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All issues Volume 35 / No Suppl. 1 (2003) Genet. Sel. Evol., 35 Suppl. 1 (2003) S137-S145 References
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Issue
Genet. Sel. Evol.
Volume 35, Number Suppl. 1, 2003
Second International Symposium on Candidate Genes for Animal Health
Page(s) S137 - S145
DOI https://doi.org/10.1051/gse:2003022

References

  1. Bayés M., Hartung A.J., Ezer S., Pispa J., Thesleff I., Srivastava A.K., Kere J., The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats, Hum. Mol. Genet. 7 (1998) 1661-1669.
  2. Braun U., Ansari H.A., Hediger R., Süss U., Ehrensperger F., Hypotrichosis and oligodontia associated with a chromosomal Xq-deletion in a Simmental/Red Holstein crossbreed [German], Tierärztl. Prax. 16 (1988) 39-44.
  3. Chen Y., Molloy S.S., Thomas L., Gambee J., Bachinger H.P., Ferguson B., Zonana J., Thomas G., Morris N.P., Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia, Proc. Natl. Acad. Sci. USA 98 (2001) 7218-7223.
  4. Drieux H., Priouzeau M., Thiéry G., Priouzeau M.L., Hypotrichose congénitale avec anodontie, acérie et macroglossie chez le veau, Rec. Med. Vet. 126 (1950) 385-399.
  5. Drögemüller C., Distl O., Leeb T., Partial deletion of the bovine ED1 gene causes anhidrotic ectodermal dysplasia in cattle, Genome Res. 11 (2001) 1699-1705.
  6. Drögemüller C., Kuiper H., Peters M., Guionaud S., Distl O., Leeb T., Congenital hypotrichosis with anodontia in cattle: A genetic, clinical and histological analysis, Vet. Dermatol. 13 (2002) 307-313.
  7. Drögemüller C., Peters M., Pohlenz J., Distl O., Leeb T., A single point mutation within the ED1 gene disrupts correct splicing at two different splice sites and leads to anhidrotic ectodermal dysplasia in cattle, J. Mol. Med. 80 (2002) 319-323.
  8. Drögemüller C., Kuiper H., Leeb T., Peters M., Pohlenz J., Distl O., Congenital hypotrichosis and oligodontia in cattle [German], Tierärztl. Prax. 31 (2003) 70-76.
  9. Elomaa O., Pulkkinen K., Hannelius U., Mikkola M., Saarialho-Kere U., Kere J., Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein, Hum. Mol. Genet. 10 (2001) 953-962.
  10. Ezer S., Bayés M., Elomaa O., Schlessinger D., Kere J., Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells, Hum. Mol. Genet. 8 (1999) 2079-2086.
  11. Ferguson B.M., Brockdorff N., Formstone E., Ngyuen T., Kronmiller J.E., Zonana J., Cloning of Tabby, the murine homolog of the human EDA gene: evidence for a membrane-associated protein with a short collagenous domain, Hum. Mol. Genet. 6 (1997) 1589-1594.
  12. Headon D.J., Overbeek P.A., Involvement of a novel Tnf receptor homologue in hair follicle induction, Nat. Genet. 22 (1999) 370-374.
  13. Headon D.J., Emmal S.A., Ferguson B.M., Tucker A.S., Justice M.J., Sharpe P.T., Zonana J., Overbeek P.A., Gene defect in ectodermal dysplasia implicates a death domain adapter in development, Nature 414 (2001) 913-916.
  14. Kere J., Srivastava A.K., Montonen O., Zonana J., Thomas N., Ferguson B., Munoz F., Morgan D., Clarke A., Baybayan P., Chen E.Y., Ezer S., Saarialho-Kere U., de la Chapelle A., Schlessinger D., X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein, Nat. Genet. 13 (1996) 409-416.
  15. Koppinen P., Pispa J., Laurikkala J., Thesleff I., Mikkola M.L., Signalling and subcellular localization of the TNF receptor Edar, Exp. Cell. Res. 269 (2001) 180-192.
  16. Kumar A., Eby M.T., Sinha S., Jasmin A., Chaudhary P.M., The ectodermal dysplasia receptor activates the nuclear factor-kappaB, JNK and cell death pathways and binds to ectodysplasin, J. Biol. Chem. 276 (2001) 2668-2677.
  17. Locksley R.M., Killeen N., Lenardo M.J., The TNF and TNF receptor superfamilies: integrating mammalian biology, Cell 104 (2001) 487-501.
  18. Mikkola M.L., Pispa J., Pekkanen M., Paulin L., Nieminen P., Kere J., Thesleff I., Ectodysplasin, a protein required for epithelial morphogenesis, is a novel TNF homologue and promotes cell-matrix adhesion, Mech. Dev. 88 (1999) 133-146.
  19. Monreal A.W., Zonana J., Ferguson B., Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations, Am. J. Hum. Genet. 63 (1998) 380-389.
  20. Monreal A.W., Ferguson B.M., Headon D.J., Street S.L., Overbeek P.A., Zonana J., Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia, Nat. Genet. 22 (1999) 366-369.
  21. Nicholas F.W., Genetic databases: online catalogues of inherited disorders, Rev. Sci. Tech. 17 (1998) 346-350.
  22. Online Mendelian Inheritance in Man, OMIM (TM). McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD) (2000) http://www.ncbi.nlm.nih.gov/omim/
  23. Rieck G.W., Hypotrichie-Hypodontie-Syndrom beim Rind [German], Dtsch. Tierärztl. Wschr. 92 (1985) 328-329.
  24. Schmidt-Ullrich R., Aebischer T., Hulsken J., Birchmeier W., Klemm U., Scheidereit C., Requirement of NF-kappaB/Rel for the development of hair follicles and other epidermal appendices, Development 128 (2001) 3843-3853.
  25. Schneider P., Street S.L., Gaide O., Hertig S., Tardivel A., Tschopp J., Runkel L., Alevizopoulos K., Ferguson B.M., Zonana J., Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A, J. Biol. Chem. 276 (2001) 18819-18827.
  26. Selmanowitz V.J., Ectodermal dysplasias in cattle - Analogues in man, Br. J. Dermatol. 84 (1970) 258-265.
  27. Srivastava A.K., Pispa J., Hartung A.J., Du Y., Ezer S., Jenks T., Shimada T., Pekkanen M., Mikkola M.L., Ko M.S.H., Thesleff I., Kere J., Schlessinger D., The tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains, Proc. Natl. Acad. Sci. USA 94 (1997) 13069-13074.
  28. Srivastava A.K., Durmowicz M.C., Hartung A.J., Hudson J., Ouzts L.V., Donovan D.M., Cui C.Y., Schlessinger D., Ectodysplasin-A1 is sufficient to rescue both hair growth and sweat glands in tabby mice, Hum. Mol. Genet. 10 (2001) 2973-2981.
  29. Wijeratne W.V.S., O'Toole D., Wood L., Harkness J.W., A genetic, pathological and virological study of congenital hypotrichosis and incisor anodontia in cattle, Vet. Rec. 122 (1988) 149-152.
  30. Yan M., Wang L.C., Hymowitz S.G., Schilbach S., Lee J., Goddard A., de Vos A.M., Gao W.Q., Dixit V.M., Two-amino acid molecular switch in an epithelial morphogen that regulates binding to two distinct receptors, Science 290 (2000) 523-527.
  31. Yan M., Zhang Z., Brady J.F., Schilbach S., Fairbrother W.J., Dixit V.M., Identification of a novel death domain-containing adaptor molecule for ectodysplasin-A receptor that is mutated in crinkled mice, Curr. Biol. 12 (2002) 409-413.
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