Citation Impact
Citing Papers
Extended-resolution structured illumination imaging of endocytic and cytoskeletal dynamics
2015 ScienceNobel
De novo design of allosterically switchable protein assemblies
2024 StandoutNatureNobel
Computationally designed sensors detect endogenous Ras activity and signaling effectors at subcellular resolution
2024 StandoutNobel
Mass photometry enables label-free tracking and mass measurement of single proteins on lipid bilayers
2021
Concerted changes in transcripts in the prefrontal cortex precede neuropathology in Alzheimer's disease
2010
Control of autophagy initiation by phosphoinositide 3‐phosphatase jumpy
2009
Regulation of the Voltage Gated K<sup>+</sup> Channel K<sub>v1.3</sub> by Recombinant Human Klotho Protein
2014 Standout
Ca2+ channels and skeletal muscle diseases
2010
Multiple phases of chondrocyte enlargement underlie differences in skeletal proportions
2013 StandoutNature
Calcium's Role in Mechanotransduction during Muscle Development
2014 Standout
Descending control of pain
2002 Standout
Mammalian phosphoinositide kinases and phosphatases
2009 StandoutNobel
Physiology of Cell Volume Regulation in Vertebrates
2009
Diverse roles of the actin cytoskeleton in striated muscle
2009
Super-resolution microscopy demystified
2018 Standout
Inositol and higher inositol phosphates in neural tissues: homeostasis, metabolism and functional significance
2002
Confirmation of five novel susceptibility loci for Systemic Lupus Erythematosus (SLE) and integrated network analysis of 82 SLE susceptibility loci
2017
Biological Functions of Autophagy Genes: A Disease Perspective
2019 Standout
Mice lacking microRNA 133a develop dynamin 2–dependent centronuclear myopathy
2011
Metazoan MicroRNAs
2018 Standout
Glial transporters for glutamate, glycine, and GABA: II. GABA transporters
2001
The cytoprotective role of taurine in exercise-induced muscle injury
2002
A novel PtdIns3P and PtdIns(3,5)P2 phosphatase with an inactivating variant in centronuclear myopathy
2006
Leishmania donovani Targets Dicer1 to Downregulate miR-122, Lower Serum Cholesterol, and Facilitate Murine Liver Infection
2013
Fluorescence nanoscopy in cell biology
2017 StandoutNobel
Congenital disorders of autophagy: an emerging novel class of inborn errors of neuro-metabolism
2015
SWELL1, a Plasma Membrane Protein, Is an Essential Component of Volume-Regulated Anion Channel
2014 StandoutNobel
Differential Regulation of Lipoprotein and Hepatitis C Virus Secretion by Rab1b
2017 StandoutNobel
Down-Regulation of the Myoinositol Transporter SMIT by JAK2
2012
Molecular mechanism and physiological functions of clathrin-mediated endocytosis
2011 Standout
Current knowledge of the pre‐autophagosomal structure (PAS)
2010 StandoutNobel
The neuronal endopeptidase ECEL1 is associated with a distinct form of recessive distal arthrogryposis
2012
Macrophage Cytokines: Involvement in Immunity and Infectious Diseases
2014 Standout
Gasdermins: Effectors of Pyroptosis
2017 Standout
Glial transporters for glutamate, glycine and GABA I. Glutamate transporters
2001
Phase Separation by Low Complexity Domains Promotes Stress Granule Assembly and Drives Pathological Fibrillization
2015 Standout
Single-cell transcriptomic analysis of Alzheimer’s disease
2019 StandoutNature
LRRC8 Proteins Form Volume-Regulated Anion Channels that Sense Ionic Strength
2016 StandoutNobel
Atg9 Vesicles Recruit Vesicle-tethering Proteins Trs85 and Ypt1 to the Autophagosome Formation Site
2012 StandoutNobel
Physiology and Pathophysiology of Carnosine
2013 Standout
Lipid droplet breakdown requires Dynamin 2 for vesiculation of autolysosomal tubules in hepatocytes
2013
Filming Biomolecular Processes by High-Speed Atomic Force Microscopy
2014
Role of Rab GTPases in Membrane Traffic and Cell Physiology
2011
Quantifying the Dynamics of Protein Self-Organization Using Deep Learning Analysis of Atomic Force Microscopy Data
2020 StandoutNobel
Amyloid β peptide cleavage by kallikrein 7 attenuates fibril growth and rescues neurons from Aβ-mediated toxicity in vitro
2013 StandoutNobel
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis
2013 StandoutNobel
Fiber Types in Mammalian Skeletal Muscles
2011 Standout
Rotational dynamics and transition mechanisms of surface-adsorbed proteins
2022 StandoutNobel
Engineering Biomolecular Self‐Assembly at Solid–Liquid Interfaces
2020 StandoutNobel
Welander distal myopathy is caused by a mutation in the RNA‐binding protein TIA1
2012
Autophagy pathway: Cellular and molecular mechanisms
2017 Standout
Atg14: A Key Player in Orchestrating Autophagy
2011 StandoutNobel
Lipid Peroxidation: Production, Metabolism, and Signaling Mechanisms of Malondialdehyde and 4-Hydroxy-2-Nonenal
2014 Standout
Disentangling Rotational Dynamics and Ordering Transitions in a System of Self-Organizing Protein Nanorods via Rotationally Invariant Latent Representations
2021 StandoutNobel
FluoSTEPs: Fluorescent biosensors for monitoring compartmentalized signaling within endogenous microdomains
2021
PtdIns 3-Kinase Orchestrates Autophagosome Formation in Yeast
2011 StandoutNobel
The Role of Atg Proteins in Autophagosome Formation
2011 StandoutNobel
Works of Marc Bitoun being referenced
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene
2007
Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset
2007
Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis
2009
Taurine Down‐Regulates Basal and Osmolarity‐Induced Gene Expression of Its Transporter, but Not the Gene Expression of Its Biosynthetic Enzymes, in Astrocyte Primary Cultures
2000
Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsy
2010
Gene expression of taurine transporter and taurine biosynthetic enzymes in brain of rats with acute or chronic hyperosmotic plasma
2000
Dynamin 2 and human diseases
2010
Neuromuscular expression of the BTB/POZ and zinc finger protein myoneurin
2003
Mutations in dynamin 2 cause dominant centronuclear myopathy
2005
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization
2010
Actin scaffolding by clathrin heavy chain is required for skeletal muscle sarcomere organization
2014
A Centronuclear Myopathy – Dynamin 2 Mutation Impairs Autophagy in Mice
2012
A NEW CENTRONUCLEAR MYOPATHY PHENOTYPE DUE TO A NOVEL DYNAMIN 2 MUTATION
2009
A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice
2010
An alternative mechanism of clathrin-coated pit closure revealed by ion conductance microscopy
2012
Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscle
2019
Gene expression of the transporters and biosynthetic enzymes of the osmolytes in astrocyte primary cultures exposed to hyperosmotic conditions
2000