BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

693 related articles for article (PubMed ID: 29409891)

  • 1. Hereditary galactosemia.
    Demirbas D; Coelho AI; Rubio-Gozalbo ME; Berry GT
    Metabolism; 2018 Jun; 83():188-196. PubMed ID: 29409891
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The molecular basis of galactosemia - Past, present and future.
    Timson DJ
    Gene; 2016 Sep; 589(2):133-41. PubMed ID: 26143117
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare cases of galactose metabolic disorders: identification of more than two mutations per patient.
    Schulpis KH; Thodi G; Chatzidaki M; Iakovou K; Molou E; Dotsikas Y; Loukas YL
    J Pediatr Endocrinol Metab; 2017 Oct; 30(10):1119-1120. PubMed ID: 28902631
    [No Abstract]   [Full Text] [Related]  

  • 4. Pathophysiology and targets for treatment in hereditary galactosemia: A systematic review of animal and cellular models.
    Haskovic M; Coelho AI; Bierau J; Vanoevelen JM; Steinbusch LKM; Zimmermann LJI; Villamor-Martinez E; Berry GT; Rubio-Gozalbo ME
    J Inherit Metab Dis; 2020 May; 43(3):392-408. PubMed ID: 31808946
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Galactosemia: when is it a newborn screening emergency?
    Berry GT
    Mol Genet Metab; 2012 May; 106(1):7-11. PubMed ID: 22483615
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular basis of disorders of human galactose metabolism: past, present, and future.
    Novelli G; Reichardt JK
    Mol Genet Metab; 2000; 71(1-2):62-5. PubMed ID: 11001796
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The fundamental importance of human galactose metabolism: lessons from genetics and biochemistry.
    Petry KG; Reichardt JK
    Trends Genet; 1998 Mar; 14(3):98-102. PubMed ID: 9540406
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Epimerase-deficiency galactosemia is not a binary condition.
    Openo KK; Schulz JM; Vargas CA; Orton CS; Epstein MP; Schnur RE; Scaglia F; Berry GT; Gottesman GS; Ficicioglu C; Slonim AE; Schroer RJ; Yu C; Rangel VE; Keenan J; Lamance K; Fridovich-Keil JL
    Am J Hum Genet; 2006 Jan; 78(1):89-102. PubMed ID: 16385452
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Galactose and cataract.
    Stambolian D
    Surv Ophthalmol; 1988; 32(5):333-49. PubMed ID: 3043741
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Distinct roles of galactose-1P in galactose-mediated growth arrest of yeast deficient in galactose-1P uridylyltransferase (GALT) and UDP-galactose 4'-epimerase (GALE).
    Mumma JO; Chhay JS; Ross KL; Eaton JS; Newell-Litwa KA; Fridovich-Keil JL
    Mol Genet Metab; 2008 Feb; 93(2):160-71. PubMed ID: 17981065
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Galactosemia: Biochemistry, Molecular Genetics, Newborn Screening, and Treatment.
    Succoio M; Sacchettini R; Rossi A; Parenti G; Ruoppolo M
    Biomolecules; 2022 Jul; 12(7):. PubMed ID: 35883524
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Drosophila melanogaster Models of Galactosemia.
    Daenzer JM; Fridovich-Keil JL
    Curr Top Dev Biol; 2017; 121():377-395. PubMed ID: 28057307
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Galactosemia].
    Owada M
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):647-51. PubMed ID: 3270877
    [No Abstract]   [Full Text] [Related]  

  • 15. Coordinated movement, neuromuscular synaptogenesis and trans-synaptic signaling defects in Drosophila galactosemia models.
    Jumbo-Lucioni PP; Parkinson WM; Kopke DL; Broadie K
    Hum Mol Genet; 2016 Sep; 25(17):3699-3714. PubMed ID: 27466186
    [TBL] [Abstract][Full Text] [Related]  

  • 16. GALT Deficiency Galactosemia.
    Anderson S
    MCN Am J Matern Child Nurs; 2018; 43(1):44-51. PubMed ID: 29215423
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Galactosemia].
    Ohtake A; Amemiya S
    Nihon Rinsho; 2006 Sep; Suppl 3():215-9. PubMed ID: 17022534
    [No Abstract]   [Full Text] [Related]  

  • 18. The ability of an LC-MS/MS-based erythrocyte GALT enzyme assay to predict the phenotype in subjects with GALT deficiency.
    Demirbas D; Huang X; Daesety V; Feenstra S; Haskovic M; Qi W; Gubbels CS; Hecht L; Levy HL; Waisbren SE; Berry GT
    Mol Genet Metab; 2019 Apr; 126(4):368-376. PubMed ID: 30718057
    [TBL] [Abstract][Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 35.