-
2
-
-
0023725932
-
Hypotrichose und Oligodontie, verbunden mit einer Xq-Deletion, bei einem Kalb der schweizerischen Fleckviehrasse
-
Braun, U., Ansari, H.A., Hediger, R. et al. Hypotrichose und Oligodontie, verbunden mit einer Xq-Deletion, bei einem Kalb der schweizerischen Fleckviehrasse. Tierärztliche Praxis 1988; 16: 39-44.
-
(1988)
Tierärztliche Praxis
, vol.16
, pp. 39-44
-
-
Braun, U.1
Ansari, H.A.2
Hediger, R.3
-
3
-
-
0004623027
-
Hypotrichose congénitale avec anodontie, acérie et macroglossie chez le veau
-
Drieux, H., Priouzeau, M., Thiéry, G. et al. Hypotrichose congénitale avec anodontie, acérie et macroglossie chez le veau. Recueil de Médecine Vétérinaire 1950; 126: 385-99.
-
(1950)
Recueil de Médecine Vétérinaire
, vol.126
, pp. 385-399
-
-
Drieux, H.1
Priouzeau, M.2
Thiéry, G.3
-
4
-
-
0024285403
-
A genetical, pathological and virological study of congenital hypotrichosis and incisor anodontia in cattle
-
Wijeratne, W.V.S., O'Toole, D., Wood, L. et al. A genetical, pathological and virological study of congenital hypotrichosis and incisor anodontia in cattle. Veterinary Record 1988; 122: 149-52.
-
(1988)
Veterinary Record
, vol.122
, pp. 149-152
-
-
Wijeratne, W.V.S.1
O'Toole, D.2
Wood, L.3
-
5
-
-
0040920369
-
-
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)
-
Online Mendelian Inheritance in Man, Omim (TM). McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, 2000, National Library of Medicine (Bethesda, MD), available at: http:// www.ncbi.nlm.nih.gov/omim/
-
(2000)
Online Mendelian Inheritance in Man
-
-
-
6
-
-
0014833344
-
Clinical spectrum of anhidrotic ectodermal dysplasia
-
Reed, W.B., Lopez, D.A., Landing, B. Clinical spectrum of anhidrotic ectodermal dysplasia. Archives of Dermatology 1970; 102: 134-43.
-
(1970)
Archives of Dermatology
, vol.102
, pp. 134-143
-
-
Reed, W.B.1
Lopez, D.A.2
Landing, B.3
-
7
-
-
9344250077
-
X-Linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein
-
Kere, J., Srivastava, A.K., Montonen, O. et al. X-Linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nature Genetics 1996; 13: 409-16.
-
(1996)
Nature Genetics
, vol.13
, pp. 409-416
-
-
Kere, J.1
Srivastava, A.K.2
Montonen, O.3
-
8
-
-
0032231350
-
Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations
-
Monreal, A., 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. American Journal of Human Genetics 1998; 63: 380-9.
-
(1998)
American Journal of Human Genetics
, vol.63
, pp. 380-389
-
-
Monreal, A.1
Zonana, J.2
Ferguson, B.3
-
9
-
-
0031716740
-
The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats
-
Bayés, M., Hartung, A.J., Ezer, S. et al. The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats. Human Molecular Genetics 1998; 7: 1661-9.
-
(1998)
Human Molecular Genetics
, vol.7
, pp. 1661-1669
-
-
Bayés, M.1
Hartung, A.J.2
Ezer, S.3
-
10
-
-
0035379554
-
Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A
-
Schneider, P., Street, S.L., Gaide, O. et al. Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A. Journal of Biological Chemistry 2001; 276: 18819-27.
-
(2001)
Journal of Biological Chemistry
, vol.276
, pp. 18819-18827
-
-
Schneider, P.1
Street, S.L.2
Gaide, O.3
-
11
-
-
0034981134
-
Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia
-
Vincent, M.C., Biancalana, V., Ginisty, D. et al. Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia. European Journal of Human Genetics 2001; 9: 355-63.
-
(2001)
European Journal of Human Genetics
, vol.9
, pp. 355-363
-
-
Vincent, M.C.1
Biancalana, V.2
Ginisty, D.3
-
12
-
-
12644310324
-
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
-
Srivastava, A.K., Pispa, J., Hartung, A.J. et al. 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. Proceedings of the National Academy of Sciences of the USA 1997; 94: 13069-74.
-
(1997)
Proceedings of the National Academy of Sciences of the USA
, vol.94
, pp. 13069-13074
-
-
Srivastava, A.K.1
Pispa, J.2
Hartung, A.J.3
-
13
-
-
0032852542
-
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
-
Ezer, S., Bayés, M., Elomaa, O. et al. 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. Human Molecular Genetics 1999; 8: 2079-86.
-
(1999)
Human Molecular Genetics
, vol.8
, pp. 2079-2086
-
-
Ezer, S.1
Bayés, M.2
Elomaa, O.3
-
14
-
-
0035871196
-
Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein
-
Elomaa, O., Pulkkinen, K., Hannelius, U. et al. Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein. Human Molecular Genetics 2001; 10: 953-62.
-
(2001)
Human Molecular Genetics
, vol.10
, pp. 953-962
-
-
Elomaa, O.1
Pulkkinen, K.2
Hannelius, U.3
-
15
-
-
0034485688
-
Identification of a highly polymorphic microsatellite within the bovine ectodysplasin a (ED1) gene on BTa Xq22-24
-
Drögemüller, C, Distl, O., Leeb, T. Identification of a highly polymorphic microsatellite within the bovine ectodysplasin A (ED1) gene on BTA Xq22-24. Animal Genetics 2000; 31: 416.
-
(2000)
Animal Genetics
, vol.31
, pp. 416
-
-
Drögemüller, C.1
Distl, O.2
Leeb, T.3
-
16
-
-
0034938390
-
Assignment of the bovine ectodysplasin a gene (ED1) to bovine Xq22-q24 by fluorescence in situ hybridization
-
Kuiper, H., Kutschke, L., Drögemüller, C. et al. Assignment of the bovine ectodysplasin A gene (ED1) to bovine Xq22-q24 by fluorescence in situ hybridization. Cytogenetics and Cell Genetics 2001; 92: 356-9.
-
(2001)
Cytogenetics and Cell Genetics
, vol.92
, pp. 356-359
-
-
Kuiper, H.1
Kutschke, L.2
Drögemüller, C.3
-
17
-
-
0034756444
-
Partial deletion of the bovine ED1 gene causes anhidrotic ectodermal dysplasia in cattle
-
Drögemüller, C, Distl, O., Leeb, T. Partial deletion of the bovine ED1 gene causes anhidrotic ectodermal dysplasia in cattle. Genome Research 2001; 11: 1699-705.
-
(2001)
Genome Research
, vol.11
, pp. 1699-1705
-
-
Drögemüller, C.1
Distl, O.2
Leeb, T.3
-
19
-
-
0039007930
-
Genetische Untersuchung von kongenitaler Hypotrichose mit Anodontie bei Deutschen Holstein Kälbern
-
Distl, O., Drögemüller, C., Kuiper, H. et al. Genetische Untersuchung von kongenitaler Hypotrichose mit Anodontie bei Deutschen Holstein Kälbern. Tierärztliche Umschau 2000; 55: 72-9.
-
(2000)
Tierärztliche Umschau
, vol.55
, pp. 72-79
-
-
Distl, O.1
Drögemüller, C.2
Kuiper, H.3
-
20
-
-
0025351528
-
Induction of sweat glands by epidermal growth factor in murine X-linked anhidrotic ectodermal dysplasia
-
Blecher, S.R., Kapalanga, J., Lalonde, D. Induction of sweat glands by epidermal growth factor in murine X-linked anhidrotic ectodermal dysplasia. Nature 1990; 345: 542-4.
-
(1990)
Nature
, vol.345
, pp. 542-544
-
-
Blecher, S.R.1
Kapalanga, J.2
Lalonde, D.3
-
21
-
-
0345978521
-
A note on six kinds of genetic hypotrichosis in cattle
-
Hutt, EB. A note on six kinds of genetic hypotrichosis in cattle. Journal of Heredity 1963; 54: 186-7.
-
(1963)
Journal of Heredity
, vol.54
, pp. 186-187
-
-
Hutt, E.B.1
-
22
-
-
0006952049
-
Streaked hairlessness in Holstein-Friesian cattle
-
Eldridge, F.E., Atkeson, EW. Streaked hairlessness in Holstein-Friesian cattle. Journal of Heredity 1953; 44: 265-71.
-
(1953)
Journal of Heredity
, vol.44
, pp. 265-271
-
-
Eldridge, F.E.1
Atkeson, E.W.2
|