Jalali S - Search Results

1

Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration.

Friedman JS, Chang B, Kannabiran C, Chakarova C, Singh HP, Jalali S, Hawes NL, Branham K, Othman M, Filippova E, Thompson DA, Webster AR, Andréasson S, Jacobson SG, Bhattacharya SS, Heckenlively JR, Swaroop A. Friedman JS, et al. Among authors: jalali s. Am J Hum Genet. 2006 Dec;79(6):1059-70. doi: 10.1086/510021. Epub 2006 Oct 23. Am J Hum Genet. 2006. PMID: 17186464 Free PMC article.

2

Screening for homozygosity by descent in families with autosomal recessive retinitis pigmentosa.

Lalitha K, Jalali S, Kadakia T, Kannabiran C. Lalitha K, et al. Among authors: jalali s. J Genet. 2002 Aug;81(2):59-63. doi: 10.1007/BF02715901. J Genet. 2002. PMID: 12532037

3

Homozygous null mutations in the ABCA4 gene in two families with autosomal recessive retinal dystrophy.

Singh HP, Jalali S, Hejtmancik JF, Kannabiran C. Singh HP, et al. Among authors: jalali s. Am J Ophthalmol. 2006 May;141(5):906-13. doi: 10.1016/j.ajo.2005.12.009. Epub 2006 Mar 20. Am J Ophthalmol. 2006. PMID: 16546111

4

Share, learn and get together: knowledge and information interactions at the XLV International Symposium of ISCEV - Hyderabad, India, 25-29 August 2007.

Jalali S, Kondo M, Narayanan R, Kannabiran C, McCulloch DL. Jalali S, et al. Doc Ophthalmol. 2007 Jul;115(1):1-2. doi: 10.1007/s10633-007-9068-7. Doc Ophthalmol. 2007. PMID: 17661099 Free article. No abstract available.

5

Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening.

Singh HP, Jalali S, Narayanan R, Kannabiran C. Singh HP, et al. Among authors: jalali s. Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4065-71. doi: 10.1167/iovs.09-3479. Epub 2009 Apr 1. Invest Ophthalmol Vis Sci. 2009. PMID: 19339744 Free PMC article.

6

Posterior microphthalmos pigmentary retinopathy syndrome.

Pehere N, Jalali S, Deshmukh H, Kannabiran C. Pehere N, et al. Among authors: jalali s. Doc Ophthalmol. 2011 Apr;122(2):127-32. doi: 10.1007/s10633-011-9266-1. Epub 2011 Mar 18. Doc Ophthalmol. 2011. PMID: 21416382

7

Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23.

Kannabiran C, Singh HP, Jalali S. Kannabiran C, et al. Among authors: jalali s. Hum Genet. 2012 May;131(5):717-23. doi: 10.1007/s00439-011-1115-5. Epub 2011 Nov 15. Hum Genet. 2012. PMID: 22083234

8

Mutations in TULP1, NR2E3, and MFRP genes in Indian families with autosomal recessive retinitis pigmentosa.

Kannabiran C, Singh H, Sahini N, Jalali S, Mohan G. Kannabiran C, et al. Among authors: jalali s. Mol Vis. 2012;18:1165-74. Epub 2012 May 4. Mol Vis. 2012. PMID: 22605927 Free PMC article.

9

NMNAT1 mutations cause Leber congenital amaurosis.

Falk MJ, Zhang Q, Nakamaru-Ogiso E, Kannabiran C, Fonseca-Kelly Z, Chakarova C, Audo I, Mackay DS, Zeitz C, Borman AD, Staniszewska M, Shukla R, Palavalli L, Mohand-Said S, Waseem NH, Jalali S, Perin JC, Place E, Ostrovsky J, Xiao R, Bhattacharya SS, Consugar M, Webster AR, Sahel JA, Moore AT, Berson EL, Liu Q, Gai X, Pierce EA. Falk MJ, et al. Among authors: jalali s. Nat Genet. 2012 Sep;44(9):1040-5. doi: 10.1038/ng.2361. Epub 2012 Jul 29. Nat Genet. 2012. PMID: 22842227 Free PMC article.

10

Mutation of SPATA7 in a family with autosomal recessive early-onset retinitis pigmentosa.

Kannabiran C, Palavalli L, Jalali S. Kannabiran C, et al. Among authors: jalali s. J Mol Genet Med. 2012;6:301-3. doi: 10.4172/1747-0862.1000053. Epub 2012 Dec 12. J Mol Genet Med. 2012. PMID: 23300508 Free PMC article. No abstract available.

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