157 related articles for article (PubMed ID: 31751289)
1. A New Terminal Nonsense Mutation of the Cathepsin C Gene in a Patient With Atypical Papillon-Lefèvre Syndrome.
Moura AL; Regateiro FS; Peres Resende E; Coimbra Silva H; Gonçalo M; Todo Bom A; Faria E
J Investig Allergol Clin Immunol; 2020 Apr; 30(2):151-153. PubMed ID: 31751289
[No Abstract] [Full Text] [Related]
2. The novel CTSC homozygous nonsense mutation p.Lys106X in a patient with Papillon-Lefèvre syndrome with all permanent teeth remaining at over 40 years of age.
Kobayashi T; Sugiura K; Takeichi T; Akiyama M
Br J Dermatol; 2013 Oct; 169(4):948-50. PubMed ID: 23662908
[No Abstract] [Full Text] [Related]
3. 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]
4. 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]
5. Gene symbol: CTSC. Disease: Papillon-Lefevre syndrome.
de Haar SF; Mir M; Nguyen M; Kazemi B; Ramezani GH; Everts V; Beertsen W
Hum Genet; 2005 May; 116(6):545. PubMed ID: 15991336
[No Abstract] [Full Text] [Related]
6. A novel large deletion combined with a nonsense mutation in a Chinese child with Papillon-Lefèvre syndrome.
Wu W; Chen B; Chen X; Chen L; Yi L; Wang Y; Yan F; Sun W
J Periodontal Res; 2016 Jun; 51(3):376-80. PubMed ID: 26385525
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. High immunoglobulin E in a Chinese Papillon-Lefèvre syndrome patient with novel compound mutations of cathepsin C.
Wen X; Wang X; Duan X
J Dermatol; 2012 Jul; 39(7):664-5. PubMed ID: 22221209
[No Abstract] [Full Text] [Related]
9. 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]
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. 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]
12. Functional Cathepsin C mutations cause different Papillon-Lefèvre syndrome phenotypes.
Noack B; Görgens H; Schacher B; Puklo M; Eickholz P; Hoffmann T; Schackert HK
J Clin Periodontol; 2008 Apr; 35(4):311-6. PubMed ID: 18294227
[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. Novel compound heterozygous mutations in CTSC gene cause Papillon-Lefèvre syndrome with high serum immunoglobulin E.
Li Z; Liu J; Fang S; Zhu H; Zhang X; Cai J; Li B; Xu Y
J Dermatol Sci; 2014 Dec; 76(3):258-60. PubMed ID: 25450092
[No Abstract] [Full Text] [Related]
15. Cathepsin C gene 5'-untranslated region mutation in papillon-lefèvre syndrome.
Kosem R; Debeljak M; Repič Lampret B; Kansky A; Battelino T; Trebušak Podkrajšek K
Dermatology; 2012; 225(3):193-203. PubMed ID: 23108224
[TBL] [Abstract][Full Text] [Related]
16. 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]
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. Novel CTSC mutations in a patient with Papillon-Lefèvre syndrome with recurrent pyoderma and minimal oral and palmoplantar involvement.
Castori M; Madonna S; Giannetti L; Floriddia G; Milioto M; Amato S; Castiglia D
Br J Dermatol; 2009 Apr; 160(4):881-3. PubMed ID: 18945301
[No Abstract] [Full Text] [Related]
19. Description of two new cathepsin C gene mutations in patients with Papillon-Lefèvre syndrome.
Wani AA; Devkar N; Patole MS; Shouche YS
J Periodontol; 2006 Feb; 77(2):233-7. PubMed ID: 16460249
[TBL] [Abstract][Full Text] [Related]
20. Haim Munk syndrome and Papillon Lefevre syndrome--allelic mutations in cathepsin C with variation in phenotype.
Rai R; Thiagarajan S; Mohandas S; Natarajan K; Shanmuga Sekar C; Ramalingam S
Int J Dermatol; 2010 May; 49(5):541-3. PubMed ID: 20534088
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
