Marquardt A - Search Results

1

Solution structure of hpTX2, a toxin from Heteropoda venatoria spider that blocks Kv4.2 potassium channel.

Bernard C, Legros C, Ferrat G, Bischoff U, Marquardt A, Pongs O, Darbon H. Bernard C, et al. Among authors: marquardt a. Protein Sci. 2000 Nov;9(11):2059-67. Protein Sci. 2000. PMID: 11152117 Free PMC article.

2

Functional expression of a rat homologue of the voltage gated either á go-go potassium channel reveals differences in selectivity and activation kinetics between the Drosophila channel and its mammalian counterpart.

Ludwig J, Terlau H, Wunder F, Brüggemann A, Pardo LA, Marquardt A, Stühmer W, Pongs O. Ludwig J, et al. Among authors: marquardt a. EMBO J. 1994 Oct 3;13(19):4451-8. doi: 10.1002/j.1460-2075.1994.tb06767.x. EMBO J. 1994. PMID: 7925287 Free PMC article.

3

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

4

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

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

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

7

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

8

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

9

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.

10

cDNA cloning, genomic structure, and chromosomal localization of three members of the human fatty acid desaturase family.

Marquardt A, Stöhr H, White K, Weber BH. Marquardt A, et al. Genomics. 2000 Jun 1;66(2):175-83. doi: 10.1006/geno.2000.6196. Genomics. 2000. PMID: 10860662

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