Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes (English)
- New search for: Li, W.
- New search for: Wang, X.
- New search for: Fan, W.
- New search for: Zhao, P.
- New search for: Chan, Y. C.
- New search for: Chen, S.
- New search for: Zhang, S.
- New search for: Guo, X.
- New search for: Zhang, Y.
- New search for: Li, Y.
- New search for: Li, W.
- New search for: Wang, X.
- New search for: Fan, W.
- New search for: Zhao, P.
- New search for: Chan, Y. C.
- New search for: Chen, S.
- New search for: Zhang, S.
- New search for: Guo, X.
- New search for: Zhang, Y.
- New search for: Li, Y.
In:
HUMAN MOLECULAR GENETICS
;
21
, 1
;
32-45
;
2012
-
ISSN:
- Article (Journal) / Print
-
Title:Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes
-
Contributors:
-
Published in:HUMAN MOLECULAR GENETICS ; 21, 1 ; 32-45
-
Publisher:
- New search for: Oxford University Press
-
Publication date:2012-01-01
-
Size:14 pages
-
ISSN:
-
Type of media:Article (Journal)
-
Type of material:Print
-
Language:English
- New search for: 572.8
- Further information on Dewey Decimal Classification
-
Classification:
DDC: 572.8 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 21, Issue 1
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.
- 1
-
ALS mutations in FUS cause neuronal dysfunction and death in Caenorhabditis elegans by a dominant gain-of-function mechanismMurakami, Tetsuro / Yang, Seung-Pil / Xie, Lin / Kawano, Taizo / Fu, Donald / Mukai, Asuka / Bohm, Christopher / Chen, Fusheng / Robertson, Janice / Suzuki, Hiroshi et al. | 2012
- 10
-
The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome casesChiesa, Nicoletta / De Crescenzo, Agostina / Mishra, Kankadeb / Perone, Lucia / Carella, Massimo / Palumbo, Orazio / Mussa, Alessandro / Sparago, Angela / Cerrato, Flavia / Russo, Silvia et al. | 2012
- 26
-
Cardiovascular defects in a mouse model of HOXA1 syndromeMakki, Nadja / Capecchi, Mario R. et al. | 2012
- 32
-
Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromesLi, Wen / Wang, Xianming / Fan, Wenxia / Zhao, Ping / Chan, Yau-Chi / Chen, Shen / Zhang, Shiqiang / Guo, Xiangpeng / Zhang, Ya / Li, Yanhua et al. | 2012
- 46
-
What are the determinants of gene expression levels and breadths in the human genome?Park, Jungsun / Xu, Ke / Park, Taesung / Yi, Soojin V. et al. | 2012
- 57
-
Retrotransposon activation contributes to fragile X premutation rCGG-mediated neurodegenerationTan, Huiping / Qurashi, Abrar / Poidevin, Mickael / Nelson, David L. / Li, He / Jin, Peng et al. | 2012
- 66
-
Thymidine kinase 2 mutations in autosomal recessive progressive external ophthalmoplegia with multiple mitochondrial DNA deletionsTyynismaa, Henna / Sun, Ren / Ahola-Erkkilä, Sofia / Almusa, Henrikki / Pöyhönen, Rosanna / Korpela, Mari / Honkaniemi, Jari / Isohanni, Pirjo / Paetau, Anders / Wang, Liya et al. | 2012
- 76
-
Protein interacting with C kinase (PICK1) is a suppressor of spinocerebellar ataxia 3-associated neurodegeneration in DrosophilaMcGurk, Leeanne / Bonini, Nancy M. et al. | 2012
- 85
-
Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNAIle mutation causing hypertrophic cardiomyopathyPerli, Elena / Giordano, Carla / Tuppen, Helen A.L. / Montopoli, Monica / Montanari, Arianna / Orlandi, Maurizia / Pisano, Annalinda / Catanzaro, Daniela / Caparrotta, Laura / Musumeci, Beatrice et al. | 2012
- 101
-
IRE1 plays an essential role in ER stress-mediated aggregation of mutant huntingtin via the inhibition of autophagy fluxLee, H. / Noh, J. Y. / Oh, Y. / Kim, Y. / Chang, J. W. / Chung, C. W. / Lee, S. T. / Kim, M. / Ryu, H. / Jung, Y. K. et al. | 2012
- 115
-
Mitochondrial complex III stabilizes complex I in the absence of NDUFS4 to provide partial activityCalvaruso, Maria Antonietta / Willems, Peter / van den Brand, Mariël / Valsecchi, Federica / Kruse, Shane / Palmiter, Richard / Smeitink, Jan / Nijtmans, Leo et al. | 2012
- 121
-
Impaired functionality and homing of Fancg-deficient hematopoietic stem cellsBarroca, Vilma / Mouthon, Marc André / Lewandowski, Daniel / Brunet de la Grange, Philippe / Gauthier, Laurent Robert / Pflumio, Françoise / Boussin, François Dominique / Arwert, Fre / Riou, Lydia / Allemand, Isabelle et al. | 2012
- 136
-
Arginine methylation by PRMT1 regulates nuclear-cytoplasmic localization and toxicity of FUS/TLS harbouring ALS-linked mutationsTradewell, Miranda L. / Yu, Zhenbao / Tibshirani, Michael / Boulanger, Marie-Chloé / Durham, Heather D. / Richard, Stéphane et al. | 2012
- 150
-
Charcot-Marie-Tooth disease CMT4A: GDAP1 increases cellular glutathione and the mitochondrial membrane potentialNoack, Rebecca / Frede, Svenja / Albrecht, Philipp / Henke, Nadine / Pfeiffer, Annika / Knoll, Katrin / Dehmel, Thomas / Meyer zu Hörste, Gerd / Stettner, Mark / Kieseier, Bernd C. et al. | 2012
- 163
-
Transcriptional responses to loss or gain of function of the leucine-rich repeat kinase 2 (LRRK2) gene uncover biological processes modulated by LRRK2 activityNikonova, Elena V. / Xiong, Yulan / Tanis, Keith Q. / Dawson, Valina L. / Vogel, Robert L. / Finney, Eva M. / Stone, David J. / Reynolds, Ian J. / Kern, Jonathan T. / Dawson, Ted M. et al. | 2012
- 175
-
Dysfunctions in endosomal-lysosomal and autophagy pathways underlie neuropathology in a mouse model for Lafora diseasePuri, Rajat / Suzuki, Toshimitsu / Yamakawa, Kazuhiro / Ganesh, Subramaniam et al. | 2012
- 185
-
Severe neuromuscular denervation of clinically relevant muscles in a mouse model of spinal muscular atrophyLing, Karen K. Y. / Gibbs, Rebecca M. / Feng, Zhihua / Ko, Chien-Ping et al. | 2012
- 196
-
Survival of pancreatic beta cells is partly controlled by a TCF7L2-p53-p53INP1-dependent pathwayZhou, Yuedan / Zhang, Enming / Berggreen, Christine / Jing, Xingjun / Osmark, Peter / Lang, Stefan / Cilio, Corrado M. / Göransson, Olga / Groop, Leif / Renström, Erik et al. | 2012
- 208
-
Reprogramming somatic cells into iPS cells activates LINE-1 retroelement mobilityWissing, Silke / Muñoz-Lopez, Martin / Macia, Angela / Yang, Zhiyuan / Montano, Mauricio / Collins, William / Garcia-Perez, Jose Luis / Moran, John V. / Greene, Warner C. et al. | 2012
- 219
-
Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some lociSinger, Heike / Walier, Maja / Nüsgen, Nicole / Meesters, Christian / Schreiner, Felix / Woelfle, Joachim / Fimmers, Rolf / Wienker, Thomas / Kalscheuer, Vera M. / Becker, Tim et al. | 2012
- NP
-
Contents Page| 2012
- NP-c
-
Subscription Page| 2012
- NP-a
-
Cover Page| 2012
- NP-b
-
Editorial Board| 2012