Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 90

1.

Antisense STAT3 inhibitor decreases viability of myelodysplastic and leukemic stem cells.

Shastri A, Choudhary G, Teixeira M, Gordon-Mitchell S, Ramachandra N, Bernard L, Bhattacharyya S, Lopez R, Pradhan K, Giricz O, Ravipati G, Wong LF, Cole S, Bhagat TD, Feld J, Dhar Y, Bartenstein M, Thiruthuvanathan VJ, Wickrema A, Ye BH, Frank DA, Pellagatti A, Boultwood J, Zhou T, Kim Y, MacLeod AR, Epling-Burnette PK, Ye M, McCoon P, Woessner R, Steidl U, Will B, Verma A.

J Clin Invest. 2018 Dec 3;128(12):5479-5488. doi: 10.1172/JCI120156. Epub 2018 Nov 5.

2.

STAT3 inhibition as a therapeutic strategy for leukemia.

Kanna R, Choudhary G, Ramachandra N, Steidl U, Verma A, Shastri A.

Leuk Lymphoma. 2018 Sep;59(9):2068-2074. doi: 10.1080/10428194.2017.1397668. Epub 2017 Nov 22. Review.

PMID:
29164994
3.

Detection of First-Line Drug Resistance Mutations and Drug-Protein Interaction Dynamics from Tuberculosis Patients in South India.

Nachappa SA, Neelambike SM, Amruthavalli C, Ramachandra NB.

Microb Drug Resist. 2018 May;24(4):377-385. doi: 10.1089/mdr.2017.0048. Epub 2017 Aug 16.

PMID:
28813625
4.

Epigenetically Aberrant Stroma in MDS Propagates Disease via Wnt/β-Catenin Activation.

Bhagat TD, Chen S, Bartenstein M, Barlowe AT, Von Ahrens D, Choudhary GS, Tivnan P, Amin E, Marcondes AM, Sanders MA, Hoogenboezem RM, Kambhampati S, Ramachandra N, Mantzaris I, Sukrithan V, Laurence R, Lopez R, Bhagat P, Giricz O, Sohal D, Wickrema A, Yeung C, Gritsman K, Aplan P, Hochedlinger K, Yu Y, Pradhan K, Zhang J, Greally JM, Mukherjee S, Pellagatti A, Boultwood J, Will B, Steidl U, Raaijmakers MHGP, Deeg HJ, Kharas MG, Verma A.

Cancer Res. 2017 Sep 15;77(18):4846-4857. doi: 10.1158/0008-5472.CAN-17-0282. Epub 2017 Jul 6.

5.

Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approach.

Suresh RV, Lingaiah K, Veerappa AM, Ramachandra NB.

Indian J Med Res. 2017 Jan;145(1):39-50. doi: 10.4103/ijmr.IJMR_965_14.

6.

Genome-Based Identification of Heterotic Patterns in Rice.

Beukert U, Li Z, Liu G, Zhao Y, Ramachandra N, Mirdita V, Pita F, Pillen K, Reif JC.

Rice (N Y). 2017 Dec;10(1):22. doi: 10.1186/s12284-017-0163-4. Epub 2017 May 19.

7.

High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts.

Murthy MN, Veerappa AM, Seshachalam KB, Ramachandra NB.

Neurol Res. 2016 Sep;38(9):775-85. doi: 10.1080/01616412.2016.1204105. Epub 2016 Jul 11.

PMID:
27399248
8.

A newly evolved Drosophila Cytorace-9 shows trade-off between longevity and immune response.

Sinam YM, Chatterjee A, Ranjini MS, Poojari A, Nagarajan A, Ramachandra NB, Nongthomba U.

Infect Genet Evol. 2016 Oct;44:1-7. doi: 10.1016/j.meegid.2016.06.025. Epub 2016 Jun 13.

PMID:
27306321
9.

Pexmetinib: A Novel Dual Inhibitor of Tie2 and p38 MAPK with Efficacy in Preclinical Models of Myelodysplastic Syndromes and Acute Myeloid Leukemia.

Bachegowda L, Morrone K, Winski SL, Mantzaris I, Bartenstein M, Ramachandra N, Giricz O, Sukrithan V, Nwankwo G, Shahnaz S, Bhagat T, Bhattacharyya S, Assal A, Shastri A, Gordon-Mitchell S, Pellagatti A, Boultwood J, Schinke C, Yu Y, Guha C, Rizzi J, Garrus J, Brown S, Wollenberg L, Hogeland G, Wright D, Munson M, Rodriguez M, Gross S, Chantry D, Zou Y, Platanias L, Burgess LE, Pradhan K, Steidl U, Verma A.

Cancer Res. 2016 Aug 15;76(16):4841-4849. doi: 10.1158/0008-5472.CAN-15-3062. Epub 2016 Jun 10.

10.

Copy Number Variation of UGT 2B Genes in Indian Families Using Whole Genome Scans.

Veerappa AM, Padakannaya P, Ramachandra NB.

J Nucleic Acids. 2016;2016:1648527. doi: 10.1155/2016/1648527. Epub 2016 Mar 22.

11.
12.
13.

Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations.

Prabhanjan M, Suresh RV, Murthy MN, Ramachandra NB.

Diabetes Res Clin Pract. 2016 Mar;113:160-70. doi: 10.1016/j.diabres.2015.12.015. Epub 2016 Jan 13.

PMID:
26830856
14.

Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.

Veerappa AM, Suresh RV, Vishweswaraiah S, Lingaiah K, Murthy M, Manjegowda DS, Padakannaya P, Ramachandra NB.

Genet Res (Camb). 2015 Sep 22;97:e18. doi: 10.1017/S0016672315000191.

PMID:
26390810
15.

IL-10 and IL-17F Promoter Single Nucleotide Polymorphism and Asthma: A Case-Control Study in South India.

Raeiszadeh Jahromi S, Mahesh PA, Jayaraj BS, Holla AD, Vishweswaraiah S, Ramachandra NB.

Lung. 2015 Oct;193(5):739-47. doi: 10.1007/s00408-015-9753-3. Epub 2015 Jun 25.

PMID:
26108303
16.

Family history & the risk for adult onset asthma.

Davoodi P, Mahesh PA, Holla AD, Ramachandra NB.

Indian J Med Res. 2015 Mar;141(3):361-3. No abstract available.

17.

Global spectrum of copy number variations reveals genome organizational plasticity and proposes new migration routes.

Veerappa AM, Vishweswaraiah S, Lingaiah K, Murthy M, Suresh RV, Manjegowda DS, Ramachandra NB.

PLoS One. 2015 Apr 24;10(4):e0121846. doi: 10.1371/journal.pone.0121846. eCollection 2015.

18.

An understanding of spinocerebellar ataxia.

Ramachandra NB, Kusuma L.

Indian J Med Res. 2015 Feb;141(2):148-50. No abstract available.

19.

IL8-CXCR2 pathway inhibition as a therapeutic strategy against MDS and AML stem cells.

Schinke C, Giricz O, Li W, Shastri A, Gordon S, Barreyro L, Bhagat T, Bhattacharyya S, Ramachandra N, Bartenstein M, Pellagatti A, Boultwood J, Wickrema A, Yu Y, Will B, Wei S, Steidl U, Verma A.

Blood. 2015 May 14;125(20):3144-52. doi: 10.1182/blood-2015-01-621631. Epub 2015 Mar 25. Erratum in: Blood. 2015 Jul 16;126(3):425. Barreryo, Laura [corrected to Barreyro, Laura].

20.

An insight into the understanding of 5-HTR2A variants leading to schizophrenia.

Lingaiah K, Ramachandra NB.

Indian J Med Res. 2014 Dec;140(6):713-5. No abstract available.

21.

Copy number variation burden on asthma subgenome in normal cohorts identifies susceptibility markers.

Vishweswaraiah S, Veerappa AM, Mahesh PA, Jahromi SR, Ramachandra NB.

Allergy Asthma Immunol Res. 2015 May;7(3):265-75. doi: 10.4168/aair.2015.7.3.265. Epub 2014 Dec 18.

22.

Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family.

Manjegowda DS, Prasad M, Veerappa AM, Ramachandra NB.

Genet Res (Camb). 2014 Oct 10;96:e12. doi: 10.1017/S0016672314000159.

PMID:
25579819
23.

Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays.

Veerappa AM, Lingaiah K, Vishweswaraiah S, Murthy MN, Suresh RV, Manjegowda DS, Ramachandra NB.

Genet Res (Camb). 2014 Dec 16;96:e17. doi: 10.1017/S0016672314000202.

PMID:
25578402
24.

Development of Rapid Automatized Naming (RAN) in Simultaneous Kannada-English Biliterate Children.

Siddaiah A, Saldanha M, Venkatesh SK, Ramachandra NB, Padakannaya P.

J Psycholinguist Res. 2016 Feb;45(1):177-87. doi: 10.1007/s10936-014-9338-y. Epub 2014 Nov 19.

PMID:
25408516
25.

Insertion-deletions burden in copy number polymorphisms of the Tibetan population.

Veerappa AM, Vishweswaraiah S, Lingaiah K, Murthy NM, Suresh RV, Belur K, Ramachandra NB, Tejaswini, Patel NB, Gowda PK.

Indian J Hum Genet. 2014 Apr;20(2):166-74. doi: 10.4103/0971-6866.142888.

26.

Roles of the troponin isoforms during indirect flight muscle development in Drosophila.

Singh SH, Kumar P, Ramachandra NB, Nongthomba U.

J Genet. 2014 Aug;93(2):379-88.

27.

Molecular interaction network and pathway studies of ADAM33 potentially relevant to asthma.

Vishweswaraiah S, Veerappa AM, Mahesh PA, Jayaraju BS, Krishnarao CS, Ramachandra NB.

Ann Allergy Asthma Immunol. 2014 Oct;113(4):418-24.e1. doi: 10.1016/j.anai.2014.07.009. Epub 2014 Aug 22.

PMID:
25155083
28.

Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics.

Veerappa AM, Saldanha M, Padakannaya P, Ramachandra NB.

Am J Med Genet B Neuropsychiatr Genet. 2014 Oct;165B(7):572-80. doi: 10.1002/ajmg.b.32260. Epub 2014 Aug 19.

PMID:
25139666
29.

Serum levels of IL-10, IL-17F and IL-33 in patients with asthma: a case-control study.

Raeiszadeh Jahromi S, Mahesh PA, Jayaraj BS, Madhunapantula SR, Holla AD, Vishweswaraiah S, Ramachandra NB.

J Asthma. 2014 Dec;51(10):1004-13. doi: 10.3109/02770903.2014.938353. Epub 2014 Jul 18.

PMID:
24960440
30.

Egg-derived tyrosine phosphatase as a potential biomarker for muscle ageing and degeneration in Drosophila melanogaster.

Singh SH, Ramachandra NB, Nongthomba U.

J Genet Genomics. 2014 Apr 20;41(4):221-4. doi: 10.1016/j.jgg.2014.01.008. Epub 2014 Feb 3. No abstract available.

PMID:
24780620
31.

Divergence of the gene aly in experimentally evolved cytoraces, the members of the nasuta-albomicans complex of Drosophila.

Radhika PN, Ramachandra NB.

Insect Mol Biol. 2014 Aug;23(4):435-43. doi: 10.1111/imb.12091. Epub 2014 Mar 20.

PMID:
24645631
32.

Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia.

Veerappa AM, Saldanha M, Padakannaya P, Ramachandra NB.

Am J Med Genet B Neuropsychiatr Genet. 2013 Dec;162B(8):889-97. doi: 10.1002/ajmg.b.32199. Epub 2013 Sep 20.

PMID:
24591081
33.

Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression.

Veerappa AM, Murthy MN, Vishweswaraiah S, Lingaiah K, Suresh RV, Nachappa SA, Prashali N, Yadav SN, Srikanta MA, Manjegowda DS, Seshachalam KB, Ramachandra NB.

PLoS One. 2014 Feb 28;9(2):e90391. doi: 10.1371/journal.pone.0090391. eCollection 2014.

34.

Association of socio-economic status with family history in adult patients with asthma.

Davoodi P, Mahesh PA, Holla AD, Ramachandra NB.

Indian J Med Res. 2013 Oct;138(4):497-503.

35.

Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population.

Venkatesh SK, Siddaiah A, Padakannaya P, Ramachandra NB.

Psychiatr Genet. 2014 Feb;24(1):10-20. doi: 10.1097/YPG.0000000000000009.

PMID:
24362368
36.

Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with developmental dyslexia.

Venkatesh SK, Siddaiah A, Padakannaya P, Ramachandra NB.

Gene. 2013 Oct 25;529(2):215-9. doi: 10.1016/j.gene.2013.08.017. Epub 2013 Aug 14.

PMID:
23954868
37.

Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays.

Veerappa AM, Vishweswaraiah S, Lingaiah K, Murthy M, Manjegowda DS, Nayaka R, Ramachandra NB.

PLoS One. 2013 Jul 3;8(7):e66843. doi: 10.1371/journal.pone.0066843. Print 2013.

38.

Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosome.

Veerappa AM, Padakannaya P, Ramachandra NB.

Funct Integr Genomics. 2013 Aug;13(3):285-93. doi: 10.1007/s10142-013-0323-6. Epub 2013 May 26.

PMID:
23708688
39.

Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity.

Veerappa AM, Saldanha M, Padakannaya P, Ramachandra NB.

J Hum Genet. 2013 Aug;58(8):539-47. doi: 10.1038/jhg.2013.47. Epub 2013 May 16.

PMID:
23677055
40.

Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population.

Venkatesh SK, Siddaiah A, Padakannaya P, Ramachandra NB.

J Hum Genet. 2013 Aug;58(8):531-8. doi: 10.1038/jhg.2013.46. Epub 2013 May 16.

PMID:
23677054
41.

Rapid evolution of a few members of nasuta-albomicans complex of Drosophila: study on two candidate genes, Sod1 and Rpd3.

Ranjini MS, Ramachandra NB.

J Mol Evol. 2013 May;76(5):311-23. doi: 10.1007/s00239-013-9560-5. Epub 2013 Apr 26.

PMID:
23619741
42.

Membrane topology of yeast alkaline ceramidase YPC1.

Ramachandra N, Conzelmann A.

Biochem J. 2013 Jun 15;452(3):585-94. doi: 10.1042/BJ20130085.

PMID:
23445175
43.

Adaptation of low-resolution methods for the study of yeast microsomal polytopic membrane proteins: a methodological review.

Bochud A, Ramachandra N, Conzelmann A.

Biochem Soc Trans. 2013 Feb 1;41(1):35-42. doi: 10.1042/BST20120212. Review.

PMID:
23356255
44.

Functional analysis of the genes encoding diaminopropionate ammonia lyase in Escherichia coli and Salmonella enterica serovar Typhimurium.

Kalyani JN, Ramachandra N, Kachroo AH, Mahadevan S, Savithri HS.

J Bacteriol. 2012 Oct;194(20):5604-12. Epub 2012 Aug 17.

45.

Serum levels of interleukin-13 and interferon-gamma from adult patients with asthma in Mysore.

Davoodi P, Mahesh PA, Holla AD, Vijayakumar GS, Jayaraj BS, Chandrashekara S, Ramachandra NB.

Cytokine. 2012 Nov;60(2):431-7. doi: 10.1016/j.cyto.2012.05.012. Epub 2012 Jun 12.

PMID:
22698804
46.

Mutations in Drosophila myosin rod cause defects in myofibril assembly.

Salvi SS, Kumar RP, Ramachandra NB, Sparrow JC, Nongthomba U.

J Mol Biol. 2012 May 25;419(1-2):22-40. doi: 10.1016/j.jmb.2012.02.025. Epub 2012 Feb 24.

PMID:
22370558
47.

Differential susceptibility of a few members of the nasuta-albomicans complex of Drosophila to paraquat-induced lethality and oxidative stress.

Ranjini MS, Hosamani R, Muralidhara, Ramachandra NB.

Genome. 2011 Oct;54(10):829-35. doi: 10.1139/g11-049. Epub 2011 Sep 30.

PMID:
21961920
48.

An understanding of the genetic basis of asthma.

Bijanzadeh M, Mahesh PA, Ramachandra NB.

Indian J Med Res. 2011 Aug;134:149-61. Review.

49.

GATA4 specific nonsynonymous single-nucleotide polymorphisms in congenital heart disease patients of Mysore, India.

Dinesh SM, Lingaiah K, Savitha MR, Krishnamurthy B, Narayanappa D, Ramachandra NB.

Genet Test Mol Biomarkers. 2011 Oct;15(10):715-20. doi: 10.1089/gtmb.2010.0278. Epub 2011 Jun 1.

PMID:
21631294
50.

Aurora A is a repressed effector target of the chromatin remodeling protein INI1/hSNF5 required for rhabdoid tumor cell survival.

Lee S, Cimica V, Ramachandra N, Zagzag D, Kalpana GV.

Cancer Res. 2011 May 1;71(9):3225-35. doi: 10.1158/0008-5472.CAN-10-2167. Epub 2011 Apr 26.

Supplemental Content

Loading ...
Support Center