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Full Electronic Band Structure Characterization of Al-Doped ZnO Nanocrystalline Films Through Simulation.
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- Journal of Electronic Materials, 2024, v. 53, n. 10, p. 5885, doi. 10.1007/s11664-024-11331-2
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- Article
An Innovative Model for Electronic Band Structure Analysis of Doped and Un-Doped ZnO.
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- Journal of Electronic Materials, 2021, v. 50, n. 4, p. 2417, doi. 10.1007/s11664-021-08756-4
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- Article
Genetic Association of ACE2 rs2285666 Polymorphism With COVID-19 Spatial Distribution in India.
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- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.564741
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- Article
Role of common sarcomeric gene polymorphisms in genetic susceptibility to left ventricular dysfunction.
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- Journal of Genetics, 2016, v. 95, n. 2, p. 263, doi. 10.1007/s12041-016-0623-4
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- Article
PERFORMANCE INVESTIGATION OF FULLY VERTICAL ORGANIC MATERIAL BASED MULTI-LAYER OLEDs.
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- i-Manager's Journal on Material Science, 2018, v. 5, n. 4, p. 23, doi. 10.26634/jms.5.4.13969
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- Article
Atomistic nonlinear carrier dynamics in Ge.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-32732-z
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- Article
A novel biallelic frameshift variant in C2orf69 causing developmental regression, seizures, microcephaly, autistic features, and hypertonia.
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- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 9, p. 2446, doi. 10.1002/ajmg.a.63310
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- Article
Organic anion transporter 1B1 (SLCO1B1) polymorphism and gallstone formation: High incidence of Exon4 CA genotype in female patients in North India.
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- Hepatology Research, 2011, v. 41, n. 1, p. 71, doi. 10.1111/j.1872-034X.2010.00736.x
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- Article
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-45948-y
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- Article
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-45948-y
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- Article
Multi-Analytic Approach Elucidates Significant Role of Hormonal and Hepatocanalicular Transporter Genetic Variants in Gallstone Disease in North Indian Population.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0059173
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- Article
Significant Role of Estrogen and Progesterone Receptor Sequence Variants in Gallbladder Cancer Predisposition: A Multi-Analytical Strategy.
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- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0040162
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- Article
Association of 25 bp Deletion in MYBPC3 Gene with Left Ventricle Dysfunction in Coronary Artery Disease Patients.
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- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0024123
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- Article
Cigarette smoking and its effect on coagulation profile, hematological parameters, and oxygen saturation in healthy blood donor.
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- Asian Journal of Medical Sciences, 2024, v. 15, n. 8, p. 140, doi. 10.3126/ajms.v15i8.65345
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- Article
A study of the alteration in hematological parameters and liver function test with respect to the severity of dengue fever.
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- Asian Journal of Medical Sciences, 2021, v. 12, n. 3, p. 93, doi. 10.3126/ajms.v12i3.33027
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- Article
Report of four novel variants in ASNS causing asparagine synthetase deficiency and review of literature.
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- Congenital Anomalies, 2018, v. 58, n. 5, p. 181, doi. 10.1111/cga.12275
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- Article
In silico characterization and identification of compound heterozygous variants in H/ACA Ribonucleoprotein Assembly Factor ( SHQ1) from Indian population.
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- Journal of Family Medicine & Primary Care, 2024, v. 13, n. 1, p. 208, doi. 10.4103/jfmpc.jfmpc_979_23
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- Article
Genetic and linguistic non-correspondence suggests evidence for collective social climbing in the Kol tribe of South Asia.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-61941-z
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- Article
The peopling of Lakshadweep Archipelago.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-43384-3
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- Article
Most frequent South Asian haplotypes of ACE2 share identity by descent with East Eurasian populations.
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- PLoS ONE, 2020, v. 15, n. 9, p. 1, doi. 10.1371/journal.pone.0238255
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- Article
Correction to: The immunogenetics of COVID-19.
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- 2023
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- Correction Notice
The immunogenetics of COVID-19.
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- Immunogenetics, 2023, v. 75, n. 3, p. 309, doi. 10.1007/s00251-022-01284-3
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- Article
Impact of renin-angiotensin-aldosterone system gene polymorphisms on left ventricular dysfunction in coronary artery disease patients.
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- Disease Markers, 2012, v. 32, n. 1, p. 33, doi. 10.1155/2012/854150
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- Article
Effect of genetic variant (rs11887534) in ABCG8 gene in coronary artery disease and response to atorvastatin therapy.
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- Disease Markers, 2010, v. 28, n. 5, p. 307, doi. 10.1155/2010/357304
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- Article
Historic migration to South Asia in the last two millennia: A case of Jewish and Parsi populations.
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- Journal of Biosciences, 2019, v. 44, n. 3, p. N.PAG, doi. 10.1007/s12038-019-9873-7
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- Article
Genetic Diversity and Spatiotemporal Distribution of SARS-CoV-2 Alpha Variant in India.
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- COVID, 2023, v. 3, n. 4, p. 472, doi. 10.3390/covid3040035
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- Article
Publisher Correction: The major genetic risk factor for severe COVID‑19 does not show any association among South Asian populations.
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- 2021
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- Correction Notice
The major genetic risk factor for severe COVID-19 does not show any association among South Asian populations.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-91711-4
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- Article
An innovative technique for electronic transport model of group-III nitrides.
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- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-75588-3
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- Article
De novo dominant ASXL3 mutations alter H2A deubiquitination and transcription in Bainbridge-Ropers syndrome.
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- Human Molecular Genetics, 2016, v. 25, n. 3, p. 597, doi. 10.1093/hmg/ddv499
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- Article
Tin di-selenide and zinc oxide based SPR biosensor for detection of DNA hybridization, anemia and abnormality in urine.
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- Optical & Quantum Electronics, 2022, v. 54, n. 6, p. 1, doi. 10.1007/s11082-022-03759-9
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- Article
Genotype–phenotype correlations in individuals with pathogenic <italic>RERE</italic> variants.
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- Human Mutation, 2018, v. 39, n. 5, p. 666, doi. 10.1002/humu.23400
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- Article
Role of ABCG8 D19H (rs11887534) variant in gallstone susceptibility in northern India A Srivastava et al. ABCG8 D19H polymorphism and gallstone disease.
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- Journal of Gastroenterology & Hepatology, 2010, v. 25, n. 11, p. 1758, doi. 10.1111/j.1440-1746.2010.06349.x
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- Article