128 related articles for article (PubMed ID: 19292718)
1. A novel 3017-bp deletion mutation in the FERMT1 (KIND1) gene in a Chinese family with Kindler syndrome.
Zhou C; Song S; Zhang J
Br J Dermatol; 2009 May; 160(5):1119-22. PubMed ID: 19292718
[No Abstract] [Full Text] [Related]
2. A novel large FERMT1 (KIND1) gene deletion in Kindler syndrome.
Has C; Yordanova I; Balabanova M; Kazandjieva J; Herz C; Kohlhase J; Bruckner-Tuderman L
J Dermatol Sci; 2008 Dec; 52(3):209-12. PubMed ID: 18835760
[No Abstract] [Full Text] [Related]
3. Novel and recurrent KIND1 mutations in two patients with Kindler syndrome and severe mucosal involvement.
Mansur AT; Elcioglu NH; Aydingöz IE; Akkaya AD; Serdar ZA; Herz C; Bruckner-Tuderman L; Has C
Acta Derm Venereol; 2007; 87(6):563-5. PubMed ID: 17989907
[No Abstract] [Full Text] [Related]
4. Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome.
Martignago BC; Lai-Cheong JE; Liu L; McGrath JA; Cestari TF
Br J Dermatol; 2007 Dec; 157(6):1281-4. PubMed ID: 17916195
[No Abstract] [Full Text] [Related]
5. C-terminally truncated kindlin-1 leads to abnormal adhesion and migration of keratinocytes.
Has C; Ludwig RJ; Herz C; Kern JS; Ussar S; Ochsendorf FR; Kaufmann R; Schumann H; Kohlhase J; Bruckner-Tuderman L
Br J Dermatol; 2008 Nov; 159(5):1192-6. PubMed ID: 18652585
[TBL] [Abstract][Full Text] [Related]
6. Unusual molecular findings in Kindler syndrome.
Arita K; Wessagowit V; Inamadar AC; Palit A; Fassihi H; Lai-Cheong JE; Pourreyron C; South AP; McGrath JA
Br J Dermatol; 2007 Dec; 157(6):1252-6. PubMed ID: 17854379
[TBL] [Abstract][Full Text] [Related]
7. A novel frameshift mutation in the KIND1 gene in Turkish siblings with Kindler syndrome.
Kaçar N; Semerci N; Ergin S; Pascucci M; Zambruno G; Castiglia D
Br J Dermatol; 2008 Jun; 158(6):1375-7. PubMed ID: 18410424
[No Abstract] [Full Text] [Related]
8. Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene.
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
J Invest Dermatol; 2006 Aug; 126(8):1776-83. PubMed ID: 16675959
[TBL] [Abstract][Full Text] [Related]
9. An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene.
Sethuraman G; Fassihi H; Ashton GH; Bansal A; Kabra M; Sharma VK; McGrath JA
Clin Exp Dermatol; 2005 May; 30(3):286-8. PubMed ID: 15807691
[TBL] [Abstract][Full Text] [Related]
10. Kindler syndrome: a new mutation and new diagnostic possibilities.
Burch JM; Fassihi H; Jones CA; Mengshol SC; Fitzpatrick JE; McGrath JA
Arch Dermatol; 2006 May; 142(5):620-4. PubMed ID: 16702500
[TBL] [Abstract][Full Text] [Related]
11. Novel and recurrent FERMT1 gene mutations in Kindler syndrome.
Techanukul T; Sethuraman G; Zlotogorski A; Horev L; Macarov M; Trainer A; Fong K; Lens M; Medenica L; Ramesh V; McGrath JA; Lai-Cheong JE
Acta Derm Venereol; 2011 May; 91(3):267-70. PubMed ID: 21336475
[TBL] [Abstract][Full Text] [Related]
12. Novel KIND1 gene mutation in Kindler syndrome with severe gastrointestinal tract involvement.
Sadler E; Klausegger A; Muss W; Deinsberger U; Pohla-Gubo G; Laimer M; Lanschuetzer C; Bauer JW; Hintner H
Arch Dermatol; 2006 Dec; 142(12):1619-24. PubMed ID: 17178989
[TBL] [Abstract][Full Text] [Related]
13. Chronic colitis due to an epithelial barrier defect: the role of kindlin-1 isoforms.
Kern JS; Herz C; Haan E; Moore D; Nottelmann S; von Lilien T; Greiner P; Schmitt-Graeff A; Opitz OG; Bruckner-Tuderman L; Has C
J Pathol; 2007 Dec; 213(4):462-70. PubMed ID: 17955455
[TBL] [Abstract][Full Text] [Related]
14. Kindler syndrome pathogenesis and fermitin family homologue 1 (kindlin-1) function.
D'Souza MA; Kimble RM; McMillan JR
Dermatol Clin; 2010 Jan; 28(1):115-8. PubMed ID: 19945623
[TBL] [Abstract][Full Text] [Related]
15. A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome.
Gao Y; Bai JL; Liu XY; Qu YJ; Cao YY; Wang JC; Jin YW; Wang H; Song F
J Zhejiang Univ Sci B; 2015 Nov; 16(11):957-62. PubMed ID: 26537214
[TBL] [Abstract][Full Text] [Related]
16. Kindler syndrome: extension of FERMT1 mutational spectrum and natural history.
Has C; Castiglia D; del Rio M; Diez MG; Piccinni E; Kiritsi D; Kohlhase J; Itin P; Martin L; Fischer J; Zambruno G; Bruckner-Tuderman L
Hum Mutat; 2011 Nov; 32(11):1204-12. PubMed ID: 21936020
[TBL] [Abstract][Full Text] [Related]
17. Expression of exon-8-skipped kindlin-1 does not compensate for defects of Kindler syndrome.
Natsuga K; Nishie W; Shinkuma S; Nakamura H; Matsushima Y; Tatsuta A; Komine M; Shimizu H
J Dermatol Sci; 2011 Jan; 61(1):38-44. PubMed ID: 21146372
[TBL] [Abstract][Full Text] [Related]
18. New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndrome.
Fuchs-Telem D; Nousbeck J; Singer A; McGrath JA; Sarig O; Sprecher E
Clin Exp Dermatol; 2014 Apr; 39(3):361-7. PubMed ID: 24635080
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Retrospective diagnosis of Kindler syndrome in a 37-year-old man.
Thomson MA; Ashton GH; McGrath JA; Eady RA; Moss C
Clin Exp Dermatol; 2006 Jan; 31(1):45-7. PubMed ID: 16309479
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
