X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (54) 54
index medicus (40) 40
genetics & heredity (35) 35
india (25) 25
male (18) 18
microbiology (18) 18
biochemistry (17) 17
genomics (17) 17
genes (16) 16
beer (15) 15
chemistry (15) 15
compositions or test papers therefor (15) 15
condition-responsive control in microbiological orenzymological processes (15) 15
enzymology (15) 15
genomes (15) 15
measuring or testing processes involving enzymes, nucleicacids or microorganisms (15) 15
metallurgy (15) 15
mutation or genetic engineering (15) 15
processes of preparing such compositions (15) 15
spirits (15) 15
vinegar (15) 15
wine (15) 15
female (13) 13
genome, human (13) 13
genotype (13) 13
mutation (13) 13
alleles (12) 12
biochemistry & molecular biology (12) 12
polymorphism, single nucleotide (12) 12
research (12) 12
disease (11) 11
evolutionary biology (11) 11
genetic aspects (11) 11
phenotype (11) 11
ataxia (10) 10
gene (10) 10
genetic variation (10) 10
spinocerebellar ataxia (10) 10
spinocerebellar ataxias - genetics (10) 10
animals (9) 9
haplotypes (9) 9
population (9) 9
population genetics (9) 9
adult (8) 8
analysis (8) 8
biotechnology & applied microbiology (8) 8
gene-expression (8) 8
polymorphism, single nucleotide - genetics (8) 8
compositions thereof (7) 7
culture media (7) 7
evolution (7) 7
expression (7) 7
gene frequency (7) 7
genetics (7) 7
genome (7) 7
indian population (7) 7
linkage disequilibrium (7) 7
medicine, ayurvedic (7) 7
microorganisms or enzymes (7) 7
nerve tissue proteins - genetics (7) 7
propagating, preserving or maintaining microorganisms (7) 7
ayurveda (6) 6
databases, genetic (6) 6
disease susceptibility (6) 6
dna (6) 6
dominant cerebellar-ataxia (6) 6
genetic diversity (6) 6
genetics, population (6) 6
india - epidemiology (6) 6
life sciences (6) 6
microbial genetics and genomics (6) 6
polymorphism, genetic (6) 6
adolescent (5) 5
alu elements (5) 5
alu elements - genetics (5) 5
animal genetics and genomics (5) 5
ataxins (5) 5
ayurgenomics (5) 5
base sequence (5) 5
cag repeat (5) 5
cell biology (5) 5
diversity (5) 5
expansion (5) 5
genetic predisposition to disease (5) 5
human genetics (5) 5
medicine (5) 5
medicine, research & experimental (5) 5
molecular analysis (5) 5
molecular sequence data (5) 5
oligonucleotide array sequence analysis (5) 5
pedigree (5) 5
polymorphism (5) 5
polymorphisms (5) 5
populations (5) 5
prakriti (5) 5
protein (5) 5
sca7 (5) 5
transcription, genetic (5) 5
transposable elements (5) 5
african continental ancestry group - genetics (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


BMC Genomics, ISSN 1471-2164, 08/2012, Volume 13, Issue 1, pp. 426 - 426
Journal Article
Journal Article
Journal Article
Clinical Genetics, ISSN 0009-9163, 12/2019, Volume 96, Issue 6, pp. 566 - 574
Over 100 genetically distinct causal known loci for hereditary ataxia phenotype poses a challenge for diagnostic work‐up for ataxia patients in a clinically... 
targeted sequencing | autosomal recessive cerebellar ataxia | ataxia genetics | whole exome sequencing | India | Cerebellum | Ataxia | Phenotypes | Cerebellar ataxia
Journal Article
Journal of Genetics, ISSN 0022-1333, 03/2016, Volume 95, Issue 1, pp. 209 - 228
Ayurveda, an ancient Indian system of medicine documented and practised since 1500 B.C., follows a systems approach that has interesting parallels with... 
prakriti | trisutra | system biology | ayurgenomics | tridosha | P4 medicine | human individuality | Medicine, Ayurvedic | Genome, Human | Humans | Precision Medicine | Analysis | Precision medicine | Genomics
Journal Article
Journal Article
Briefings in Functional Genomics, ISSN 2041-2649, 09/2011, Volume 10, Issue 5, p. 294
Non-coding RNAs (ncRNAs) are increasingly being implicated in diverse functional roles. Majority of these ncRNAs have their origin in the repetitive elements... 
Genomics | Primates | Genomes | Ribonucleic acid--RNA | Binding sites
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2010, Volume 107, Issue 44, pp. 18961 - 18966
Journal Article
Indian Journal of Medical Research, ISSN 0971-5916, 2015, Volume 142, Issue 2, pp. 187 - 198
Background & objectives : Spinocerebellar ataxia 7 (SCA7) is a rare form of neurodegenerative disorder with the clinical manifestation of cerebellar ataxia and... 
SCA7 | Indian population | Genotype-phenotype correlation | CAG repeats | Spinocerebellar ataxia | Consortia | Haplotypes | Neurology | Population | Ataxia | Genomes | Mutation | Deoxyribonucleic acid--DNA
Journal Article