194 related articles for article (PubMed ID: 24586202)
1. The Caenorhabditis elegans iodotyrosine deiodinase ortholog SUP-18 functions through a conserved channel SC-box to regulate the muscle two-pore domain potassium channel SUP-9.
de la Cruz IP; Ma L; Horvitz HR
PLoS Genet; 2014 Feb; 10(2):e1004175. PubMed ID: 24586202
[TBL] [Abstract][Full Text] [Related]
2. sup-9, sup-10, and unc-93 may encode components of a two-pore K+ channel that coordinates muscle contraction in Caenorhabditis elegans.
de la Cruz IP; Levin JZ; Cummins C; Anderson P; Horvitz HR
J Neurosci; 2003 Oct; 23(27):9133-45. PubMed ID: 14534247
[TBL] [Abstract][Full Text] [Related]
3. Genetic interactions between UNC-17/VAChT and a novel transmembrane protein in Caenorhabditis elegans.
Mathews EA; Mullen GP; Hodgkin J; Duerr JS; Rand JB
Genetics; 2012 Dec; 192(4):1315-25. PubMed ID: 23051648
[TBL] [Abstract][Full Text] [Related]
4. The RNA-binding protein SUP-12 controls muscle-specific splicing of the ADF/cofilin pre-mRNA in C. elegans.
Anyanful A; Ono K; Johnsen RC; Ly H; Jensen V; Baillie DL; Ono S
J Cell Biol; 2004 Nov; 167(4):639-47. PubMed ID: 15545320
[TBL] [Abstract][Full Text] [Related]
5. Muscle-specific splicing factors ASD-2 and SUP-12 cooperatively switch alternative pre-mRNA processing patterns of the ADF/cofilin gene in Caenorhabditis elegans.
Ohno G; Ono K; Togo M; Watanabe Y; Ono S; Hagiwara M; Kuroyanagi H
PLoS Genet; 2012; 8(10):e1002991. PubMed ID: 23071450
[TBL] [Abstract][Full Text] [Related]
6. Two Paralogous Tetraspanins TSP-12 and TSP-14 Function with the ADAM10 Metalloprotease SUP-17 to Promote BMP Signaling in Caenorhabditis elegans.
Wang L; Liu Z; Shi H; Liu J
PLoS Genet; 2017 Jan; 13(1):e1006568. PubMed ID: 28068334
[TBL] [Abstract][Full Text] [Related]
7. Locomotion Behavior Is Affected by the Gα
Gottschling DC; Döring F; Lüersen K
Genetics; 2017 May; 206(1):283-297. PubMed ID: 28341653
[TBL] [Abstract][Full Text] [Related]
8. Three new classes of mutations in the Caenorhabditis elegans muscle gene sup-9.
Levin JZ; Horvitz HR
Genetics; 1993 Sep; 135(1):53-70. PubMed ID: 8224828
[TBL] [Abstract][Full Text] [Related]
9. Crystal structure of iodotyrosine deiodinase, a novel flavoprotein responsible for iodide salvage in thyroid glands.
Thomas SR; McTamney PM; Adler JM; Laronde-Leblanc N; Rokita SE
J Biol Chem; 2009 Jul; 284(29):19659-67. PubMed ID: 19436071
[TBL] [Abstract][Full Text] [Related]
10. Behavioral genetics of caenorhabditis elegans unc-103-encoded erg-like K(+) channel.
Reiner DJ; Weinshenker D; Tian H; Thomas JH; Nishiwaki K; Miwa J; Gruninger T; Leboeuf B; Garcia LR
J Neurogenet; 2006; 20(1-2):41-66. PubMed ID: 16807195
[TBL] [Abstract][Full Text] [Related]
11. KChIP-like auxiliary subunits of Kv4 channels regulate excitability of muscle cells and control male turning behavior during mating in Caenorhabditis elegans.
Chen X; Ruan MY; Cai SQ
J Neurosci; 2015 Feb; 35(5):1880-91. PubMed ID: 25653349
[TBL] [Abstract][Full Text] [Related]
12. Allele-specific suppression in Caenorhabditis elegans reveals details of EMS mutagenesis and a possible moonlighting interaction between the vesicular acetylcholine transporter and ERD2 receptors.
Mathews EA; Stroud D; Mullen GP; Gavriilidis G; Duerr JS; Rand JB; Hodgkin J
Genetics; 2021 Aug; 218(4):. PubMed ID: 33914877
[TBL] [Abstract][Full Text] [Related]
13. Dissection of K+ currents in Caenorhabditis elegans muscle cells by genetics and RNA interference.
Santi CM; Yuan A; Fawcett G; Wang ZW; Butler A; Nonet ML; Wei A; Rojas P; Salkoff L
Proc Natl Acad Sci U S A; 2003 Nov; 100(24):14391-6. PubMed ID: 14612577
[TBL] [Abstract][Full Text] [Related]
14. A mechanistic basis for the coordinated regulation of pharyngeal morphogenesis in Caenorhabditis elegans by LIN-35/Rb and UBC-18-ARI-1.
Mani K; Fay DS
PLoS Genet; 2009 Jun; 5(6):e1000510. PubMed ID: 19521497
[TBL] [Abstract][Full Text] [Related]
15. Cell excitability necessary for male mating behavior in Caenorhabditis elegans is coordinated by interactions between big current and ether-a-go-go family K(+) channels.
LeBoeuf B; Garcia LR
Genetics; 2012 Mar; 190(3):1025-41. PubMed ID: 22174070
[TBL] [Abstract][Full Text] [Related]
16. Evidence for functional redundancy between C. elegans ADAM proteins SUP-17/Kuzbanian and ADM-4/TACE.
Jarriault S; Greenwald I
Dev Biol; 2005 Nov; 287(1):1-10. PubMed ID: 16197940
[TBL] [Abstract][Full Text] [Related]
17. Mutations in the Caenorhabditis elegans U2AF large subunit UAF-1 alter the choice of a 3' splice site in vivo.
Ma L; Horvitz HR
PLoS Genet; 2009 Nov; 5(11):e1000708. PubMed ID: 19893607
[TBL] [Abstract][Full Text] [Related]
18. Genetic screening in C. elegans identifies rho-GTPase activating protein 6 as novel HERG regulator.
Potet F; Petersen CI; Boutaud O; Shuai W; Stepanovic SZ; Balser JR; Kupershmidt S
J Mol Cell Cardiol; 2009 Feb; 46(2):257-67. PubMed ID: 19038263
[TBL] [Abstract][Full Text] [Related]
19. Resistance to volatile anesthetics by mutations enhancing excitatory neurotransmitter release in Caenorhabditis elegans.
Hawasli AH; Saifee O; Liu C; Nonet ML; Crowder CM
Genetics; 2004 Oct; 168(2):831-43. PubMed ID: 15514057
[TBL] [Abstract][Full Text] [Related]
20. Clozapine, nimodipine and endosulfan differentially suppress behavioral defects caused by gain-of-function mutations in a two-pore domain K
Kasap M; Dwyer DS
Neurosci Res; 2021 Sep; 170():41-49. PubMed ID: 32681854
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
