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Research | 3 July 2020 | Open
Investigations of an inducible intact dystrophin gene excision system in cardiac and skeletal muscle in vivo
Scientific Reports 10 , 1–12

Rights & permissionsfor article Investigations of an inducible intact dystrophin gene excision system in cardiac and skeletal muscle in vivo . Opens in a new window.
News and Views | 1 August 2008
Unraveling the ribbon synapse
- Jakob S Satz
- & Kevin P Campbell
Nature Neuroscience 11 , 857–859

Rights & permissionsfor article Unraveling the ribbon synapse . Opens in a new window.
Research | 25 July 2002
Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy
- Steven A. Moore
- , Fumiaki Saito
- , Jianguo Chen
- , Daniel E. Michele
- , Michael D. Henry
- , Albee Messing
- , Ronald D. Cohn
- , Susan E. Ross-Barta
- , Steve Westra
- , Roger A. Williamson
- , Toshinori Hoshi
- & Kevin P. Campbell
Nature 418 , 422–425

Rights & permissionsfor article Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy . Opens in a new window.
Research | 30 January 1997
Direct binding of G-protein βλ complex to voltage-dependent calcium channels
Nature 385 , 446–450

Rights & permissionsfor article Direct binding of G-protein βλ complex to voltage-dependent calcium channels . Opens in a new window.
Research | 1 December 1994
Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice
Nature Genetics 8 , 340–344

Rights & permissionsfor article Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice . Opens in a new window.
Research | 6 June 2004
LARGE can functionally bypass α-dystroglycan glycosylation defects in distinct congenital muscular dystrophies
- Rita Barresi
- , Daniel E Michele
- , Motoi Kanagawa
- , Hollie A Harper
- , Sherri A Dovico
- , Jakob S Satz
- , Steven A Moore
- , Wenli Zhang
- , Harry Schachter
- , Jan P Dumanski
- , Ronald D Cohn
- , Ichizo Nishino
- & Kevin P Campbell
Nature Medicine 10 , 696–703

Rights & permissionsfor article LARGE can functionally bypass α-dystroglycan glycosylation defects in distinct congenital muscular dystrophies . Opens in a new window.
Research | 24 May 1990
Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle
Nature 345 , 315–319

Rights & permissionsfor article Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle . Opens in a new window.
Research | 20 July 1989
Induction of calcium currents by the expression of the α₁-subunit of the dihydropyridine receptor from skeletal muscle
Nature 340 , 233–236

Rights & permissionsfor article Induction of calcium currents by the expression of the α1-subunit of the dihydropyridine receptor from skeletal muscle . Opens in a new window.
Research | 24 September 1992
Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy
Nature 359 , 320–322

Rights & permissionsfor article Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy . Opens in a new window.
Research | 16 March 1989
Association of dystrophin and an integral membrane glycoprotein
- Kevin P. Campbell
- & Steven D. Kahl
Nature 338 , 259–262

Rights & permissionsfor article Association of dystrophin and an integral membrane glycoprotein . Opens in a new window.
Research | 19 January 2011
Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene
European Journal of Human Genetics 19 , 452–457

Rights & permissionsfor article Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene . Opens in a new window.
Research | 10 December 1992
Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle
Nature 360 , 588–591

Rights & permissionsfor article Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle . Opens in a new window.
Research | 23 July 1998
A neuronal ryanodine receptor mediates light-induced phase delays of the circadian clock
Nature 394 , 381–384

Rights & permissionsfor article A neuronal ryanodine receptor mediates light-induced phase delays of the circadian clock . Opens in a new window.
Research | 3 March 1994
Calcium channel β-subunit binds to a conserved motif in the I–II cytoplasmic linker of the α1-subunit
Nature 368 , 67–70

Rights & permissionsfor article Calcium channel β-subunit binds to a conserved motif in the I–II cytoplasmic linker of the α1-subunit . Opens in a new window.
Research | 31 December 1987
Subcellular fractionation of dystrophin to the triads of skeletal muscle
Nature 330 , 754–758

Rights & permissionsfor article Subcellular fractionation of dystrophin to the triads of skeletal muscle . Opens in a new window.
Research | 25 July 2002
Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophies
- Daniel E. Michele
- , Rita Barresi
- , Motoi Kanagawa
- , Fumiaki Saito
- , Ronald D. Cohn
- , Jakob S. Satz
- , James Dollar
- , Ichizo Nishino
- , Richard I. Kelley
- , Hannu Somer
- , Volker Straub
- , Katherine D. Mathews
- , Steven A. Moore
- & Kevin P. Campbell
Nature 418 , 417–421

Rights & permissionsfor article Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophies . Opens in a new window.
Research | 8 May 2003
Defective membrane repair in dysferlin-deficient muscular dystrophy
- Dimple Bansal
- , Katsuya Miyake
- , Steven S. Vogel
- , Séverine Groh
- , Chien-Chang Chen
- , Roger Williamson
- , Paul L. McNeil
- & Kevin P. Campbell
Nature 423 , 168–172

Rights & permissionsfor article Defective membrane repair in dysferlin-deficient muscular dystrophy . Opens in a new window.
Research | 1 March 1999
Enteroviral protease 2A cleaves dystrophin: Evidence of cytoskeletal disruption in an acquired cardiomyopathy
Nature Medicine 5 , 320–326

Rights & permissionsfor article Enteroviral protease 2A cleaves dystrophin: Evidence of cytoskeletal disruption in an acquired cardiomyopathy . Opens in a new window.
27 April 2011
Improved genotyping of the dysferlin null mouse
Protocol Exchange

Rights & permissionsfor article Improved genotyping of the dysferlin null mouse . Opens in a new window.
1 June 1995
Expression of Deletion-Containing Dystrophins in mdx Muscle: Implications for Gene Therapy and Dystrophin Function
Pediatric Research 37 , 693–700

Rights & permissionsfor article Expression of Deletion-Containing Dystrophins in mdx Muscle: Implications for Gene Therapy and Dystrophin Function . Opens in a new window.
Research | 19 August 1993
Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity
Nature 364 , 725–729

Rights & permissionsfor article Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity . Opens in a new window.
Research | 26 October 2008
Sarcolemma-localized nNOS is required to maintain activity after mild exercise
Nature 456 , 511–515

Rights & permissionsfor article Sarcolemma-localized nNOS is required to maintain activity after mild exercise . Opens in a new window.
News and Views | 28 November 1996
Utrophin to the rescue
- Kevin P. Campbell
- & Rachelle H. Crosbie
Nature 384 , 308–309

Rights & permissionsfor article Utrophin to the rescue . Opens in a new window.
Research | 15 August 2016
Structural basis of laminin binding to the LARGE glycans on dystroglycan
- David C Briggs
- , Takako Yoshida-Moriguchi
- , Tianqing Zheng
- , David Venzke
- , Mary E Anderson
- , Andrea Strazzulli
- , Marco Moracci
- , Liping Yu
- , Erhard Hohenester
- & Kevin P Campbell
Nature Chemical Biology 12 , 810–814

Rights & permissionsfor article Structural basis of laminin binding to the LARGE glycans on dystroglycan . Opens in a new window.
Research | 16 October 2013
LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy
Nature 503 , 136–140

Rights & permissionsfor article LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy . Opens in a new window.
Research | 2 May 2010
Substitutions in woolly mammoth hemoglobin confer biochemical properties adaptive for cold tolerance
- Kevin L Campbell
- , Jason E E Roberts
- , Laura N Watson
- , Jörg Stetefeld
- , Angela M Sloan
- , Anthony V Signore
- , Jesse W Howatt
- , Jeremy R H Tame
- , Nadin Rohland
- , Tong-Jian Shen
- , Jeremy J Austin
- , Michael Hofreiter
- , Chien Ho
- , Roy E Weber
- & Alan Cooper
Nature Genetics 42 , 536–540

Rights & permissionsfor article Substitutions in woolly mammoth hemoglobin confer biochemical properties adaptive for cold tolerance . Opens in a new window.
Research | 1 November 1995
β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12
- Leland E. Lim
- , Franck Duclos
- , Odile Broux
- , Nathalie Bourg
- , Yoshihide Sunada
- , Valérie Allamand
- , Jon Meyer
- , Isabelle Richard
- , Carolyn Moomaw
- , Clive Slaughter
- , Fernando M.S. Tomé
- , Michel Fardeau
- , Charles E. Jackson
- , Jacques S. Beckmann
- & Kevin P. Campbell
Nature Genetics 11 , 257–265

Rights & permissionsfor article β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12 . Opens in a new window.
Research | 22 April 2012
ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome
- Tobias Willer
- , Hane Lee
- , Mark Lommel
- , Takako Yoshida-Moriguchi
- , Daniel Beltran Valero de Bernabe
- , David Venzke
- , Sebahattin Cirak
- , Harry Schachter
- , Jiri Vajsar
- , Thomas Voit
- , Francesco Muntoni
- , Andrea S Loder
- , William B Dobyns
- , Thomas L Winder
- , Sabine Strahl
- , Katherine D Mathews
- , Stanley F Nelson
- , Steven A Moore
- & Kevin P Campbell
Nature Genetics 44 , 575–580

Rights & permissionsfor article ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome . Opens in a new window.
Research | 1 December 1994
Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy
Nature Genetics 8 , 333–339

Rights & permissionsfor article Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy . Opens in a new window.
Research | 1 August 1998
The mouse stargazer gene encodes a neuronal Ca²⁺-channel γ subunit
Nature Genetics 19 , 340–347

Rights & permissionsfor article The mouse stargazer gene encodes a neuronal Ca2+-channel γ subunit . Opens in a new window.
Research | 20 February 1992
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
Nature 355 , 696–702

Rights & permissionsfor article Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix . Opens in a new window.
Research | 13 May 2007
RIM1 confers sustained activity and neurotransmitter vesicle anchoring to presynaptic Ca²⁺ channels
- Shigeki Kiyonaka
- , Minoru Wakamori
- , Takafumi Miki
- , Yoshitsugu Uriu
- , Mio Nonaka
- , Haruhiko Bito
- , Aaron M Beedle
- , Emiko Mori
- , Yuji Hara
- , Michel De Waard
- , Motoi Kanagawa
- , Makoto Itakura
- , Masami Takahashi
- , Kevin P Campbell
- & Yasuo Mori
Nature Neuroscience 10 , 691–701

Rights & permissionsfor article RIM1 confers sustained activity and neurotransmitter vesicle anchoring to presynaptic Ca2+ channels . Opens in a new window.

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Investigations of an inducible intact dystrophin gene excision system in cardiac and skeletal muscle in vivo

Unraveling the ribbon synapse

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy

Direct binding of G-protein βλ complex to voltage-dependent calcium channels

Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice

LARGE can functionally bypass α-dystroglycan glycosylation defects in distinct congenital muscular dystrophies

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

Induction of calcium currents by the expression of the α₁-subunit of the dihydropyridine receptor from skeletal muscle

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

Association of dystrophin and an integral membrane glycoprotein

Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene

Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle

A neuronal ryanodine receptor mediates light-induced phase delays of the circadian clock

Calcium channel β-subunit binds to a conserved motif in the I–II cytoplasmic linker of the α1-subunit

Subcellular fractionation of dystrophin to the triads of skeletal muscle

Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophies

Defective membrane repair in dysferlin-deficient muscular dystrophy

Enteroviral protease 2A cleaves dystrophin: Evidence of cytoskeletal disruption in an acquired cardiomyopathy

Improved genotyping of the dysferlin null mouse

Expression of Deletion-Containing Dystrophins in mdx Muscle: Implications for Gene Therapy and Dystrophin Function

Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity

Sarcolemma-localized nNOS is required to maintain activity after mild exercise

Utrophin to the rescue

Structural basis of laminin binding to the LARGE glycans on dystroglycan

LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy

Substitutions in woolly mammoth hemoglobin confer biochemical properties adaptive for cold tolerance

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy

The mouse stargazer gene encodes a neuronal Ca²⁺-channel γ subunit

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

RIM1 confers sustained activity and neurotransmitter vesicle anchoring to presynaptic Ca²⁺ channels

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