324 related articles for article (PubMed ID: 25244098)
1. Papillon-Lefèvre syndrome patient reveals species-dependent requirements for neutrophil defenses.
Sørensen OE; Clemmensen SN; Dahl SL; Østergaard O; Heegaard NH; Glenthøj A; Nielsen FC; Borregaard N
J Clin Invest; 2014 Oct; 124(10):4539-48. PubMed ID: 25244098
[TBL] [Abstract][Full Text] [Related]
2. A rare CTSC mutation in Papillon-Lefèvre Syndrome results in abolished serine protease activity and reduced NET formation but otherwise normal neutrophil function.
Sanchez Klose FP; Björnsdottir H; Dahlstrand Rudin A; Persson T; Khamzeh A; Sundqvist M; Thorbert-Mros S; Dieckmann R; Christenson K; Bylund J
PLoS One; 2021; 16(12):e0261724. PubMed ID: 34932608
[TBL] [Abstract][Full Text] [Related]
3. Papillon-Lefèvre syndrome: correlating the molecular, cellular, and clinical consequences of cathepsin C/dipeptidyl peptidase I deficiency in humans.
Pham CT; Ivanovich JL; Raptis SZ; Zehnbauer B; Ley TJ
J Immunol; 2004 Dec; 173(12):7277-81. PubMed ID: 15585850
[TBL] [Abstract][Full Text] [Related]
4. Lack of cathelicidin processing in Papillon-Lefèvre syndrome patients reveals essential role of LL-37 in periodontal homeostasis.
Eick S; Puklo M; Adamowicz K; Kantyka T; Hiemstra P; Stennicke H; Guentsch A; Schacher B; Eickholz P; Potempa J
Orphanet J Rare Dis; 2014 Sep; 9():148. PubMed ID: 25260376
[TBL] [Abstract][Full Text] [Related]
5. Processing of Neutrophil α-Defensins Does Not Rely on Serine Proteases In Vivo.
Glenthøj A; Nickles K; Cowland J; Borregaard N
PLoS One; 2015; 10(5):e0125483. PubMed ID: 25945506
[TBL] [Abstract][Full Text] [Related]
6. Prolonged pharmacological inhibition of cathepsin C results in elimination of neutrophil serine proteases.
Guarino C; Hamon Y; Croix C; Lamort AS; Dallet-Choisy S; Marchand-Adam S; Lesner A; Baranek T; Viaud-Massuard MC; Lauritzen C; Pedersen J; Heuzé-Vourc'h N; Si-Tahar M; Fıratlı E; Jenne DE; Gauthier F; Horwitz MS; Borregaard N; Korkmaz B
Biochem Pharmacol; 2017 May; 131():52-67. PubMed ID: 28193451
[TBL] [Abstract][Full Text] [Related]
7. Clinical, genetic, and biochemical findings in two siblings with Papillon-Lefèvre Syndrome.
Cagli NA; Hakki SS; Dursun R; Toy H; Gokalp A; Ryu OH; Hart PS; Hart TC
J Periodontol; 2005 Dec; 76(12):2322-9. PubMed ID: 16332247
[TBL] [Abstract][Full Text] [Related]
8. Two patients with Papillon-Lefèvre syndrome without periodontal involvement of the permanent dentition.
Umlauft J; Schnabl D; Blunder S; Moosbrugger-Martinz V; Kapferer-Seebacher I; Zschocke J; Schmuth M; Gruber R
J Dermatol; 2021 Apr; 48(4):537-541. PubMed ID: 33580910
[TBL] [Abstract][Full Text] [Related]
9. Characterization of neutrophil function in Papillon-Lefèvre syndrome.
Roberts H; White P; Dias I; McKaig S; Veeramachaneni R; Thakker N; Grant M; Chapple I
J Leukoc Biol; 2016 Aug; 100(2):433-44. PubMed ID: 26957212
[TBL] [Abstract][Full Text] [Related]
10. Protein modeling of cathepsin C mutations found in Papillon-Lefèvre syndrome.
Moghaddasian M; Arab H; Dadkhah E; Boostani H; Babak AR; Abbaszadegan MR
Gene; 2014 Mar; 538(1):182-7. PubMed ID: 24374475
[TBL] [Abstract][Full Text] [Related]
11. NSP4 is stored in azurophil granules and released by activated neutrophils as active endoprotease with restricted specificity.
Perera NC; Wiesmüller KH; Larsen MT; Schacher B; Eickholz P; Borregaard N; Jenne DE
J Immunol; 2013 Sep; 191(5):2700-7. PubMed ID: 23904161
[TBL] [Abstract][Full Text] [Related]
12. Loss-of-function mutations in cathepsin C in two families with Papillon-Lefèvre syndrome are associated with deficiency of serine proteinases in PMNs.
de Haar SF; Jansen DC; Schoenmaker T; De Vree H; Everts V; Beertsen W
Hum Mutat; 2004 May; 23(5):524. PubMed ID: 15108292
[TBL] [Abstract][Full Text] [Related]
13. A novel mutation in the cathepsin C gene in a Pakistani family with Papillon-Lefevre syndrome.
Kurban M; Cheng T; Wajid M; Kiuru M; Shimomura Y; Christiano AM
J Eur Acad Dermatol Venereol; 2010 Aug; 24(8):967-9. PubMed ID: 20236208
[TBL] [Abstract][Full Text] [Related]
14. A novel mutation of the cathepsin C gene in a thai family with Papillon-Lefevre syndrome.
Nitta H; Wara-Aswapati N; Lertsirivorakul J; Nakamura T; Yamamoto M; Izumi Y; Nakamura T; Ishikawa I
J Periodontol; 2005 Mar; 76(3):492-6. PubMed ID: 15857086
[TBL] [Abstract][Full Text] [Related]
15. Novel mutations of cathepsin C gene in two Chinese patients with Papillon-Lefèvre syndrome.
Yang Y; Bai X; Liu H; Li L; Cao C; Ge L
J Dent Res; 2007 Aug; 86(8):735-8. PubMed ID: 17652201
[TBL] [Abstract][Full Text] [Related]
16. Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome.
Hart TC; Hart PS; Bowden DW; Michalec MD; Callison SA; Walker SJ; Zhang Y; Firatli E
J Med Genet; 1999 Dec; 36(12):881-7. PubMed ID: 10593994
[TBL] [Abstract][Full Text] [Related]
17. [Novel mutations of cathepsin C gene in two Chinese patients with Papillon-Lefèvre syndrome].
Yang Y; Bai XW; Liu HS; Cao CF; Ge LH
Zhonghua Kou Qiang Yi Xue Za Zhi; 2006 Oct; 41(10):602-5. PubMed ID: 17129448
[TBL] [Abstract][Full Text] [Related]
18. Biochemical and mutational analyses of the cathepsin c gene (CTSC) in three North American families with Papillon Lefèvre syndrome.
Zhang Y; Hart PS; Moretti AJ; Bouwsma OJ; Fisher EM; Dudlicek L; Pettenati MJ; Hart TC
Hum Mutat; 2002 Jul; 20(1):75. PubMed ID: 12112662
[TBL] [Abstract][Full Text] [Related]
19. Papillon-Lefèvre syndrome with homozygous nonsense mutation of cathepsin C gene presenting with late-onset periodontitis.
Ragunatha S; Ramesh M; Anupama P; Kapoor M; Bhat M
Pediatr Dermatol; 2015; 32(2):292-4. PubMed ID: 24894642
[TBL] [Abstract][Full Text] [Related]
20. A novel mutation of the cathepsin C gene in Papillon-Lefèvre syndrome.
Cury VF; Costa JE; Gomez RS; Boson WL; Loures CG; De ML
J Periodontol; 2002 Mar; 73(3):307-12. PubMed ID: 11922261
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
