(Q28191257)

2

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E B Lane

3

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G Melino

4

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D H Felix

5

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C S Munro

6

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W H McLean

Journal of Dental Research

7

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language of work or name

English

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publication date

March 2001

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published in

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volume

80

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issue

3

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page(s)

919-23

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cites work

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White sponge naevus of the mucosa: clinical and linkage data

21 January 2018

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Human keratin diseases: hereditary fragility of specific epithelial tissues

21 January 2018

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Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene.

21 January 2018

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Keratin expression in the normal nail unit: markers of regional differentiation.

21 January 2018

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Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

21 January 2018

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White sponge nevus (leukoedema exfoliativum mucosae oris): Ultrastructural observations

21 January 2018

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Peptides from the Conserved Ends of the Rod Domain of Desmin Disassemble Intermediate Filaments and Reveal Unexpected Structural Features: A Circular Dichroism, Fourier Transform Infrared, and Electron Microscopic Study

21 January 2018

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The intermediate filament protein consensus motif of helix 2B: its atomic structure and contribution to assembly

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Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation

21 January 2018

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Epidermolysis Bullosa Simplex (Dowling-Meara Type) Is a Genetic Disease Characterized by an Abnormal Keratin-Filament Network Involving Keratins K5 and K14

21 January 2018

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Do the ends justify the mean? Proline mutations at the ends of the keratin coiled-coil rod segment are more disruptive than internal mutations

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Oral tetracycline rinse improves symptoms of white sponge nevus

21 January 2018

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Retrovirus-mediated transgenic keratin expression in cultured fibroblasts: Specific domain functions in keratin stabilization and filament formation

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Ultrastructure of the white sponge nevus

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Intermediate filaments in disease

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Keratin 16 and keratin 17 mutations cause pachyonychia congenita

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The catalog of human cytokeratins: patterns of expression in normal epithelia, tumors and cultured cells

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Mouse keratin 4 is necessary for internal epithelial integrity

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Keratin 13 point mutation underlies the hereditary mucosal epithelial disorder white sponge nevus

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A mutation in the mucosal keratin K4 is associated with oral white sponge nevus

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Identification of two novel mutations in keratin 13 as the cause of white sponge naevus.

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Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stress

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A glutamine insertion in the 1A alpha helical domain of the keratin 4 gene in a familial case of white sponge nevus

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Cell type heterogeneity of cytokeratin expression in complex epithelia and carcinomas as demonstrated by monoclonal antibodies specific for cytokeratins nos. 4 and 13.

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The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing

21 January 2018

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Isolation, sequence and expression of the gene encoding human keratin 13

21 January 2018

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