Marquardt A - Search Results

1

VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies.

White K, Marquardt A, Weber BH. White K, et al. Among authors: marquardt a. Hum Mutat. 2000;15(4):301-8. doi: 10.1002/(SICI)1098-1004(200004)15:4<301::AID-HUMU1>3.0.CO;2-N. Hum Mutat. 2000. PMID: 10737974 Review.

2

Three novel human VMD2-like genes are members of the evolutionary highly conserved RFP-TM family.

Stöhr H, Marquardt A, Nanda I, Schmid M, Weber BH. Stöhr H, et al. Among authors: marquardt a. Eur J Hum Genet. 2002 Apr;10(4):281-4. doi: 10.1038/sj.ejhg.5200796. Eur J Hum Genet. 2002. PMID: 12032738

3

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: marquardt a. Nat Genet. 1997 Oct;17(2):164-70. doi: 10.1038/ng1097-164. Nat Genet. 1997. PMID: 9326935

4

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. Among authors: marquardt a. Genome Res. 1998 Jan;8(1):48-56. doi: 10.1101/gr.8.1.48. Genome Res. 1998. PMID: 9445487 Free PMC article.

5

Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease).

Marquardt A, Stöhr H, Passmore LA, Krämer F, Rivera A, Weber BH. Marquardt A, et al. Hum Mol Genet. 1998 Sep;7(9):1517-25. doi: 10.1093/hmg/7.9.1517. Hum Mol Genet. 1998. PMID: 9700209

6

Refined mapping of the gene encoding the p127 kDa UV-damaged DNA-binding protein (DDB1) within 11q12-q13.1 and its exclusion in Best's vitelliform macular dystrophy.

Stöhr H, Marquardt A, Rivera A, Kellner U, Weber BH. Stöhr H, et al. Among authors: marquardt a. Eur J Hum Genet. 1998 Jul-Aug;6(4):400-5. doi: 10.1038/sj.ejhg.5200196. Eur J Hum Genet. 1998. PMID: 9781049

7

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. Among authors: marquardt a. Cytogenet Cell Genet. 2000;88(3-4):211-6. doi: 10.1159/000015552. Cytogenet Cell Genet. 2000. PMID: 10828591

8

A sequence-ready high-resolution physical map of the best macular dystrophy gene region in 11q12-q13.

Cooper PR, Nowak NJ, Higgins MJ, Simpson SA, Marquardt A, Stoehr H, Weber BH, Gerhard DS, de Jong PJ, Shows TB. Cooper PR, et al. Among authors: marquardt a. Genomics. 1997 Apr 15;41(2):185-92. doi: 10.1006/geno.1997.4660. Genomics. 1997. PMID: 9143493

9

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: marquardt a. Cytogenet Cell Genet. 1998;81(1):12-7. doi: 10.1159/000015001. Cytogenet Cell Genet. 1998. PMID: 9691169

10

Transcript map of a 900-kb genomic region in Xp22.1-p22.2: identification of 12 novel genes.

Warneke-Wittstock R, Marquardt A, Gehrig A, Sauer CG, Gessler M, Weber BH. Warneke-Wittstock R, et al. Among authors: marquardt a. Genomics. 1998 Jul 1;51(1):59-67. doi: 10.1006/geno.1998.5382. Genomics. 1998. PMID: 9693033

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