相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation
Aaron Y. L. Cheung et al.
HUMAN MOLECULAR GENETICS (2011)
Meta-analysis of the heterogeneity of X chromosome inactivation in human pluripotent stem cells
Tal Bruck et al.
STEM CELL RESEARCH (2011)
Derivation of Pre-X Inactivation Human Embryonic Stem Cells under Physiological Oxygen Concentrations
Christopher J. Lengner et al.
CELL (2010)
A Model for Neural Development and Treatment of Rett Syndrome Using Human Induced Pluripotent Stem Cells
Maria C. N. Marchetto et al.
CELL (2010)
Pluripotency and Cellular Reprogramming: Facts, Hypotheses, Unresolved Issues
Jacob H. Hanna et al.
CELL (2010)
Female Human iPSCs Retain an Inactive X Chromosome
Jason Tchieu et al.
CELL STEM CELL (2010)
Rett Syndrome Microglia Damage Dendrites and Synapses by the Elevated Release of Glutamate
Izumi Maezawa et al.
JOURNAL OF NEUROSCIENCE (2010)
Variations of X Chromosome Inactivation Occur in Early Passages of Female Human Embryonic Stem Cells
Tamar Dvash et al.
PLOS ONE (2010)
Neural differentiation of human induced pluripotent stem cells follows developmental principles but with variable potency
Bao-Yang Hu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Human embryonic stem cells with biological and epigenetic characteristics similar to those of mouse ESCs
Jacob Hanna et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Epigenetic reprogramming and induced pluripotency
Konrad Hochedlinger et al.
DEVELOPMENT (2009)
Rett Syndrome Astrocytes Are Abnormal and Spread MeCP2 Deficiency through Gap Junctions
Izumi Maezawa et al.
JOURNAL OF NEUROSCIENCE (2009)
Induced pluripotent stem cells from a spinal muscular atrophy patient
Allison D. Ebert et al.
NATURE (2009)
Modelling pathogenesis and treatment of familial dysautonomia using patient-specific iPSCs
Gabsang Lee et al.
NATURE (2009)
Live cell imaging distinguishes bona fide human iPS cells from partially reprogrammed cells
Elayne M. Chan et al.
NATURE BIOTECHNOLOGY (2009)
Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology
Nurit Ballas et al.
NATURE NEUROSCIENCE (2009)
A Robust Approach to Identifying Tissue-Specific Gene Expression Regulatory Variants Using Personalized Human Induced Pluripotent Stem Cells
Je-Hyuk Lee et al.
PLOS GENETICS (2009)
Defining molecular cornerstones during fibroblast to iPS cell reprogramming in mouse
Matthias Stadtfeld et al.
CELL STEM CELL (2008)
Marked differences in differentiation propensity among human embryonic stem cell lines
Kenji Osafune et al.
NATURE BIOTECHNOLOGY (2008)
Generation of human-induced pluripotent stem cells
In-Hyun Park et al.
NATURE PROTOCOLS (2008)
X-chromosome inactivation and epigenetic fluidity in human embryonic stem cells
Susana S. Silva et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
MeCP2, a key contributor to neurological disease, activates and represses transcription
Maria Chahrour et al.
SCIENCE (2008)
Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons
John T. Dimos et al.
SCIENCE (2008)
Reprogramming of human somatic cells to pluripotency with defined factors
In-Hyun Park et al.
NATURE (2008)
Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes
Dag H. Yasui et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Mechanisms of disease: neurogenetics of MeCP2 deficiency
U Francke
NATURE CLINICAL PRACTICE NEUROLOGY (2006)
Differentiation of human embryonic stem cells to neural lineages in adherent culture by blocking bone morphogenetic protein signaling
L Gerrard et al.
STEM CELLS (2005)
Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders
RC Samaco et al.
HUMAN MOLECULAR GENETICS (2004)
X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of Rett syndrome
JI Young et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
被撤回的出版物: A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos (Retracted article. See vol. 73, pg. 1083, 2019)
I Stancheva et al.
MOLECULAR CELL (2003)
RettBASE:: The IRSA MECP2 variation data-base -: A new mutation database in evolution
J Christodoulou et al.
HUMAN MUTATION (2003)
Role of histone H3 lysine 27 methylation in X inactivation
K Plath et al.
SCIENCE (2003)
The role of different X-inactivation pattern on the variable clinical phenotype with Rett syndrome
T Ishii et al.
BRAIN & DEVELOPMENT (2001)
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
J Guy et al.
NATURE GENETICS (2001)
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
RZ Chen et al.
NATURE GENETICS (2001)