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 *

258 related articles for article (PubMed ID: 32474749)

  • 21. Erythroid glucose transporters.
    Montel-Hagen A; Sitbon M; Taylor N
    Curr Opin Hematol; 2009 May; 16(3):165-72. PubMed ID: 19346941
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The Glut1 and Glut4 glucose transporters are differentially expressed during perinatal and postnatal erythropoiesis.
    Montel-Hagen A; Blanc L; Boyer-Clavel M; Jacquet C; Vidal M; Sitbon M; Taylor N
    Blood; 2008 Dec; 112(12):4729-38. PubMed ID: 18796630
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Glucose transporter-1 deficiency syndrome can cause various clinical symptoms].
    Larsen J; Stubbings V; Møller RS; Hjalgrim H
    Ugeskr Laeger; 2013 Dec; 175(50A):V04130248. PubMed ID: 25353328
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Novel mutation in a patient with late onset GLUT1 deficiency syndrome.
    Juozapaite S; Praninskiene R; Burnyte B; Ambrozaityte L; Skerliene B
    Brain Dev; 2017 Apr; 39(4):352-355. PubMed ID: 27927575
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Facilitated glucose transporter protein type 1 (GLUT1) deficiency syndrome: impaired glucose transport into brain-- a review.
    Klepper J; Voit T
    Eur J Pediatr; 2002 Jun; 161(6):295-304. PubMed ID: 12029447
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Functional studies of the T295M mutation causing Glut1 deficiency: glucose efflux preferentially affected by T295M.
    Wang D; Yang H; Shi L; Ma L; Fujii T; Engelstad K; Pascual JM; De Vivo DC
    Pediatr Res; 2008 Nov; 64(5):538-43. PubMed ID: 18614966
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Glucose transporter isoforms GLUT1 and GLUT3 transport dehydroascorbic acid.
    Rumsey SC; Kwon O; Xu GW; Burant CF; Simpson I; Levine M
    J Biol Chem; 1997 Jul; 272(30):18982-9. PubMed ID: 9228080
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Implications of aberrant temperature-sensitive glucose transport via the glucose transporter deficiency mutant (GLUT1DS) T295M for the alternate-access and fixed-site transport models.
    Cunningham P; Naftalin RJ
    J Membr Biol; 2013 Jun; 246(6):495-511. PubMed ID: 23740044
    [TBL] [Abstract][Full Text] [Related]  

  • 29. GLUT-1 deficiency without epilepsy--an exceptional case.
    Overweg-Plandsoen WC; Groener JE; Wang D; Onkenhout W; Brouwer OF; Bakker HD; De Vivo DC
    J Inherit Metab Dis; 2003; 26(6):559-63. PubMed ID: 14605501
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Towards a more palatable treatment for Glut1 deficiency syndrome.
    Brockmann K
    Dev Med Child Neurol; 2011 Jul; 53(7):580-1. PubMed ID: 21585366
    [No Abstract]   [Full Text] [Related]  

  • 31. A Different SLC2A1 Gene Mutation in Glut 1 Deficiency Syndrome: c.734A>C.
    Çolak R; Alkan Özdemir S; Yangın Ergon E; Kağnıcı M; Çalkavur Ş
    Balkan Med J; 2017 Dec; 34(6):580-583. PubMed ID: 28443597
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Red blood cells as glucose carriers to the human brain: Modulation of cerebral activity by erythrocyte exchange transfusion in Glut1 deficiency (G1D).
    Wang RC; Lee EE; De Simone N; Kathote G; Primeaux S; Avila A; Yu DM; Johnson M; Good LB; Jakkamsetti V; Sarode R; Holland AA; Pascual JM
    J Cereb Blood Flow Metab; 2023 Mar; 43(3):357-368. PubMed ID: 36523131
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The clinical and biochemical hallmarks generally associated with GLUT1DS may be caused by defects in genes other than SLC2A1.
    Sánchez-Lijarcio O; Yubero D; Leal F; Couce ML; González Gutiérrez-Solana L; López-Laso E; García-Cazorla À; Pías-Peleteiro L; de Azua Brea B; Ibáñez-Micó S; Mateo-Martínez G; Troncoso-Schifferli M; Witting-Enriquez S; Ugarte M; Artuch R; Pérez B
    Clin Genet; 2022 Jul; 102(1):40-55. PubMed ID: 35388452
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Glucose transporter 1 deficiency syndrome and hemiplegic migraines as a dominant presenting clinical feature.
    Mohammad SS; Coman D; Calvert S
    J Paediatr Child Health; 2014 Dec; 50(12):1025-6. PubMed ID: 25440161
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [GLUT-1 deficiency syndrome].
    Zavala M; Castillo V; Gonzalez M; Castillo S
    Rev Neurol; 2019 Aug; 69(4):178-179. PubMed ID: 31334562
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Another Case of Glucose Transporter 1 Deficiency Syndrome with Periventricular Calcification, Cataracts, Hemolysis, and Pseudohyperkalemia.
    Shibata T; Kobayashi K; Yoshinaga H; Ono H; Shinpo M; Kagitani-Shimono K
    Neuropediatrics; 2017 Oct; 48(5):390-393. PubMed ID: 28582795
    [No Abstract]   [Full Text] [Related]  

  • 37. Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome.
    Ivanova N; Peycheva V; Kamenarova K; Kancheva D; Tsekova I; Aleksandrova I; Hristova D; Litvinenko I; Todorova D; Sarailieva G; Dimova P; Tomov V; Bozhinova V; Mitev V; Kaneva R; Jordanova A
    Seizure; 2018 Jan; 54():41-44. PubMed ID: 29223885
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutational and functional analysis of Glucose transporter I deficiency syndrome.
    Nakamura S; Osaka H; Muramatsu S; Aoki S; Jimbo EF; Yamagata T
    Mol Genet Metab; 2015 Nov; 116(3):157-62. PubMed ID: 26304067
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Disease-associated Glut1 single amino acid substitute mutations S66F, R126C, and T295M constitute Glut1-deficiency states in vitro.
    Wong HY; Law PY; Ho YY
    Mol Genet Metab; 2007 Feb; 90(2):193-8. PubMed ID: 17052934
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Inherited epithelial transporter disorders--an overview.
    Bergeron MJ; Simonin A; Bürzle M; Hediger MA
    J Inherit Metab Dis; 2008 Apr; 31(2):178-87. PubMed ID: 18415698
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.