Epithelial Biology Laboratory
E. Birgitte Lane has not added Biography.
If you are E. Birgitte Lane and would like to personalize this page please email our Author Liaison for assistance.
Deletion of the cytoplasmatic domain of BP180/collagen XVII causes a phenotype with predominant features of epidermolysis bullosa simplex.
The Journal of investigative dermatology Jan, 2002 | Pubmed ID: 11851893
Characterization of early assembly intermediates of recombinant human keratins.
Journal of structural biology Jan-Feb, 2002 | Pubmed ID: 12064936
Defolliculated (dfl): a dominant mouse mutation leading to poor sebaceous gland differentiation and total elimination of pelage follicles.
The Journal of investigative dermatology Jul, 2002 | Pubmed ID: 12164921
Cloning of human, murine, and marsupial keratin 7 and a survey of K7 expression in the mouse.
Biochemical and biophysical research communications Oct, 2002 | Pubmed ID: 12359226
Keratin mutations of epidermolysis bullosa simplex alter the kinetics of stress response to osmotic shock.
Journal of cell science Nov, 2002 | Pubmed ID: 12376565
Long-range polymerase chain reaction for specific full-length amplification of the human keratin 14 gene and novel keratin 14 mutations in epidermolysis bullosa simplex patients.
The Journal of investigative dermatology Mar, 2003 | Pubmed ID: 12603865
Observation of keratin particles showing fast bidirectional movement colocalized with microtubules.
Journal of cell science Apr, 2003 | Pubmed ID: 12640027
Phenotypes, genotypes and their contribution to understanding keratin function.
Trends in genetics : TIG May, 2003 | Pubmed ID: 12711220
The quest for the function of simple epithelial keratins.
BioEssays : news and reviews in molecular, cellular and developmental biology Aug, 2003 | Pubmed ID: 12879445
Conformational changes in the rod domain of human keratin 8 following heterotypic association with keratin 18 and its implication for filament stability.
Biochemistry Feb, 2004 | Pubmed ID: 14756564
Keratin 8/18 breakdown and reorganization during apoptosis.
Experimental cell research Jul, 2004 | Pubmed ID: 15194421
Mechanical stress induces profound remodelling of keratin filaments and cell junctions in epidermolysis bullosa simplex keratinocytes.
Journal of cell science Oct, 2004 | Pubmed ID: 15454576
Stress models for the study of intermediate filament function.
Methods in cell biology , 2004 | Pubmed ID: 15646621
Two families with Greither's syndrome caused by a keratin 1 mutation.
Journal of the American Academy of Dermatology Nov, 2005 | Pubmed ID: 16227096
Clinical and pathological features of pachyonychia congenita.
The journal of investigative dermatology. Symposium proceedings / the Society for Investigative Dermatology, Inc. [and] European Society for Dermatological Research Oct, 2005 | Pubmed ID: 16250204
Mutation S233L in the 1B domain of keratin 1 causes epidermolytic palmoplantar keratoderma with "tonotubular" keratin.
The Journal of investigative dermatology Mar, 2006 | Pubmed ID: 16439967
Association of Shh and Ptc with keratin localization in the initiation of the formation of circumvallate papilla and von Ebner's gland.
Cell and tissue research Aug, 2006 | Pubmed ID: 16552524
New consensus nomenclature for mammalian keratins.
The Journal of cell biology Jul, 2006 | Pubmed ID: 16831889
Epidermolysis bullosa simplex in Scotland caused by a spectrum of keratin mutations.
The Journal of investigative dermatology Mar, 2007 | Pubmed ID: 17039244
Intermediate filaments and stress.
Experimental cell research Jun, 2007 | Pubmed ID: 17524394
Multiple self-healing squamous epithelioma in different ethnic groups: more than a founder mutation disorder?
The Journal of investigative dermatology Oct, 2007 | Pubmed ID: 17554363
Ninein is released from the centrosome and moves bi-directionally along microtubules.
Journal of cell science Sep, 2007 | Pubmed ID: 17698918
A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita.
Journal of dermatological science Dec, 2007 | Pubmed ID: 17719747
Molecular force spectroscopy of homophilic nectin-1 interactions.
Biochemical and biophysical research communications Nov, 2007 | Pubmed ID: 17822670
The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases.
Human mutation Mar, 2008 | Pubmed ID: 18033728
Unique and recurrent mutations in the filaggrin gene in Singaporean Chinese patients with ichthyosis vulgaris.
The Journal of investigative dermatology Jul, 2008 | Pubmed ID: 18239616
Dual-specificity phosphatases in the hypo-osmotic stress response of keratin-defective epithelial cell lines.
Experimental cell research Jun, 2008 | Pubmed ID: 18410923
Therapeutic siRNAs for dominant genetic skin disorders including pachyonychia congenita.
Journal of dermatological science Sep, 2008 | Pubmed ID: 18495438
The intermediate filament network in cultured human keratinocytes is remarkably extensible and resilient.
PloS one , 2008 | Pubmed ID: 18523546
Association of skin barrier genes within the PSORS4 locus is enriched in Singaporean Chinese with early-onset psoriasis.
The Journal of investigative dermatology Mar, 2009 | Pubmed ID: 18787534
Keratin K6c mutations cause focal palmoplantar keratoderma.
The Journal of investigative dermatology Feb, 2010 | Pubmed ID: 19609311
Severe keratin 5 and 14 mutations induce down-regulation of junction proteins in keratinocytes.
Experimental cell research Oct, 2009 | Pubmed ID: 19616543
ERK involvement in resistance to apoptosis in keratinocytes with mutant keratin.
The Journal of investigative dermatology Mar, 2010 | Pubmed ID: 19847192
A novel mutation in the kinase domain of KIT in an Indian family with a mild piebaldism phenotype.
Journal of dermatological science Sep, 2010 | Pubmed ID: 20688482
Immunohistochemical localization of cytokeratins in the junctional region of ectoderm and endoderm.
Anatomical record (Hoboken, N.J. : 2007) Nov, 2010 | Pubmed ID: 20818615
Filaggrin null mutations are not a protective factor for acne vulgaris.
The Journal of investigative dermatology Jun, 2011 | Pubmed ID: 21326297
Keratin 14-null cells as a model to test the efficacy of gene therapy approaches in epithelial cells.
The Journal of investigative dermatology Jul, 2011 | Pubmed ID: 21326298
Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1.
Nature genetics Apr, 2011 | Pubmed ID: 21358634
Developmental expression of the fermitin/kindlin gene family in Xenopus laevis embryos.
Developmental dynamics : an official publication of the American Association of Anatomists Aug, 2011 | Pubmed ID: 21761481
Validation of GWAS loci for atopic dermatitis in a Singapore Chinese population.
The Journal of investigative dermatology May, 2012 | Pubmed ID: 22318392
The mechanical behavior of mutant K14-R125P keratin bundles and networks in NEB-1 keratinocytes.
PloS one , 2012 | Pubmed ID: 22363617
Keratins and disease at a glance.
Journal of cell science Sep, 2012 | Pubmed ID: 23104737
'See-saw' expression of microRNA-198 and FSTL1 from a single transcript in wound healing.
Nature Mar, 2013 | Pubmed ID: 23395958
Lamin B1 fluctuations have differential effects on cellular proliferation and senescence.
The Journal of cell biology Mar, 2013 | Pubmed ID: 23439683
Generation and characterisation of keratin 7 (K7) knockout mice.
PloS one , 2013 | Pubmed ID: 23741325
Making more matrix: enhancing the deposition of dermal-epidermal junction components in vitro and accelerating organotypic skin culture development, using macromolecular crowding.
Tissue engineering. Part A Jan, 2015 | Pubmed ID: 25058150
Characterization of fetal keratinocytes, showing enhanced stem cell-like properties: a potential source of cells for skin reconstruction.
Stem cell reports Aug, 2014 | Pubmed ID: 25254345
Assays to Study Consequences of Cytoplasmic Intermediate Filament Mutations: The Case of Epidermal Keratins.
Methods in enzymology , 2016 | Pubmed ID: 26795473
Direct organelle thermometry with fluorescence lifetime imaging microscopy in single myotubes.
Chemical communications (Cambridge, England) Mar, 2016 | Pubmed ID: 26977478
SOBRE A JoVE
Copyright © 2024 MyJoVE Corporation. Todos os direitos reservados