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.
147 related articles for article (PubMed ID: 24090639)
41. Caveolins bind to (Na+, K+)/H+ exchanger NHE7 by a novel binding module. Lin PJ; Williams WP; Kobiljski J; Numata M Cell Signal; 2007 May; 19(5):978-88. PubMed ID: 17207967 [TBL] [Abstract][Full Text] [Related]
42. An inside job: how endosomal Na(+)/H(+) exchangers link to autism and neurological disease. Kondapalli KC; Prasad H; Rao R Front Cell Neurosci; 2014; 8():172. PubMed ID: 25002837 [TBL] [Abstract][Full Text] [Related]
43. The Na(+)/H (+) exchanger NHE5 is sorted to discrete intracellular vesicles in the central and peripheral nervous systems. Lukashova V; Jinadasa T; Ilie A; Verbich D; Cooper E; Orlowski J Adv Exp Med Biol; 2013; 961():397-410. PubMed ID: 23224898 [TBL] [Abstract][Full Text] [Related]
45. Functional role of cysteine residues in the Na+/H+ exchanger effects of mutation of cysteine residues on targeting and activity of the Na+/H+ exchanger. Wang H; Singh D; Fliegel L Arch Biochem Biophys; 1998 Oct; 358(1):116-24. PubMed ID: 9750172 [TBL] [Abstract][Full Text] [Related]
46. Novel SLC9A6 mutations in two families with Christianson syndrome. Riess A; Rossier E; Krüger R; Dufke A; Beck-Woedl S; Horber V; Alber M; Gläser D; Riess O; Tzschach A Clin Genet; 2013 Jun; 83(6):596-7. PubMed ID: 22931061 [No Abstract] [Full Text] [Related]
47. 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]
48. Late endosomal cholesterol accumulation leads to impaired intra-endosomal trafficking. Sobo K; Le Blanc I; Luyet PP; Fivaz M; Ferguson C; Parton RG; Gruenberg J; van der Goot FG PLoS One; 2007 Sep; 2(9):e851. PubMed ID: 17786222 [TBL] [Abstract][Full Text] [Related]
49. Syndrome of X linked intellectual disability, epilepsy, progressive brain atrophy and large head associated with Padmanabha H; Saini AG; Sahu JK; Singhi P BMJ Case Rep; 2017 Dec; 2017():. PubMed ID: 29275387 [No Abstract] [Full Text] [Related]
50. X-linked Angelman-like syndrome caused by Slc9a6 knockout in mice exhibits evidence of endosomal-lysosomal dysfunction. Strømme P; Dobrenis K; Sillitoe RV; Gulinello M; Ali NF; Davidson C; Micsenyi MC; Stephney G; Ellevog L; Klungland A; Walkley SU Brain; 2011 Nov; 134(Pt 11):3369-83. PubMed ID: 21964919 [TBL] [Abstract][Full Text] [Related]
51. Proline residues in transmembrane segment IV are critical for activity, expression and targeting of the Na+/H+ exchanger isoform 1. Slepkov ER; Chow S; Lemieux MJ; Fliegel L Biochem J; 2004 Apr; 379(Pt 1):31-8. PubMed ID: 14680478 [TBL] [Abstract][Full Text] [Related]
52. 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]
53. Ketamine promotes the amyloidogenic pathway by regulating endosomal pH. Ren W; Lou H; Ren X; Wen G; Wu X; Xia X; Wang S; Yu X; Yan L; Zhang G; Yao J; Lu Y; Wu X Toxicology; 2022 Apr; 471():153163. PubMed ID: 35378374 [TBL] [Abstract][Full Text] [Related]
54. L1 syndrome diagnosis complemented with functional analysis of L1CAM variants located to the two N-terminal Ig-like domains. Christaller WA; Vos Y; Gebre-Medhin S; Hofstra RM; Schäfer MK Clin Genet; 2017 Jan; 91(1):115-120. PubMed ID: 26891472 [TBL] [Abstract][Full Text] [Related]
55. Christianson syndrome: A novel splicing variant of SLC9A6 causes exon skipping in a Chinese boy and a literature review. Zhang X; Wu X; Liu H; Song T; Jiang Y; He H; Yang S; Xie Y J Clin Lab Anal; 2022 Jan; 36(1):e24123. PubMed ID: 34791706 [TBL] [Abstract][Full Text] [Related]
56. Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Lizarraga SB; Ma L; Maguire AM; van Dyck LI; Wu Q; Ouyang Q; Kavanaugh BC; Nagda D; Livi LL; Pescosolido MF; Schmidt M; Alabi S; Cowen MH; Brito-Vargas P; Hoffman-Kim D; Gamsiz Uzun ED; Schlessinger A; Jones RN; Morrow EM Sci Transl Med; 2021 Feb; 13(580):. PubMed ID: 33568516 [TBL] [Abstract][Full Text] [Related]
57. Emerging links between endosomal pH and cancer. Ko M; Quiñones-Hinojosa A; Rao R Cancer Metastasis Rev; 2020 Jun; 39(2):519-534. PubMed ID: 32253638 [TBL] [Abstract][Full Text] [Related]
58. Enhanced activity of human serotonin transporter variants associated with autism. Prasad HC; Steiner JA; Sutcliffe JS; Blakely RD Philos Trans R Soc Lond B Biol Sci; 2009 Jan; 364(1514):163-73. PubMed ID: 18957375 [TBL] [Abstract][Full Text] [Related]
59. 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]
60. IQSEC2-Associated Intellectual Disability and Autism. Levy NS; Umanah GKE; Rogers EJ; Jada R; Lache O; Levy AP Int J Mol Sci; 2019 Jun; 20(12):. PubMed ID: 31234416 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]