206 related articles for article (PubMed ID: 18003898)
1. An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line.
Zvaritch E; Depreux F; Kraeva N; Loy RE; Goonasekera SA; Boncompagni S; Kraev A; Gramolini AO; Dirksen RT; Franzini-Armstrong C; Seidman CE; Seidman JG; Maclennan DH
Proc Natl Acad Sci U S A; 2007 Nov; 104(47):18537-42. PubMed ID: 18003898
[TBL] [Abstract][Full Text] [Related]
2. A retrograde signal from RyR1 alters DHP receptor inactivation and limits window Ca2+ release in muscle fibers of Y522S RyR1 knock-in mice.
Andronache Z; Hamilton SL; Dirksen RT; Melzer W
Proc Natl Acad Sci U S A; 2009 Mar; 106(11):4531-6. PubMed ID: 19246389
[TBL] [Abstract][Full Text] [Related]
3. Ryanodine modification of RyR1 retrogradely affects L-type Ca(2+) channel gating in skeletal muscle.
Bannister RA; Beam KG
J Muscle Res Cell Motil; 2009; 30(5-6):217-23. PubMed ID: 19802526
[TBL] [Abstract][Full Text] [Related]
4. Muscle weakness in Ryr1I4895T/WT knock-in mice as a result of reduced ryanodine receptor Ca2+ ion permeation and release from the sarcoplasmic reticulum.
Loy RE; Orynbayev M; Xu L; Andronache Z; Apostol S; Zvaritch E; MacLennan DH; Meissner G; Melzer W; Dirksen RT
J Gen Physiol; 2011 Jan; 137(1):43-57. PubMed ID: 21149547
[TBL] [Abstract][Full Text] [Related]
5. Excitation--contraction uncoupling by a human central core disease mutation in the ryanodine receptor.
Avila G; O'Brien JJ; Dirksen RT
Proc Natl Acad Sci U S A; 2001 Mar; 98(7):4215-20. PubMed ID: 11274444
[TBL] [Abstract][Full Text] [Related]
6. Ca2+ release in muscle fibers expressing R4892W and G4896V type 1 ryanodine receptor disease mutants.
Lefebvre R; Legrand C; Groom L; Dirksen RT; Jacquemond V
PLoS One; 2013; 8(1):e54042. PubMed ID: 23308296
[TBL] [Abstract][Full Text] [Related]
7. A malignant hyperthermia-inducing mutation in RYR1 (R163C): consequent alterations in the functional properties of DHPR channels.
Bannister RA; Estève E; Eltit JM; Pessah IN; Allen PD; López JR; Beam KG
J Gen Physiol; 2010 Jun; 135(6):629-40. PubMed ID: 20479108
[TBL] [Abstract][Full Text] [Related]
8. Ca2+-dependent excitation-contraction coupling triggered by the heterologous cardiac/brain DHPR beta2a-subunit in skeletal myotubes.
Sheridan DC; Carbonneau L; Ahern CA; Nataraj P; Coronado R
Biophys J; 2003 Dec; 85(6):3739-57. PubMed ID: 14645065
[TBL] [Abstract][Full Text] [Related]
9. Functional and biochemical properties of ryanodine receptor type 1 channels from heterozygous R163C malignant hyperthermia-susceptible mice.
Feng W; Barrientos GC; Cherednichenko G; Yang T; Padilla IT; Truong K; Allen PD; Lopez JR; Pessah IN
Mol Pharmacol; 2011 Mar; 79(3):420-31. PubMed ID: 21156754
[TBL] [Abstract][Full Text] [Related]
10. Multiple regions of RyR1 mediate functional and structural interactions with alpha(1S)-dihydropyridine receptors in skeletal muscle.
Protasi F; Paolini C; Nakai J; Beam KG; Franzini-Armstrong C; Allen PD
Biophys J; 2002 Dec; 83(6):3230-44. PubMed ID: 12496092
[TBL] [Abstract][Full Text] [Related]
11. Ca2+ current and charge movements in skeletal myotubes promoted by the beta-subunit of the dihydropyridine receptor in the absence of ryanodine receptor type 1.
Ahern CA; Sheridan DC; Cheng W; Mortenson L; Nataraj P; Allen P; De Waard M; Coronado R
Biophys J; 2003 Feb; 84(2 Pt 1):942-59. PubMed ID: 12547776
[TBL] [Abstract][Full Text] [Related]
12. Junctional trafficking and restoration of retrograde signaling by the cytoplasmic RyR1 domain.
Polster A; Perni S; Filipova D; Moua O; Ohrtman JD; Bichraoui H; Beam KG; Papadopoulos S
J Gen Physiol; 2018 Feb; 150(2):293-306. PubMed ID: 29284662
[TBL] [Abstract][Full Text] [Related]
13. Gene dose influences cellular and calcium channel dysregulation in heterozygous and homozygous T4826I-RYR1 malignant hyperthermia-susceptible muscle.
Barrientos GC; Feng W; Truong K; Matthaei KI; Yang T; Allen PD; Lopez JR; Pessah IN
J Biol Chem; 2012 Jan; 287(4):2863-76. PubMed ID: 22139840
[TBL] [Abstract][Full Text] [Related]
14. Triad proteins and intracellular Ca2+ transients during development of human skeletal muscle cells in aneural and innervated cultures.
Tanaka H; Furuya T; Kameda N; Kobayashi T; Mizusawa H
J Muscle Res Cell Motil; 2000; 21(6):507-26. PubMed ID: 11206130
[TBL] [Abstract][Full Text] [Related]
15. Conformational coupling of DHPR and RyR1 in skeletal myotubes is influenced by long-range allosterism: evidence for a negative regulatory module.
Lee EH; Lopez JR; Li J; Protasi F; Pessah IN; Kim DH; Allen PD
Am J Physiol Cell Physiol; 2004 Jan; 286(1):C179-89. PubMed ID: 13679303
[TBL] [Abstract][Full Text] [Related]
16. Expression levels of RyR1 and RyR3 control resting free Ca2+ in skeletal muscle.
Perez CF; López JR; Allen PD
Am J Physiol Cell Physiol; 2005 Mar; 288(3):C640-9. PubMed ID: 15548569
[TBL] [Abstract][Full Text] [Related]
17. A central core disease mutation in the Ca
Chirasani VR; Xu L; Addis HG; Pasek DA; Dokholyan NV; Meissner G; Yamaguchi N
Am J Physiol Cell Physiol; 2019 Aug; 317(2):C358-C365. PubMed ID: 31166712
[TBL] [Abstract][Full Text] [Related]
18. Ryanodine receptor type 1 (RyR1) mutations C4958S and C4961S reveal excitation-coupled calcium entry (ECCE) is independent of sarcoplasmic reticulum store depletion.
Hurne AM; O'Brien JJ; Wingrove D; Cherednichenko G; Allen PD; Beam KG; Pessah IN
J Biol Chem; 2005 Nov; 280(44):36994-7004. PubMed ID: 16120606
[TBL] [Abstract][Full Text] [Related]
19. Effects of conformational peptide probe DP4 on bidirectional signaling between DHPR and RyR1 calcium channels in voltage-clamped skeletal muscle fibers.
Olojo RO; Hernández-Ochoa EO; Ikemoto N; Schneider MF
Biophys J; 2011 May; 100(10):2367-77. PubMed ID: 21575570
[TBL] [Abstract][Full Text] [Related]
20. Orthograde dihydropyridine receptor signal regulates ryanodine receptor passive leak.
Eltit JM; Li H; Ward CW; Molinski T; Pessah IN; Allen PD; Lopez JR
Proc Natl Acad Sci U S A; 2011 Apr; 108(17):7046-51. PubMed ID: 21482776
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
