BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 26458004)

  • 1. The role of cathepsin K in oral and maxillofacial disorders.
    Wen X; Yi LZ; Liu F; Wei JH; Xue Y
    Oral Dis; 2016 Mar; 22(2):109-15. PubMed ID: 26458004
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and animal research findings in pycnodysostosis and gene mutations of cathepsin K from 1996 to 2011.
    Xue Y; Cai T; Shi S; Wang W; Zhang Y; Mao T; Duan X
    Orphanet J Rare Dis; 2011 May; 6():20. PubMed ID: 21569238
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Not all pycnodysostosis-related mutants of human cathepsin K are inactive - crystal structure and biochemical studies of an active mutant I249T.
    Roy S; Das Chakraborty S; Biswas S
    FEBS J; 2018 Nov; 285(22):4265-4280. PubMed ID: 30199612
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel CTSK mutation resulting in an entire exon 2 skipping in a Thai girl with pycnodysostosis.
    Utokpat P; Panmontha W; Tongkobpetch S; Suphapeetiporn K; Shotelersuk V
    Pediatr Int; 2013 Oct; 55(5):651-5. PubMed ID: 24134756
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dental Abnormalities Caused by Novel Compound Heterozygous CTSK Mutations.
    Xue Y; Wang L; Xia D; Li Q; Gao S; Dong M; Cai T; Shi S; He L; Hu K; Mao T; Duan X
    J Dent Res; 2015 May; 94(5):674-81. PubMed ID: 25731711
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial pycnodysostosis: identification of a novel mutation in the CTSK gene (cathepsin K).
    Toral-López J; Gonzalez-Huerta LM; Sosa B; Orozco S; González HP; Cuevas-Covarrubias SA
    J Investig Med; 2011 Feb; 59(2):277-80. PubMed ID: 21099701
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Pycnodysostosis, a case report].
    Nassar K; Janani S; Rachidi W; Mkinsi O
    Presse Med; 2015 Nov; 44(11):1193-6. PubMed ID: 26456945
    [No Abstract]   [Full Text] [Related]  

  • 8. Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect.
    Otaify GA; Abdel-Hamid MS; Mehrez MI; Aboul-Ezz E; Zaki MS; Aglan MS; Temtamy SA
    Osteoporos Int; 2018 Aug; 29(8):1833-1841. PubMed ID: 29796728
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Mutation in CTSK Gene in an Autosomal Recessive Pycnodysostosis Family of Chinese Origin.
    Huang X; Qi X; Li M; Wang O; Jiang Y; Xing X; Hu YY; Xia W
    Calcif Tissue Int; 2015 May; 96(5):373-8. PubMed ID: 25725806
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ichthyosis vulgaris and pycnodysostosis: an unusual occurrence.
    Kshirsagar VY; Ahmed M; Nagarsenkar S; Sahoo K; Shah KB
    Acta Med Acad; 2012; 41(2):214-8. PubMed ID: 23331396
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The silencing of cathepsin K used in gene therapy for periodontal disease reveals the role of cathepsin K in chronic infection and inflammation.
    Chen W; Gao B; Hao L; Zhu G; Jules J; MacDougall MJ; Wang J; Han X; Zhou X; Li YP
    J Periodontal Res; 2016 Oct; 51(5):647-60. PubMed ID: 26754272
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Distribution of Cathepsin K in Late Stage of Tooth Germ Development and Its Function in Degrading Enamel Matrix Proteins in Mouse.
    Jiang T; Liu F; Wang WG; Jiang X; Wen X; Hu KJ; Xue Y
    PLoS One; 2017; 12(1):e0169857. PubMed ID: 28095448
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease.
    Sayed Amr K; El-Bassyouni HT; Abdel Hady S; Mostafa MI; Mehrez MI; Coviello D; El-Kamah GY
    Genes (Basel); 2021 Sep; 12(10):. PubMed ID: 34680947
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Increased Bone Resorption during Lactation in Pycnodysostosis.
    Jansen IDC; Papapoulos SE; Bravenboer N; de Vries TJ; Appelman-Dijkstra NM
    Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33670411
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Pycnodysostosis: a rare disease with frequent fractures].
    Sánchez Lázaro JA; Linares Álvarez L
    Semergen; 2014 Apr; 40(3):e47-50. PubMed ID: 23759316
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Heparan sulfate selectively inhibits the collagenase activity of cathepsin K.
    Zhang X; Luo Y; Hao H; Krahn JM; Su G; Dutcher R; Xu Y; Liu J; Pedersen LC; Xu D
    Matrix Biol; 2024 May; 129():15-28. PubMed ID: 38548090
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pycnodysostosis with novel gene mutation and sporadic medullary thyroid carcinoma: A case report.
    Shi X; Huang C; Xiao F; Liu W; Zeng J; Li X
    Medicine (Baltimore); 2017 Dec; 96(50):e8730. PubMed ID: 29390266
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel missense mutation in cathepsin K (CTSK) gene in a consanguineous Pakistani family with pycnodysostosis.
    Khan B; Ahmed Z; Ahmad W
    J Investig Med; 2010 Jun; 58(5):720-4. PubMed ID: 20305575
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and genetic characterization of three Russian patients with pycnodysostosis due to pathogenic variants in the CTSK gene.
    Markova TV; Kenis V; Melchenko E; Guseva D; Osipova D; Galeeva N; Nagornova T; Dadali EL
    Mol Genet Genomic Med; 2022 May; 10(5):e1904. PubMed ID: 35315254
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multiple Fractures and Impaired Bone Fracture Healing in a Patient with Pycnodysostosis and Hypophosphatasia.
    Hepp N; Frederiksen AL; Dunø M; Jørgensen NR; Langdahl B; Vedtofte P; Hove HB; Hindsø K; Jensen JB
    Calcif Tissue Int; 2019 Dec; 105(6):681-686. PubMed ID: 31489468
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.