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.
186 related articles for article (PubMed ID: 23508127)
1. Genes for endosomal NHE6 and NHE9 are misregulated in autism brains. Schwede M; Garbett K; Mirnics K; Geschwind DH; Morrow EM Mol Psychiatry; 2014 Mar; 19(3):277-9. PubMed ID: 23508127 [No Abstract] [Full Text] [Related]
2. Christianson syndrome protein NHE6 modulates TrkB endosomal signaling required for neuronal circuit development. Ouyang Q; Lizarraga SB; Schmidt M; Yang U; Gong J; Ellisor D; Kauer JA; Morrow EM Neuron; 2013 Oct; 80(1):97-112. PubMed ID: 24035762 [TBL] [Abstract][Full Text] [Related]
3. The Na+/H+ exchanger NHE6 modulates endosomal pH to control processing of amyloid precursor protein in a cell culture model of Alzheimer disease. Prasad H; Rao R J Biol Chem; 2015 Feb; 290(9):5311-27. PubMed ID: 25561733 [TBL] [Abstract][Full Text] [Related]
4. Functional evaluation of autism-associated mutations in NHE9. Kondapalli KC; Hack A; Schushan M; Landau M; Ben-Tal N; Rao R Nat Commun; 2013; 4():2510. PubMed ID: 24065030 [TBL] [Abstract][Full Text] [Related]
5. Genes for endosomal pH regulators NHE6 and NHE9 are dysregulated in the substantia nigra in Parkinson's disease. Prasad H Gene; 2024 Nov; 927():148737. PubMed ID: 38945311 [TBL] [Abstract][Full Text] [Related]
6. Effect of disease-associated SLC9A9 mutations on protein-protein interaction networks: implications for molecular mechanisms for ADHD and autism. Zhang-James Y; Vaudel M; Mjaavatten O; Berven FS; Haavik J; Faraone SV Atten Defic Hyperact Disord; 2019 Mar; 11(1):91-105. PubMed ID: 30927234 [TBL] [Abstract][Full Text] [Related]
7. GGA1 interacts with the endosomal Na+/H+ exchanger NHE6 governing localization to the endosome compartment. Ma L; Kasula RK; Ouyang Q; Schmidt M; Morrow EM J Biol Chem; 2024 Aug; 300(8):107552. PubMed ID: 39002678 [TBL] [Abstract][Full Text] [Related]
8. Loss of Christianson Syndrome Na Pescosolido MF; Ouyang Q; Liu JS; Morrow EM J Neurosci; 2021 Nov; 41(44):9235-9256. PubMed ID: 34526390 [TBL] [Abstract][Full Text] [Related]
9. A Christianson syndrome-linked deletion mutation (∆(287)ES(288)) in SLC9A6 disrupts recycling endosomal function and elicits neurodegeneration and cell death. Ilie A; Gao AY; Reid J; Boucher A; McEwan C; Barrière H; Lukacs GL; McKinney RA; Orlowski J Mol Neurodegener; 2016 Sep; 11(1):63. PubMed ID: 27590723 [TBL] [Abstract][Full Text] [Related]