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8. Induction of senescence pathways in Kindler syndrome primary keratinocytes. Piccinni E; Di Zenzo G; Maurelli R; Dellambra E; Teson M; Has C; Zambruno G; Castiglia D Br J Dermatol; 2013 May; 168(5):1019-26. PubMed ID: 23278235 [TBL] [Abstract][Full Text] [Related]
9. Partial loss of epithelial phenotype in kindlin-1-deficient keratinocytes. Qu H; Wen T; Pesch M; Aumailley M Am J Pathol; 2012 Apr; 180(4):1581-92. PubMed ID: 22326752 [TBL] [Abstract][Full Text] [Related]
10. Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients. Guerrero-Aspizua S; Conti CJ; Escamez MJ; Castiglia D; Zambruno G; Youssefian L; Vahidnezhad H; Requena L; Itin P; Tadini G; Yordanova I; Martin L; Uitto J; Has C; Del Rio M Orphanet J Rare Dis; 2019 Jul; 14(1):183. PubMed ID: 31340837 [TBL] [Abstract][Full Text] [Related]
11. Focal adhesions in the skin: lessons learned from skin fragility disorders. Has C; He Y Eur J Dermatol; 2017 Jun; 27(S1):8-11. PubMed ID: 28690212 [TBL] [Abstract][Full Text] [Related]
12. UV-B-induced cutaneous inflammation and prospects for antioxidant treatment in Kindler syndrome. Maier K; He Y; Wölfle U; Esser PR; Brummer T; Schempp C; Bruckner-Tuderman L; Has C Hum Mol Genet; 2016 Dec; 25(24):5339-5352. PubMed ID: 27798104 [TBL] [Abstract][Full Text] [Related]
13. Colocalization of kindlin-1, kindlin-2, and migfilin at keratinocyte focal adhesion and relevance to the pathophysiology of Kindler syndrome. Lai-Cheong JE; Ussar S; Arita K; Hart IR; McGrath JA J Invest Dermatol; 2008 Sep; 128(9):2156-65. PubMed ID: 18528435 [TBL] [Abstract][Full Text] [Related]
14. FERMT1 promoter mutations in patients with Kindler syndrome. Has C; Chmel N; Levati L; Neri I; Sonnenwald T; Pigors M; Godbole K; Dudhbhate A; Bruckner-Tuderman L; Zambruno G; Castiglia D Clin Genet; 2015 Sep; 88(3):248-54. PubMed ID: 25156791 [TBL] [Abstract][Full Text] [Related]
15. Kindlin-1 and -2 have overlapping functions in epithelial cells implications for phenotype modification. He Y; Esser P; Heinemann A; Bruckner-Tuderman L; Has C Am J Pathol; 2011 Mar; 178(3):975-82. PubMed ID: 21356350 [TBL] [Abstract][Full Text] [Related]
16. Induction of phenotype modifying cytokines by FERMT1 mutations. Heinemann A; He Y; Zimina E; Boerries M; Busch H; Chmel N; Kurz T; Bruckner-Tuderman L; Has C Hum Mutat; 2011 Apr; 32(4):397-406. PubMed ID: 21309038 [TBL] [Abstract][Full Text] [Related]
17. Kindler syndrome: a focal adhesion genodermatosis. Lai-Cheong JE; Tanaka A; Hawche G; Emanuel P; Maari C; Taskesen M; Akdeniz S; Liu L; McGrath JA Br J Dermatol; 2009 Feb; 160(2):233-42. PubMed ID: 19120339 [TBL] [Abstract][Full Text] [Related]
18. Single Amino Acid Deletion in Kindlin-1 Results in Partial Protein Degradation Which Can Be Rescued by Chaperone Treatment. Maier K; He Y; Esser PR; Thriene K; Sarca D; Kohlhase J; Dengjel J; Martin L; Has C J Invest Dermatol; 2016 May; 136(5):920-929. PubMed ID: 26827766 [TBL] [Abstract][Full Text] [Related]