Citation Impact
Citing Papers
Visualizing enveloping layer glycans during zebrafish early embryogenesis
2010 StandoutNobel
TRP Channels as Potential Drug Targets
2017
Plants send small RNAs in extracellular vesicles to fungal pathogen to silence virulence genes
2018 StandoutScience
Angiotensin II causes hypertension and cardiac hypertrophy through its receptors in the kidney
2006 StandoutNobel
Structural basis for the recognition of SARS-CoV-2 by full-length human ACE2
2020 StandoutScience
Membrane curvature regulates the spatial distribution of bulky glycoproteins
2022 StandoutNobel
A Gain-of-Function Mutation in TRPA1 Causes Familial Episodic Pain Syndrome
2010
Latrophilins Function as Heterophilic Cell-adhesion Molecules by Binding to Teneurins
2013 StandoutNobel
Two Distinct Populations of Exosomes Are Released from LIM1863 Colon Carcinoma Cell-derived Organoids
2012
Wiskott-Aldrich syndrome protein regulates autophagy and inflammasome activity in innate immune cells
2017
CD9-Positive Microvesicles Mediate the Transfer of Molecules to Bovine Spermatozoa during Epididymal Maturation
2013
CNNM2 Mutations Cause Impaired Brain Development and Seizures in Patients with Hypomagnesemia
2014
Structure of the TRPA1 ion channel suggests regulatory mechanisms
2015 StandoutNatureNobel
Biogenesis of the Posterior Pole Is Mediated by the Exosome/Microvesicle Protein-sorting Pathway
2011
Mechanisms of SARS-CoV-2 entry into cells
2021 Standout
Discoveries in structure and physiology of mechanically activated ion channels
2020 StandoutNatureNobel
Angiotensin II Directly Stimulates ENaC Activity in the Cortical Collecting Duct via AT1 Receptors
2002
Exosomes from human saliva as a source of microRNA biomarkers
2009
SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor
2020 Standout
Myasthenia Gravis
2016 Standout
Increased Basal Activity Is a Key Determinant in the Severity of Human Skeletal Dysplasia Caused by TRPV4 Mutations
2011
Highly-purified exosomes and shed microvesicles isolated from the human colon cancer cell line LIM1863 by sequential centrifugal ultrafiltration are biochemically and functionally distinct
2015
Sialic acids in human health and disease
2008
Transient receptor potential channelopathies
2010
Exosomes: proteomic insights and diagnostic potential
2009
Exosomes: Extracellular organelles important in intercellular communication
2010 Standout
O-Pair Search with MetaMorpheus for O-glycopeptide characterization
2020 StandoutNobel
Neuromuscular junction disorders
2016
Guillain–Barré Syndrome
2012 Standout
Exosomes as new diagnostic tools in CNS diseases
2015
Improved biochemical strategies for targeted delivery of taxoids
2007
Gold nanoparticles in nanomedicine: preparations, imaging, diagnostics, therapies and toxicity
2009 Standout
Hypoxia and Hypoxia Signaling in Tissue Repair and Fibrosis
2012
International Union of Basic and Clinical Pharmacology. LXXVI. Current Progress in the Mammalian TRP Ion Channel Family
2010
Biological Functions of Autophagy Genes: A Disease Perspective
2019 Standout
Hermansky–Pudlak syndrome: a disease of protein trafficking and organelle function
2006
Mitochondria: In Sickness and in Health
2012 Standout
Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene
2002
Hypoxia and the extracellular matrix: drivers of tumour metastasis
2014 StandoutNobel
Shedding light on the cell biology of extracellular vesicles
2018 Standout
OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
2014 Standout
The Subsystems Approach to Genome Annotation and its Use in the Project to Annotate 1000 Genomes
2005 Standout
Chronic Health Conditions in Adult Survivors of Childhood Cancer
2006 Standout
Revealing the human mucinome
2022 StandoutNobel
Distinct roles for the kidney and systemic tissues in blood pressure regulation by the renin-angiotensin system
2005 StandoutNobel
A Cell-Penetrating Scorpion Toxin Enables Mode-Specific Modulation of TRPA1 and Pain
2019 StandoutNobel
TRPV1 structures in distinct conformations reveal activation mechanisms
2013 StandoutNatureNobel
Exosomes – vesicular carriers for intercellular communication
2009 Standout
TRPV4-pathy, a novel channelopathy affecting diverse systems
2010
Respiratory muscle weakness in peripheral neuropathies
2010
Glycosylation in health and disease
2019
Structure of the TRPV1 ion channel determined by electron cryo-microscopy
2013 StandoutNatureNobel
Expression and regulation of the neutral amino acid transporter B0AT1 in rat small intestine
2017
Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition
2005
Communication by Extracellular Vesicles: Where We Are and Where We Need to Go
2016 Standout
Long-term Complications Following Childhood and Adolescent Cancer: Foundations for Providing Risk-based Health Care for Survivors
2004
FLRT Proteins Are Endogenous Latrophilin Ligands and Regulate Excitatory Synapse Development
2012
Airway Mucus Function and Dysfunction
2010 Standout
CD39 and CD73 in immunity and inflammation
2013 Standout
Mitochondria: The Next (Neurode)Generation
2011
Mutations in theAUH gene cause 3-methylglutaconic aciduria type I
2003
Myasthenia gravis and the neuromuscular junction
2013
Characteristics and Progression of Hearing Loss in Children with Down Syndrome
2017
Identification of a Potential Peptide Inhibitor of SARS-CoV-2 Targeting its Entry into the Host Cells
2020
Gold nanoparticles in biomedical applications: recent advances and perspectives
2011 Standout
Inhibition of SARS-CoV-2 Infections in Engineered Human Tissues Using Clinical-Grade Soluble Human ACE2
2020 Standout
Chronic Kidney Disease
2016 Standout
Autophagy and human diseases
2013
Small RNAs are modified with N-glycans and displayed on the surface of living cells
2021 StandoutNobel
The Cell Biology of Hermansky–Pudlak Syndrome: Recent Advances
2005
Slc15a4, AP-3, and Hermansky-Pudlak syndrome proteins are required for Toll-like receptor signaling in plasmacytoid dendritic cells
2010 StandoutNobel
Down Syndrome
2020 Standout
Extracellular vesicles: Exosomes, microvesicles, and friends
2013 Standout
Regulated Airway Goblet Cell Mucin Secretion
2007
Proteomic comparison defines novel markers to characterize heterogeneous populations of extracellular vesicle subtypes
2016 Standout
Magnesium in Man: Implications for Health and Disease
2014 Standout
Mice with mutations of Dock7 have generalized hypopigmentation and white-spotting but show normal neurological function
2009 StandoutNobel
Walking the interactome for candidate prioritization in exome sequencing studies of Mendelian diseases
2014
Electron-Based Dissociation Is Needed for O-Glycopeptides Derived from OpeRATOR Proteolysis
2020 StandoutNobel
Cryo-EM and X-ray structures of TRPV4 reveal insight into ion permeation and gating mechanisms
2018
Genetic and epigenetic factors influencing chronic kidney disease
2014
Abnormal water metabolism in mice lacking the type 1A receptor for ANG II
2000 StandoutNobel
The biology , function , and biomedical applications of exosomes
2020 StandoutScience
A γGT-AT1Areceptor transgene protects renal cortical structure in AT1receptor-deficient mice
2004 StandoutNobel
Colloidal gold nanoparticles: a novel nanoparticle platform for developing multifunctional tumor‐targeted drug delivery vectors
2006
Role and mechanism of angiotensin‐converting enzyme 2 in acute lung injury in coronavirus disease 2019
2020
Phosphoproteins in extracellular vesicles as candidate markers for breast cancer
2017
Emerging Targets in Photopharmacology
2016 StandoutNobel
Structural insight into TRPV5 channel function and modulation
2019 StandoutNobel
Regulation of Sodium Balance and Blood Pressure by the AT1AReceptor for Angiotensin II
2000 StandoutNobel
Extracellular vesicles in diagnosis and therapy of kidney diseases
2016
Structural and Biochemical Consequences of Disease-Causing Mutations in the Ankyrin Repeat Domain of the Human TRPV4 Channel
2012
Distinct roles for the kidney and systemic tissues in blood pressure regulation by the renin-angiotensin system
2005 StandoutNobel
Chemical Glycoproteomics
2016 StandoutNobel
Works of Robert Kleta being referenced
Description of familial keloids in five pedigrees: evidence for autosomal dominant inheritance and phenotypic heterogeneity
2009
Regulation of Na+/H+ exchange by diadenosine polyphosphates, angiotensin II, and vasopressin in rat cortical collecting duct.
1995
The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel
2011
Biochemical and molecular analyses of infantile free sialic acid storage disease in North American children
2003
Cellular, Molecular and Clinical Characterization of Patients with Hermansky–Pudlak Syndrome Type 5
2004
Rab27b is Up‐Regulated in Human Griscelli Syndrome Type II Melanocytes and Linked to the Actin Cytoskeleton via Exon F‐Myosin Va Transcripts
2004
Large-Scale Proteomics and Phosphoproteomics of Urinary Exosomes
2008
Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility
2010
Type III 3-Methylglutaconic Aciduria (Optic Atrophy Plus Syndrome, or Costeff Optic Atrophy Syndrome): Identification of the OPA3 Gene and Its Founder Mutation in Iraqi Jews
2001
OPA3, mutated in 3-methylglutaconic aciduria type III, encodes two transcripts targeted primarily to mitochondria
2010
Phospholipase A2 Receptor (PLA2R1) Sequence Variants in Idiopathic Membranous Nephropathy
2013
A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis
2012
Mutations in TRPV4 cause Charcot-Marie-Tooth disease type 2C
2009
Tissue-Specific Amino Acid Transporter Partners ACE2 and Collectrin Differentially Interact With Hartnup Mutations
2008
Development of ifosfamide-induced nephrotoxicity: prospective follow-up in 75 patients
1999
A candidate gene for autoimmune myasthenia gravis
2012
KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function
2010
Familial hypomagnesemia-hypercalciuria in 2 siblings.
2001
2013
Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1
2016
Neurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome
2013
Generation and validation of a zebrafish model of EAST (Epilepsy, ataxia, sensorineural deafness and tubulopathy) syndrome
2013
Pharmacological treatment of nephropathic cystinosis with cysteamine
2004
Galactosylation of IgA1 Is Associated with Common Variation in C1GALT1
2017