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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.
Polisetti, Naresh and Agarwal, Prasoon and Khan, Imran and Kondaiah, Paturu and Sangwan, Virender S and Vemuganti, Geeta K (2010) Gene expression profile of epithelial cells and mesenchymal cells derived from limbal explant culture. In: Molecular Vision, 16 (136). pp. 1227-1240.
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 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.
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.
Venkatesh, CP and Pillai, VS and Raghunath, A and Prakash, VS and Vathsala, R and Kumar, A and Pericak-Vance, Margaret A (2002) Clinical phenotype and linkage analysis of the congenital fibrosis of the extraocular muscles in an Indian family. In: Molecular Vision, 8 . pp. 294-297.
