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58349116039
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Kindler syndrome: A focal adhesion genodermatosis
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Lai-Cheong JE, Tanaka A, Hawche G, Emanuel P, Maari C, Taskesen M, Akdeniz S, Liu L, McGrath JA: Kindler syndrome: a focal adhesion genodermatosis. Br J Dermatol 2009; 160: 233-242.
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Akdeniz, S.7
Liu, L.8
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Kindlins: Essential regulators of integrin signalling and cellmatrix adhesion
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Larjava H, Plow EF, Wu C: Kindlins: essential regulators of integrin signalling and cellmatrix adhesion. EMBO Rep 2008; 9: 1203-1208.
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Larjava, H.1
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33845990287
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Kindlin-1 is a phosphoprotein involved in regulation of polarity, proliferation, and motility of epidermal keratinocytes
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Herz C, Aumailley M, Schulte C, Schlotzer- Schrehardt U, Bruckner-Tuderman L, Has C: Kindlin-1 is a phosphoprotein involved in regulation of polarity, proliferation, and motility of epidermal keratinocytes. J Biol Chem 2006; 281: 36082-36090.
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Herz, C.1
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Schlotzer-Schrehardt, U.4
Bruckner-Tuderman, L.5
Has, C.6
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33746115677
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Molecular basis of Kindler syndrome in Italy: Novel and recurrent Alu/ Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene
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Has C, Wessagowit V, Pascucci M, Baer C, Didona B, Wilhelm C, Pedicelli C, Locatelli A, Kohlhase J, Ashton GH, Tadini G, Zambruno G, Bruckner-Tuderman L, McGrath JA, Castiglia D: Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/ Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene. J Invest Dermatol 2006; 126: 1776-1783.
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Has, C.1
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Baer, C.4
Didona, B.5
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Pedicelli, C.7
Locatelli, A.8
Kohlhase, J.9
Ashton, G.H.10
Tadini, G.11
Zambruno, G.12
Bruckner-Tuderman, L.13
McGrath, J.A.14
Castiglia, D.15
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5
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73549105028
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Kindlin-1 is required for rhoGTPase-mediated lamellipodia formation in keratinocytes
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Has C, Herz C, Zimina E, Qu HY, He Y, Zhang ZG, Wen TT, Gache Y, Aumailley M, Bruckner-Tuderman L: Kindlin-1 is required for rhoGTPase-mediated lamellipodia formation in keratinocytes. Am J Pathol 2009; 175: 1442-1452.
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Has, C.1
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He, Y.5
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Wen, T.T.7
Gache, Y.8
Aumailley, M.9
Bruckner-Tuderman, L.10
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6
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54249105508
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C-terminally truncated kindlin-1 leads to abnormal adhesion and migration of keratinocytes
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Has C, Ludwig RJ, Herz C, Kern JS, Ussar S, Ochsendorf FR, Kaufmann R, Schumann H, Kohlhase J, Bruckner-Tuderman L: C-terminally truncated kindlin-1 leads to abnormal adhesion and migration of keratinocytes. Br J Dermatol 2008; 159: 1192-1196.
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Has, C.1
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Ussar, S.5
Ochsendorf, F.R.6
Kaufmann, R.7
Schumann, H.8
Kohlhase, J.9
Bruckner-Tuderman, L.10
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7
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38849119897
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Novel and recurrent KIND1 mutations in two patients with Kindler syndrome and severe mucosal involvement
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Mansur AT, Elcioglu NH, Aydingoz IE, Akkaya AD, Serdar ZA, Herz C, Bruckner-Tuderman L, Has C: Novel and recurrent KIND1 mutations in two patients with Kindler syndrome and severe mucosal involvement. Acta Derm Venereol 2007; 87: 563-565.
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Acta Derm Venereol
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Mansur, A.T.1
Elcioglu, N.H.2
Aydingoz, I.E.3
Akkaya, A.D.4
Serdar, Z.A.5
Herz, C.6
Bruckner-Tuderman, L.7
Has, C.8
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8
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36148942525
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Unusual molecular findings in Kindler syndrome
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Arita K, Wessagowit V, Inamadar AC, Palit A, Fassihi H, Lai-Cheong JE, Pourreyron C, South AP, McGrath JA: Unusual molecular findings in Kindler syndrome. Br J Dermatol 2007; 157: 1252-1256.
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Arita, K.1
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Palit, A.4
Fassihi, H.5
Lai-Cheong, J.E.6
Pourreyron, C.7
South, A.P.8
McGrath, J.A.9
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9
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A presumptive case of Kindler syndrome with a new clinical finding
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Satter EK: A presumptive case of Kindler syndrome with a new clinical finding. Pediatr Dermatol 2008; 25: 646-648.
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Satter, E.K.1
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53349162122
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A novel large FERMT1 (KIND1) gene deletion in Kindler syndrome
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Has C, Yordanova I, Balabanova M, Kazandjieva J, Herz C, Kohlhase J, Bruckner-Tuderman L: A novel large FERMT1 (KIND1) gene deletion in Kindler syndrome. J Dermatol Sci 2008; 52: 209-212.
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J Dermatol Sci
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Has, C.1
Yordanova, I.2
Balabanova, M.3
Kazandjieva, J.4
Herz, C.5
Kohlhase, J.6
Bruckner-Tuderman, L.7
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11
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9144226774
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Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome
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Ashton GH, McLean WH, South AP, Oyama N, Smith FJ, Al-Suwaid R, Al-Ismaily A, Atherton DJ, Harwood CA, Leigh IM, Moss C, Didona B, Zambruno G, Patrizi A, Eady RA, McGrath JA: Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome. J Invest Dermatol 2004; 122: 78-83.
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Ashton, G.H.1
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Al-Suwaid, R.6
Al-Ismaily, A.7
Atherton, D.J.8
Harwood, C.A.9
Leigh, I.M.10
Moss, C.11
Didona, B.12
Zambruno, G.13
Patrizi, A.14
Eady, R.A.15
McGrath, J.A.16
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12
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0141993502
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Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorder
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Lanschuetzer CM, Muss WH, Emberger M, Pohla-Gubo G, Klausegger A, Bauer JW, Hintner H: Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorder. J Cutan Pathol 2003; 30: 553-560.
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Lanschuetzer, C.M.1
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Emberger, M.3
Pohla-Gubo, G.4
Klausegger, A.5
Bauer, J.W.6
Hintner, H.7
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13
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Aggressive squamous cell carcinoma in Kindler syndrome
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Emanuel PO, Rudikoff D, Phelps RG: Aggressive squamous cell carcinoma in Kindler syndrome. Skinmed 2006; 5: 305-307.
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Emanuel, P.O.1
Rudikoff, D.2
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15
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0035724198
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Kindler syndrome complicated by squamous cell carcinoma of the hard palate: Successful treatment with high-dose radiation therapy and granulocyte-macrophage colony-stimulating factor
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Lotem M, Raben M, Zeltser R, Landau M, Sela M, Wygoda M, Tochner ZA: Kindler syndrome complicated by squamous cell carcinoma of the hard palate: successful treatment with high-dose radiation therapy and granulocyte-macrophage colony-stimulating factor. Br J Dermatol 2001; 144: 1284-1286.
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Lotem, M.1
Raben, M.2
Zeltser, R.3
Landau, M.4
Sela, M.5
Wygoda, M.6
Tochner, Z.A.7
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