Genetics of atopic dermatitis

Immunology and Allergy Clinics of North America

Volumn 22, Issue 2, 2002, Pages 199-209

  Cookson, William O C M ^a   Harper, John I ^b   Moffatt, Miriam F ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b Hospital for Children   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; RANTES;

ANTIGEN PRESENTING CELL; ATOPIC DERMATITIS; CHROMOSOME 17Q; CHROMOSOME 1Q; CHROMOSOME 20P; CHROMOSOME 3Q; DENDRITIC CELL; EPIDERMIS; GENE EXPRESSION; GENE MAPPING; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENETIC RISK; HUMAN; INFECTION; LANGHANS GIANT CELL; NETHERTON DISEASE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PSORIASIS; REVIEW; SKIN; T LYMPHOCYTE;

EID: 0036313270     PISSN: 08898561     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0889-8561(01)00005-4     Document Type: Review

References (77)

1. Worldwide variations in the prevalence of symptoms of atopic eczema in the International Study of Asthma and Allergies in Childhood
2. The cost of atopic eczema
3. Atopic eczema: Its social and financial costs
4. Possible influences of Staphylococcus aureus on atopic dermatitis-the colonizing features and the effects of staphylococcal enterotoxins
5. Immunoglobulin E in dermatoses: Levels in atopic dermatitis and urticaria
6. Association of atopic dermatitis to the beta subunit of the high affinity immunoglobulin E receptor
7. Exposure to farming in early life and development of asthma and allergy: A cross-sectional survey
8. Atopic dermatitis: A genetic-epidemiologic study in a population-based twin sample
9. Atopic dermatitis: A genetic-epidemiologic study in a population-based twin sample
10. The future of genetic studies of complex human diseases
11. Genetic linkage of childhood atopic dermatitis to psoriasis susceptibility loci
12. A major susceptibility locus for atopic dermatitis maps to chromosome 3q21
13. The alliance of genes and environment in asthma and allergy
14. Contributing factors to the pathobiology: The genetics of asthma
15. Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases
16. Searching for psoriasis susceptibility genes in Italy: Genome scan and evidence for a new locus on chromosome 1
17. Gene for familial psoriasis susceptibility mapped to the distal end of human chromosome 17q
18. Identification of a major susceptibility locus on chromosome 6p and evidence for further disease loci revealed by a two stage genome-wide search in psoriasis
19. Psoriasis susceptibility locus in chromosome region 3q21 identified in patients from southwest Sweden
20. Analysis of three suggested psoriasis susceptibility loci in a large Swedish set of families: Confirmation of linkage to chromosome 6p (HLA region), and to 17q, but not to 4q
21. Evidence that a locus for familial psoriasis maps to chromosome 4q
22. Evidence for two psoriasis susceptibility loci (HLA and 17q) and two novel candidate regions (16q and 20p) by genome-wide scan
23. Psoriasis
24. Psoriasis in an unselected series of twins
25. Natural history of psoriasis in 61 twin pairs
26. Linkage between atopy and the IgE high-affinity receptor gene at 11q13 in atopic dermatitis families
27. Evidence for linkage of chromosome 5q31-q33 and 13q12-q14 markers to atopic dermatitis
28. Genes encoding structural proteins of epidermal cornification and S100 calcium-binding proteins form a gene complex ("epidermal differentiation complex") on human chromosome 1q21
29. Assignment of psoriasin to human chromosomal band 1q21: Coordinate overexpression of clustered genes in psoriasis
30. Expression of the SPRR cornification genes is differentially affected by carcinogenic transformation
31. The proteins elafin, filaggrin, keratin intermediate filaments, loricrin, and small proline-rich proteins 1 and 2 are isodipeptide cross-linked components of the human epidermal cornified cell envelope
32. Human trichohyalin gene is clustered with the genes for other epidermal structural proteins and calcium-binding proteins at chromosomal locus 1q21
33. Profilaggrin is a major epidermal calcium-binding protein
34. Psoriasin: A novel chemotactic protein
35. Psoriasin (S100A7)
36. A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome
37. Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
38. Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12
39. A susceptibility locus for epidermodysplasia verruciformis, an abnormal predisposition to infection with the oncogenic human papillomavirus type 5, maps to chromosome 17qter in a region containing a psoriasis locus
40. Genome-wide search for asthma susceptibility loci in a founder population: The Collaborative Study on the Genetics of Asthma
41. A genome-wide search for linkage to asthma: German Asthma Genetics Group
42. A new variant of the β subunit of the high affinity receptor for Immunoglobulin E (FcεRI-E237G): Associations with measures of atopy and bronchial hyperresponsiveness
43. Association between atopic asthma and a coding variant of Fc epsilon RI beta in a Japanese population
44. Linkage of high-affinity IgE receptor gene with bronchial hyperreactivity, even in absence of atopy
45. Fc epsilon RI-beta polymorphism and total serum IgE levels in endemically parasitized Australian aborigines
46. Association between atopy and variants of the β subunit of the high affinity immunoglobulin E receptor
47. Signalling through the high-affinity IgE receptor Fc epsilon RI
48. Association between genetic variants of mast-cell chymase and eczema
49. No evidence for an association between a variant of the mast cell chymase gene and atopic dermatitis based on case-control and haplotype-relative-risk analyses
50. Absence of association between a variant of the mast cell chymase gene and atopic dermatitis in an Italian population
51. Atopic dermatitis is associated with a functional mutation in the promoter of the C-C chemokine RANTES
52. A clinical and immunological study of Netherton's syndrome
53. Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome
54. LEKTI, a novel 15-domain type of human serine proteinase inhibitor
55. Linkage analysis of IL4 and other chromosome 5q31.1 markers and total serum immunoglobulin E concentrations
56. Evidence for a locus regulating total serum IgE levels mapping to chromosome 5
57. Gene polymorphism in Netherton and common atopic disease
58. Reaction of mast cell proteases tryptase and chymase with protease activated receptors (PARs) on keratinocytes and fibroblasts
59. Mite allergens groups I-VII: A catalogue of enzymes
60. Identification of complement factor 5 as a susceptibility locus for experimental allergic asthma
61. Activation of human serum complement with allergens: I. Generation of C3a, C4a, and C5a and induction of human neutrophil aggregation
62. Characterization by phenotype of families with atopic dermatitis
63. Analysis of familial aggregation of atopic eczema and other atopic diseases by odds ratio regression models
64. Atopic dermatitis may be linked to whether a child is first- or second-born and/or the age of the mother
65. Incidence and predictors of atopic dermatitis in an open birth cohort in Sisimiut, Greenland
66. The genetics of asthma. Maternal effects in atopic disease
67. Differences in risk of insulin-dependent diabetes in offspring of diabetic mothers and diabetic fathers
68. Family history as a risk factor for rheumatoid arthritis: A case-control study
69. Differences in risk of Crohn's disease in offspring of mothers and fathers with inflammatory bowel disease
70. Genetics of psoriasis: Paternal inheritance and a locus on chromosome 6p
71. Excessive paternal transmission in psoriatic arthritis
72. The role of allergy in the development of asthma
73. Genomic imprinting
74. The skin as an organ of immunity
75. The skin immune system (SIS): Distribution and immunophenotype of lymphocyte subpopulations in normal human skin