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Number of items: 50.

Conference Poster

Ali, Mahmood and Prabhakara, MG and Babu, M and Bajaj, V and Manjunath, GB and Vasan, SS and Prasannakumar, KM and Kumar, Arun (2005) Cytogenetic and molecular analysis of infertile males from Bangalore, India. In: 15th Annual Meeting of ISSRF and Symposium on Trends in Molecular and Applied Approaches to Reproduction, 4-6 February, 2005, Kolkata,India, p. 79.

Dorairaj, SK and Ramesh, TK and Manjunath, GB and Gupta, SK and Ali, Mahmood and Shah, M and Aruna, AR and Kumar, Arun (2004) Genetic analysis of CYP1B1, MYOC, OPTN and OPTC genes in glaucoma patients from South India. In: 54th Annual meeting of the American Society of Human Genetics, October 28-30, Toronto, Canada, 2098/F4-383.

Prabhakara, MG and Babu, M and Ali, Mahmood and Bajaj, V and Manjunath, GB and Khare, S and Prasannakumar, KM and Kumar, Arun (2004) Genetic analysis of infertile males from Bangalore, India. In: 54th Annual meeting of the American Society of Human Genetics, October 28-30, Toronto, Canada, 920/T-182.

Kumar, Arun and Prabhakara, MG and Ali, Mahmood and Babu, M and Bajaj, V and Kumar, Prasanna (2004) Genetic analysis of males with idiopathic infertility from Bangalore. In: 14th Annual meeting of the Indian Society for the Study of Reproduction and Fertility, Jan 23-25, 2004, Bangalore, India, 94-Poster 40.

Ali, Mahmood and Kumar, Arun (2004) Imprinting and Transcriptional Regulation Mechanism of the SLC22A18 gene from human chromosome segment 11p15.5. In: 28th All India Cell Biology Conference and Symposium on Genome Biology, Dec 1-3, 2004, Chandigarh, India, p. 70.

Bajaj, V and Ankita, I and Ali, Mahmood and Kumar, Arun (2004) Nature and Mechanism of Genomic Imprinting: Studies on the Human Imprinted Region on Chromosome 11p15.5. In: Annual Meeting of the Indian Society of Developmental Biologists - 2004 and Symosium on Development, Epigenetics and Plasticity, Dec 21-23, 2004, Bangalore, India, p. 47.

Ali, Mahmood and Markandaya, M and Girimaji, SC and Shukla, AK and Sacchidanand, S and Kumar, Arun (2003) Mutational analysis of the TSC2 gene in 23 TSC families from India. In: 53rd Annual Meeting of the American Society of Human Genetics, November 4-8, Convention Center, Los Angeles, U.S.A, p. 2219.

Ali, Mahmood and Girimaji, SC and Kumar, Arun (2003) Promoter characterization of the TSC1 gene. In: 10th Congress of Federation of Asian & Oceanian Biochemists and Molecular Biologists, December 7-11, Indian Institute of Science, Bangalore, India, P2-06.

Ali, Mahmood and Girimaji, SC and Kumar, Arun (2002) Isolation and characterization of the TSC1 gene promoter. In: XVI All India cell Biology Conference and Symposium, 12-14 December, 2002, Navi Mumbai, India, AP6-68.

Journal Article

Pradhan, Shalmali Avinash and Rather, Mohammad Iqbal and Tiwari, Ankana and Bhat, Vishwanath Kumble and Kumar, Arun (2014) Evidence that TSC2 acts as a transcription factor and binds to and represses the promoter of Epiregulin. In: NUCLEIC ACIDS RESEARCH, 42 (10). pp. 6243-6255.

Rather, Mohammad Iqbal and Swamy, Shivananda and Gopinath, Kodaganur S. and Kumar, Arun (2014) Transcriptional Repression of Tumor Suppressor CDC73, Encoding an RNA Polymerase II Interactor, by Wilms Tumor 1 Protein (WT1) Promotes Cell Proliferation IMPLICATION FOR CANCER THERAPEUTICS. In: JOURNAL OF BIOLOGICAL CHEMISTRY, 289 (2). pp. 968-976.

Shah, Mohd Hussain and Bhat, Vishwanath and Shetty, Jyoti S and Kumar, Arun (2014) Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome. In: MOLECULAR VISION, 20 . pp. 790-796.

Kodaganur, Srinivas Gopinath and Kapoor, Saketh and Veerappa, Avinash M and Tontanahal, Sagar Jagannath and Sarda, Astha and Yathish, S and Prakash, Ravi D and Kumar, Arun (2013) Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature. In: Molecular Vision, 19 . pp. 1694-1706.

Kodaganur, Srinivas G and Tontanahal, Sagar J and Sarda, Astha and Shah, Mohd H and Bhat, Vishwanath and Kumar, Arun (2013) Clinical phenotype and the lack of mutations in the CHRNG, CHRND, and CHRNA1 genes in two Indian families with Escobar syndrome. In: Clinical Dysmorphology, 22 (2). pp. 54-58.

Rather, Mohammad Iqbal and Nagashri, Mathighatta N and Swamy, Shivananda S and Gopinath, Kodaganur S and Kumar, Arun (2013) Oncogenic MicroRNA-155 Down-regulates Tumor Suppressor CDC73 and Promotes Oral Squamous Cell Carcinoma Cell Proliferation IMPLICATIONS FOR CANCER THERAPEUTICS. In: JOURNAL OF BIOLOGICAL CHEMISTRY, 288 (1). pp. 608-618.

Venkatesh, Thejaswini and Nagashri, Mathighatta Nagaraj and Swamy, Shivananda S and Mohiyuddin, Azeem SM and Gopinath, Kodaganur S and Kumar, Arun (2013) Primary Microcephaly Gene MCPH1 Shows Signatures of Tumor Suppressors and Is Regulated by miR-27a in Oral Squamous Cell Carcinoma. In: PLOS ONE, 8 (3).

Kapoor, Saketh and Bindu, Parayil Sankaran and Taly, Arun B. and Sinha, Sanjib and Gayathri, Narayanappa and Rani, S. Vasantha and Chandak, Giriraj Ratan and Kumar, Arun (2012) Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy. In: MOLECULAR VISION, 18 (211-14). pp. 2022-2032.

Singhmar, Pooja and Kumar, Arun (2011) Angelman Syndrome Protein UBE3A Interacts with Primary Microcephaly Protein ASPM, Localizes to Centrosomes and Regulates Chromosome Segregation. In: PLos One, 6 (5).

Kumar, Arun and Duvvari, Maheswara R and Prabhakaran, Venkatesh C and Shetty, Jyoti S and Murthy, Gowri J and Blanton, Susan Halloran (2010) A homozygous mutation in LTBP2 causes isolated microspherophakia. In: Human Genetics, 128 (4). pp. 365-371.

Kumar, Arun and Duvvari, Maheswara R and Prabhakaran, Venkatesh C and Murthy, Gowri J and Blanton, Susan H (2010) A homozygous mutation in LTBP2 causes isolated microspherophakia. In: Human Genetics, 128 (4). pp. 365-371.

Frio, Thomas Rio and Panek, Sylwia and Iseli, Christian and Di Gioia, Silvio Alessandro and Kumar, Arun and Gal, Andreas and Rivolta, Carlo (2009) Ultra high throughput sequencing excludes MDH1 as candidate gene for RP28-linked retinitis pigmentosa. In: Molecular Vision, 15 (278-81). pp. 2627-2633.

Frio, Thomas Rio and Panek, Sylwia and Iseli, Christian and Di Gioia, Silvio Alessandro and Kumar, Arun and Gal, Andreas and Rivolta, Carlo (2009) Ultra high throughput sequencing excludes MDH1 as candidate gene for RP28-linked retinitis pigmentosa. In: Molecular Vision, 15 (278-81). pp. 2627-2632.

Kumar, Arun and Girimaji, Satish C and Duvvari, Mahesh R and Blanton, Susan (2009) Mutations in STIL, Encoding a Pericentriolar and Centrosomal Protein, Cause Primary Microcephaly. In: American Journal Of Human Genetics, 84 (2). pp. 286-290.

Kumar, Arun and Girimaji, Satish C and Duvvari, Mahesh R and Blanton, Susan H (2009) Mutations in STIL, Encoding a Pericentriolar and Centrosomal Protein, Cause Primary Microcephaly. In: The American Journal of Human Genetics, 84 (2). 286-290 .

Ali, Abdullah Mahmood and Bajaj, Vineeta and Gopinath, KS and Kumar, Arun (2009) Characterization of the human SLC22A18 gene promoter and its regulation by the transcription factor Sp1. In: Gene, 429 (1-2). pp. 37-43.

Ali, Abdullah Mahmood and Bajaj, Vineeta and Gopinath, KS and Kumar, Arun (2009) Characterization of the human SLC22A18 gene promoter and its regulation by the transcription factor Sp1. In: Gene, 429 (1-2). pp. 37-43.

Bajaj, Vineeta and Singhmar, Pooia and Kumar, Arun (2008) Promoter characterization and regulation of expression of an imprinted gene SLC22A18AS. In: Gene, 424 (1-2). pp. 40-47.

Chakraborty, Sanjukta and Mohiyuddin, AzeemSM and Gopinath, KS and Kumar, Arun (2008) Involvement of TSC genes and differential expression of other members of the mTOR signaling pathway in oral squamous cell carcinoma. In: BMC Cancer, 8 (163). 163-1-163-12.

Kumar, Arun and Dorairaj, Syril Kumar and Prabhakaran, Venkatesh C and Prakash, Ravi D and Chakraborty, Sanjukta (2007) Identification of genes associated with tumorigenesis of meibomian cell carcinoma by microarray analysis. In: Genomics, 90 (5). pp. 559-566.

Chakraborty, Sanjukta and Khare, Sonal and Dorairaj, Syril Kumar and Prabhakaran, Venkatesh C and Prakash, Ravi D and Kumar, Arun (2007) Identification of genes associated with tumorigenesis of retinoblastoma by microarray analysis. In: Genomics, 90 (3). pp. 344-353.

Kumar, Arun and Bhattacharjee, Soma and Ravi Prakash, Durgappa and Sadanand, Chethan Sitarampur (2007) Genetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: two novel mutations in SLC4A11. In: Molecular Vision, 13 . pp. 39-46.

Kumar, Arun and Basavaraj, Manjunath G and Gupta, Santosh K and Qamar, Imteyaz and Ali, Abdullah Mahmood and Bajaj, Vineeta and Ramesh, TK and Prakash, Ravi D and Shetty, Jyoti S and Dorairaj, Syril K (2007) Role of CYP1B1, MYOC, OPTN and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients. In: Molecular Vision, 13 (73). pp. 667-676.

Ali, Mahmood and Girimaji, SC and Markandaya, M and Shukla, AK and Sacchidanand, S and Kumar, Arun (2005) Mutation and polymorphism analysis of TSC1 and TSC2 genes in Indian patients with tuberous sclerosis complex. In: Acta Neurologica Scandinavica, 111 (1). pp. 54-63.

Ali, Mahmood and Venkatesh, Conjeevaram P and Ragunath, Anitha and Kumar, Arun (2004) Mutation analysis of the KIF21A gene in an Indian family with CFEOM1: implication of CpG methylation for most frequent mutations. In: Ophthalmic Genetics, 25 (4). pp. 247-255.

Kumar, Arun and Babu, Mohan and Kimberling, William J and Venkatesh, Conjeevaram Prabhakaran (2004) Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A. In: Molecular Vision, 10 . pp. 910-916.

Kumar, Arun and Babu, Mohan and Raghunath, Anitha and Venkatesh, Conjeevaram Prabhakaran (2004) Genetic analysis of a five generation Indian family with BPES: A novel missense mutation (p.Y215C). In: Molecular Vision, 10 . pp. 445-449.

Kumar, Arun and Shetty, Jyoti and Kumar, Bharath and Blanton, Susan Halloran (2004) Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family. In: Molecular Vision, 10 (49-50). pp. 399-402.

Kumar, Arun and Shetty, Jyoti and Kumar, Bharath and Blanton, Susan Halloran (2004) Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family. In: Molecular Vision, 10 . pp. 399-402.

Bajaj, Vineeta and Markandaya, Manjunath and Krishna, Lingegowda and Kumar, Arun (2004) Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5. In: BMC Genetics, 5 (13). pp. 1-4.

Astbury, Caroline and Christ, Laurie A and Aughton, David J and Cassidy, Suzanne B and Kumar, Arun and Eichler, Evan E and Schwartz, Stuart (2004) Detection of deletions in de novo balanced chromosome rearrangements: Further evidence for their role in phenotypic abnormalities. In: Genetics In Medicine, 6 (2). pp. 81-89.

Ali, Mahmood and Girimaji, Satish C and Kumar, Arun (2003) Identification of a core promoter and a novel isoform of the human TSCI gene transcript and structural comparison with mouse homolog. In: Gene, 320 . pp. 145-154.

Ali, Mahmood and Girimaji, Satish C and Kumar, Arun (2003) Identification of a core promoter and a novel isoform of the human TSC1 gene transcript and structural comparison with mouse homolog. In: Gene, 320 . pp. 145-154.

Selvaraju, Veeriah and Markandaya, Manjunath and Prasad, Pullabatla Venkata Siva and Sathyan, Parthasarathy and Sethuraman, Gomathy and Srivastava, Satish Chandra and Thakker, Nalin and Kumar, Arun (2003) Mutation analysis of the cathepsin C gene in Indian families with Papillon-Lefèvre syndrome. In: BMC Medical Genetics, 4 (5). pp. 1-8.

Kumar, Arun and Markandaya, M and Girimaji, SC (2002) Primary microcephaly: microcephalin and ASPM determine the size of the human brain. In: Journal of Biosciences, 27 (7). pp. 629-632.

Kumar, Arun and Girimaji, SC (2001) Tuberous sclerosis complex: A Drosophila connection. In: Journal of Biosciences, 26 (3). pp. 285-287.

Kumar, Arun (2001) Retinitis pigmentosa: mutations in a receptor tyrosine kinase gene, MERTK. In: Journal of Biosciences, 26 (1). pp. 3-5.

Kumar, Arun (2000) Alzheimer’s disease:amyloid beta-peptide antibody vaccine as plaque remover. In: Journal of Biosciences, 25 (4). pp. 315-316.

Kumar, Arun (2000) Rett and ICF syndromes: methylation moves into medicine. In: Journal of Biosciences, 25 (3). pp. 213-214.

Kumar, Arun and Minocha, Vijay K and Sasikumar, K and Mujumdar, PP (1999) Fuzzy optimization model for water quality management of a river system - Closure. In: Journal of Water Resources Planning And Management, 125 (3). pp. 179-180.

Kumar, Arun (1999) Genomic imprinting: mom and dad (epi) genetics. In: Journal of Biosciences, 24 (1). pp. 4-6.

This list was generated on Sun Sep 21 16:03:33 2014 IST.