E. Birgitte Lane

Epithelial Biology Laboratory, Institute of Medical Biology, A*STAR

Affiliated withInstitute of Medical Biology, A*STAR

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 14	2016

Other Publications

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