180 related articles for article (PubMed ID: 30771446)
1. 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]
2. 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]
3. Cln3 function is linked to osmoregulation in a Dictyostelium model of Batten disease.
Mathavarajah S; McLaren MD; Huber RJ
Biochim Biophys Acta Mol Basis Dis; 2018 Nov; 1864(11):3559-3573. PubMed ID: 30251676
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Recent Insights into NCL Protein Function Using the Model Organism
McLaren MD; Mathavarajah S; Huber RJ
Cells; 2019 Feb; 8(2):. PubMed ID: 30717401
[TBL] [Abstract][Full Text] [Related]
7. Loss of Cln3 function in the social amoeba Dictyostelium discoideum causes pleiotropic effects that are rescued by human CLN3.
Huber RJ; Myre MA; Cotman SL
PLoS One; 2014; 9(10):e110544. PubMed ID: 25330233
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Cln3-mutations underlying juvenile neuronal ceroid lipofuscinosis cause significantly reduced levels of Palmitoyl-protein thioesterases-1 (Ppt1)-protein and Ppt1-enzyme activity in the lysosome.
Appu AP; Bagh MB; Sadhukhan T; Mondal A; Casey S; Mukherjee AB
J Inherit Metab Dis; 2019 Sep; 42(5):944-954. PubMed ID: 31025705
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Secretion and function of Cln5 during the early stages of Dictyostelium development.
Huber RJ; Mathavarajah S
Biochim Biophys Acta Mol Cell Res; 2018 Jul; 1865(10):1437-1450. PubMed ID: 30048658
[TBL] [Abstract][Full Text] [Related]
12. Human iPSC models of neuronal ceroid lipofuscinosis capture distinct effects of TPP1 and CLN3 mutations on the endocytic pathway.
Lojewski X; Staropoli JF; Biswas-Legrand S; Simas AM; Haliw L; Selig MK; Coppel SH; Goss KA; Petcherski A; Chandrachud U; Sheridan SD; Lucente D; Sims KB; Gusella JF; Sondhi D; Crystal RG; Reinhardt P; Sterneckert J; Schöler H; Haggarty SJ; Storch A; Hermann A; Cotman SL
Hum Mol Genet; 2014 Apr; 23(8):2005-22. PubMed ID: 24271013
[TBL] [Abstract][Full Text] [Related]
13. A mouse mutant deficient in both neuronal ceroid lipofuscinosis-associated proteins CLN3 and TPP1.
Sleat DE; Banach-Petrosky W; Larrimore KE; Nemtsova Y; Wiseman JA; Najafi A; Johnson D; Poole TA; Takahashi K; Cooper JD; Lobel P
J Inherit Metab Dis; 2023 Jul; 46(4):720-734. PubMed ID: 37078466
[TBL] [Abstract][Full Text] [Related]
14. An altered transcriptome underlies
Kim WD; Huber RJ
Front Genet; 2022; 13():1045738. PubMed ID: 36437924
[TBL] [Abstract][Full Text] [Related]
15. Loss of CLN3, the gene mutated in juvenile neuronal ceroid lipofuscinosis, leads to metabolic impairment and autophagy induction in retinal pigment epithelium.
Zhong Y; Mohan K; Liu J; Al-Attar A; Lin P; Flight RM; Sun Q; Warmoes MO; Deshpande RR; Liu H; Jung KS; Mitov MI; Lin N; Butterfield DA; Lu S; Liu J; Moseley HNB; Fan TWM; Kleinman ME; Wang QJ
Biochim Biophys Acta Mol Basis Dis; 2020 Oct; 1866(10):165883. PubMed ID: 32592935
[TBL] [Abstract][Full Text] [Related]
16. Molecular networking in the neuronal ceroid lipofuscinoses: insights from mammalian models and the social amoeba Dictyostelium discoideum.
Huber RJ
J Biomed Sci; 2020 May; 27(1):64. PubMed ID: 32430003
[TBL] [Abstract][Full Text] [Related]
17. Mutated genes in juvenile and variant late infantile neuronal ceroid lipofuscinoses encode lysosomal proteins.
Vesa J; Peltonen L
Curr Mol Med; 2002 Aug; 2(5):439-44. PubMed ID: 12125809
[TBL] [Abstract][Full Text] [Related]
18. A novel c.1135_1138delCTGT mutation in CLN3 leads to juvenile neuronal ceroid lipofuscinosis.
Drack AV; Miller JN; Pearce DA
J Child Neurol; 2013 Sep; 28(9):1112-6. PubMed ID: 23877479
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]