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 *

117 related articles for article (PubMed ID: 8446427)

  • 21. Molecular abnormalities of collagen.
    Pope FM; Nicholls AC
    J Clin Pathol Suppl (R Coll Pathol); 1978; 12():95-104. PubMed ID: 103936
    [No Abstract]   [Full Text] [Related]  

  • 22. Further defining the phenotypic spectrum of B4GALT7 mutations.
    Salter CG; Davies JH; Moon RJ; Fairhurst J; Bunyan D; ; Foulds N
    Am J Med Genet A; 2016 Jun; 170(6):1556-63. PubMed ID: 26940150
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Biochemical and thermodynamic characterization of mutated β1,4-galactosyltransferase 7 involved in the progeroid form of the Ehlers-Danlos syndrome.
    Rahuel-Clermont S; Daligault F; Piet MH; Gulberti S; Netter P; Branlant G; Magdalou J; Lattard V
    Biochem J; 2010 Dec; 432(2):303-11. PubMed ID: 20809901
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Galactosyltransferase I is a gene responsible for progeroid variant of Ehlers-Danlos syndrome: molecular cloning and identification of mutations.
    Furukawa K; Okajima T
    Biochim Biophys Acta; 2002 Dec; 1573(3):377-81. PubMed ID: 12417421
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Hypomorphic zebrafish models mimic the musculoskeletal phenotype of β4GalT7-deficient Ehlers-Danlos syndrome.
    Delbaere S; Van Damme T; Syx D; Symoens S; Coucke P; Willaert A; Malfait F
    Matrix Biol; 2020 Jul; 89():59-75. PubMed ID: 31862401
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [The Ehlers-Danlos syndrome].
    Blom WA
    Ned Tijdschr Geneeskd; 1983 Jun; 127(24):1054-8. PubMed ID: 6877411
    [No Abstract]   [Full Text] [Related]  

  • 29. The Specific Role of Dermatan Sulfate as an Instructive Glycosaminoglycan in Tissue Development.
    Mizumoto S; Yamada S
    Int J Mol Sci; 2022 Jul; 23(13):. PubMed ID: 35806490
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. The molecular basis of classic Ehlers-Danlos syndrome: a comprehensive study of biochemical and molecular findings in 48 unrelated patients.
    Malfait F; Coucke P; Symoens S; Loeys B; Nuytinck L; De Paepe A
    Hum Mutat; 2005 Jan; 25(1):28-37. PubMed ID: 15580559
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Systematic investigation of the skin in Chst14-/- mice: A model for skin fragility in musculocontractural Ehlers-Danlos syndrome caused by CHST14 variants (mcEDS-CHST14).
    Hirose T; Mizumoto S; Hashimoto A; Takahashi Y; Yoshizawa T; Nitahara-Kasahara Y; Takahashi N; Nakayama J; Takehana K; Okada T; Nomura Y; Yamada S; Kosho T; Watanabe T
    Glycobiology; 2021 Feb; 31(2):137-150. PubMed ID: 32601684
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Ehlers-Danlos features with progeroid facies and mild mental retardation. Further delineation of the syndrome.
    Hernández A; Aguirre-Negrete MG; González-Flores S; Reynoso-Luna MC; Fragoso R; Nazará Z; Tapia-Arizmendi G; Cantú JM
    Clin Genet; 1986 Dec; 30(6):456-61. PubMed ID: 3815877
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Ehlers-Danlos syndrome type I. Ultrastructural study].
    Paradisi M; Giubilei L; Canzona F; Angelo C; Onetti Muda A; Puddu P
    Minerva Pediatr; 1997 May; 49(5):215-9. PubMed ID: 9340484
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition.
    Mao JR; Taylor G; Dean WB; Wagner DR; Afzal V; Lotz JC; Rubin EM; Bristow J
    Nat Genet; 2002 Apr; 30(4):421-5. PubMed ID: 11925569
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Thrombin regulates vascular smooth muscle cell proteoglycan synthesis via PAR-1 and multiple downstream signalling pathways.
    Ivey ME; Little PJ
    Thromb Res; 2008; 123(2):288-97. PubMed ID: 18571697
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Decorin inhibits cell migration through a process requiring its glycosaminoglycan side chain.
    Merle B; Durussel L; Delmas PD; Clézardin P
    J Cell Biochem; 1999 Dec; 75(3):538-46. PubMed ID: 10536375
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Critical roles of glycosaminoglycan side chains of cartilage proteoglycan (aggrecan) in antigen recognition and presentation.
    Glant TT; Buzás EI; Finnegan A; Negroiu G; Cs-Szabó G; Mikecz K
    J Immunol; 1998 Apr; 160(8):3812-9. PubMed ID: 9558085
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Vascular Ehlers-Danlos syndromes--biochemical and molecular-genetic investigations].
    Lund AM
    Ugeskr Laeger; 2006 Feb; 168(9):915-20. PubMed ID: 16513057
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Three arginine to cysteine substitutions in the pro-alpha (I)-collagen chain cause Ehlers-Danlos syndrome with a propensity to arterial rupture in early adulthood.
    Malfait F; Symoens S; De Backer J; Hermanns-Lê T; Sakalihasan N; Lapière CM; Coucke P; De Paepe A
    Hum Mutat; 2007 Apr; 28(4):387-95. PubMed ID: 17211858
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.