Dryja TP - Search Results

1

Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1).

Berson EL, Grimsby JL, Adams SM, McGee TL, Sweklo E, Pierce EA, Sandberg MA, Dryja TP. Berson EL, et al. Among authors: dryja tp. Invest Ophthalmol Vis Sci. 2001 Sep;42(10):2217-24. Invest Ophthalmol Vis Sci. 2001. PMID: 11527933

2

Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosis.

Rivolta C, Ayyagari R, Sieving PA, Berson EL, Dryja TP. Rivolta C, et al. Among authors: dryja tp. Mol Vis. 2003 Feb 18;9:49-51. Mol Vis. 2003. PMID: 12592226 Free article.

3

Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa.

McLaughlin ME, Sandberg MA, Berson EL, Dryja TP. McLaughlin ME, et al. Among authors: dryja tp. Nat Genet. 1993 Jun;4(2):130-4. doi: 10.1038/ng0693-130. Nat Genet. 1993. PMID: 8394174

4

A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens.

Kajiwara K, Sandberg MA, Berson EL, Dryja TP. Kajiwara K, et al. Among authors: dryja tp. Nat Genet. 1993 Mar;3(3):208-12. doi: 10.1038/ng0393-208. Nat Genet. 1993. PMID: 8485575

5

Evaluation of the human gene encoding recoverin in patients with retinitis pigmentosa or an allied disease.

Parminder AH, Murakami A, Inana G, Berson EL, Dryja TP. Parminder AH, et al. Among authors: dryja tp. Invest Ophthalmol Vis Sci. 1997 Mar;38(3):704-9. Invest Ophthalmol Vis Sci. 1997. PMID: 9071225

6

Evaluation of the rhodopsin kinase gene in patients with retinitis pigmentosa.

Yamamoto S, Khani SC, Berson EL, Dryja TP. Yamamoto S, et al. Among authors: dryja tp. Exp Eye Res. 1997 Aug;65(2):249-53. doi: 10.1006/exer.1997.9998. Exp Eye Res. 1997. PMID: 9268593

7

Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa.

Dryja TP, Hahn LB, Kajiwara K, Berson EL. Dryja TP, et al. Invest Ophthalmol Vis Sci. 1997 Sep;38(10):1972-82. Invest Ophthalmol Vis Sci. 1997. PMID: 9331261

8

Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele.

McGee TL, Devoto M, Ott J, Berson EL, Dryja TP. McGee TL, et al. Among authors: dryja tp. Am J Hum Genet. 1997 Nov;61(5):1059-66. doi: 10.1086/301614. Am J Hum Genet. 1997. PMID: 9345108 Free PMC article.

9

Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa.

Hagstrom SA, North MA, Nishina PL, Berson EL, Dryja TP. Hagstrom SA, et al. Among authors: dryja tp. Nat Genet. 1998 Feb;18(2):174-6. doi: 10.1038/ng0298-174. Nat Genet. 1998. PMID: 9462750

10

Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.

Morimura H, Fishman GA, Grover SA, Fulton AB, Berson EL, Dryja TP. Morimura H, et al. Among authors: dryja tp. Proc Natl Acad Sci U S A. 1998 Mar 17;95(6):3088-93. doi: 10.1073/pnas.95.6.3088. Proc Natl Acad Sci U S A. 1998. PMID: 9501220 Free PMC article.

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