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 *

131 related articles for article (PubMed ID: 37742391)

  • 1. Loss of mfsd8 alters the secretome during Dictyostelium aggregation.
    Huber RJ; Gray J; Kim WD
    Eur J Cell Biol; 2023 Dec; 102(4):151361. PubMed ID: 37742391
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mfsd8 localizes to endocytic compartments and influences the secretion of Cln5 and cathepsin D in Dictyostelium.
    Huber RJ; Mathavarajah S; Yap SQ
    Cell Signal; 2020 Jun; 70():109572. PubMed ID: 32087303
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mfsd8 Modulates Growth and the Early Stages of Multicellular Development in
    Yap SQ; Kim WD; Huber RJ
    Front Cell Dev Biol; 2022; 10():930235. PubMed ID: 35756993
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Using the social amoeba Dictyostelium to study the functions of proteins linked to neuronal ceroid lipofuscinosis.
    Huber RJ
    J Biomed Sci; 2016 Nov; 23(1):83. PubMed ID: 27881166
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Gene disruption of Mfsd8 in mice provides the first animal model for CLN7 disease.
    Damme M; Brandenstein L; Fehr S; Jankowiak W; Bartsch U; Schweizer M; Hermans-Borgmeyer I; Storch S
    Neurobiol Dis; 2014 May; 65():12-24. PubMed ID: 24423645
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of Cln3 impacts protein secretion in the social amoeba Dictyostelium.
    Huber RJ
    Cell Signal; 2017 Jul; 35():61-72. PubMed ID: 28365442
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An altered transcriptome underlies
    Kim WD; Huber RJ
    Front Genet; 2022; 13():1045738. PubMed ID: 36437924
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comparative transcriptomics reveals mechanisms underlying cln3-deficiency phenotypes in Dictyostelium.
    Huber RJ; Mathavarajah S
    Cell Signal; 2019 Jun; 58():79-90. PubMed ID: 30771446
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cln5 is secreted and functions as a glycoside hydrolase in Dictyostelium.
    Huber RJ; Mathavarajah S
    Cell Signal; 2018 Jan; 42():236-248. PubMed ID: 29128403
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis.
    Kousi M; Siintola E; Dvorakova L; Vlaskova H; Turnbull J; Topcu M; Yuksel D; Gokben S; Minassian BA; Elleder M; Mole SE; Lehesjoki AE
    Brain; 2009 Mar; 132(Pt 3):810-9. PubMed ID: 19201763
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis.
    Sharifi A; Kousi M; Sagné C; Bellenchi GC; Morel L; Darmon M; Hulková H; Ruivo R; Debacker C; El Mestikawy S; Elleder M; Lehesjoki AE; Jalanko A; Gasnier B; Kyttälä A
    Hum Mol Genet; 2010 Nov; 19(22):4497-514. PubMed ID: 20826447
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Partial genetic suppression of a loss-of-function mutant of the neuronal ceroid lipofuscinosis-associated protease TPP1 in Dictyostelium discoideum.
    Phillips JE; Gomer RH
    Dis Model Mech; 2015 Feb; 8(2):147-56. PubMed ID: 25540127
    [TBL] [Abstract][Full Text] [Related]  

  • 13. AAV9/MFSD8 gene therapy is effective in preclinical models of neuronal ceroid lipofuscinosis type 7 disease.
    Chen X; Dong T; Hu Y; Shaffo FC; Belur NR; Mazzulli JR; Gray SJ
    J Clin Invest; 2022 Mar; 132(5):. PubMed ID: 35025759
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rett-like onset in late-infantile neuronal ceroid lipofuscinosis (CLN7) caused by compound heterozygous mutation in the MFSD8 gene and review of the literature data on clinical onset signs.
    Craiu D; Dragostin O; Dica A; Hoffman-Zacharska D; Gos M; Bastian AE; Gherghiceanu M; Rolfs A; Nahavandi N; Craiu M; Iliescu C
    Eur J Paediatr Neurol; 2015 Jan; 19(1):78-86. PubMed ID: 25439737
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Aberrant adhesion impacts early development in a Dictyostelium model for juvenile neuronal ceroid lipofuscinosis.
    Huber RJ; Myre MA; Cotman SL
    Cell Adh Migr; 2017 Jul; 11(4):399-418. PubMed ID: 27669405
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The novel neuronal ceroid lipofuscinosis gene MFSD8 encodes a putative lysosomal transporter.
    Siintola E; Topcu M; Aula N; Lohi H; Minassian BA; Paterson AD; Liu XQ; Wilson C; Lahtinen U; Anttonen AK; Lehesjoki AE
    Am J Hum Genet; 2007 Jul; 81(1):136-46. PubMed ID: 17564970
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia.
    Geier EG; Bourdenx M; Storm NJ; Cochran JN; Sirkis DW; Hwang JH; Bonham LW; Ramos EM; Diaz A; Van Berlo V; Dokuru D; Nana AL; Karydas A; Balestra ME; Huang Y; Russo SP; Spina S; Grinberg LT; Seeley WW; Myers RM; Miller BL; Coppola G; Lee SE; Cuervo AM; Yokoyama JS
    Acta Neuropathol; 2019 Jan; 137(1):71-88. PubMed ID: 30382371
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mechanisms regulating the intracellular trafficking and release of CLN5 and CTSD.
    Huber RJ; Kim WD; Wilson-Smillie MLDM
    Traffic; 2024 Jan; 25(1):e12925. PubMed ID: 38272448
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neuronal ceroid lipofuscinosis associated with an MFSD8 mutation in Chihuahuas.
    Ashwini A; D'Angelo A; Yamato O; Giordano C; Cagnotti G; Harcourt-Brown T; Mhlanga-Mutangadura T; Guo J; Johnson GS; Katz ML
    Mol Genet Metab; 2016 Aug; 118(4):326-32. PubMed ID: 27211611
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The conserved cellular roles of CLN proteins: Novel insights from Dictyostelium discoideum.
    Remtulla AAN; Huber RJ
    Eur J Cell Biol; 2023 Jun; 102(2):151305. PubMed ID: 36917916
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.