A two-motif isoform of the major calcium channel subunit in skeletal muscle

[1]  P. Ellinor,et al.  Molecular cloning of multiple subtypes of a novel rat brain isoform of the α 1 subunit of the voltage-dependent calcium channel , 1991, Neuron.

[2]  R. MacKinnon.  Determination of the subunit stoichiometry of a voltage-activated potassium channel , 1991, Nature.

[3]  R. MacKinnon,et al.  Mutations affecting internal TEA blockade identify the probable pore-forming region of a K+ channel , 1991, Science.

[4]  A. Brown,et al.  Exchange of conduction pathways between two related K+ channels , 1991, Science.

[5]  C. Stevens.  Making a submicroscopic hole in one , 1991, Nature.

[6]  T. Schwarz,et al.  Alteration of ionic selectivity of a K+ channel by mutation of the H5 region , 1991, Nature.

[7]  B. Flucher,et al.  Localization of the α 1 and α 2 subunits of the dihydropyridine receptor and ankyrin in skeletal muscle triads , 1990, Neuron.

[8]  B. Adams,et al.  Regions of the skeletal muscle dihydropyridine receptor critical for excitation–contraction coupling , 1990, Nature.

[9]  Richard W. Aldrich,et al.  Mixing and matching , 1990, Nature.

[10]  Yuh Nung Jan,et al.  Evidence for the formation of heteromultimeric potassium channels in Xenopus oocytes , 1990, Nature.

[11]  B. Sakmann,et al.  Heteromultimeric channels formed by rat brain potassium-channel proteins , 1990, Nature.

[12]  R. North,et al.  Heteropolymeric potassium channels expressed in xenopus oocytes from cloned subunits , 1990, Neuron.

[13]  S. Narumiya,et al.  Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channel , 1989, Nature.

[14]  F. Conti,et al.  Structural parts involved in activation and inactivation of the sodium channel , 1989, Nature.

[15]  H. Takeshima,et al.  Primary structure and expression from complementary DNA of skeletal muscle ryanodine receptor , 1989, Nature.

[16]  K. Campbell,et al.  Structural evidence for direct interaction between the molecular components of the transverse tubule/sarcoplasmic reticulum junction in skeletal muscle , 1988, The Journal of cell biology.

[17]  W. Catterall,et al.  Structure and function of voltage-sensitive ion channels. , 1988, Science.

[18]  K. Campbell,et al.  Sequence and expression of MRNAs encoding the α1 and α2 subunits of a DHP-sensitive calcium channel , 1988 .

[19]  W. Huse,et al.  Lambda ZAP: a bacteriophage lambda expression vector with in vivo excision properties. , 1988, Nucleic acids research.

[20]  J. Tam,et al.  Synthetic peptide vaccine design: synthesis and properties of a high-density multiple antigenic peptide system. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[21]  J. Tam,et al.  Antibody specific to the alpha subunit of the guanine nucleotide-binding regulatory protein Go: developmental appearance and immunocytochemical localization in brain. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[22]  S. Hasegawa,et al.  Post‐natal disappearance of transient calcium channels in mouse skeletal muscle: effects of denervation and culture. , 1988, The Journal of physiology.

[23]  C. Knudson,et al.  Effect of postnatal development on calcium currents and slow charge movement in mammalian skeletal muscle , 1988, The Journal of general physiology.

[24]  R. Gibbs,et al.  Generation of cDNA probes directed by amino acid sequence: cloning of urate oxidase. , 1988, Science.

[25]  J. Frelinger,et al.  A simple, rapid method for the purification of poly A+ RNA. , 1988, BioTechniques.

[26]  K. Mullis,et al.  Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. , 1988, Science.

[27]  Harold P. Erickson,et al.  Purification and reconstitution of the calcium release channel from skeletal muscle , 1988, Nature.

[28]  A. Brown,et al.  Monoclonal antibody to the alpha 1-subunit of the dihydropyridine-binding complex inhibits calcium currents in BC3H1 myocytes. , 1988, The Journal of biological chemistry.

[29]  K. Campbell,et al.  Purified ryanodine receptor from skeletal muscle sarcoplasmic reticulum is the Ca2+-permeable pore of the calcium release channel. , 1987, The Journal of biological chemistry.

[30]  S. Froehner,et al.  Monoclonal antibody identifies a 200-kDa subunit of the dihydropyridine-sensitive calcium channel. , 1987, The Journal of biological chemistry.

[31]  V. Flockerzi,et al.  Primary structure of the receptor for calcium channel blockers from skeletal muscle , 1987, Nature.

[32]  G. Meissner,et al.  Monoclonal antibody specific for the transverse tubular membrane of skeletal muscle activates the dihydropyridine-sensitive Ca2+ channel. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[33]  K. Campbell,et al.  Structural characterization of the 1,4-dihydropyridine receptor of the voltage-dependent Ca2+ channel from rabbit skeletal muscle. Evidence for two distinct high molecular weight subunits. , 1987, The Journal of biological chemistry.

[34]  E. Ríos,et al.  Involvement of dihydropyridine receptors in excitation–contraction coupling in skeletal muscle , 1987, Nature.

[35]  S. Fleischer,et al.  Purification of the ryanodine receptor and identity with feet structures of junctional terminal cisternae of sarcoplasmic reticulum from fast skeletal muscle. , 1987, The Journal of biological chemistry.

[36]  F. Hofmann,et al.  Purified dihydropyridine-binding site from skeletal muscle t-tubules is a functional calcium channel , 1986, Nature.

[37]  P. E. Wilson,et al.  Monoclonal antibody specific for the T-tubule of skeletal muscle. , 1986, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[38]  M. Lazdunski,et al.  Solubilization of the nitrendipine receptor from skeletal muscle transverse tubule membranes. Interactions with specific inhibitors of the voltage-dependent Ca2+ channel. , 1984, European journal of biochemistry.

[39]  W. Almers,et al.  Calcium depletion in frog muscle tubules: the decline of calcium current under maintained depolarization. , 1981, The Journal of physiology.

[40]  E. Stefani,et al.  Inward calcium current in twitch muscle fibres of the frog. , 1978, The Journal of physiology.

[41]  W. Chandler,et al.  Voltage Dependent Charge Movement in Skeletal Muscle: a Possible Step in Excitation–Contraction Coupling , 1973, Nature.

[42]  S. Schiaffino,et al.  COORDINATED DEVELOPMENT OF THE SARCOPLASMIC RETICULUM AND T SYSTEM DURING POSTNATAL DIFFERENTIATION OF RAT SKELETAL MUSCLE , 1969, The Journal of cell biology.

[43]  B. Nadal-Ginard,et al.  Generation of protein isoform diversity by alternative splicing: mechanistic and biological implications. , 1987, Annual review of cell biology.

[44]  C. Ragan,et al.  Techniques for the Analysis of Membrane Proteins , 1986 .