212 related articles for article (PubMed ID: 29410039)
1. Autophagic dysfunction in patients with Papillon-Lefèvre syndrome is restored by recombinant cathepsin C treatment.
Bullón P; Castejón-Vega B; Román-Malo L; Jimenez-Guerrero MP; Cotán D; Forbes-Hernandez TY; Varela-López A; Pérez-Pulido AJ; Giampieri F; Quiles JL; Battino M; Sánchez-Alcázar JA; Cordero MD
J Allergy Clin Immunol; 2018 Oct; 142(4):1131-1143.e7. PubMed ID: 29410039
[TBL] [Abstract][Full Text] [Related]
2. Analysis of urinary cathepsin C for diagnosing Papillon-Lefèvre syndrome.
Hamon Y; Legowska M; Fergelot P; Dallet-Choisy S; Newell L; Vanderlynden L; Kord Valeshabad A; Acrich K; Kord H; Charalampos T; Morice-Picard F; Surplice I; Zoidakis J; David K; Vlahou A; Ragunatha S; Nagy N; Farkas K; Széll M; Goizet C; Schacher B; Battino M; Al Farraj Aldosari A; Wang X; Liu Y; Marchand-Adam S; Lesner A; Kara E; Korkmaz-Icöz S; Moss C; Eickholz P; Taieb A; Kavukcu S; Jenne DE; Gauthier F; Korkmaz B
FEBS J; 2016 Feb; 283(3):498-509. PubMed ID: 26607765
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Cathepsin C role in inflammatory gastroenterological, renal, rheumatic, and pulmonary disorders.
Aghdassi AA; Pham C; Zierke L; Mariaule V; Korkmaz B; Rhimi M
Biochimie; 2024 Jan; 216():175-180. PubMed ID: 37758158
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C.
Hart TC; Hart PS; Michalec MD; Zhang Y; Firatli E; Van Dyke TE; Stabholz A; Zlotogorski A; Shapira L; Soskolne WA
J Med Genet; 2000 Feb; 37(2):88-94. PubMed ID: 10662807
[TBL] [Abstract][Full Text] [Related]
7. Clinical and molecular analysis in Papillon-Lefèvre syndrome.
Machado RA; Cuadra-Zelaya FJM; Martelli-Júnior H; Miranda RT; Casarin RCV; Corrêa MG; Nociti F; Coletta RD
Am J Med Genet A; 2019 Oct; 179(10):2124-2131. PubMed ID: 31282082
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Novel point mutations, deletions, and polymorphisms in the cathepsin C gene in nine families from Europe and North Africa with Papillon-Lefèvre syndrome.
Lefèvre C; Blanchet-Bardon C; Jobard F; Bouadjar B; Stalder JF; Cure S; Hoffmann A; Prud'Homme JF; Fischer J
J Invest Dermatol; 2001 Dec; 117(6):1657-61. PubMed ID: 11886537
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Long-term change of disease behavior in Papillon-Lefèvre syndrome: seven years follow-up.
Wang X; Liu Y; Liu Y; Dong G; Kenney EB; Liu Q; Ma Z; Wang Q
Eur J Med Genet; 2015 Mar; 58(3):184-7. PubMed ID: 25497043
[TBL] [Abstract][Full Text] [Related]
12. 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]
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 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]
15. 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]
16. Eponym: Papillon-Lefevre syndrome.
Dalgıc B; Bukulmez A; Sarı S
Eur J Pediatr; 2011 Jun; 170(6):689-91. PubMed ID: 21165749
[TBL] [Abstract][Full Text] [Related]
17. Potential Role of the Mitochondria for the Dermatological Treatment of Papillon-Lefèvre.
Castejón-Vega B; Battino M; Quiles JL; Bullon B; Cordero MD; Bullón P
Antioxidants (Basel); 2021 Jan; 10(1):. PubMed ID: 33445524
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Novel cathepsin C mutation in a Brazilian family with Papillon-Lefèvre syndrome: case report and mutation update.
Pallos D; Acevedo AC; Mestrinho HD; Cordeiro I; Hart TC
J Dent Child (Chic); 2010; 77(1):36-41. PubMed ID: 20359428
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]