Citation Impact

Citing Papers

Histone demethylase KDM6A directly senses oxygen to control chromatin and cell fate
2019 StandoutScienceNobel
Visualizing enveloping layer glycans during zebrafish early embryogenesis
2010 StandoutNobel
Cyclic GMP-AMP Synthase Is a Cytosolic DNA Sensor That Activates the Type I Interferon Pathway
2012 StandoutScience
Human cerebral organoids recapitulate gene expression programs of fetal neocortex development
2015 StandoutNobel
The biomass distribution on Earth
2018 Standout
Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq
2015 StandoutScience
The mucin-selective protease StcE enables molecular and functional analysis of human cancer-associated mucins
2019 StandoutNobel
In vivo gene editing in dystrophic mouse muscle and muscle stem cells
2015 Science
Accelerated Evolution of Conserved Noncoding Sequences in Humans
2006 StandoutScienceNobel
Dystroglycan is required for polarizing the epithelial cells and the oocyte in Drosophila
2002
In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy
2015 Science
Dystroglycan Function Requires Xylosyl- and Glucuronyltransferase Activities of LARGE
2012 Science
The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition
2016
Cerebral cortex expansion and folding: what have we learned?
2016
Eukaryotic opportunists dominate the deep-subsurface biosphere in South Africa
2015
The promise and challenge of therapeutic genome editing
2020 StandoutNatureNobel
Understanding Human Glycosylation Disorders: Biochemistry Leads the Charge
2013
Bioorthogonal Chemistry: Fishing for Selectivity in a Sea of Functionality
2009 StandoutNobel
An FHL1-containing complex within the cardiomyocyte sarcomere mediates hypertrophic biomechanical stress responses in mice
2008
The multifunctional roles of the four-and-a-half-LIM only protein FHL2
2006
Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy
2002 Nature
Circular RNAs are a large class of animal RNAs with regulatory potency
2013 StandoutNature
Physical Principles of Membrane Shape Regulation by the Glycocalyx
2019 StandoutNobel
Non-viral gene delivery in skeletal muscle: a protein factory
2003
The cancer glycocalyx mechanically primes integrin-mediated growth and survival
2014 StandoutNatureNobel
Screening for antisense modulation of dystrophin pre-mRNA splicing
2002
Dystroglycan: important player in skeletal muscle and beyond
2005
Glycobiology of the neuromuscular junction
2003
The complexities of dystroglycan
2001
Protozoan Community Structure in a Fractal Soil Environment
2001
Muscular dystrophies involving the dystrophin–glycoprotein complex: an overview of current mouse models
2002
The muscular dystrophies
2002 Standout
Protein glycosylation in disease: new insights into the congenital muscular dystrophies
2003
Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study
2011 Standout
Gamma oscillations in the hippocampus require high complex I gene expression and strong functional performance of mitochondria
2010
Genetic defects in the human glycome
2006
DNA extraction procedures meaningfully influence qPCR-based mtDNA copy number determination
2009
Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy
2007 StandoutNobel
Notch Signaling: A Dance of Proteins Changing Partners
2000
Muscular dystrophies, the cytoskeleton and cell adhesion
2002
Micro-dystrophin cDNA ameliorates dystrophic phenotypes when introduced into mdx mice as a transgene
2002
Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members
2004
The dystroglycan complex: From biology to cancer
2005
Comprehensive classification of nucleotidyltransferase fold proteins: identification of novel families and their representatives in human
2009
Four-and-a-Half LIM Domain Proteins Inhibit Transactivation by Hypoxia-inducible Factor 1
2012 StandoutNobel
Protein O-Mannosylation in the Murine Brain: Occurrence of Mono-O-Mannosyl Glycans and Identification of New Substrates
2016
Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation
2010 Standout
Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1
2010
The MicroRNA miR-1 Regulates a MEF-2-Dependent Retrograde Signal at Neuromuscular Junctions
2008 StandoutNobel
The zebrafish as a model for muscular dystrophy and congenital myopathy
2003
Enterochromaffin Cells Are Gut Chemosensors that Couple to Sensory Neural Pathways
2017 StandoutNobel
Arthrogryposis: A Review and Update
2009
Density and Diversity of Protozoa in Some Arid Australian Soils
2002
Genetic suppression of phenotypes arising from mutations in dystrophin-related genes in Caenorhabditis elegans
2000
Targeting Dystroglycan in the Brain
2003
A Forward Genetics Screen in Mice Identifies Recessive Deafness Traits and Reveals That Pejvakin Is Essential for Outer Hair Cell Function
2007
A diverse range of gene products are effectors of the type I interferon antiviral response
2011 StandoutNatureNobel
The AAV-mediated and RNA-guided CRISPR/Cas9 system for gene therapy of DMD and BMD
2017
Fast gapped-read alignment with Bowtie 2
2012 Standout
Dystrophin Is Required for Appropriate Retrograde Control of Neurotransmitter Release at theDrosophilaNeuromuscular Junction
2006
The protein-labeling reagent FLASH-EDT 2 binds not only to CCXXCC motifs but also non-specifically to endogenous cysteine-rich proteins
2001
Inhibition of dystroglycan binding to laminin disrupts the PI3K/AKT pathway and survival signaling in muscle cells
2002
Molecular mechanisms of muscular dystrophies: old and new players
2006
N6-methyladenosine-dependent regulation of messenger RNA stability
2013 StandoutNature
Hsp72 preserves muscle function and slows progression of severe muscular dystrophy
2012 Nature
The role of cytoskeletal proteins in cardiomyopathies
1998
Muscular dystrophies: genes to pathogenesis
2003
The Hallmarks of Aging
2013 Standout
Pharmacological significance of glycosylation in therapeutic proteins
2009
Disease mutations in CMP-sialic acid transporter SLC35A1 result in abnormal  -dystroglycan O-mannosylation, independent from sialic acid
2014
β-Dystrobrevin, a New Member of the Dystrophin Family
1997
Emerging Strategies in the Treatment of Duchenne Muscular Dystrophy
2018
A Putative Src Homology 3 Domain Binding Motif but Not the C-terminal Dystrophin WW Domain Binding Motif Is Required for Dystroglycan Function in Cellular Polarity in Drosophila
2007 StandoutNobel
Removal of dystroglycan causes severe muscular dystrophy in zebrafish embryos
2002
Glycobiology of neuromuscular disorders
2003
Matrix Elasticity Directs Stem Cell Lineage Specification
2006 Standout
Small RNAs are modified with N-glycans and displayed on the surface of living cells
2021 StandoutNobel
Induction, assembly, maturation and maintenance of a postsynaptic apparatus
2001
α-Neurexins couple Ca2+ channels to synaptic vesicle exocytosis
2003 StandoutNatureNobel
Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy
2017
Human disorders of cortical development: from past to present
2006
Characterization of transposable elements in the genome of rice (Oryza sativa L.) using Representational Difference Analysis (RDA)
2002
Soluble amyloid precursor protein (APP) regulates transthyretin and Klotho gene expression without rescuing the essential function of APP
2010 StandoutNobel
The map-based sequence of the rice genome
2005 StandoutNature
Cardiac-Specific LIM Protein FHL2 Modifies the Hypertrophic Response to β-Adrenergic Stimulation
2001
A catechol- O -methyltransferase that is essential for auditory function in mice and humans
2008 StandoutNobel
In Vivo Imaging of Membrane-Associated Glycans in Developing Zebrafish
2008 StandoutScienceNobel
Modeling and automation of sequencing-based characterization of RNA structure
2011 StandoutNobel
Protozoa from aboveground and ground soils of a tropical rain forest in Puerto Rico
2006
B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycan
2014
Massive Idiosyncratic Exon Skipping Corrects the Nonsense Mutation in Dystrophic Mouse Muscle and Produces Functional Revertant Fibers by Clonal Expansion
2000
CRISPR Correction of Duchenne Muscular Dystrophy
2018
Cyclin-dependent kinases regulate lysosomal degradation of hypoxia-inducible factor 1α to promote cell-cycle progression
2014 StandoutNobel
Tissue Cells Feel and Respond to the Stiffness of Their Substrate
2005 StandoutScience
Dystroglycan: from biosynthesis to pathogenesis of human disease
2006
Muscle-specific expression of insulin-like growth factor I counters muscle decline in mdx mice
2002
Fluorophore Targeting to Cellular Proteins via Enzyme-Mediated Azide Ligation and Strain-Promoted Cycloaddition
2012 StandoutNobel
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis
2013 StandoutNobel
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
Role of Glycosylation in Development
2004
New Biarsenical Ligands and Tetracysteine Motifs for Protein Labeling in Vitro and in Vivo:  Synthesis and Biological Applications
2002 StandoutNobel
Imaging the glycome
2008 StandoutNobel
Protozoa of biological soil crusts of a cool desert in Utah
2007
Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein
2001 StandoutNobel
Fhl-1, a New Key Protein in Pulmonary Hypertension
2008
Protein Glycoengineering Enabled by the Versatile Synthesis of Aminooxy Glycans and the Genetically Encoded Aldehyde Tag
2011 StandoutNobel
Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewal
2012 StandoutNobel
Friends Not Foes: CTLA-4 Blockade and mTOR Inhibition Cooperate during CD8+ T Cell Priming To Promote Memory Formation and Metabolic Readiness
2015 StandoutNobel
Functional characteristics of dystrophic skeletal muscle: insights from animal models
2002
Mechanisms in Protein O-Glycan Biosynthesis and Clinical and Molecular Aspects of Protein O-Glycan Biosynthesis Defects: A Review
2006
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
2013 Standout
Autoimmune Dilated Cardiomyopathy in PD-1 Receptor-Deficient Mice
2001 StandoutScienceNobel
Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in body-wide skeletal muscles
2004 StandoutNobel
Myotubes differentiate optimally on substrates with tissue-like stiffness
2004
Chemical Glycoproteomics
2016 StandoutNobel
Computational design of a red fluorophore ligase for site-specific protein labeling in living cells
2014 StandoutNobel
Recombination signal sequence-binding protein Jκ alters mesodermal cell fate decisions by suppressing cardiomyogenesis
2003 StandoutNobel
The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation
2014

Works of S. Brown being referenced

Lack of myostatin results in excessive muscle growth but impaired force generation
2007
Dystrophin : gene, protein, and cell biology
1997
Guide to the methods of study and identification of soil gymnamoebae
2004
Diversity of gymnamoebae in grassland soil in southern Scotland
2004
Skeletal muscle pathology in autosomal dominant Emery‐Dreifuss muscular dystrophy with lamin A/C mutations
2001
FHL3 Is an Actin-binding Protein That Regulates α-Actinin-mediated Actin Bundling
2003
Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy
2005
The Cardiac Expression of Striated Muscle LIM Protein 1 (SLIM1) is Restricted to the Outflow Tract of the Developing Heart
1999
Phenotypic spectrum associated with mutations in the fukutin‐related protein gene
2003
Transgenic Overexpression of LARGE Induces α-Dystroglycan Hyperglycosylation in Skeletal and Cardiac Muscle
2010
Muscular dystrophies due to glycosylation defects
2011
Multiple Cosmopolitan Ecotypes within a Microbial Eukaryote Morphospecies
2006
Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan
2001
Profound skeletal muscle depletion of α-dystroglycan in Walker-Warburg syndrome
2003
Four and a Half LIM Protein 1 Binds Myosin-binding Protein C and Regulates Myosin Filament Formation and Sarcomere Assembly
2006
Non‐sarcolemmal Muscular Dystrophies
2001
Utrophin-Dystrophin-Deficient Mice as a Model for Duchenne Muscular Dystrophy
1997
The dystrophin–glycoprotein complex in brain development and disease
2012
Characterization of Two Isoforms of the Skeletal Muscle LIM Protein 1, SLIM1
1999
Defective glycosylation in congenital muscular dystrophies
2004
A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of α-dystroglycan
2003
Genetic correction of dystrophin deficiency and skeletal muscle remodeling in adult MDX mouse via transplantation of retroviral producer cells.
1997
Immunohistological intensity measurements as a tool to assess sarcolemma‐associated protein expression
2009
Abnormalities in α-Dystroglycan Expression in MDC1C and LGMD2I Muscular Dystrophies
2004
Defective glycosylation in muscular dystrophy
2002
Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human
2007
Enhanced expression of recombinant dystrophin following intramuscular injection of Epstein–Barr virus (EBV)-based mini-chromosome vectors in mdx mice
1999
Role of LIM Domains in Mediating Signaling Protein Interactions
2001
Estimating the Growth Potential of the Soil Protozoan Community
2000
Congenital muscular dystrophies
2002
FKRP gene mutations cause congenital muscular dystrophy, mental retardation, and cerebellar cysts
2003
Skeletal muscle LIM protein 1 (SLIM1/FHL1) induces α5β1-integrin-dependent myocyte elongation
2003
FHL3 binds MyoD and negatively regulates myotube formation
2007
Brief communication. First evaluation of nuclear DNA content in Setaria genus by flow cytometry
1998
Skeletal muscle LIM protein 1 regulates integrin-mediated myoblast adhesion, spreading, and migration
2003
Muscular dystrophies due to defective glycosylation of dystroglycan.
2007
Identification of FHL1 as a regulator of skeletal muscle mass: implications for human myopathy
2008
Dystrophic phenotype induced in vitro by antibody blockade of muscle α-dystroglycan-laminin interaction
1999
A reevaluation of the amoeba genus Vahlkampfia based on SSUrDNA sequences
1999
Rankless by CCL
2026