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。CD22 blockade restores homeostatic microglial phagocytosis in ageing brains
John V. Pluvinage et al.
NATURE (2019)
CAG Repeat Not Polyglutamine Length Determines Timing of Huntington's Disease Onset
Jong-Min Lee et al.
CELL (2019)
REST, a master transcriptional regulator in neurodegenerative disease
Jee-Yeon Hwang et al.
CURRENT OPINION IN NEUROBIOLOGY (2018)
Microglia activation in Niemann-Pick disease, type C1 is amendable to therapeutic intervention
Antony Cougnoux et al.
HUMAN MOLECULAR GENETICS (2018)
Rett syndrome: a neurological disorder with metabolic components
Stephanie M. Kyle et al.
OPEN BIOLOGY (2018)
The ZZ-type zinc finger of ZZZ3 modulates the ATAC complex-mediated histone acetylation and gene activation
Wenyi Mi et al.
NATURE COMMUNICATIONS (2018)
Whole exome sequencing of ENU-induced thrombosis modifier mutations in the mouse
Kart Tomberg et al.
PLOS GENETICS (2018)
Spotlight on protein N-terminal acetylation
Rasmus Ree et al.
EXPERIMENTAL AND MOLECULAR MEDICINE (2018)
The histone demethylase JMJD2A regulates the expression of BDNF and mediates neuropathic pain in mice
Junfei Zhou et al.
EXPERIMENTAL CELL RESEARCH (2017)
Spindlin I is essential for metaphase II stage maintenance and chromosomal stability in porcine oocytes
Jeong-Woo Choi et al.
MOLECULAR HUMAN REPRODUCTION (2017)
PRDM15 safeguards naive pluripotency by transcriptionally regulating WNT and MAPK-ERK signaling
Slim Mzoughi et al.
NATURE GENETICS (2017)
THE ROLE OF CELSR3 IN THE DEVELOPMENT OF CENTRAL SOMATOSENSORY PROJECTIONS FROM DORSAL ROOT GANGLIA
Feifei Wang et al.
NEUROSCIENCE (2017)
Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor loci
Randal J. Westrick et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)
REST corepressors RCOR1 and RCOR2 and the repressor INSM1 regulate the proliferation-differentiation balance in the developing brain
Caitlin E. Monaghan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)
Evidence for opposing roles of Celsr3 and Vangl2 in glutamatergic synapse formation
Sonal Thakar et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)
Histone peptide microarray screen of chromo and Tudor domains defines new histone lysine methylation interactions
Erin K. Shanle et al.
EPIGENETICS & CHROMATIN (2017)
Maternal expression of the histone demethylase Kdm4a is crucial for pre-implantation development
Aditya Sankar et al.
DEVELOPMENT (2017)
Celsr3 and Fzd3 Organize a Pioneer Neuron Scaffold to Steer Growing Thalamocortical Axons
Jia Feng et al.
CEREBRAL CORTEX (2016)
DNA Double Strand Breaks: A Common Theme in Neurodegenerative Diseases
Daniela Merlo et al.
CURRENT ALZHEIMER RESEARCH (2016)
MeCP2 co-ordinates liver lipid metabolism with the NCoR1/HDAC3 corepressor complex
Stephanie M. Kyle et al.
HUMAN MOLECULAR GENETICS (2016)
Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes
Paul D. Ross et al.
HUMAN MOLECULAR GENETICS (2016)
MRN, CtIP, and BRCA1 mediate repair of topoisomerase II-DNA adducts
Tomas Aparicio et al.
JOURNAL OF CELL BIOLOGY (2016)
flexsurv: A Platform for Parametric Survival Modeling in R
Christopher H. Jackson
JOURNAL OF STATISTICAL SOFTWARE (2016)
Biochemical reconstitution of TET1-TDG-BER-dependent active DNA demethylation reveals a highly coordinated mechanism
Alain R. Weber et al.
NATURE COMMUNICATIONS (2016)
Tet Enzymes Regulate Telomere Maintenance and Chromosomal Stability of Mouse ESCs
Jiao Yang et al.
CELL REPORTS (2016)
Activity-Induced DNA Breaks Govern the Expression of Neuronal Early-Response Genes
Ram Madabhushi et al.
CELL (2015)
Fitting Linear Mixed-Effects Models Using lme4
Douglas Bates et al.
JOURNAL OF STATISTICAL SOFTWARE (2015)
A mechanism for the suppression of homologous recombination in G1 cells
Alexandre Orthwein et al.
NATURE (2015)
BRUCE regulates DNA double-strand break response by promoting USP8 deubiquitination of BRIT1
Chunmin Ge et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
Catalytic and Noncatalytic Roles of the CtIP Endonuclease in Double-Strand Break End Resection
Nodar Makharashvili et al.
MOLECULAR CELL (2014)
DNA Damage and Its Links to Neurodegeneration
Ram Madabhushi et al.
NEURON (2014)
Cholesterol Metabolism Is Altered in Rett Syndrome: A Study on Plasma and Primary Cultured Fibroblasts Derived from Patients
Marco Segatto et al.
PLOS ONE (2014)
MeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis?
Elisa Bellini et al.
FRONTIERS IN CELLULAR NEUROSCIENCE (2014)
Dendritic spine dysgenesis in Rett syndrome
Xin Xu et al.
FRONTIERS IN NEUROANATOMY (2014)
Rett-causing mutations reveal two domains critical for MeCP2 function and for toxicity in MECP2 duplication syndrome mice
Laura Dean Heckman et al.
ELIFE (2014)
Emerging roles of the corepressors NCoR1 and SMRT in homeostasis
Adrienne Mottis et al.
GENES & DEVELOPMENT (2013)
Apolipoproteins E and AV mediate lipoprotein clearance by hepatic proteoglycans
Jon C. Gonzales et al.
JOURNAL OF CLINICAL INVESTIGATION (2013)
A Cell Cycle-Dependent Regulatory Circuit Composed of 53BP1-RIF1 and BRCA1-CtIP Controls DNA Repair Pathway Choice
Cristina Escribano-Diaz et al.
MOLECULAR CELL (2013)
A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome
Christie M. Buchovecky et al.
NATURE GENETICS (2013)
Physiologic brain activity causes DNA double-strand breaks in neurons, with exacerbation by amyloid-β
Elsa Suberbielle et al.
NATURE NEUROSCIENCE (2013)
Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor
Matthew J. Lyst et al.
NATURE NEUROSCIENCE (2013)
A Tudor Domain Protein SPINDLIN1 Interacts with the mRNA-Binding Protein SERBP1 and Is Involved in Mouse Oocyte Meiotic Resumption
Ting Gang Chew et al.
PLOS ONE (2013)
A Novel Role for Tm7sf2 Gene in Regulating TNFα Expression
Ilaria Bellezza et al.
PLOS ONE (2013)
A role for metabolism in Rett syndrome pathogenesis New clinical findings and potential treatment targets
Monica J. Justice et al.
RARE DISEASES (2013)
Acetoacetyl-CoA synthetase is essential for normal neuronal development
Shinya Hasegawa et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2012)
PRDM proteins: Important players in differentiation and disease
Cathrine K. Fog et al.
BIOESSAYS (2012)
The Prdm family: expanding roles in stem cells and development
Tobias Hohenauer et al.
DEVELOPMENT (2012)
Preclinical research in Rett syndrome: setting the foundation for translational success
David M. Katz et al.
DISEASE MODELS & MECHANISMS (2012)
CDK targeting of NBS1 promotes DNA-end resection, replication restart and homologous recombination
Jacob Falck et al.
EMBO REPORTS (2012)
Rett networked database: An integrated clinical and genetic network of rett syndrome databases
Elisa Grillo et al.
HUMAN MUTATION (2012)
Acetoacetyl-CoA synthetase, a ketone body-utilizing enzyme, is controlled by SREBP-2 and affects serum cholesterol levels
Shinya Hasegawa et al.
MOLECULAR GENETICS AND METABOLISM (2012)
clusterMaker: a multi-algorithm clustering plugin for Cytoscape
John H. Morris et al.
BMC BIOINFORMATICS (2011)
Synaptic microcircuit dysfunction in genetic models of neurodevelopmental disorders: focus on Mecp2 and Met
Gordon M. G. Shepherd et al.
CURRENT OPINION IN NEUROBIOLOGY (2011)
Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations
Kirstine Ravn et al.
ORPHANET JOURNAL OF RARE DISEASES (2011)
Repressor element 1 silencing transcription factor (REST) controls radial migration and temporal neuronal specification during neocortical development
Gail Mandel et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Fast and accurate long-read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2010)
EphB-Mediated Degradation of the RhoA GEF Ephexin5 Relieves a Developmental Brake on Excitatory Synapse Formation
Seth S. Margolis et al.
CELL (2010)
Partial silencing of methyl cytosine protein binding 2 (MECP2) in mesenchymal stem cells induces senescence with an increase in damaged DNA
Tiziana Squillaro et al.
FASEB JOURNAL (2010)
Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels in Olfactory Sensory Neurons Regulate Axon Extension and Glomerular Formation
Arie S. Mobley et al.
JOURNAL OF NEUROSCIENCE (2010)
L1 retrotransposition in neurons is modulated by MeCP2
Alysson R. Muotri et al.
NATURE (2010)
DNA resection in eukaryotes: deciding how to fix the break
Pablo Huertas
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2010)
The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function
David Warde-Farley et al.
NUCLEIC ACIDS RESEARCH (2010)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Mouse models of DNA double-strand break repair and neurological disease
Pierre-Olivier Frappart et al.
DNA REPAIR (2008)
Liver-specific deletion of histone deacetylase 3 disrupts metabolic transcriptional networks
Sarah K. Knutson et al.
EMBO JOURNAL (2008)
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
Ivana Matera et al.
HUMAN MOLECULAR GENETICS (2008)
The actin-binding protein Abp1 controls dendritic spine morphology and is important for spine head and synapse formation
Akvile Haeckel et al.
JOURNAL OF NEUROSCIENCE (2008)
MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number
Hsiao-Tuan Chao et al.
NEURON (2007)
Lipid specific activation of the murine P4-ATPase Atp8a1 (ATPase II)
JK Paterson et al.
BIOCHEMISTRY (2006)
Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse
JL Moran et al.
GENOME RESEARCH (2006)
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
Thierry Bienvenu et al.
NATURE REVIEWS GENETICS (2006)
REST and its corepressors mediate plasticity of neuronal gene chromatin throughout neurogenesis
N Ballas et al.
CELL (2005)
The Birc6 (Bruce) gene regulates p53 and the mitochondrial pathway of apoptosis and is essential for mouse embryonic development
JY Ren et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Suppressor screen in Mpl-/- mice:: c-Myb mutation causes supraphysiological production of platelets in the absence of thrombopoietin signaling
MR Carpinelli et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Rett syndrome: A prototypical neurodevelopmental disorder
JL Neul et al.
NEUROSCIENTIST (2004)
BRUCE, a giant E2/E3 ubiquitin ligase and inhibitor of apoptosis protein of the trans-Golgi network, is required for normal placenta development and mouse survival
K Lotz et al.
MOLECULAR AND CELLULAR BIOLOGY (2004)
Functional genetic analysis of mouse chromosome 11
BT Kile et al.
NATURE (2003)
Knockout of the cholesterol 24-hydroxylase gene in mice reveals a brain-specific mechanism of cholesterol turnover
EG Lund et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Cytoscape: A software environment for integrated models of biomolecular interaction networks
P Shannon et al.
GENOME RESEARCH (2003)
Balanced X chromosome inactivation patterns in the Rett syndrome brain
MD Shahbazian et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
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)
分享论文
