Items where Author is "Ramachandra, N. B."

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Article

Nachappa, S. A. and Neelambike, S. M. and Amruthavalli, C. 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 (Larchmont, N.Y.), 24 (4). pp. 377-385.

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

Megha, Murthy N. and Ramachandra, N. B. (2017) Prioritization of differentially expressed genes in substantia nigra transcriptomes of Parkinson's disease reveals key protein interactions and pathways. Meta Gene, 14. 12 - 18. ISSN 2214-5400

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

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

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

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

Ananda, S. and Marita Saldanha and Shyamala, K. V. and Ramachandra, N. B. and Padakannaya, P. (2016) Development of rapid automatized naming (ran) in simultaneous kannada-english biliterate children. Journal of Psycholinguistic Research, 45 (1). pp. 177-187. ISSN 1573-6555

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.

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

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

Vishweswaraiah, S. and Veerappa, A. M. and Mahesh, P. A. and Jahromi, S. R. and Ramachandra, N. B. (2015) Copy number variation burden on asthma subgenome in normal cohorts identifies susceptibility markers. ALLERGY ASTHMA & IMMUNOLOGY RESEARCH, 7 (3). pp. 265-275. ISSN 2092-7363

Manjegowda, D. S. and Karunakar, P. and Ramachandra, N. B. (2015) Effect of structural changes in proteins derived from gata4 nonsynonymous single nucleotide polymorphisms in congenital heart disease. Indian Journal of Pharmaceutical Sciences, 77 (6). pp. 735-741. ISSN 0250-474X

Davoodi, P. and Mahesh, P. A. and Holla, A. D. and Ramachandra, N. B. (2015) Family history & the risk for adult onset asthma. INDIAN JOURNAL OF MEDICAL RESEARCH, 141. pp. 361-363. ISSN 0971-5916

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

Veerappa, A. M. and Vishweswaraiah, S. and Lingaiah, K. and Murthy, M. and Suresh, R. V. and Manjegowda, D. S. and Ramachandra, N. B. (2015) Global spectrum of copy number variations reveals genome organizational plasticity and proposes new migration routes. PLOS ONE, 10 (4). ISSN 1932-6203

Jahromi, S. R. and Mahesh, P. A. and Jayaraj, B. S. and Holla, A. D. and Vishweswaraiah, S. and Ramachandra, N. B. (2015) Il-10 and il-17f promoter single nucleotide polymorphism and asthma: a case-control study in south india. LUNG, 193 (5). pp. 739-747. ISSN 1432-1750

Jahromi, S. R. and Mahesh, P. A. and Jayaraj, B. S. and Holla, A. D. and Vishweswaraiah, S. and Ramachandra, N. B. (2015) Single nucleotide polymorphism and asthma: A study on the genetic basis of asthma. EUROPEAN RESPIRATORY JOURNAL, 46 (59). ISSN 1399-3003

Davoodi, P. and Mahesh, P. A. and Holla, A. D. and Ramachandra, N. B. (2015) A preliminary study on the association of single nucleotide polymorphisms of interleukin 4 (IL4), IL13, IL4 receptor alpha (IL4R alpha) & toll-like receptor 4 (TLR4) genes with asthma in Indian adults. Indian Journal of Medical Research, 142. pp. 674-679.

Davoodi, Parisa and Mahesh, P. A. and Amrutha, D. Holla and Ramachandra, N. B. (2015) A preliminary study on the association of single nucleotide polymorphisms of interleukin 4 (IL4), IL13, IL4 receptor alpha (IL4Rα) & Toll-like receptor 4 (TLR4) genes with asthma in Indian adults. Indian Journal of Medical Research, 142 (6). pp. 675-680. ISSN 0975-9174

Ramachandra, N. B. and Kusuma, L. (2015) An understanding of spinocerebellar ataxia. INDIAN JOURNAL OF MEDICAL RESEARCH, 141. pp. 148-150. ISSN 0971-5916

Venkatesh, S. K. and Siddaiah, A. and Padakannaya, P. and Ramachandra, N. B. (2014) Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population. Psychiatric Genetics, 24 (1). pp. 10-20.

Saldanha, M. and Siddaiah, A. and Veerappa, A. M. and Ramachandra, N. B. and Padakannaya, P. (2014) Catch them before they fall: A simple test of sight-word and pseudo-word reading in Kannada for a quick and early assessment. SAGE Open, 4 (4). ISSN 2158-2440

Veerappa, A. M. and Murthy, M. and Vishweswaraiah, S. and Lingaiah, K. and Suresh, R. V. and Nachappa, S. A. and Prashali, N. and Yadav, S. N. and Srikanta, M. A. and Manjegowda, D. S. and Seshachalam, K. B. and Ramachandra, N. B. (2014) Copy number variations burden on mirna genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression. PLoS ONE, 9 (2). ISSN 1932-6203

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 0962-1075

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

Singh, S. H. and Ramachandra, N. B. and Nongthomba, U. (2014) Egg-derived tyrosine phosphatase as a potential biomarker for muscle ageing and degeneration in Drosophila melanogaster. Journal of Genetics and Genomics, 41 (4). pp. 221-224. ISSN 16738527

Veerappa, A. M. and Saldanha, M. and Padakannaya, 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 1552-4841

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

Manjegowda, D. S. and Prasad, M. and Veerappa, A. M. and Ramachandra, N. B. (2014) Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family. Genetics Research, 96. ISSN 0016-6723

Veerappa, A. M. and Lingaiah, K. and Vishweswaraiah, S. and Murthy, M. N. and Suresh, R. V. and Manjegowda, D. S. and Ramachandra, N. B. (2014) Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays. Genetics Research, 96. ISSN 0016-6723

Avinash, M. V. and Sangeetha, V. and Kusuma, L. and Megha Murthy, N. and Raviraj, V. S. and Keshava, B. and Ramachandra, N. B. and Tejaswini, T. and Niveditha, B. Patel and Supriya Gowda, P. K. (2014) Insertion-deletions burden in copy number polymorphisms of the Tibetan population. Indian Journal of Human Genetics, 20 (2). pp. 166-174.

Vishweswaraiah, S. and Veerappa, A. M. and Mahesh, P. A. and Jayaraj, B. S. and Krishnarao, C. S. and Ramachandra, N. B. (2014) Molecular interaction network and pathway studies of ADAM33 potentially relevant to asthma. Annals of Allergy, Asthma and Immunology, 113 (4). 418-424.e1. ISSN 1081-1206

Singh, S. H. and Kumar, P. and Ramachandra, N. B. and Nongthomba, U. (2014) Roles of the troponin isoforms during indirect flight muscle development in Drosophila. Journal of Genetics, 93 (2). pp. 379-388.

Raeiszadeh Jahromi, S. and Mahesh, P. A. and Jayaraj, B. S. and Madhunapantula, S. R. V. and Holla, A. D. and Vishweswaraiah, S. 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.

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

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.

Lingaiah, K. and Ramachandra, N. B. (2014) An insight into the understanding of 5-HTR2A variants leading to schizophrenia. Indian Journal of Medical Research, 140 (DEC). pp. 713-715. ISSN 0971-5916

Venkatesh, S. K. and Siddaiah, A. and Padakannaya, P. and Ramachandra, N. B. (2013) Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population. Journal of Human Genetics, 58 (8). pp. 531-538. ISSN 1434-5161

Davoodi, P. and Mahesh, P. A. and Holla, A. D. and Ramachandra, N. B. (2013) Association of socio-economic status with family history in adult patients with asthma. Indian Journal of Medical Research, 138 (4). pp. 497-503. ISSN 0971-5916

Veerappa, A. M. and Padakannaya, P. and Ramachandra, N. B. (2013) Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the y chromosome. Functional and Integrative Genomics, 13 (3). pp. 285-293. ISSN 1438-793X

Veerappa, A. M. and Saldanha, M. and Padakannaya, P. and Ramachandra, N. B. (2013) Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity. Journal of Human Genetics, 58 (8). pp. 539-547. ISSN 1434-5161

Veerappa, A. M. and Saldanha, M. and Padakannaya, P. and Ramachandra, N. B. (2013) Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 162 (8). pp. 889-897. ISSN 1552-4841

Venkatesh, S. K. and Siddaiah, A. and Padakannaya, P. and Ramachandra, N. B. (2013) Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with Developmental Dyslexia. Gene, 529 (2). pp. 215-219.

Ranjini, M. S. and Ramachandra, N. B. (2013) Rapid evolution of a few members of nasuta-albomicans complex of drosophila: Study on two candidate genes, Sod1 and Rpd3. Journal of Molecular Evolution, 76 (5). pp. 311-323. ISSN 1432-1432

Veerappa, A. M. and Vishweswaraiah, S. and Lingaiah, K. and Murthy, M. and Manjegowda, D. S. and Nayaka, R. and Ramachandra, N. B. (2013) Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays. PLoS ONE, 8 (7).

Thongatabam, B. and Ramachandra, N. B. (2012) Genomic introgression in laboratory evolved hybrid races, Cytorace 1 and Fissioncytorace-1 of Nasuta-albomicans complex (NAC) of Drosophila (Insecta, Diptera) as revealed by RAPD and ISSR markers. Italian Journal of Zoology, 79 (4). pp. 520-529. ISSN 1748-5851

Sheetal Salvi, S. and Kumar, R. Pravin and Ramachandra, N. B. and Sparrow, John C. and Nongthomba, Upendra (2012) Mutations in Drosophila Myosin rod cause defects in Myofibril assembly. Journal of Molecular Biology, 419 (1). 22 - 40. ISSN 1089-8638

Davoodi, Parisa and Mahesh, P. A. and Amrutha, D. Holla and Vijayakumar, G. S. and Jayaraj, B. S. and Chandrashekara, S. and Ramachandra, N. B. (2012) Serum levels of interleukin-13 and interferon-gamma from adult patients with asthma in Mysore. Cytokine, 60 (2). 431 - 437. ISSN 1096-0023

Ranjini, M. S. and Ramachandra, N. B. (2011) Differential response to hormesis by laboratory evolved short-lived and long-lived cytoraces of nasuta-albomicans complex of Drosophila. ITALIAN JOURNAL OF ZOOLOGY, 78 (1). pp. 70-81. ISSN 1125-0003

Ranjini, M. S. and Hosamani, R. and Muralidhara and Ramachandra, N. B. (2011) Differential susceptibility of a few members of nasuta-albomicans complex of drosophila to paraquat-induced lethality and oxidative stress. GENOME, 54 (10). pp. 829-835.

Dinesh, S. M. and Lingaiah, K. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2011) GATA4 specific nonsynonymous single-nucleotide polymorphisms in congenital heart disease patients of Mysore, India. GENETIC TESTING AND MOLECULAR BIOMARKERS, 15 (10). pp. 715-720.

Kusuma, L. and Dinesh, S. M. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2011) A maiden report on CRELD1 single-nucleotide polymorphism association in congenital heart disease patients of Mysore, South India. GENETIC TESTING AND MOLECULAR BIOMARKERS, 15 (7-8). pp. 483-487.

Bijanzadeh, M. and Mahesh, P. A. and Ramachandra, N. B. (2011) An understanding of the genetic basis of asthma. INDIAN JOURNAL OF MEDICAL RESEARCH, 134 (2). pp. 149-161. ISSN 0971-5916

Kusuma, L. and Bharath, A. Parshwanath and Savitha, R. M. and Balasundaram Krishnamurthy and Ramachandra, N. B. (2010) A rare case of congenital heart disease with ambiguous genitalia. Indian Journal of Human Genetics, 16 (3). pp. 166-168. ISSN 1998-362X

Mahdi, Bijanzadeh and Mahesh, P. A. and Savitha, M. R. and Pradeep Kumar, B. S. and Jayaraj and Ramachandra, N. B. (2010) Inheritance patterns, consanguinity & risk for asthma. Indian Journal of Heterocyclic Chemistry, 132 (1). pp. 48-55. ISSN 0971-1627

Bijaya, Thongatabam and Ramachandra, N. B. (2010) Racial divergence of a rare laboratory evolved centromeric fission Cytorace of nasuta-albomicans complex of Drosophila. Indian Journal of Experimental Biology, 48 (5). pp. 511-517. ISSN 0975-1009

Malini, Suttur S. and Ramachandra, N. B. (2010) Young Mothers Produce More Chromosomal Syndrome Babies in Mysore, South India. International Journal of Human Genetics, 10 (1-3). pp. 105-112. ISSN 0972-3757

Dinesh, S. M. and Kusuma, L. and Smitha, R. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2010) Single-Nucleotide Polymorphisms of NKX2.5 Found in Congenital Heart Disease Patients of Mysore, South India. Genetic Testing and Molecular Biomarkers, 14 (6). pp. 873-879. ISSN 1945-0257

Ranjini, M. S. and Ramachandra, N. B. (2009) Evolution of short-lived and long-lived races of drosophila in the envrons of laboratory. Indian Journal of Gerontology, 23 (4). pp. 381-398. ISSN 0971-4189

Pushpa Saviour and Padakannaya, Prakash and Nishanimutt, S. and Ramachandra, N. B. (2009) Familial patterns and biological markers of dyslexia. International Journal of Human Genetics, 9 (1). pp. 21-29. ISSN 0972-3757

Bijanzadeh, Mahdi and Ramachandra, N. B. and Mahesh, P. A. and Savitha, M. R. and Manjunath, B. S. and Jayaraj, B. S. (2009) Lack of association between asthma and ABO blood group. LUNG, 187 (6). pp. 389-392. ISSN 1432-1750

Malini, S. S. and Savitha, M. and Balasundaram, K. and Ramachandra, N. B. (2009) Rare association of turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex. Indian Journal of Human Genetics, 15 (2). pp. 75-77. ISSN 1998-362x

Bijanzadeh, Mahdi and Ramachandra, N. B. and Mahesh, P. A. and Savitha, M. R. and Vijayakumar, G. S. and Pradeep Kumar and Manjunath, B. S. and Jayaraj, B. S. (2009) Soluble intercellular adhesion molecule-1 and e-selectin in patients with asthma exacerbation. LUNG, 187 (5). pp. 315-320. ISSN 1432-1750

Pushpa Saviour and Satish Kumar and Kiran, U. and Ravuri, R. R. and Rao, V. R. and Ramachandra, N. B. (2008) Allelic variants of DYX1C1 are not associated with dyslexia in India. Indian Journal of Human Genetics, 14 (3). pp. 99-102. ISSN 1998-362X

Ponnappa, K. C. and Pushpa Saviour and Ramachandra, N. B. and Manjunatha Kini, R. and Veerabasappa Gowda, T. (2008) INN-toxin, a highly lethal peptide from the venom of Indian cobra (Naja naja) venom—Isolation, characterization and pharmacological actions. Peptides, 29 (11). 1893 - 1900. ISSN 1873-5169

Smitha, R. and Savitha, M. R. and Krishnamurthy, Balasundaram and Doddaiah, Narayanappa and Prasanth, S. N. and Ramachandra, N. B. (2007) Association between pericentric inversion in chromosome 9 and congenital heart defects. International Journal of Human Genetics, 7 (3). pp. 241-248. ISSN 0972-3757

Malini, S. S. and Smitha, R. and Ramachandra, N. B. (2007) Evolution of phenylthiocarbamide taster trait in Mysore, South India. Indian Journal of Human Genetics, 13 (1). pp. 16-20. ISSN 1998-362X

Harini, B. P. and Ramachandra, N. B. (2007) Newly evolved cytoraces of nasuta-albondcans complex of Drosophila live better than their parents as revealed by life-history trait analysis at three different temperatures. Current Science, 93 (3). pp. 348-356. ISSN 0011-3891

Harini, B. P. and Ramachandra, N. B. (2007) Newly evolved cytoraces of nasuta–albomicans complex of drosophila live better than their parents as revealed by life-history trait analysis at three different temperatures. Current Science, 93 (3). pp. 348-356. ISSN 0011-3891

Malini, S. S. and Ramachandra, N. B. (2007) Possible risk factors for down Syndrome and sex chromosomal aneuploidy in Mysore, South India. Indian Journal of Human Genetics, 13 (3). pp. 102-108. ISSN 1998-362X

Babu, Sajesh and Ramachandra, N. B. (2007) Screen for new mutations on the 2nd chromosome involved in indirect flight muscle development in Drosophila melanogaster. Genome, 50 (4). pp. 343-350. ISSN 1480-3321

Savitha, M. R. and Krishnamurthy, B. and Ashok, D. A. and Ramachandra, N. B. (2007) Self abortion of attacks in patients with hot water epilepsy. Indian Pediatrics, 44 (4). p. 298. ISSN 0974-7559

Smitha, R. and Harshavardhan Gawde, M. and Hyderi, Abbas and Savitha, M. R. and Patel, Zareen M. and Krishnamurthy, Balasundaram and Ramachandra, N. B. (2006) De novo isochromosome 18p in a female dysmorphic child. Journal of Applied Genetics, 47 (4). pp. 397-401. ISSN 2190-3883

Smitha, R. and Ramachandra, N. B. (2006) Parental consanguinity increases congenital heart diseases in South India. Annals of Human Biology, 33 (5-6). pp. 519-528. ISSN 1464-5033

Saviour, P. and Ramachandra, N. B. (2006) Biological basis of dyslexia:a maturing perspective. Current Science, 90 (2). pp. 168-175. ISSN 0011-3891

Malini, S. S. and Ramachandra, N. B. (2006) Influence of advanced age of maternal grandmothers on down syndrome. BMC Medical Genetics, 7 (1). p. 4. ISSN 1471-2350

Harini, B. P. and Ramachandra, N. B. (2003) Racial divergence in the foreleg bristles of four members of the nasuta-albomicans complex of Drosophila. Current Science, 85 (10). pp. 1444-1450.

Harini, B. P. and Ramachandra, N. B. (2003) Evolutionary experimentation through hybridization under laboratory condition in Drosophila:evidence for recombinational speciation. BMC Evolutionary Biology, 3 (20). ISSN 1471-2148

Mahesh, G. and Ramachandra, N. B. and Ranganath, H. A. (2000) Patterns of replication in the neo-sex chromosomes of Drosophila nasuta albomicans. Journal of Biosciences, 25 (3). pp. 229-234. ISSN 0250-5991

Harini, B. P. and Ramachandra, N. B. (2000) Racial divergence in body weight: A study in the four members of newly evolved nasuta-albomicans complex of Drosophila. Current Science, 78 (3). pp. 342-344. ISSN 0011-3891

Tanuja, M. T. and Ramachandra, N. B. and Ranganath, H. A. (1999) Evolution of a recent neo-Y sex chromosome in a laboratory population of Drosophila. Journal of Genetics, 78 (2). pp. 81-85. ISSN 0022-1333

Nongthomba, U. and Ramachandra, N. B. (1999) A direct screen identifies new flight muscle mutants on the Drosophila second chromosome. Genetics, 153 (1). pp. 261-274. ISSN 0016-6731

Ramachandra, N. B. and Ranganath, H. A. (1990) The chromosomes of 2 drosophila races - drosophila-nasuta-nasuta and drosophila-nasuta-albomicana .5. introgression and the evolution of new karyotypes. Journal of Zoological Systematics and Evolutionary Research, 28 (1). pp. 62-68.

This list was generated on Sun Mar 7 15:05:35 2021 IST.