183 related articles for article (PubMed ID: 36055242)
21. Functional Assessment
Ouyang Q; Joesch-Cohen L; Mishra S; Riaz HA; Schmidt M; Morrow EM
eNeuro; 2019; 6(6):. PubMed ID: 31676550
[TBL] [Abstract][Full Text] [Related]
22. Sodium-hydrogen exchanger 6 (NHE6) deficiency leads to hearing loss, via reduced endosomal signalling through the BDNF/Trk pathway.
Kucharava K; Brand Y; Albano G; Sekulic-Jablanovic M; Glutz A; Xian X; Herz J; Bodmer D; Fuster DG; Petkovic V
Sci Rep; 2020 Feb; 10(1):3609. PubMed ID: 32107410
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Acid indigestion in the endosome: linking signaling dysregulation to neurodevelopmental disorders.
Yap CC; Winckler B
Neuron; 2013 Oct; 80(1):4-6. PubMed ID: 24094097
[TBL] [Abstract][Full Text] [Related]
26. A new family with an SLC9A6 mutation expanding the phenotypic spectrum of Christianson syndrome.
Masurel-Paulet A; Piton A; Chancenotte S; Redin C; Thauvin-Robinet C; Henrenger Y; Minot D; Creppy A; Ruffier-Bourdet M; Thevenon J; Kuentz P; Lehalle D; Curie A; Blanchard G; Ghosn E; Bonnet M; Archimbaud-Devilliers M; Huet F; Perret O; Philip N; Mandel JL; Faivre L
Am J Med Genet A; 2016 Aug; 170(8):2103-10. PubMed ID: 27256868
[TBL] [Abstract][Full Text] [Related]
27. 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
bioRxiv; 2023 Nov; ():. PubMed ID: 37986849
[TBL] [Abstract][Full Text] [Related]
28. SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.
Gilfillan GD; Selmer KK; Roxrud I; Smith R; Kyllerman M; Eiklid K; Kroken M; Mattingsdal M; Egeland T; Stenmark H; Sjøholm H; Server A; Samuelsson L; Christianson A; Tarpey P; Whibley A; Stratton MR; Futreal PA; Teague J; Edkins S; Gecz J; Turner G; Raymond FL; Schwartz C; Stevenson RE; Undlien DE; Strømme P
Am J Hum Genet; 2008 Apr; 82(4):1003-10. PubMed ID: 18342287
[TBL] [Abstract][Full Text] [Related]
29. Novel c.1505_1509dupCTGCC pathogenic variation in a male case with Christianson syndrome.
Yalcintepe S; Gurkan H
Clin Dysmorphol; 2021 Jan; 30(1):36-38. PubMed ID: 33278113
[TBL] [Abstract][Full Text] [Related]
30. Deletion of the sodium/hydrogen exchanger 6 causes low bone volume in adult mice.
Schnyder D; Albano G; Kucharczyk P; Dolder S; Siegrist M; Anderegg M; Pathare G; Hofstetter W; Baron R; Fuster DG
Bone; 2021 Dec; 153():116178. PubMed ID: 34508879
[TBL] [Abstract][Full Text] [Related]
31. NHE6 depletion corrects ApoE4-mediated synaptic impairments and reduces amyloid plaque load.
Pohlkamp T; Xian X; Wong CH; Durakoglugil MS; Werthmann GC; Saido TC; Evers BM; White CL; Connor J; Hammer RE; Herz J
Elife; 2021 Oct; 10():. PubMed ID: 34617884
[TBL] [Abstract][Full Text] [Related]
32. The Na+/H+ exchanger NHE6 in the endosomal recycling system is involved in the development of apical bile canalicular surface domains in HepG2 cells.
Ohgaki R; Matsushita M; Kanazawa H; Ogihara S; Hoekstra D; van Ijzendoorn SC
Mol Biol Cell; 2010 Apr; 21(7):1293-304. PubMed ID: 20130086
[TBL] [Abstract][Full Text] [Related]
33. Complex Neurological Phenotype in Female Carriers of
Pescosolido MF; Kavanaugh BC; Pochet N; Schmidt M; Jerskey BA; Rogg JM; De Jager PL; Young-Pearse TL; Liu JS; Morrow EM
Mol Neuropsychiatry; 2019 Apr; 5(2):98-108. PubMed ID: 31192222
[TBL] [Abstract][Full Text] [Related]
34. Dual degradation mechanisms ensure disposal of NHE6 mutant protein associated with neurological disease.
Roxrud I; Raiborg C; Gilfillan GD; Strømme P; Stenmark H
Exp Cell Res; 2009 Oct; 315(17):3014-27. PubMed ID: 19619532
[TBL] [Abstract][Full Text] [Related]
35. Enhanced recruitment of endosomal Na+/H+ exchanger NHE6 into Dendritic spines of hippocampal pyramidal neurons during NMDA receptor-dependent long-term potentiation.
Deane EC; Ilie AE; Sizdahkhani S; Das Gupta M; Orlowski J; McKinney RA
J Neurosci; 2013 Jan; 33(2):595-610. PubMed ID: 23303939
[TBL] [Abstract][Full Text] [Related]
36. The expanding phenotypic spectrum of female SLC9A6 mutation carriers: a case series and review of the literature.
Sinajon P; Verbaan D; So J
Hum Genet; 2016 Aug; 135(8):841-50. PubMed ID: 27142213
[TBL] [Abstract][Full Text] [Related]
37. Na+/H+ exchanger isoform 6 (NHE6/SLC9A6) is involved in clathrin-dependent endocytosis of transferrin.
Xinhan L; Matsushita M; Numaza M; Taguchi A; Mitsui K; Kanazawa H
Am J Physiol Cell Physiol; 2011 Dec; 301(6):C1431-44. PubMed ID: 21881004
[TBL] [Abstract][Full Text] [Related]
38. Histone deacetylase-mediated regulation of endolysosomal pH.
Prasad H; Rao R
J Biol Chem; 2018 May; 293(18):6721-6735. PubMed ID: 29567836
[TBL] [Abstract][Full Text] [Related]
39. Functional analysis of two SLC9A6 frameshift variants in lymphoblastoid cells from patients with Christianson syndrome.
He H; Zhang H; Chen H; He F; Yin F; Stauber T; Zou X; Peng J
CNS Neurosci Ther; 2023 Dec; 29(12):4059-4069. PubMed ID: 37381736
[TBL] [Abstract][Full Text] [Related]
40. A mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition.
Garbern JY; Neumann M; Trojanowski JQ; Lee VM; Feldman G; Norris JW; Friez MJ; Schwartz CE; Stevenson R; Sima AA
Brain; 2010 May; 133(Pt 5):1391-402. PubMed ID: 20395263
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
