Christopher A. Walsh Division of Genetics, Department of Medicine Boston Children's Hospital Biography Publications Institution JoVE Articles Christopher A. Walsh has not added a biography. If you are Christopher A. Walsh and would like to personalize this page please email our Author Liaison for assistance. Publications Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan American Journal of Human Genetics. Feb, 2013 | Pubmed ID: 23453667 Using Whole-Exome Sequencing to Identify Inherited Causes of Autism Neuron. Jan, 2013 | Pubmed ID: 23352163 Schizencephaly: Association with Young Maternal Age, Alcohol Use, and Lack of Prenatal Care Journal of Child Neurology. Feb, 2013 | Pubmed ID: 23266945 Delineation of the Clinical, Molecular and Cellular Aspects of Novel JAM3 Mutations Underlying the Autosomal Recessive Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts Human Mutation. Mar, 2013 | Pubmed ID: 23255084 Microcephaly Gene Links Trithorax and REST/NRSF to Control Neural Stem Cell Proliferation and Differentiation Cell. Nov, 2012 | Pubmed ID: 23178126 Single-neuron Sequencing Analysis of L1 Retrotransposition and Somatic Mutation in the Human Brain Cell. Oct, 2012 | Pubmed ID: 23101622 Common Genetic Variants, Acting Additively, Are a Major Source of Risk for Autism Molecular Autism. 2012 | Pubmed ID: 23067556 CHMP1A Encodes an Essential Regulator of BMI1-INK4A in Cerebellar Development Nature Genetics. Nov, 2012 | Pubmed ID: 23023333 Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations As a Cause of Walker-Warburg Syndrome American Journal of Human Genetics. Sep, 2012 | Pubmed ID: 22958903 Molecular Basis for Specific Regulation of Neuronal Kinesin-3 Motors by Doublecortin Family Proteins Molecular Cell. Sep, 2012 | Pubmed ID: 22857951 Homozygous PLCB1 Deletion Associated with Malignant Migrating Partial Seizures in Infancy Epilepsia. Aug, 2012 | Pubmed ID: 22690784 Whole-exome Sequencing and Homozygosity Analysis Implicate Depolarization-regulated Neuronal Genes in Autism PLoS Genetics. 2012 | Pubmed ID: 22511880 Impact of PNKP Mutations Associated with Microcephaly, Seizures and Developmental Delay on Enzyme Activity and DNA Strand Break Repair Nucleic Acids Research. Aug, 2012 | Pubmed ID: 22508754 Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations Neuron. Apr, 2012 | Pubmed ID: 22500628 Expanding the Spectrum of Rearrangements Involving Chromosome 19: a Mild Phenotype Associated with a 19p13.12-p13.13 Deletion American Journal of Medical Genetics. Part A. Apr, 2012 | Pubmed ID: 22419660 Variable Disease Severity in Saudi Arabian and Sudanese Families with C.3924 + 2 T > C Mutation of LAMA2 BMC Research Notes. 2011 | Pubmed ID: 22166137 Phenotypic Heterogeneity in Woodhouse-Sakati Syndrome: Two New Families with a Mutation in the C2orf37 Gene American Journal of Medical Genetics. Part A. Nov, 2011 | Pubmed ID: 21964978 Neurogenesis at the Brain-cerebrospinal Fluid Interface Annual Review of Cell and Developmental Biology. 2011 | Pubmed ID: 21801012 Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism Neuron. Jun, 2011 | Pubmed ID: 21658581 COL4A1 Mutations Cause Ocular Dysgenesis, Neuronal Localization Defects, and Myopathy in Mice and Walker-Warburg Syndrome in Humans PLoS Genetics. May, 2011 | Pubmed ID: 21625620 Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly [corrected] American Journal of Human Genetics. May, 2011 | Pubmed ID: 21529751 The Cerebrospinal Fluid Provides a Proliferative Niche for Neural Progenitor Cells Neuron. Mar, 2011 | Pubmed ID: 21382550 What Disorders of Cortical Development Tell Us About the Cortex: One Plus One Does Not Always Make Two Current Opinion in Genetics & Development. Jun, 2011 | Pubmed ID: 21288712 A Forward Genetic Screen with a Thalamocortical Axon Reporter Mouse Yields Novel Neurodevelopment Mutants and a Distinct Emx2 Mutant Phenotype Neural Development. 2011 | Pubmed ID: 21214893 A Homozygous Mutation in the Tight-junction Protein JAM3 Causes Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts American Journal of Human Genetics. Dec, 2010 | Pubmed ID: 21109224 SOBP is Mutated in Syndromic and Nonsyndromic Intellectual Disability and is Highly Expressed in the Brain Limbic System American Journal of Human Genetics. Nov, 2010 | Pubmed ID: 21035105 Allelic Diversity in Human Developmental Neurogenetics: Insights into Biology and Disease Neuron. Oct, 2010 | Pubmed ID: 20955932 Candidate Gene Sequencing of LHX2, HESX1, and SOX2 in a Large Schizencephaly Cohort American Journal of Medical Genetics. Part A. Nov, 2010 | Pubmed ID: 20949537 Mutations in WDR62, Encoding a Centrosome-associated Protein, Cause Microcephaly with Simplified Gyri and Abnormal Cortical Architecture Nature Genetics. Nov, 2010 | Pubmed ID: 20890278 Mutation in PQBP1 is Associated with Periventricular Heterotopia American Journal of Medical Genetics. Part A. Nov, 2010 | Pubmed ID: 20886605 Cux1 and Cux2 Regulate Dendritic Branching, Spine Morphology, and Synapses of the Upper Layer Neurons of the Cortex Neuron. May, 2010 | Pubmed ID: 20510857 Deletions of NRXN1 (neurexin-1) Predispose to a Wide Spectrum of Developmental Disorders American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. Jun, 2010 | Pubmed ID: 20468056 Cdk5rap2 Regulates Centrosome Function and Chromosome Segregation in Neuronal Progenitors Development (Cambridge, England). Jun, 2010 | Pubmed ID: 20460369 Developmental and Degenerative Features in a Complicated Spastic Paraplegia Annals of Neurology. Apr, 2010 | Pubmed ID: 20437587 The Apical Complex Couples Cell Fate and Cell Survival to Cerebral Cortical Development Neuron. Apr, 2010 | Pubmed ID: 20399730 The Exon Junction Complex Component Magoh Controls Brain Size by Regulating Neural Stem Cell Division Nature Neuroscience. May, 2010 | Pubmed ID: 20364144 Genetic Malformations of the Human Frontal Lobe Epilepsia. Feb, 2010 | Pubmed ID: 20331705 Clinical Genetic Testing for Patients with Autism Spectrum Disorders Pediatrics. Apr, 2010 | Pubmed ID: 20231187 Mutations in PNKP Cause Microcephaly, Seizures and Defects in DNA Repair Nature Genetics. Mar, 2010 | Pubmed ID: 20118933 Tgif1 and Tgif2 Regulate Nodal Signaling and Are Required for Gastrulation Development (Cambridge, England). Jan, 2010 | Pubmed ID: 20040491 The Syndrome of Perisylvian Polymicrogyria with Congenital Arthrogryposis Brain & Development. Aug, 2010 | Pubmed ID: 19751967 A Truncating Mutation of TRAPPC9 is Associated with Autosomal-recessive Intellectual Disability and Postnatal Microcephaly American Journal of Human Genetics. Dec, 2009 | Pubmed ID: 20004763 Detecting Natural Selection by Empirical Comparison to Random Regions of the Genome Human Molecular Genetics. Dec, 2009 | Pubmed ID: 19783549 Transcription Factor Lmo4 Defines the Shape of Functional Areas in Developing Cortices and Regulates Sensorimotor Control Developmental Biology. Mar, 2009 | Pubmed ID: 19111533 Bilateral Frontoparietal Polymicrogyria, Lennox-Gastaut Syndrome, and GPR56 Gene Mutations Epilepsia. Jun, 2009 | Pubmed ID: 19016831 Disruption of Neural Progenitors Along the Ventricular and Subventricular Zones in Periventricular Heterotopia Human Molecular Genetics. Feb, 2009 | Pubmed ID: 18996916 Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome American Journal of Human Genetics. Dec, 2008 | Pubmed ID: 19026396 Autism and Brain Development Cell. Oct, 2008 | Pubmed ID: 18984148 Sequence Analysis of P21-activated Kinase 3 (PAK3) in Chronic Schizophrenia with Cognitive Impairment Schizophrenia Research. Dec, 2008 | Pubmed ID: 18805672 Ethnically Diverse Causes of Walker-Warburg Syndrome (WWS): FCMD Mutations Are a More Common Cause of WWS Outside of the Middle East Human Mutation. Nov, 2008 | Pubmed ID: 18752264 Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry Science (New York, N.Y.). Jul, 2008 | Pubmed ID: 18621663 Identification of Neural Outgrowth Genes Using Genome-wide RNAi PLoS Genetics. Jul, 2008 | Pubmed ID: 18604272 Donnai-Barrow Syndrome (DBS/FOAR) in a Child with a Homozygous LRP2 Mutation Due to Complete Chromosome 2 Paternal Isodisomy American Journal of Medical Genetics. Part A. Jul, 2008 | Pubmed ID: 18553518 Consistent Chromosome Abnormalities Identify Novel Polymicrogyria Loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2 American Journal of Medical Genetics. Part A. Jul, 2008 | Pubmed ID: 18536050 GPR56 Regulates Pial Basement Membrane Integrity and Cortical Lamination The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. May, 2008 | Pubmed ID: 18509043 Lis1-Nde1-dependent Neuronal Fate Control Determines Cerebral Cortical Size and Lamination Human Molecular Genetics. Aug, 2008 | Pubmed ID: 18469343 Association Between Microdeletion and Microduplication at 16p11.2 and Autism The New England Journal of Medicine. Feb, 2008 | Pubmed ID: 18184952 Cux-2 Controls the Proliferation of Neuronal Intermediate Precursors of the Cortical Subventricular Zone Cerebral Cortex (New York, N.Y. : 1991). Aug, 2008 | Pubmed ID: 18033766 Severe Muscle-eye-brain Disease is Associated with a Homozygous Mutation in the POMGnT1 Gene European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society. Mar, 2008 | Pubmed ID: 17881266 Genes That Control the Size of the Cerebral Cortex Novartis Foundation Symposium. 2007 | Pubmed ID: 18494253 A Novel Form of Lethal Microcephaly with Simplified Gyral Pattern and Brain Stem Hypoplasia American Journal of Medical Genetics. Part A. Dec, 2007 | Pubmed ID: 17975804 Development of a Focused Oligonucleotide-array Comparative Genomic Hybridization Chip for Clinical Diagnosis of Genomic Imbalance Clinical Chemistry. Dec, 2007 | Pubmed ID: 17901113 Doublecortin is Expressed in Articular Chondrocytes Biochemical and Biophysical Research Communications. Nov, 2007 | Pubmed ID: 17897623 A Comparative Proteomic Analysis of Human and Rat Embryonic Cerebrospinal Fluid Journal of Proteome Research. Sep, 2007 | Pubmed ID: 17696520 Mutations in LRP2, Which Encodes the Multiligand Receptor Megalin, Cause Donnai-Barrow and Facio-oculo-acoustico-renal Syndromes Nature Genetics. Aug, 2007 | Pubmed ID: 17632512 A 2-Mb Critical Region Implicated in the Microcephaly Associated with Terminal 1q Deletion Syndrome American Journal of Medical Genetics. Part A. Aug, 2007 | Pubmed ID: 17603806 Disease-associated Mutations Affect GPR56 Protein Trafficking and Cell Surface Expression Human Molecular Genetics. Aug, 2007 | Pubmed ID: 17576745 NFIA Haploinsufficiency is Associated with a CNS Malformation Syndrome and Urinary Tract Defects PLoS Genetics. May, 2007 | Pubmed ID: 17530927 Comprehensive EMX2 Genotyping of a Large Schizencephaly Case Series American Journal of Medical Genetics. Part A. Jun, 2007 | Pubmed ID: 17506092 Comment on "Ongoing Adaptive Evolution of ASPM, a Brain Size Determinant in Homo Sapiens" Science (New York, N.Y.). Apr, 2007 | Pubmed ID: 17446375 Both Doublecortin and Doublecortin-like Kinase Play a Role in Cortical Interneuron Migration The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. Apr, 2007 | Pubmed ID: 17409252 Insights into the Gyrification of Developing Ferret Brain by Magnetic Resonance Imaging Journal of Anatomy. Jan, 2007 | Pubmed ID: 17229284 The Role of RELN in Lissencephaly and Neuropsychiatric Disease American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. Jan, 2007 | Pubmed ID: 16958033 Filamin A (FLNA) is Required for Cell-cell Contact in Vascular Development and Cardiac Morphogenesis Proceedings of the National Academy of Sciences of the United States of America. Dec, 2006 | Pubmed ID: 17172441 Brain Evolution and Uniqueness in the Human Genome Cell. Sep, 2006 | Pubmed ID: 16990130 Molecular Approaches to Brain Asymmetry and Handedness Nature Reviews. Neuroscience. Aug, 2006 | Pubmed ID: 16858393 Deletion of Chromosome 1p36 is Associated with Periventricular Nodular Heterotopia American Journal of Medical Genetics. Part A. Aug, 2006 | Pubmed ID: 16835933 Mutated Nup62 Causes Autosomal Recessive Infantile Bilateral Striatal Necrosis Annals of Neurology. Aug, 2006 | Pubmed ID: 16786527 Genomic and Evolutionary Analyses of Asymmetrically Expressed Genes in Human Fetal Left and Right Cerebral Cortex Cerebral Cortex (New York, N.Y. : 1991). Jul, 2006 | Pubmed ID: 16766703 An Autosomal Recessive Form of Spastic Cerebral Palsy (CP) with Microcephaly and Mental Retardation American Journal of Medical Genetics. Part A. Jul, 2006 | Pubmed ID: 16761294 Periventricular Nodular Heterotopia and Williams Syndrome American Journal of Medical Genetics. Part A. Jun, 2006 | Pubmed ID: 16691586 Impaired Proliferation and Migration in Human Miller-Dieker Neural Precursors Annals of Neurology. Jul, 2006 | Pubmed ID: 16642511 Cerebellar Ataxia with Progressive Improvement Archives of Neurology. Apr, 2006 | Pubmed ID: 16606775 Impaired Neuronal Positioning and Dendritogenesis in the Neocortex After Cell-autonomous Dab1 Suppression The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. Feb, 2006 | Pubmed ID: 16467525 Neocortical Neuronal Arrangement in Miller Dieker Syndrome Acta Neuropathologica. May, 2006 | Pubmed ID: 16456669 Genetic Interactions Between Doublecortin and Doublecortin-like Kinase in Neuronal Migration and Axon Outgrowth Neuron. Jan, 2006 | Pubmed ID: 16387638 Periventricular Heterotopia: New Insights into Ehlers-Danlos Syndrome Clinical Medicine & Research. Nov, 2005 | Pubmed ID: 16303888 Genotype-phenotype Analysis of Human Frontoparietal Polymicrogyria Syndromes Annals of Neurology. Nov, 2005 | Pubmed ID: 16240336 Molecular Insights into Human Brain Evolution Nature. Sep, 2005 | Pubmed ID: 16136130 Characterization of Rho-GDIgamma and Rho-GDIalpha MRNA in the Developing and Mature Brain with an Analysis of Mice with Targeted Deletions of Rho-GDIgamma Brain Research. Aug, 2005 | Pubmed ID: 16054116 The Microcephaly ASPM Gene is Expressed in Proliferating Tissues and Encodes for a Mitotic Spindle Protein Human Molecular Genetics. Aug, 2005 | Pubmed ID: 15972725 Cytoplasmic LEK1 is a Regulator of Microtubule Function Through Its Interaction with the LIS1 Pathway Proceedings of the National Academy of Sciences of the United States of America. Jun, 2005 | Pubmed ID: 15939891 Early Asymmetry of Gene Transcription in Embryonic Human Left and Right Cerebral Cortex Science (New York, N.Y.). Jun, 2005 | Pubmed ID: 15894532 EMX2-independent Familial Schizencephaly: Clinical and Genetic Analyses American Journal of Medical Genetics. Part A. Jun, 2005 | Pubmed ID: 15887302 Targeted Disruption of Tgif, the Mouse Ortholog of a Human Holoprosencephaly Gene, Does Not Result in Holoprosencephaly in Mice Molecular and Cellular Biology. May, 2005 | Pubmed ID: 15831469 A Centrosomal Mechanism Involving CDK5RAP2 and CENPJ Controls Brain Size Nature Genetics. Apr, 2005 | Pubmed ID: 15793586 Mutations in POMT1 Are Found in a Minority of Patients with Walker-Warburg Syndrome American Journal of Medical Genetics. Part A. Feb, 2005 | Pubmed ID: 15637732 Directed Migration of Neural Stem Cells to Sites of CNS Injury by the Stromal Cell-derived Factor 1alpha/CXC Chemokine Receptor 4 Pathway Proceedings of the National Academy of Sciences of the United States of America. Dec, 2004 | Pubmed ID: 15608062 The Many Faces of Filamin: a Versatile Molecular Scaffold for Cell Motility and Signalling Nature Cell Biology. Nov, 2004 | Pubmed ID: 15516996 Mitotic Spindle Regulation by Nde1 Controls Cerebral Cortical Size Neuron. Oct, 2004 | Pubmed ID: 15473967 Expression of Cux-1 and Cux-2 in the Subventricular Zone and Upper Layers II-IV of the Cerebral Cortex The Journal of Comparative Neurology. Nov, 2004 | Pubmed ID: 15452856 Abnormal Cerebellar Development and Axonal Decussation Due to Mutations in AHI1 in Joubert Syndrome Nature Genetics. Sep, 2004 | Pubmed ID: 15322546 A Novel Signaling Mechanism in Brain Development Pediatric Research. Sep, 2004 | Pubmed ID: 15269343 Genetics of Disorders of Cortical Development Neuroimaging Clinics of North America. May, 2004 | Pubmed ID: 15182816 Etiological Heterogeneity of Familial Periventricular Heterotopia and Hydrocephalus Brain & Development. Aug, 2004 | Pubmed ID: 15165674 Genetic Basis of Developmental Malformations of the Cerebral Cortex Archives of Neurology. May, 2004 | Pubmed ID: 15148137 Accelerated Evolution of the ASPM Gene Controlling Brain Size Begins Prior to Human Brain Expansion PLoS Biology. May, 2004 | Pubmed ID: 15045028 G Protein-coupled Receptor-dependent Development of Human Frontal Cortex Science (New York, N.Y.). Mar, 2004 | Pubmed ID: 15044805 Development Current Opinion in Neurobiology. Feb, 2004 | Pubmed ID: 15018931 The Hyh Mutation Uncovers Roles for Alpha Snap in Apical Protein Localization and Control of Neural Cell Fate Nature Genetics. Mar, 2004 | Pubmed ID: 14758363 Mutations in ARFGEF2 Implicate Vesicle Trafficking in Neural Progenitor Proliferation and Migration in the Human Cerebral Cortex Nature Genetics. Jan, 2004 | Pubmed ID: 14647276 Mapping Form and Function in the Human Brain: the Emerging Field of Functional Neuroimaging in Cortical Malformations Epilepsy & Behavior : E&B. Dec, 2003 | Pubmed ID: 14698694 Protein-truncating Mutations in ASPM Cause Variable Reduction in Brain Size American Journal of Human Genetics. Nov, 2003 | Pubmed ID: 14574646 Developmental Genetic Malformations of the Cerebral Cortex Current Neurology and Neuroscience Reports. Sep, 2003 | Pubmed ID: 12914687 Increased Neuronal Production, Enlarged Forebrains and Cytoarchitectural Distortions in Beta-catenin Overexpressing Transgenic Mice Cerebral Cortex (New York, N.Y. : 1991). Jun, 2003 | Pubmed ID: 12764034 Markers of Cellular Proliferation Are Expressed in Cortical Tubers Annals of Neurology. May, 2003 | Pubmed ID: 12731003 Bilateral Frontoparietal Polymicrogyria: Clinical and Radiological Features in 10 Families with Linkage to Chromosome 16 Annals of Neurology. May, 2003 | Pubmed ID: 12730993 The DCX-domain Tandems of Doublecortin and Doublecortin-like Kinase Nature Structural Biology. May, 2003 | Pubmed ID: 12692530 Characterization of Foxp2 and Foxp1 MRNA and Protein in the Developing and Mature Brain The Journal of Comparative Neurology. May, 2003 | Pubmed ID: 12687690 Reelin is Expressed in the Accessory Olfactory System, but is Not a Guidance Cue for Vomeronasal Axons Brain Research. Developmental Brain Research. Feb, 2003 | Pubmed ID: 12586436 Cryptic T(1;12)(q44;p13.3) Translocation in a Previously Described Syndrome with Polymicrogyria, Segregating As an Apparently X-linked Trait American Journal of Medical Genetics. Part A. Feb, 2003 | Pubmed ID: 12548742 Bilateral Periventricular Nodular Heterotopia Due to Filamin 1 Gene Mutation: Widespread Glomeruloid Microvascular Anomaly and Dysplastic Cytoarchitecture in the Cerebral Cortex Acta Neuropathologica. Dec, 2002 | Pubmed ID: 12410386 Filamin A and Filamin B Are Co-expressed Within Neurons During Periods of Neuronal Migration and Can Physically Interact Human Molecular Genetics. Nov, 2002 | Pubmed ID: 12393796 Mutations in the O-mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome American Journal of Human Genetics. Nov, 2002 | Pubmed ID: 12369018 ASPM is a Major Determinant of Cerebral Cortical Size Nature Genetics. Oct, 2002 | Pubmed ID: 12355089 Doublecortin is Required in Mice for Lamination of the Hippocampus but Not the Neocortex The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. Sep, 2002 | Pubmed ID: 12196578 Regulation of Cerebral Cortical Size by Control of Cell Cycle Exit in Neural Precursors Science (New York, N.Y.). Jul, 2002 | Pubmed ID: 12130776 Smooth, Rough and Upside-down Neocortical Development Current Opinion in Genetics & Development. Jun, 2002 | Pubmed ID: 12076676 Evidence of Common Progenitors and Patterns of Dispersion in Rat Striatum and Cerebral Cortex The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. May, 2002 | Pubmed ID: 12019320 Mapping of the Mouse Hyh Gene to a YAC/BAC Contig on Proximal Chromosome 7 Mammalian Genome : Official Journal of the International Mammalian Genome Society. May, 2002 | Pubmed ID: 12016511 An Autosomal Recessive Form of Bilateral Frontoparietal Polymicrogyria Maps to Chromosome 16q12.2-21 American Journal of Human Genetics. Apr, 2002 | Pubmed ID: 11845408 Dissected Serebral Kortikal Eksplantlarından ile kullanım için Kemirgen Embriyolar arasından Beyin Omurilik Sıvısı İzolasyonu Mauro W. Zappaterra1, Anthony S. LaMantia2, Christopher A. Walsh3,4, Maria K. Lehtinen5 1Department of Physical Medicine and Rehabilitation, VA Greater Los Angeles Healthcare System, 2Department of Pharmacology and Physiology, Institute for Neuroscience, The George Washington University School of Medicine and Health Sciences, 3Division of Genetics, Department of Medicine, Boston Children's Hospital, 4Howard Hughes Medical Institute, Boston Children's Hospital, 5Department of Pathology, Boston Children's Hospital, Harvard Medical School JoVE 50333 Neuroscience
Dissected Serebral Kortikal Eksplantlarından ile kullanım için Kemirgen Embriyolar arasından Beyin Omurilik Sıvısı İzolasyonu Mauro W. Zappaterra1, Anthony S. LaMantia2, Christopher A. Walsh3,4, Maria K. Lehtinen5 1Department of Physical Medicine and Rehabilitation, VA Greater Los Angeles Healthcare System, 2Department of Pharmacology and Physiology, Institute for Neuroscience, The George Washington University School of Medicine and Health Sciences, 3Division of Genetics, Department of Medicine, Boston Children's Hospital, 4Howard Hughes Medical Institute, Boston Children's Hospital, 5Department of Pathology, Boston Children's Hospital, Harvard Medical School JoVE 50333 Neuroscience
