Morris-Rosendahl DJ - Search Results

1

Association between hSKCa3 and schizophrenia not confirmed by transmission disequilibrium test in 193 offspring/parents trios.

Wittekindt O, Schwab SG, Burgert E, Knapp M, Albus M, Lerer B, Hallmayer J, Rietschel M, Segman R, Borrmann M, Lichtermann D, Crocq MA, Maier W, Morris-Rosendahl DJ, Wildenauer DB. Wittekindt O, et al. Mol Psychiatry. 1999 May;4(3):267-70. doi: 10.1038/sj.mp.4000495. Mol Psychiatry. 1999. PMID: 10395217

2

Isolation of a novel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: a candidate for schizophrenia and bipolar disorder?

Chandy KG, Fantino E, Wittekindt O, Kalman K, Tong LL, Ho TH, Gutman GA, Crocq MA, Ganguli R, Nimgaonkar V, Morris-Rosendahl DJ, Gargus JJ. Chandy KG, et al. Mol Psychiatry. 1998 Jan;3(1):32-7. doi: 10.1038/sj.mp.4000353. Mol Psychiatry. 1998. PMID: 9491810

3

The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia.

Wittekindt O, Jauch A, Burgert E, Schärer L, Holtgreve-Grez H, Yvert G, Imbert G, Zimmer J, Hoehe MR, Macher JP, Chiaroni P, van Calker D, Crocq MA, Morris-Rosendahl DJ. Wittekindt O, et al. Neurogenetics. 1998 Aug;1(4):259-65. doi: 10.1007/s100480050038. Neurogenetics. 1998. PMID: 10732800 Clinical Trial.

4

Analysis of the CAG repeats in the SCA1 and B37 genes in schizophrenic and bipolar I disorder patients: tentative association between B37 and schizophrenia.

Morris-Rosendahl DJ, Burgert E, Uyanik G, Mayerova A, Duval F, Macher JP, Crocq MA. Morris-Rosendahl DJ, et al. Am J Med Genet. 1997 May 31;74(3):324-30. doi: 10.1002/(sici)1096-8628(19970531)74:3<324::aid-ajmg15>3.0.co;2-q. Am J Med Genet. 1997. PMID: 9184318

5

No association between the tyrosine hydroxylase microsatellite marker HUMTH01 and schizophrenia or bipolar I disorder.

Burgert E, Crocq MA, Bausch E, Macher JP, Morris-Rosendahl DJ. Burgert E, et al. Psychiatr Genet. 1998 Summer;8(2):45-8. doi: 10.1097/00041444-199800820-00002. Psychiatr Genet. 1998. PMID: 9686421

6

An apamin- and scyllatoxin-insensitive isoform of the human SK3 channel.

Wittekindt OH, Visan V, Tomita H, Imtiaz F, Gargus JJ, Lehmann-Horn F, Grissmer S, Morris-Rosendahl DJ. Wittekindt OH, et al. Mol Pharmacol. 2004 Mar;65(3):788-801. doi: 10.1124/mol.65.3.788. Mol Pharmacol. 2004. PMID: 14978258

7

hSKCa3: a candidate gene for schizophrenia?

Meissner B, Purmann S, Schürmann M, Zühlke C, Lencer R, Arolt V, Müller-Myhsok B, Morris-Rosendahl DJ, Schwinger E. Meissner B, et al. Psychiatr Genet. 1999 Jun;9(2):91-6. Psychiatr Genet. 1999. PMID: 10412188

8

Mutation screening of the KCNN3 gene reveals a rare frameshift mutation.

Bowen T, Williams N, Norton N, Spurlock G, Wittekindt OH, Morris-Rosendahl DJ, Williams H, Brzustowicz L, Hoogendoorn B, Zammit S, Jones G, Sanders RD, Jones LA, McCarthy G, Jones S, Bassett A, Cardno AG, Owen MJ, O'Donovan MC. Bowen T, et al. Mol Psychiatry. 2001 May;6(3):259-60. doi: 10.1038/sj.mp.4000128. Mol Psychiatry. 2001. PMID: 11326292 No abstract available.

9

A novel non-neuronal hSK3 isoform with a dominant-negative effect on hSK3 currents.

Wittekindt OH, Dreker T, Morris-Rosendahl DJ, Lehmann-Horn F, Grissmer S. Wittekindt OH, et al. Cell Physiol Biochem. 2004;14(1-2):23-30. doi: 10.1159/000076923. Cell Physiol Biochem. 2004. PMID: 14976403

10

Serotonin transporter (5-HTT) gene polymorphisms are not associated with susceptibility to mood disorders.

Hoehe MR, Wendel B, Grunewald I, Chiaroni P, Levy N, Morris-Rosendahl D, Macher JP, Sander T, Crocq MA. Hoehe MR, et al. Am J Med Genet. 1998 Feb 7;81(1):1-3. doi: 10.1002/(sici)1096-8628(19980207)81:1<1::aid-ajmg1>3.0.co;2-2. Am J Med Genet. 1998. PMID: 9514579

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