Humphries MM - Search Results

1

Protection of photoreceptors in a mouse model of RP10.

Tam LC, Kiang AS, Chadderton N, Kenna PF, Campbell M, Humphries MM, Farrar GJ, Humphries P. Tam LC, et al. Among authors: humphries p, humphries mm. Adv Exp Med Biol. 2010;664:559-65. doi: 10.1007/978-1-4419-1399-9_64. Adv Exp Med Biol. 2010. PMID: 20238059

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: humphries p. 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

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. Among authors: humphries p, humphries mm. 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.

4

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. Among authors: humphries p, humphries mm. Genomics. 1992 Nov;14(3):805-7. doi: 10.1016/s0888-7543(05)80193-4. Genomics. 1992. PMID: 1427912

5

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: humphries p, humphries mm. Am J Hum Genet. 1992 Mar;50(3):634-9. Am J Hum Genet. 1992. PMID: 1539599 Free PMC article.

6

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. Among authors: humphries p, humphries mm. Nature. 1991 Dec 12;354(6353):478-80. doi: 10.1038/354478a0. Nature. 1991. PMID: 1749427

7

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. Among authors: humphries p, humphries mm. Genomics. 1991 Dec;11(4):1170-1. Genomics. 1991. PMID: 1783387 No abstract available.

8

Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6.

Farrar GJ, Jordan SA, Kenna P, Humphries MM, Kumar-Singh R, McWilliam P, Allamand V, Sharp E, Humphries P. Farrar GJ, et al. Among authors: humphries p, humphries mm. Genomics. 1991 Dec;11(4):870-4. doi: 10.1016/0888-7543(91)90009-4. Genomics. 1991. PMID: 1783395

9

Human nidogen gene: identification of multiple RFLP and exclusion as candidate gene in a family with epidermolysis bullosa (EBS2) with evidence for linkage to chromosome 1.

Humphries M, Nagayoshi T, Sheils D, Humphries P, Uitto J. Humphries M, et al. J Invest Dermatol. 1990 Nov;95(5):568-70. doi: 10.1111/1523-1747.ep12505546. J Invest Dermatol. 1990. PMID: 1977802 Free article.

10

Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneity.

Farrar GJ, McWilliam P, Bradley DG, Kenna P, Lawler M, Sharp EM, Humphries MM, Eiberg H, Conneally PM, Trofatter JA, et al. Farrar GJ, et al. Among authors: humphries mm. Genomics. 1990 Sep;8(1):35-40. doi: 10.1016/0888-7543(90)90223-h. Genomics. 1990. PMID: 2081598

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