Daiger SP - Search Results

1

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

Blanton SH, Heckenlively JR, Cottingham AW, Friedman J, Sadler LA, Wagner M, Friedman LH, Daiger SP. Blanton SH, et al. Among authors: daiger sp. Genomics. 1991 Dec;11(4):857-69. doi: 10.1016/0888-7543(91)90008-3. Genomics. 1991. PMID: 1783394

2

Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa.

Bowne SJ, Sullivan LS, Blanton SH, Cepko CL, Blackshaw S, Birch DG, Hughbanks-Wheaton D, Heckenlively JR, Daiger SP. Bowne SJ, et al. Among authors: daiger sp. Hum Mol Genet. 2002 Mar 1;11(5):559-68. doi: 10.1093/hmg/11.5.559. Hum Mol Genet. 2002. PMID: 11875050 Free PMC article.

3

Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families.

Sullivan LS, Bowne SJ, Birch DG, Hughbanks-Wheaton D, Heckenlively JR, Lewis RA, Garcia CA, Ruiz RS, Blanton SH, Northrup H, Gire AI, Seaman R, Duzkale H, Spellicy CJ, Zhu J, Shankar SP, Daiger SP. Sullivan LS, et al. Among authors: daiger sp. Invest Ophthalmol Vis Sci. 2006 Jul;47(7):3052-64. doi: 10.1167/iovs.05-1443. Invest Ophthalmol Vis Sci. 2006. PMID: 16799052 Free PMC article.

4

Genomic rearrangements of the PRPF31 gene account for 2.5% of autosomal dominant retinitis pigmentosa.

Sullivan LS, Bowne SJ, Seaman CR, Blanton SH, Lewis RA, Heckenlively JR, Birch DG, Hughbanks-Wheaton D, Daiger SP. Sullivan LS, et al. Among authors: daiger sp. Invest Ophthalmol Vis Sci. 2006 Oct;47(10):4579-88. doi: 10.1167/iovs.06-0440. Invest Ophthalmol Vis Sci. 2006. PMID: 17003455 Free PMC article.

5

A tight linkage cluster, with two new RFLPs (D8S96 and D8S108), in the interval 8cen-q13.

Cottingham AW, Sadler LA, Blanton SH, Wagner MJ, Wells DE, Heckenlively JR, Daiger SP. Cottingham AW, et al. Among authors: daiger sp. Nucleic Acids Res. 1992 Mar 25;20(6):1426. doi: 10.1093/nar/20.6.1426. Nucleic Acids Res. 1992. PMID: 1348578 Free PMC article.

6

Human chromosome 8 linkage map based on short tandem repeat polymorphisms: effect of genotyping errors.

Tomfohrde J, Wood S, Schertzer M, Wagner MJ, Wells DE, Parrish J, Sadler LA, Blanton SH, Daiger SP, Wang Z, et al. Tomfohrde J, et al. Among authors: daiger sp. Genomics. 1992 Sep;14(1):144-52. doi: 10.1016/s0888-7543(05)80297-6. Genomics. 1992. PMID: 1427821

7

Linkage between Rh blood group and autosomal dominant retinitis pigmentosa in ten Chinese families.

Fei YJ, Blanton SH, Daiger SP, Luo CR. Fei YJ, et al. Among authors: daiger sp. Chin Med J (Engl). 1992 Jun;105(6):486-9. Chin Med J (Engl). 1992. PMID: 1451549

8

Dinucleotide repeat polymorphism at the human tissue plasminogen activator gene (PLAT).

Sadler LA, Blanton SH, Daiger SP. Sadler LA, et al. Among authors: daiger sp. Nucleic Acids Res. 1991 Nov 11;19(21):6058. doi: 10.1093/nar/19.21.6058-a. Nucleic Acids Res. 1991. PMID: 1945894 Free PMC article.

9

Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q.

Blanton SH, Cottingham AW, Giesenschlag N, Heckenlively JR, Humphries P, Daiger SP. Blanton SH, et al. Among authors: daiger sp. Genomics. 1990 Sep;8(1):179-81. doi: 10.1016/0888-7543(90)90243-n. Genomics. 1990. PMID: 2081594

10

DNA linkage studies of degenerative retinal diseases.

Daiger SP, Heckenlively JR, Lewis RA, Pelias MZ. Daiger SP, et al. Prog Clin Biol Res. 1987;247:147-62. Prog Clin Biol Res. 1987. PMID: 3317443 Review.

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