Transduction of 3'-flanking sequences is common in L1 retrotransposition (English)
- New search for: Goodier, John L.
- New search for: Ostertag, Eric M.
- New search for: Kazazian, Haig H.
- New search for: Goodier, John L.
- New search for: Ostertag, Eric M.
- New search for: Kazazian, Haig H.
In:
Human molecular genetics
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9
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653-
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2000
- Article (Journal) / Electronic Resource
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Title:Transduction of 3'-flanking sequences is common in L1 retrotransposition
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Contributors:
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Published in:Human molecular genetics ; 9, 4 ; 653-
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Publisher:
- New search for: Oxford University Press
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Publication date:2000-03-01
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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 9, Issue 4
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.
- 463
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The np 3243 MELAS mutation: damned if you aminoacylate, damned if you don'tJacobs, Howard T. / Holt, Ian J. et al. | 2000
- 467
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Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patientsBörner, G. Valentin / Zeviani, Massimo / Tiranti, Valeria / Carrara, Franco / Hoffmann, Sabine / Gerbitz, Klaus Dieter / Lochmüller, Hanns / Pongratz, Dieter / Klopstock, Thomas / Melberg, Atle et al. | 2000
- 477
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Functional analysis of ARHGAP6, a novel GTPase-activating protein for RhoAPrakash, Siddharth K. / Paylor, Richard / Jenna, Sarah / Lamarche-Vane, Nathalie / Armstrong, Dawna L. / Xu, Bisong / Mancini, Michael A. / Zoghbi, Huda Y. et al. | 2000
- 489
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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysisShaikh, Tamim H. / Kurahashi, Hiroki / Saitta, Sulagna C. / OHare, Anna Mizrahy / Hu, Ping / Roe, Bruce A. / Driscoll, Deborah A. / McDonald-McGinn, Donna M. / Zackai, Elaine H. / Budarf, Marcia L. et al. | 2000
- 503
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Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in miceWheeler, Vanessa C. / White, Jacqueline K. / Gutekunst, Claire-Anne / Vrbanac, Vladimir / Weaver, Meredith / Li, Xiao-Jiang / Li, Shi-Hua / Yi, Hong / Vonsattel, Jean-Paul / Gusella, James F. et al. | 2000
- 515
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Genome-wide variation in recombination in female meiosis: a risk factor for non-disjunction of chromosome 21Brown, Amanda Savage / Feingold, Eleanor / Broman, Karl W. / Sherman, Stephanie L. et al. | 2000
- 525
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A functional analysis of a natural variant of intercellular adhesion molecule-1 (ICAM-1Kilifi)Craig, Alister / Fernandez-Reyes, Delmiro / Mesri, Mehdi / McDowall, Alison / Altieri, Dario C. / Hogg, Nancy / Newbold, Christopher et al. | 2000
- 531
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Mapping of X-linked progressive retinal atrophy (XLPRA), the canine homolog of retinitis pigmentosa 3 (RP3)Zeiss, Caroline J. / Ray, Kunal / Acland, Gregory M. / Aguirre, Gustavo D. et al. | 2000
- 539
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Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin associationBérubé, Nathalie G. / Smeenk, Cecilia A. / Picketts, David J. et al. | 2000
- 549
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Genetic variants of IL-13 signalling and human asthma and atopyHeinzmann, A. / Mao, X.-Q. / Akaiwa, M. / Kreomer, R.T. / Gao, P.-S. / Ohshima, K. / Umeshita, R. / Abe, Y. / Braun, S. / Yamashita, T. et al. | 2000
- 561
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Developmentally distinct effects on human {varepsilon}-, {gamma}- and {delta}-globin levels caused by the absence or altered position of the human {beta}-globin gene in YAC transgenic miceBauchwitz, Robert / Costantini, Frank et al. | 2000
- 575
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A genetic risk factor for mouse neural tube defects: defining the embryonic basisFleming, Angeleen / Copp, Andrew J. et al. | 2000
- 583
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A new gene involved in DNA double-strand break repair and V(D)J recombination is located on human chromosome 10pMoshous, Despina / Li, Lanying / Chasseval, Régina de / Philippe, Noel / Jabado, Nada / Cowan, Morton J. / Fischer, Alain / Villartay, Jean-Pierre de et al. | 2000
- 589
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An imprinted locus associated with transient neonatal diabetes mellitusGardner, Rebecca J. / Mackay, Deborah J.G. / Mungall, Andrew J. / Polychronakos, Constantin / Siebert, Reiner / Shield, Julian P.H. / Temple, I. Karen / Robinson, David O. et al. | 2000
- 597
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Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2Kondo, Tadashi / Bobek, Miroslav P. / Kuick, Rork / Lamb, Barbara / Zhu, Xiaoxiang / Narayan, Ajita / Bourchis, Déborah / Viegas-Péquignot, Evani / Ehrlich, Melanie / Hanash, Samir M. et al. | 2000
- 605
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Constitutive and regulated modes of splicing produce six major myotonic dystrophy protein kinase (DMPK) isoforms with distinct propertiesGroenen, Patricia J.T.A. / Wansink, Derick G. / Coerwinkel, Marga / van den Broek, Walther / Jansen, Gert / Wieringa, Bé et al. | 2000
- 617
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Expression of the human CFTR gene from episomal oriP-EBNA1-YACs in mouse cellsHuertas, Dori / Howe, Steve / McGuigan, Amanda / Huxley, Clare et al. | 2000
- 631
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{beta}-globin YAC transgenes exhibit uniform expression levels but position effect variegation in miceAlami, Raouf / Greally, John M. / Tanimoto, Keiji / Hwang, Steven / Feng, Yong-Qing / Engel, James D. / Fiering, Steven / Bouhassira, Eric E. et al. | 2000
- 637
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Spectrum of SPG4 mutations in autosomal dominant spastic paraplegiaFonknechten, Nùria / Mavel, Delphine / Byrne, Paula / Davoine, Claire-Sophie / Cruaud, Corinne / Boentsch, Dominikus / Samson, Delphine / Coutinho, Paula / Hutchinson, Michael / Monagle, Paul Mc et al. | 2000
- 645
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Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS ratDCruz, Patricia M. / Yasumura, Douglas / Weir, Jessica / Matthes, Michael T. / Abderrahim, Hadi / LaVail, Matthew M. / Vollrath, Douglas et al. | 2000
- 653
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Transduction of 3'-flanking sequences is common in L1 retrotranspositionGoodier, John L. / Ostertag, Eric M. / Kazazian, Haig H. et al. | 2000
- 659
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Corrigendum| 2000