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Items: 18

1.

A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function.

Schwander M, Sczaniecka A, Grillet N, Bailey JS, Avenarius M, Najmabadi H, Steffy BM, Federe GC, Lagler EA, Banan R, Hice R, Grabowski-Boase L, Keithley EM, Ryan AF, Housley GD, Wiltshire T, Smith RJ, Tarantino LM, Müller U.

J Neurosci. 2007 Feb 28;27(9):2163-75.

2.

Neurobiology of schizophrenia.

Ross CA, Margolis RL, Reading SA, Pletnikov M, Coyle JT.

Neuron. 2006 Oct 5;52(1):139-53. Review.

3.
4.

Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond.

Tunbridge EM, Harrison PJ, Weinberger DR.

Biol Psychiatry. 2006 Jul 15;60(2):141-51. Epub 2006 Feb 14. Review.

PMID:
16476412
5.

Association of Ala72Ser polymorphism with COMT enzyme activity and the risk of schizophrenia in Koreans.

Lee SG, Joo Y, Kim B, Chung S, Kim HL, Lee I, Choi B, Kim C, Song K.

Hum Genet. 2005 Mar;116(4):319-28. Epub 2005 Jan 12.

PMID:
15645182
6.

Identification of Lps2 as a key transducer of MyD88-independent TIR signalling.

Hoebe K, Du X, Georgel P, Janssen E, Tabeta K, Kim SO, Goode J, Lin P, Mann N, Mudd S, Crozat K, Sovath S, Han J, Beutler B.

Nature. 2003 Aug 14;424(6950):743-8. Epub 2003 Jul 20.

PMID:
12872135
7.

Effect of dopamine uptake inhibition on brain catecholamine levels and locomotion in catechol-O-methyltransferase-disrupted mice.

Huotari M, Santha M, Lucas LR, Karayiorgou M, Gogos JA, Männistö PT.

J Pharmacol Exp Ther. 2002 Dec;303(3):1309-16.

8.

A highly significant association between a COMT haplotype and schizophrenia.

Shifman S, Bronstein M, Sternfeld M, Pisanté-Shalom A, Lev-Lehman E, Weizman A, Reznik I, Spivak B, Grisaru N, Karp L, Schiffer R, Kotler M, Strous RD, Swartz-Vanetik M, Knobler HY, Shinar E, Beckmann JS, Yakir B, Risch N, Zak NB, Darvasi A.

Am J Hum Genet. 2002 Dec;71(6):1296-302. Epub 2002 Oct 25.

9.

Brain catecholamine metabolism in catechol-O-methyltransferase (COMT)-deficient mice.

Huotari M, Gogos JA, Karayiorgou M, Koponen O, Forsberg M, Raasmaja A, Hyttinen J, Männistö PT.

Eur J Neurosci. 2002 Jan;15(2):246-56.

PMID:
11849292
10.

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

Murphy KC, Jones LA, Owen MJ.

Arch Gen Psychiatry. 1999 Oct;56(10):940-5.

PMID:
10530637
11.

Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior.

Gogos JA, Morgan M, Luine V, Santha M, Ogawa S, Pfaff D, Karayiorgou M.

Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):9991-6.

12.

Chemical synaptic transmission in the cochlea.

Puel JL.

Prog Neurobiol. 1995 Dec;47(6):449-76. Review.

PMID:
8787031
13.

Hyperlocomotion and indifference to cocaine and amphetamine in mice lacking the dopamine transporter.

Giros B, Jaber M, Jones SR, Wightman RM, Caron MG.

Nature. 1996 Feb 15;379(6566):606-12.

PMID:
8628395
14.

Neurotransmitters and neuromodulators of the mammalian cochlea.

Eybalin M.

Physiol Rev. 1993 Apr;73(2):309-73. Review. No abstract available.

PMID:
8097330
15.

Genomic organization of the human catechol O-methyltransferase gene and its expression from two distinct promoters.

Tenhunen J, Salminen M, Lundström K, Kiviluoto T, Savolainen R, Ulmanen I.

Eur J Biochem. 1994 Aug 1;223(3):1049-59.

16.

A type VII myosin encoded by the mouse deafness gene shaker-1.

Gibson F, Walsh J, Mburu P, Varela A, Brown KA, Antonio M, Beisel KW, Steel KP, Brown SD.

Nature. 1995 Mar 2;374(6517):62-4.

PMID:
7870172
17.

Defective myosin VIIA gene responsible for Usher syndrome type 1B.

Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston MD, et al.

Nature. 1995 Mar 2;374(6517):60-1.

PMID:
7870171
18.

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

Karayiorgou M, Morris MA, Morrow B, Shprintzen RJ, Goldberg R, Borrow J, Gos A, Nestadt G, Wolyniec PS, Lasseter VK, et al.

Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7612-6.

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