Disruption of two novel genes by a translocation co-segregating with schizophrenia (English)
- New search for: Millar, J. Kirsty
- New search for: Wilson-Annan, Julie C.
- New search for: Anderson, Susan
- New search for: Christie, Sheila
- New search for: Taylor, Martin S.
- New search for: Semple, Colin A. M.
- New search for: Devon, Rebecca S.
- New search for: Clair, David M. St
- New search for: Muir, Walter J.
- New search for: Blackwood, Douglas H. R.
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- New search for: Millar, J. Kirsty
- New search for: Wilson-Annan, Julie C.
- New search for: Anderson, Susan
- New search for: Christie, Sheila
- New search for: Taylor, Martin S.
- New search for: Semple, Colin A. M.
- New search for: Devon, Rebecca S.
- New search for: Clair, David M. St
- New search for: Muir, Walter J.
- New search for: Blackwood, Douglas H. R.
- New search for: Porteous, David J.
In:
Human molecular genetics
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9
, 9
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1415-
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2000
- Article (Journal) / Electronic Resource
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Title:Disruption of two novel genes by a translocation co-segregating with schizophrenia
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Contributors:Millar, J. Kirsty ( author ) / Wilson-Annan, Julie C. ( author ) / Anderson, Susan ( author ) / Christie, Sheila ( author ) / Taylor, Martin S. ( author ) / Semple, Colin A. M. ( author ) / Devon, Rebecca S. ( author ) / Clair, David M. St ( author ) / Muir, Walter J. ( author ) / Blackwood, Douglas H. R. ( author )
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Published in:Human molecular genetics ; 9, 9 ; 1415-
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Publisher:
- New search for: Oxford University Press
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Publication date:2000-05-22
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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 9, Issue 9
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.
- 1259
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Decreased expression of striatal signaling genes in a mouse model of Huntington's diseaseLuthi-Carter, Ruth / Strand, Andrew / Peters, Nikki L. / Solano, Steven M. / Hollingsworth, Zane R. / Menon, Anil S. / Frey, Ariel S. / Spektor, Boris S. / Penney, Ellen B. / Schilling, Gabriele et al. | 2000
- 1273
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A transcription-activating polymorphism in the ACHE promoter associated with acute sensitivity to anti-acetylcholinesterasesShapira, Michael / Tur-Kaspa, Ilan / Bosgraaf, Leonard / Livni, Nadav / Grant, Alastair D. / Grisaru, Dan / Korner, Mira / Ebstein, Richard P. / Soreq, Hermona et al. | 2000
- 1283
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Biochemical and structural analysis of missense mutations in N-acetylgalactosamine-6-sulfate sulfatase causing mucopolysaccharidosis IVA phenotypesSukegawa, Kazuko / Nakamura, Haruki / Kato, Zenichiro / Tomatsu, Shunji / Montaño, Adriana M. / Fukao, Toshiyuki / Toietta, Gabriele / Tortora, Paolo / Orii, Tadao / Kondo, Naomi et al. | 2000
- 1291
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Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21Herr, Mathias / Dudbridge, Frank / Zavattari, Patrizia / Cucca, Francesco / Guja, Cristian / March, Ruth / Campbell, R. Duncan / Barnett, Anthony H. / Bain, Stephen C. / Todd, John A. et al. | 2000
- 1303
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A novel protein with RNA-binding motifs interacts with ataxin-2Shibata, Hiroki / Huynh, Duong P. / Pulst, Stefan-M. et al. | 2000
- 1315
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Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham StudyShearman, Amanda M. / Ordovas, Jose M. / Cupples, L. Adrienne / Schaefer, Ernst J. / Harmon, Michael D. / Shao, Yujun / Keen, J. Dianne / DeStefano, Anita L. / Joost, Oscar / Wilson, Peter W. F. et al. | 2000
- 1321
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Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 geneVeugelers, Mark / Cat, Bart De / Muyldermans, Sin Ya / Reekmans, Gunter / Delande, Nathalie / Frints, Suzanne / Legius, Eric / Fryns, Jean-Pierre / Schrander-Stumpel, Connie / Weidle, Bernhard et al. | 2000
- 1329
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A full genome scan for age-related maculopathyWeeks, Daniel E. / Conley, Yvette P. / Mah, Tammy S. / Paul, T. Otis / Morse, Lawrence / Ngo-Chang, Julilani / Dailey, J.P. / Ferrell, Robert E. / Gorin, Michael B. et al. | 2000
- 1351
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KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformationEerola, Iiro / Plate, Karl H. / Spiegel, Roland / Boon, Laurence M. / Mulliken, John B. / Vikkula, Miikka et al. | 2000
- 1357
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Dystrophin and utrophin influence fiber type composition and post-synaptic membrane structureRafael, Jill A. / Townsend, Elizabeth R. / Squire, Sarah E. / Potter, Allyson C. / Chamberlain, Jeffrey S. / Davies, Kay E. et al. | 2000
- 1369
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Rett syndrome: analysis of MECP2 and clinical characterization of 31 patientsHuppke, P. / Laccone, F. / Krämer, N. / Engel, W. / Hanefeld, F. et al. | 2000
- 1377
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MECP2 mutations account for most cases of typical forms of Rett syndromeBienvenu, Thierry / Carrié, Alain / de Roux, Nicolas / Vinet, Marie-Claude / Jonveaux, Philippe / Couvert, Philippe / Villard, Laurent / Arzimanoglou, Alexis / Beldjord, Cherif / Fontes, Michel et al. | 2000
- 1385
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Spectrum of {Delta}7-dehydrocholesterol reductase mutations in patients with the Smith-Lemli-Opitz (RSH) syndromeYu, Hongwei / Lee, Mi-Hye / Starck, Lena / Elias, Ellen R. / Irons, Mira / Salen, Gerald / Patel, Shailendra B. / Tint, G. Stephen et al. | 2000
- 1393
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Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2ATagawa, Kazuhiko / Taya, Choji / Hayashi, Yukiko / Nakagawa, Masahiro / Ono, Yasuko / Fukuda, Rie / Karasuyama, Hajime / Toyama-Sorimachi, Noriko / Katsui, Yukiko / Hata, Shoji et al. | 2000
- 1403
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Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cellsHewett, Jeffrey / Gonzalez-Agosti, Charo / Slater, Damien / Ziefer, Philipp / Li, Sang / Bergeron, Daniele / Jacoby, David J. / Ozelius, Laurie J. / Ramesh, Vijaya / Breakefield, Xandra O. et al. | 2000
- 1415
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Disruption of two novel genes by a translocation co-segregating with schizophreniaMillar, J. Kirsty / Wilson-Annan, Julie C. / Anderson, Susan / Christie, Sheila / Taylor, Martin S. / Semple, Colin A. M. / Devon, Rebecca S. / Clair, David M. St / Muir, Walter J. / Blackwood, Douglas H. R. et al. | 2000
- 1425
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Linkage and linkage disequilibrium in chromosome band 1p36 in American Chaldeans with inflammatory bowel diseaseCho, Judy H. / Nicolae, Dan L. / Ramos, Richard / Fields, Carter T. / Rabenau, Karen / Corradino, Sarah / Brant, Steven R. / Espinosa, Rafael / LeBeau, Michelle / Hanauer, Stephen B. et al. | 2000
- 1433
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Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamineYanagisawa, Hiroko / Bundo, Miki / Miyashita, Toshiyuki / Okamura-Oho, Yuko / Tadokoro, Keiko / Tokunaga, Katsushi / Yamada, Masao et al. | 2000
- 1443
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Barhl1, a gene belonging to a new subfamily of mammalian homeobox genes, is expressed in migrating neurons of the CNSBulfone, Alessandro / Menguzzato, Emilio / Broccoli, Vania / Marchitiello, Anna / Gattuso, Claudio / Mariani, Margherita / Consalez, Gian Giacomo / Martinez, Salvador / Ballabio, Andrea / Banfi, Sandro et al. | 2000
- 1453
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Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)Muchir, Antoine / Bonne, Gisèle / van der Kooi, Anneke J. / van Meegen, Mia / Baas, Frank / Bolhuis, Pieter A. / de Visser, Marianne / Schwartz, Ketty et al. | 2000
- 1461
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Corrigendum| 2000