-
1
-
-
0027290687
-
Inherited epidermolysis bullosa. Clinical features, molecular genetics and pathoetiologic mechanisms
-
Uitto, J., Christiano, A.M. Inherited epidermolysis bullosa. Clinical features, molecular genetics and pathoetiologic mechanisms. Dermatologic Clinics 1993; 11: 549-63.
-
(1993)
Dermatologic Clinics
, vol.11
, pp. 549-563
-
-
Uitto, J.1
Christiano, A.M.2
-
2
-
-
18344413641
-
Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5)
-
Aberdam, D., Galliano, M.-F., Vailly, J. et al. Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5). Nature Genetics 1994; 6: 299-304.
-
(1994)
Nature Genetics
, vol.6
, pp. 299-304
-
-
Aberdam, D.1
Galliano, M.-F.2
Vailly, J.3
-
3
-
-
0028568985
-
A homozygous nonsense mutation in the beta 3 chain gene of laminin 5 (LAMB3) in Herlitz junctional epidermolysis bullosa
-
Pulkkinen, L., Christiano, A.M., Gerecke, D. et al. A homozygous nonsense mutation in the beta 3 chain gene of laminin 5 (LAMB3) in Herlitz junctional epidermolysis bullosa. Genomics 1994; 24: 357-60.
-
(1994)
Genomics
, vol.24
, pp. 357-360
-
-
Pulkkinen, L.1
Christiano, A.M.2
Gerecke, D.3
-
4
-
-
0028180092
-
Mutations of the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa
-
Pulkkinen, L., Christiano, A.M., Airenne, T., Haakana, H., Tryggvason, K., Uitto, J. Mutations of the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa. Nature Genetics 1994; 6: 293-8
-
(1994)
Nature Genetics
, vol.6
, pp. 293-298
-
-
Pulkkinen, L.1
Christiano, A.M.2
Airenne, T.3
Haakana, H.4
Tryggvason, K.5
Uitto, J.6
-
5
-
-
0028899779
-
Identification of a homozygous exon-skipping mutation in the LAMC2 gene in a patient with Herlitz's junctional epidermolysis bullosa
-
Vailly, J., Pulkkinen, L., Christiano, A.M. et al. Identification of a homozygous exon-skipping mutation in the LAMC2 gene in a patient with Herlitz's junctional epidermolysis bullosa. Journal of Investigative Dermatology 1995; 104: 434-7.
-
(1995)
Journal of Investigative Dermatology
, vol.104
, pp. 434-437
-
-
Vailly, J.1
Pulkkinen, L.2
Christiano, A.M.3
-
6
-
-
0029044045
-
A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosa
-
Kivirikko, S., McGrath, J.A., Baudoin, C. et al. A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosa. Human Molecular Genetics 1995; 4: 959-62.
-
(1995)
Human Molecular Genetics
, vol.4
, pp. 959-962
-
-
Kivirikko, S.1
McGrath, J.A.2
Baudoin, C.3
-
7
-
-
0029150295
-
A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: Prenatal exclusion in a fetus at risk
-
McGrath, J.A., Kivirikko, S., Ciatti, S. et al. A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at risk. Genomics 1995; 29: 282-4.
-
(1995)
Genomics
, vol.29
, pp. 282-284
-
-
McGrath, J.A.1
Kivirikko, S.2
Ciatti, S.3
-
8
-
-
0028909571
-
Identification of a homozygous one-basepair deletion in exon 14 of the LAMB3 gene in a patient with Herlitz junctional epidermolysis bullosa and prenatal diagnosis in a family at risk for recurrence
-
Vailly, J., Pulkkinen, L., Miquel, C. et al. Identification of a homozygous one-basepair deletion in exon 14 of the LAMB3 gene in a patient with Herlitz junctional epidermolysis bullosa and prenatal diagnosis in a family at risk for recurrence. Journal of Investigative Dermatology 1995; 104: 462-6.
-
(1995)
Journal of Investigative Dermatology
, vol.104
, pp. 462-466
-
-
Vailly, J.1
Pulkkinen, L.2
Miquel, C.3
-
9
-
-
0030029420
-
Mutational hotspots in the LAMB3 gene in the lethal (Herlitz) type of junctional epidermolysis bullosa
-
Kivirikko, S., Mcgrath, J.A., Pulkkinen, L., Uitto, J., Christiano, A.M. Mutational hotspots in the LAMB3 gene in the lethal (Herlitz) type of junctional epidermolysis bullosa. Human Molecular Genetics 1996; 5: 231-7.
-
(1996)
Human Molecular Genetics
, vol.5
, pp. 231-237
-
-
Kivirikko, S.1
Mcgrath, J.A.2
Pulkkinen, L.3
Uitto, J.4
Christiano, A.M.5
-
10
-
-
0028930755
-
180-kD bullous pemphigoid antigen (BP180) is deficient in generalized atrophic benign epidermolysis bullosa
-
Jonkman, M.F., De Jong, M.C., Heeres, K. et al. 180-kD bullous pemphigoid antigen (BP180) is deficient in generalized atrophic benign epidermolysis bullosa. Journal of Clinical investigation 1995; 95: 1345-52.
-
(1995)
Journal of Clinical Investigation
, vol.95
, pp. 1345-1352
-
-
Jonkman, M.F.1
De Jong, M.C.2
Heeres, K.3
-
11
-
-
0029145676
-
Diminished expression of the extracellular domain of bullous pemphigoid antigen 2 (BPAG2) in the epidermal basement membrane of patients with generalized atrophic benign epidermolysis bullosa
-
Pohla-Gubo, G., Lazarova, Z., Giudice, G.J. et al. Diminished expression of the extracellular domain of bullous pemphigoid antigen 2 (BPAG2) in the epidermal basement membrane of patients with generalized atrophic benign epidermolysis bullosa. Experimental Dermatology 1995; 4: 199-206.
-
(1995)
Experimental Dermatology
, vol.4
, pp. 199-206
-
-
Pohla-Gubo, G.1
Lazarova, Z.2
Giudice, G.J.3
-
12
-
-
13344282732
-
Generalized atrophic benign epidermolysis bullosa: Either 180 kD bullous pemphigoid antigen or laminin-5 deficiency
-
Jonkman, M.F., Dejong, M.C.J.M., Heeres, K. et al. Generalized atrophic benign epidermolysis bullosa: Either 180 kD bullous pemphigoid antigen or laminin-5 deficiency. Archives of Dermatology 1996; 132: 145-50.
-
(1996)
Archives of Dermatology
, vol.132
, pp. 145-150
-
-
Jonkman, M.F.1
Dejong, M.C.J.M.2
Heeres, K.3
-
13
-
-
0028919592
-
Altered laminin 5 expression due to mutations in the gene encoding the beta 3 chain (LAMB3) in generalized atrophic benign epidermolysis bullos
-
McGrath, J.A., Pulkkinen, L., Christiano, A.M., Leigh, I.M., Eady, R.A.J., Uitto, J. Altered laminin 5 expression due to mutations in the gene encoding the beta 3 chain (LAMB3) in generalized atrophic benign epidermolysis bullos. Journal of Investigative Dermatology 1995; 104: 467-74.
-
(1995)
Journal of Investigative Dermatology
, vol.104
, pp. 467-474
-
-
McGrath, J.A.1
Pulkkinen, L.2
Christiano, A.M.3
Leigh, I.M.4
Eady, R.A.J.5
Uitto, J.6
-
14
-
-
0030138012
-
Compound heterozygosity for nonsense and missense mutations in the LAMB3 gene in nonlethal junctional epidermolysis bullosa
-
McGrath, J.A., Christiano, A.M., Pulkkinen, L., Eady, R.A.J., Uitto, J. Compound heterozygosity for nonsense and missense mutations in the LAMB3 gene in nonlethal junctional epidermolysis bullosa. Journal of Investigative Dermatology 1996; 106: 1157-9.
-
(1996)
Journal of Investigative Dermatology
, vol.106
, pp. 1157-1159
-
-
McGrath, J.A.1
Christiano, A.M.2
Pulkkinen, L.3
Eady, R.A.J.4
Uitto, J.5
-
15
-
-
0029121987
-
Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1) in generalized atrophic benign epidermolysis bullosa
-
McGrath, J.A., Gatalica, B., Christiano, A.M. et al. Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1) in generalized atrophic benign epidermolysis bullosa. Nature Genetics; 11: 83-6.
-
Nature Genetics
, vol.11
, pp. 83-86
-
-
McGrath, J.A.1
Gatalica, B.2
Christiano, A.M.3
-
16
-
-
3743134384
-
Mutations in the 180-kD bullous pemphigoid antigen gene (BPAG2/COL17A1) underlie generalized atrophic benign epidermolysis bullosa
-
Abstract
-
McGrath, J.A., Christiano, A.M., Gatalica, B. et al. Mutations in the 180-kD bullous pemphigoid antigen gene (BPAG2/COL17A1) underlie generalized atrophic benign epidermolysis bullosa. Journal of Investigative Dermatology; 105: 449 [Abstract].
-
Journal of Investigative Dermatology
, vol.105
, pp. 449
-
-
McGrath, J.A.1
Christiano, A.M.2
Gatalica, B.3
-
17
-
-
0029873761
-
A homozygous deletion mutation in the gene encoding the 180-kDa bullous pemphigoid antigen (BPAG2) in a family with generalized atrophic benign epidermolysis bullosa
-
McGrath, J.A., Darling, T., Gatalica, B. et al. A homozygous deletion mutation in the gene encoding the 180-kDa bullous pemphigoid antigen (BPAG2) in a family with generalized atrophic benign epidermolysis bullosa. Journal of Investigative Dermatology 1996; 106: 771-4.
-
(1996)
Journal of Investigative Dermatology
, vol.106
, pp. 771-774
-
-
McGrath, J.A.1
Darling, T.2
Gatalica, B.3
-
18
-
-
3743105200
-
Mutations in the bullous pemphigoid antigen 2 (BPAG2) gene in five Austrian families with generalized atrophic benign epidermolysis bullosa (GABEB)
-
Abstract
-
Darling, T., McGrath, J.A., Yee, C. et al. Mutations in the bullous pemphigoid antigen 2 (BPAG2) gene in five Austrian families with generalized atrophic benign epidermolysis bullosa (GABEB). Journal of Investigative Dermatology 1996; 106: 842 [Abstract].
-
(1996)
Journal of Investigative Dermatology
, vol.106
, pp. 842
-
-
Darling, T.1
McGrath, J.A.2
Yee, C.3
-
19
-
-
0029897474
-
Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition
-
McGrath, J.A., Gatalica, B., Li, K.H. et al. Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition. American Journal of Pathology 1996; 148: 1787-96.
-
(1996)
American Journal of Pathology
, vol.148
, pp. 1787-1796
-
-
McGrath, J.A.1
Gatalica, B.2
Li, K.H.3
-
20
-
-
0028989243
-
Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresia
-
Vidal, F., Aberdam, D., Miquel, C. et al. Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresia. Nature Genetics 1995; 10: 229-34.
-
(1995)
Nature Genetics
, vol.10
, pp. 229-234
-
-
Vidal, F.1
Aberdam, D.2
Miquel, C.3
-
21
-
-
0029990621
-
Deficiency of the integrin beta 4 subunit in junctional epidermolysis bullosa with pyloric atresia: Consequences for hemidesmosome formation and adhesion properties
-
Niessen, C.M., Vanderraaijhelmer, L.M.H., Hulsman, E.H.M., Vanderneut, R., Jonkman, M.F., Sonnenberg, A. Deficiency of the integrin beta 4 subunit in junctional epidermolysis bullosa with pyloric atresia: Consequences for hemidesmosome formation and adhesion properties. Journal of Cell Science 1996; 109: 1695-706.
-
(1996)
Journal of Cell Science
, vol.109
, pp. 1695-1706
-
-
Niessen, C.M.1
Vanderraaijhelmer, L.M.H.2
Hulsman, E.H.M.3
Vanderneut, R.4
Jonkman, M.F.5
Sonnenberg, A.6
-
22
-
-
3743090781
-
A deletion in the cDNA sequence encoding the pemphigoid antigen BP180 underlies a benign form of junctional epidermolysis bullosa
-
Abstract
-
Chavanas, S., Gache, Y., Blanchet-Bardon, C., Ortonne, J.P., Meneguzzi, G. A deletion in the cDNA sequence encoding the pemphigoid antigen BP180 underlies a benign form of junctional epidermolysis bullosa. Journal of Investigative Dermatology 1995; 105: 449 [Abstract].
-
(1995)
Journal of Investigative Dermatology
, vol.105
, pp. 449
-
-
Chavanas, S.1
Gache, Y.2
Blanchet-Bardon, C.3
Ortonne, J.P.4
Meneguzzi, G.5
-
23
-
-
0025050901
-
19-DEJ-1, a monoclonal antibody to the hemidesmosome-anchoring filament complex, is the only reliable immunohistochemical probe for all major forms of junctional epidermolysis bullosa
-
Fine, J.D. 19-DEJ-1, a monoclonal antibody to the hemidesmosome-anchoring filament complex, is the only reliable immunohistochemical probe for all major forms of junctional epidermolysis bullosa. Archives of Dermatology 1990; 126: 1187-90.
-
(1990)
Archives of Dermatology
, vol.126
, pp. 1187-1190
-
-
Fine, J.D.1
-
24
-
-
3743074107
-
Uncein, a cell membrane-associated anchoring filament component, is biochemically similar to kalinin but differs markedly in its in vitro expression by normal and non-Herlitz junctional epidermolysis bullosa (JEB) human keratinocyte monolayers
-
(Abstract 62) North Carolina: Chapel Hill
-
Zeng, L., Daniels, A., Riddelle, K., Fine, J.-D. Uncein, a cell membrane-associated anchoring filament component, is biochemically similar to kalinin but differs markedly in its in vitro expression by normal and non-Herlitz junctional epidermolysis bullosa (JEB) human keratinocyte monolayers (Abstract 62). International Symposium on Epidermolysis Bullosa. North Carolina: Chapel Hill, 1994: 80.
-
(1994)
International Symposium on Epidermolysis Bullosa
, pp. 80
-
-
Zeng, L.1
Daniels, A.2
Riddelle, K.3
Fine, J.-D.4
-
25
-
-
0026712482
-
Expression of integrin alpha 6-beta 4 in junctional epidermolysis bullosa
-
Jonkman, M.F., De Jong, M.C.J.M., Heeres, K., Sonnenberg, A. Expression of integrin alpha 6-beta 4 in junctional epidermolysis bullosa. Journal of Investigative Dermatology 1992; 99: 489-96.
-
(1992)
Journal of Investigative Dermatology
, vol.99
, pp. 489-496
-
-
Jonkman, M.F.1
De Jong, M.C.J.M.2
Heeres, K.3
Sonnenberg, A.4
-
26
-
-
0029864911
-
Human amnion contains a novel laminin variant, laminin 7 which like laminin 6, covalently associates with laminin 5 to promote stable epithelial-stromal attachment
-
Champliaud, M.F., Lunstrum, G.P., Rousselle, P., Nishiyama, T., Keene, D.R., Burgeson, R.E. Human amnion contains a novel laminin variant, laminin 7 which like laminin 6, covalently associates with laminin 5 to promote stable epithelial-stromal attachment. Journal of Cell Biology 1996; 132: 1189-98.
-
(1996)
Journal of Cell Biology
, vol.132
, pp. 1189-1198
-
-
Champliaud, M.F.1
Lunstrum, G.P.2
Rousselle, P.3
Nishiyama, T.4
Keene, D.R.5
Burgeson, R.E.6
-
27
-
-
0029970497
-
LAD-1, the linear IgA bullous dermatosis autoantigen, is a novel 120-kDa anchoring filament protein synthesized by epidermal cells
-
Marinkovich, M.P., Taylor, T.B., Keene, D.R., Burgeson, R.E., Zone, J.J. LAD-1, the linear IgA bullous dermatosis autoantigen, is a novel 120-kDa anchoring filament protein synthesized by epidermal cells. Journal of Investigative Dermatology 1996; 106: 734-8.
-
(1996)
Journal of Investigative Dermatology
, vol.106
, pp. 734-738
-
-
Marinkovich, M.P.1
Taylor, T.B.2
Keene, D.R.3
Burgeson, R.E.4
Zone, J.J.5
-
28
-
-
0029996248
-
97-kDa linear IgA bullous dermatosis (LAD) antigen localizes to the lamina lucida of the epidermal basement membrane
-
Ishiko, A., Shimizu, H., Masunaga, T. et al. 97-kDa linear IgA bullous dermatosis (LAD) antigen localizes to the lamina lucida of the epidermal basement membrane. Journal of Investigative Dermatology 1996; 106: 739-43.
-
(1996)
Journal of Investigative Dermatology
, vol.106
, pp. 739-743
-
-
Ishiko, A.1
Shimizu, H.2
Masunaga, T.3
-
29
-
-
3743090782
-
LAD-1 is absent in a subset of generalized atrophic benign junctional epidermolysis bullosa patients
-
Abstract
-
Marinkovich, M.P., Tran, H.H., Rao, S.K. et al. LAD-1 is absent in a subset of generalized atrophic benign junctional epidermolysis bullosa patients. Journal of Investigative Dermatology 1996; 106: 852 [Abstract]
-
(1996)
Journal of Investigative Dermatology
, vol.106
, pp. 852
-
-
Marinkovich, M.P.1
Tran, H.H.2
Rao, S.K.3
-
30
-
-
0000783217
-
Cloning of the linear IgA disease gene (LADA) encoding a novel anchoring filament protein, ladinin
-
Abstract
-
Megahed, M., Motoki, K., McGrath, J., LaForgia, S., Uitto, J. Cloning of the linear IgA disease gene (LADA) encoding a novel anchoring filament protein, ladinin. Journal of Investigative Dermatology 1996; 106: 832 [Abstract].
-
(1996)
Journal of Investigative Dermatology
, vol.106
, pp. 832
-
-
Megahed, M.1
Motoki, K.2
McGrath, J.3
LaForgia, S.4
Uitto, J.5
-
31
-
-
0028811442
-
Altered expression of a new antigen of the dermal-epidermal junction (NU-T2 DEJ Ag) in junctional epidermolysis bullosa
-
Tadini, G., Kanitakis, J., Cavalli, R., Schmitt, D., Cambiaghi, S., Berti, E. Altered expression of a new antigen of the dermal-epidermal junction (NU-T2 DEJ Ag) in junctional epidermolysis bullosa. Archives of Dermatological Research 1995; 287: 699-704.
-
(1995)
Archives of Dermatological Research
, vol.287
, pp. 699-704
-
-
Tadini, G.1
Kanitakis, J.2
Cavalli, R.3
Schmitt, D.4
Cambiaghi, S.5
Berti, E.6
-
32
-
-
0024220724
-
Hereditary junctional mechanobullous disease in a foal
-
Frame, S.R., Harrington, D.D., Fessier, J., Frame, P.F. Hereditary junctional mechanobullous disease in a foal. Journal of the American Veterinary Medical Association 1988; 193: 1420-4.
-
(1988)
Journal of the American Veterinary Medical Association
, vol.193
, pp. 1420-1424
-
-
Frame, S.R.1
Harrington, D.D.2
Fessier, J.3
Frame, P.F.4
-
33
-
-
0023779559
-
Ultrastructure of junctional epidermolysis bullosa in Belgian foals
-
Johnson, G.C., Kohn, C.W., Johnson, C.W., Garry, F., Scott, D., Martin, S. Ultrastructure of junctional epidermolysis bullosa in Belgian foals. Journal of Comparative Pathology 1988; 98: 329-36.
-
(1988)
Journal of Comparative Pathology
, vol.98
, pp. 329-336
-
-
Johnson, G.C.1
Kohn, C.W.2
Johnson, C.W.3
Garry, F.4
Scott, D.5
Martin, S.6
-
34
-
-
0024694901
-
Mechanobullous disease in two Belgian foals
-
Kohn, C.W., Johnson, G.C., Garry, F., Johnson, C.W., Martin, S. Mechanobullous disease in two Belgian foals. Equine Veterinary Journal 1989; 21: 297-301.
-
(1989)
Equine Veterinary Journal
, vol.21
, pp. 297-301
-
-
Kohn, C.W.1
Johnson, G.C.2
Garry, F.3
Johnson, C.W.4
Martin, S.5
-
35
-
-
0010527888
-
Epidermolyse bulleuse jonctionnelle létale chez le cheval de trait
-
Gourreau, J.M., Feillou, C., Dupère, A.M., Courreau, J.F., Alliot, A., Menguy, R. Epidermolyse bulleuse jonctionnelle létale chez le cheval de trait. Point Vétérinaire 1990; 22: 65-7.
-
(1990)
Point Vétérinaire
, vol.22
, pp. 65-67
-
-
Gourreau, J.M.1
Feillou, C.2
Dupère, A.M.3
Courreau, J.F.4
Alliot, A.5
Menguy, R.6
-
36
-
-
0347218121
-
Junctional epidermolysis bullosa (epitheliogenesis imperfecta) in French foals
-
von Tscharner, C., Halliwell, R. E. W., eds. London: Baillière Tindall, [Abstract]
-
Gourreau, J.M., Feillou, C., Morand, M., Alliot, A. Junctional epidermolysis bullosa (epitheliogenesis imperfecta) in French foals. In: von Tscharner, C., Halliwell, R. E. W., eds. Advances in Veterinary Dermatology, Vol. 1. London: Baillière Tindall, 1990: 464 [Abstract].
-
(1990)
Advances in Veterinary Dermatology
, vol.1
, pp. 464
-
-
Gourreau, J.M.1
Feillou, C.2
Morand, M.3
Alliot, A.4
-
37
-
-
0029286464
-
Epidermolysis bullosa bei einem kalb
-
Stocker, H., Lott, G., Straumann, U., Rusch, P. Epidermolysis bullosa bei einem kalb. Tierarztliche Praxis 1995; 23: 123-6.
-
(1995)
Tierarztliche Praxis
, vol.23
, pp. 123-126
-
-
Stocker, H.1
Lott, G.2
Straumann, U.3
Rusch, P.4
-
38
-
-
0346588168
-
A hereditary junctional mechanobullous disease in the cat
-
Montréal, Canada, [Abstract]
-
Johnstone, I., Mason, K., Sutton, R. A hereditary junctional mechanobullous disease in the cat. Proceedings of the 2nd World Congress of Veterinary Dermatology. Montréal, Canada, 1992: 111 [Abstract].
-
(1992)
Proceedings of the 2nd World Congress of Veterinary Dermatology
, pp. 111
-
-
Johnstone, I.1
Mason, K.2
Sutton, R.3
-
40
-
-
0023679117
-
A disease resembling junctional epidermolysis bullosa in a toy Poodle
-
Dunstan, R.W., Sills, R.C., Wilkinson, J.E., Paller, A.S., Hashimoto, K.H. A disease resembling junctional epidermolysis bullosa in a toy Poodle. American Journal of Dermatopathology 1988; 10: 442-7.
-
(1988)
American Journal of Dermatopathology
, vol.10
, pp. 442-447
-
-
Dunstan, R.W.1
Sills, R.C.2
Wilkinson, J.E.3
Paller, A.S.4
Hashimoto, K.H.5
-
41
-
-
0028073704
-
The epitope for anti-type VII collagen monoclonal antibody (LH7:2) locates at the central region of the N-terminal non-collagenous domain of type VII collagen
-
Tanaka, T., Takahashi, T., Furukawa, F., Imamura, S. The epitope for anti-type VII collagen monoclonal antibody (LH7:2) locates at the central region of the N-terminal non-collagenous domain of type VII collagen. British Journal of Dermatology 1994; 131: 472-6.
-
(1994)
British Journal of Dermatology
, vol.131
, pp. 472-476
-
-
Tanaka, T.1
Takahashi, T.2
Furukawa, F.3
Imamura, S.4
-
42
-
-
0021689226
-
Monoclonal antibodies to human type IV collagen: Useful reagents to demonstrate the heterotrimeric nature of the molecule
-
Odermatt, B.F., Lang, A.B., Rüttner, J.R., Wintherhalten, K.H., Treb, B. Monoclonal antibodies to human type IV collagen: useful reagents to demonstrate the heterotrimeric nature of the molecule. Proceedings of the National Academy of Science 1984; 81: 7343-7.
-
(1984)
Proceedings of the National Academy of Science
, vol.81
, pp. 7343-7347
-
-
Odermatt, B.F.1
Lang, A.B.2
Rüttner, J.R.3
Wintherhalten, K.H.4
Treb, B.5
-
43
-
-
0025149542
-
Epithelial integrin alpha 6-beta 4: Complete primary structure of alpha 6 and variant forms of beta 4
-
Tamura, R.N., Rozzo, C., Starr, L. Epithelial integrin alpha 6-beta 4: complete primary structure of alpha 6 and variant forms of beta 4. Journal of Cell Biology 1990; 111: 1593-604.
-
(1990)
Journal of Cell Biology
, vol.111
, pp. 1593-1604
-
-
Tamura, R.N.1
Rozzo, C.2
Starr, L.3
-
44
-
-
0027242415
-
The matrix secreted by 804G cells contains laminin-related components that participate in hemidesmosome assembly in vitro
-
Langhofer, M., Hopkinson, S.B., Jones, J.C.R. The matrix secreted by 804G cells contains laminin-related components that participate in hemidesmosome assembly in vitro. Journal of Cell Science 1993; 105: 753-64.
-
(1993)
Journal of Cell Science
, vol.105
, pp. 753-764
-
-
Langhofer, M.1
Hopkinson, S.B.2
Jones, J.C.R.3
-
45
-
-
0026730506
-
Cytoplasmic domain of the 180-kD bullous pemphigoid antigen, a hemidesmosomal component: Molecular and cell biologic characterization
-
Hopkinson, S.B., Riddelle, K.S., Jones, J.C.R. Cytoplasmic domain of the 180-kD bullous pemphigoid antigen, a hemidesmosomal component: molecular and cell biologic characterization. Journal of Investigative Dermatology 1992; 99: 264-70.
-
(1992)
Journal of Investigative Dermatology
, vol.99
, pp. 264-270
-
-
Hopkinson, S.B.1
Riddelle, K.S.2
Jones, J.C.R.3
-
46
-
-
0029339154
-
Canine bullous pemphigoid (BP) - Identification of the 180 kD canine BP antigen by circulating autoantibodies
-
Iwasaki, T., Olivry, T., Lapiere, J.C. et al. Canine bullous pemphigoid (BP) - identification of the 180 kD canine BP antigen by circulating autoantibodies. Veterinary Pathology 1995; 32: 387-93.
-
(1995)
Veterinary Pathology
, vol.32
, pp. 387-393
-
-
Iwasaki, T.1
Olivry, T.2
Lapiere, J.C.3
-
47
-
-
0028267893
-
Herlitz junctional epidermolysis bullosa keratinocytes display heterogeneous defects of nicein/kalinin gene expression
-
Baudoin, C., Miquel, C., Blanchet-Bardon, C., Gambini, C., Meneguzzi, G., Ortonne, J.P. Herlitz junctional epidermolysis bullosa keratinocytes display heterogeneous defects of nicein/kalinin gene expression. Journal of Clinical Investigation 1994; 93: 862-9.
-
(1994)
Journal of Clinical Investigation
, vol.93
, pp. 862-869
-
-
Baudoin, C.1
Miquel, C.2
Blanchet-Bardon, C.3
Gambini, C.4
Meneguzzi, G.5
Ortonne, J.P.6
-
48
-
-
0024811825
-
An immunocytochemical technique offering increased sensitivity and lowered cost with a streptavidin-horseradish peroxidase conjugate
-
Cartun, R.W., Pedersen, C. An immunocytochemical technique offering increased sensitivity and lowered cost with a streptavidin-horseradish peroxidase conjugate. Journal of Histotechnology 1989; 12: 273-7.
-
(1989)
Journal of Histotechnology
, vol.12
, pp. 273-277
-
-
Cartun, R.W.1
Pedersen, C.2
-
49
-
-
0028910129
-
Investigation of epidermotropism in canine mycosis fungoides: Expression of intercellular adhesion molecule-1 (ICAM-1) and beta-2 integrins
-
Olivry, T., Moore, P.F., Naydan, D.K., Danilenko, D.M., Affolter, V.K. Investigation of epidermotropism in canine mycosis fungoides: Expression of intercellular adhesion molecule-1 (ICAM-1) and beta-2 integrins. Archives of Dermatological Research 1995; 287: 186-92.
-
(1995)
Archives of Dermatological Research
, vol.287
, pp. 186-192
-
-
Olivry, T.1
Moore, P.F.2
Naydan, D.K.3
Danilenko, D.M.4
Affolter, V.K.5
-
51
-
-
0021794196
-
Epidermolysis bullosa: Variability of expression of cicatricial pemphigoid, bullous pemphigoid, and epidermolysis bullosa acquisita antigens in clinically uninvolved skin
-
Fine, J.D. Epidermolysis bullosa: variability of expression of cicatricial pemphigoid, bullous pemphigoid, and epidermolysis bullosa acquisita antigens in clinically uninvolved skin. Journal of Investigative Dermatology 1985; 85: 47-9.
-
(1985)
Journal of Investigative Dermatology
, vol.85
, pp. 47-49
-
-
Fine, J.D.1
-
52
-
-
3743140928
-
Epidermolyse bulleuse jonctionelle familiale chez des chiots Berger de Beauce
-
Paris, [Abstract]. PMCAC edition, Paris
-
Fontaine, J., Rémy, I., Clercx, C. Epidermolyse bulleuse jonctionelle familiale chez des chiots Berger de Beauce. Congrès Annuel de la Conférence Nationale des Vétérinaires Spécialistes des Petits Animaux. Paris, 1992: 310 [Abstract]. PMCAC edition, Paris.
-
(1992)
Congrès Annuel de la Conférence Nationale des Vétérinaires Spécialistes des Petits Animaux
, pp. 310
-
-
Fontaine, J.1
Rémy, I.2
Clercx, C.3
-
53
-
-
0026067709
-
Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa - A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry
-
Fine, J.-D., Bauer, E.A., Briggaman, R.A. et al. Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa - A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry. Journal of the American Academy of Dermatology 1991; 24: 119-35.
-
(1991)
Journal of the American Academy of Dermatology
, vol.24
, pp. 119-135
-
-
Fine, J.-D.1
Bauer, E.A.2
Briggaman, R.A.3
-
56
-
-
0027430326
-
Ultrastructural findings in epidermolysis bullosa
-
Smith, L.T. Ultrastructural findings in epidermolysis bullosa. Archives of Dermatology 1993; 129: 1578-84.
-
(1993)
Archives of Dermatology
, vol.129
, pp. 1578-1584
-
-
Smith, L.T.1
-
57
-
-
0022631878
-
Hemidesmosome heterogeneity in junctional epidermolysis bullosa revealed by morphometric analysis
-
Tidman, M., Eady, R. Hemidesmosome heterogeneity in junctional epidermolysis bullosa revealed by morphometric analysis. Journal of Investigative Dermatology 1986; 86: 51-6.
-
(1986)
Journal of Investigative Dermatology
, vol.86
, pp. 51-56
-
-
Tidman, M.1
Eady, R.2
-
58
-
-
0029793261
-
Absence of detectable α6 integrin in pyloric atresia-junctional epidermolysis bullosa syndrome. Application of prenatal diagnosis in a family at risk for recurrence
-
Shimizu, H., Suzumori, K., Hatta, N., Nishikawa, T. Absence of detectable α6 integrin in pyloric atresia-junctional epidermolysis bullosa syndrome. Application of prenatal diagnosis in a family at risk for recurrence. Archives of Dermatology 1996; 132: 919-25.
-
(1996)
Archives of Dermatology
, vol.132
, pp. 919-925
-
-
Shimizu, H.1
Suzumori, K.2
Hatta, N.3
Nishikawa, T.4
-
59
-
-
3743146379
-
Homozygous α6 integrin gene mutation in epidermolysis bullosa with congenital pyloric atresia
-
Abstract
-
Uitto, J., Kimonis, V.E., Xu, Y., Spanou, E.N., Pulkkinen, L. Homozygous α6 integrin gene mutation in epidermolysis bullosa with congenital pyloric atresia. Journal of Investigative Dermatology 1997; 108: 541[Abstract].
-
(1997)
Journal of Investigative Dermatology
, vol.108
, pp. 541
-
-
Uitto, J.1
Kimonis, V.E.2
Xu, Y.3
Spanou, E.N.4
Pulkkinen, L.5
-
60
-
-
3743102989
-
A homozygous mutation in the gene encoding integrin α6 in junctional epidermolysis bullosa with pyloric atresia
-
Abstract
-
D'Alessio, M., Ruzzi, L., Gagnoux-Palacios, L. et al. A homozygous mutation in the gene encoding integrin α6 in junctional epidermolysis bullosa with pyloric atresia. Journal of Investigative Dermatology 1997; 108: 542 [Abstract].
-
(1997)
Journal of Investigative Dermatology
, vol.108
, pp. 542
-
-
D'Alessio, M.1
Ruzzi, L.2
Gagnoux-Palacios, L.3
|