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Arun Kumar

Research Profile

Geographic Areas

India

Procedures

Concepts & Ideas

Chemicals & Drugs

Physiology

Disorders

Anatomy

Tumor Cell Line

Phenomena

Polymorphism, Single-Stranded Conformational

Co-author Network

Publications

TOP 3
Srinivas G Kodaganur; Astha Sarda; Mohd H Shah; Sagar J Tontanahal; Vishwanath Bhat; Arun Kumar
Clinical phenotype and the lack of mutations in the CHRNG, CHRND, and CHRNA1 genes in two Indian families with Escobar syndrome.
Mohammad Iqbal Rather; Shivananda S Swamy; Kodaganur S Gopinath; Mathighatta N Nagashri; Arun Kumar
Oncogenic microRNA-155 down-regulates tumor suppressor CDC73 and promotes oral squamous cell carcinoma cell proliferation: implications for cancer therapeutics.
Thejaswini Venkatesh; Kodaganur S Gopinath; S M Azeem Mohiyuddin; Mathighatta Nagaraj Nagashri; Shivananda S Swamy; Arun Kumar
Primary microcephaly gene MCPH1 shows signatures of tumor suppressors and is regulated by miR-27a in oral squamous cell carcinoma.

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All Publications

2013: Srinivas G Kodaganur; Astha Sarda; Mohd H Shah; Sagar J Tontanahal; Vishwanath Bhat; Arun Kumar
Clinical phenotype and the lack of mutations in the CHRNG, CHRND, and CHRNA1 genes in two Indian families with Escobar syndrome.
Clinical dysmorphology 2013;22(2):54-8.
2013: Mohammad Iqbal Rather; Shivananda S Swamy; Kodaganur S Gopinath; Mathighatta N Nagashri; Arun Kumar
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(1):608-18.
2013: Thejaswini Venkatesh; Kodaganur S Gopinath; S M Azeem Mohiyuddin; Mathighatta Nagaraj Nagashri; Shivananda S Swamy; Arun Kumar
Primary microcephaly gene MCPH1 shows signatures of tumor suppressors and is regulated by miR-27a in oral squamous cell carcinoma.
PloS one 2013;8(3):e54643.
2011: Shalmali Pradhan; M N Nagashri; K S Gopinath; Arun Kumar
Expression profiling of CYP1B1 in oral squamous cell carcinoma: counterintuitive downregulation in tumors.
PloS one 2011;6(11):e27914.
2011: Pooja Singhmar; Arun Kumar
Angelman syndrome protein UBE3A interacts with primary microcephaly protein ASPM, localizes to centrosomes and regulates chromosome segregation.
PloS one 2011;6(5):e20397.
2010: Arun Kumar; Maheswara R Duvvari; Venkatesh C Prabhakaran; Jyoti S Shetty; Gowri J Murthy; S Blanton
A homozygous mutation in LTBP2 causes isolated microspherophakia.
Human genetics 2010;128(4):365-71.
2009: Arun Kumar; Satish Girimaji; Mahesh R Duvvari; S Blanton
Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly.
American journal of human genetics 2009;84(2):286-90.
2009: Abdullah Ali; Vineeta Bajaj; K S Gopinath; Arun Kumar
Characterization of the human SLC22A18 gene promoter and its regulation by the transcription factor Sp1.
Gene 2009;429(1-2):37-43.
2008: Vineeta Bajaj; Pooja Singhmar; Arun Kumar
Promoter characterization and regulation of expression of an imprinted gene SLC22A18AS.
Gene 2008;424(1-2):40-7.
2008: Chakraborty Sanjukta; S M Azeem Mohiyuddin; K S Gopinath; Arun Kumar
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.
2007: Arun Kumar; Syril Kumar Dorairaj; Venkatesh C Prabhakaran; D Ravi Prakash; Chakraborty Sanjukta
Identification of genes associated with tumorigenesis of meibomian cell carcinoma by microarray analysis.
Genomics 2007;90(5):559-66.
2007: Chakraborty Sanjukta; Sonal Khare; Syril Dorairaj; Venkatesh C Prabhakaran; D Ravi Prakash; Arun Kumar
Identification of genes associated with tumorigenesis of retinoblastoma by microarray analysis.
Genomics 2007;90(3):344-53.
2007: Arun Kumar; Manjunath G Basavaraj; Santosh K Gupta; Imteyaz Qamar; Abdullah Ali; Vineeta Bajaj; T K Ramesh; D Ravi Prakash; Jyoti Shetty; Syril Dorairaj
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():667-76.
2007: Arun Kumar; Soma Bhattacharjee; D Ravi Prakash; Chethan Sitarampur Sadanand
Genetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: two novel mutations in SLC4A11.
Molecular vision 2007;13():39-46.
2004: Abdullah Ali; Conjeevaram Prabhakaran Venkatesh; Anitha Ragunath; Arun Kumar
Mutation analysis of the KIF21A gene in an Indian family with CFEOM1: implication of CpG methylation for most frequent mutations.
Ophthalmic genetics 2004;25(4):247-55.
2004: Arun Kumar; Mohan Babu; William J Kimberling; Conjeevaram Prabhakaran Venkatesh
Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A.
Molecular vision 2004;10():910-6.
2004: Arun Kumar; Mohan Babu; Anitha Raghunath; Conjeevaram Prabhakaran Venkatesh
Genetic analysis of a five generation Indian family with BPES: a novel missense mutation (p.Y215C).
Molecular vision 2004;10():445-9.
2004: Arun Kumar; Jyoti Shetty; Bharath Kumar; S Blanton
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.
2004: Vineeta Bajaj; Manjunath Markandaya; Lingegowda Krishna; Arun Kumar
Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5.
BMC genetics 2004;5():13.
2003: Abdullah Ali; Satish Girimaji; Arun Kumar
Identification of a core promoter and a novel isoform of the human TSC1 gene transcript and structural comparison with mouse homolog.
Gene 2003;320():145-54.
2003: Veeriah Selvaraju; Manjunath Markandaya; Pullabatla Venkata Siva Prasad; Parthasarathy Sathyan; Gomathy Sethuraman; Satish Chandra Srivastava; Nalin Thakker; Arun Kumar
Mutation analysis of the cathepsin C gene in Indian families with Papillon-Lefèvre syndrome.
BMC medical genetics 2003;4():5.
2002: Arun Kumar; Manjunath Markandaya; Satish Girimaji
Primary microcephaly: microcephalin and ASPM determine the size of the human brain.
Journal of biosciences 2002;27(7):629-32.
2002: Conjeevaram Prabhakaran Venkatesh; V S Pillai; A Raghunath; V S Prakash; R Vathsala; Margaret Pericak-Vance; Arun Kumar
Clinical phenotype and linkage analysis of the congenital fibrosis of the extraocular muscles in an Indian family.
Molecular vision 2002;8():294-7.