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STXBP1
Oegtp - Epilepsy Test Requisition Lab Use Only: Patient Information
Epileptic Mechanisms Shared by Alzheimer's Disease
Abstracts from the 51St European Society of Human Genetics Conference: Electronic Posters
Supplementary Table 2
STXBP1 Analysis for Early Infantile Epileptic Encephalopathy
Deciphering the Molecular Profile of Plaques, Memory Decline And
Downregulation of Carnitine Acyl-Carnitine Translocase by Mirnas
Structural Analysis of De Novo STXBP1 Mutation in Complex with Syntaxin 1A
STXBP1 Disorders Scientific
De Novo STXBP1 Mutations in Mental Retardation and Nonsyndromic
STXBP1 Encephalopathy with Epilepsy
Single-Cell Rnaseq Reveals Cell Adhesion Molecule Profiles in Electrophysiologically Defined Neurons
ADX609 3301 Athena Newborndx Gene Panel Update 3-30-20.Indd
The Trans-SNARE-Regulating Function of Munc18-1 Is Essential to Synaptic Exocytosis
How Alternative Splicing Affects Membrane-Trafficking Dynamics R
Diagnostic Exome Sequencing Provides a Molecular Diagnosis for a Significant Proportion of Patients with Epilepsy
Identifying Factors That Conctribute to Phenotypic Heterogeneity in Melanoma Progression
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Top View
Disorders of STXBP1?
Syntaxin 3 Is Essential for Photoreceptor Outer Segment Protein Trafficking and Survival
S41467-018-04466-4.Pdf
STXBP1 Reduces the Inhibitory Impact of Syntaxin-1A On
Deep Sequencing Regarding R105, a Mosaic Variant in MECP2 Exon 1
Table 8. 341 Human Cdnas Used for Hierarchical Clustering of DNA
AUTS2 Confers Gene Activation to Polycomb Group Proteins in the CNS
STXBP1 Gene Syntaxin Binding Protein 1
STXBP1 Encephalopathy Connecting Neurodevelopmental Disorders with Α-Synucleinopathies?
De Novo Mutations in the Gene Encoding STXBP1 (MUNC18-1) Cause Early Infantile Epileptic Encephalopathy
Volume 27 / Number 1 / March 2019 Volume 27 / Number 1 March 2019 Pages 1-31
Table S-1 Mpkccd Transcriptome
Sakano Wang 2017 Proteomic Analyses of Nucleus Lam.Pdf
Novel MITF Targets Identified Using a Two-Step DNA Microarray Strategy
Genetic Neonatal-Onset Epilepsies and Developmental/Epileptic Encephalopathies with Movement Disorders: a Systematic Review
Proteomic Analysis of Membrane Microdomain-Associated Proteins in the Dorsolateral Prefrontal Cortex in Schizophrenia and Bipola
The Role of Micrornas in Metabolic Syndrome-Related Oxidative Stress
Novel 9Q34.11 Gene Deletions Encompassing Combinations of Four Mendelian Disease Genes: STXBP1, SPTAN1, ENG, and TOR1A