| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/HUMU.20981 |
| P698 | PubMed publication ID | 19267394 |
| P50 | author | Leena Bruckner-Tuderman | Q1812122 |
| P2093 | author name string | Thomas M Magin | |
| Claudia Wohlenberg | |||
| Ursula Reuter | |||
| Wera Roth | |||
| P2860 | cites work | Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease | Q24540828 |
| p120-catenin mediates inflammatory responses in the skin | Q24647606 | ||
| Macrophage inflammatory protein 3alpha is involved in the constitutive trafficking of epidermal langerhans cells | Q24671761 | ||
| The MSP receptor regulates alpha6beta4 and alpha3beta1 integrins via 14-3-3 proteins in keratinocyte migration | Q28201887 | ||
| CCL27-CCR10 interactions regulate T cell-mediated skin inflammation | Q28217086 | ||
| Thymus and activation regulated chemokine (TARC)/CCL17 and skin diseases | Q28253402 | ||
| Good cop, bad cop: the different faces of NF-kappaB | Q28291669 | ||
| Acquisition of immune function during the development of the Langerhans cell network in neonatal mice | Q28366015 | ||
| Keratin 17 modulates hair follicle cycling in a TNFalpha-dependent fashion | Q28585367 | ||
| A keratin cytoskeletal protein regulates protein synthesis and epithelial cell growth | Q28592102 | ||
| The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases. | Q30366056 | ||
| Regulation of dendritic cell recruitment by chemokines | Q34505316 | ||
| Keratins: a structural scaffold with emerging functions. | Q35076346 | ||
| Keratins and skin disorders | Q35923500 | ||
| The basal keratin network of stratified squamous epithelia: defining K15 function in the absence of K14. | Q36235624 | ||
| Current insights into the formation and breakdown of hemidesmosomes. | Q36498608 | ||
| Langerhans cells renew in the skin throughout life under steady-state conditions | Q36505129 | ||
| Catenins: keeping cells from getting their signals crossed | Q36644519 | ||
| Structural and regulatory functions of keratins. | Q36791981 | ||
| Diseases of epidermal keratins and their linker proteins | Q36832566 | ||
| Loss of p120 catenin and links to mitotic alterations, inflammation, and skin cancer | Q36899976 | ||
| Complete cytolysis and neonatal lethality in keratin 5 knockout mice reveal its fundamental role in skin integrity and in epidermolysis bullosa simplex | Q38762092 | ||
| p120 Catenin is required for growth factor-dependent cell motility and scattering in epithelial cells | Q39788653 | ||
| KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome | Q40042316 | ||
| Constitutive expression and regulated release of the transmembrane chemokine CXCL16 in human and murine skin | Q40158221 | ||
| An autocrine/paracrine loop linking keratin 14 aggregates to tumor necrosis factor alpha-mediated cytotoxicity in a keratinocyte model of epidermolysis bullosa simplex | Q40609811 | ||
| A usual frameshift and delayed termination codon mutation in keratin 5 causes a novel type of epidermolysis bullosa simplex with migratory circinate erythema. | Q42446267 | ||
| Targeted deletion of the integrin beta4 signaling domain suppresses laminin-5-dependent nuclear entry of mitogen-activated protein kinases and NF-kappaB, causing defects in epidermal growth and migration | Q42480617 | ||
| New insights into the molecular basis of desmoplakin- and desmin-related cardiomyopathies. | Q50708085 | ||
| TNF-mediated inflammatory skin disease in mice with epidermis-specific deletion of IKK2 | Q57198247 | ||
| Induction of Inflammatory Cytokines by a Keratin Mutation and their Repression by a Small Molecule in a Mouse Model for EBS | Q59591354 | ||
| A frequent functional SNP in theMMP1promoter is associated with higher disease severity in recessive dystrophic epidermolysis bullosa | Q61843807 | ||
| P433 | issue | 5 | |
| P921 | main subject | epidermolysis bullosa | Q923020 |
| P304 | page(s) | 832-841 | |
| P577 | publication date | 2009-05-01 | |
| P1433 | published in | Human Mutation | Q5937269 |
| P1476 | title | Cytokines as genetic modifiers in K5-/- mice and in human epidermolysis bullosa simplex | |
| P478 | volume | 30 |
| Q27320939 | A Drosophila Model of Epidermolysis Bullosa Simplex. |
| Q84210782 | Animal models of epidermolysis bullosa: update 2010 |
| Q36631641 | Animal models of skin disease for drug discovery. |
| Q35759101 | Deconstructing the skin: cytoarchitectural determinants of epidermal morphogenesis |
| Q26852211 | Defining keratin protein function in skin epithelia: epidermolysis bullosa simplex and its aftermath |
| Q33888515 | Directed expression of a chimeric type II keratin partially rescues keratin 5-null mice |
| Q52615636 | Expression signature of epidermolysis bullosa simplex. |
| Q46103260 | Induction of phenotype modifying cytokines by FERMT1 mutations. |
| Q38768002 | Keratin 8-deletion induced colitis predisposes to murine colorectal cancer enforced by the inflammasome and IL-22 pathway |
| Q35125858 | Keratin gene mutations in disorders of human skin and its appendages |
| Q36580507 | Keratin intermediate filament proteins - novel regulators of inflammation and immunity in skin |
| Q38332150 | Keratins and skin disease. |
| Q28591014 | Keratins regulate protein biosynthesis through localization of GLUT1 and -3 upstream of AMP kinase and Raptor |
| Q33713926 | Mechanisms of fibroblast cell therapy for dystrophic epidermolysis bullosa: high stability of collagen VII favors long-term skin integrity |
| Q50875254 | Pro-Inflammatory Chemokines and Cytokines Dominate the Blister Fluid Molecular Signature in Patients with Epidermolysis Bullosa and Affect Leukocyte and Stem Cell Migration. |
| Q28393706 | Progress towards genetic and pharmacological therapies for keratin genodermatoses: current perspective and future promise |
| Q34319779 | The expanding significance of keratin intermediate filaments in normal and diseased epithelia |
| Q39740388 | The ubiquitin ligase CHIP/STUB1 targets mutant keratins for degradation. |
| Q64248984 | Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases |
| Q52625823 | Verrucous carcinoma in epidermolysis bullosa simplex is possibly associated with a novel mutation in the keratin 5 gene. |
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