4.5 Article

A VPS13D spastic ataxia mutation disrupts the conserved adaptor-binding site in yeast Vps13

Related references

Note: Only part of the references are listed.
Article Multidisciplinary Sciences

Coming together to define membrane contact sites

Luca Scorrano et al.

NATURE COMMUNICATIONS (2019)

Article Clinical Neurology

Recessive mutations in >VPS13D cause childhood onset movement disorders

Julie Gauthier et al.

ANNALS OF NEUROLOGY (2018)

Article Clinical Neurology

Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects

Eunju Seong et al.

ANNALS OF NEUROLOGY (2018)

Article Biochemistry & Molecular Biology

Vps13D Encodes a Ubiquitin-Binding Protein that Is Required for the Regulation of Mitochondrial Size and Clearance

Allyson L. Anding et al.

CURRENT BIOLOGY (2018)

Article Cell Biology

Competitive organelle-specific adaptors recruit Vps13 to membrane contact sites

Bjorn D. M. Bean et al.

JOURNAL OF CELL BIOLOGY (2018)

Article Multidisciplinary Sciences

Insights into autophagosome biogenesis from structural and biochemical analyses of the ATG2A-WIPI4 complex

Saikat Chowdhury et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2018)

Article Multidisciplinary Sciences

The Atg2-Atg18 complex tethers pre-autophagosomal membranes to the endoplasmic reticulum for autophagosome formation

Tetsuya Kotani et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2018)

Review Biochemistry & Molecular Biology

WD40 Repeat Proteins: Signalling Scaffold with Diverse Functions

Buddhi Prakash Jain et al.

PROTEIN JOURNAL (2018)

Review Multidisciplinary Sciences

Here, there, and everywhere: The importance of ER membrane contact sites

Haoxi Wu et al.

SCIENCE (2018)

Article Biochemistry & Molecular Biology

Differential requirement for ATG2A domains for localization to autophagic membranes and lipid droplets'

Norito Tamura et al.

FEBS LETTERS (2017)

Article Cell Biology

Vps13-Mcp1 interact at vacuole-mitochondria interfaces and bypass ER-mitochondria contact sites

Arun T. John Peter et al.

JOURNAL OF CELL BIOLOGY (2017)

Review Clinical Neurology

Mitochondria-associated membranes as hubs for neurodegeneration

Michiel Krols et al.

ACTA NEUROPATHOLOGICA (2016)

Article Cell Biology

Yeast Vps13 promotes mitochondrial function and is localized at membrane contact sites

Jae-Sook Park et al.

MOLECULAR BIOLOGY OF THE CELL (2016)

Review Neurosciences

There's Something Wrong with my MAM; the ER-Mitochondria Axis and Neurodegenerative Diseases

Sebastien Paillusson et al.

TRENDS IN NEUROSCIENCES (2016)

Article Cell Biology

ER-mitochondrial junctions can be bypassed by dominant mutations in the endosomal protein Vps13

Alexander B. Lang et al.

JOURNAL OF CELL BIOLOGY (2015)

Letter Biochemical Research Methods

The I-TASSER Suite: protein structure and function prediction

Jianyi Yang et al.

NATURE METHODS (2015)

Article Cell Biology

Toward a Comprehensive Map of the Effectors of Rab GTPases

Alison K. Gillingham et al.

DEVELOPMENTAL CELL (2014)

Article Multidisciplinary Sciences

Crystal structure of EML1 reveals the basis for Hsp90 dependence of oncogenic EML4-ALK by disruption of an atypical β-propeller domain

Mark W. Richards et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)

Article Multidisciplinary Sciences

Computational design of a self-assembling symmetrical β-propeller protein

Arnout R. D. Voet et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)

Article Neurosciences

Using Whole-Exome Sequencing to Identify Inherited Causes of Autism

Timothy W. Yu et al.

NEURON (2013)

Article Biochemistry & Molecular Biology

Structure-based Analyses Reveal Distinct Binding Sites for Atg2 and Phosphoinositides in Atg18

Yasunori Watanabe et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2012)

Article Cell Biology

VPS13 regulates membrane morphogenesis during sporulation in Saccharomyces cerevisiae

Jae-Sook Park et al.

JOURNAL OF CELL SCIENCE (2012)

Article Biochemistry & Molecular Biology

Two-Site Recognition of Phosphatidylinositol 3-Phosphate by PROPPINs in Autophagy

Sulochanadevi Baskaran et al.

MOLECULAR CELL (2012)

Article Biochemical Research Methods

Fiji: an open-source platform for biological-image analysis

Johannes Schindelin et al.

NATURE METHODS (2012)

Article Biochemistry & Molecular Biology

Cohen Syndrome-associated Protein, COH1, Is a Novel, Giant Golgi Matrix Protein Required for Golgi Integrity

Wenke Seifert et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2011)

Review Biochemistry & Molecular Biology

The many blades of the β-propeller proteins: conserved but versatile

Cammy K. -M. Chen et al.

TRENDS IN BIOCHEMICAL SCIENCES (2011)

Review Cell Biology

Structure and function of WD40 domain proteins

Chao Xu et al.

PROTEIN & CELL (2011)

Article Chemistry, Multidisciplinary

Optimized Measurement Temperature Gives Access to the Solution Structure of a 49 kDa Homohexameric β-Propeller

Ilka Varnay et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2010)

Article Genetics & Heredity

Deletions in the VPS13B(COH1) Gene as a Cause of Cohen Syndrome

I. Balikova et al.

HUMAN MUTATION (2009)

Article Biochemistry & Molecular Biology

Reconstruction of functional β-propeller lectins via homo-oligomeric assembly of shorter fragments

Itamar Yadid et al.

JOURNAL OF MOLECULAR BIOLOGY (2007)

Article Genetics & Heredity

Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndrome

W Seifert et al.

JOURNAL OF MEDICAL GENETICS (2006)

Article Biotechnology & Applied Microbiology

Analysis of the human VPS13 gene family

A Velayos-Baeza et al.

GENOMICS (2004)

Article Genetics & Heredity

Delineation of Cohen syndrome following a large-scale genotype-phenotype screen

J Kolehmainen et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2004)

Article Biochemistry & Molecular Biology

The structure of Aip1p, a WD repeat protein that regulates cofilin-mediated actin depolymerization

WC Voegtli et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2003)

Article Biochemistry & Molecular Biology

Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis

C Dobson-Stone et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2002)

Article Genetics & Heredity

A conserved sorting-associated protein is mutant in chorea-acanthocytosis

L Rampoldi et al.

NATURE GENETICS (2001)