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Items: 14

1.

CMV promoter is inadequate for expression of mutant human RyR2 in transgenic rabbits.

Wakula P, Bisping E, Kockskämper J, Post H, Brauer S, Deuter M, Oehlmann R, Besenfelder U, Lai FA, Brem G, Pieske B.

J Pharmacol Toxicol Methods. 2011 Mar-Apr;63(2):180-5. doi: 10.1016/j.vascn.2010.09.007. Epub 2010 Sep 29.

PMID:
20883803
2.

Alternatively spliced transcripts of the thymus-specific protease PRSS16 are differentially expressed in human thymus.

Luther C, Wienhold W, Oehlmann R, Heinemann MK, Melms A, Tolosa E.

Genes Immun. 2005 Feb;6(1):1-7.

PMID:
15592422
3.

PCR bias in ecological analysis: a case study for quantitative Taq nuclease assays in analyses of microbial communities.

Becker S, Böger P, Oehlmann R, Ernst A.

Appl Environ Microbiol. 2000 Nov;66(11):4945-53.

4.

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

Gasser T, Müller-Myhsok B, Wszolek ZK, Oehlmann R, Calne DB, Bonifati V, Bereznai B, Fabrizio E, Vieregge P, Horstmann RD.

Nat Genet. 1998 Mar;18(3):262-5.

PMID:
9500549
5.
6.

Genetic complexity and Parkinson's disease.

Gasser T, Müller-Myhsok B, Wszolek ZK, Dürr A, Vaughan JR, Bonifati V, Meco G, Bereznai B, Oehlmann R, Agid Y, Brice A, Wood N.

Science. 1997 Jul 18;277(5324):388-9; author reply 389. No abstract available.

PMID:
9518367
7.

Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan.

Veske A, Oehlmann R, Younus F, Mohyuddin A, Müller-Myhsok B, Mehdi SQ, Gal A.

Hum Mol Genet. 1996 Jan;5(1):165-8.

PMID:
8789456
8.

Oguchi disease: suggestion of linkage to markers on chromosome 2q.

Maw MA, John S, Jablonka S, Müller B, Kumaramanickavel G, Oehlmann R, Denton MJ, Gal A.

J Med Genet. 1995 May;32(5):396-8.

9.

Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan.

Leutelt J, Oehlmann R, Younus F, van den Born LI, Weber JL, Denton MJ, Mehdi SQ, Gal A.

Clin Genet. 1995 Mar;47(3):122-4.

PMID:
7634534
10.

Missense rhodopsin mutation in a family with recessive RP.

Kumaramanickavel G, Maw M, Denton MJ, John S, Srikumari CR, Orth U, Oehlmann R, Gal A.

Nat Genet. 1994 Sep;8(1):10-1. No abstract available.

PMID:
7987385
11.

Genetic linkage mapping of multiple epiphyseal dysplasia to the pericentromeric region of chromosome 19.

Oehlmann R, Summerville GP, Yeh G, Weaver EJ, Jimenez SA, Knowlton RG.

Am J Hum Genet. 1994 Jan;54(1):3-10.

12.

Localization of the Krabbe disease gene (GALC) on chromosome 14 by multipoint linkage analysis.

Oehlmann R, Zlotogora J, Wenger DA, Knowlton RG.

Am J Hum Genet. 1993 Dec;53(6):1250-5.

13.

Exclusion of type II and type VI procollagen gene mutations in a five-generation family with multiple epiphyseal dysplasia.

Weaver EJ, Summerville GP, Yeh G, Hervada-Page M, Oehlmann R, Rothman R, Jimenez SA, Knowlton RG.

Am J Med Genet. 1993 Feb 1;45(3):345-52.

PMID:
8094597
14.

Amplified DNA in cells of genetic melanoma of Xiphophorus.

Schwab M, Oehlmann R, Brüderlein S, Wakamatsu Y.

Oncogene. 1989 Feb;4(2):139-44.

PMID:
2927944

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