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 *

397 related articles for article (PubMed ID: 19727438)

  • 41. Biotinidase deficiency: initial clinical features and rapid diagnosis.
    Wolf B; Heard GS; Weissbecker KA; McVoy JR; Grier RE; Leshner RT
    Ann Neurol; 1985 Nov; 18(5):614-7. PubMed ID: 4073853
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Biotin uptake into human peripheral blood mononuclear cells increases early in the cell cycle, increasing carboxylase activities.
    Stanley JS; Mock DM; Griffin JB; Zempleni J
    J Nutr; 2002 Jul; 132(7):1854-9. PubMed ID: 12097659
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Sodium-dependent multivitamin transporter gene is regulated at the chromatin level by histone biotinylation in human Jurkat lymphoblastoma cells.
    Zempleni J; Gralla M; Camporeale G; Hassan YI
    J Nutr; 2009 Jan; 139(1):163-6. PubMed ID: 19056636
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Mutational hotspot in the human biotinidase gene causes profound biotinidase deficiency.
    Pomponio RJ; Reynolds TR; Cole H; Buck GA; Wolf B
    Nat Genet; 1995 Sep; 11(1):96-8. PubMed ID: 7550325
    [TBL] [Abstract][Full Text] [Related]  

  • 45. High frequency of biotinidase deficiency in Italian population identified by newborn screening.
    Funghini S; Tonin R; Malvagia S; Caciotti A; Donati MA; Morrone A; la Marca G
    Mol Genet Metab Rep; 2020 Dec; 25():100689. PubMed ID: 33312878
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Biotin-responsive multiple carboxylase deficiency in an 8-year-old boy with normal serum biotinidase and fibroblast holocarboxylase-synthetase activities.
    Holme E; Jacobson CE; Kristiansson B
    J Inherit Metab Dis; 1988; 11(3):270-6. PubMed ID: 3148068
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Biotin deficiency reduces expression of SLC19A3, a potential biotin transporter, in leukocytes from human blood.
    Vlasova TI; Stratton SL; Wells AM; Mock NI; Mock DM
    J Nutr; 2005 Jan; 135(1):42-7. PubMed ID: 15623830
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Biotin regulates the genetic expression of holocarboxylase synthetase and mitochondrial carboxylases in rats.
    Rodríguez-Meléndez R; Cano S; Méndez ST; Velázquez A
    J Nutr; 2001 Jul; 131(7):1909-13. PubMed ID: 11435506
    [TBL] [Abstract][Full Text] [Related]  

  • 49. K4, K9 and K18 in human histone H3 are targets for biotinylation by biotinidase.
    Kobza K; Camporeale G; Rueckert B; Kueh A; Griffin JB; Sarath G; Zempleni J
    FEBS J; 2005 Aug; 272(16):4249-59. PubMed ID: 16098205
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Holocarboxylase synthetase 1 physically interacts with histone h3 in Arabidopsis.
    Chen X; Chou HH; Wurtele ES
    Scientifica (Cairo); 2013; 2013():983501. PubMed ID: 24278788
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Biotin supply affects expression of biotin transporters, biotinylation of carboxylases and metabolism of interleukin-2 in Jurkat cells.
    Manthey KC; Griffin JB; Zempleni J
    J Nutr; 2002 May; 132(5):887-92. PubMed ID: 11983808
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Partial Biotinidase Deficiency Revealed Imbalances in Acylcarnitines Profile at Tandem Mass Spectrometry Newborn Screening.
    Cicalini I; Pieragostino D; Rizzo C; Verrocchio S; Semeraro D; Zucchelli M; Di Michele S; Dionisi-Vici C; Stuppia L; De Laurenzi V; Bucci I; Rossi C
    Int J Environ Res Public Health; 2021 Feb; 18(4):. PubMed ID: 33572391
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Biotinidase and its roles in biotin metabolism.
    Hymes J; Wolf B
    Clin Chim Acta; 1996 Nov; 255(1):1-11. PubMed ID: 8930409
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Biotin availability regulates expression of the sodium-dependent multivitamin transporter and the rate of biotin uptake in HepG2 cells.
    Pacheco-Alvarez D; Solórzano-Vargas RS; González-Noriega A; Michalak C; Zempleni J; León-Del-Río A
    Mol Genet Metab; 2005 Aug; 85(4):301-7. PubMed ID: 15905112
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.
    Burri BJ; Sweetman L; Nyhan WL
    J Clin Invest; 1981 Dec; 68(6):1491-5. PubMed ID: 6798072
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Multiple carboxylase deficiency].
    Andersen JB; Haagerup A; Christensen E
    Ugeskr Laeger; 1998 Feb; 160(8):1151-7. PubMed ID: 9492625
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Lactic acidosis in biotin-responsive multiple carboxylase deficiency caused by holocarboxylase synthetase deficiency of early and late onset.
    Sherwood WG; Saunders M; Robinson BH; Brewster T; Gravel RA
    J Pediatr; 1982 Oct; 101(4):546-50. PubMed ID: 6811711
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Transplacental transport and tissue distribution of biotin in mice at midgestation.
    Taniguchi A; Watanabe T
    Congenit Anom (Kyoto); 2008 Jun; 48(2):57-62. PubMed ID: 18452485
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Biotinidase deficiency. Progressive encephalopathy curable with biotin].
    Héron B; Gautier A; Dulac O; Ponsot G
    Arch Fr Pediatr; 1993 Dec; 50(10):875-8. PubMed ID: 8053766
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Clinical findings and biochemical and molecular analysis of four patients with holocarboxylase synthetase deficiency.
    Morrone A; Malvagia S; Donati MA; Funghini S; Ciani F; Pela I; Boneh A; Peters H; Pasquini E; Zammarchi E
    Am J Med Genet; 2002 Jul; 111(1):10-8. PubMed ID: 12124727
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.