Stöhr H - Search Results

1

Abnormal vessel formation in the choroid of mice lacking tissue inhibitor of metalloprotease-3.

Janssen A, Hoellenriegel J, Fogarasi M, Schrewe H, Seeliger M, Tamm E, Ohlmann A, May CA, Weber BH, Stöhr H. Janssen A, et al. Among authors: stohr h. Invest Ophthalmol Vis Sci. 2008 Jul;49(7):2812-22. doi: 10.1167/iovs.07-1444. Epub 2008 Apr 11. Invest Ophthalmol Vis Sci. 2008. PMID: 18408187

2

A recombination event excludes the ROM1 locus from the Best's vitelliform macular dystrophy region.

Stöhr H, Weber BH. Stöhr H, et al. Hum Genet. 1995 Feb;95(2):219-22. doi: 10.1007/BF00209406. Hum Genet. 1995. PMID: 7860071

3

(ATTT)n-tetranucleotide repeat polymorphism in the 5'-flanking region of the UGB gene.

Stöhr H, Weber BH. Stöhr H, et al. Hum Mol Genet. 1994 Nov;3(11):2086. Hum Mol Genet. 1994. PMID: 7874146 No abstract available.

4

Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy.

Weber BH, Vogt G, Pruett RC, Stöhr H, Felbor U. Weber BH, et al. Among authors: stohr h. Nat Genet. 1994 Dec;8(4):352-6. doi: 10.1038/ng1294-352. Nat Genet. 1994. PMID: 7894485

5

A case of nonpenetrance in Best's disease.

Weber BH, Stöhr H, Walker D. Weber BH, et al. Among authors: stohr h. Am J Ophthalmol. 1994 Sep 15;118(3):398-9. doi: 10.1016/s0002-9394(14)72970-8. Am J Ophthalmol. 1994. PMID: 8085602 No abstract available.

6

A novel Ser156Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy with unusual clinical features.

Felbor U, Stöhr H, Amann T, Schönherr U, Weber BH. Felbor U, et al. Among authors: stohr h. Hum Mol Genet. 1995 Dec;4(12):2415-6. doi: 10.1093/hmg/4.12.2415. Hum Mol Genet. 1995. PMID: 8634721 No abstract available.

7

A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy.

Felbor U, Stöhr H, Amann T, Schönherr U, Apfelstedt-Sylla E, Weber BH. Felbor U, et al. Among authors: stohr h. J Med Genet. 1996 Mar;33(3):233-6. doi: 10.1136/jmg.33.3.233. J Med Genet. 1996. PMID: 8728699 Free PMC article.

8

Genomic organization of the human tissue inhibitor of metalloproteinases-3 (TIMP3).

Stöhr H, Roomp K, Felbor U, Weber BH. Stöhr H, et al. Genome Res. 1995 Dec;5(5):483-7. doi: 10.1101/gr.5.5.483. Genome Res. 1995. PMID: 8808469 Free article.

9

A gene map of the Best's vitelliform macular dystrophy region in chromosome 11q12-q13.1.

Stöhr H, Marquardt A, Rivera A, Cooper PR, Nowak NJ, Shows TB, Gerhard DS, Weber BH. Stöhr H, et al. Genome Res. 1998 Jan;8(1):48-56. doi: 10.1101/gr.8.1.48. Genome Res. 1998. PMID: 9445487 Free PMC article.

10

cDNA cloning and genomic structure of a novel gene (C11orf9) localized to chromosome 11q12-->q13.1 which encodes a highly conserved, potential membrane-associated protein.

Stöhr H, Marquardt A, White K, Weber BH. Stöhr H, et al. Cytogenet Cell Genet. 2000;88(3-4):211-6. doi: 10.1159/000015552. Cytogenet Cell Genet. 2000. PMID: 10828591

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

136 results

Search Page

Filters