Campbell, Kevin P. - Department of Physiology and Biophysics, University of Iowa

• 3676 Journal of Physiology (1995), 485.3, pp.619-634 619 * To whom correspondence should be addressed.
• THE JOURNAL OF BIOLOCXCAL CHEMISTRY Vol. 265. No. 17, Issue of June 15. pp. 10118-10124,199O 0 1990 by The American Society for Biochemistry and Molecular Biology, Inc. Printed in U.S. A.
• Introduction In intact tissue, many types of epithelial cells are routinely
• Purified Ryanodine Receptor from Rabbit Skeletal Muscle Is the Calcium-Release
• Caveolin-3 is not an integral component of the dystrophin glycoprotein complex
• Subunit Heterogeneity in N-type Ca2 (Received for publication, September 1, 1995, and in revised form, October 19, 1995)
• Localization of the High Affinity Calcium Binding Intrinsic Glycoprotein in Sarcoplasmic Reticulum
• The Voltage-dependent Calcium Channel Subunit Contains Two Stable Interacting Domains*
• reward contingency automatically (616 times) without any indication to the monkey. There were various types of error trial: failing to fixate the fixation point, breaking
• Neurobiology of Disease Transcriptional Upregulation of Cav3.2 Mediates
• Y. Fukuyama, M. Osawa and K. Saito(Eds.), Congenital Muscular Dyrfrophies O 1997 Elsevier Science B.V. All rights reserved
• Human Molecular Genetics doi:10.1093/hmg/ddn009
• The sarcoglycan complex in limb-girdle muscular dystrophy Leland E. Lim and Kevin P. Campbell ,
• 10. R. A. Williamson et al., Hum. Mol. Genet. 6, 831 11. Y. Sunada, S. M. Bernier, C. A. Kozak, Y. Yamada, K. P.
• Expression, Localization and Functions in Acrosome Reaction
• -Dystroglycan can mediate arenavirus infection in the absence of -dystroglycan
• Cell, Vol. 117, 953964, June 25, 2004, Copyright 2004 by Cell Press Molecular Recognition by LARGE Is Essential
• Dystrophin-Glycoprotein Complex Is Highly Enriched in Isolated Skeletal Muscle Sarcolemma
• 4047Research Article Introduction
• Cell, Vol. 110, 639648, September 6, 2002, Copyright 2002 by Cell Press Disruption of Dag1 in Differentiated
• 340 nature genetics volume 19 august 1998 The mouse stargazer gene encodes
• J Mol Cell Cardiol 22, 1477-1485 (1990) Identification and Characterization of Proteins in Sarcoplasmic
• 2007LANDESBIOSCIENCE.DONOTDISTRIBUTE. 144 Channels 2007;Vol.1Issue3
• Dp71 can restore the dystrophin-associated glycoprotein complex in
• Research Article 3683 Introduction
• Communication Vol. 268, No. 16, Issue of June 5, pp. 11496-11499, 1993 THEJOURNALOF BIOLOGICAL CHEMISTRY
• The dystrophinglycoprotein complex (DGC) is a multisubunit complex that connects the cytoskeleton of a muscle fiber to its
• Triadin, a Linker for Calsequestrin and the Ryanodine Receptor
• RIM1 confers sustained activity and neurotransmitter vesicle anchoring to presynaptic Ca2+ channels
• The Histochemical Society, Inc. 0022-1554/98/$3.30 449 Volume 46(4): 449457, 1998
• The Rockefeller University Press, 0021-9525/97/10/375/11 $2.00 The Journal of Cell Biology, Volume 139, Number 2, October 20, 1997 375385
• Transmembrane Auxiliary Subunits of Voltage-dependent
• Insulin Resistance in Striated Muscle-specific Integrin Receptor 1-deficient Mice*
• Case report Further evidence of Fukutin mutations as a cause of childhood onset
• Introduction The sarcolemmal basement membrane is a plasma membrane-
• Research article TheJournalofClinicalInvestigation http://www.jci.org Volume117 Number7 July2007 1805
• 1998 Oxford University Press 823829Human Molecular Genetics, 1998, Vol. 7, No. 5 mdx muscle pathology is independent of nNOS
• Volume I 65 PROTEIN COMPONENTS AND THEIR ROLES IN SARCOPLASMIC
• BMC Physiology (2001) 1:8 http://www.biomedcentral.com/1472-6793/1/8 BMC Physiology (2001) 1:8Research article
• 2005 FASEB The FASEB Journal express article 10.1096/fj.05-4678fje. Published online November 23, 2005.
• Reprint Series 7 October 1988, Volume 242, pp. 99-102
• Reprinted from Calcium Channels: Structure and Function Volume 560 of the Annals of the New York Academy of Sciences
• A 4 Isoform-specific Interaction Site in the Carboxyl-terminal Region of the Voltage-dependent Ca2
• Gene Therapy (2000) 7, 13851391 2000 Macmillan Publishers Ltd All rights reserved 0969-7128/00 $15.00
• Biochemical Characterization and Molecular Cloning of Cardiac Triadin*
• Poster Papers Monoclonal Antibody Characterization
• Loss of -Dystroglycan Laminin Binding in Epithelium-derived Cancers Is Caused by Silencing
• Communication THE JOURNAL. OF BIOLOGKAL CHEMISTRY
• Evidence for a 95 kDa Short Form of the 1A Subunit Associated with the -Conotoxin MVIIC Receptor of the P/Q-type
• The CaV3.2 T-Type Ca2 Channel Is Required for Pressure
• The Rockefeller University Press, 0021-9525/99/04/153/13 $2.00 The Journal of Cell Biology, Volume 145, Number 1, April 5, 1999 153165
• Compositional Differences between Infant and Adult Human Corneal Basement Membranes
• Ultrastructural Localization of Calsequestrin in Adult Rat Atrial and Ventricular Muscle Cells
• Genes, Brain and Behavior (2007) 6: 425431 # 2006 The Authors Journal Compilation # 2006 Blackwell Publishing Ltd
• THE JOURNAL OF BIOLOGICALC H E Y ~ Y 0 1987by TheAmerican Society for Biochemistryand Molecular Biology.he.
• Contact-Dependent Regulation of N-Type Calcium Channel Subunits during Synaptogenesis
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• Identification of Three Subunits of the High Affinity -Conotoxin MVIIC-sensitive Ca2
• Evidence for the Presence of Calsequestrin in Both Peripheral and Interior Regions of Sheep Purkinje
• THEJOURNALOF BIOLOGICALCHEMISTRY Vol. 257, No. 3, Issue of February 10. pp. 123-1246. 1982
• Dystroglycan Matrix Receptor Function in Cardiac Myocytes Is Important for Limiting Activity-Induced
• Intracellular Accumulation and Reduced Sarcolemmal Expression of Dysferlin in
• Cell Calcium 46 (2009) 282292 Contents lists available at ScienceDirect
• Cellular/Molecular Inhibition of Recombinant N-Type CaV Channels by the 2
• Adenosine A3 receptor stimulation induces protection of skeletal muscle from eccentric exercise-mediated injury
• FEBS Letters 352 (1994) 49-53 0014-5793/94/$7.00 1994 Federation of European Biochemical Societies. All rights reserved.
• 1997 Oxford University Press 747752Human Molecular Genetics, 1997, Vol. 6, No. 5 Mild congenital muscular dystrophy in two patients
• THEJOURNALOF BIOLOGICAL CHEMISTRY Q 1989by The American Society for Biochemistry and Molecular Biology, Inc.
• Cell, Vol. 80, 675-679, March 10, 1995, Copyright 1995 by Cell Press Three Muscular Dystrophies: Review
• The Ca2+-releaseChannelJRyanodineReceptor Is Localized in Junctional and Corbular SarcoplasmicReticulum in CardiacMuscle
• Brief Communications 6 4 Integrin and Dystroglycan Cooperate to Stabilize the
• JOURNAL OF VIROLOGY, 0022-538X/01/$04.00 0 DOI: 10.1128/JVI.75.1.448457.2001
• JOURNAL OF VIROLOGY, May 2002, p. 51405146 Vol. 76, No. 10 0022-538X/02/$04.00 0 DOI: 10.1128/JVI.76.10.51405146.2002
• Workshop report 114th ENMC International Workshop on Congenital Muscular Dystrophy
• J Mol Cell Cardiol 29, 3175-3188 (1997) Feature Article
• INTRODUCTION Differentiation of the neuromuscular junction (NMJ) depends
• Structural determinants of calcium channel subunit Hongyan Liu, Kevin f? Campbell
• Pestic. Sci. 1998, 54, 345352 Characterisation of Antibody Models of the
• Neurobiology of Disease Distinct Functions of Glial and Neuronal Dystroglycan in the
• CARDIOMYOPATHY Exercise-Induced Left Ventricular Systolic Dysfunction
• Functional Glycosylation of Dystroglycan Is Crucial for Thymocyte Development in the Mouse
• Cellular/Molecular Involvement of Ca2
• O-Mannosyl Phosphorylation of Alpha-Dystroglycan Is Required for
• R E S E A R C H A R T I C L E A Comparative Study of a-Dystroglycan Glycosylation in
• Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif
• Sarcoglycan Complex IMPLICATIONS FOR METABOLIC DEFECTS
• Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel
• Sarcolemma-localized nNOS is required to maintain activity after mild exercise
• Neurobiology of Disease Brain and Eye Malformations Resembling WalkerWarburg
• FUKUTIN-RELATED PROTEIN ASSOCIATES WITH THE SARCOLEMMAL DYSTROPHIN-GLYCOPROTEIN COMPLEX*
• JOURNAL OF VIROLOGY, June 2007, p. 56855695 Vol. 81, No. 11 0022-538X/07/$08.00 0 doi:10.1128/JVI.02574-06
• J Physiol 574.2 (2006) pp 415430 415 CaV3.2 is the major molecular substrate for redox
• Copyright @ 2006 by the American Association of Neuropathologists, Inc. Unauthorized reproduction of this article is prohibited. ORIGINAL ARTICLE
• Fukutin Gene Mutations Cause Dilated Cardiomyopathy with Minimal
• A functional AMPA receptorcalcium channel complex in the postsynaptic membrane
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• JOURNAL OF VIROLOGY, Nov. 2005, p. 1428214296 Vol. 79, No. 22 0022-538X/05/$08.00 0 doi:10.1128/JVI.79.22.1428214296.2005
• Development/Plasticity/Repair Both Laminin and Schwann Cell Dystroglycan Are
• Disruption of perlecan binding and matrix assembly by post-translational or genetic disruption of dystroglycan function
• Centronuclear myopathy in mice lacking a novel muscle-specific protein kinase
• Aberrant glycosylation of a-dystroglycan causes defective binding of laminin in the muscle of chicken muscular dystrophy
• Cell stiffness and receptors: evidence for cytoskeletal subnetworks Hayden Huang,1
• Laminin isoforms differentially regulate adhesion, spreading, proliferation, and ERK activation of h1 integrin-null cells
• Neuron, Vol. 42, 387399, May 13, 2004, Copyright 2004 by Cell Press Structural Analysis of the Voltage-Dependent
• Modified Cardiovascular L-type Channels in Mice Lacking the Voltage-dependent Ca2
• Abnormal Coronary Function in Mice Deficient in 1H T-type
• Phenotypic heterogeneity in the stargazin allelic series Verity A. Letts,1
• Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in
• Neuron, Vol. 38, 747758, June 5, 2003, Copyright 2003 by Cell Press Unique Role of Dystroglycan in Peripheral
• Molecular Biology of the Cell Vol. 14, 20882103, May 2003
• former determine the tree structure related to the efficiency of the webs, and the latter form the loops involved in network robustness.
• 1 Subunit Interactions within the Skeletal Muscle L-type Voltage-gated Calcium Channels*
• Molecular characterization of a two-domain form of the neuronal voltage-gated P/Q-type calcium channel K12.1 subunit
• [CANCER RESEARCH 62, 71027109, December 1, 2002] A Role for Dystroglycan in Epithelial Polarization: Loss of Function in Breast
• Long-term regulation of voltage-gated Ca2 channels by gabapentin
• Dystroglycan Is Selectively Associated with Inhibitory GABAergic Synapses But Is Dispensable for Their Differentiation
• Differentiation (2001) 69:121134 C Blackwell Wissenschafts-Verlag 2001 ORIGINAL ARTICLE
• The Rockefeller University Press, 0021-9525/2001/10/301/10 $5.00 The Journal of Cell Biology, Volume 155, Number 2, October 15, 2001 301310
• Intramembrane charge movements and excitation contraction coupling expressed by two-domain
• INTRODUCTION ECM molecules are integral to tissue form and function. They
• J. Exp. Med. The Rockefeller University Press 0022-1007/2000/11/1249/12 $5.00 Volume 192, Number 9, November 6, 2000 12491260
• Dystroglycan Overexpression in Vivo Alters Acetylcholine Receptor Aggregation
• Expression of -Sarcoglycan in Smooth Muscle and Its Interaction with the Smooth Muscle Sarcoglycan-Sarcospan Complex*
• Neuron, Vol. 25, 279293, February, 2000, Copyright 2000 by Cell Press Maturation and Maintenance
• MOLECULAR AND CELLULAR BIOLOGY, 0270-7306/00/$04.00 0
• Molecular Cell, Vol. 5, 141151, January, 2000, Copyright 2000 by Cell Press Disruption of the -Sarcoglycan Gene Reveals
• -Sarcoglycan Replaces -Sarcoglycan in Smooth Muscle to Form a Unique Dystrophin-Glycoprotein Complex*
• Assembly of the Sarcoglycan INSIGHTS FOR MUSCULAR DYSTROPHY*
• Cell, Vol. 95, 859870, December 11, 1998, Copyright 1998 by Cell Press A Role for Dystroglycan
• Role of -Dystroglycan as a Schwann Cell Receptor for
• Nature Macmillan Publishers Ltd 1998 letters to nature
• b-Sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate
• Dissection of Functional Domains of the Voltage-Dependent Ca2 Channel 2 Subunit
• Extracellular Interaction of the Voltage-dependent Channel 2 and 1 Subunits*
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• DEVELOPMENTAL BIOLOGY 181, 156167 (1997) ARTICLE NO. DB968430
• In vivo muscle gene transfer of full-lengthdystrophin PR Clemens et a1
• Forced Expression of Dystrophin Deletion Constructs Reveals Structure-Function Correlations
• CLINICAL AND MOLECULAR PATHOLOGICAL FEATURES OF SEVERE
• Neuropathology and Applied Neurobiology 1996, 22, 30-3 7 Ultrastructural localization of adhalin, a-dystroglycan
• Journal of Neurochemistry Lippincott-Raven Publishers, Philadelphia
• C h d Heterogeneity of A d h h Deficiency Lucia Morandi, MD,* Rita Barresi, PhD,* Claudia Di Blasi, PhD,* Daniel Jung, PhD,?
• FEBS 16670 FEBS Letters 381 (1996) 15-20 Absence of y-sarcoglycan (35 DAG) in autosomal recessive muscular
• Neuron, Vol. 16, 431440, February, 1996, Copyright 1996 by Cell Press Dual Function of the Voltage-Dependent Ca2
• FEBS 16621 FEBS Letters 380 (1996) 272-276 Identification of critical amino acids involved in a,-p interaction in
• BRIEF REPORT: DEFICIENCY OF A DYSTROPHIN-ASSOCIATED
• Neurosensory Hearing Loss in Secondary Adhalinopathy By K. Oexle', R. Herrmann', Catherine~ o d 8 ,F. ~eturc4,CII.Hiibner', 1.-C. Kaplan3,Y.~ i z u n o ~ ,E. Ozawa4,
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• Identification and Characterization of the Dystrophin Anchoring Site on -Dystroglycan*
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• Neuron, Vol. 15, 115-126, July, 1995, Copyright O 1995 by Cell Press Rapsyn May Function as a Link between
• Non-Muscle oL-DystroglycanIs Involved in Epithelial Development
• 01995 Oxford University Press Human Molecular Genetics, 1995, Vol. 4, No. 7 1163-1167 A common missense mutation in the adhalin gene in
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• The Rockefeller University Press, 0021-9525/95/05/1093/9 $2.00 The Journal of Cell Biology, Volume 129, Number 4, May 1995 1093-1101 1093
• THE JOURNAL OF BIOLOGICAL CHEMISTRY Vol. 270, No. 16, Issue of April 21, pp. 9027-9030, 1995
• 1994 Oxford University Press Human Molecular Genetics, 1994, Vol. 3, No. 10 1725-1733 *To whom correspondence should be addressed
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• 0960&8966(94)E0023-2 EXPRESSION OF DYSTROPHIN-ASSOCIATED GLYCOPROTEINS
• Cortical Localization ofa Calcium Release Channel in Sea Urchin Eggs
• Dystrophin-associated Proteins Are Greatly Reduced in Skeletal Muscle from mdx Mice
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• Biochem. J. (1990) 270, 545-548 (Printed in Great Britain) 545 Sequence similarity of calreticulin with a Ca2+
• Identification of Novel Proteins Unique to Either Transverse Tubules (TS28) or the Sarcolemma (SL50) in Rabbit Skeletal Muscle
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• Plant Physiol. (1989) 91,1259-1261 Received for publication July 6, 1989 0032-0889/89/91 /1259/03/$01.00/0 and in revised form August 18, 1989
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• Structural Evidence for Direct Interaction between the Molecular Components of the Transverse Tubule/
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• Evidence for the Presence of Calsequestrin in Two Structurally Different Regions of
• THEJOURNALOF BIOLOGICALCHEMISTRY Vol. 258, No. 18, Issue of September 25, pp. 11267-11273,1983
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• DIDS INHIBITION OF SARCOPLASMIC RETICULUM ANION EFFLUX AND CALCIUM TRANSPORT
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• Communication THE Joua~ai OF H,o,.oc,cai CHEM,STHV
• nature neuroscience volume 11 | number 8 | AuGuST 2008 857 news and views
• Subunit of Voltage-activated Calcium Channels*
• Dystrophin-Glycoprotein Complex: Post-translational
• Skeletal Muscle Basement Membrane-Sarcolemma-Cytoskeleton Interaction Minireview Series*
• INVITED REVIEW ABSTRACT: Muscular dystrophies represent a heterogeneous group of disorders, which have been largely classified by clinical phenotype. In the
• Dystroglycan connects the extracellular matrix and cytoskeleton. Key findings in the past year indicate that
• Journal of Neuroscience Research 42528-538 (1995) Dystroglycan Expression in the Wild Type and
• Dystrophin-glycoprotein complex: molecular organization and critical roles in skeletal muscle
• tients who are homozygous for null mutations and did not express adhalin. Missense mutations resulted in
• Clin Biochem, Vol. 23, pp. 159-166, 1990 0009-9120/90 $3.00 + .00 Printed in Canada. All rights reserved. Copyright 1990 The Canadian Society of Clinical Chemists.
• The Calcium Channel: Structure, Function and Implications
• Calsequestrin DAVID H. MacLENNAN
• Reprinted from Trends in Biochemical Sciences Elsevier/North-Holland Biomedical Press 1979
• Reprinted from Calcium Binding Proteins and Calcium Function (R.H. Wasserman et al., eds.).
• Dystroglycan Is Involved in Laminin-1-Stimulated Motility of
• Journal of Neuropathology and Experimental Neurology Copyright O 1995 by the American Association of Neuropathologists
• Sarcospan, the 25-kDa Transmembrane Component of
• The Rockefeller University Press, 0021-9525/2000/09/1399/11 $5.00 The Journal of Cell Biology, Volume 150, Number 6, September 18, 2000 13991409
• C-Terminal Titin Deletions Cause a Novel Early-Onset Myopathy with Fatal
• THE JOURNAL OF BIOLOGICAL CHEMISTRY Vol. 269, No. 45, Issue of November 11, pp. 28359-28365, 1994 1994 by The American Society for Biochemistry and Molecular Biology, Inc. Printed in U.S.A.
• THE ,JOURNAL OF BIOLOGICALCHEMISTqY 0 1987by The Amencan Socxetyof BlologxalChemists, Inc.
• Contrast Agent-Enhanced Magnetic Resonance Imaging of Skeletal Muscle Damage in Animal Models
• Loss of sarcolemma nNOS in sarcoglycan-deficient RACHELLE H. CROSBIE1,2
• 320 NATURE MEDICINE VOLUME 5 NUMBER 3 MARCH 1999 Heart failure is a leading cause of cardiovascular mortality in the
• Other names Dystroglycan, 156dystrophin-associatedglycoprotein(DAG),43DAG, SL156,
• Molecular Biology of the Cell Vol. 18, 44934507, November 2007
• Cell Motility and the Cytoskeleton 9:164-174 (1988) A Monoclonal Antibody to the Ca2+
• THEJOURNALOF BIOLOGICALCHEMISTRY 0 1992by The American Society for Biochemistry and Molecular Biology,Inc.
• 0 1995 Oxford University Press Human Molecular Genetics, 1995, Vol.4, No. 8 1245-2250 Expression of human full-length and
• Reprinted from Trends in NeuroSciences-October, 1988 Vol. 11, No. 10 1988, Elsevier Publications, Cambridge 0378 -5912/88/$02.00 425 The biochemistry and molecular biology of the
• Communication Vol. 259, No. 9, Issue of May 10,pp. 53&1-5387,1984 THEJOURNALOF BIOLOGICALCHEMISTRY
• Adhalin Gene Mutations in Patients with Autosomal Recessive Childhood Onset Muscular Dystrophy with Adhalin Deficiency
• Auxiliary subunits: essential components of the voltage-gated calcium channel complex
• Neuron, Vol. 7, 17-25, July, 1991, Copyright 1991 by Cell Press The Brain Ryanodine Receptor
• Neuron, Vol. 25, 533535, March, 2000, Copyright 2000 by Cell Press Letter to the Editor
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• Reprinted from Biochemistry, 1989, 28, 4830. Copyright 1989 by the American Chemical Society and reprinted by permission of the copyright owner.
• Congenital Muscular Dystrophy with Rigid Spine Syndrome: A Clinical, Pathological,
• ade (11). The varied and unusual polyhedra of this sequence illustrate how certain sym-
• Neurobiology of Disease Visual Impairment in the Absence of Dystroglycan
• Molecular Cell, Vol. 1, 841848, May, 1998, Copyright 1998 by Cell Press Functional Rescue of the Sarcoglycan Complex
• THEJOURNAL OF &OLOGiCAL CWF"STRY IC) 1987by The American Society for Biochemistry and MolecularBiology, Inc,
• Congenital muscular dystrophy with glycosylation defects of a-dystroglycan in Japan
• Acknowledgements We thank J. Flanagan, S. Prouty, S. Cutshall and D. Venzke for technical support. We also
• 696 VOLUME 10 | NUMBER 7 | JULY 2004 NATURE MEDICINE Fukuyama congenital muscular dystrophy (FCMD), muscle-eye-brain
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• A Role of Dystroglycan in Schwannoma Cell Adhesion to Laminin* (Received for publication, September 13, 1996, and in revised form, March 3, 1997)
• Communication Vol. 264, No. 3 Issue of January 25, pp. 1345-1348,1989 THEJOURNALOF BIOLOGICALCHEMISTRY
• Reactive oxygen species deglycosilate glomerular a-dystroglycan
• JOURNAL OF VIROLOGY, June 2008, p. 60346038 Vol. 82, No. 12 0022-538X/08/$08.00 0 doi:10.1128/JVI.00100-08
• POSSIBLE SITES OF ION FLOW IN THE SARCOPLASMIC RETICULUM MEMBRANE
• Dysferlin and muscle membrane repair Renzhi Han and Kevin P Campbell
• Human Molecular Genetics, 1994, Vol. 3, No. 12 2269 * To whom correspondence should be addressed * To whom correspondence should be addressed
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• Communication Val. 262.No.17,Iseue of June 15,pp. 7943-7946,1987 THE JOURNALOF BIOLOGICALCHEMISTRY
• Dysferlin and the plasma membrane repair in muscular dystrophy
• Communication Vol. 262 No. 14 Issue of May 15 pp. 64fX+3 1987 THEJOURNALOF BIOLOGICALCHEMISTRY
• 1111111111 TOPICS~ 2 0 ~ Glycosylation of dystroglycan and congenital muscular dystrophies
• [CANCER RESEARCH 64, 61526159, September 1, 2004] Proteolytic Enzymes and Altered Glycosylation Modulate Dystroglycan Function in
• The Rockefeller University Press, 0021-9525/98/09/1461/11 $2.00 The Journal of Cell Biology, Volume 142, Number 6, September 21, 1998 14611471
• 1993 Oxford University Press 20192022Human Molecular Genetics, 1996, Vol. 5, No. 12 A founder mutation in the -sarcoglycan gene of
• Biochem. J. (1989) 263, 605-608 (Printed in Great Britain) 605 The identification of sarcoplasmic reticulum terminal cisternae
• INTRODUCTION Duchenne muscular dystrophy (DMD) is a progressive, X-
• Introduction Dilated cardiomyopathy, one of the
• Biosynthesis of dystroglycan: processing of a precursor propeptide Kathleen H. Holta
• Advances in Cyclic Nucleotide and Protein Phosphorylation Research, Vol. 17,
• Characterization of -Sarcoglycan, a Novel Component of the Oligomeric Sarcoglycan Complex Involved in
• Communication Vol. 264,No. 8,Issue of March 15,pp. 4269-4272,1989 0 1989by The American Society for Biochemistry and Molecular Biology, Inc.
• POMT1 mutation results in defective glycosylation and loss of laminin-binding
• Characterization of aquaporin-4 in muscle and muscular dystrophy
• Long-term Skeletal Muscle Protection After Gene Transfer in a Mouse Model of LGMD-2D
• The Rockefeller University Press, 0021-9525/2001/07/435/11 $5.00 The Journal of Cell Biology, Volume 154, Number 2, July 23, 2001 435445
• Nephrol Dial Transplant (2010) 25: 478484 doi: 10.1093/ndt/gfp465
• Neuron, Vol. 13, 505-506, September, 1994, Copyright 1994 by Cell Press Matters Arising
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• Biochemical Characterization of the Epithelial Dystroglycan Complex*
• Muscles of mice deficient in -sarcoglycan maintain large masses and near control force values throughout the life span
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• Cell, Vol. 98, 465474, August 20, 1999, Copyright 1999 by Cell Press Disruption of the SarcoglycanSarcospan Complex
• PGC-1 regulates the neuromuscular junction program and ameliorates
• Biochemical and Biophysical Evidence for 2 Subunit Association with Neuronal Voltage-activated Ca2
• Case report A novel POMT2 mutation causes mild congenital
• ION PATHWAYS IN PROTEINS OF THE SARCOPLASMIC RETICULUM *
• Our understanding of the structure and function of dystroglycan, a cell surface laminin/agrin receptor, has
• THEJOURNAL OF BIOLOGICAL CHEMISTRY 0 1991 by The American Society for Biochemistry and Molecular Biology, Inc
• Rab3-interacting Molecule Isoforms Lacking the Rab3-binding Domain Induce Long Lasting Currents but
• LETTERS TO NATURE NATURE VOL. 330 24/31 DECEMBER 1987
• Neural Regulation of -Dystroglycan Biosynthesis and Glycosylation in Skeletal Muscle
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• 1997 Oxford University Press 831841Human Molecular Genetics, 1997, Vol. 6, No. 6 Dystroglycan is essential for early embryonic
• Journal of Cardiovascular Pharmacology 12(Suppl. 4):S86-S90 1988 Raven Press, Ltd., New York
• Reprint Series 27 April 1990, Volume 248, pp. 490-492
• BRIEF COMMUNICATION c1-Dependent Down-regulation of Recombinant
• THE JOURNAL OF BIOLOGICAL CHEMISTRY Vol. 270, No. 10, Issue of March 10, pp. 4975-4978, 1995
• Ultrastructural Localization of Calsequestrin in Rat Skeletal Muscle by
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