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1 CACNL1A3, encoding the alpha-subunit of the dihydropyridine receptor.
2 ures from which emerge tubes enriched in the dihydropyridine receptor.
3 il of the voltage sensor of EC coupling, the dihydropyridine receptor.
4 lpha) subunit, and the alpha2 subunit of the dihydropyridine receptor.
5 d because RyR1s are under the control of the dihydropyridine receptor.
6 presence of a normal pattern of triadin and dihydropyridine receptor.
7 g embryos lacking the alpha1S subunit of the dihydropyridine receptor.
8 he II-III loop of the alpha 1 subunit of the dihydropyridine receptor.
9 d by the localization of actin filaments and dihydropyridine receptors.
10 l coupling with the t-tubule voltage-sensing dihydropyridine receptors.
11 (endo)plasmic reticulum calcium-ATPase1, and dihydropyridine receptors.
13 ng various regions of the II-III loop of the dihydropyridine receptor alpha 1 subunit, only one pepti
14 90 of the II-III loop of the skeletal muscle dihydropyridine receptor alpha(1) subunit (DHPR, alpha(1
16 Glu(724)-Pro(760) (peptide C) region of the dihydropyridine receptor alpha1 II-III loop is important
20 nsgenic variants of the alpha subunit of the dihydropyridine receptor (alpha1sDHPR) resulted in appro
21 The alpha2/delta1 subunit forms part of the dihydropyridine receptor, an essential protein complex f
22 peptide (termed peptide A (pA)) of alpha(1s)-dihydropyridine receptor and are thought to act at a com
23 a functional linkage between the sarcolemmal dihydropyridine receptor and the SR ryanodine receptor.
25 interactions with the L-type Ca(2+) channel (dihydropyridine receptor) and FK506-binding protein 12 a
26 n Ca2+ sparks is mediated by the sarcolemmal dihydropyridine receptor but is also independent of Ca2+
28 may be vital for the targeting of the muscle dihydropyridine receptor complex to the transverse tubul
29 king of CaV1.1, the principal subunit of the dihydropyridine receptor (DHPR) (L-type Ca(2+) channel),
30 (mdg/mdg), a mutation of the skeletal muscle dihydropyridine receptor (DHPR) alpha 1 subunit, has ser
31 reases the expression of the skeletal muscle dihydropyridine receptor (DHPR) alpha(1) subunit by regu
32 -III cytoplasmic loop of the skeletal muscle dihydropyridine receptor (DHPR) alpha(1)-subunit is esse
33 been described in the cytosolic loops of the dihydropyridine receptor (DHPR) alpha1S pore subunit and
34 FRU) in rat cardiac muscle consisting of one dihydropyridine receptor (DHPR) and eight ryanodine rece
36 er-channel signaling between the sarcolemmal dihydropyridine receptor (DHPR) and the ryanodine recept
37 on between the voltage-gated calcium channel dihydropyridine receptor (DHPR) and the ryanodine recept
38 In skeletal muscle, coupling between the 1,4-dihydropyridine receptor (DHPR) and the type 1 ryanodine
39 involves conformational coupling between the dihydropyridine receptor (DHPR) and the type 1 ryanodine
40 in EC coupling mode are not due to shifts in dihydropyridine receptor (DHPR) and/or ryanodine recepto
41 ockout cells lacking the beta subunit of the dihydropyridine receptor (DHPR) are devoid of slow L-typ
42 imeras consisting of the homologous skeletal dihydropyridine receptor (DHPR) beta1a subunit and the h
45 t of myotubes from mice lacking the skeletal dihydropyridine receptor (DHPR) beta1a subunit, was inve
47 1a subunit is a cytoplasmic component of the dihydropyridine receptor (DHPR) complex that plays an es
49 de (KKERKLARTA) is a fragment of the cardiac dihydropyridine receptor (DHPR) from the cytosolic loop
52 between ryanodine receptor type 1 (RyR1) and dihydropyridine receptor (DHPR) in skeletal muscle serve
55 ests that the cytoplasmic II-III loop of the dihydropyridine receptor (DHPR) is the primary source of
58 revious studies have shown that the skeletal dihydropyridine receptor (DHPR) pore subunit Ca(V)1.1 (a
59 region of the beta1a subunit of the skeletal dihydropyridine receptor (DHPR) to the mechanism of exci
60 ation then dissociates them from the tubular dihydropyridine receptor (DHPR) voltage sensors that pro
61 oupling, the four-domain pore subunit of the dihydropyridine receptor (DHPR) was cut in the cytoplasm
62 ceptor 1 and dysgenic myotubes that lack the dihydropyridine receptor (DHPR), and is independent of t
63 d TBBPA on ryanodine receptor type 1 (RyR1), dihydropyridine receptor (DHPR), and sarcoplasmic/endopl
64 s with key modulators - proteins such as the dihydropyridine receptor (DHPR), FKBP12/12.6, and calmod
65 between the ryanodine receptor (RyR) and the dihydropyridine receptor (DHPR), two proteins essential
66 e CICR cascade by increasing the fidelity of dihydropyridine receptor (DHPR)--ryanodine receptor (RyR
69 We found that a functional skeletal muscle dihydropyridine receptor (DHPR, the L-type Ca(2+) channe
70 ticulum Ca(2+) release channel) and alpha(1S)dihydropyridine receptor (DHPR, the surface membrane vol
71 traction coupling involves the activation of dihydropyridine receptors (DHPR) and type-1 ryanodine re
75 tage-gated L-type calcium channel (Ca(v)1.1; dihydropyridine receptor, DHPR) was determined using ele
76 ) essential for bidirectional signaling with dihydropyridine receptors (DHPRs) and for the organizati
77 in muscle relies on the interaction between dihydropyridine receptors (DHPRs) and RyRs within Ca(2+)
78 Rs): those at the periphery colocalized with dihydropyridine receptors (DHPRs) and those at the cell
79 c calcium release units, dCRUs) that contain dihydropyridine receptors (DHPRs) and triadin, two essen
81 cle involves conformational coupling between dihydropyridine receptors (DHPRs) in the plasma membrane
82 quires communication between voltage-sensing dihydropyridine receptors (DHPRs) in transverse tubule m
83 tly targeted to junctions and interacts with dihydropyridine receptors (DHPRs) inducing their arrange
84 d by 2 well-identified calcium channels: the dihydropyridine receptors (DHPRs) that act as voltage se
85 echnique and expression of truncated/mutated dihydropyridine receptors (DHPRs) to investigate whether
86 ontrol: plasma membrane calcium channels, or dihydropyridine receptors (DHPRs), and SR calcium releas
87 Rs): those at the periphery colocalized with dihydropyridine receptors (DHPRs), and those at the cell
88 pective roles of ryanodine receptors (RyRs), dihydropyridine receptors (DHPRs), inositol-1,4,5-trisph
89 tain two proteins essential to e-c coupling: dihydropyridine receptors (DHPRs), L-type Ca(2+) channel
90 Rs), or SR calcium release channels, and the dihydropyridine receptors (DHPRs), or L-type calcium cha
94 Coupling between L-type Ca(2+) channels (dihydropyridine receptors, DHPRs) and ryanodine receptor
95 skeletal muscle, L-type calcium channels (or dihydropyridine receptors, DHPRs) are coupled functional
96 ) and the surface membrane calcium channels (dihydropyridine receptors, DHPRs) in myocardium from the
97 action of surface membrane calcium channels (dihydropyridine receptors; DHPRs) with the calcium relea
99 , and possibly in RyR's interaction with the dihydropyridine receptor in excitation-contraction coupl
100 n of the skeletal muscle L-type Ca2+ channel/dihydropyridine receptor in response to insulin-like gro
102 and Ca(2+)-CaM at a critical region for RYR1-dihydropyridine receptor interaction are suggestive of a
104 , including alpha-actinin, the Ca-ATPase and dihydropyridine receptors, is not affected, even at site
105 An allosteric interaction between RyR1 and dihydropyridine receptors located in the plasma membrane
106 line receptors, whereas relaxed mutants lack dihydropyridine receptor-mediated release of internal ca
108 ons or junctions), where the voltage-sensing dihydropyridine receptor of the surface membrane interac
109 evels or in SERCA2b (smooth muscle isoform), dihydropyridine receptor, or alpha-actin mRNA levels in
110 Understanding which cytosolic domains of the dihydropyridine receptor participate in excitation-contr
111 lcium channels to be cloned, skeletal muscle dihydropyridine receptors remain the only ones not funct
112 the L-type voltage-gated Ca(2+) channel (1,4-dihydropyridine receptor) serves as the voltage sensor f
113 S6 and IVS6 interact to form a high affinity dihydropyridine receptor site on L-type Ca2+ channels.
115 Thus, we conclude that the alpha(2)delta(1) dihydropyridine receptor subunit is physiologically nece
116 A) partial knockdown of the alpha(2)delta(1) dihydropyridine receptor subunits cause a significant in
117 nd III of the alpha1 subunit of the skeletal dihydropyridine receptor (the II-III loop) interacts wit
118 well as Ca(2+)-dependent regulation via the dihydropyridine receptor, the ryanodine receptor, and tr
119 2/delta, beta 1, and gamma) skeletal muscle dihydropyridine receptor transduces transverse tubule me
120 diment with membrane vesicles containing the dihydropyridine receptor, which is consistent with earli