169
huntington's chorea (167) 167
genotype (166) 166
nucleic acid conformation (164) 164
age (160) 160
ctg repeat (160) 160
dna - chemistry (159) 159
triplet repeats (159) 159
deoxyribonucleic acid--dna (158) 158
saccharomyces-cerevisiae (153) 153
neurodegeneration (151) 151
escherichia-coli (147) 147
mismatch repair (146) 146
multidisciplinary sciences (146) 146
medicine (145) 145
genomic instability (144) 144
mutations (144) 144
expression (143) 143
huntington disease (139) 139
dna methylation (138) 138
gene frequency (136) 136
models, genetic (135) 135
rna-binding proteins (135) 135
biology (134) 134
polymorphism, genetic (134) 134
dna replication (131) 131
huntingtons disease (131) 131
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (2869) 2869
Spanish (16) 16
Japanese (14) 14
Russian (9) 9
Chinese (4) 4
French (2) 2
German (2) 2
Polish (2) 2
Czech (1) 1
Hebrew (1) 1
Korean (1) 1
Norwegian (1) 1
Portuguese (1) 1
Serbian (1) 1
Ukrainian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Molecular Therapy, ISSN 1525-0016, 01/2017, Volume 25, Issue 1, pp. 24 - 43
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2017, Volume 114, Issue 40, pp. E8392 - E8401
Journal Article
DEVELOPMENT, ISSN 0950-1991, 01/2018, Volume 145, Issue 2, pp. dev156844 - dev156844
Journal Article
Journal Article
PLoS Genetics, ISSN 1553-7390, 02/2013, Volume 9, Issue 2, pp. e1003280 - e1003280
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 04/2018, Volume 46, Issue 7, pp. 3498 - 3516
Abstract Simple sequence repeats (SSRs) are found throughout the genome, and under some conditions can change in length over time. Germline and somatic... 
RNA-POLYMERASE-II | GENOME INSTABILITY | HUMAN-CELLS | ELONGATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | COUPLED DNA-REPAIR | GROUP D HELICASE | EFFICIENT REPAIR | CAG REPEAT CONTRACTION | DAMAGE | TRINUCLEOTIDE REPEAT | Index Medicus | Genome Integrity, Repair and
Journal Article