Gehrig A - Search Results

1

Inactivation of the murine X-linked juvenile retinoschisis gene, Rs1h, suggests a role of retinoschisin in retinal cell layer organization and synaptic structure.

Weber BH, Schrewe H, Molday LL, Gehrig A, White KL, Seeliger MW, Jaissle GB, Friedburg C, Tamm E, Molday RS. Weber BH, et al. Among authors: gehrig a. Proc Natl Acad Sci U S A. 2002 Apr 30;99(9):6222-7. doi: 10.1073/pnas.092528599. Proc Natl Acad Sci U S A. 2002. PMID: 11983912 Free PMC article.

2

Isolation and characterization of the murine X-linked juvenile retinoschisis (Rs1h) gene.

Gehrig AE, Warneke-Wittstock R, Sauer CG, Weber BH. Gehrig AE, et al. Mamm Genome. 1999 Mar;10(3):303-7. doi: 10.1007/s003359900991. Mamm Genome. 1999. PMID: 10051329

3

Genome-wide expression profiling of the retinoschisin-deficient retina in early postnatal mouse development.

Gehrig A, Langmann T, Horling F, Janssen A, Bonin M, Walter M, Poths S, Weber BH. Gehrig A, et al. Invest Ophthalmol Vis Sci. 2007 Feb;48(2):891-900. doi: 10.1167/iovs.06-0641. Invest Ophthalmol Vis Sci. 2007. PMID: 17251492 Free article.

4

Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisis.

Gehrig A, White K, Lorenz B, Andrassi M, Clemens S, Weber BH. Gehrig A, et al. Clin Genet. 1999 Jun;55(6):461-5. doi: 10.1034/j.1399-0004.1999.550611.x. Clin Genet. 1999. PMID: 10450864

5

The role of caspases in photoreceptor cell death of the retinoschisin-deficient mouse.

Gehrig A, Janssen A, Horling F, Grimm C, Weber BH. Gehrig A, et al. Cytogenet Genome Res. 2006;115(1):35-44. doi: 10.1159/000094799. Cytogenet Genome Res. 2006. PMID: 16974082

6

Positional cloning of the gene associated with X-linked juvenile retinoschisis.

Sauer CG, Gehrig A, Warneke-Wittstock R, Marquardt A, Ewing CC, Gibson A, Lorenz B, Jurklies B, Weber BH. Sauer CG, et al. Among authors: gehrig a. Nat Genet. 1997 Oct;17(2):164-70. doi: 10.1038/ng1097-164. Nat Genet. 1997. PMID: 9326935

7

Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies.

Felbor U, Gehrig A, Sauer CG, Marquardt A, Köhler M, Schmid M, Weber BH. Felbor U, et al. Among authors: gehrig a. Cytogenet Cell Genet. 1998;81(1):12-7. doi: 10.1159/000015001. Cytogenet Cell Genet. 1998. PMID: 9691169

8

Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration.

Krämer F, White K, Pauleikhoff D, Gehrig A, Passmore L, Rivera A, Rudolph G, Kellner U, Andrassi M, Lorenz B, Rohrschneider K, Blankenagel A, Jurklies B, Schilling H, Schütt F, Holz FG, Weber BH. Krämer F, et al. Among authors: gehrig a. Eur J Hum Genet. 2000 Apr;8(4):286-92. doi: 10.1038/sj.ejhg.5200447. Eur J Hum Genet. 2000. PMID: 10854112

9

Identifying differentially expressed genes in the mammalian retina and the retinal pigment epithelium by suppression subtractive hybridization.

Schulz HL, Rahman FA, Fadl El Moula FM, Stojic J, Gehrig A, Weber BH. Schulz HL, et al. Among authors: gehrig a. Cytogenet Genome Res. 2004;106(1):74-81. doi: 10.1159/000078564. Cytogenet Genome Res. 2004. PMID: 15218245

10

Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1).

Gehrig A, Felbor U, Kelsell RE, Hunt DM, Maumenee IH, Weber BH. Gehrig A, et al. J Med Genet. 1998 Aug;35(8):641-5. doi: 10.1136/jmg.35.8.641. J Med Genet. 1998. PMID: 9719369 Free PMC article.

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