X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (68846) 68846
Publication (6440) 6440
Newspaper Article (4102) 4102
Book Review (2375) 2375
Book Chapter (483) 483
Conference Proceeding (440) 440
Dissertation (183) 183
Magazine Article (38) 38
Web Resource (30) 30
Data Set (21) 21
Paper (18) 18
Newsletter (17) 17
Reference (17) 17
Government Document (14) 14
Trade Publication Article (14) 14
Streaming Video (5) 5
Book / eBook (2) 2
Journal / eJournal (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
haplotypes (56124) 56124
index medicus (56112) 56112
humans (42935) 42935
female (25965) 25965
male (25929) 25929
genetics & heredity (18304) 18304
genetic aspects (14129) 14129
alleles (14008) 14008
adult (13978) 13978
genotype (13763) 13763
polymorphism, single nucleotide (13458) 13458
animals (13434) 13434
middle aged (12879) 12879
genetics (11842) 11842
gene frequency (11004) 11004
research (10940) 10940
genes (10552) 10552
genetic variation (10370) 10370
polymorphism (9464) 9464
haplotypes - genetics (9439) 9439
genetic predisposition to disease (9432) 9432
analysis (9371) 9371
linkage disequilibrium (8889) 8889
mutation (8349) 8349
haplotype (8062) 8062
population (7827) 7827
polymorphism, genetic (7806) 7806
aged (7767) 7767
phylogeny (7705) 7705
case-control studies (7606) 7606
biochemistry & molecular biology (7301) 7301
population genetics (7164) 7164
association (7022) 7022
molecular sequence data (6854) 6854
risk factors (6835) 6835
immunology (6786) 6786
dna (6491) 6491
base sequence (6344) 6344
mitochondrial dna (6271) 6271
evolutionary biology (6227) 6227
research article (6124) 6124
genetic research (6115) 6115
polymerase chain reaction (5801) 5801
evolution (5783) 5783
genomes (5751) 5751
genetic diversity (5579) 5579
adolescent (5444) 5444
sequence analysis, dna (5396) 5396
genetics, population (5355) 5355
phenotype (5316) 5316
genomics (5219) 5219
pedigree (5182) 5182
disease (5046) 5046
dna, mitochondrial - genetics (4968) 4968
expression (4881) 4881
polymorphism, single nucleotide - genetics (4781) 4781
gene (4776) 4776
medicine (4753) 4753
risk (4713) 4713
studies (4702) 4702
multidisciplinary sciences (4700) 4700
deoxyribonucleic acid--dna (4613) 4613
child (4602) 4602
susceptibility (4482) 4482
single nucleotide polymorphisms (4424) 4424
polymorphisms (4311) 4311
ecology (4284) 4284
genetic markers (4249) 4249
biology (4193) 4193
single-nucleotide polymorphism (4028) 4028
phylogeography (3868) 3868
life sciences (3862) 3862
science (3800) 3800
asian continental ancestry group - genetics (3625) 3625
chromosome mapping (3564) 3564
populations (3536) 3536
article (3378) 3378
physiological aspects (3321) 3321
identification (3311) 3311
models, genetic (3308) 3308
gene expression (3264) 3264
mice (3235) 3235
abridged index medicus (3196) 3196
chromosomes (3134) 3134
cell biology (3017) 3017
young adult (2996) 2996
genetic association studies (2894) 2894
genetic polymorphisms (2886) 2886
evolution, molecular (2860) 2860
diversity (2821) 2821
polymorphism, restriction fragment length (2819) 2819
proteins (2794) 2794
health aspects (2776) 2776
neurosciences (2752) 2752
genetic linkage (2740) 2740
oncology (2718) 2718
human genetics (2717) 2717
geography (2715) 2715
major histocompatibility complex (2572) 2572
china (2571) 2571
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (71954) 71954
Chinese (628) 628
Russian (339) 339
Spanish (203) 203
Japanese (192) 192
French (149) 149
German (118) 118
Korean (90) 90
Portuguese (55) 55
Polish (40) 40
Czech (17) 17
Italian (16) 16
Hungarian (15) 15
Croatian (11) 11
Ukrainian (8) 8
Persian (6) 6
Slovak (6) 6
Swedish (6) 6
Turkish (6) 6
Norwegian (4) 4
Catalan (3) 3
Dutch (3) 3
Lithuanian (3) 3
Serbian (2) 2
Welsh (2) 2
Arabic (1) 1
Bulgarian (1) 1
Danish (1) 1
Greek (1) 1
Romanian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Artificial Cells, Nanomedicine, and Biotechnology, ISSN 2169-1401, 12/2019, Volume 47, Issue 1, pp. 1471 - 1475
Purpose: This study was aimed to study the hypothesis that forkhead box O1 (FOXO1) gene rs17446614 and rs17592236 single nucleotide polymorphisms (SNPs)... 
haplotypes | polymorphisms | FOXO1 | diabetic nephropathy | MATERIALS SCIENCE, BIOMATERIALS | GLYCOGEN-SYNTHESIS | GLUCONEOGENESIS | METABOLISM | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ENGINEERING, BIOMEDICAL
Journal Article
Scientific reports, ISSN 2045-2322, 06/2019, Volume 9, Issue 1, pp. 8296 - 12
In this association study on chromosome 11, the data from 12,537 Korean individuals within the Health Examinee (HEXA) and the Korea Association Resource (KARE)... 
Haplotypes | Genetic analysis | Molecular dynamics | Chromosome 11 | Population studies | Single-nucleotide polymorphism | Gene loci | Genomes | Genetic diversity
Journal Article
BMC CANCER, ISSN 1471-2407, 04/2019, Volume 19, Issue 1, pp. 357 - 357
Background: Osteosarcoma is the most common malignant bone tumor in children. Survival remains poor among histologically poor responders, and there is a need... 
SURVIVAL | PROGNOSTIC-FACTORS | Whole genome sequencing | Childhood cancers | TOXICITY | POLYMORPHISM | Drug resistance | IFOSFAMIDE | CHEMOTHERAPY | ETOPOSIDE | ONCOLOGY | Osteosarcoma | EXTREMITY | Genetics | EXPRESSION | Pharmacogenomics | Haplotypes | Usage | Genetic research | Genetic aspects | Research | Nucleotide sequencing | Drug therapy | DNA sequencing
Journal Article
ALGORITHMS FOR MOLECULAR BIOLOGY, ISSN 1748-7188, 05/2019, Volume 14, Issue 1, pp. 13 - 13
Journal Article
BMC BIOINFORMATICS, ISSN 1471-2105, 06/2019, Volume 20, Issue 1, pp. 364 - 364
Journal Article
Journal Article
Acta neuropathologica communications, ISSN 2051-5960, 03/2019, Volume 7, Issue 1, pp. 47 - 47
First-degree family members refused genetic examination. [...]the case reported here differs from previously described cases because of the presence of a rapid... 
Prion diseases | R208H | Mutation | Neuropathology | Genetic Creutzfeldt-Jakob disease | Dementia | HAPLOTYPE | NEUROSCIENCES | Creutzfeldt-Jakob disease | Haplotypes | Proteins | Genotype & phenotype | Insomnia | BSE | Patients | Polymorphism
Journal Article
Journal Article
BMC MEDICAL GENETICS, ISSN 1471-2350, 07/2019, Volume 20, Issue 1, pp. 118 - 118
BackgroundRecessive mutations of coding regions and splice sites of the SLC26A4 gene cause hearing loss with enlargement of the vestibular aqueduct (EVA). Some... 
Deafness | DFNB4 | PENDRED-SYNDROME | VARIANTS | SYNDROMIC HEARING-LOSS | GENOTYPE | Pendred syndrome | Hearing | Noncoding | MUTATION | GENETICS & HEREDITY | SLC26A4 | Haplotype | ASSOCIATION | Genetic aspects | Research | Gene mutations | Vestibular apparatus | Hearing loss
Journal Article
Nature Communications, ISSN 2041-1723, 12/2019, Volume 10, Issue 1, pp. 628 - 14
Analysis of antibody repertoires by high-throughput sequencing is of major importance in understanding adaptive immune responses. Our knowledge of variations... 
REPERTOIRE | CELLS | MULTIDISCIPLINARY SCIENCES | SEQUENCE | GERMLINE GENE | IMMUNOGLOBULIN | DIVERSITY | INFERENCE | REGION | REVEALS | Haplotypes | Immune response | Copy number | Genes | Test procedures | Inference | Gene deletion | Loci | Heterozygosity | Next-generation sequencing | Clonal deletion | Lymphocytes B | Deletion | Bayesian analysis | Genotypes | Index Medicus
Journal Article
RETROVIROLOGY, ISSN 1742-4690, 05/2019, Volume 16, Issue 1, pp. 14 - 14
Bovine leukemia virus (BLV) causes enzootic bovine leukosis and is closely related to the human T-lymphotropic virus. Bovine major histocompatibility complex... 
BLV INFECTION PROFILES | MILK-PRODUCTION | ALLELES | SUBCLINICAL PROGRESSION | CATTLE | HAPLOTYPES | IDENTIFICATION | BoLA-DQA1 | Bovine leukemia virus | BoLA-DRB3 | Proviral load | DAIRY | VIROLOGY | RESISTANCE | BOLA | Japanese Holstein | Surveys | Disease transmission | Major histocompatibility complex | Analysis | Development and progression | Disease susceptibility | Genetic aspects | Research | Diagnosis | Index Medicus
Journal Article