DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation (English)
- New search for: Morris, Jill A.
- New search for: Kandpal, Geeta
- New search for: Ma, Lei
- New search for: Austin, Christopher P.
- New search for: Morris, Jill A.
- New search for: Kandpal, Geeta
- New search for: Ma, Lei
- New search for: Austin, Christopher P.
In:
Human molecular genetics
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12
, 13
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1591-
;
2003
- Article (Journal) / Electronic Resource
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Title:DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation
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Contributors:Morris, Jill A. ( author ) / Kandpal, Geeta ( author ) / Ma, Lei ( author ) / Austin, Christopher P. ( author )
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Published in:Human molecular genetics ; 12, 13 ; 1591-
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Publisher:
- New search for: Oxford University Press
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Publication date:2003-07-01
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 12, Issue 13
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1463
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CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behaviorFrints, Suzanna G. M. / Marynen, Peter / Hartmann, Dieter / Fryns, Jean-Pierre / Steyaert, Jean / Schachner, Melitta / Rolf, Bettina / Craessaerts, Katleen / Snellinx, An / Hollanders, Karen et al. | 2003
- 1475
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Protein kinase-A activity in PRKAR1A-mutant cells, and regulation of mitogen-activated protein kinases ERK1/2Robinson-White, Audrey / Hundley, Thomas R. / Shiferaw, Miriam / Bertherat, Jérôme / Sandrini, Fabiano / Stratakis, Constantine A. et al. | 2003
- 1485
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Expansion of the polyQ repeat in ataxin-2 alters its Golgi localization, disrupts the Golgi complex and causes cell deathHuynh, Duong P. / Yang, Hai-Tao / Vakharia, Hema / Nguyen, Dung / Pulst, Stefan M. et al. | 2003
- 1497
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Transglutaminase potentiates ligand-dependent proteasome dysfunction induced by polyglutamine-expanded androgen receptorMandrusiak, Lisa M. / Beitel, Lenore K. / Wang, Xiaoling / Scanlon, Thomas C. / Chevalier-Larsen, Erica / Merry, Diane E. / Trifiro, Mark A. et al. | 2003
- 1507
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True XP group E patients have a defective UV-damaged DNA binding protein complex and mutations in DDB2 which reveal the functional domains of its p48 productRapic-Otrin, Vesna / Navazza, Valentina / Nardo, Tiziana / Botta, Elena / McLenigan, Mary / Bisi, Dawn C. / Levine, Arthur S. / Stefanini, Miria et al. | 2003
- 1523
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The Menkes disease ATPase (ATP7A) is internalized via a Rac1-regulated, clathrin- and caveolae-independent pathwayCobbold, Christian / Coventry, Julie / Ponnambalam, Sreenivasan / Monaco, Anthony P. et al. | 2003
- 1535
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Dentatorubral-pallidoluysian atrophy protein is phosphorylated by c-Jun NH2-terminal kinaseOkamura-Oho, Yuko / Miyashita, Toshiyuki / Nagao, Kazuaki / Shima, Seigo / Ogata, Yukie / Katada, Toshiaki / Nishina, Hiroshi / Yamada, Masao et al. | 2003
- 1543
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Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retinaDalloz, Cécile / Sarig, Rachel / Fort, Patrice / Yaffe, David / Bordais, Agnès / Pannicke, Thomas / Grosche, Jens / Mornet, Dominique / Reichenbach, Andreas / Sahel, José et al. | 2003
- 1555
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Selective striatal neuronal loss in a YAC128 mouse model of Huntington diseaseSlow, Elizabeth J. / van Raamsdonk, Jeremy / Rogers, Daniel / Coleman, Sarah H. / Graham, Rona K. / Deng, Yu / Oh, Rosemary / Bissada, Nagat / Hossain, Sazzad M. / Yang, Yu-Zhou et al. | 2003
- 1569
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Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regionsSandovici, Ionel / Leppert, Mark / Hawk, Patricia Red / Suarez, Alexander / Linares, Yendi / Sapienza, Carmen et al. | 2003
- 1579
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Genetic modifiers interact with maternal determinants in vascular development of Tgfb1-/- miceTang, Yang / McKinnon, Margaret L. / Leong, Li Ming / Rusholme, Sarah A. B. / Wang, Susana / Akhurst, Rosemary J. et al. | 2003
- 1591
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DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutationMorris, Jill A. / Kandpal, Geeta / Ma, Lei / Austin, Christopher P. et al. | 2003
- 1609
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Distinct chaperone mechanisms can delay the formation of aggresomes by the myopathy-causing R120G {alpha}B-crystallin mutantChávez Zobel, Aura T. / Loranger, Anne / Marceau, Normand / Thériault, Jimmy R. / Lambert, Herman / Landry, Jacques et al. | 2003
- 1621
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Nucleocytoplasmic transport signals affect the age at onset of abnormalities in knock-in mice expressing polyglutamine within an ectopic protein contextJackson, Walker S. / Tallaksen-Greene, Sara J. / Albin, Roger L. / Detloff, Peter J. et al. | 2003
- 1631
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Lathosterolosis: an inborn error of human and murine cholesterol synthesis due to lathosterol 5-desaturase deficiencyKrakowiak, Patrycja A. / Wassif, Christopher A. / Kratz, Lisa / Cozma, Diana / Kovárová, Martina / Harris, Ginny / Grinberg, Alexander / Yang, Yinzi / Hunter, Alasdair G.W. / Tsokos, Maria et al. | 2003