301 related articles for article (PubMed ID: 15590704)
21. Loss of proteolytically processed filaggrin caused by epidermal deletion of Matriptase/MT-SP1.
List K; Szabo R; Wertz PW; Segre J; Haudenschild CC; Kim SY; Bugge TH
J Cell Biol; 2003 Nov; 163(4):901-10. PubMed ID: 14638864
[TBL] [Abstract][Full Text] [Related]
22. Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families.
Bitoun E; Chavanas S; Irvine AD; Lonie L; Bodemer C; Paradisi M; Hamel-Teillac D; Ansai S; Mitsuhashi Y; Taïeb A; de Prost Y; Zambruno G; Harper JI; Hovnanian A
J Invest Dermatol; 2002 Feb; 118(2):352-61. PubMed ID: 11841556
[TBL] [Abstract][Full Text] [Related]
23. A heterozygous null mutation combined with the G1258A polymorphism of SPINK5 causes impaired LEKTI function and abnormal expression of skin barrier proteins.
Di WL; Hennekam RC; Callard RE; Harper JI
Br J Dermatol; 2009 Aug; 161(2):404-12. PubMed ID: 19438860
[TBL] [Abstract][Full Text] [Related]
24. Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome.
Chavanas S; Bodemer C; Rochat A; Hamel-Teillac D; Ali M; Irvine AD; Bonafé JL; Wilkinson J; Taïeb A; Barrandon Y; Harper JI; de Prost Y; Hovnanian A
Nat Genet; 2000 Jun; 25(2):141-2. PubMed ID: 10835624
[TBL] [Abstract][Full Text] [Related]
25. Murine filaggrin-2 is involved in epithelial barrier function and down-regulated in metabolically induced skin barrier dysfunction.
Hansmann B; Ahrens K; Wu Z; Proksch E; Meyer-Hoffert U; Schröder JM
Exp Dermatol; 2012 Apr; 21(4):271-6. PubMed ID: 22417302
[TBL] [Abstract][Full Text] [Related]
26. SPINK5 and Netherton syndrome: novel mutations, demonstration of missing LEKTI, and differential expression of transglutaminases.
Raghunath M; Tontsidou L; Oji V; Aufenvenne K; Schürmeyer-Horst F; Jayakumar A; Ständer H; Smolle J; Clayman GL; Traupe H
J Invest Dermatol; 2004 Sep; 123(3):474-83. PubMed ID: 15304086
[TBL] [Abstract][Full Text] [Related]
27. A de novo variant in the ASPRV1 gene in a dog with ichthyosis.
Bauer A; Waluk DP; Galichet A; Timm K; Jagannathan V; Sayar BS; Wiener DJ; Dietschi E; Müller EJ; Roosje P; Welle MM; Leeb T
PLoS Genet; 2017 Mar; 13(3):e1006651. PubMed ID: 28249031
[TBL] [Abstract][Full Text] [Related]
28. Matriptase/MT-SP1 is required for postnatal survival, epidermal barrier function, hair follicle development, and thymic homeostasis.
List K; Haudenschild CC; Szabo R; Chen W; Wahl SM; Swaim W; Engelholm LH; Behrendt N; Bugge TH
Oncogene; 2002 May; 21(23):3765-79. PubMed ID: 12032844
[TBL] [Abstract][Full Text] [Related]
29. rAAV2-mediated restoration of LEKTI in LEKTI-deficient cells from Netherton patients.
Roedl D; Oji V; Buters JT; Behrendt H; Braun-Falco M
J Dermatol Sci; 2011 Mar; 61(3):194-8. PubMed ID: 21251800
[TBL] [Abstract][Full Text] [Related]
30. Netherton syndrome with ichthyosis linearis circumflexa and trichorrhexis invaginatum.
Ng E; Hale CS; Meehan SA; Cohen DE
Dermatol Online J; 2014 Dec; 20(12):. PubMed ID: 25526335
[TBL] [Abstract][Full Text] [Related]
31. LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome.
Bitoun E; Micheloni A; Lamant L; Bonnart C; Tartaglia-Polcini A; Cobbold C; Al Saati T; Mariotti F; Mazereeuw-Hautier J; Boralevi F; Hohl D; Harper J; Bodemer C; D'Alessio M; Hovnanian A
Hum Mol Genet; 2003 Oct; 12(19):2417-30. PubMed ID: 12915442
[TBL] [Abstract][Full Text] [Related]
32. The content of free amino acids in the stratum corneum is increased in senile xerosis.
Takahashi M; Tezuka T
Arch Dermatol Res; 2004 Mar; 295(10):448-52. PubMed ID: 14762669
[TBL] [Abstract][Full Text] [Related]
33. Filaggrin in the frontline: role in skin barrier function and disease.
Sandilands A; Sutherland C; Irvine AD; McLean WH
J Cell Sci; 2009 May; 122(Pt 9):1285-94. PubMed ID: 19386895
[TBL] [Abstract][Full Text] [Related]
34. Epidermal-specific defect of GPI anchor in Pig-a null mice results in Harlequin ichthyosis-like features.
Hara-Chikuma M; Takeda J; Tarutani M; Uchida Y; Holleran WM; Endo Y; Elias PM; Inoue S
J Invest Dermatol; 2004 Sep; 123(3):464-9. PubMed ID: 15304084
[TBL] [Abstract][Full Text] [Related]
35. LEKTI demonstrable by immunohistochemistry of the skin: a potential diagnostic skin test for Netherton syndrome.
Ong C; O'Toole EA; Ghali L; Malone M; Smith VV; Callard R; Harper JI
Br J Dermatol; 2004 Dec; 151(6):1253-7. PubMed ID: 15606522
[TBL] [Abstract][Full Text] [Related]
36. Ichthyosis vulgaris: identification of a defect in synthesis of filaggrin correlated with an absence of keratohyaline granules.
Sybert VP; Dale BA; Holbrook KA
J Invest Dermatol; 1985 Mar; 84(3):191-4. PubMed ID: 2579164
[TBL] [Abstract][Full Text] [Related]
37. Caspase-14 protects against epidermal UVB photodamage and water loss.
Denecker G; Hoste E; Gilbert B; Hochepied T; Ovaere P; Lippens S; Van den Broecke C; Van Damme P; D'Herde K; Hachem JP; Borgonie G; Presland RB; Schoonjans L; Libert C; Vandekerckhove J; Gevaert K; Vandenabeele P; Declercq W
Nat Cell Biol; 2007 Jun; 9(6):666-74. PubMed ID: 17515931
[TBL] [Abstract][Full Text] [Related]
38. A compound heterozygous mutation of the SPINK5 gene in a Taiwanese boy with Netherton syndrome.
Chao SC; Tsai YM; Lee JY
J Formos Med Assoc; 2003 Jun; 102(6):418-23. PubMed ID: 12923596
[TBL] [Abstract][Full Text] [Related]
39. An update on molecular aspects of the non-syndromic ichthyoses.
Akiyama M; Shimizu H
Exp Dermatol; 2008 May; 17(5):373-82. PubMed ID: 18341575
[TBL] [Abstract][Full Text] [Related]
40. Altered stratum corneum barrier and enhanced percutaneous immune responses in filaggrin-null mice.
Kawasaki H; Nagao K; Kubo A; Hata T; Shimizu A; Mizuno H; Yamada T; Amagai M
J Allergy Clin Immunol; 2012 Jun; 129(6):1538-46.e6. PubMed ID: 22409988
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
