Narayanan V - Search Results

1

Cognitive dysfunction in NF1 knock-out mice may result from altered vesicular trafficking of APP/DRD3 complex.

Donarum EA, Halperin RF, Stephan DA, Narayanan V. Donarum EA, et al. Among authors: narayanan v. BMC Neurosci. 2006 Mar 8;7:22. doi: 10.1186/1471-2202-7-22. BMC Neurosci. 2006. PMID: 16524466 Free PMC article.

2

Identification of somatic chromosomal abnormalities in hypothalamic hamartoma tissue at the GLI3 locus.

Craig DW, Itty A, Panganiban C, Szelinger S, Kruer MC, Sekar A, Reiman D, Narayanan V, Stephan DA, Kerrigan JF. Craig DW, et al. Among authors: narayanan v. Am J Hum Genet. 2008 Feb;82(2):366-74. doi: 10.1016/j.ajhg.2007.10.006. Epub 2008 Jan 31. Am J Hum Genet. 2008. PMID: 18252217 Free PMC article.

3

Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation.

Jentarra GM, Olfers SL, Rice SG, Srivastava N, Homanics GE, Blue M, Naidu S, Narayanan V. Jentarra GM, et al. Among authors: narayanan v. BMC Neurosci. 2010 Feb 17;11:19. doi: 10.1186/1471-2202-11-19. BMC Neurosci. 2010. PMID: 20163734 Free PMC article.

4

Skewed allele-specific expression of the NF1 gene in normal subjects: a possible mechanism for phenotypic variability in neurofibromatosis type 1.

Jentarra GM, Rice SG, Olfers S, Rajan C, Saffen DM, Narayanan V. Jentarra GM, et al. Among authors: narayanan v. J Child Neurol. 2012 Jun;27(6):695-702. doi: 10.1177/0883073811423439. Epub 2011 Nov 8. J Child Neurol. 2012. PMID: 22068829

5

Improved methods for RNAseq-based alternative splicing analysis.

Halperin RF, Hegde A, Lang JD, Raupach EA; C4RCD Research Group; Legendre C, Liang WS, LoRusso PM, Sekulic A, Sosman JA, Trent JM, Rangasamy S, Pirrotte P, Schork NJ. Halperin RF, et al. Sci Rep. 2021 May 24;11(1):10740. doi: 10.1038/s41598-021-89938-2. Sci Rep. 2021. PMID: 34031440 Free PMC article.

6

Mapping of the human P84 gene to the subtelomeric region of chromosome 20p.

Eckert C, Olinsky S, Cummins J, Stephan D, Narayanan V. Eckert C, et al. Among authors: narayanan v. Somat Cell Mol Genet. 1997 Jul;23(4):297-301. doi: 10.1007/BF02674421. Somat Cell Mol Genet. 1997. PMID: 9542532

7

Evidence for population variation in TSC1 and TSC2 gene expression.

Jentarra GM, Rice SG, Olfers S, Saffen D, Narayanan V. Jentarra GM, et al. Among authors: narayanan v. BMC Med Genet. 2011 Feb 23;12:29. doi: 10.1186/1471-2350-12-29. BMC Med Genet. 2011. PMID: 21345208 Free PMC article.

8

Tuberous sclerosis complex: genetics to pathogenesis.

Narayanan V. Narayanan V. Pediatr Neurol. 2003 Nov;29(5):404-9. doi: 10.1016/j.pediatrneurol.2003.09.002. Pediatr Neurol. 2003. PMID: 14684235 Review.

9

Epigenetics, autism spectrum, and neurodevelopmental disorders.

Rangasamy S, D'Mello SR, Narayanan V. Rangasamy S, et al. Among authors: narayanan v. Neurotherapeutics. 2013 Oct;10(4):742-56. doi: 10.1007/s13311-013-0227-0. Neurotherapeutics. 2013. PMID: 24104594 Free PMC article. Review.

10

Genetic aspects of neurocutaneous disorders.

Jentarra G, Snyder SL, Narayanan V. Jentarra G, et al. Among authors: narayanan v. Semin Pediatr Neurol. 2006 Mar;13(1):43-7. doi: 10.1016/j.spen.2006.01.010. Semin Pediatr Neurol. 2006. PMID: 16818175 Review.

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