Farrar GJ - Search Results

1

siRNA targeting Schlemm's canal endothelial tight junctions enhances outflow facility and reduces IOP in a steroid-induced OHT rodent model.

Cassidy PS, Kelly RA, Reina-Torres E, Sherwood JM, Humphries MM, Kiang AS, Farrar GJ, O'Brien C, Campbell M, Stamer WD, Overby DR, Humphries P, O'Callaghan J. Cassidy PS, et al. Among authors: farrar gj. Mol Ther Methods Clin Dev. 2020 Oct 31;20:86-94. doi: 10.1016/j.omtm.2020.10.022. eCollection 2021 Mar 12. Mol Ther Methods Clin Dev. 2020. PMID: 33376757 Free PMC article.

2

Alu polymorphism in the human type I Keratin (KRT14) gene.

Humphries MM, Sheils DM, Jordan SA, Farrar GJ, Kumar-Singh R, Humphries P. Humphries MM, et al. Among authors: farrar gj. Hum Mol Genet. 1992 Sep;1(6):453. doi: 10.1093/hmg/1.6.453. Hum Mol Genet. 1992. PMID: 1284533 No abstract available.

3

Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutions.

Jordan SA, Farrar GJ, Kenna P, Humphries P. Jordan SA, et al. Among authors: farrar gj. Hum Mutat. 1992;1(3):240-7. doi: 10.1002/humu.1380010311. Hum Mutat. 1992. PMID: 1301931

4

Autosomal dominant retinitis pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked family.

Farrar GJ, Findlay JB, Kumar-Singh R, Kenna P, Humphries MM, Sharpe E, Humphries P. Farrar GJ, et al. Hum Mol Genet. 1992 Dec;1(9):769-71. doi: 10.1093/hmg/1.9.769. Hum Mol Genet. 1992. PMID: 1302614 No abstract available.

5

Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree.

Farrar GJ, Kenna P, Jordan SA, Kumar-Singh R, Humphries MM, Sharp EM, Sheils D, Humphries P. Farrar GJ, et al. Genomics. 1992 Nov;14(3):805-7. doi: 10.1016/s0888-7543(05)80193-4. Genomics. 1992. PMID: 1427912

6

Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin.

Jordan SA, Farrar GJ, Kumar-Singh R, Kenna P, Humphries MM, Allamand V, Sharp EM, Humphries P. Jordan SA, et al. Among authors: farrar gj. Am J Hum Genet. 1992 Mar;50(3):634-9. Am J Hum Genet. 1992. PMID: 1539599 Free PMC article.

7

On the molecular genetics of retinitis pigmentosa.

Humphries P, Kenna P, Farrar GJ. Humphries P, et al. Among authors: farrar gj. Science. 1992 May 8;256(5058):804-8. doi: 10.1126/science.1589761. Science. 1992. PMID: 1589761 Review.

8

A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa.

Farrar GJ, Kenna P, Jordan SA, Kumar-Singh R, Humphries MM, Sharp EM, Sheils DM, Humphries P. Farrar GJ, et al. Nature. 1991 Dec 12;354(6353):478-80. doi: 10.1038/354478a0. Nature. 1991. PMID: 1749427

9

A sequence polymorphism in the human peripherin/RDS gene.

Farrar GJ, Kenna P, Jordan SA, Kumar-Singh R, Humphries P. Farrar GJ, et al. Nucleic Acids Res. 1991 Dec 25;19(24):6982. doi: 10.1093/nar/19.24.6982-a. Nucleic Acids Res. 1991. PMID: 1762948 Free PMC article.

10

Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic origin.

Farrar GJ, Kenna P, Redmond R, Shiels D, McWilliam P, Humphries MM, Sharp EM, Jordan S, Kumar-Singh R, Humphries P. Farrar GJ, et al. Genomics. 1991 Dec;11(4):1170-1. Genomics. 1991. PMID: 1783387 No abstract available.

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