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DEPDC5
Acute Knockdown of Depdc5 Leads to Synaptic Defects in Mtor-Related Epileptogenesis
DEPDC5 Takes a Second Hit in Familial Focal Epilepsy
The Genetics of Bipolar Disorder
Stranded Breaks in Drosophila Youheng Wei1,2†, Lucia Bettedi1†, Chun-Yuan Ting1, Kuikwon Kim1, Yingbiao Zhang1, Jiadong Cai2, Mary a Lilly1*
Epileptic Spasms Are a Feature of DEPDC5 Mtoropathy
Epigenetic Mechanisms Are Involved in the Oncogenic Properties of ZNF518B in Colorectal Cancer
Engineered Type 1 Regulatory T Cells Designed for Clinical Use Kill Primary
Epileptic Spasms Are a Feature of DEPDC5 Mtoropathy
VIEW Open Access the Role of Ubiquitination and Deubiquitination in Cancer Metabolism Tianshui Sun1, Zhuonan Liu2 and Qing Yang1*
Germline and Somatic Mutations in the MTOR Gene in Focal Cortical Dysplasia and Epilepsy
Mutations in Mtor Regulator DEPDC5 Cause Focal Epilepsy with Brain
UC Berkeley UC Berkeley Electronic Theses and Dissertations
Variation in Protein Coding Genes Identifies Information Flow
Supplemental Solier
Multiple Rare Variants in Typical and Atypical Rolandic Epilepsy – a Genetic Analysis
Regulation of Body Size and Growth Control
Mutations of DEPDC5 Cause Autosomal Dominant Focal Epilepsies
Title: DEPDC5-Related Epilepsy Genereview Table 3 Authors: Baulac S, Weckhuysen S Date: September 2016
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From Emerging Basic Science Toward Solutions for People’S Wellbeing
DEPDC5 Gene DEP Domain Containing 5
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Non-Canonical Mtor-Independent Role of DEPDC5 In
Familial Cortical Dysplasia Type IIA Caused by a Germline Mutation in DEPDC5 Thomas Scerri1, Jessica R
Dentification of New Genetic Syndromes with Epilepsy by Whole
Genome-Wide Association Analyses Identify Genotype-By-Environment Interactions of Growth Traits in Simmental Cattle
Mutational Inactivation of Mtorc1 Repressor Gene DEPDC5 in Human Gastrointestinal Stromal Tumors
The Role of Ubiquitination in Tumorigenesis and Targeted Drug Discovery
The Stress–Wnt-Signaling Axis: a Hypothesis for Attention-Deficit Hyperactivity Disorder and Therapy Approaches
The Roles of Ubiquitin in Mediating Autophagy
Integration of Cistromic and Transcriptomic Analyses Identifies Nphs2, Mafb, and Magi2 As Wilms' Tumor 1 Target Genes in Podoc
The GATOR1 Complex Regulates Metabolic Homeostasis and the Response to Nutrient Stress in Drosophila Melanogaster
Identification of DEP Domain-Containing Proteins by a Machine Learning Method and Experimental Analysis of Their Expression in Human HCC Tissues
A Splicing Variation in NPRL2 Causing Familial Focal Epilepsy With
Integrated Data Analysis Reveals Uterine Leiomyoma Subtypes with Distinct Driver Pathways and Biomarkers
Diagnostic Exome Sequencing in Non-Acquired Focal Epilepsies Highlights a Major Role of GATOR1 Complex Genes
The Landscape of Epilepsy-Related GATOR1 Variants
Dissecting the Genetic Basis of Comorbid Epilepsy Phenotypes In
Mammalian Target of Rapamycin Pathway Mutations Cause
Association of MTOR Mutations with Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism
Inbred Mouse Strains Expression in Primary Immunocytes Across
DEPDC5 As a Potential Therapeutic Target for Epilepsy
RUNX1-EVI1 Disrupts Lineage Determination and the Cell Cycle by Interfering with RUNX1 and EVI1 Driven Gene Regulatory Networks
Comparative Genetic Screens in Human Cells Reveal New Regulatory
Analyzing Presymptomatic Tissue to Gain Insights Into the Molecular and Mechanistic Origins of Late-Onset Degenerative Trinucleotide Repeat Disease
L'approche Basée Sur Le Génotype Déterminé Par Séquençage Haut
Involvement of Calcium, Ras, MAPK, PI3K-Akt and Mtor Signaling Pathways in Autism Spectrum Disorders
Supplemental Material
FKBP39 Controls Nutrient Dependent Nprl3 Expression and TORC1
TORC1 Regulators Iml1/GATOR1 and GATOR2 Control Meiotic