Auteurs
Analysis
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Analysis
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Serveur d'exploration sur les relations entre la France et l'Australie - Analysis (UK)

Index « Auteurs » - entrée « Sandra T. Cooper »
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Sandra Suske < Sandra T. Cooper < Sandra Turner  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 2.
Ident.Authors (with country if any)Title
000F56 (2015) Michaela Yuen [Australie] ; Sandra T. Cooper [Australie] ; Steve B. Marston [Royaume-Uni] ; Kristen J. Nowak [Australie] ; Elyshia Mcnamara [Australie] ; Nancy Mokbel [Australie, Liban] ; Biljana Ilkovski [Australie] ; Gianina Ravenscroft [Australie] ; John Rendu [France] ; Josine M. De Winter [Pays-Bas] ; Lars Klinge [Allemagne] ; Alan H. Beggs [États-Unis] ; Kathryn N. North [Australie] ; Coen A. C. Ottenheijm [Pays-Bas] ; Nigel F. Clarke [Australie]Muscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibres
002643 (2010) Nigel F. Clarke [Australie] ; Leigh B. Waddell [Australie] ; Sandra T. Cooper [Australie] ; Margaret Perry [Australie] ; Robert L. L. Smith [Australie] ; Andrew J. Kornberg [Australie] ; Francesco Muntoni [Royaume-Uni] ; Suzanne Lillis [Royaume-Uni] ; Volker Straub [Royaume-Uni] ; Kate Bushby [Royaume-Uni] ; Michela Guglieri [Royaume-Uni] ; Mary D. King [Irlande (pays)] ; Michael A. Farrell [Irlande (pays)] ; Isabelle Marty [France] ; Joel Lunardi [France] ; Nicole Monnier [France] ; Kathryn N. North [Australie]Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion

List of associated KwdEn.i

Nombre de
documents		Descripteur
2Mutation
1Abnormality
1Actins (genetics)
1Actins (metabolism)
1Adolescent
1Adult
1Autosomal recessive inheritance
1Biopsy
1Calcium (metabolism)
1Central core disease
1Cftd
1Cftd patients
1Child
1Child health
1Child, Preschool
1Clarke
1Common cause
1Congenital
1Congenital fiber type disproportion
1Congenital myopathies
1Congenital myopathy
1Convergent strabismus
1Core myopathy
1Disproportion
1European descent
1Female
1Fiber diameter
1Fiber hypotrophy
1Fiber size
1Fiber size disproportion
1Fibers diam
1Generalised
1Generalised muscle
1Genetic causes
1Genetic testing
1Histological
1Humans
1Hypotrophy
1Infant
1Jungbluth
1Main histological abnormality
1Male
1Malignant hyperthermia
1Middle Aged
1Monnier
1Muscle Contraction (physiology)
1Muscle Fibers, Slow-Twitch (metabolism)
1Muscle Weakness (genetics)
1Muscle Weakness (metabolism)
1Muscle samples
1Muscular Atrophy (genetics)
1Muscular Atrophy (metabolism)
1Muscular Diseases (genetics)
1Muscular Diseases (metabolism)
1Myopathy
1Myosins (genetics)
1Myosins (metabolism)
1Neuromuscul disord
1Ophthalmoplegia
1Protein Isoforms
1Protein studies
1Ptosis
1Receptor
1Recessive
1Recessive mutations
1Recessive ryr1 mutations
1Respiratory failure
1Ryanodine
1Ryanodine receptor type
1Ryr1
1Ryr1 cause cftd
1Ryr1 gene
1Ryr1 gene analysis
1Ryr1 levels
1Ryr1 mutations
1Second biopsy
1Sequence changes
1Sequencing genomic
1Tropomyosin (genetics)
1Tropomyosin (metabolism)

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HfdIndexSelect -h $EXPLOR_AREA/Data/UK/Analysis/Author.i  \
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