USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder
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Vesicular Trafficking to the Immune Synapse: How to Assemble Receptor-Tailored Pathways from a Basic Building SetModulation of the p53/MDM2 interplay by HAUSP inhibitorsDeubiquitinating enzymes Ubp2 and Ubp15 regulate endocytosis by limiting ubiquitination and degradation of ARTsCellular functions of WASP family proteins at a glance.Stabilization of histone demethylase PHF8 by USP7 promotes breast carcinogenesis.Current Perspectives in Autism Spectrum Disorder: From Genes to Therapy.A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes.Lessons learned from additional research analyses of unsolved clinical exome cases.Endosomal system genetics and autism spectrum disorders: A literature review.Autism genetics - an overview.De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder.Integration of cellular ubiquitin and membrane traffic systems: focus on deubiquitylases.A Comprehensive Guide to the MAGE Family of Ubiquitin Ligases.Cellular and disease functions of the Prader-Willi Syndrome gene MAGEL2.Protein deubiquitinase USP7 is required for osteogenic differentiation of human adipose-derived stem cells.PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic Proteins.Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features.Prader-Willi Syndrome and Schaaf-Yang Syndrome: Neurodevelopmental Diseases Intersecting at the MAGEL2 Gene.A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy.USP7 small-molecule inhibitors interfere with ubiquitin binding.The Prader-Willi syndrome proteins MAGEL2 and necdin regulate leptin receptor cell surface abundance through ubiquitination pathways.Sorting nexin 27 interactome in T-lymphocytes identifies zona occludens-2 dynamic redistribution at the immune synapse.Deubiquitylating enzymes and drug discovery: emerging opportunities.Chromosomal microarray analysis in the genetic evaluation of 279 patients with syndromic obesity.Endosomal Receptor Trafficking: Retromer and Beyond.Whole-exome Sequencing Helps the Diagnosis and Treatment in Children with Neurodevelopmental Delay Accompanied Unexplained Dyspnea.Clinical Significance of Ubiquitin Specific Protease 7 (USP7) in Predicting Prognosis of Hepatocellular Carcinoma and its Functional Mechanisms.HRS-WASH axis governs actin-mediated endosomal recycling and cell invasion.Prioritized High-Confidence Risk Genes for Intellectual Disability Reveal Molecular Convergence During Brain Development
P2860
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P2860
USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder
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2015 nî lūn-bûn
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2015 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի սեպտեմբերին հրատարակված գիտական հոդված
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2015年の論文
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2015年論文
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2015年論文
@zh-hant
2015年論文
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2015年論文
@zh-mo
2015年論文
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2015年论文
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name
USP7 Acts as a Molecular Rheos ...... an Neurodevelopmental Disorder
@ast
USP7 Acts as a Molecular Rheos ...... an Neurodevelopmental Disorder
@en
USP7 Acts as a Molecular Rheos ...... an Neurodevelopmental Disorder
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type
label
USP7 Acts as a Molecular Rheos ...... an Neurodevelopmental Disorder
@ast
USP7 Acts as a Molecular Rheos ...... an Neurodevelopmental Disorder
@en
USP7 Acts as a Molecular Rheos ...... an Neurodevelopmental Disorder
@nl
prefLabel
USP7 Acts as a Molecular Rheos ...... an Neurodevelopmental Disorder
@ast
USP7 Acts as a Molecular Rheos ...... an Neurodevelopmental Disorder
@en
USP7 Acts as a Molecular Rheos ...... an Neurodevelopmental Disorder
@nl
P2093
P2860
P1433
P1476
USP7 Acts as a Molecular Rheos ...... an Neurodevelopmental Disorder
@en
P2093
Ankita Patel
Bertrand Isidor
Christian P Schaaf
Ian D Krantz
Jean P Pfotenhauer
Jill A Rosenfeld
Klementina Fon Tacer
Margarita S Saenz
Michael D Fountain
P2860
P304
P356
10.1016/J.MOLCEL.2015.07.033
P407
P577
2015-09-17T00:00:00Z