Citation Impact
Citing Papers
Pten Deficiency in Melanocytes Results in Resistance to Hair Graying and Susceptibility to Carcinogen-Induced Melanomagenesis
2008 StandoutNobel
WGCNA: an R package for weighted correlation network analysis
2008 Standout
β-Catenin Controls Hair Follicle Morphogenesis and Stem Cell Differentiation in the Skin
2001 Standout
Integrated Weighted Gene Co-expression Network Analysis with an Application to Chronic Fatigue Syndrome
2008
Potent and Selective Triazole-Based Inhibitors of the Hypoxia-Inducible Factor Prolyl-Hydroxylases with Activity in the Murine Brain
2015 StandoutNobel
Interleukin-6 protects hepatocytes from CCl4-mediated necrosis and apoptosis in mice by reducing MMP-2 expression
2005
Atopic Dermatitis
2008 Standout
Mutations in the NF-κB signaling pathway: implications for human disease
2006
Control of Cyclin D1 and Breast Tumorigenesis by the EglN2 Prolyl Hydroxylase
2009 StandoutNobel
Liver fibrosis
2005 Standout
Association of differentially expressed genes with activation of mouse hepatic stellate cells by high-density cDNA mircoarray
2004
MicroRNA-205 Maintains T Cell Development following Stress by Regulating Forkhead Box N1 and Selected Chemokines
2016
Progressive activation of TH2/TH22 cytokines and selective epidermal proteins characterizes acute and chronic atopic dermatitis
2012
Role for ELOVL3 and Fatty Acid Chain Length in Development of Hair and Skin Function
2004 StandoutNobel
Cellulose nanomaterials review: structure, properties and nanocomposites
2011 Standout
Evaluation, Treatment, and Prevention of Vitamin D Deficiency: an Endocrine Society Clinical Practice Guideline
2011 Standout
Obesity-induced gut microbial metabolite promotes liver cancer through senescence secretome
2013 StandoutNature
Atopic dermatitis
2015 Standout
Molecular characterization of homozygous variegate porphyria
1998
Shared Principles in NF-κB Signaling
2008 Standout
PAR1 antagonism protects against experimental liver fibrosis. Role of proteinase receptors in stellate cell activation
2004
Secreted and Transmembrane Wnt Inhibitors and Activators
2012
Porphyrias
2010 Standout
Cryopreservation of hepatic stellate cells
2005
Homozygous Variegate Porphyria: 20 y Follow-Up and Characterization of Molecular Defect
2001
Stem cells find their niche
2001 StandoutNature
Oxygen sensing by HIF hydroxylases
2004 StandoutNobel
Immortal Activated Human Hepatic Stellate Cells Generated by Ectopic Telomerase Expression
2002
MiR-21 Simultaneously Regulates ERK1 Signaling in HSC Activation and Hepatocyte EMT in Hepatic Fibrosis
2014
Structurally Mapping Endogenous Heme in the CcmCDE Membrane Complex for Cytochrome c Biogenesis
2018 StandoutNobel
Discoidin Domain Receptor 2 Interacts with Src and Shc following Its Activation by Type I Collagen
2002
JmjC-domain-containing proteins and histone demethylation
2006
What a difference a hydroxyl makes: mutant IDH, (R)-2-hydroxyglutarate, and cancer
2013 StandoutNobel
The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
1999
Effect of bradykinin metabolism inhibitors on evoked hypotension in rats: rank efficacy of enzymes associated with bradykinin‐mediated angioedema
2007
Structural and functional features of central nervous system lymphatic vessels
2015 StandoutNature
Variegate Porphyria in Western Europe: Identification of PPOX Gene Mutations in 104 Families, Extent of Allelic Heterogeneity, and Absence of Correlation between Phenotype and Type of Mutation
1999
Vitamin D and the skin
2010
Metazoan MicroRNAs
2018 Standout
Two to Tango: Regulation of Mammalian Iron Metabolism
2010 Standout
DDR2 receptor promotes MMP-2–mediated proliferation and invasion by hepatic stellate cells
2001
Epidermal Nerve Fibers Modulate Keratinocyte Growth via Neuropeptide Signaling in an Innervated Skin Model
2013
Histone demethylation by a family of JmjC domain-containing proteins
2005 StandoutNature
Wnt/β-Catenin Signaling and Disease
2012 Standout
Wnt/β-Catenin Signaling: Components, Mechanisms, and Diseases
2009 Standout
Cytochrome P450 2E1-derived Reactive Oxygen Species Mediate Paracrine Stimulation of Collagen I Protein Synthesis by Hepatic Stellate Cells
2002
Roles of JUMONJI in mouse embryonic development
2004
Causes of epidermal filaggrin reduction and their role in the pathogenesis of atopic dermatitis
2014
TNF-α and Th2 Cytokines Induce Atopic Dermatitis–Like Features on Epidermal Differentiation Proteins and Stratum Corneum Lipids in Human Skin Equivalents
2014
The nuclear receptor SHP mediates inhibition of hepatic stellate cells by FXR and protects against liver fibrosis
2004
Adenosine A2Areceptors play a role in the pathogenesis of hepatic cirrhosis
2006
Human hepatic stellate cell lines, LX-1 and LX-2: new tools for analysis of hepatic fibrosis
2004
Proangiogenic Role of Tumor–Activated Hepatic Stellate Cells in Experimental Melanoma Metastasis
2003
Differential expression genes analyzed by cDNA array in the regulation of rat hepatic fibrogenesis
2006
Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relatives
2009
EMT: 2016
2016 Standout
Hypoxia-inducible Factor (HIF) Asparagine Hydroxylase Is Identical to Factor Inhibiting HIF (FIH) and Is Related to the Cupin Structural Family
2002 StandoutNobel
Identification of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies
2011 Standout
WNT Signaling in the Control of Hair Growth and Structure
1999
Mechanisms of fibrosis: therapeutic translation for fibrotic disease
2012 Standout
Liver Retinol Transporter and Receptor for Serum Retinol-binding Protein (RBP4)
2012
GFAP promoter directs lacZ expression specifically in a rat hepatic stellate cell line
2006
The Biology of Hair Follicles
1999 Standout
Diagnosis and treatment of the hepatic porphyrias
2003
Structure of Factor-inhibiting Hypoxia-inducible Factor (HIF) Reveals Mechanism of Oxidative Modification of HIF-1α
2003 StandoutNobel
Angiotensin–Neprilysin Inhibition versus Enalapril in Heart Failure
2014 Standout
Leptin in hepatic fibrosis: Evidence for increased collagen production in stellate cells and lean littermates of ob/ob mice
2002
Heme in pathophysiology: a matter of scavenging, metabolism and trafficking across cell membranes
2014
Nanoparticles, Proteins, and Nucleic Acids: Biotechnology Meets Materials Science
2001 Standout
The Retinoblastoma Binding Protein RBP2 Is an H3K4 Demethylase
2007 StandoutNobel
Mouse R-spondin2 is required for apical ectodermal ridge maintenance in the hindlimb
2007
Liver fibrosis: searching for cell model answers
2007
Cancer-related inflammation
2008 StandoutNature
Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humans
1998
JmjC: cupin metalloenzyme-like domains in jumonji, hairless and phospholipase A2β
2001
Hepatic Stellate Cells: Protean, Multifunctional, and Enigmatic Cells of the Liver
2008 Standout
Wnt/β-Catenin Signaling, Disease, and Emerging Therapeutic Modalities
2017 Standout
The Polycomb complex PRC2 and its mark in life
2011 StandoutNature
Chronic tophaceous gout as the first manifestation of gout in two cases and a review of the literature
2017
Generalized lymphedema associated with neurologic signs (GLANS) syndrome: A new entity?
2014
Autosomal recessive erythropoietic protoporphyria in the United Kingdom: prevalence and relationship to liver disease
2004
PAV-1, a new rat hepatic stellate cell line converts retinol into retinoic acid, a process altered by ethanol
2002
The hairless mouse in skin research
2008
Nanostructure of cellulose microfibrils in spruce wood
2011 Standout
FOXP3: Of Mice and Men
2005
Familial and Sporadic Porphyria Cutanea Tarda: Characterization and Diagnostic Strategies
2009
DDR2 receptor promotes MMP-2–mediated proliferation and invasion by hepatic stellate cells
2001
The Maize Primary Cell Wall Microfibril: A New Model Derived from Direct Visualization
2006
Structure of the STRA6 receptor for retinol uptake
2016 StandoutScienceNobel
Methylation: lost in hydroxylation?
2005
Expansion of FOXP3high regulatory T cells by human dendritic cells (DCs) in vitro and after injection of cytokine-matured DCs in myeloma patients
2006 StandoutNobel
Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
1999
Control of skin cancer by the circadian rhythm
2011 StandoutNobel
Emerging Challenges in Regulatory T Cell Function and Biology
2007 StandoutScienceNobel
Reduced filaggrin expression is accompanied by increased Staphylococcus aureus colonization of epidermal skin models
2014
Gout
2021 Standout
Scraggly, a new hair loss mutation on mouse Chromosome 19
1999
Controls of Hair Follicle Cycling
2001 Standout
Tissue-specific contributions of Tmem79 to atopic dermatitis and mast cell-mediated histaminergic itch
2018 StandoutNobel
Phospholipase A2Enzymes: Physical Structure, Biological Function, Disease Implication, Chemical Inhibition, and Therapeutic Intervention
2011 Standout
Plakoglobin Suppresses Epithelial Proliferation and Hair Growth in Vivo
2000 StandoutNobel
The gene gun: current applications in cutaneous gene therapy
2000
Biomass Recalcitrance: Engineering Plants and Enzymes for Biofuels Production
2007 StandoutScience
Works of Jorge Frank being referenced
RSPO4 Is the Major Gene in Autosomal-Recessive Anonychia and Mutations Cluster in the Furin-Like Cysteine-Rich Domains of the Wnt Signaling Ligand R-spondin 4
2007
Lymphedema in Prader–Willi syndrome
2008
Homozygous Variegate Porphyria: Identification of Mutations on Both Alleles of the Protoporphyrinogen Oxidase Gene in a Severely Affected Proband
1998
Variegate Porphyria: Identification of a Nonsense Mutation in the Protoporphyrinogen Oxidase Gene
1998
The molecular basis of porphyria cutanea tarda in Chile: Identification and functional characterization of mutations in the uroporphyrinogen decarboxylase gene
2004
European porphyria initiative (EPI): a platform to develop a common approach to the management of porphyrias and to promote research in the field
2006
Porphyria cutanea tarda – When skin meets liver
2010
IL-31 regulates differentiation and filaggrin expression in human organotypic skin models
2011
Mutations in the Gene Encoding the Wnt-Signaling Component R-Spondin 4 (RSPO4) Cause Autosomal Recessive Anonychia
2006
Phenotype Diversity in Familial Cylindromatosis: A Frameshift Mutation in the Tumor Suppressor Gene CYLD Underlies Different Tumors of Skin Appendages
2002
Molecular heterogeneity of familial porphyria cutanea tarda in Spain: characterization of 10 novel mutations in the UROD gene
2007
Tophi as first clinical sign of gout
2008
Treatment of acute edema attacks in hereditary angioedema with a bradykinin receptor-2 antagonist (Icatibant)
2007
Ancestral Founder Mutation of the Nude (FOXN1) Gene in Congenital Severe Combined Immunodeficiency Associated with Alopecia in Southern Italy Population
2004
Diagnosis and Treatment of the Acute Porphyrias: An Interdisciplinary Challenge
2001
Recurrent missense mutation in the protoporphyrinogen oxidase gene underlies variegate porphyria
1998
Alopecia Universalis Associated with a Mutation in the Human hairless Gene
1998 Science
Human equivalent of the mouse Nude/SCID phenotype: long-term evaluation of immunologic reconstitution after bone marrow transplantation
2001
Molecular basis of variegate porphyria: a missense mutation in the protoporphyrinogen oxidase gene.
1998
Erythropoietic protoporphyria: identification of novel mutations in the ferrochelatase gene and comparison of biochemical markers versus molecular analysis as diagnostic strategies.
1999
An immortalized rat liver stellate cell line (HSC-T6): a new cell model for the study of retinoid metabolism in vitro
2000