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Kurt G Beam Jr.

TitleProfessor
InstitutionUniversity of Colorado Denver - Anschutz Medical Campus
DepartmentSOM - Physiology
Phone3037244542

     Bibliographic 
     selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Polster A, Nelson BR, Olson EN, Beam KG. Stac3 has a direct role in skeletal muscle-type excitation-contraction coupling that is disrupted by a myopathy-causing mutation. Proc Natl Acad Sci U S A. 2016 Sep 27; 113(39):10986-91.
      View in: PubMed
    2. Bannister RA, Sheridan DC, Beam KG. Distinct Components of Retrograde Ca(V)1.1-RyR1 Coupling Revealed by a Lethal Mutation in RyR1. Biophys J. 2016 Feb 23; 110(4):912-21.
      View in: PubMed
    3. Ohrtman JD, Romberg CF, Moua O, Bannister RA, Levinson SR, Beam KG. Apparent lack of physical or functional interaction between CaV1.1 and its distal C terminus. J Gen Physiol. 2015 Apr; 145(4):303-14.
      View in: PubMed
    4. Polster A, Perni S, Bichraoui H, Beam KG. Stac adaptor proteins regulate trafficking and function of muscle and neuronal L-type Ca2+ channels. Proc Natl Acad Sci U S A. 2015 Jan 13; 112(2):602-6.
      View in: PubMed
    5. Bannister RA, Beam KG. Impaired gating of an L-Type Ca(2+) channel carrying a mutation linked to malignant hyperthermia. Biophys J. 2013 May 07; 104(9):1917-22.
      View in: PubMed
    6. Szpyt J, Lorenzon N, Perez CF, Norris E, Allen PD, Beam KG, Samsó M. Three-dimensional localization of the a and ß subunits and of the II-III loop in the skeletal muscle L-type Ca2+ channel. J Biol Chem. 2012 Dec 21; 287(52):43853-61.
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    7. Polster A, Ohrtman JD, Beam KG, Papadopoulos S. Fluorescence resonance energy transfer (FRET) indicates that association with the type I ryanodine receptor (RyR1) causes reorientation of multiple cytoplasmic domains of the dihydropyridine receptor (DHPR) a(1S) subunit. J Biol Chem. 2012 Nov 30; 287(49):41560-8.
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    8. Bannister RA, Beam KG. Ca(V)1.1: The atypical prototypical voltage-gated Ca²? channel. Biochim Biophys Acta. 2013 Jul; 1828(7):1587-97.
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    9. Cherednichenko G, Zhang R, Bannister RA, Timofeyev V, Li N, Fritsch EB, Feng W, Barrientos GC, Schebb NH, Hammock BD, Beam KG, Chiamvimonvat N, Pessah IN. Triclosan impairs excitation-contraction coupling and Ca2+ dynamics in striated muscle. Proc Natl Acad Sci U S A. 2012 Aug 28; 109(35):14158-63.
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    10. Eltit JM, Bannister RA, Moua O, Altamirano F, Hopkins PM, Pessah IN, Molinski TF, López JR, Beam KG, Allen PD. Malignant hyperthermia susceptibility arising from altered resting coupling between the skeletal muscle L-type Ca2+ channel and the type 1 ryanodine receptor. Proc Natl Acad Sci U S A. 2012 May 15; 109(20):7923-8.
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    11. Sheridan DC, Moua O, Lorenzon NM, Beam KG. Bimolecular fluorescence complementation and targeted biotinylation provide insight into the topology of the skeletal muscle Ca ( 2+) channel ß1a subunit. Channels (Austin). 2012 Jan-Feb; 6(1):26-40.
      View in: PubMed
    12. Bannister RA, Beam KG. Properties of Na+ currents conducted by a skeletal muscle L-type Ca2+ channel pore mutant (SkEIIIK). Channels (Austin). 2011 May-Jun; 5(3):262-8.
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    13. Beam KG, Bannister RA. Looking for answers to EC coupling's persistent questions. J Gen Physiol. 2010 Jul; 136(1):7-12.
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    14. Bannister RA, Estève E, Eltit JM, Pessah IN, Allen PD, López JR, Beam KG. A malignant hyperthermia-inducing mutation in RYR1 (R163C): consequent alterations in the functional properties of DHPR channels. J Gen Physiol. 2010 Jun; 135(6):629-40.
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    15. Estève E, Eltit JM, Bannister RA, Liu K, Pessah IN, Beam KG, Allen PD, López JR. A malignant hyperthermia-inducing mutation in RYR1 (R163C): alterations in Ca2+ entry, release, and retrograde signaling to the DHPR. J Gen Physiol. 2010 Jun; 135(6):619-28.
      View in: PubMed
    16. Bannister RA, Beam KG. Ryanodine modification of RyR1 retrogradely affects L-type Ca(2+) channel gating in skeletal muscle. J Muscle Res Cell Motil. 2009; 30(5-6):217-23.
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    17. Bannister RA, Beam KG. The cardiac alpha(1C) subunit can support excitation-triggered Ca2+ entry in dysgenic and dyspedic myotubes. Channels (Austin). 2009 Jul-Aug; 3(4):268-73.
      View in: PubMed
    18. Bannister RA, Papadopoulos S, Haarmann CS, Beam KG. Effects of inserting fluorescent proteins into the alpha1S II-III loop: insights into excitation-contraction coupling. J Gen Physiol. 2009 Jul; 134(1):35-51.
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    19. Bannister RA, Pessah IN, Beam KG. The skeletal L-type Ca(2+) current is a major contributor to excitation-coupled Ca(2+) entry. J Gen Physiol. 2009 Jan; 133(1):79-91.
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    20. Ohrtman J, Ritter B, Polster A, Beam KG, Papadopoulos S. Sequence differences in the IQ motifs of CaV1.1 and CaV1.2 strongly impact calmodulin binding and calcium-dependent inactivation. J Biol Chem. 2008 Oct 24; 283(43):29301-11.
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    21. Bannister RA, Grabner M, Beam KG. The alpha(1S) III-IV loop influences 1,4-dihydropyridine receptor gating but is not directly involved in excitation-contraction coupling interactions with the type 1 ryanodine receptor. J Biol Chem. 2008 Aug 22; 283(34):23217-23.
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    22. Lorenzon NM, Beam KG. Disease causing mutations of calcium channels. Channels (Austin). 2008 May-Jun; 2(3):163-79.
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    23. Bannister RA, Colecraft HM, Beam KG. Rem inhibits skeletal muscle EC coupling by reducing the number of functional L-type Ca2+ channels. Biophys J. 2008 Apr 01; 94(7):2631-8.
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    24. Gach MP, Cherednichenko G, Haarmann C, Lopez JR, Beam KG, Pessah IN, Franzini-Armstrong C, Allen PD. Alpha2delta1 dihydropyridine receptor subunit is a critical element for excitation-coupled calcium entry but not for formation of tetrads in skeletal myotubes. Biophys J. 2008 Apr 15; 94(8):3023-34.
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    25. Lorenzon NM, Beam KG. Accessibility of targeted DHPR sites to streptavidin and functional effects of binding on EC coupling. J Gen Physiol. 2007 Oct; 130(4):379-88.
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    26. Sheridan DC, Takekura H, Franzini-Armstrong C, Beam KG, Allen PD, Perez CF. Bidirectional signaling between calcium channels of skeletal muscle requires multiple direct and indirect interactions. Proc Natl Acad Sci U S A. 2006 Dec 26; 103(52):19760-5.
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    27. Leuranguer V, Papadopoulos S, Beam KG. Organization of calcium channel beta1a subunits in triad junctions in skeletal muscle. J Biol Chem. 2006 Feb 10; 281(6):3521-7.
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    28. Bannister RA, Beam KG. The alpha1S N-terminus is not essential for bi-directional coupling with RyR1. Biochem Biophys Res Commun. 2005 Oct 14; 336(1):134-41.
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    29. Hurne AM, O'Brien JJ, Wingrove D, Cherednichenko G, Allen PD, Beam KG, Pessah IN. Ryanodine receptor type 1 (RyR1) mutations C4958S and C4961S reveal excitation-coupled calcium entry (ECCE) is independent of sarcoplasmic reticulum store depletion. J Biol Chem. 2005 Nov 04; 280(44):36994-7004.
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    30. Cherednichenko G, Hurne AM, Fessenden JD, Lee EH, Allen PD, Beam KG, Pessah IN. Conformational activation of Ca2+ entry by depolarization of skeletal myotubes. Proc Natl Acad Sci U S A. 2004 Nov 02; 101(44):15793-8.
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    31. Lorenzon NM, Haarmann CS, Norris EE, Papadopoulos S, Beam KG. Metabolic biotinylation as a probe of supramolecular structure of the triad junction in skeletal muscle. J Biol Chem. 2004 Oct 15; 279(42):44057-64.
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    32. Papadopoulos S, Leuranguer V, Bannister RA, Beam KG. Mapping sites of potential proximity between the dihydropyridine receptor and RyR1 in muscle using a cyan fluorescent protein-yellow fluorescent protein tandem as a fluorescence resonance energy transfer probe. J Biol Chem. 2004 Oct 15; 279(42):44046-56.
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    33. Leuranguer V, Dirksen RT, Beam KG. Potentiated L-type Ca2+ channels rectify. J Gen Physiol. 2003 Jun; 121(6):541-50.
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    34. Wilkens CM, Beam KG. Insertion of alpha1S II-III loop and C terminal sequences into alpha1H fails to restore excitation-contraction coupling in dysgenic myotubes. J Muscle Res Cell Motil. 2003; 24(1):99-109.
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    35. Protasi F, Paolini C, Nakai J, Beam KG, Franzini-Armstrong C, Allen PD. Multiple regions of RyR1 mediate functional and structural interactions with alpha(1S)-dihydropyridine receptors in skeletal muscle. Biophys J. 2002 Dec; 83(6):3230-44.
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    36. O'Brien JJ, Feng W, Allen PD, Chen SR, Pessah IN, Beam KG. Ca2+ activation of RyR1 is not necessary for the initiation of skeletal-type excitation-contraction coupling. Biophys J. 2002 May; 82(5):2428-35.
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    37. Proenza C, O'Brien J, Nakai J, Mukherjee S, Allen PD, Beam KG. Identification of a region of RyR1 that participates in allosteric coupling with the alpha(1S) (Ca(V)1.1) II-III loop. J Biol Chem. 2002 Feb 22; 277(8):6530-5.
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    38. Wilkens CM, Grabner M, Beam KG. Potentiation of the cardiac L-type Ca(2+) channel (alpha(1C)) by dihydropyridine agonist and strong depolarization occur via distinct mechanisms. J Gen Physiol. 2001 Nov; 118(5):495-508.
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    39. Stroffekova K, Proenza C, Beam KG. The protein-labeling reagent FLASH-EDT2 binds not only to CCXXCC motifs but also non-specifically to endogenous cysteine-rich proteins. Pflugers Arch. 2001 Sep; 442(6):859-66.
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    40. Wilkens CM, Kasielke N, Flucher BE, Beam KG, Grabner M. Excitation-contraction coupling is unaffected by drastic alteration of the sequence surrounding residues L720-L764 of the alpha 1S II-III loop. Proc Natl Acad Sci U S A. 2001 May 08; 98(10):5892-7.
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    41. Lorenzon NM, Grabner M, Suda N, Beam KG. Structure and targeting of RyR1: implications from fusion of green fluorescent protein at the amino-terminal. Arch Biochem Biophys. 2001 Apr 01; 388(1):13-7.
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    42. Proenza C, Wilkens CM, Beam KG. Excitation-contraction coupling is not affected by scrambled sequence in residues 681-690 of the dihydropyridine receptor II-III loop. J Biol Chem. 2000 Sep 29; 275(39):29935-7.
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    43. Proenza C, Wilkens C, Lorenzon NM, Beam KG. A carboxyl-terminal region important for the expression and targeting of the skeletal muscle dihydropyridine receptor. J Biol Chem. 2000 Jul 28; 275(30):23169-74.
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    44. Suda N, Dirksen RT, Gonzalez A, Beam KG. Low serum promotes maturation of excitation-contraction coupling in myotubes. Pflugers Arch. 2000 Mar; 439(5):555-8.
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    45. Lorenzon NM, Beam KG. Calcium channelopathies. Kidney Int. 2000 Mar; 57(3):794-802.
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    46. Pan F, Beam KG. The absence of resurgent sodium current in mouse spinal neurons. Brain Res. 1999 Dec 04; 849(1-2):162-8.
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    47. Dirksen RT, Beam KG. Role of calcium permeation in dihydropyridine receptor function. Insights into channel gating and excitation-contraction coupling. J Gen Physiol. 1999 Sep; 114(3):393-403.
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    48. Grabner M, Dirksen RT, Suda N, Beam KG. The II-III loop of the skeletal muscle dihydropyridine receptor is responsible for the Bi-directional coupling with the ryanodine receptor. J Biol Chem. 1999 Jul 30; 274(31):21913-9.
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    49. Beam K. Calcium channel splicing: mind your Ps and Qs. Nat Neurosci. 1999 May; 2(5):393-4.
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    50. Nakai J, Tanabe T, Konno T, Adams B, Beam KG. Localization in the II-III loop of the dihydropyridine receptor of a sequence critical for excitation-contraction coupling. J Biol Chem. 1998 Sep 25; 273(39):24983-6.
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    51. García KD, Sprunger LK, Meisler MH, Beam KG. The sodium channel Scn8a is the major contributor to the postnatal developmental increase of sodium current density in spinal motoneurons. J Neurosci. 1998 Jul 15; 18(14):5234-9.
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    52. Lorenzon NM, Lutz CM, Frankel WN, Beam KG. Altered calcium channel currents in Purkinje cells of the neurological mutant mouse leaner. J Neurosci. 1998 Jun 15; 18(12):4482-9.
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    53. Nakai J, Sekiguchi N, Rando TA, Allen PD, Beam KG. Two regions of the ryanodine receptor involved in coupling with L-type Ca2+ channels. J Biol Chem. 1998 May 29; 273(22):13403-6.
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    54. Grabner M, Dirksen RT, Beam KG. Tagging with green fluorescent protein reveals a distinct subcellular distribution of L-type and non-L-type Ca2+ channels expressed in dysgenic myotubes. Proc Natl Acad Sci U S A. 1998 Feb 17; 95(4):1903-8.
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    55. Dirksen RT, Nakai J, Gonzalez A, Imoto K, Beam KG. The S5-S6 linker of repeat I is a critical determinant of L-type Ca2+ channel conductance. Biophys J. 1997 Sep; 73(3):1402-9.
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    56. García J, Nakai J, Imoto K, Beam KG. Role of S4 segments and the leucine heptad motif in the activation of an L-type calcium channel. Biophys J. 1997 Jun; 72(6):2515-23.
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    57. Nakai J, Ogura T, Protasi F, Franzini-Armstrong C, Allen PD, Beam KG. Functional nonequality of the cardiac and skeletal ryanodine receptors. Proc Natl Acad Sci U S A. 1997 Feb 04; 94(3):1019-22.
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    58. Beam KG, Franzini-Armstrong C. Functional and structural approaches to the study of excitation-contraction coupling. Methods Cell Biol. 1997; 52:283-306.
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    59. García KD, Mynlieff M, Sanders DB, Beam KG, Walrond JP. Lambert-Eaton sera reduce low-voltage and high-voltage activated Ca2+ currents in murine dorsal root ganglion neurons. Proc Natl Acad Sci U S A. 1996 Aug 20; 93(17):9264-9.
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    60. García KD, Beam KG. Reduction of calcium currents by Lambert-Eaton syndrome sera: motoneurons are preferentially affected, and L-type currents are spared. J Neurosci. 1996 Aug 15; 16(16):4903-13.
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    61. Adams BA, Tanabe T, Beam KG. Ca2+ current activation rate correlates with alpha 1 subunit density. Biophys J. 1996 Jul; 71(1):156-62.
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    62. Dirksen RT, Beam KG. Unitary behavior of skeletal, cardiac, and chimeric L-type Ca2+ channels expressed in dysgenic myotubes. J Gen Physiol. 1996 Jun; 107(6):731-42.
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    63. Gallant EM, Balog EM, Beam KG. Slow calcium current is not reduced in malignant hyperthermic porcine myotubes. Muscle Nerve. 1996 Apr; 19(4):450-5.
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    64. Nakai J, Dirksen RT, Nguyen HT, Pessah IN, Beam KG, Allen PD. Enhanced dihydropyridine receptor channel activity in the presence of ryanodine receptor. Nature. 1996 Mar 07; 380(6569):72-5.
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    65. Dirksen RT, Beam KG. Single calcium channel behavior in native skeletal muscle. J Gen Physiol. 1995 Feb; 105(2):227-47.
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    66. García J, Beam KG. Calcium transients associated with the T type calcium current in myotubes. J Gen Physiol. 1994 Dec; 104(6):1113-28.
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    67. Adams BA, Mori Y, Kim MS, Tanabe T, Beam KG. Heterologous expression of BI Ca2+ channels in dysgenic skeletal muscle. J Gen Physiol. 1994 Nov; 104(5):985-96.
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    68. Takekura H, Bennett L, Tanabe T, Beam KG, Franzini-Armstrong C. Restoration of junctional tetrads in dysgenic myotubes by dihydropyridine receptor cDNA. Biophys J. 1994 Aug; 67(2):793-803.
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    69. Mynlieff M, Beam KG. Adenosine acting at an A1 receptor decreases N-type calcium current in mouse motoneurons. J Neurosci. 1994 Jun; 14(6):3628-34.
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    70. Nakai J, Adams BA, Imoto K, Beam KG. Critical roles of the S3 segment and S3-S4 linker of repeat I in activation of L-type calcium channels. Proc Natl Acad Sci U S A. 1994 Feb 01; 91(3):1014-8.
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    71. García J, Beam KG. Measurement of calcium transients and slow calcium current in myotubes. J Gen Physiol. 1994 Jan; 103(1):107-23.
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    72. García J, Tanabe T, Beam KG. Relationship of calcium transients to calcium currents and charge movements in myotubes expressing skeletal and cardiac dihydropyridine receptors. J Gen Physiol. 1994 Jan; 103(1):125-47.
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    73. Mori Y, Niidome T, Fujita Y, Mynlieff M, Dirksen RT, Beam KG, Iwabe N, Miyata T, Furutama D, Furuichi T, et al. Molecular diversity of voltage-dependent calcium channel. Ann N Y Acad Sci. 1993 Dec 20; 707:87-108.
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    74. Tanabe T, Mikami A, Niidome T, Numa S, Adams BA, Beam KG. Structure and function of voltage-dependent calcium channels from muscle. Ann N Y Acad Sci. 1993 Dec 20; 707:81-6.
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    75. Chaudhari N, Beam KG. mRNA for cardiac calcium channel is expressed during development of skeletal muscle. Dev Biol. 1993 Feb; 155(2):507-15.
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    76. Beam KG, Adams BA, Niidome T, Numa S, Tanabe T. Function of a truncated dihydropyridine receptor as both voltage sensor and calcium channel. Nature. 1992 Nov 12; 360(6400):169-71.
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    77. Mynlieff M, Beam KG. Developmental expression of voltage-dependent calcium currents in identified mouse motoneurons. Dev Biol. 1992 Aug; 152(2):407-10.
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    78. Mynlieff M, Beam KG. Characterization of voltage-dependent calcium currents in mouse motoneurons. J Neurophysiol. 1992 Jul; 68(1):85-92.
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    79. Tanabe T, Adams BA, Numa S, Beam KG. Repeat I of the dihydropyridine receptor is critical in determining calcium channel activation kinetics. Nature. 1991 Aug 29; 352(6338):800-3.
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    80. McCobb DP, Beam KG. Action potential waveform voltage-clamp commands reveal striking differences in calcium entry via low and high voltage-activated calcium channels. Neuron. 1991 Jul; 7(1):119-27.
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    81. Adams BA, Beam KG. Contractions of dysgenic skeletal muscle triggered by a potentiated, endogenous calcium current. J Gen Physiol. 1991 Apr; 97(4):687-96.
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    82. McCobb DP, Best PM, Beam KG. The differentiation of excitability in embryonic chick limb motoneurons. J Neurosci. 1990 Sep; 10(9):2974-84.
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    83. Adams BA, Tanabe T, Mikami A, Numa S, Beam KG. Intramembrane charge movement restored in dysgenic skeletal muscle by injection of dihydropyridine receptor cDNAs. Nature. 1990 Aug 09; 346(6284):569-72.
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    84. Tanabe T, Beam KG, Adams BA, Niidome T, Numa S. Regions of the skeletal muscle dihydropyridine receptor critical for excitation-contraction coupling. Nature. 1990 Aug 09; 346(6284):567-9.
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    85. Adams BA, Beam KG. Muscular dysgenesis in mice: a model system for studying excitation-contraction coupling. FASEB J. 1990 Jul; 4(10):2809-16.
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    86. Tanabe T, Mikami A, Numa S, Beam KG. Cardiac-type excitation-contraction coupling in dysgenic skeletal muscle injected with cardiac dihydropyridine receptor cDNA. Nature. 1990 Mar 29; 344(6265):451-3.
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    87. Numa S, Tanabe T, Takeshima H, Mikami A, Niidome T, Nishimura S, Adams BA, Beam KG. Molecular insights into excitation-contraction coupling. Cold Spring Harb Symp Quant Biol. 1990; 55:1-7.
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    88. Chaudhari N, Beam KG. Fibroblasts fuse with myotubes developing in culture. Adv Exp Med Biol. 1990; 280:131-6; discussion 136-7.
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    89. Chaudhari N, Delay R, Beam KG. Restoration of normal function in genetically defective myotubes by spontaneous fusion with fibroblasts. Nature. 1989 Oct 05; 341(6241):445-7.
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    90. Adams BA, Beam KG. A novel calcium current in dysgenic skeletal muscle. J Gen Physiol. 1989 Sep; 94(3):429-44.
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    91. Chaudhari N, Beam KG. The muscular dysgenesis mutation in mice leads to arrest of the genetic program for muscle differentiation. Dev Biol. 1989 Jun; 133(2):456-67.
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    92. McCobb DP, Best PM, Beam KG. Development alters the expression of calcium currents in chick limb motoneurons. Neuron. 1989 Jun; 2(6):1633-43.
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    93. Courbin P, Koenig J, Ressouches A, Beam KG, Powell JA. Rescue of excitation-contraction coupling in dysgenic muscle by addition of fibroblasts in vitro. Neuron. 1989 Apr; 2(4):1341-50.
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    94. Knudson CM, Chaudhari N, Sharp AH, Powell JA, Beam KG, Campbell KP. Specific absence of the alpha 1 subunit of the dihydropyridine receptor in mice with muscular dysgenesis. J Biol Chem. 1989 Jan 25; 264(3):1345-8.
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    95. Beam KG, Tanabe T, Numa S. Structure, function, and regulation of the skeletal muscle dihydropyridine receptor. Ann N Y Acad Sci. 1989; 560:127-37.
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    96. Tanabe T, Beam KG, Powell JA, Numa S. Restoration of excitation-contraction coupling and slow calcium current in dysgenic muscle by dihydropyridine receptor complementary DNA. Nature. 1988 Nov 10; 336(6195):134-9.
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    97. Kinnamon SC, Dionne VE, Beam KG. Apical localization of K+ channels in taste cells provides the basis for sour taste transduction. Proc Natl Acad Sci U S A. 1988 Sep; 85(18):7023-7.
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    98. Beam KG. Duchenne muscular dystrophy. Localizing the gene product. Nature. 1988 Jun 30; 333(6176):798-9.
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    99. Beam KG, Knudson CM. Effect of postnatal development on calcium currents and slow charge movement in mammalian skeletal muscle. J Gen Physiol. 1988 Jun; 91(6):799-815.
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    100. Beam KG, Knudson CM. Calcium currents in embryonic and neonatal mammalian skeletal muscle. J Gen Physiol. 1988 Jun; 91(6):781-98.
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    101. Caldwell JH, Campbell DT, Beam KG. Na channel distribution in vertebrate skeletal muscle. J Gen Physiol. 1986 Jun; 87(6):907-32.
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    102. Beam KG, Knudson CM, Powell JA. A lethal mutation in mice eliminates the slow calcium current in skeletal muscle cells. Nature. 1986 Mar 13-19; 320(6058):168-70.
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    103. Beam KG, Caldwell JH, Campbell DT. Na channels in skeletal muscle concentrated near the neuromuscular junction. Nature. 1985 Feb 14-20; 313(6003):588-90.
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    104. Simon BJ, Beam KG. Slow charge movement in mammalian skeletal muscle. J Gen Physiol. 1985 Jan; 85(1):1-19.
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    105. Simon BJ, Beam KG. The influence of transverse tubular delays on the kinetics of charge movement in mammalian skeletal muscle. J Gen Physiol. 1985 Jan; 85(1):21-42.
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    106. Donaldson PL, Beam KG. Calcium currents in a fast-twitch skeletal muscle of the rat. J Gen Physiol. 1983 Oct; 82(4):449-68.
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    107. Beam KG, Donaldson PL. A quantitative study of potassium channel kinetics in rat skeletal muscle from 1 to 37 degrees C. J Gen Physiol. 1983 Apr; 81(4):485-512.
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    108. Beam KG, Donaldson PL. Slow components of potassium tail currents in rat skeletal muscle. J Gen Physiol. 1983 Apr; 81(4):513-30.
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    109. Simon BJ, Beam KG. Charge movement in a fast twitch skeletal muscle from rat. Biophys J. 1983 Feb; 41(2):223-6.
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    110. Nestler EJ, Beam KG, Greengard P. Nicotinic cholinergic stimulation increases cyclic GMP levels in vertebrate skeletal muscle. Nature. 1978 Oct 05; 275(5679):451-3.
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    111. Beam KG, Nestler EJ, Greengard P. Increased cyclic GMP levels associated with contraction in muscle fibres of the giant barnacle. Nature. 1977 Jun 09; 267(5611):534-6.
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    112. Beam KG. A voltage-clamp study of the effect of two lidocaine derivatives on the time course of end-plate currents. J Physiol. 1976 Jun; 258(2):279-300.
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    113. Beam KG, Greengard P. Cyclic nucleotides, protein phosphorylation and synaptic function. Cold Spring Harb Symp Quant Biol. 1976; 40:157-68.
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