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JOURNAL OF INVESTIGATIVE DERMATOLOGY
Rivista
Codice:
E092388
ISSN:
0022-202X
Dati Generali
Dati Generali
Pubblicazioni (33)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
A new role for the human vascular endothelial growth factor receptor-1: Direct involvement in endothelial cell adhesion and migration
Abstract
A stop codon in xeroderma pigmentosum group C families in Turkey and Italy: molecular genetic evidence for a common ancestor.
Articolo
Actin reorganization is abnormal and cellular ATP is decreased in Hailey-Hayley keratinocytes.
Articolo
Antimicrobial Properties Of Distinctin In An Experimental Model Of MRSA-Infected Wounds.
Articolo
Association of Melanocortin-1 Receptor Variants with Pigmentary Traits in Humans: A Pooled Analysis from the M-Skip Project
Articolo
Bmi-1 reduction plays a key role in physiological and premature aging of primary human keratinocytes.
Articolo
Clinical significance of PCR-positive mRNA markers in peripheral blood and regional nodes of malignant melanoma (MM) patients
Abstract
Cockayne Syndrome Type a (CSA) Protein Protects Primary Human Keratinocytes from Senescence.
Articolo
Combining Type I Interferons and 5-Aza-2 '-Deoxycitidine to Improve Anti-Tumor Response against Melanoma
Articolo
DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and Cockayne syndrome resemble xeroderma pigmentosum cells
Articolo
Differential modulation of Ku70/80 DNA-binding activity in a patient with multiple basal cell carcinomas.
Articolo
EDA2R Is Associated with Androgenetic Alopecia.
Articolo
Endocannabinoid Tone Regulates Human Sebocyte Biology
Articolo
Evidence for a cell adhesion role of human vascular endothelial growth factor receptor-1
Articolo
Expression and function of nerve growth factor and nerve growth factor receptor on cultured keratinocytes
Articolo
Expression of the Collagen VI alpha5 and alpha6 Chains in Normal Human Skin and in Skin of Patients with Collagen VI-Related Myopathies
Articolo
High-frequency microsatellite instability is associated with defective DNA mismatch repair in human melanoma.
Articolo
High-mobility group box 1 protein in human and murine skin: involvement in wound healing.
Articolo
Human Keratinocyte ATP2C1 localizes to the Golgi and controls Golgi Ca2+ stores.
Articolo
IKK alpha Is a p63 Transcriptional Target Involved in the Pathogenesis of Ectodermal Dysplasias
Articolo
IKKalpha Is a p63 Transcriptional Target Involved in the Pathogenesis of Ectodermal Dysplasias.
Articolo
Identification of BRAF 3'UTR Isoforms in Melanoma
Articolo
Low levels of genetic heterogeneity in matched lymph node metastases from melanoma patients
Articolo
MUTATIONS IN ERBB4 MAY PLAY A MINOR ROLE IN MELANOMA PATHOGENESIS
Articolo
Mimetic peptides of suppressor of cytokine signaling (SOCS)1 impair inflammatory responses of epidermal keratinocytes in vitro and in a mouse skin model of allergic contact dermatitis
Articolo
Molecular genetic analysis in a large group of families and sporadic cases affected by Incontinentia Pigmenti: Genomic rearrangement, new mutations and genotype-phenotype correlations
Abstract
Mutations in ERBB4 may have a minor role in melanoma pathogenesis
Articolo
Nectin-4 Mutations Causing Ectodermal Dysplasia with Syndactyly Perturb the Rac1 Pathway and the Kinetics of Adherens Junction Formation
Articolo
Nerve growth factor is increased in psoriatic skin
Articolo
POF1B Localizes to Desmosomes and Regulates Cell Adhesion in Human Intestinal and Keratinocyte Cell Lines
Articolo
Radiosensitization of human melanoma cell by ribozyme-mediated inhibition of survivin expression
Articolo
Soluble vascular endothelial growth factor-1 could represent a positive mediator in the angiogenic process
Abstract
Two New XPD Patients Compound Heterozygous for the Same Mutation Demonstrate Diverse Clinical Features.
Articolo
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