Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
Chen, Richard Z., Akbarian, Schahram, Tudor, Matthew, Jaenisch, Rudolf·2001·Nature Genetics
DOI 10.1038/85906
Cited by (1,001)
Items 101–200 of 1,001
- Deletion of Mecp2 in Sim1-Expressing Neurons Reveals a Critical Role for MeCP2 in Feeding Behavior, Aggression, and the Response to StressFyffe, Sharyl L., Neul, Jeff L., Samaco, Rodney C., Chao, Hsiao-Tuan, Ben-Shachar, Shay, Moretti, Paolo, McGill, Bryan E., Goulding, Evan H., Sullivan, Elinor, Tecott, Laurence H. et al. · 2008 · Neuron
- Genetic Alterations of DNA Methylation Machinery in Human DiseasesTewfik Hamidi, Anup Kumar Singh, Taiping Chen · 2015 · Epigenomics
- Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalitiesRodney C. Samaco, Caleigh Mandel‐Brehm, Hsiao-Tuan Chao, Christopher Scott Ward, Sharyl L. Fyffe-Maricich, Jun Tao Ren, Κ. Hyland, Christina Thaller B, Stephen M. Maricich, Peter Humphreys et al. · 2009 · Proceedings of the National Academy of Sciences
- Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivoHao Li, Jonathan C. Radford, Michael J. Ragusa, Katherine L. Shea, Scott R. McKercher, Jeffrey D. Zaremba, Walid Soussou, Zhiguo Nie, Yeon‐Joo Kang, Nobuki Nakanishi et al. · 2008 · Proceedings of the National Academy of Sciences
- Rett syndrome: insights into genetic, molecular and circuit mechanismsJacque Pak Kan Ip, Nikolaos Mellios, Mriganka Sur · 2018 · Nature reviews. Neuroscience
- Brain-Derived Neurotrophic Factor Expression and Respiratory Function Improve after Ampakine Treatment in a Mouse Model of Rett SyndromeMichaël Ogier, Hong Wang, Elizabeth J. Hong, Qifang Wang, Michael E. Greenberg, David Miles Katz · 2007 · Journal of Neuroscience
- NKCC1 Chloride Importer Antagonists Attenuate Many Neurological and Psychiatric DisordersYehezkel Ben‐Ari · 2017 · Trends in Neurosciences
- Monogenic causes of X-linked mental retardationJamel Chelly, Jean‐Louis Mandel · 2001 · Nature Reviews Genetics
- Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neuronsSmrt, Richard D., Eaves-Egenes, Julialea, Barkho, Basam Z., Santistevan, Nicholas J., Zhao, Chunmei, Aimone, James B., Gage, Fred H., Zhao, Xinyu · 2007 · Neurobiology of Disease
- Postnatal Loss of Methyl-CpG Binding Protein 2 in the Forebrain is Sufficient to Mediate Behavioral Aspects of Rett Syndrome in MiceTerry Gemelli, Olivier Berton, Erika D. Nelson, Linda I. Perrotti, Rudolf Jaenisch, Lisa M. Monteggia · 2005 · Biological Psychiatry
- Methyl-CpG binding proteins: specialized transcriptional repressors or structural components of chromatin?Thomas Clouaire, Irina Stancheva · 2008 · Cellular and Molecular Life Sciences
- Reading the unique DNA methylation landscape of the brain: Non-CpG methylation, hydroxymethylation, and MeCP2Kinde, Benyam, Gabel, Harrison W., Gilbert, Caitlin S., Griffith, Eric C., Greenberg, Michael E. · 2015 · Proceedings of the National Academy of Sciences
- A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndromeBuchovecky, Christie M, Turley, Stephen D, Brown, Hannah M, Kyle, Stephanie M, McDonald, Jeffrey G, Liu, Benny, Pieper, Andrew A, Huang, Wenhui, Katz, David M, Russell, David W et al. · 2013 · Nature Genetics
- Early Defects of GABAergic Synapses in the Brain Stem of a MeCP2 Mouse Model of Rett SyndromeLucian Medrihan, Evangelia Tantalaki, Gayane Aramuni, Vardanush Sargsyan, Irina Dudanova, Markus Missler, Weiqi Zhang · 2007 · Journal of Neurophysiology
- Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responsesGoffin, Darren, Allen, Megan, Zhang, Le, Amorim, Maria, Wang, I-Ting Judy, Reyes, Arith-Ruth S, Mercado-Berton, Amy, Ong, Caroline, Cohen, Sonia, Hu, Linda et al. · 2012 · Nature Neuroscience
- Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological functionJifang Tao, Keping Hu, Qiang Chang, Hao Wu, Nicholas E. Sherman, Keri Martinowich, Robert J. Klose, Carolyn Schanen, Rudolf Jaenisch, Weidong Wang et al. · 2009 · Proceedings of the National Academy of Sciences
- An AT-hook domain in MeCP2 determines the clinical course of Rett syndrome and related disordersBaker, Steven Andrew, Chen, Lin, Wilkins, Angela Dawn, Yu, Peng, Lichtarge, Olivier, Zoghbi, Huda Yahya · 2013 · Cell
- Common marmoset as a new model animal for neuroscience research and genome editing technologyNoriyuki Kishi, Kenya Sato, Erika Sasaki, Hideyuki Okano · 2014 · Development Growth & Differentiation
- Reduced AKT/mTOR signaling and protein synthesis dysregulation in a Rett syndrome animal modelRicciardi, Sara, Boggio, Elena M., Grosso, Stefano, Lonetti, Giuseppina, Forlani, Greta, Stefanelli, Gilda, Calcagno, Eleonora, Morello, Noemi, Landsberger, Nicoletta, Biffo, Stefano et al. · 2011 · Human Molecular Genetics
- The Ski protein family is required for MeCP2-mediated transcriptional repression.Kokura, Kenji, Kaul, Sunil C., Wadhwa, Renu, Nomura, Teruaki, Khan, Md Matiullah, Shinagawa, Toshie, Yasukawa, Takashi, Colmenares, Clemencia, Ishii, Shunsuke · 2001 · Journal of Biological Chemistry
- Delayed Maturation of Neuronal Architecture and Synaptogenesis in Cerebral Cortex of<i>Mecp2</i>-Deficient MiceFukuda, Tetsuya, Itoh, Masayuki, Ichikawa, Tomio, Washiyama, Kazuo, Goto, Yu-ichi · 2005 · Journal of Neuropathology & Experimental Neurology
- MECP2 disorders: from the clinic to mice and backLombardi, Laura Marie, Baker, Steven Andrew, Zoghbi, Huda Yahya · 2015 · Journal of Clinical Investigation
- Dicer loss in striatal neurons produces behavioral and neuroanatomical phenotypes in the absence of neurodegenerationTrinna L. Cuellar, Tigwa H. Davis, Peter T. Nelson, Gabriel B. Loeb, Brian D. Harfe, Erik M. Ullian, Michael T. McManus · 2008 · Proceedings of the National Academy of Sciences
- Systemic Delivery of MeCP2 Rescues Behavioral and Cellular Deficits in Female Mouse Models of Rett SyndromeSaurabh K. Garg†, Daniel T. Lioy, Hélène Cheval, James C. McGann, John M. Bissonnette, Matthew J. Murtha, Kevin D. Foust, Brian K. Kaspar, Adrian Peter Bird, Gail Mandel · 2013 · Journal of Neuroscience
- Molecular genetics of autism spectrum disorderJeremy M. Veenstra-VanderWeele, Edwin H. Cook · 2004 · Molecular Psychiatry
- Gene expression analysis exposes mitochondrial abnormalities in a mouse model of Rett syndromeKriaucionis, Skirmantas, Paterson, Andrew, Curtis, John, Guy, Jacky, MacLeod, Nikki, Bird, Adrian · 2006 · Molecular and Cellular Biology
- MeCP2-Dependent Transcriptional Repression Regulates Excitatory NeurotransmissionErika D. Nelson, Ege T. Kavalali, Lisa M. Monteggia · 2006 · Current Biology
- G ENETIC E FFECTS OF M ETHYLATION D IETSIgnatia B. Van den Veyver · 2002 · Annual Review of Nutrition
- High-Throughput, High-Resolution Mapping of Protein Localization in Mammalian Brain by In Vivo Genome EditingTakayasu Mikuni, Jun Nishiyama, Ye Sun, Naomi Kamasawa, Ryohei Yasuda · 2016 · Cell
- Rett syndrome: a neurological disorder with metabolic componentsKyle, Stephanie M., Vashi, Neeti, Justice, Monica J. · 2018 · Open Biology
- Rett syndrome: clinical review and genetic updateLinda S. Weaving, C J Ellaway, Jozef Gécz, John Christodoulou · 2005 · Journal of Medical Genetics
- Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndromeKun‐Yong Kim, Eriona Hysolli, In‐Hyun Park · 2011 · Proceedings of the National Academy of Sciences
- Neurophysiology and Regulation of the Balance Between Excitation and Inhibition in Neocortical CircuitsRoberta Tatti, Melissa S. Haley, Olivia K. Swanson, Tenzin Tselha, Arianna Maffei · 2016 · Biological Psychiatry
- The Role of MeCP2 in Brain Development and Neurodevelopmental DisordersMichael L. Gonzales, Janine M. LaSalle · 2010 · Current Psychiatry Reports
- Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of miceGregory J. Pelka, Catherine M. Watson, Tania Radziewic, Melinda Hayward, Hooshang Lahooti, John Christodoulou, Patrick Tam · 2006 · Brain
- Preclinical research in Rett syndrome: setting the foundation for translational successKatz, David M., Berger-Sweeney, Joanne E., Eubanks, James H., Justice, Monica J., Neul, Jeffrey L., Pozzo-Miller, Lucas, Blue, Mary E., Christian, Diana, Crawley, Jacqueline N., Giustetto, Maurizio et al. · 2012 · Disease Models & Mechanisms
- Ventral hippocampal projections to the medial prefrontal cortex regulate social memoryPhillips, Mary L, Robinson, Holly Anne, Pozzo-Miller, Lucas · 2019 · eLife
- Clinical and biological progress over 50 years in Rett syndromeHelen Leonard, Stuart Cobb, Jenny Anne Downs · 2016 · Nature Reviews Neurology
- Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus MonkeysChen, Yongchang, Yu, Juehua, Niu, Yuyu, Qin, Dongdong, Liu, Hailiang, Li, Gang, Hu, Yingzhou, Wang, Jiaojian, Lu, Yi, Kang, Yu et al. · 2017 · Cell
- Genetic controls balancing excitatory and inhibitory synaptogenesis in neurodevelopmental disorder modelsGatto · 2010 · Frontiers in Synaptic Neuroscience
- Isogenic Pairs of Wild Type and Mutant Induced Pluripotent Stem Cell (iPSC) Lines from Rett Syndrome Patients as In Vitro Disease ModelGene E. Ananiev, Emily Cunningham Williams, Hongda Li, Qiang Chang · 2011 · PLoS ONE
- Gene Expression Profiling in Postmortem Rett Syndrome Brain: Differential Gene Expression and Patient ClassificationCarlo Colantuoni, Ok‐Hee Jeon, Karim Hyder, Alex A. Chenchik, Anis H. Khimani, Vinodh Narayanan, Eric P. Hoffman, Walter E. Kaufmann, Sakkubai Naidu, Jonathan Pevsner · 2001 · Neurobiology of Disease
- Wild-type microglia do not reverse pathology in mouse models of Rett syndromeJieqi Wang, Eike Wegener, Teng-Wei Huang, Smitha P. Sripathy, Hector De Jesús‐Cortés, Pin Xu, Stephanie Tran, Whitney Knobbe, Vid Leko, Jeremiah K. Britt et al. · 2015 · Nature
- Early Environmental Enrichment Moderates the Behavioral and Synaptic Phenotype of MeCP2 Null MiceGiuseppina Lonetti, Andrea Angelucci, Laura Morando, Elena Maria Boggio, Maurizio Giustetto, Tommaso Pizzorusso · 2010 · Biological Psychiatry
- Mutant astrocytes differentiated from Rett syndrome patients-specific iPSCs have adverse effects on wild-type neuronsEmily Cunningham Williams, Xiaofen Zhong, Ahmed Mohamed, Ronghui Li, Yan Liu, Qiping Dong, Gene E. Ananiev, Jonathan Chern Choong Mok, Benjamin Ray Lin, Jianfeng Lü et al. · 2014 · Human Molecular Genetics
- Evidence that direct inhibition of transcription factor binding is the prevailing mode of gene and repeat repression by DNA methylationSebastian Kaluscha, Silvia Domcke, Christiane Wirbelauer, Michael Beda Stadler, Sevi Durdu, Lukas Burger, Dirk Schübeler · 2022 · Nature Genetics
- Rett Syndrome and MeCP2: Linking Epigenetics and Neuronal FunctionMona D. Shahbazian, Huda Yahya Zoghbi · 2002 · The American Journal of Human Genetics
- Role of BDNF epigenetics in activity-dependent neuronal plasticityKarpova, Nina N. · 2014 · Neuropharmacology
- Mapping Pathological Phenotypes in a Mouse Model of CDKL5 DisorderElena Amendola, Yang Zhan, Camilla Mattucci, Enrico Castroflorio, Eleonora Calcagno, Claudia Fuchs, Giuseppina Lonetti, Davide Silingardi, Alexei L. Vyssotski, Dominika Farley et al. · 2014 · PLoS ONE
- Behavioral and anatomical abnormalities in Mecp2 mutant mice: A model for Rett syndromeNancy A. Stearns, Laura R. Schaevitz, Heather L. Bowling, Nupur Nag, U.V. Berger, Joanne E. Berger-Sweeney · 2007 · Neuroscience
- MeCP2 Is Critical for Maintaining Mature Neuronal Networks and Global Brain Anatomy during Late Stages of Postnatal Brain Development and in the Mature Adult BrainMinh Vu Chuong Nguyen, Fu Du, Christy A. Felice, Xiu Shan, A. Nigam, Gail Mandel, J. K. Robinson, Nurit Ballas · 2012 · Journal of Neuroscience
- Advances in behavioral genetics: mouse models of autismSheryl S. Moy, Jessica J. Nadler · 2007 · Molecular Psychiatry
- Reversing Neurodevelopmental Disorders in AdultsEhninger, Dan, Li, Weidong, Fox, Kevin, Stryker, Michael P., Silva, Alcino J. · 2008 · Neuron
- Ablation of de novo DNA methyltransferase Dnmt3a in the nervous system leads to neuromuscular defects and shortened lifespanSuzanne P. Nguyen, Konstantinos Meletis, Dongdong Fu, Sonal Jhaveri, Rudolf Jaenisch · 2007 · Developmental Dynamics
- Isolation of neuronal chromatin from brain tissueJiang, Yan, Matevossian, Anouch, Huang, Hsien-Sung, Straubhaar, Juerg, Akbarian, Schahram · 2008 · BMC Neuroscience
- Environmental enrichment ameliorates a motor coordination deficit in a mouse model of Rett syndrome –<i>Mecp2</i>gene dosage effects and BDNF expressionKondo, Mari, Gray, Laura J., Pelka, Gregory J., Christodoulou, John, Tam, Patrick P. L., Hannan, Anthony J. · 2008 · European Journal of Neuroscience
- DNA Methylation in Plants: Relationship to Small RNAs and Histone Modifications, and Functions in Transposon InactivationHidetoshi Saze, Kazuo Tsugane, Tatsuo Kanno, Takehiro Nishimura · 2012 · Plant and Cell Physiology
- Methyl-CpG-binding protein 2 represses LINE-1 expression and retrotransposition but not Alu transcriptionFang Yu · 2001 · Nucleic Acids Research
- A partial loss of function allele of Methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndromeRodney C. Samaco, John Denis Fryer, Jun Tao Ren, Sharyl L. Fyffe-Maricich, H.-T. Chao, Y. Sun, John J. Greer, Huda Yahya Zoghbi, Jeffrey Lorenz Neul · 2008 · Human Molecular Genetics
- The Rett Syndrome Behaviour Questionnaire (RSBQ): refining the behavioural phenotype of Rett syndromeRebecca H. Mount, Tony Charman, Richard Patrick Hastings, Sheena Reilly, Hilary Cass · 2002 · Journal of Child Psychology and Psychiatry
- Breathing disorders in Rett syndrome: Progressive neurochemical dysfunction in the respiratory network after birthDavid Miles Katz, Mathias Dutschmann, Jan‐Marino Ramirez, Ge´rard Hilaire · 2009 · Respiratory Physiology & Neurobiology
- Induced pluripotent stem cells (iPSCs) and neurological disease modeling: progress and promisesMaria Carolina Marchetto, Kristen Brennand, Leah F. Boyer, Fred H. Gage · 2011 · Human Molecular Genetics
- Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndromeUlrike A. Nuber, Skirmantas Kriaučionis, Tim C. Roloff, Jacky Guy, Jim Selfridge, Christine Steinhoff, Ralph Schulz, Bettina Lipkowitz, Hans‐Hilger Ropers, Megan C. Holmes et al. · 2005 · Human Molecular Genetics
- DNA hypomethylation restricted to the murine forebrain induces cortical degeneration and impairs postnatal neuronal maturationHutnick, Leah K., Golshani, Peyman, Namihira, Masakasu, Xue, Zhigang, Matynia, Anna, Yang, X. William, Silva, Alcino J., Schweizer, Felix E., Fan, Guoping · 2009 · Human Molecular Genetics
- The Impact of MeCP2 Loss- or Gain-of-Function on Synaptic PlasticityElisa S. Na, Erika D. Nelson, Ege T. Kavalali, Lisa M. Monteggia · 2012 · Neuropsychopharmacology
- Female Mecp2+/− mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studiesRodney C. Samaco, Christopher Michael McGraw, Christopher Scott Ward, Yaling Sun, Jeffrey Lorenz Neul, Huda Yahya Zoghbi · 2012 · Human Molecular Genetics
- Genome-wide analysis reveals methyl-CpG–binding protein 2–dependent regulation of microRNAs in a mouse model of Rett syndromeHao Wu, Jifang Tao, Pauline J. Chen, Atif Shahab, Weihong Ge, Ronald P. Hart, Xiaoan Ruan, Yijun Ruan, Yi Eve Sun · 2010 · Proceedings of the National Academy of Sciences
- The Role of DNA Methylation in the Central Nervous System and Neuropsychiatric DisordersJian Feng, Guoping Fan · 2009 · International review of neurobiology
- Multiple Modes of Interaction between the Methylated DNA Binding Protein MeCP2 and ChromatinNikitina Tv, Xi Shi, Rajarshi P. Ghosh, Rachel A. Horowitz-Scherer, Jeffrey C. Hansen, Christopher L. F. Woodcock · 2006 · Molecular and Cellular Biology
- Exogenous Brain-Derived Neurotrophic Factor Rescues Synaptic Dysfunction inMecp2-Null MiceDavid D. Kline, Michaël Ogier, Diana Lee Kunze, David Miles Katz · 2010 · Journal of Neuroscience
- Synaptic Imbalance, Stereotypies, and Impaired Social Interactions in Mice with Altered Neuroligin 2 ExpressionRochelle M. Hines, Long‐Jun Wu, Dustin J. Hines, Hendrik W. Steenland, S. Mansour, Regina Dahlhaus, Roshni Rebecca Singaraja, Xiaoxia Cao, Esther M. Sammler, Sheriar G. Hormuzdi et al. · 2008 · Journal of Neuroscience
- The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cellsJung, Benjamin P., Jugloff, Denis G.M., Zhang, Guangming, Logan, Richard, Brown, Stephanie, Eubanks, James H. · 2003 · Journal of Neurobiology
- BDNF deregulation in Rett syndromeWei Li, Lucas D. Pozzo‐Miller · 2013 · Neuropharmacology
- Advances in understanding of Rett syndrome and MECP2 duplication syndrome: prospects for future therapiesAlexander J. Sandweiss, Vicky L. Brandt, Huda Yahya Zoghbi · 2020 · The Lancet Neurology
- RettBASE: The IRSA MECP2 variation database—a new mutation database in evolutionJohn Christodoulou, Andrew J. Grimm, Tony Maher, Bruce Bennetts · 2003 · Human Mutation
- Rett Syndrome and MeCP2Vichithra R. B. Liyanage, Mojgan Rastegar · 2014 · NeuroMolecular Medicine
- The Molecular Basis of MeCP2 Function in the BrainRebekah Tillotson, Adrian Peter Bird · 2019 · Journal of Molecular Biology
- The contribution of GABAergic dysfunction to neurodevelopmental disordersKartik Ramamoorthi, Yingxi Lin · 2011 · Trends in Molecular Medicine
- Zebrafish as an Animal Model for Drug Discovery in Parkinson’s Disease and Other Movement Disorders: A Systematic ReviewRita L. Vaz, Tiago F. Outeiro, Joaquim José Ferreira · 2018 · Frontiers in Neurology
- Components of the DNA Methylation System of Chromatin Control Are RNA-binding ProteinsLinda Jeffery, Sara Nakielny · 2004 · Journal of Biological Chemistry
- Rett Syndrome: A Prototypical Neurodevelopmental DisorderJeffrey Lorenz Neul, Huda Yahya Zoghbi · 2004 · The Neuroscientist
- Epigenetic dysregulation in cognitive disordersJohannes Gräff, Isabelle M. Mansuy · 2009 · European Journal of Neuroscience
- Comparative study of methyl-CpG-binding domain proteinsTim C. Roloff, Hans‐Hilger Ropers, Ulrike A. Nuber · 2003 · BMC Genomics
- Loss of Histone Deacetylase 2 Improves Working Memory and Accelerates Extinction LearningMichael J. Morris, Melissa Mahgoub, Elisa S. Na, Heena Pranav, Lisa M. Monteggia · 2013 · Journal of Neuroscience
- Brain Plasticity and Disease: A Matter of InhibitionLaura Baroncelli, Chiara Braschi, Maria Spolidoro, Tatjana Begenisic, Lamberto Maffei, Alessandro Sale · 2011 · Neural Plasticity
- Behavioral profiles of mouse models for autism spectrum disordersElodie Ey, Claire S. Leblond, Thomas Bourgeron · 2011 · Autism Research
- Substance P-Mediated Modulation of Pacemaker Properties in the Mammalian Respiratory NetworkFernando Peña‐Ortega, Jan‐Marino Ramirez · 2004 · Journal of Neuroscience
- Morphological and functional reversal of phenotypes in a mouse model of Rett syndromeRobinson, Lianne, Guy, Jacky, McKay, Leanne, Brockett, Emma, Spike, Rosemary C., Selfridge, Jim, De Sousa, Dina, Merusi, Cara, Riedel, Gernot, Bird, Adrian et al. · 2012 · Brain
- Modeling psychiatric disorders for developing effective treatmentsKaiser, Tobias, Feng, Guoping · 2015 · Nature Medicine
- Improved Survival and Reduced Phenotypic Severity Following AAV9/MECP2 Gene Transfer to Neonatal and Juvenile Male Mecp2 Knockout MiceKamal K.E. Gadalla, Mark E.S. Bailey, ROSEMARY C. SPIKE, Paul D. Ross, Kenton Woodard, Sahana Nagabhushan Kalburgi, Lavanya Bachaboina, Jie V. Deng, Anne E. West, Richard Jude Samulski et al. · 2012 · Molecular Therapy
- Impaired Cerebellar Development and Function in Mice Lacking CAPS2, a Protein Involved in Neurotrophin ReleaseTetsushi Sadakata, Wataru Kakegawa, Akira Mizoguchi, Miwa Washida, Ritsuko Katoh‐Semba, Fumihiro Shutoh, Takehito Okamoto, Hisako Nakashima, Kazushi Kimura, Mika Tanaka et al. · 2007 · Journal of Neuroscience
- Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2−/y knockout miceGeorg Martin Stettner, Peter Huppke, Cornelia Brendel, Diethelm Wolfgang Richter, Jutta Gärtner, Mathias Dutschmann · 2007 · The Journal of Physiology
- Dysregulation of Brain-Derived Neurotrophic Factor Expression and Neurosecretory Function in<i>Mecp2</i>Null MiceWang, Hong, Chan, Shyue-an, Ogier, Michael, Hellard, David, Wang, Qifang, Smith, Corey, Katz, David M. · 2006 · The Journal of Neuroscience
- Increased binding of MeCP2 to the GAD1 and RELN promoters may be mediated by an enrichment of 5-hmC in autism spectrum disorder (ASD) cerebellumZhubi, A, Chen, Y, Dong, E, Cook, E H, Guidotti, A, Grayson, D R · 2014 · Translational Psychiatry
- Brain Activity Mapping in
<i>Mecp2</i>
Mutant Mice Reveals Functional Deficits in Forebrain Circuits, Including Key Nodes in the Default Mode Network, that are Reversed with Ketamine TreatmentKron, Miriam, Howell, C. James, Adams, Ian T., Ransbottom, Michael, Christian, Diana, Ogier, Michael, Katz, David M. · 2012 · The Journal of Neuroscience
- The MeCP2‐null mouse hippocampus displays altered basal inhibitory rhythms and is prone to hyperexcitabilityLiang Zhang, Jiwei He, Denis G.M. Jugloff, James H. Eubanks · 2007 · Hippocampus
- Conditional alleles in mice: Practical considerations for tissue‐specific knockoutsKin Ming Kwan · 2002 · genesis
- Enhanced synapse remodelling as a common phenotype in mouse models of autismIsshiki, Masaaki, Tanaka, Shinji, Kuriu, Toshihiko, Tabuchi, Katsuhiko, Takumi, Toru, Okabe, Shigeo · 2014 · Nature Communications
- Loss of MeCP2 in Parvalbumin-and Somatostatin-Expressing Neurons in Mice Leads to Distinct Rett Syndrome-like PhenotypesAya Ito, Kerstin Ure, Hongmei Chen, John W. Swann, Huda Yahya Zoghbi · 2015 · Neuron
- The influences of diet and exercise on mental health through hormesisFernando Gómez‐Pinilla · 2007 · Ageing Research Reviews