Saxena R - Search Results

1

Variability in CYP2C9 allele frequency: a pilot study of its predicted impact on warfarin response among healthy South and North Indians.

Nahar R, Deb R, Saxena R, Puri RD, Verma IC. Nahar R, et al. Among authors: saxena r. Pharmacol Rep. 2013;65(1):187-94. doi: 10.1016/s1734-1140(13)70977-0. Pharmacol Rep. 2013. PMID: 23563037 Free article.

2

Genetic counseling and prenatal diagnosis in India--experience at Sir Ganga Ram Hospital.

Verma IC, Saxena R, Lall M, Bijarnia S, Sharma R. Verma IC, et al. Among authors: saxena r. Indian J Pediatr. 2003 Apr;70(4):293-7. doi: 10.1007/BF02723582. Indian J Pediatr. 2003. PMID: 12793304

3

Establishment of tyrosinase sequence database in normally pigmented Indians and Japanese for rapid determination of novel mutations.

Miyamura Y, Verma IC, Saxena R, Murase A, Kono M, Suzuki T, Yasue S, Shibata S, Sakakibara A, Tomita Y. Miyamura Y, et al. Among authors: saxena r. J Dermatol Sci. 2005 Sep;39(3):167-73. doi: 10.1016/j.jdermsci.2005.03.004. J Dermatol Sci. 2005. PMID: 15885985

4

Leber's hereditary optic neuropathy with molecular characterization in two Indian families.

Verma IC, Bijarnia S, Saxena R, Kohli S, Puri RD, Thomas E, Chowdhary D, Jha SN, Grover AK. Verma IC, et al. Among authors: saxena r. Indian J Ophthalmol. 2005 Sep;53(3):167-71. doi: 10.4103/0301-4738.16674. Indian J Ophthalmol. 2005. PMID: 16137960 Free article.

5

Prenatal diagnosis of phenylketonuria.

Kohli S, Saxena R, Thomas E, Rao P, Verma IC. Kohli S, et al. Among authors: saxena r. Indian J Med Res. 2005 Nov;122(5):400-3. Indian J Med Res. 2005. PMID: 16456253

6

Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations.

Verma IC, Kleanthous M, Saxena R, Fucharoen S, Winichagoon P, Raizuddin S, Khan SN, Akbari MT, Izadyar M, Kotea N, Old JM, Ioannou PA, Khan B. Verma IC, et al. Among authors: saxena r. Hemoglobin. 2007;31(4):439-52. doi: 10.1080/03630260701641245. Hemoglobin. 2007. PMID: 17994378

7

Conformational change of UGT1A1 by a novel missense mutation (p.L131P) causing Crigler-Najjar syndrome type I.

Maruo Y, Verma IC, Matsui K, Takahashi H, Mimura Y, Ota Y, Mori A, Saxena R, Sato H, Takeuchi Y. Maruo Y, et al. Among authors: saxena r. J Pediatr Gastroenterol Nutr. 2008 Mar;46(3):308-11. doi: 10.1097/MPG.0b013e3181638c8b. J Pediatr Gastroenterol Nutr. 2008. PMID: 18376249 No abstract available.

8

Molecular studies of achondroplasia.

Nahar R, Saxena R, Kohli S, Puri R, Verma IC. Nahar R, et al. Among authors: saxena r. Indian J Orthop. 2009 Apr;43(2):194-6. doi: 10.4103/0019-5413.50856. Indian J Orthop. 2009. PMID: 19838370 Free PMC article.

9

Gene changes in Duchenne muscular dystrophy: comparison of multiplex PCR and multiplex ligation-dependent probe amplification techniques.

Kohli S, Saxena R, Thomas E, Singh J, Verma IC. Kohli S, et al. Among authors: saxena r. Neurol India. 2010 Nov-Dec;58(6):852-6. doi: 10.4103/0028-3886.73744. Neurol India. 2010. PMID: 21150048 Free article.

10

Mutation studies in the CFTR gene in Asian Indian subjects with congenital bilateral absence of vas deferens: report of two novel mutations and four novel variants.

Sachdeva K, Saxena R, Majumdar A, Chadha S, Verma IC. Sachdeva K, et al. Among authors: saxena r. Genet Test Mol Biomarkers. 2011 May;15(5):307-12. doi: 10.1089/gtmb.2010.0156. Epub 2011 Jan 22. Genet Test Mol Biomarkers. 2011. PMID: 21254931

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