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.
291 related articles for article (PubMed ID: 17989217)
1. Activating mutation in a mucolipin transient receptor potential channel leads to melanocyte loss in varitint-waddler mice. Xu H; Delling M; Li L; Dong X; Clapham DE Proc Natl Acad Sci U S A; 2007 Nov; 104(46):18321-6. PubMed ID: 17989217 [TBL] [Abstract][Full Text] [Related]
2. A helix-breaking mutation in TRPML3 leads to constitutive activity underlying deafness in the varitint-waddler mouse. Grimm C; Cuajungco MP; van Aken AF; Schnee M; Jörs S; Kros CJ; Ricci AJ; Heller S Proc Natl Acad Sci U S A; 2007 Dec; 104(49):19583-8. PubMed ID: 18048323 [TBL] [Abstract][Full Text] [Related]
3. TRPML3 mutations cause impaired mechano-electrical transduction and depolarization by an inward-rectifier cation current in auditory hair cells of varitint-waddler mice. van Aken AF; Atiba-Davies M; Marcotti W; Goodyear RJ; Bryant JE; Richardson GP; Noben-Trauth K; Kros CJ J Physiol; 2008 Nov; 586(22):5403-18. PubMed ID: 18801844 [TBL] [Abstract][Full Text] [Related]
4. The varitint-waddler mouse phenotypes and the TRPML3 ion channel mutation: cause and consequence. Cuajungco MP; Samie MA Pflugers Arch; 2008 Nov; 457(2):463-73. PubMed ID: 18504603 [TBL] [Abstract][Full Text] [Related]
5. The varitint-waddler (Va) deafness mutation in TRPML3 generates constitutive, inward rectifying currents and causes cell degeneration. Nagata K; Zheng L; Madathany T; Castiglioni AJ; Bartles JR; García-Añoveros J Proc Natl Acad Sci U S A; 2008 Jan; 105(1):353-8. PubMed ID: 18162548 [TBL] [Abstract][Full Text] [Related]
6. Drosophila TRPML forms PI(3,5)P2-activated cation channels in both endolysosomes and plasma membrane. Feng X; Huang Y; Lu Y; Xiong J; Wong CO; Yang P; Xia J; Chen D; Du G; Venkatachalam K; Xia X; Zhu MX J Biol Chem; 2014 Feb; 289(7):4262-72. PubMed ID: 24375408 [TBL] [Abstract][Full Text] [Related]
7. Gain-of-function mutation in TRPML3 causes the mouse Varitint-Waddler phenotype. Kim HJ; Li Q; Tjon-Kon-Sang S; So I; Kiselyov K; Muallem S J Biol Chem; 2007 Dec; 282(50):36138-42. PubMed ID: 17962195 [TBL] [Abstract][Full Text] [Related]
8. Cryo-electron microscopy structure of the lysosomal calcium-permeable channel TRPML3. Hirschi M; Herzik MA; Wie J; Suo Y; Borschel WF; Ren D; Lander GC; Lee SY Nature; 2017 Oct; 550(7676):411-414. PubMed ID: 29019979 [TBL] [Abstract][Full Text] [Related]
10. Life and death of sensory hair cells expressing constitutively active TRPML3. Grimm C; Jörs S; Heller S J Biol Chem; 2009 May; 284(20):13823-13831. PubMed ID: 19299509 [TBL] [Abstract][Full Text] [Related]
11. TRPML3 and hearing loss in the varitint-waddler mouse. Atiba-Davies M; Noben-Trauth K Biochim Biophys Acta; 2007 Aug; 1772(8):1028-31. PubMed ID: 17329082 [TBL] [Abstract][Full Text] [Related]
12. Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice. Di Palma F; Belyantseva IA; Kim HJ; Vogt TF; Kachar B; Noben-Trauth K Proc Natl Acad Sci U S A; 2002 Nov; 99(23):14994-9. PubMed ID: 12403827 [TBL] [Abstract][Full Text] [Related]
14. A novel mode of TRPML3 regulation by extracytosolic pH absent in the varitint-waddler phenotype. Kim HJ; Li Q; Tjon-Kon-Sang S; So I; Kiselyov K; Soyombo AA; Muallem S EMBO J; 2008 Apr; 27(8):1197-205. PubMed ID: 18369318 [TBL] [Abstract][Full Text] [Related]
15. Properties of the TRPML3 channel pore and its stable expansion by the Varitint-Waddler-causing mutation. Kim HJ; Yamaguchi S; Li Q; So I; Muallem S J Biol Chem; 2010 May; 285(22):16513-20. PubMed ID: 20378547 [TBL] [Abstract][Full Text] [Related]
16. The tissue-specific expression of TRPML2 (MCOLN-2) gene is influenced by the presence of TRPML1. Samie MA; Grimm C; Evans JA; Curcio-Morelli C; Heller S; Slaugenhaupt SA; Cuajungco MP Pflugers Arch; 2009 Nov; 459(1):79-91. PubMed ID: 19763610 [TBL] [Abstract][Full Text] [Related]
17. Heteromultimeric TRPML channel assemblies play a crucial role in the regulation of cell viability models and starvation-induced autophagy. Zeevi DA; Lev S; Frumkin A; Minke B; Bach G J Cell Sci; 2010 Sep; 123(Pt 18):3112-24. PubMed ID: 20736310 [TBL] [Abstract][Full Text] [Related]
18. Differential mechanisms of action of the mucolipin synthetic agonist, ML-SA1, on insect TRPML and mammalian TRPML1. Feng X; Xiong J; Lu Y; Xia X; Zhu MX Cell Calcium; 2014 Dec; 56(6):446-56. PubMed ID: 25266962 [TBL] [Abstract][Full Text] [Related]
19. Constitutive activity of the human TRPML2 channel induces cell degeneration. Lev S; Zeevi DA; Frumkin A; Offen-Glasner V; Bach G; Minke B J Biol Chem; 2010 Jan; 285(4):2771-82. PubMed ID: 19940139 [TBL] [Abstract][Full Text] [Related]
20. Genetic inactivation of Trpml3 does not lead to hearing and vestibular impairment in mice. Jörs S; Grimm C; Becker L; Heller S PLoS One; 2010 Dec; 5(12):e14317. PubMed ID: 21179200 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]