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 *

142 related articles for article (PubMed ID: 8098071)

  • 1. Impaired hexose uptake by diploid skin fibroblasts from galactosaemic patients. Connection with cell growth and amino acid metabolism, and possible bearing on late-onset clinical symptoms.
    Wolfrom C; Raynaud N; Kadhom N; Poggi J; Soni T; Gautier M
    J Inherit Metab Dis; 1993; 16(1):78-90. PubMed ID: 8098071
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Glutamine dependency of human skin fibroblasts: modulation by hexoses.
    Wolfrom C; Kadhom N; Polini G; Poggi J; Moatti N; Gautier M
    Exp Cell Res; 1989 Aug; 183(2):303-18. PubMed ID: 2767153
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Galactose and glucose metabolism in galactokinase deficient, galactose-1-P-uridyl transferase deficient and normal human fibroblasts.
    Friedman TB; Yarkin RJ; Merril CR
    J Cell Physiol; 1975 Jun; 85(3):569-78. PubMed ID: 167035
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Culture of galactosaemic fibroblasts in the presence of galactose: effect of inosine.
    Pourci ML; Mangeot M; Soni T; Lemonnier A
    J Inherit Metab Dis; 1990; 13(6):819-28. PubMed ID: 2079832
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Deficit of uridine diphosphate galactose in galactosaemia.
    Ng WG; Xu YK; Kaufman FR; Donnell GN
    J Inherit Metab Dis; 1989; 12(3):257-66. PubMed ID: 2515367
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Respective effects of glucose and glutamine on the glutamine synthetase activity of human skin fibroblasts.
    Soni T; Wolfrom C; Guerroui S; Raynaud N; Poggi J; Moatti N; Gautier M
    Mol Cell Biochem; 1991 Apr; 102(2):149-54. PubMed ID: 1679192
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diagnosis of inherited disorders of galactose metabolism.
    Cuthbert C; Klapper H; Elsas L
    Curr Protoc Hum Genet; 2008 Jan; Chapter 17():Unit 17.5. PubMed ID: 18428423
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Metabolic cooperation in cocultures of fibroblasts from patients with various abnormalities of galactose metabolism].
    Kadhom N; Brivet M; Baptista J; Gautier M; Lemonnier A
    C R Acad Sci III; 1989; 308(17):453-8. PubMed ID: 2543487
    [TBL] [Abstract][Full Text] [Related]  

  • 9. UDP-glucose and UDP-galactose concentrations in cultured skin fibroblasts of patients with classical galactosaemia.
    Keevill NJ; Holton JB; Allen JT
    J Inherit Metab Dis; 1994; 17(1):23-6. PubMed ID: 8051935
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Galactose metabolism in transferase-deficient galactosaemic and normal long-term lymphoid cell lines.
    Beratis NG; Wilbur L
    J Inherit Metab Dis; 1987; 10(4):347-58. PubMed ID: 2831430
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Galactosemia: alterations in sulfate metabolism secondary to galactose-1-phosphate uridyltransferase deficiency.
    Tedesco TA; Miller KL
    Science; 1979 Sep; 205(4413):1395-7. PubMed ID: 472754
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Uridine diphosphate hexoses in leukocytes and fibroblasts of classic galactosemics and patients with other metabolic diseases.
    Gibson JB; Reynolds RA; Palmieri MJ; States B; Berry GT; Segal S
    Pediatr Res; 1994 Nov; 36(5):613-8. PubMed ID: 7877880
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ultrastructural features of human galactosaemic fibroblasts: effects of different nutritional environments.
    Johnson JB; Noguchi PD; Petricciani JC
    Cytobios; 1976; 17(67-68):159-70. PubMed ID: 201432
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Low efficiency of [14C]galactose incorporation by galactosemic skin fibroblasts: relationship with neurological sequelae.
    Kadhom N; Baptista J; Brivet M; Wolfrom C; Gautier M
    Biochem Med Metab Biol; 1994 Aug; 52(2):140-4. PubMed ID: 7993662
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Endogenous galactose formation in galactose-1-phosphate uridyltransferase deficiency.
    Schadewaldt P; Kamalanathan L; Hammen HW; Kotzka J; Wendel U
    Arch Physiol Biochem; 2014 Dec; 120(5):228-39. PubMed ID: 25268296
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Use of a genetic variant to study the hexose transport properties of human skin fibroblasts.
    Mesmer OT; Gordon BA; Rupar CA; Lo TC
    Biochem J; 1990 Feb; 265(3):823-9. PubMed ID: 2306216
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in the galactose-1-phosphate uridyltransferase gene of two families with mild galactosaemia variants.
    Sommer M; Gathof BS; Podskarbi T; Giugliani R; Kleinlein B; Shin YS
    J Inherit Metab Dis; 1995; 18(5):567-76. PubMed ID: 8598637
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Defective galactosylation of proteins in cultured skin fibroblasts from galactosaemic patients.
    Dobbie JA; Holton JB; Clamp JR
    Ann Clin Biochem; 1990 May; 27 ( Pt 3)():274-5. PubMed ID: 2382964
    [No Abstract]   [Full Text] [Related]  

  • 19. [Galactose-1-phosphate uridyltransferase deficiency].
    Okano Y; Isshiki G
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):15-21. PubMed ID: 9589977
    [No Abstract]   [Full Text] [Related]  

  • 20. Clinical features of galactokinase deficiency: a review of the literature.
    Bosch AM; Bakker HD; van Gennip AH; van Kempen JV; Wanders RJ; Wijburg FA
    J Inherit Metab Dis; 2002 Dec; 25(8):629-34. PubMed ID: 12705493
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.