Items where Subject is "B Life Science > Genetics and Genomics"

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Creators | Item Type
Jump to: A | J | M | N | R | S | T | V | Y
Number of items at this level: 20.

A

Ashitha, S. N. and Avinash, M. V. and Ramachandra, N. B. (2017) Whole exome sequencing of discordant diseases in Monozygotic twins with Down syndrome reveals mutations for Congenital Heart Defect and epileptic seizures. Meta Gene, 12. 134 - 137. ISSN 2214-5400

Avinash, M. V. and Prakash, P. and Ramachandra, N. B. (2016) Copy number variation of UGT 2B genes in Indian families using whole genome scans. Journal of Nucleic Acids. ISSN 2090-021X

Avinash, M. V. and Saldanha, Marita and Prakash, P. and Ramachandra, N. B. (2014) Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 165 (7). pp. 572-580. ISSN 1552-485X

J

Jahromi, Sareh Raeiszadeh and Mahesh, P. A. and Jayaraj, B. S. and Madhunapantula, Subba Rao V. and Amrutha D. Holla and Sangeetha, V. and Ramachandra, N. B. (2014) Serum levels of IL-10, IL-17F and IL-33 in patients with asthma: a case–control study. Journal of Asthma, 51 (10). pp. 1004-1013. ISSN 1532-4303

M

Manasa Prabhanjan and Suresh, Raviraj V. and Megha, N. Murthy and Ramachandra, N. B. (2016) Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations. Diabetes Research and Clinical Practice, 113. 160 - 170. ISSN 1872-8227

Megha Murthy, N. and Avinash, M. V. and Seshachalam, K. B. and Ramachandra, N. B. (2016) High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts. Neurological Research, 38 (9). pp. 775-785.

Megha Murthy, N. and Blauwendraat, Cornelis and Hardy, John and Sebastian, Guelfi and Lewis, Patrick A. and Trabzuni, Daniah (2017) Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson's disease on chromosome 7p15.3. Neurogenetics, 18 (3). pp. 121-133. ISSN 1364-6753

Mysore, Keshava and Shyamala, Baragur and Reichert, Heinrich and Rodrigues, Veronica (2010) Comparative Analysis of Olfactory System Organization in Flies and Social Hymenopterans. Journal of Neurogenetics, 24. p. 31. ISSN 0167-7063,

N

Naik, Srilata Puru and Mahesh, P. A. and Jayaraj, B. S. and Madhunapantula, SubbaRao V. and Jahromi, Sarah Raeiszadeh and Yadav, Manish Kumar (2017) Evaluation of inflammatory markers interleukin-6 (IL-6) and matrix metalloproteinase-9 (MMP-9) in asthma. Journal of Asthma, 54 (6). pp. 584-593. ISSN 1532-4303

R

Radhika, P. N. and Ramachandra, N. B. (2014) Divergence of the gene aly in experimentally evolved cytoraces, the members of the nasuta-albomicans complex of Drosophila. Insect Molecular Biology, 23 (4). pp. 435-443. ISSN 1365-2583

Raeiszadeh Jahromi, Sareh and Bijanzadeh, Mahdi and Mahesh, P. A. and Sangeetha, V. and Ramachandra, N. B. (2014) Single nucleotide polymorphism and Asthma: from conformational variations to structural alternations. Molecular and Biochemical Diagnosis Journal, 1 (2). pp. 63-75.

S

Sinam, Y. M. and Arunita Chatterjee and Ranjini, M. S. and Adarsh Poojari and Aarthi Nagarajan and Ramachandra, N. B. and Upendra, N. (2016) A newly evolved drosophila cytorace-9 shows trade-off between longevity and immune response. Infection, Genetics and Evolution, 44. 1 - 7. ISSN 1567-7257

Somanna, A. N. and Sumana, M. N. and Chokkanna, A. and Ramachandra, N. B. (2018) Detection of first-line drug resistance mutations and drug–protein interaction dynamics from tuberculosis patients in South India. Microbial Drug Resistance, 24 (4). pp. 377-385. ISSN 1931-8448

Suresh, R. V. and Narayannapa and Savitha and Ambika S. Udupa and Kusuma, L. and Sunil Kumar, P. and Ramachandra, N. B. (2017) Association of RFC1 A80G gene polymorphism with advanced maternal age in risk of Down syndrome. Current Medicine Research and Practice, 7 (1). 6 - 10. ISSN 2352-0817

Suresh, Raviraj V. and Kusuma, L. and Avinash, M. V. and Ramachandra, N. B. (2017) Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: a copy number variation approach. Indian Journal of Medical Research, 145 (1). pp. 39-50. ISSN 0975-9174

T

Tejaswini, Prakash and Avinash, V. and Ramachandra, N. B. (2017) Complex interaction between HNRNPD mutations and risk polymorphisms is associated with discordant Crohn’s disease in monozygotic twins. Autoimmunity, 50 (5). pp. 275-276. ISSN 1607-842X

Tejaswini, Prakash and Avinash, V. and Ramachandra, N. B. (2017) Complex interaction between HNRNPD mutations and risk polymorphisms is associated with discordant Crohn’s disease in monozygotic twins. Autoimmunity, 50 (5). pp. 275-276. ISSN 1607-842X

V

Veerappa, A. M. and Suresh, R. V. and Vishweswaraiah, S. and Lingaiah, K. and Murthy, M. and Manjegowda, D. S. and Padakannaya, P. and Ramachandra, N. B. (2015) Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization. GENETICS RESEARCH, 97. ISSN 1469-5073

Y

Yogita Kattimani and Avinash, M. V. (2018) Complex interaction between mutant HNRNPA1 and gE of varicella zoster virus in pathogenesis of multiple sclerosis. Autoimmunity, 51 (4). pp. 147-151. ISSN 1607-842X

Yogita Kattimani and Avinash, M. V. (2018) Dysregulation of NRXN1 by mutant MIR8485 leads to calcium overload in pre-synapses inducing neurodegeneration in Multiple sclerosis. Multiple Sclerosis and Related Disorders, 22. 153 - 156. ISSN 2211-0356

This list was generated on Tue Oct 22 22:01:16 2019 IST.