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CADPS2
Primate Specific Retrotransposons, Svas, in the Evolution of Networks That Alter Brain Function
Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing
Identification of Potential Key Genes and Pathway Linked with Sporadic Creutzfeldt-Jakob Disease Based on Integrated Bioinformatics Analyses
REVIEW ARTICLE the Genetics of Autism
CADPS2 (NM 001009571) Human Tagged ORF Clone – RC220606
Impaired Secretion of Brain-Derived Neurotrophic Factor and Neuropsy- Chiatric Diseases Naoki Adachi and Hiroshi Kunugi*
Advances in Autism Genetics: on the Threshold of a New Neurobiology
Reduced Axonal Localization of a Caps2 Splice Variant Impairs Axonal Release of BDNF and Causes Autistic-Like Behavior in Mice
Molecular Mechanisms: Mutations Make Medley of Symptoms
An Integrative Analysis of Non-Coding Regulatory DNA Variations Associated with Autism Spectrum Disorder
The Role of Neurotrophic Factors in Autism T Nickl-Jockschat and TM Michel Department of Psychiatry and Psychotherapy, RWTH Aachen University, Aachen, Germany
Novel Neuroprotective Loci Modulating Ischemic Stroke Volume in Wild-Derived Inbred Mouse Strains
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Gene Amplifications at Chromosome 7 of the Human Gastric Cancer Genome
And Post-Symptomatic Frontotemporal Dementia-Like Mice with TDP-43
Genome-Wide Association Study and Pathway Analysis for Female Fertility Traits in Iranian Holstein Cattle
Single-Cell RNA-Seq of Mouse Dopaminergic Neurons Informs Candidate Gene Selection For
Maternally Inherited Genetic Variants of CADPS2 Are Present in Autism Spectrum Disorders and Intellectual Disability Patients
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The Cancer Genome Atlas Dataset-Based Analysis of Aberrantly Expressed Genes by Geneanalytics in Thymoma Associated Myasthenia Gravis: Focusing on T Cells
216141 2 En Bookbackmatter 461..490
Behavioural Phenotyping Assays for Mouse Models of Autism
Chromosomal Deletion in 7Q31.2-31.32 Involving Ca2+-Dependent Activator Protein for Secretion Gene in a Patient with Cerebellar Ataxia: a Case Report
A Functional Polymorphism of the Brain Derived Neurotrophic Factor Gene and Cortical Anatomy in Autism Spectrum Disorder
7Q31.32 Partial Duplication First Report of a Child with Dysmorphism
Single-Cell Sequencing of the Human Midbrain Reveals Glial Activation and a Neuronal State Specific to Parkinson’S Disease
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Human Tagged ORF Clone Lentiviral Particle – RC220606L4V
Convergent Functional Genomic Studies of Omega-3 Fatty Acids in Stress Reactivity, Bipolar Disorder and Alcoholism
Aspects of Excitatory/Inhibitory Synapses in Multiple Brain Regions Are Correlated with Levels of Brain-Derived Neurotrophic Factor/ Neurotrophin-3
Supporting Information Appendix SI Materials and Methods
Deletion Involving the 7Q31-32 Band at the CADPS2 Gene Locus in a Patient with Autism Spectrum Disorder and Recurrent Psychotic Syndrome Triggered by Stress
Mouse Models of Mutations and Variations in Autism Spectrum Disorder-Associated Genes: Mice Expressing Caps2/Cadps2 Copy Number and Alternative Splicing Variants
The Pennsylvania State University Schreyer
Single-Cell Sequencing of the Human Midbrain Reveals Glial Activation and a Neuronal State Specific to Parkinson’S Disease
Analysis of Gene Expression in Ca2+-Dependent
Genome-Wide Identification of Conserved Regulatory Function in Diverged Sequences
Genome-Wide Copy Number Variant Analysis for Congenital Ventricular Septal Defects in Chinese Han Population
Analysis of Gene Expression in Ca2+-Dependent Activator Protein
Supplementary Table 1. a Full List of Cancer Genes
1 Abnormal Social Behaviors and Dysfunction of Autism-Related Genes