Propping P - Search Results

1

Genetic variation in human 5-HT receptors: potential pathogenetic and pharmacological role.

Göthert M, Propping P, Bönisch H, Brüss M, Nöthen MM. Göthert M, et al. Among authors: propping p. Ann N Y Acad Sci. 1998 Dec 15;861:26-30. doi: 10.1111/j.1749-6632.1998.tb10169.x. Ann N Y Acad Sci. 1998. PMID: 9928235 Review.

2

Genetic variation of CNS receptors--a new perspective for pharmacogenetics.

Propping P, Nöthen MM. Propping P, et al. Pharmacogenetics. 1995 Oct;5(5):318-25. doi: 10.1097/00008571-199510000-00008. Pharmacogenetics. 1995. PMID: 8563773 Review. No abstract available.

3

Modified ligand binding to the naturally occurring Cys-124 variant of the human serotonin 5-HT1B receptor.

Brüss M, Bönisch H, Bühlen M, Nöthen MM, Propping P, Göthert M. Brüss M, et al. Among authors: propping p. Pharmacogenetics. 1999 Feb;9(1):95-102. Pharmacogenetics. 1999. PMID: 10208648

4

Schizophrenia: genetic tools for unraveling the nature of a complex disorder.

Propping P, Nöthen MM. Propping P, et al. Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7607-8. doi: 10.1073/pnas.92.17.7607. Proc Natl Acad Sci U S A. 1995. PMID: 7644462 Free PMC article. Review. No abstract available.

5

Identification of genetic variation in the human serotonin 1D beta receptor gene.

Nöthen MM, Erdmann J, Shimron-Abarbanell D, Propping P. Nöthen MM, et al. Among authors: propping p. Biochem Biophys Res Commun. 1994 Dec 15;205(2):1194-200. doi: 10.1006/bbrc.1994.2792. Biochem Biophys Res Commun. 1994. PMID: 7802650

6

Metabotropic glutamate receptor 3 (GRM3) gene variation is not associated with schizophrenia or bipolar affective disorder in the German population.

Martí SB, Cichon S, Propping P, Nöthen M. Martí SB, et al. Among authors: propping p. Am J Med Genet. 2002 Jan 8;114(1):46-50. doi: 10.1002/ajmg.1624. Am J Med Genet. 2002. PMID: 11840505

7

Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder.

Jamra RA, Klein K, Villela AW, Becker T, Schulze TG, Schmael C, Deschner M, Klopp N, Illig T, Propping P, Cichon S, Rietschel M, Nöthen MM, Schumacher J. Jamra RA, et al. Among authors: propping p. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):663-5. doi: 10.1002/ajmg.b.30358. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16823801

8

Association of major depression with rare functional variants in norepinephrine transporter and serotonin1A receptor genes.

Haenisch B, Linsel K, Brüss M, Gilsbach R, Propping P, Nöthen MM, Rietschel M, Fimmers R, Maier W, Zobel A, Höfels S, Guttenthaler V, Göthert M, Bönisch H. Haenisch B, et al. Among authors: propping p. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):1013-6. doi: 10.1002/ajmg.b.30912. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19105200

9

Association versus linkage studies in psychosis genetics.

Nöthen MM, Propping P, Fimmers R. Nöthen MM, et al. Among authors: propping p. J Med Genet. 1993 Aug;30(8):634-7. doi: 10.1136/jmg.30.8.634. J Med Genet. 1993. PMID: 8411047 Free PMC article. No abstract available.

10

Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: identification of two naturally occurring receptor variants and association analysis in schizophrenia.

Erdmann J, Shimron-Abarbanell D, Rietschel M, Albus M, Maier W, Körner J, Bondy B, Chen K, Shih JC, Knapp M, Propping P, Nöthen MM. Erdmann J, et al. Among authors: propping p. Hum Genet. 1996 May;97(5):614-9. doi: 10.1007/BF02281871. Hum Genet. 1996. PMID: 8655141

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