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Risk Factors for Aneurysmal Subarachnoid Hemorrhage in an Indian Population.
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- Cerebrovascular Diseases, 2010, v. 29, n. 3, p. 268, doi. 10.1159/000275501
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- Publication type:
- Article
Association of matrix metalloproteinase 2 and matrix metalloproteinase 9 gene polymorphism in aggressive and nonaggressive odontogenic lesions: A pilot study.
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- Journal of Oral & Maxillofacial Pathology (0973029X), 2019, v. 23, n. 1, p. 158, doi. 10.4103/jomfp.JOMFP_2_17
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- Publication type:
- Article
C12orf57 pathogenic variants: a unique cause of developmental encephalopathy in a south Indian child.
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- Journal of Genetics, 2022, v. 101, n. 2, p. 1, doi. 10.1007/s12041-022-01371-0
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- Article
Compositional profile of mucosal bacteriome of smokers and smokeless tobacco users.
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- Clinical Oral Investigations, 2022, v. 26, n. 2, p. 1647, doi. 10.1007/s00784-021-04137-7
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- Publication type:
- Article
Evidence of association of serotonin transporter gene polymorphisms with schizophrenia in a South Indian population.
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- Journal of Human Genetics, 2009, v. 54, n. 9, p. 538, doi. 10.1038/jhg.2009.76
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- Publication type:
- Article
c-myc oncogene expression and cell proliferation in mixed oligo-astrocytoma.
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- International Journal of Cancer, 1996, v. 65, n. 6, p. 730, doi. 10.1002/(SICI)1097-0215(19960315)65:6<730::AID-IJC3>3.0.CO;2-#
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- Publication type:
- Article
DNA Methyl Transferase (DNMT) Gene Polymorphisms Could Be a Primary Event in Epigenetic Susceptibility to Schizophrenia.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0098182
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- Publication type:
- Article
Genetic Association Analysis of ATP Binding Cassette Protein Family Reveals a Novel Association of <i>ABCB1</i> Genetic Variants with Epilepsy Risk, but Not with Drug-Resistance.
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- PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0089253
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- Publication type:
- Article
An Immunological Perspective to Non-syndromic Sensorineural Hearing Loss.
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- Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02848
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- Publication type:
- Article
Ethnic variation and the relevance of homozygous RNF 213 p.R4810.K variant in the phenotype of Indian Moya moya disease.
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- PLoS ONE, 2020, v. 15, n. 12, p. 1, doi. 10.1371/journal.pone.0243925
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- Publication type:
- Article
Genetic variation in Asiatic lions and Indian tigers.
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- Electrophoresis, 1997, v. 18, n. 9, p. 1693, doi. 10.1002/elps.1150180938
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- Publication type:
- Article
Circadian rhythm of homocysteine is hCLOCK genotype dependent.
- Published in:
- Molecular Biology Reports, 2014, v. 41, n. 6, p. 3597, doi. 10.1007/s11033-014-3223-5
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- Publication type:
- Article
Lack of association of Lysyl oxidase ( LOX) gene polymorphisms with intracranial aneurysm in a south Indian population.
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- Molecular Biology Reports, 2013, v. 40, n. 10, p. 5869, doi. 10.1007/s11033-013-2693-1
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- Publication type:
- Article
Ethnic and region-specific genetic risk variants of stroke and its comorbid conditions can define the variations in the burden of stroke and its phenotypic traits.
- Published in:
- eLife, 2024, p. 1, doi. 10.7554/eLife.94088
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- Publication type:
- Article
Polymorphic variants of mismatch repair gene human MutS homologue-2 influence oral squamous cell carcinoma in a South Indian population.
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- Clinical Cancer Investigation Journal, 2015, v. 4, n. 2, p. 170, doi. 10.4103/2278-0513.150614
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- Publication type:
- Article
Microsatellite instability in D2S123 flanking the hMSH2 gene in oral squamous cell carcinoma in South India.
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- Clinical Cancer Investigation Journal, 2015, v. 4, n. 1, p. 22, doi. 10.4103/2278-0513.149031
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- Publication type:
- Article
Genetic Affinities and Adaptation of the South-West Coast Populations of India.
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- Genome Biology & Evolution, 2023, v. 15, n. 12, p. 1, doi. 10.1093/gbe/evad225
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- Publication type:
- Article
Understanding Pharmaco-Epigenomic Response of Antipsychotic Drugs Using Genome-Wide MicroRNA Expression Profile in Liver Cell Line.
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- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.786632
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- Article
Genetic gateways to COVID‐19 infection: Implications for risk, severity, and outcomes.
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- FASEB Journal, 2020, v. 34, n. 7, p. 8787, doi. 10.1096/fj.202001115R
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- Publication type:
- Article
An interpretable block-attention network for identifying regulatory feature interactions.
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- Briefings in Bioinformatics, 2023, v. 24, n. 4, p. 1, doi. 10.1093/bib/bbad250
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- Publication type:
- Article
Role of endothelial nitric oxide synthase gene polymorphisms in predicting aneurysmal subarachnoid hemorrhage in South Indian patients.
- Published in:
- Disease Markers, 2008, v. 24, n. 6, p. 333, doi. 10.1155/2008/193590
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- Publication type:
- Article
Association of Single Nucleotide Gene Polymorphism at Interleukin-1β +3954, -511, and -31 in Chronic Periodontitis and Aggressive Periodontitis in Dravidian Ethnicity.
- Published in:
- Journal of Periodontology, 2010, v. 81, n. 1, p. 62, doi. 10.1902/jop.2009.090256
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- Publication type:
- Article
A Case-Control Study on the Association of Human Leukocyte Antigen-A*9 and -B* 15 Alleles With Generalized Aggressive Periodontitis in an Indian Population.
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- Journal of Periodontology, 2006, v. 77, n. 12, p. 1954, doi. 10.1902/jop.2006.040411
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- Publication type:
- Article
Pharmacogenetic evaluation of ABCB1, Cyp2C9, Cyp2C19 and methylene tetrahydrofolate reductase polymorphisms in teratogenicity of anti-epileptic drugs in women with epilepsy.
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- Annals of Indian Academy of Neurology, 2014, v. 17, n. 3, p. 259, doi. 10.4103/0972-2327.138475
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- Publication type:
- Article
Molecular signatures of cell cycle transcripts in the pathogenesis of Glial tumors.
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- Journal of Carcinogenesis, 2004, v. 3, n. 1, p. 11, doi. 10.1186/1477-3163-3-11
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- Publication type:
- Article
Universal protocol for generating 100bp size standard for endless usage.
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- Electronic Journal of Biotechnology, 2008, v. 11, n. 2, p. 1, doi. 10.2225/vol11-issue2-fulltext-10
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- Article
Population dynamics of the Teak defoliator (Hyblaea puera Cramer) in Nilambur teak plantations using Randomly Amplified Gene Encoding Primers (RAGEP).
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- BMC Ecology, 2005, v. 5, p. 1, doi. 10.1186/1472-6785-5-1
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- Publication type:
- Article
Genomic selection signatures in autism spectrum disorder identifies cognitive genomic tradeoff and its relevance in paradoxical phenotypes of deficits versus potentialities.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-89798-w
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- Article
Differences in the bacteriome of swab, saliva, and tissue biopsies in oral cancer.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-020-80859-0
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- Article
Comprehensive Genetic Study of a Monozygotic Triplet Discordant for Autism Spectrum Disorder.
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- Neurology India, 2024, v. 72, n. 2, p. 384, doi. 10.4103/ni.ni_349_22
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- Publication type:
- Article
Contribution from MHC-Mediated Risk in Schizophrenia Can Reflect a More Ethnic-Specific Genetic and Comorbid Background.
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- Cells (2073-4409), 2022, v. 11, n. 17, p. 2695, doi. 10.3390/cells11172695
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- Article
Pro-inflammatory cytokines and their epistatic interactions in genetic susceptibility to schizophrenia.
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- 2016
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- Publication type:
- journal article
Pathogenesis of intracranial aneurysm is mediated by proinflammatory cytokine TNFA and IFNG and through stochastic regulation of IL10 and TGFB1 by comorbid factors.
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- Journal of Neuroinflammation, 2015, v. 12, n. 1, p. 1, doi. 10.1186/s12974-015-0354-0
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- Publication type:
- Article
Erratum to: Pathogenesis of intracranial aneurysm is mediated by proinflammatory cytokine TNFA and IFNG and through stochastic regulation of IL10 and TGFB1 by comorbid factors.
- Published in:
- 2015
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- Publication type:
- corrected article
Pathogenesis of intracranial aneurysm is mediated by proinflammatory cytokine TNFA and IFNG and through stochastic regulation of IL10 and TGFB1 by comorbid factors.
- Published in:
- Journal of Neuroinflammation, 2015, v. 12, n. 1, p. 1, doi. 10.1186/s12974-015-0354-0
- By:
- Publication type:
- Article
Pathogenesis of intracranial aneurysm is mediated by proinflammatory cytokine TNFA and IFNG and through stochastic regulation of IL10 and TGFB1 by comorbid factors.
- Published in:
- Journal of Neuroinflammation, 2015, v. 12, n. 1, p. 1, doi. 10.1186/s12974-015-0354-0
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- Publication type:
- Article
Genetics of Adolescent Suicide: A Literature review.
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- Journal of Indian Association for Child & Adolescent Mental Health, 2021, v. 17, n. 2, p. 135, doi. 10.1177/0973134220210209
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- Publication type:
- Article
Pro-inflammatory cytokine response pre-dominates immuno-genetic pathway in development of rheumatoid arthritis.
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- Molecular Biology Reports, 2020, v. 47, n. 11, p. 8669, doi. 10.1007/s11033-020-05909-2
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- Article
Genetic association of DNMT variants can play a critical role in defining the methylation patterns in autism.
- Published in:
- IUBMB Life, 2019, v. 71, n. 7, p. 901, doi. 10.1002/iub.2021
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- Publication type:
- Article
Disruption of circadian rhythm and risk of autism spectrum disorder: role of immune-inflammatory, oxidative stress, metabolic and neurotransmitter pathways.
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- Reviews in the Neurosciences, 2022, v. 33, n. 1, p. 93, doi. 10.1515/revneuro-2021-0022
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- Publication type:
- Article
Understanding the role of genetic variability in LRRK2 in Indian population.
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- 2019
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- Publication type:
- journal article
Methylome-wide and meQTL analysis helps to distinguish treatment response from non-response and pathogenesis markers in schizophrenia.
- Published in:
- Frontiers in Psychiatry, 2024, p. 1, doi. 10.3389/fpsyt.2024.1297760
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- Publication type:
- Article
Haloperidol induces pharmacoepigenetic response by modulating miRNA expression, global DNA methylation and expression profiles of methylation maintenance genes and genes involved in neurotransmission in neuronal cells.
- Published in:
- PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0184209
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- Publication type:
- Article
Cytokine gene polymorphism (interleukin-1β +3954, Interleukin-6 [-597/-174] and tumor necrosis factor-α -308) in chronic periodontitis with and without type 2 diabetes mellitus.
- Published in:
- Indian Journal of Dental Research, 2014, v. 25, n. 3, p. 375, doi. 10.4103/0970-9290.138343
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- Publication type:
- Article
Transforming growth factor-β-1 polymorphisms are infrequent but exist at selected loci in oral submucous fibrosis.
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- Indian Journal of Dental Research, 2010, v. 21, n. 3, p. 413, doi. 10.4103/0970-9290.70815
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- Publication type:
- Article
5-Hydroxytryptamine (serotonin) 2A receptor gene polymorphism is associated with schizophrenia.
- Published in:
- Indian Journal of Medical Research, 2014, v. 140, n. 6, p. 736
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- Publication type:
- Article