Standout Papers
- Expanding the scope of N → S acyl transfer in native peptide sequences (2015)
- Persistent kallikrein 5 activation induces atopic dermatitis-like skin architecture independent of PAR2 activity (2017)
- Sunflower trypsin inhibitor (SFTI-1) analogues of synthetic and biological origin via N→S acyl transfer: potential inhibitors of human Kallikrein-5 (KLK5) (2014)
- Tissue Kallikrein Inhibitors Based on the Sunflower Trypsin Inhibitor Scaffold – A Potential Therapeutic Intervention for Skin Diseases (2016)
Citation Impact
Citing Papers
Widespread Parallel Evolution in Sticklebacks by Repeated Fixation of Ectodysplasin Alleles
2005 StandoutScience
Signaling from β1- and β2-adrenergic receptors is defined by differential interactions with PDE4
2008 StandoutNobel
The International Scientific Association of Probiotics and Prebiotics (ISAPP) consensus statement on the definition and scope of postbiotics
2021 Standout
Exploring chemoselective S-to-N acyl transfer reactions in synthesis and chemical biology
2017
The history and advances in cancer immunotherapy: understanding the characteristics of tumor-infiltrating immune cells and their therapeutic implications
2020 Standout
Down-Regulation of Na+/K+ATPase Activity by Human Parvovirus B19 Capsid Protein VP1
2013 Standout
Genetic Heterogeneity in Erythrokeratodermia Variabilis: Novel Mutations in the Connexin Gene GJB4 (Cx30.3) and Genotype-Phenotype Correlations
2003
Dynamic changes in connexin expression correlate with key events in the wound healing process
2003
Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria
2002
Connexin disorders of the skin
2005
Gap junction diseases of the skin
2004
Determination of free and total (free plus protein-bound) melatonin in plasma and cerebrospinal fluid by high-performance liquid chromatography with fluorescence detection
2002
Elucidating the principles of the molecular organization of heteropolymeric tight junction strands
2011
Expanding The Phenotypic Spectrum of Cx26 Disorders: Bart–Pumphrey Syndrome is Caused by a Novel Missense Mutation in GJB2
2004
Hidradenitis suppurativa: A comprehensive review
2009 Standout
Inhibition of JNK Promotes Differentiation of Epidermal Keratinocytes
2006
Connexin disorders of the ear, skin, and lens
2004
TRPV3 in keratinocytes transmits temperature information to sensory neurons via ATP
2009 StandoutNobel
Functional Analysis of a Novel I71N Mutation in the <i>GJB2</i> Gene Among Southern Egyptians Causing Autosomal Recessive Hearing Loss
2010
The International Scientific Association for Probiotics and Prebiotics (ISAPP) consensus statement on the definition and scope of synbiotics
2020 Standout
Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects
2020 Standout
Functional Domain Mapping and Selective Trans-dominant Effects Exhibited by Cx26 Disease-causing Mutations
2004
Roles of Met-34, Cys-64, and Arg-75 in the Assembly of Human Connexin 26
2003
Protease inhibition as new therapeutic strategy for GI diseases
2016
Transport and Function of Cx26 Mutants Involved in Skin and Deafness Disorders
2003
A Deafness-Associated Mutant Human Connexin 26 Improves the Epithelial Barrier In Vitro
2007
Hereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new era
2015 Standout
Mitochondrial transfer from bone-marrow–derived stromal cells to pulmonary alveoli protects against acute lung injury
2012 Standout
Biological Functions of Autophagy Genes: A Disease Perspective
2019 Standout
Metalloproteinases and their natural inhibitors in inflammation and immunity
2013
A Lactobacillus rhamnosus GG-derived Soluble Protein, p40, Stimulates Ligand Release from Intestinal Epithelial Cells to Transactivate Epidermal Growth Factor Receptor
2013
Sensorineural hearing loss in children
2005 Standout
Constitutive Autophagy and Nucleophagy during Epidermal Differentiation
2016
Revealing the human mucinome
2022 StandoutNobel
Remodelling the extracellular matrix in development and disease
2014 Standout
Proteases and small intestinal barrier function in health and disease
2014
Physiology and Pathophysiology of Purinergic Neurotransmission
2007 Standout
Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome
2002
Structures of membrane proteins
2010 StandoutNobel
Connexin gene pathology
2003
Tetracysteine Genetic Tags Complexed with Biarsenical Ligands as a Tool for Investigating Gap Junction Structure and Dynamics
2003 StandoutNobel
The skin: an indispensable barrier
2008 Standout
SWELL1, a Plasma Membrane Protein, Is an Essential Component of Volume-Regulated Anion Channel
2014 StandoutNobel
Dysbiosis and Staphylococcus aureus Colonization Drives Inflammation in Atopic Dermatitis
2015
Nuevos modelos experimentales para el estudio de la homeostasis y la enfermedad cutánea
2014
Novel Connexin 43 (GJA1) mutation causes oculo–dento–digital dysplasia with curly hair
2004
Structural and Functional Similarities of Calcium Homeostasis Modulator 1 (CALHM1) Ion Channel with Connexins, Pannexins, and Innexins*
2013
Connexin30 mutations responsible for hidrotic ectodermal dysplasia cause abnormal hemichannel activity
2004
AKAP79-mediated Targeting of the Cyclic AMP-dependent Protein Kinase to the β1-Adrenergic Receptor Promotes Recycling and Functional Resensitization of the Receptor
2006
Cytochrome P450 enzymes in drug metabolism: Regulation of gene expression, enzyme activities, and impact of genetic variation
2013 Standout
Mutation of a Conserved Threonine in the Third Transmembrane Helix of α- and β-Connexins Creates a Dominant-negative Closed Gap Junction Channel
2005
Mutations in the gene for connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on connexin 30
2003
Identification of Cyclobutane Pyrimidine Dimer-Responsive Genes Using UVB-Irradiated Human Keratinocytes Transfected with In Vitro-Synthesized Photolyase mRNA
2015 StandoutNobel
Proteases and the gut barrier
2012
A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract
2003
The human skin microbiome
2018 Standout
The prevalence of connexin 26 ( GJB2 ) mutations in the Chinese population
2002
Gene therapies for inherited skin disorders
2014
A novel connexin 26 gene mutation associated with features of the keratitis-ichthyosis-deafness syndrome and the follicular occlusion triad
2004
Targeted epidermal expression of mutant Connexin 26(D66H) mimics true Vohwinkel syndrome and provides a model for the pathogenesis of dominant connexin disorders
2003
Wound repair and regeneration: Mechanisms, signaling, and translation
2014 Standout
Fluorescence lifetime imaging microscopy (FLIM) to quantify protein–protein interactions inside cells
2006
Structure of the human volume regulated anion channel
2018 StandoutNobel
2003
Regulatory T Cells and Human Disease
2020 StandoutNobel
New Experimental Models of Skin Homeostasis and Diseases
2014
Seven Post-synthetic Covalent Reactions in Tandem Leading to Enzyme-like Complexity within Metal–Organic Framework Crystals
2016 StandoutNobel
Visualization of mycobacterial membrane dynamics in live cells
2017 StandoutNobel
Oculodentodigital Dysplasia-causing Connexin43 Mutants Are Non-functional and Exhibit Dominant Effects on Wild-type Connexin43
2005
Fluorescence Lifetime Measurements and Biological Imaging
2010 Standout
Ca2+ waves in keratinocytes are transmitted to sensory neurons: the involvement of extracellular ATP and P2Y2 receptor activation
2004
Three-dimensional structure of a human connexin26 gap junction channel reveals a plug in the vestibule
2007
An intact connexin N-terminus is required for function but not gap junction formation
2008
CONNEXINS AND CELL SIGNALING IN DEVELOPMENT AND DISEASE
2004
Advances in Fmoc solid‐phase peptide synthesis
2016
Plasma Membrane Channels Formed by Connexins: Their Regulation and Functions
2003
Going Round in Circles with N→S Acyl Transfer
2017 StandoutNobel
Computation-Guided Rational Design of a Peptide Motif That Reacts with Cyanobenzothiazoles via Internal Cysteine–Lysine Relay
2018 StandoutNobel
Advanced Fluorescence Microscopy Techniques—FRAP, FLIP, FLAP, FRET and FLIM
2012
Molecular Genetics of Hearing Loss
2001
Genetic variants of Adam17 differentially regulate TGFβ signaling to modify vascular pathology in mice and humans
2014
Life cycle of connexins in health and disease
2006 Standout
TRP ION CHANNELS AND TEMPERATURE SENSATION
2006 StandoutNobel
Emerging issues of connexin channels: biophysics fills the gap
2001
Translating Immunology into Therapeutic Concepts for Inflammatory Bowel Disease
2018
Extrapineal melatonin: sources, regulation, and potential functions
2014 Standout
Claudins and the Modulation of Tight Junction Permeability
2013 Standout
trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation
2001
Clinical Practice Guideline: Sudden Hearing Loss (Update)
2019 Standout
The gut-brain axis: interactions between enteric microbiota, central and enteric nervous systems.
2015 Standout
Mechanisms of Cx43 and Cx26 transport to the plasma membrane and gap junction regeneration
2005
Altered connexin expression and wound healing in the epidermis of connexin-deficient mice
2003
Diverse gap junctions modulate distinct mechanisms for fiber cell formation during lens development and cataractogenesis
2006 StandoutNobel
Genetics of Sensory Mechanotransduction
2002 StandoutNobel
Works of Wei‐Li Di being referenced
Multiple Epidermal Connexins are Expressed in Different Keratinocyte Subpopulations Including Connexin 31
2001
Cellular Mechanisms of Mutant Connexins in Skin Disease and Hearing Loss
2003
Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutations
2002
Ex-vivo Gene Therapy Restores LEKTI Activity and Corrects the Architecture of Netherton Syndrome-derived Skin Grafts
2010
Connexin 26 Expression and Mutation Analysis in Epidermal Disease
2001
Inflammatory Skin and Bowel Disease Linked toADAM17Deletion
2011
The pineal and extra‐pineal origins of 5‐sulphatoxy N‐acetyl‐serotonin in humans
1999
Quantitative fluorescence resonance energy transfer (FRET) measurement with acceptor photobleaching and spectral unmixing
2004
AKT1-mediated Lamin A/C degradation is required for nuclear degradation and normal epidermal terminal differentiation
2015
Connexin Mutations in Skin Disease and Hearing Loss
2001
An enzyme immunoassay for 6‐sulphatoxy‐melatonin in human urine
1996
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss
2001
Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysis
2005
Functional studies of human skin disease- and deafness-associated connexin 30 mutations
2002
Radioimmunoassay of bound and free melatonin in plasma
1998
Expanding the scope of N → S acyl transfer in native peptide sequences
2015 StandoutNobel
HPLC assay of melatonin in plasma with fluorescence detection
1993
Aberrant gating, but a normal expression pattern, underlies the recessive phenotype of the deafness mutant Connexin26M34T
2004