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 *

143 related articles for article (PubMed ID: 27730712)

  • 1. Stimulus-dependent NETosis by neutrophils from a Papillon-Lefèvre Syndrome patient.
    Batinica M; Stephan A; Steiger J; Tantcheva-Poόr I; Eming SA; Fabri M
    J Eur Acad Dermatol Venereol; 2017 May; 31(5):e239-e241. PubMed ID: 27730712
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Papillon-Lefèvre syndrome and malignant melanoma.
    Cook GP
    Dermatology; 2009; 219(2):187-8. PubMed ID: 19506350
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. [Recurrent European missense mutation in a Hungarian pedigree with Papillon-Lefèvre syndrome].
    Vályi P; Farkas K; Tripolszki K; Sulák A; Széll M; Nagy N; Nagy K
    Fogorv Sz; 2014 Sep; 107(3):87-92. PubMed ID: 25509509
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Papillon-Lefevre syndrome: clinical presentation and a brief review.
    Dhanrajani PJ
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Jul; 108(1):e1-7. PubMed ID: 19540439
    [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. 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]  

  • 11. 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]  

  • 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. 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]  

  • 14. Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patients.
    Zhang Y; Lundgren T; Renvert S; Tatakis DN; Firatli E; Uygur C; Hart PS; Gorry MC; Marks JJ; Hart TC
    J Med Genet; 2001 Feb; 38(2):96-101. PubMed ID: 11158173
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Demonstration of altered splicing with the IVS3-1G --> a mutation of cathepsin C.
    Nusier M; Zhang Y; Yassin O; Hart TC; Hart PS
    Mol Genet Metab; 2002 Mar; 75(3):280-3. PubMed ID: 11914041
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [Papillon-Lefèvre syndrome: A new case].
    Martinho S; Levade T; Fergelot P; Stephan JL
    Arch Pediatr; 2017 Apr; 24(4):360-362. PubMed ID: 28242153
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.