Koehler M - Search Results

1

Association of the Ghrelin receptor gene region with left ventricular hypertrophy in the general population: results of the MONICA/KORA Augsburg Echocardiographic Substudy.

Baessler A, Kwitek AE, Fischer M, Koehler M, Reinhard W, Erdmann J, Riegger G, Doering A, Schunkert H, Hengstenberg C. Baessler A, et al. Among authors: koehler m. Hypertension. 2006 May;47(5):920-7. doi: 10.1161/01.HYP.0000215180.32274.c8. Epub 2006 Mar 27. Hypertension. 2006. PMID: 16567594

2

Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease.

Baessler A, Fischer M, Mayer B, Koehler M, Wiedmann S, Stark K, Doering A, Erdmann J, Riegger G, Schunkert H, Kwitek AE, Hengstenberg C. Baessler A, et al. Among authors: koehler m. Hum Mol Genet. 2007 Apr 15;16(8):887-99. doi: 10.1093/hmg/ddm033. Epub 2007 Feb 26. Hum Mol Genet. 2007. PMID: 17324965

3

Genetic variants within the LPIN1 gene, encoding lipin, are influencing phenotypes of the metabolic syndrome in humans.

Wiedmann S, Fischer M, Koehler M, Neureuther K, Riegger G, Doering A, Schunkert H, Hengstenberg C, Baessler A. Wiedmann S, et al. Among authors: koehler m. Diabetes. 2008 Jan;57(1):209-17. doi: 10.2337/db07-0083. Epub 2007 Oct 16. Diabetes. 2008. PMID: 17940119

4

Mapping and genomic characterization of the gene encoding diacylglycerol kinase gamma (DAGK3): assessment of its role in dominant optic atrophy (OPA1).

Stöhr H, Klein J, Gehrig A, Koehler MR, Jurklies B, Kellner U, Leo-Kottler B, Schmid M, Weber BH. Stöhr H, et al. Among authors: koehler mr. Hum Genet. 1999 Jan;104(1):99-105. doi: 10.1007/s004390050917. Hum Genet. 1999. PMID: 10071200

5

Yeast artificial chromosome mapping of the cystinosis locus on chromosome 17p by fluorescence in situ hybridization.

Stec I, Peters U, Harms E, Koehler MR, Schmid M, Deufel T. Stec I, et al. Among authors: koehler mr. Hum Genet. 1996 Sep;98(3):321-2. doi: 10.1007/s004390050215. Hum Genet. 1996. PMID: 8707302

6

Assignment of the membrane-associated modulator of the Na(+)-sugar cotransport systems gene RSC1A1 to human chromosome 1p36.1 by in situ hybridization.

Koehler MR, Lambotte S, Koepsell H, Schmid M. Koehler MR, et al. Cytogenet Cell Genet. 1996;73(4):341-2. doi: 10.1159/000134371. Cytogenet Cell Genet. 1996. PMID: 8751391 No abstract available.

7

Assignment of the germ cell cyritestin gene 2 (CYRN2) to human chromosome 16q12.1 by fluorescence in situ hybridization to 5-azacytidine induced, partially decondensed chromosomes.

Koehler MR, von Beust G, Engel W, Schmid M. Koehler MR, et al. Cytogenet Cell Genet. 1997;77(3-4):178-9. doi: 10.1159/000134569. Cytogenet Cell Genet. 1997. PMID: 9284909 No abstract available.

8

Conserved synteny between the chicken Z sex chromosome and human chromosome 9 includes the male regulatory gene DMRT1: a comparative (re)view on avian sex determination.

Nanda I, Zend-Ajusch E, Shan Z, Grützner F, Schartl M, Burt DW, Koehler M, Fowler VM, Goodwin G, Schneider WJ, Mizuno S, Dechant G, Haaf T, Schmid M. Nanda I, et al. Among authors: koehler m. Cytogenet Cell Genet. 2000;89(1-2):67-78. doi: 10.1159/000015567. Cytogenet Cell Genet. 2000. PMID: 10894941

9

Assignment of the human melanoma inhibitory activity gene (MIA) to 19q13.32-q13.33 by fluorescence in situ hybridization (FISH).

Koehler MR, Bosserhoff A, von Beust G, Bauer A, Blesch A, Buettner R, Schlegel J, Bogdahn U, Schmid M. Koehler MR, et al. Genomics. 1996 Jul 1;35(1):265-7. doi: 10.1006/geno.1996.0352. Genomics. 1996. PMID: 8661134 No abstract available.

10

Roct1, a rat polyspecific transporter gene for the excretion of cationic drugs, maps to chromosome 1q11-12.

Koehler MR, Gorboulev V, Koepsell H, Steinlein C, Schmid M. Koehler MR, et al. Mamm Genome. 1996 Mar;7(3):247-8. doi: 10.1007/s003359900074. Mamm Genome. 1996. PMID: 8833261 No abstract available.

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