E. Birgitte Lane

Deletion of the cytoplasmatic domain of BP180/collagen XVII causes a phenotype with predominant features of epidermolysis bullosa simplex.

Characterization of early assembly intermediates of recombinant human keratins.

Defolliculated (dfl): a dominant mouse mutation leading to poor sebaceous gland differentiation and total elimination of pelage follicles.

Cloning of human, murine, and marsupial keratin 7 and a survey of K7 expression in the mouse.

Keratin mutations of epidermolysis bullosa simplex alter the kinetics of stress response to osmotic shock.

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.

Observation of keratin particles showing fast bidirectional movement colocalized with microtubules.

Phenotypes, genotypes and their contribution to understanding keratin function.

The quest for the function of simple epithelial keratins.

Conformational changes in the rod domain of human keratin 8 following heterotypic association with keratin 18 and its implication for filament stability.

Keratin 8/18 breakdown and reorganization during apoptosis.

Mechanical stress induces profound remodelling of keratin filaments and cell junctions in epidermolysis bullosa simplex keratinocytes.

Stress models for the study of intermediate filament function.

Two families with Greither's syndrome caused by a keratin 1 mutation.

Clinical and pathological features of pachyonychia congenita.

Mutation S233L in the 1B domain of keratin 1 causes epidermolytic palmoplantar keratoderma with "tonotubular" keratin.

Association of Shh and Ptc with keratin localization in the initiation of the formation of circumvallate papilla and von Ebner's gland.

New consensus nomenclature for mammalian keratins.

Epidermolysis bullosa simplex in Scotland caused by a spectrum of keratin mutations.

Intermediate filaments and stress.

Multiple self-healing squamous epithelioma in different ethnic groups: more than a founder mutation disorder?

Ninein is released from the centrosome and moves bi-directionally along microtubules.

A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita.

Molecular force spectroscopy of homophilic nectin-1 interactions.

The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases.

Unique and recurrent mutations in the filaggrin gene in Singaporean Chinese patients with ichthyosis vulgaris.

Dual-specificity phosphatases in the hypo-osmotic stress response of keratin-defective epithelial cell lines.

Therapeutic siRNAs for dominant genetic skin disorders including pachyonychia congenita.

The intermediate filament network in cultured human keratinocytes is remarkably extensible and resilient.

Association of skin barrier genes within the PSORS4 locus is enriched in Singaporean Chinese with early-onset psoriasis.

Keratin K6c mutations cause focal palmoplantar keratoderma.

Severe keratin 5 and 14 mutations induce down-regulation of junction proteins in keratinocytes.

ERK involvement in resistance to apoptosis in keratinocytes with mutant keratin.

A novel mutation in the kinase domain of KIT in an Indian family with a mild piebaldism phenotype.

Immunohistochemical localization of cytokeratins in the junctional region of ectoderm and endoderm.

Filaggrin null mutations are not a protective factor for acne vulgaris.

Keratin 14-null cells as a model to test the efficacy of gene therapy approaches in epithelial cells.

Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1.

Developmental expression of the fermitin/kindlin gene family in Xenopus laevis embryos.

Validation of GWAS loci for atopic dermatitis in a Singapore Chinese population.

The mechanical behavior of mutant K14-R125P keratin bundles and networks in NEB-1 keratinocytes.

Keratins and disease at a glance.

'See-saw' expression of microRNA-198 and FSTL1 from a single transcript in wound healing.

Lamin B1 fluctuations have differential effects on cellular proliferation and senescence.

Generation and characterisation of keratin 7 (K7) knockout mice.

Making more matrix: enhancing the deposition of dermal-epidermal junction components in vitro and accelerating organotypic skin culture development, using macromolecular crowding.

Characterization of fetal keratinocytes, showing enhanced stem cell-like properties: a potential source of cells for skin reconstruction.

Assays to Study Consequences of Cytoplasmic Intermediate Filament Mutations: The Case of Epidermal Keratins.

Direct organelle thermometry with fluorescence lifetime imaging microscopy in single myotubes.