The epidermis: rising to the surface

Current Opinion in Genetics and Development

Volumn 4, Issue 5, 1994, Pages 725-736

  Fuchs, Elaine ^a   Byrne, Carolyn ^a  

^a UNIVERSITY OF CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN; KERATIN; LAMININ; RETINOIC ACID BINDING PROTEIN; TRANSCRIPTION FACTOR; TRANSFORMING GROWTH FACTOR ALPHA;

CELL DIFFERENTIATION; CELL NUCLEUS MEMBRANE; CONGENITAL SKIN DISEASE; CYTOSKELETON; DEVELOPMENTAL GENETICS; EMBRYO DEVELOPMENT; EPIDERMIS; HEMIDESMOSOME; NONHUMAN; PRIORITY JOURNAL; REVIEW; SKIN SURFACE; TRANSGENE;

ANIMAL; BASE SEQUENCE; CELL DIFFERENTIATION; CELL DIVISION; DNA; EPIDERMIS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HUMAN; KERATIN; MOLECULAR SEQUENCE DATA; SKIN DISEASES; STEM CELLS; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; TRANSCRIPTION FACTORS;

EID: 0028089871     PISSN: 0959437X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0959-437X(94)90140-X     Document Type: Article

References (70)

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2. Intermediate Filaments: Structure, Dynamics, Function, and Disease
3. Programming Gene Expression in Developing Epidermis
4. Retinoid-Mediated Transcriptional Regulation of Keratin Genes in Human Epidermal and Squamous Cell Carcinoma Cells
5. Mutant Keratin Expression in Transgenic Mice Causes Marked Abnormalities Resembling a Human Genetic Skin Disease
6. Point Mutations in Human Keratin 14 Genes of Epidermolysis Bullosa Simplex Patients: Genetic and Functional Analyses
7. Do the Ends Justify the Means? Proline Mutations at the Ends of the Keratin Coiled-Coil Rod Segment are More Disruptive than Internal Mutations
8. Epidermolysis Bullosa Simplex: Evidence in Two Families for Keratin Gene Abnormalities
9. A Mutation in the Conserved Helix Termination Peptide of Keratin 5 in Hereditary Skin Blistering
10. The Genetic Basis of Epidermolytic Hyperkeratosis: A Disorder of Differentiation-Specific Epidermal Keratin Genes
11. A Leucine → Proline Mutation in the H1 Subdomain of Keratin 1 Causes Epidermolytic Hyperkeratosis
12. Mutations in the Rod Domains of Keratins 1 and 10 in Epidermolytic Hyperkeratosis
13. Intermediate Filaments and Disease: Mutations that Cripple Cell Strength
14. Epidermolytic Palmoplantar Keratoderma Cosegregates with a Keratin 9 Mutation in a Pedigree with Breast and Ovarian Cancer
15. Keratin 9 Gene Mutations in Epidermolytic Palmoplantar Keratoderma (EPPK)
16. Genetic and Clinical Mosaicism in a Type of Epidermal Nevus
17. Variants of the Heavy Neurofilament Subunit are Associated with the Development of Amyotrophic Lateral Sclerosis
18. Desmosomes and Hemidesmosomes
19. The Beta 4 Subunit Cytoplasmic Domain Mediates the Interaction of alpha 6 Beta 4 Integrin with the Cytoskeleton of Hemidesmosomes
20. Herlitz's junctional epidermolysis bullosa is Genetically Linked to Mutations in the Gene for the γ2 Subunit (LAMC2) of Nicein/Kalinin (Laminin 5)
21. Mutations in the γ2 chain gene (LAMC2) of Kalinin/Laminin 5 in the Junctional Forms of Epidermolysis Bullosa
22. A Homozygous Insertion- Deletion in the Type VII Collagen Gene (COL7A1) in Hallopeau-Siemens Dystrophic Epidermolysis Bullosa
23. Stratification-Related Expression of Isoforms of the Desmosomal Cadherins in Human Epidermis
24. Nomenclature of the Desmosomal Cadherins
25. Functional Analysis of Desmoplakin Domains: Specification of the Interaction with Keratin Versus Vimentin Intermediate Filament Networks
26. Contributions of Cytoplasmic Domains of Desmosomal Cadherins to Desmosome Assembly and Intermediate Filament Anchorage
27. Autoantibodies against a Novel Epithelial Cadherin in Pemphigus Vulgaris, a Disease of Cell Adhesion
28. Structure of DSG1, the Bovine Desmosomal Cadherin Gene Encoding the Pemphigus Foliaceus Antigen. Evidence of Polymorphism
29. The Gene for Darier's Disease Maps Between D12S78 and D12S79
30. Evidence that Cadherins Play a Role in the Downregulation of Integrin Expression that Occurs During Keratinocyte Differentiation
31. Characterization of the Human Epidermal Profilaggrin Gene. Genomic Organization and Identification of an S-100-Like Calcium Binding Domain at the Amino Terminus
32. Profilaggrin is a Major Epidermal Calcium-Binding Protein
33. Identification of a Major Keratinocyte Cell Envelope Protein, Loricrin
34. Keratinocyte Transglutaminase: Differentiation Marker and Member of an Extended Family
35. Separation of Human Epidermal Stem Cells from Transit Amplifying Cells on the Basis of Differences in Integrin Function and Expression
36. Location of Stem Cells of Human Hair Follicles by Clonal Analysis
37. Label-Retaining Cells Reside in the Bulge Area of Pilosebaceous Unit: Implications for Follicular Stem Cells, Hair Cycle, and Skin Carcinogenesis
38. The Secret Life of the Hair Follicle
39. Regulation of a Human Epidermal Keratin Gene: Sequences and Nuclear Factors Involved in Keratinocyte-Specific Transcription
40. KTF-1, a Transcriptional Activator of Xenopus Embryonic Keratin Expression
41. Transcriptional Factor AP-2 is Tissue-Specific in Xenopus and is Closely Related or Identical to Keratin Transcription Factor 1 (KTF-1)
42. Probing Keratinocyte and Differentiation Specificity of the K5 Promoter in Vitro and in Transgenic Mice
43. An Alternatively Spliced mRNA from the Ap-2 Gene Encodes a Negative Regulator of Transcriptional Activation by AP-2
44. Transcription Factor AP-2 is Expressed in Neural Crest Cell Lineages During Mouse Embryogenesis
45. Tissue Specific Expression of c-jun and junB During Organogenesis in the Mouse
46. Fos-IacZ Transgenic Mice: Mapping Sites of Gene Induction in the Central Nervous System
47. Stage and Tissue-Specific Expression of fosB During Mouse Development
48. Differentiation-Specific Expression of Human Keratin 1 is Mediated by a Composite AP-1/Steroid Hormone Element
49. Association of Basonuclin with Ability of Keratinocytes to Multiply and with the Absence of Terminal Differentiation
50. Skn-1a and Skn-1i Two Functionally Distinct oct-2-Related Factors Expressed in Epidermis
51. XLPOU 1 and XLPOU 2, Two Novel POU Domain Genes Expressed in the Dorsoanterior Region of Xenopus Embryos
52. Oct 6: A Regulator of Keratinocyte Gene Expression in Stratified Squamous Epithelia
53. Gradient of Homeoproteins in Developing Feather Buds
54. Patternng the Vertebrate Head: Murine Hox 2 Genes Mark Distinct Subpopulations of Premigratory and Migrating Neural Crest
55. Expression of the Hox 2.2 Homeobox Gene in Murine Embryonic Epidermis
56. The Homeodomain Gene Xenopus Distal-less- like-2 (Xdll-s) is Regulated by a Conserved Mechanism in Amphibian and Mammalian Epidermis
57. Transgenic Mice Provide New Insights into the Role of TGF-alpha During Epidermal Development and Differentiation
58. Transgenic Overexpression of Transforming Growth Factor Alpha Bypasses the Need for c-HA-ras Mutations in Mouse Skin Tumorigenesis
59. TGF Deficiency Results in Hair follicle and Eye Abnormalities in Targeted and Waved-1 Mice
60. Mice with a Null Mutation of the TGFα Gene have Abnormal Skin Architecture, Wavy Hair, and Curly Whiskers and Often Develop Corneal Inflamation
61. Biosynthesis and in Vivo Localization of the Decapentaplegic Protein DVR-6 (bone Morphogenetic Protein-6)
62. Inhibition of Skin Development by Overexpression of Transforming Growth Factor β1 in the Epidermis of Transgenic Mice
63. Loss of Expression of Transforming Growth Factor β in Skin and Skin Tumors is Associated with Hyperproliferation and a Risk for Malignant Conversion
64. Identification of the Retinoic Acid and Thyroid Hormone Receptor-Responsive Element in the Human K14 Keratin Gene
65. Developmental Expression of Murine Retinoid X Receptor (RXR) Genes
66. Role of Nuclear Retinoic Receptors in the Regulation of Gene Expression
67. Coordinate Changes in Gene Expression Which Mark the Spinous to Granular Cell Transition in Epidermis are Regulated by Protein Kinase
68. Ichthyosis Bullosa of Siemens — a Disease Involving Keratin 2e
69. Genetic Linkage of the Keratin Type II Gene Cluster with Ichthyosis Bullosa of Siemens and with Autosomal Dominant Ichthyosis Exfollativa
70. Ichthyosis Bullosa of Siemens is Caused by Mutations in the Keratin 2e Gene