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.
272 related articles for article (PubMed ID: 28365442)
1. 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]
2. 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]
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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. Microglia in juvenile neuronal ceroid lipofuscinosis are primed toward a pro-inflammatory phenotype. Xiong J; Kielian T J Neurochem; 2013 Oct; 127(2):245-58. PubMed ID: 23919525 [TBL] [Abstract][Full Text] [Related]
11. Revisiting the neuronal localization and trafficking of CLN3 in juvenile neuronal ceroid lipofuscinosis. Oetjen S; Kuhl D; Hermey G J Neurochem; 2016 Nov; 139(3):456-470. PubMed ID: 27453211 [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]
18. Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL). Järvelä I; Lehtovirta M; Tikkanen R; Kyttälä A; Jalanko A Hum Mol Genet; 1999 Jun; 8(6):1091-8. PubMed ID: 10332042 [TBL] [Abstract][Full Text] [Related]
19. Altered flurothyl seizure induction latency, phenotype, and subsequent mortality in a mouse model of juvenile neuronal ceroid lipofuscinosis/batten disease. Kriscenski-Perry E; Applegate CD; Serour A; Mhyre TR; Leonardo CC; Pearce DA Epilepsia; 2002 Oct; 43(10):1137-40. PubMed ID: 12366726 [TBL] [Abstract][Full Text] [Related]
20. A novel in-frame mutation in Sher M; Farooq M; Abdullah U; Ali Z; Faryal S; Zakaria M; Ullah F; Bukhari H; Møller RS; Tommerup N; Baig SM Int J Neurosci; 2019 Sep; 129(9):890-895. PubMed ID: 30892110 [No Abstract] [Full Text] [Related] [Next] [New Search]