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 *

162 related articles for article (PubMed ID: 25798182)

  • 1. Identification of residues/sequences in the human riboflavin transporter-2 that is important for function and cell biology.
    Subramanian VS; Kapadia R; Ghosal A; Said HM
    Nutr Metab (Lond); 2015; 12():13. PubMed ID: 25798182
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Structure/functional aspects of the human riboflavin transporter-3 (
    Subramanian VS; Sabui S; Teafatiller T; Bohl JA; Said HM
    Am J Physiol Cell Physiol; 2017 Aug; 313(2):C228-C238. PubMed ID: 28637675
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SLC52A2 [p.P141T] and SLC52A3 [p.N21S] causing Brown-Vialetto-Van Laere Syndrome in an Indian patient: First genetically proven case with mutations in two riboflavin transporters.
    Udhayabanu T; Subramanian VS; Teafatiller T; Gowda VK; Raghavan VS; Varalakshmi P; Said HM; Ashokkumar B
    Clin Chim Acta; 2016 Nov; 462():210-214. PubMed ID: 27702554
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular Mechanisms Mediating the Adaptive Regulation of Intestinal Riboflavin Uptake Process.
    Subramanian VS; Ghosal A; Kapadia R; Nabokina SM; Said HM
    PLoS One; 2015; 10(6):e0131698. PubMed ID: 26121134
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Brown-Vialetto-Van Laere and Fazio-Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritance.
    Gayathri S; Gowda VK; Udhayabanu T; O'Callaghan B; Efthymiou S; Varalakshmi P; Benakappa N; Houlden H; Ashokkumar B
    Eur J Neurol; 2021 Mar; 28(3):945-954. PubMed ID: 33325104
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of transmembrane protein 237 as a novel interactor with the intestinal riboflavin transporter-3 (RFVT-3): role in functionality and cell biology.
    Sabui S; Subramanian VS; Pham Q; Said HM
    Am J Physiol Cell Physiol; 2019 Jun; 316(6):C805-C814. PubMed ID: 30892938
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Effect of clinical mutations on functionality of the human riboflavin transporter-2 (hRFT-2).
    Nabokina SM; Subramanian VS; Said HM
    Mol Genet Metab; 2012 Apr; 105(4):652-7. PubMed ID: 22273710
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Case of Brown-Vialetto-Van Laere Syndrome Due To a Novel Mutation in
    Thulasi V; Veerapandiyan A; Pletcher BA; Tong CM; Ming X
    Child Neurol Open; 2017; 4():2329048X17725610. PubMed ID: 28856173
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: clinical course and response to riboflavin.
    Shi K; Shi Z; Yan H; Wang X; Yang Y; Xiong H; Gu Q; Wu Y; Jiang Y; Wang J
    BMC Med Genet; 2019 May; 20(1):76. PubMed ID: 31064337
    [TBL] [Abstract][Full Text] [Related]  

  • 10. In Silico Identification of a Key Residue for Substrate Recognition of the Riboflavin Membrane Transporter RFVT3.
    Dilly S; Garnier M; Solé M; Bailly R; Taib N; Bestel I
    J Chem Inf Model; 2020 Mar; 60(3):1368-1375. PubMed ID: 31922414
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Brown-Vialetto-Van Laere syndrome: a riboflavin-unresponsive patient with a novel mutation in the C20orf54 gene.
    Koy A; Pillekamp F; Hoehn T; Waterham H; Klee D; Mayatepek E; Assmann B
    Pediatr Neurol; 2012 Jun; 46(6):407-9. PubMed ID: 22633641
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Structure-function characterization of the human mitochondrial thiamin pyrophosphate transporter (hMTPPT; SLC25A19): Important roles for Ile(33), Ser(34), Asp(37), His(137) and Lys(291).
    Sabui S; Subramanian VS; Kapadia R; Said HM
    Biochim Biophys Acta; 2016 Aug; 1858(8):1883-90. PubMed ID: 27188525
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Brown-Vialetto-Van Laere Syndrome as a Mimic of Neuroimmune Disorders: 3 Cases From the Clinic and Review of the Literature.
    Allison T; Roncero I; Forsyth R; Coffman K; Pichon JL
    J Child Neurol; 2017 May; 32(6):528-532. PubMed ID: 28116953
    [TBL] [Abstract][Full Text] [Related]  

  • 14. SLC52A3, A Brown-Vialetto-van Laere syndrome candidate gene is essential for mouse development, but dispensable for motor neuron differentiation.
    Intoh A; Suzuki N; Koszka K; Eggan K
    Hum Mol Genet; 2016 May; 25(9):1814-23. PubMed ID: 26976849
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Riboflavin Treatment in Genetically Proven Brown-Vialetto-Van Laere Syndrome.
    Garg M; Kulkarni SD; Hegde AU; Shah KN
    J Pediatr Neurosci; 2018; 13(4):471-473. PubMed ID: 30937093
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Reconstitution in Proteoliposomes of the Recombinant Human Riboflavin Transporter 2 (SLC52A2) Overexpressed in
    Console L; Tolomeo M; Colella M; Barile M; Indiveri C
    Int J Mol Sci; 2019 Sep; 20(18):. PubMed ID: 31500345
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Riboflavin Transporters RFVT/SLC52A Mediate Translocation of Riboflavin, Rather than FMN or FAD, across Plasma Membrane.
    Jin C; Yao Y; Yonezawa A; Imai S; Yoshimatsu H; Otani Y; Omura T; Nakagawa S; Nakagawa T; Matsubara K
    Biol Pharm Bull; 2017; 40(11):1990-1995. PubMed ID: 29093349
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin.
    Horoz OO; Mungan NO; Yildizdas D; Hergüner Ö; Ceylaner S; Kör D; Waterham H; Coskun T
    J Pediatr Endocrinol Metab; 2016 Feb; 29(2):227-31. PubMed ID: 26444347
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sodium Butyrate Enhances Intestinal Riboflavin Uptake via Induction of Expression of Riboflavin Transporter-3 (RFVT3).
    Subramanian VS; Sabui S; Heskett CW; Said HM
    Dig Dis Sci; 2019 Jan; 64(1):84-92. PubMed ID: 30276569
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Case with Brown-Vialetto-Van Laere Syndrome: A Sudden Onset Auditory Neuropathy Spectrum Disorder.
    Mutlu B; Topçu MT; Çiprut A
    Turk Arch Otorhinolaryngol; 2019 Dec; 57(4):201-205. PubMed ID: 32128519
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.