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KCTD13
KCTD13 Is a Major Driver of Mirrored Neuroanatomical Phenotypes Associated with the 16P11.2 CNV
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Mutpred2: Inferring the Molecular and Phenotypic Impact of Amino Acid Variants
Associated 16P11.2 Deletion in Drosophila Melanogaster
Targeting the RHOA Pathway Improves Learning and Memory In
Cul3 Regulates Cytoskeleton Protein Homeostasis and Cell Migration During a Critical
A High Throughput, Functional Screen of Human Body Mass Index GWAS Loci Using Tissue-Specific Rnai Drosophila Melanogaster Crosses Thomas J
View a Copy of This Licence, Visit Mmons .Org/Licen Ses/By/4.0/
Functional Genomics Identify a Regulatory Risk Variation Rs4420550 in the 16P11.2 Schizophrenia- Associated Locus
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Spatiotemporal 16P11.2 Protein Network Implicates Cortical Late Mid-Fetal Brain Development and KCTD13- Cul3-Rhoa Pathway in Psychiatric Diseases
Chromosomal Contacts Connect Loci Associated with Autism, BMI and Head Circumference Phenotypes
Understanding the Genetic Basis of Phenotype Variability in Individuals with Neurocognitive Disorders
UNIVERSITY of CALIFORNIA Los Angeles Identification of a Multisubunit E3 Ubiquitin Ligase Required for Heterotrimeric G-Protein
Supplementary Table 1 Double Treatment Vs Single Treatment
A Novel Ribosomopathy Caused by Dysfunction of RPL10 Disrupts Neurodevelopment and Causes X-Linked Microcephaly in Humans
Prenatal Diagnosis of True Fetal Mosaicism with Small
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
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Molecular Sciences High-Resolution Chromosome Ideogram Representation of Currently Recognized Genes for Autism Spectrum Disorder
1 Clustering of Functionally-Related Genes Impacts Significantly on CNV
A Cell Type-Specific Expression Signature Predicts Haploinsufficient Autism-Susceptibility Genes
Structure and Function of Multimeric BTB Proteins and Cullin3 Substrate Adaptors
Identification of Rare Variants in KCTD13 at the Schizophrenia Risk Locus 16P11.2" (2016)
Discovering Pathways in Benign Prostate Hyperplasia: a Functional Genomics Pilot Study
Genetic Analysis of Schizophrenia and Bipolar Disorder Reveals Polygenicity but Also Suggests New Directions for Molecular Interrogation Benjamin M
KCTD: a New Gene Family Involved in Neurodevelopmental and Neuropsychiatric Disorders
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The Developmental Transcriptome of the Human Brain: Implications for Neurodevelopmental Disorders
Fish Study Links Chromosome 16 Genes to Head Size
Christina G. Perry Ph.D
A Contribution of Novel Cnvs to Schizophrenia from a Genome-Wide Study of 41,321 Subjects
Identification of Common Pathogenetic Processes Between
UC Irvine UC Irvine Electronic Theses and Dissertations
Spatiotemporal 22Q11.21 Protein Network Implicates DGCR8-Dependent Microrna Biogenesis As a Risk for Late Fetal Cortical Development in Psychiatric Diseases
Gene Expression Imputation Across Multiple Brain Regions Provides Insights Into Schizophrenia Risk
Supplementary Materials Männik Et Al