These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 22221209)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. [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]  

  • 6. 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]  

  • 7. 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]  

  • 8. [Mutational analysis of the cathepsin C gene in a family of Han nationality with Papillon-Lefevre syndrome].
    Li X; Zhang X; Zhang J; Chen Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):502-5. PubMed ID: 18841559
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 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. Genetic analysis of Papillon-Lefèvre syndrome.
    Thakker N
    Oral Dis; 2000 Sep; 6(5):263. PubMed ID: 11002405
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. Cathepsin C gene: First compound heterozygous patient with Papillon-Lefèvre syndrome and a novel symptomless mutation.
    Allende LM; García-Pérez MA; Moreno A; Corell A; Carasol M; Martínez-Canut P; Arnaiz-Villena A
    Hum Mutat; 2001 Feb; 17(2):152-3. PubMed ID: 11180601
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 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 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]  

  • 18. 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]  

  • 19. Papillon-Lefèvre syndrome: mutations and polymorphisms in the cathepsin C gene.
    Nakano A; Nomura K; Nakano H; Ono Y; LaForgia S; Pulkkinen L; Hashimoto I; Uitto J
    J Invest Dermatol; 2001 Feb; 116(2):339-43. PubMed ID: 11180012
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of cathepsin C mutations in ethnically diverse papillon-Lefèvre syndrome patients.
    Hart PS; Zhang Y; Firatli E; Uygur C; Lotfazar M; Michalec MD; Marks JJ; Lu X; Coates BJ; Seow WK; Marshall R; Williams D; Reed JB; Wright JT; Hart TC
    J Med Genet; 2000 Dec; 37(12):927-32. PubMed ID: 11106356
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.