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1 mSTRPC4 therefore probably functions as a heteromultimer.
2 methylene ATP-sensitive receptor is a P2X2/3 heteromultimer.
3 t one form of VirB11 functions as a homo- or heteromultimer.
4 trate that TRPMLs interact to form homo- and heteromultimers.
5 dulation of heterologously expressed KCNQ2/3 heteromultimers.
6 nd whether they function as homomultimers or heteromultimers.
7 ting from the loss of expression of P2X(2/3) heteromultimers.
8 odulin, suggesting that functional CaCCs are heteromultimers.
9 d K+ channel subfamilies usually do not form heteromultimers.
10 TraR function, probably by forming inactive heteromultimers.
11 d by a combination of TRP homo- and TRP-TRPL heteromultimers.
12 er more abundant subunits into CaM kinase II heteromultimers.
13 d-gated cation channels, as homomultimers or heteromultimers.
14 as wvGIRK2 homomultimers or as GIRK1-wvGIRK2 heteromultimers.
15 th in heart and brain, appear to function as heteromultimers.
17 ry (CHO) cells expressing cloned Kv7.2 + 7.3 heteromultimers and AT1 receptors studied under perforat
19 data demonstrate that TRIM5 orthologues form heteromultimers and indicate that C-terminal extensions
21 NQ3, KCNQ4, and KCNQ5 homomultimers, KCNQ2/3 heteromultimers and native M current, but not currents f
23 algamma1 forms functional channels only as a heteromultimer, and jShalgamma1 + jShal1 heteromultimers
24 s a heteromultimer, and jShalgamma1 + jShal1 heteromultimers are functional only in a 2:2 subunit sto
25 n HEK293T cells, they form homomultimers and heteromultimers, as shown by coimmunoprecipitation and i
27 yme of bacteriophage lambda, terminase, is a heteromultimer composed of a small subunit, gpNu1, and a
28 The epithelial sodium channel (ENaC) is a heteromultimer composed of three subunits, each having t
29 ltage-dependent calcium channels (VDCCs) are heteromultimers composed of a pore-forming alpha1 subuni
30 e, suggesting that GABAB receptors couple to heteromultimers composed of GIRK1 and GIRK2 channel subu
31 (BKi current), the BKi channels are largely heteromultimers composed of inactivation-competent subun
39 ly active, we demonstrate that TRPL-TRPgamma heteromultimers form a regulated phospholipase C- (PLC-)
43 Ca(2+) (LRC) channels encoded by Orai1/Orai3 heteromultimers in vascular smooth muscle cells (VSMCs).
44 We investigated whether Shaker and eag form heteromultimers in Xenopus laevis oocytes using electrop
48 in two translational start codons encoding a heteromultimer of approximately 160 to 170 kDa and havin
51 packaging enzyme of bacteriophage chi, is a heteromultimer of gpNul (21 kDa) and gpA (74 kDa) subuni
54 ed by energy-harvesting complexes, which are heteromultimers of cytoplasmic membrane proteins with ho
55 ted and basally active Na+ currents, whereas heteromultimers of GIRK2 weaver and GIRK1 appeared to ha
57 ium (KATP) channels in striated myocytes are heteromultimers of KIR6.2, a weak potassium inward recti
59 ive potassium channels (K(ATP) channels) are heteromultimers of sulfonylurea receptors (SUR) and inwa
61 ection of Q2S with either Q2L, Q3, or Q2L/Q3 heteromultimers results in attenuation of K(+) current,
63 cise MS analysis of the intact four-chain Ab heteromultimer reveals nonspecific, non-enzymatic reacti
64 ASIC2a homomultimeric channels nor ASIC1a/2a heteromultimers showed H(+)-activated [Ca(2+)](c) elevat
65 n and synaptophysin are present in homo- and heteromultimers, suggesting that a large fraction of the
66 lypeptide in the dynactin complex, a protein heteromultimer that binds to and may mediate the microtu
67 horylate adjacent subunits in the Kv channel heteromultimer that lack proline-rich SH3 domain ligand
68 ifferent Ca2+-binding affinities can lead to heteromultimers that can regulate the efficiency of exci
70 two or more DEG/ENaC subunits coassemble as heteromultimers to generate transient H(+)-gated current
73 f Kv7.2-Kv7.4 homomultimers and of Kv7.2/7.3 heteromultimers were found to be strongly dependent on t
75 kely to be mediated by Kv1.5-containing homo/heteromultimers, while I(Kv2) involves a Kv2.1 alpha-sub
76 related channel subunit, TRP-like, to form a heteromultimer with conductance characteristics distinct
78 BEC3F in various human tissues and it formed heteromultimers with APOBEC3F or APOBEC3G in the cell.
79 Box or the C-terminal B30.2/SPRY domain form heteromultimers with full-length huTRIM5alpha and are do
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