218 related articles for article (PubMed ID: 18528435)
1. 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]
2. Localization and potential function of kindlin-1 in periodontal tissues.
Petricca G; Leppilampi M; Jiang G; Owen GR; Wiebe C; Tu Y; Koivisto L; Häkkinen L; Wu C; Larjava H
Eur J Oral Sci; 2009 Oct; 117(5):518-27. PubMed ID: 19758247
[TBL] [Abstract][Full Text] [Related]
3. Kindlin binds migfilin tandem LIM domains and regulates migfilin focal adhesion localization and recruitment dynamics.
Brahme NN; Harburger DS; Kemp-O'Brien K; Stewart R; Raghavan S; Parsons M; Calderwood DA
J Biol Chem; 2013 Dec; 288(49):35604-16. PubMed ID: 24165133
[TBL] [Abstract][Full Text] [Related]
4. Kindlin-1 Regulates Keratinocyte Electrotaxis.
Zhang G; Gu Y; Begum R; Chen H; Gao X; McGrath JA; Parsons M; Song B
J Invest Dermatol; 2016 Nov; 136(11):2229-2239. PubMed ID: 27427485
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. Kindlin-1 regulates integrin dynamics and adhesion turnover.
Margadant C; Kreft M; Zambruno G; Sonnenberg A
PLoS One; 2013; 8(6):e65341. PubMed ID: 23776470
[TBL] [Abstract][Full Text] [Related]
9. Kindlin-2 phosphorylation by Src at Y193 enhances Src activity and is involved in Migfilin recruitment to the focal adhesions.
Liu Z; Lu D; Wang X; Wan J; Liu C; Zhang H
FEBS Lett; 2015 Jul; 589(15):2001-10. PubMed ID: 26037143
[TBL] [Abstract][Full Text] [Related]
10. Kindlin-1 Is required for RhoGTPase-mediated lamellipodia formation in keratinocytes.
Has C; Herz C; Zimina E; Qu HY; He Y; Zhang ZG; Wen TT; Gache Y; Aumailley M; Bruckner-Tuderman L
Am J Pathol; 2009 Oct; 175(4):1442-52. PubMed ID: 19762715
[TBL] [Abstract][Full Text] [Related]
11. Kindlin-1 Regulates Epidermal Growth Factor Receptor Signaling.
Michael M; Begum R; Chan GK; Whitewood AJ; Matthews DR; Goult BT; McGrath JA; Parsons M
J Invest Dermatol; 2019 Feb; 139(2):369-379. PubMed ID: 30248333
[TBL] [Abstract][Full Text] [Related]
12. Inhibition of cyclin-dependent kinase activity exacerbates H
Emmert H; Culley J; Brunton VG
Exp Dermatol; 2019 Sep; 28(9):1074-1078. PubMed ID: 31260568
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Kindler syndrome.
Ashton GH
Clin Exp Dermatol; 2004 Mar; 29(2):116-21. PubMed ID: 14987263
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome.
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
J Invest Dermatol; 2004 Jan; 122(1):78-83. PubMed ID: 14962093
[TBL] [Abstract][Full Text] [Related]
18. 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]
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. 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]
[Next] [New Search]
