| 1. | Rather, M. I., Swamy, S., Gopinath, K. S. and Kumar, A. Transcriptional repression of tumor suppressor CDC73, encoding an RNA polymerase II interactor, by WT1 promotes cell proliferation: implication for cancer therapeutics. The Journal of Biological Chemistry. 2013. [PubMed] |
2. | Venkatesh, T., Nagashri, M. N., Swamy, S. S., Mohiyuddin, S. M., Gopinath, K. S. and Kumar, A. Primary microcephaly gene MCPH1 shows signatures of tumor suppressors and is regulated by miR-27a in oral squamous cell carcinoma. PloS One. 2013. 8, e54643. [PubMed] | 3. | Rather, M. I., Nagashri, M. N., Swamy, S. S., Gopinath, K. S. and Kumar, A. Oncogenic microRNA-155 down-regulates tumor suppressor CDC73 and promotes oral squamous cell carcinoma cell proliferation: implications for cancer therapeutics. The Journal of Biological Chemistry. 2013. 288, 608-618. [PubMed] | 4. | Kapoor, S., Bindu, P. S., Taly, A. B., Sinha, S., Gayathri, N., Rani, S. V., Chandak, G. R. and Kumar, A. Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy. Molecular Vision. 2012. 18, 2022-2032. [PubMed] | 5. | Somasundaram, J., Krishnasamy, R., Savithri, P., Mahimairaja, S., Kumar, B. S., Sivasubramanium, K., Kumar, V. A., Poongothai, S., Coumar, M. V. and Behera, S. K. Accumulation of few heavy metals in sewage sludges, soils and plants of Coimbatore, Tamil Nadu (India). Journal of Environmental Science & Engineering. 2012. 54, 27-42. [PubMed] | 6. | Pradhan, S., Nagashri, M. N., Gopinath, K. S. and Kumar, A. Expression profiling of CYP1B1 in oral squamous cell carcinoma: counterintuitive downregulation in tumors. PloS One. 2011. 6, e27914. [PubMed] | 7. | Singhmar, P. and Kumar, A. Angelman syndrome protein UBE3A interacts with primary microcephaly protein ASPM, localizes to centrosomes and regulates chromosome segregation. PloS One. 2011. 6, e20397. [PubMed] | 8. | Kumar, A., Duvvari, M. R., Prabhakaran, V. C., Shetty, J. S., Murthy, G. J. and Blanton, S. H. A homozygous mutation in LTBP2 causes isolated microspherophakia. Human Genetics. 2010. 128, 365-371. [PubMed] | 9. | Kumar, A., Girimaji, S. C., Duvvari, M. R. and Blanton, S. H. Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly. American Journal of Human Genetics. 2009. 84, 286-290. [PubMed] | 10. | Ali, A. M., Bajaj, V., Gopinath, K. S. and Kumar, A. Characterization of the human SLC22A18 gene promoter and its regulation by the transcription factor Sp1. Gene. 2009. 429, 37-43. [PubMed] | 11. | Bajaj, V., Singhmar, P. and Kumar, A. Promoter characterization and regulation of expression of an imprinted gene SLC22A18AS. Gene. 2008. 424, 40-47. [PubMed] | 12. | Chakraborty, S., Mohiyuddin, S. M., Gopinath, K. S. and Kumar, A. Involvement of TSC genes and differential expression of other members of the mTOR signaling pathway in oral squamous cell carcinoma. BMC Cancer. 2008. 8, 163. [PubMed] | 13. | Kumar, A., Kumar, D., Prabhakaran, V. C., Prakash, D. R. and Chakraborty, S. Identification of genes associated with tumorigenesis of meibomian cell carcinoma by microarray analysis. Genomics. 2007. 90, 559-566. [PubMed] | 14. | Chakraborty, S., Khare, S., Dorairaj, S. K., Prabhakaran, V. C., Prakash, D. R. and Kumar, A. Identification of genes associated with tumorigenesis of retinoblastoma by microarray analysis. Genomics. 2007. 90, 344-353. [PubMed] | 15. | Kumar, A., Basavaraj, M. G., Gupta, S. K., Qamar, I., Ali, A. M., Bajaj, V., Ramesh, T. K., Prakash, D. R., Shetty, J. S. and Dorairaj, S. K. Role of CYP1B1, MYOC, OPTN, and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients. Molecular Vision. 2007. 13, 667-676. [PubMed] | 16. | Kumar, A., Bhattacharjee, S., Prakash, D. R. and Sadanand, C. S. Genetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: two novel mutations in SLC4A11. Molecular Vision. 2007. 13, 39-46. [PubMed] | 17. | Ali, M., Venkatesh, C., Ragunath, A. and Kumar, A. Mutation analysis of the KIF21A gene in an Indian family with CFEOM1: implication of CpG methylation for most frequent mutations. Ophthalmic Genetics. 2004. 25, 247-255. [PubMed] | 18. | Kumar, A., Babu, M., Kimberling, W. J. and Venkatesh, C. P. Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A. Molecular Vision. 2004. 10, 910-916. [PubMed] | 19. | Kumar, A., Babu, M., Raghunath, A. and Venkatesh, C. P. Genetic analysis of a five generation Indian family with BPES: a novel missense mutation (p.Y215C). Molecular Vision. 2004. 10, 445-449. [PubMed] | 20. | Kumar, A., Shetty, J., Kumar, B. and Blanton, S. H. Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family. Molecular Vision. 2004. 10, 399-402. [PubMed] | 21. | Bajaj, V., Markandaya, M., Krishna, L. and Kumar, A. Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5. BMC Genetics. 2004. 5, 13. [PubMed] | 22. | Ali, M., Girimaji, S. C. and Kumar, A. Identification of a core promoter and a novel isoform of the human TSC1 gene transcript and structural comparison with mouse homolog. Gene. 2003. 320, 145-154. [PubMed] | 23. | Selvaraju, V., Markandaya, M., Prasad, P. V., Sathyan, P., Sethuraman, G., Srivastava, S. C., Thakker, N. and Kumar, A. Mutation analysis of the cathepsin C gene in Indian families with Papillon-Lefevre syndrome. BMC Medical Genetics. 2003. 4, 5. [PubMed] | 24. | Kumar, A., Markandaya, M. and Girimaji, S. C. Primary microcephaly: microcephalin and ASPM determine the size of the human brain. Journal of Biosciences. 2002. 27, 629-632. [PubMed] |