X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (9856) 9856
Book Review (1325) 1325
Publication (954) 954
Book Chapter (140) 140
Conference Proceeding (47) 47
Dissertation (30) 30
Book / eBook (10) 10
Reference (7) 7
Newsletter (6) 6
Web Resource (6) 6
Government Document (4) 4
Newspaper Article (3) 3
Data Set (2) 2
Journal / eJournal (2) 2
Magazine Article (1) 1
Paper (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (8398) 8398
humans (7221) 7221
trinucleotide repeats (4073) 4073
male (3615) 3615
female (3222) 3222
animals (2296) 2296
genetics & heredity (2195) 2195
adult (2194) 2194
middle aged (1983) 1983
mutation (1888) 1888
neurosciences (1786) 1786
biochemistry & molecular biology (1763) 1763
trinucleotide repeat (1701) 1701
trinucleotide repeat expansion (1589) 1589
trinucleotide repeats - genetics (1490) 1490
nerve tissue proteins - genetics (1465) 1465
trinucleotide repeat expansion - genetics (1452) 1452
clinical neurology (1443) 1443
huntington disease - genetics (1335) 1335
mice (1306) 1306
alleles (1291) 1291
gene (1279) 1279
aged (1214) 1214
expansion (1172) 1172
polyglutamine (1006) 1006
base sequence (1004) 1004
genetic aspects (984) 984
huntington's disease (953) 953
disease (912) 912
proteins (908) 908
phenotype (889) 889
genetics (847) 847
molecular sequence data (837) 837
analysis (817) 817
research (812) 812
dna (806) 806
adolescent (790) 790
polymerase chain reaction (786) 786
cag repeat (780) 780
fragile x syndrome - genetics (774) 774
genes (758) 758
pedigree (736) 736
genotype (723) 723
nuclear proteins - genetics (715) 715
receptors, androgen - genetics (705) 705
polymorphism, genetic (688) 688
trinucleotide repeat diseases (673) 673
disease models, animal (666) 666
spinocerebellar ataxia (663) 663
gene expression (651) 651
myotonic dystrophy - genetics (650) 650
neurodegeneration (649) 649
neurology (640) 640
cell biology (638) 638
huntingtin protein (636) 636
nervous system diseases (616) 616
age of onset (615) 615
child (610) 610
ataxia (609) 609
huntingtons-disease (599) 599
neurodegenerative diseases (599) 599
expression (598) 598
spinocerebellar ataxias - genetics (593) 593
congenital, hereditary, and neonatal diseases and abnormalities (581) 581
instability (577) 577
article (562) 562
mice, transgenic (550) 550
peptides - genetics (546) 546
multidisciplinary sciences (544) 544
research article (534) 534
medicine (499) 499
transgenic mice (484) 484
abridged index medicus (483) 483
brain (475) 475
huntingtin (474) 474
huntington's chorea (472) 472
myotonic dystrophy (472) 472
nerve tissue proteins - metabolism (471) 471
fragile x mental retardation protein - genetics (437) 437
protein (437) 437
huntington disease - pathology (436) 436
risk factors (431) 431
biology (428) 428
dna - genetics (418) 418
case-control studies (415) 415
age (414) 414
huntingtons disease (401) 401
gene frequency (400) 400
science (393) 393
myotonic-dystrophy (391) 391
psychiatry (377) 377
cell line (376) 376
fragile x syndrome (376) 376
huntington disease (374) 374
brain - pathology (373) 373
length (371) 371
mutant huntingtin (363) 363
rna (363) 363
androgen receptor (360) 360
pathogenesis (357) 357
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (9441) 9441
Japanese (186) 186
Chinese (97) 97
German (57) 57
Spanish (57) 57
Russian (56) 56
French (34) 34
Polish (22) 22
Czech (12) 12
Dutch (12) 12
Portuguese (9) 9
Hebrew (5) 5
Hungarian (5) 5
Finnish (4) 4
Ukrainian (4) 4
Korean (3) 3
Serbian (3) 3
Swedish (3) 3
Croatian (2) 2
Danish (2) 2
Norwegian (2) 2
Slovak (2) 2
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


2004, Methods in Molecular Biology, ISBN 1588292436, Volume 277, 1 v.
The discovery that trinucleotide repeats significantly influence the age of onset and severity of a variety of hereditary neurological disorders has opened the... 
Trinucleotide repeats | Laboratory manuals | Cytology | Cell Biology | Life Sciences
Book
Genome Biology, ISSN 1474-7596, 04/2007, Volume 8, Issue 4, pp. R61 - R61
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 01/2007, Volume 35, Issue 1, pp. D80 - D87
Tandem repeats in DNA have been under intensive study for many years, first, as a consequence of their usefulness as genomic markers and DNA fingerprints and... 
SEROTONIN TRANSPORTER | INSULIN GENE | DNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | SUSCEPTIBILITY | POLYMORPHISM | DOPAMINE TRANSPORTER GENE | IDENTIFICATION | LOCUS | TRINUCLEOTIDE REPEAT | REGION | Computer Graphics | User-Computer Interface | Animals | Humans | Software | Tandem Repeat Sequences | Internet | Databases, Nucleic Acid | Cluster Analysis | Polymorphism, Genetic | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 09/2015, Volume 525, Issue 7567, pp. 56 - 61
Journal Article
2013, 2nd ed., Methods in molecular biology, ISBN 1627034102, Volume 1010
Web Resource
2013, 2nd ed., Methods in molecular biology, ISBN 1627034102, Volume 1010
Web Resource
Neuron, ISSN 0896-6273, 08/2007, Volume 55, Issue 4, pp. 556 - 564
Journal Article