Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse (English)
- New search for: Baxter, Laura L.
- New search for: Moran, Timothy H.
- New search for: Richtsmeier, Joan T.
- New search for: Troncoso, Juan
- New search for: Reeves, Roger H.
- New search for: Baxter, Laura L.
- New search for: Moran, Timothy H.
- New search for: Richtsmeier, Joan T.
- New search for: Troncoso, Juan
- New search for: Reeves, Roger H.
In:
Human molecular genetics
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9
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195-
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2000
- Article (Journal) / Electronic Resource
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Title:Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse
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Contributors:Baxter, Laura L. ( author ) / Moran, Timothy H. ( author ) / Richtsmeier, Joan T. ( author ) / Troncoso, Juan ( author ) / Reeves, Roger H. ( author )
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Published in:Human molecular genetics ; 9, 2 ; 195-
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Publisher:
- New search for: Oxford University Press
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Publication date:2000-01-22
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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 2
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.
- 149
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Neocentromeres and alpha satellite: a proposed structural code for functional human centromere DNAKoch, Jørn et al. | 2000
- 155
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Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 geneIkeda, Sakae / Shiva, Nima / Ikeda, Akihiro / Smith, Richard S. / Nusinowitz, Steven / Yan, Grace / Lin, T. Richard / Chu, Sunny / Heckenlively, John R. / North, Michael A. et al. | 2000
- 165
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Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genesFougerousse, Francoise / Bullen, Philip / Herasse, Muriel / Lindsay, Susan / Richard, Isabelle / Wilson, David / Suel, Laurence / Durand, Muriel / Robson, Steve / Abitbol, Marc et al. | 2000
- 175
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Human centromeres and neocentromeres show identical distribution patterns of >20 functionally important kinetochore-associated proteins.Saffery, Richard / Irvine, Danielle V. / Griffiths, Belinda / Kalitsis, Paul / Wordeman, Linda / Choo, K.H. Andy et al. | 2000
- 187
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Poly(ADP-ribose) polymerase at active centromeres and neocentromeres at metaphaseEarle, Elizabeth / Saxena, Alka / MacDonald, Andrew / Hudson, Damien F. / Shaffer, Lisa G. / Saffery, Richard / Cancilla, Michael R. / Cutts, Suzanne M. / Howman, Emily / Choo, K. H. Andy et al. | 2000
- 195
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Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouseBaxter, Laura L. / Moran, Timothy H. / Richtsmeier, Joan T. / Troncoso, Juan / Reeves, Roger H. et al. | 2000
- 203
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Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expressionPrawitt, Dirk / Enklaar, Thorsten / Klemm, Gabi / Gärtner, Barbara / Spangenberg, Christian / Winterpacht, Andreas / Higgins, Michael / Pelletier, Jerry / Zabel, Bernhard et al. | 2000
- 217
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Myoferlin, a candidate gene and potential modifier of muscular dystrophyDavis, Dawn Belt / Delmonte, Anthony J. / Ly, Chantal T. / McNally, Elizabeth M. et al. | 2000
- 227
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A mouse model for valproate teratogenicity: parental effects, homeotic transformations, and altered HOX expressionFaiella, Antonio / Wernig, Marius / Consalez, G. Giacomo / Hostick, Ute / Hofmann, Clementine / Hustert, Elisabeth / Boncinelli, Edoardo / Balling, Rudi / Nadeau, Joseph H. et al. | 2000
- 237
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Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1Ars, Elisabet / Serra, Eduard / García, Judit / Kruyer, Helena / Gaona, Antonia / Lázaro, Conxi / Estivill, Xavier et al. | 2000
- 249
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Restrained chondrocyte proliferation and maturation with abnormal growth plate vascularization and ossification in human FGFR-3G380R transgenic miceSegev, Orit / Chumakov, Irina / Nevo, Zvi / Givol, David / Madar-Shapiro, Liora / Sheinin, Yuri / Weinreb, Miron / Yayon, Avner et al. | 2000
- 259
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An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMNLorson, Christian L. / Androphy, Elliot J. et al. | 2000
- 267
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Inhibition of p160-mediated coactivation with increasing androgen receptor polyglutamine lengthIrvine, Ryan A. / Ma, Han / Yu, Mimi C. / Ross, Ronald K. / Stallcup, Michael R. / Coetzee, Gerhard A. et al. | 2000
- 275
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Clinical, biochemical and molecular genetic correlations in Friedreich's ataxiaBradley, J.L. / Blake, J.C. / Chamberlain, S. / Thomas, P.K. / Cooper, J.M. / Schapira, A.H.V. et al. | 2000
- 283
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Involvement of PTEN mutations in the genetic pathways of colorectal cancerogenesisGuanti, Ginevra / Resta, Nicoletta / Simone, Cristiano / Cariola, Filomena / Demma, Ignazio / Fiorente, Paola / Gentile, Mattia et al. | 2000
- 289
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A novel human odorant-binding protein gene family resulting from genomic duplicons at 9q34: differential expression in the oral and genital spheresLacazette, Eric / Gachon, Anne-Marie / Pitiot, Gilles et al. | 2000
- 303
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Alzheimer's presenilin 1 is a putative membrane receptor for rab GDP dissociation inhibitorScheper, W. / Zwart, R. / van der Sluijs, P. / Annaert, W. / Gool, W.A. van / Baas, F. et al. | 2000
- 311
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A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteinsLahn, Bruce T. / Page, David C. et al. | 2000
- 321
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Corrigendum| 2000