242 related articles for article (PubMed ID: 34932608)
21. CTSC compound heterozygous mutations in two Chinese patients with Papillon-Lefèvre syndrome.
Wu Y; Zhao L; Xu C; Wu Y
Oral Dis; 2019 Jul; 25(5):1394-1402. PubMed ID: 30908832
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. Abnormal profiles of cathepsin C secreted in urine of Papillon Lefevre syndrome patients.
Sabry S; Abouzaid MR; Mostafa MI; Abdel-Hamid MS; Saad AK; Soliman HN; Ahmed NEB
Eur J Med Genet; 2022 Oct; 65(10):104605. PubMed ID: 36058494
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Novel mutations in the cathepsin C gene in patients with pre-pubertal aggressive periodontitis and Papillon-Lefèvre syndrome.
Noack B; Görgens H; Hoffmann T; Fanghänel J; Kocher T; Eickholz P; Schackert HK
J Dent Res; 2004 May; 83(5):368-70. PubMed ID: 15111626
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis.
Toomes C; James J; Wood AJ; Wu CL; McCormick D; Lench N; Hewitt C; Moynihan L; Roberts E; Woods CG; Markham A; Wong M; Widmer R; Ghaffar KA; Pemberton M; Hussein IR; Temtamy SA; Davies R; Read AP; Sloan P; Dixon MJ; Thakker NS
Nat Genet; 1999 Dec; 23(4):421-4. PubMed ID: 10581027
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. [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]
31. Evidence for a founder mutation in the cathepsin C gene in three families with Papillon-Lefèvre syndrome.
Kurban M; Wajid M; Shimomura Y; Bahhady R; Kibbi AG; Christiano AM
Dermatology; 2009; 219(4):289-94. PubMed ID: 19816003
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Identification of novel mutation in cathepsin C gene causing Papillon-Lefèvre Syndrome in Mexican patients.
Romero-Quintana JG; Frías-Castro LO; Arámbula-Meraz E; Aguilar-Medina M; Dueñas-Arias JE; Melchor-Soto JD; Romero-Navarro JG; Ramos-Payán R
BMC Med Genet; 2013 Jan; 14():7. PubMed ID: 23311634
[TBL] [Abstract][Full Text] [Related]
34. A novel mutation in the cathepsin C (CTSC) gene in Iranian family with Papillon-Lefevre syndrome.
Ghanei M; Abbaszadegan MR; Forghanifard MM; Aarabi A; Arab H
Clin Exp Dent Res; 2021 Aug; 7(4):568-573. PubMed ID: 33586345
[TBL] [Abstract][Full Text] [Related]
35. Mutation analysis of the cathepsin C gene in Indian families with Papillon-Lefèvre syndrome.
Selvaraju V; Markandaya M; Prasad PV; Sathyan P; Sethuraman G; Srivastava SC; Thakker N; Kumar A
BMC Med Genet; 2003 Jul; 4():5. PubMed ID: 12857359
[TBL] [Abstract][Full Text] [Related]
36. A homozygous cathepsin C mutation associated with Haim-Munk syndrome.
Cury VF; Gomez RS; Costa JE; Friedman E; Boson W; De Marco L
Br J Dermatol; 2005 Feb; 152(2):353-6. PubMed ID: 15727652
[TBL] [Abstract][Full Text] [Related]
37. Papillon-Lefèvre syndrome (PLS) with novel compound heterozygous mutation in the exclusion and Peptidase C1A domains of Cathepsin C gene.
Meenu S; Pradeep B; Ramalingam S; Sairam T; Rai R; Sankaran R
Mol Biol Rep; 2020 Jul; 47(7):5681-5687. PubMed ID: 32601924
[TBL] [Abstract][Full Text] [Related]
38. Identification of a novel cathepsin C mutation (p.W185X) in a Brazilian kindred with Papillon-Lefèvre syndrome.
Hart PS; Pallos D; Zhang Y; Sanchez J; Kavamura I; Brunoni D; Hart TC
Mol Genet Metab; 2002 Jun; 76(2):145-7. PubMed ID: 12083812
[TBL] [Abstract][Full Text] [Related]
39. [Screening of CTSC gene mutations in a Chinese pedigree affected with Papillon-Lefevre syndrome].
Liu C; Tian Z; Yang Q; Ma Q; Xu X; Xiong F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):150-4. PubMed ID: 27060303
[TBL] [Abstract][Full Text] [Related]
40. Detection of an intragenic deletion expands the spectrum of CTSC mutations in Papillon-Lefèvre syndrome.
Jouary T; Goizet C; Coupry I; Redonnet-Vernhet I; Levade T; Burgelin I; Toutain A; Delaporte E; Douillard C; Lacombe D; Taieb A; Arveiler B
J Invest Dermatol; 2008 Feb; 128(2):322-5. PubMed ID: 17943190
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]