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Privacy-aware community infrastructureBlain Alison, Greally Elizabeth, Laval Steve, Blamire Andrew, Macgowan Guy, Straub Volker
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Rights: UNKNOWN · https://www.elsevier.com/tdm/userlicense/1.0/ · Source: journal-auto-sync:external:CROSSREF_ISSN
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Population frequencies of inherited neuromuscular diseases--a world survey
10.1016/0960-8966(91)90039-u · 1991
Developmental progress in Duchenne muscular dystrophy: lessons for earlier detection
10.1016/j.ejpn.2004.01.009 · 2004
Delayed diagnosis in duchenne muscular dystrophy: data from the Muscular Dystrophy Surveillance
2009
Lesson of the week: late diagnosis of Duchenne’s muscular dystrophy presenting as global developmental delay
10.1136/bmj.323.7303.37 · 2001
Standards of care for Duchenne muscular dystrophy: brief TREAT-NMD recommendations
10.1007/978-90-481-2813-6_2 · 2009
The respiratory management ofpatients with duchenne muscular dystrophy: a DMD care considerations working group specialty article
10.1002/ppul.21254 · 2010
Unresolved referenced work
2011
Duchenne Muscular Dystrophy End-Stage Respiratory Muscle Failure: Prolongation of Survival by Noninvasive Interventions
10.4187/respcare.00831 · 2011
Prevalence of cardiomyopathy in Duchenne and Becker’s muscular dystrophy
2008
The molecular defect in Duchenne muscular dystrophy
1980
Dystrophin and mutations: one gene, several proteins, multiple phenotypes
10.1016/s1474-4422(03)00585-4 · 2003
Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma
10.1212/wnl.43.4.795 · 1993
Localization of sarcoglycan, neuronal nitric oxide synthase, beta-dystroglycan, and dystrophin molecules in normal skeletal myofiber: triple immunogold labeling electron micro-scopy
10.1002/jemt.1166 · 2001
Differential targeting of nNOS and AQP4 to dystrophin-deficient sarcolemma by membrane-directed alpha-dystrobrevin
10.1242/jcs.020701 · 2008
Relocalization of neuronal nitric oxide synthase (nNOS) as a marker for complete restoration of the dystrophin associated protein complex in skeletal muscle
10.1016/s0960-8966(02)00191-8 · 2003
Dystrophin in central nervous system: a developmental, regional distribution and subcellular localization study
10.1016/0304-3940(91)90828-h · 1991
Cognitive impairment in Duchenne muscular dystrophy
10.1016/0960-8966(94)90072-8 · 1994
Association of Duchenne muscular dystrophy with autism spectrum disorder
10.1177/08830738050200100201 · 2005
Learning and Behavior in Duchenne Muscular Dystrophy for parents and educators
2011
The value of mammalian models for duchenne muscular dystrophy in developing therapeutic strategies
10.1016/s0070-2153(08)00609-1 · 2008
Towards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophy
10.1016/j.nbd.2008.03.008 · 2008
Preclinical drug trials in the mdx mouse: assessment of reliable and sensitive outcome measures
10.1002/mus.21211 · 2009
X chromosome-linked muscular dystrophy (mdx) in the mouse
10.1073/pnas.81.4.1189 · 1984
The molecular basis of muscular dystrophy in the mdx mouse: a point mutation
10.1126/science.2662404 · 1989
Contrasting effects of steroids and angiotensin-converting-enzyme inhibitors in a mouse model of dystrophin-deficient cardiomyopathy
10.1093/eurjhf/hfp028 · 2009
Performance and excitability of mdx mouse muscle at 5, and 13 wk of age
10.1152/jappl.1995.78.3.961 · 1995
Functional regeneration in the hindlimb skeletal muscle of the mdx mouse
10.1007/bf01738755 · 1988
A-utrophin up-regulation in mdx skeletal muscle is independent of regeneration
10.1016/j.nmd.2003.09.004 · 2004
Non-toxic ubiquitous over-expression of utrophin in the mdx mouse
10.1016/s0960-8966(01)00220-6 · 2001
The artificial gene Jazz, a transcriptional regulator of utrophin, corrects the dystrophic pathology in mdx mice
10.1093/hmg/ddp539 · 2010
Prevention of pathology in mdx mice by expression of utrophin: analysis using an inducible transgenic expression system
10.1093/hmg/11.26.3333 · 2002
Utrophin deficiency worsens cardiac contractile dysfunction present in dystrophin-deficient mdx mice
10.1152/ajpheart.00448.2005 · 2005
Reciprocal expression of dystrophin and utrophin in muscles of Duchenne muscular dystrophy patients, female DMD-carriers and control subjects
10.1016/0022-510x(93)90190-a · 1993
Telomere length as a tool to monitor satellite cell ampli-fication for cell-mediated gene therapy
10.1089/hum.1996.7.11-1347 · 1996
Short telomeres and stem cell exhaustion model Duchenne muscular dystrophy in mdx/mTR mice
10.1016/j.cell.2010.11.039 · 2011
Of mice and not men: differences between mouse and human immunology
10.4049/jimmunol.172.5.2731 · 2004
A chronic inflammatory response dominates the skeletal muscle molecular signature in dystrophin-deficient mdx mice
10.1093/hmg/11.3.263 · 2002
CD8(+) T-cell responses to adeno-associated virus capsid in humans
10.1038/nm1549 · 2007
Toward an oligonucleotide therapy for Duchenne muscular dystrophy: a complex deve-lopment challenge
10.1126/scitranslmed.3000512 · 2010
Optimization of peptide nucleic acid antisense oligonucleotides for local and systemic dystrophin splice correction in the mdx mouse
10.1038/mt.2009.310 · 2010
Drosophila Dystrophin is required for integrity of the musculature
10.1016/j.mod.2007.04.003 · doi-reference
Dystrophin is required for appropriate retrograde control of neurotransmitter release at the Drosophila neuromuscular junction
10.1523/jneurosci.4069-05.2006 · doi-reference
Mutations in the dystrophin-like dys-1 gene of Caenorhabditis elegans result in reduced acetylcholinesterase activity
10.1016/s0014-5793(99)01651-8 · doi-reference
Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hype-ractivity and suggest a link with cholinergic transmission
10.1007/s100480050053 · doi-reference
Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin
10.1093/hmg/ddn337 · doi-reference
Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo
10.1242/dev.00799 · doi-reference
Genes controlling and mediating locomotion behavior of the zebrafish embryo and larva
10.1242/dev.123.1.399 · doi-reference
Identification of a zebrafish model of muscular dystrophy
10.1111/j.1440-1681.2004.04030.x · doi-reference
Eccentric contraction injury in dystrophic canine muscle
10.1053/apmr.2002.35109 · doi-reference
Gait analysis using accelerometry in dystrophin-deficient dogs
10.1016/j.nmd.2009.07.014 · doi-reference
Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy
10.1016/s0092-8674(00)80532-2 · doi-reference
Impaired respiratory function in mdx and mdx/utrn(+/-) mice
10.1002/mus.21848 · doi-reference
Abnormalities in structure and function of limb skeletal muscle fibres of dystrophic mdx mice.
10.1098/rspb.1992.0058 · doi-reference
The mdx mouse skeletal muscle myopathy
10.1111/j.1365-2990.1988.tb00866.x · doi-reference
Skeletal muscle pathology in X chromosome-linked muscular dystrophy (mdx) mouse
10.1007/bf00687043 · doi-reference
Manganese-enhanced magnetic resonance imaging (MEMRI): methodological and practical considerations
10.1002/nbm.945 · doi-reference
Manganese-enhanced MRI of mouse heart during changes in inotropy
10.1002/mrm.1273 · doi-reference
Muscle damage in mdx (dystrophic) mice: role of calcium and reactive oxygen species
10.1111/j.1440-1681.2006.04394.x · doi-reference
Quantitative magnetic resonance imaging of the mdx mouse model of Duchenne muscular dystrophy
10.1002/(sici)1097-4598(199910)22:10<1367::aid-mus5>3.0.co;2-h · doi-reference
10.1016/j.ajpath.2010.11.027
10.1016/j.ajpath.2010.11.027 · doi-reference
Intolerance to ss-blockade in a mouse model of delta-sarcoglycan-deficient muscular dystrophy cardiomyopathy
10.1093/eurjhf/hfq129 · doi-reference
Steroid treatment causes deterioration of myocardial function in the {delta}-sarco-glycan-deficient mouse model for dilated cardiomyopathy
10.1093/cvr/cvn131 · doi-reference
Evans Blue Dye as an in vivo marker of myofibre damage: optimising parameters for detecting initial myofibre membrane permeability
10.1046/j.0021-8782.2001.00008.x · doi-reference
Drug screening in a zebrafish model of Duchenne muscular dystrophy
10.1073/pnas.1102116108 · doi-reference
Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology
10.1016/j.nmd.2010.08.004 · doi-reference
Dystrobrevin requires a dystrophin-binding domain to function in Caenorhabditis elegans
10.1046/j.1432-1327.2002.02780.x · doi-reference
DYC-1, a protein functionally linked to dystrophin in Caenorhabditis elegans is associated with the dense body, where it interacts with the muscle LIM domain protein ZYX-1
10.1091/mbc.e07-05-0497 · doi-reference
Embryonic expression patterns of the Drosophila dystrophin-associated glyco-protein complex orthologs
10.1016/j.modgep.2003.09.004 · doi-reference
Dystrophin and Dp71, two products of the DMD gene, show a different pattern of expression during embryonic development in zebrafish
10.1016/s0925-4773(01)00310-0 · doi-reference
Dystrobrevin and dystrophin family gene expression in zebrafish
10.1016/j.modgep.2007.10.004 · doi-reference
The dystrophin / utrophin homologues in Drosophila and in sea urchin
10.1016/s0378-1119(00)00584-9 · doi-reference
Dystrophin in adult zebrafish muscle
10.1006/bbrc.2001.5424 · doi-reference
Canine X-linked muscular dystrophy in Japan (CXMDJ
10.1538/expanim.52.93 · doi-reference
Identification of three distinguishable phenotypes in golden retriever muscular dystrophy
10.4238/vol8-2gmr581 · doi-reference
An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy
10.1016/0888-7543(92)90210-j · doi-reference
Muscular dystrophy in a litter of golden retriever dogs
10.1002/mus.880111008 · doi-reference
Progressive muscular dystrophy in a golden retriever dog: light microscope and ultrastructural features at 4 and 8 months
10.1007/bf00688053 · doi-reference