Related references
Note: Only part of the references are listed.Protein structure predictions to atomic accuracy with AlphaFold
John Jumper et al.
NATURE METHODS (2022)
Stressful steps: Progress and challenges in understanding stress-induced mRNA condensation and accumulation in stress granules
Hendrik Glauninger et al.
MOLECULAR CELL (2022)
ColabFold: making protein folding accessible to all
Milot Mirdita et al.
NATURE METHODS (2022)
Improved prediction of protein-protein interactions using AlphaFold2
P. Bryant et al.
NATURE COMMUNICATIONS (2022)
PTCHD1: Identification and Neurodevelopmental Contributions of an Autism Spectrum Disorder and Intellectual Disability Susceptibility Gene
Stephen F. Pastore et al.
GENES (2022)
Structure, function and small molecule modulation of intracellular sterol transport proteins
Laura Depta et al.
BIOORGANIC & MEDICINAL CHEMISTRY (2022)
Novel FMRP interaction networks linked to cellular stress
Mohamed S. Taha et al.
FEBS JOURNAL (2021)
Molecular mechanisms of stress granule assembly and disassembly
Sarah Hofmann et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2021)
RNA-binding protein dysfunction in neurodegeneration
Bastian Popper et al.
MOLECULAR MECHANISMS OF NEURODEGENERATION (2021)
PANTHER version 16: a revised family classification, tree-based classification tool, enhancer regions and extensive API
Huaiyu Mi et al.
NUCLEIC ACIDS RESEARCH (2021)
The Gene Ontology resource: enriching a GOld mine
Seth Carbon et al.
NUCLEIC ACIDS RESEARCH (2021)
Dispatched uses Na+ flux to power release of lipid-modified Hedgehog
Qianqian Wang et al.
NATURE (2021)
The molecular biology of FMRP: new insights into fragile X syndrome
Joel D. Richter et al.
NATURE REVIEWS NEUROSCIENCE (2021)
Patched 1 reduces the accessibility of cholesterol in the outer leaflet of membranes
Maia Kinnebrew et al.
ELIFE (2021)
Novel missense mutations in PTCHD1 alter its plasma membrane subcellular localization and cause intellectual disability and autism spectrum disorder
Judith Halewa et al.
HUMAN MUTATION (2021)
AutoDock Vina 1.2.0: New Docking Methods, Expanded Force Field, and Python Bindings
Jerome Eberhardt et al.
JOURNAL OF CHEMICAL INFORMATION AND MODELING (2021)
Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development
Ashley L. Lennox et al.
NEURON (2020)
Regulation ofRNAgranules byFMRPand implications for neurological diseases
Austin Lai et al.
TRAFFIC (2020)
Structural Basis of Low-pH-Dependent Lysosomal Cholesterol Egress by NPC1 and NPC2
Hongwu Qian et al.
CELL (2020)
Distinct Cation Gradients Power Cholesterol Transport at Different Key Points in the Hedgehog Signaling Pathway
Kostadin Petrov et al.
DEVELOPMENTAL CELL (2020)
Cholesterol access in cellular membranes controls Hedgehog signaling
Arun Radhakrishnan et al.
NATURE CHEMICAL BIOLOGY (2020)
Structural basis of sterol recognition by human hedgehog receptor PTCH1
Chao Qi et al.
SCIENCE ADVANCES (2019)
Cholesterol accessibility at the ciliary membrane controls hedgehog signaling
Maia Kinnebrew et al.
ELIFE (2019)
Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse
D. C. Ung et al.
MOLECULAR PSYCHIATRY (2018)
Structural basis for the recognition of Sonic Hedgehog by human Patchedl
Xin Gong et al.
SCIENCE (2018)
Structural Basis for Cholesterol Transport-like Activity of the Hedgehog Receptor Patched
Yunxiao Zhang et al.
CELL (2018)
Cellular Functions of the Autism Risk Factor PTCHD1 in Mice
David Tora et al.
JOURNAL OF NEUROSCIENCE (2017)
Real-time Characterization of Antibody Binding to Receptors on Living Immune Cells
Sina Bondza et al.
FRONTIERS IN IMMUNOLOGY (2017)
Thalamic reticular impairment underlies attention deficit in Ptchd1Y/- mice
Michael F. Wells et al.
NATURE (2016)
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder
A. Chaudhry et al.
CLINICAL GENETICS (2015)
SnapShot: FMRP Interacting Proteins
Emanuela Pasciuto et al.
CELL (2014)
A PTCH1 Homolog Transcriptionally Activated by p53 Suppresses Hedgehog Signaling
Jon H. Chung et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder
Santhosh Girirajan et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
lDDT: a local superposition-free score for comparing protein structures and models using distance difference tests
Valerio Mariani et al.
BIOINFORMATICS (2013)
Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega
Fabian Sievers et al.
MOLECULAR SYSTEMS BIOLOGY (2011)
Rare De Novo Variants Associated with Autism Implicate a Large Functional Network of Genes Involved in Formation and Function of Synapses
Sarah R. Gilman et al.
NEURON (2011)
New baculovirus expression tools for recombinant protein complex production
Simon Trowitzsch et al.
JOURNAL OF STRUCTURAL BIOLOGY (2010)
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto et al.
NATURE (2010)
Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability
Abdul Noor et al.
SCIENCE TRANSLATIONAL MEDICINE (2010)
AutoDock4 and AutoDockTools4: Automated Docking with Selective Receptor Flexibility
Garrett M. Morris et al.
JOURNAL OF COMPUTATIONAL CHEMISTRY (2009)
Structural variation of chromosomes in autism spectrum disorder
Christian R. Marshall et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
NPC2 facilitates bidirectional transfer of cholesterol between NPC1 and lipid bilayers, a step in cholesterol egress from lysosomes
Rodney E. Infante et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Inference of macromolecular assemblies from crystalline state
Evgeny Krissinel et al.
JOURNAL OF MOLECULAR BIOLOGY (2007)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari et al.
NATURE GENETICS (2007)
Comparison of multiple amber force fields and development of improved protein backbone parameters
Viktor Hornak et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2006)
HAN11 binds mDia1 and controls GLI1 transcriptional activity
Kazumasa Morita et al.
JOURNAL OF DERMATOLOGICAL SCIENCE (2006)
Applications for protein sequence-function evolution data: mRNA/protein expression analysis and coding SNP scoring tools
Paul D. Thomas et al.
NUCLEIC ACIDS RESEARCH (2006)
The structure of the N-terminal domain of the fragile X mental retardation protein: A platform for protein-protein interaction
A Ramos et al.
STRUCTURE (2006)
Phosphorylation of Ser640 in muscle glycogen synthase by DYRK family protein kinases
AV Skurat et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Cholesterol storage and tau pathology in Niemann-Pick type C disease in the brain
R Distl et al.
JOURNAL OF PATHOLOGY (2003)
Trafficking of cholesterol from cell bodies to distal axons in Niemann pick C1-deficient neurons
B Karten et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Share Paper
