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 *

92 related articles for article (PubMed ID: 10357109)

  • 1. Gene defect of dermatan sulfate proteoglycan of cattle affected with a variant form of Ehlers-Danlos syndrome.
    Tajima M; Miyake S; Takehana K; Kobayashi A; Yamato O; Maede Y
    J Vet Intern Med; 1999; 13(3):202-5. PubMed ID: 10357109
    [TBL] [Abstract][Full Text] [Related]  

  • 2. cDNA clone to chick corneal chondroitin/dermatan sulfate proteoglycan reveals identity to decorin.
    Li W; Vergnes JP; Cornuet PK; Hassell JR
    Arch Biochem Biophys; 1992 Jul; 296(1):190-7. PubMed ID: 1605630
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic heterogeneity and clinical variability in musculocontractural Ehlers-Danlos syndrome caused by impaired dermatan sulfate biosynthesis.
    Syx D; Van Damme T; Symoens S; Maiburg MC; van de Laar I; Morton J; Suri M; Del Campo M; Hausser I; Hermanns-Lê T; De Paepe A; Malfait F
    Hum Mutat; 2015 May; 36(5):535-47. PubMed ID: 25703627
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Occurrence of PG-Lb, a leucine-rich small chondroitin/dermatan sulphate proteoglycan in mammalian epiphyseal cartilage: molecular cloning and sequence analysis of the mouse cDNA.
    Kurita K; Shinomura T; Ujita M; Zako M; Kida D; Iwata H; Kimata K
    Biochem J; 1996 Sep; 318 ( Pt 3)(Pt 3):909-14. PubMed ID: 8836137
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Deficiency of the core proteins of dermatan sulphate proteoglycans in a variant form of Ehlers-Danlos syndrome.
    Fushimi H; Kameyama M; Shinkai H
    J Intern Med; 1989 Dec; 226(6):409-16. PubMed ID: 2562251
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A genetic defect in the biosynthesis of dermatan sulfate proteoglycan: galactosyltransferase I deficiency in fibroblasts from a patient with a progeroid syndrome.
    Quentin E; Gladen A; Rodén L; Kresse H
    Proc Natl Acad Sci U S A; 1990 Feb; 87(4):1342-6. PubMed ID: 2106134
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Defect in dermatan sulfate in urine of patients with Ehlers-Danlos syndrome caused by a CHST14/D4ST1 deficiency.
    Mizumoto S; Kosho T; Hatamochi A; Honda T; Yamaguchi T; Okamoto N; Miyake N; Yamada S; Sugahara K
    Clin Biochem; 2017 Aug; 50(12):670-677. PubMed ID: 28238810
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Histories of Dermatan Sulfate Epimerase and Dermatan 4-
    Mizumoto S; Yamada S
    Genes (Basel); 2023 Feb; 14(2):. PubMed ID: 36833436
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Recent Advances in the Pathophysiology of Musculocontractural Ehlers-Danlos Syndrome.
    Kosho T; Mizumoto S; Watanabe T; Yoshizawa T; Miyake N; Yamada S
    Genes (Basel); 2019 Dec; 11(1):. PubMed ID: 31905796
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deficiency of the decorin core protein in the variant form of Ehlers-Danlos syndrome with chronic skin ulcer.
    Wu J; Utani A; Endo H; Shinkai H
    J Dermatol Sci; 2001 Oct; 27(2):95-103. PubMed ID: 11532373
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Characterization and interactions of a fragment of the core protein of the small proteoglycan (PGII) from bovine tendon.
    Vogel KG; Koob TJ; Fisher LW
    Biochem Biophys Res Commun; 1987 Oct; 148(2):658-63. PubMed ID: 3479983
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Single-strand conformation polymorphism (SSCP) analysis of the COL3A1 gene detects a mutation that results in the substitution of glycine 1009 to valine and causes severe Ehlers-Danlos syndrome type IV.
    Nuytinck L; De Paepe A; Renard JP; Adriaens F; Leroy J
    Hum Mutat; 1994; 3(3):268-74. PubMed ID: 8019562
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Musculocontractural Ehlers-Danlos syndrome and neurocristopathies: dermatan sulfate is required for Xenopus neural crest cells to migrate and adhere to fibronectin.
    Gouignard N; Maccarana M; Strate I; von Stedingk K; Malmström A; Pera EM
    Dis Model Mech; 2016 Jun; 9(6):607-20. PubMed ID: 27101845
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Defective glycosylation of decorin and biglycan, altered collagen structure, and abnormal phenotype of the skin fibroblasts of an Ehlers-Danlos syndrome patient carrying the novel Arg270Cys substitution in galactosyltransferase I (beta4GalT-7).
    Seidler DG; Faiyaz-Ul-Haque M; Hansen U; Yip GW; Zaidi SH; Teebi AS; Kiesel L; Götte M
    J Mol Med (Berl); 2006 Jul; 84(7):583-94. PubMed ID: 16583246
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Isolation and characterization of dermatan sulphate proteoglycans from bovine sclera.
    Cöster L; Fransson LA
    Biochem J; 1981 Jan; 193(1):143-53. PubMed ID: 7305918
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and pathophysiological delineation of musculocontractural Ehlers-Danlos syndrome caused by dermatan sulfate epimerase deficiency (mcEDS-DSE): A detailed and comprehensive glycobiological and pathological investigation in a novel patient.
    Minatogawa M; Hirose T; Mizumoto S; Yamaguchi T; Nagae C; Taki M; Yamada S; Watanabe T; Kosho T
    Hum Mutat; 2022 Dec; 43(12):1829-1836. PubMed ID: 35842784
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic defects in proteoglycan biosynthesis.
    Quentin-Hoffmann E; Harrach B; Robenek H; Kresse H
    Padiatr Padol; 1993; 28(1):37-41. PubMed ID: 8446427
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IV.
    Richards AJ; Lloyd JC; Ward PN; De Paepe A; Narcisi P; Pope FM
    J Med Genet; 1991 Jul; 28(7):458-63. PubMed ID: 1895316
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Macrophage secretory products selectively stimulate dermatan sulfate proteoglycan production in cultured arterial smooth muscle cells.
    Edwards IJ; Wagner WD; Owens RT
    Am J Pathol; 1990 Mar; 136(3):609-21. PubMed ID: 2316626
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CHST14/D4ST1 deficiency: New form of Ehlers-Danlos syndrome.
    Kosho T
    Pediatr Int; 2016 Feb; 58(2):88-99. PubMed ID: 26646600
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.