About: Isabelle Marty

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Marty, Isabelle (19..-.... ; biologiste) Marty, Isabelle (19..-.... ; biologiste)
Life Event	http://www.idref.fr/112843832/birth
preferred label	Marty, Isabelle (19..-.... ; biologiste)
name	Isabelle Marty
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
Given name	Isabelle
familyName	Marty
has biographical i...tion (Deprecated)	Chargée de recherches à l'INRA d'Avignon en 2009 Spécialisée en biochimie et biologie cellulaire Examinateur d'une thèse en Sciences du Mouvement Humain à Montpellier 1 en 2013
gender	female
ORCID iD	0000-0003-3625-913X
Scopus ID	55779175800
is sameAs of	Marty, Isabelle (19..-.... ; biologiste) Marty, Isabelle (19..-.... ; biologiste) Marty, Isabelle (19..-.... ; biologiste)
is Thesis advisor of	http://www.sudoc.fr/139427651/id Fonctions des traidines dans le muscle squelettique, caractérisation de l'isoforme Trisk 32 http://www.sudoc.fr/18542032X/id http://www.sudoc.fr/143705873/id http://www.sudoc.fr/172517109/id Etude de la physiopathologie de la dystrophie musculaire tibiale et de la dystrophie des ceintures 2J et stratégies thérapeutiques http://www.sudoc.fr/112844669/id http://www.sudoc.fr/202778053/id http://www.sudoc.fr/188930728/id http://www.sudoc.fr/224736485/id http://www.sudoc.fr/223766895/id Mise en place et évolution de la paroi cellulaire du péricarpe du fruit de tomate au cours de son développement et de sa maturation http://www.sudoc.fr/246944455/id Caractérisation et rôle des isoformes de la triadine dans la physiologie des cellules musculaires http://www.sudoc.fr/270450505/id http://www.sudoc.fr/247165417/id http://www.sudoc.fr/247137146/id http://www.sudoc.fr/265632943/id
is Praeses of	http://www.sudoc.fr/263004376/id http://www.sudoc.fr/225671514/id http://www.sudoc.fr/269912460/id http://www.sudoc.fr/282135790/id
is Author of	http://www.sudoc.fr/012823414/id http://www.sudoc.fr/008858977/id Multiple determinants in voltage-dependent P/Q calcium channels control their retention in the endoplasmic reticulum Absence of beta-tropomyosin is a new cause of Escobar syndrome associated with nemaline myopathy. The calcium release complex in skeletal muscle and its associated diseases Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy N‐ WASP is required for Amphiphysin‐2/ BIN 1‐dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathy First genomic rearrangement of the RYR1 gene associated with an atypical presentation of lethal neonatal hypotonia. Functional analysis reveals splicing mutations of the CASQ2 gene in patients with CPVT: implication for genetic counselling and clinical management. DHPR α1S subunit controls skeletal muscle mass and morphogenesis http://www.sudoc.fr/245490418/id A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores. Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human. Exon skipping as a therapeutic strategy applied to an RYR1 mutation with pseudo-exon inclusion causing a severe core myopathy. Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy. Effects of sustained low-flow ischemia on myocardial function and calcium-regulating proteins in adult and senescent rat hearts Kinetics of nucleotide transport in rat heart mitochondria studied by a rapid filtration technique Caveolin 3 is associated with the calcium release complex and is modified via in vivo triadin modification. The neuronal endopeptidase ECEL1 is associated with a distinct form of recessive distal arthrogryposis. Trisk 32 regulates IP(3) receptors in rat skeletal myoblasts. Expression of the cardiac ryanodine receptor in the compensated phase of hypertrophy in rat heart mRNAs newly synthesized by tobacco mesophyll protoplasts are wound-inducible Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization. Triadin and CLIMP-63 form a link between triads and microtubules in muscle cells http://www.sudoc.fr/245547959/id Corrigendum to "22nd International Congress of the World Muscle Society, Saint Malo, France, 3rd-7th October 2017" [Neuromuscular Disorders 27S2 (2017) S51-S270] Interplay between triadin and calsequestrin in the pathogenesis of CPVT in mouse DHPR alpha1S subunit controls skeletal muscle mass and morphogenesis. Triadin: what possible function 20 years later? Triadin (Trisk 95) overexpression blocks excitation-contraction coupling in rat skeletal myotubes. Variations in the TRPV1 gene are associated to exertional heat stroke Triadin deletion induces impaired skeletal muscle function. Deletion of the microtubule-associated protein 6 (MAP6) results in skeletal muscle dysfunction Nucleotide sequence of a cDNA encoding a tobacco thioredoxin An integrated diagnosis strategy for congenital myopathies. Triadins are not triad-specific proteins: two new skeletal muscle triadins possibly involved in the architecture of sarcoplasmic reticulum. [Ryanodine receptor type 1: redox state matters] Quiescence of human muscle stem cells is favored by culture on natural biopolymeric films Étude de la topographie membranaire du transporteur mitochondrial d'adénine-nucléotides, approches immunochimique et protéolytique Topography of the membrane-bound ADP/ATP carrier assessed by enzymic proteolysis Retrograde regulation of store-operated calcium channels by the ryanodine receptor-associated protein triadin 95 in rat skeletal myotubes. The Nicotiana tabacum genome encodes two cytoplasmic thioredoxin genes which are differently expressed Ryanodine receptor 1 and associated pathologies Functional characterization of a Central Core Disease RyR1 mutation (p.Y4864H) associated with quantitative defect in RyR1 protein Transduction of the scorpion toxin maurocalcine into cells. Evidence that the toxin crosses the plasma membrane. Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion. Trisk 95 as a novel skin mirror for normal and diabetic systemic glucose level ‘Dusty core disease’ (DuCD): expanding morphological spectrum of RYR1 recessive myopathies Topography of the membrane-bound ADP/ATP carrier assessed by enzymic proteolysis Abnormal distribution of calcium-handling proteins: a novel distinctive marker in core myopathies. Modifications de l'expression génique consécutives à l'isolement de protoplastes de cellules de mésophylle de Nicotiana tabacum Triadin binding to the C-terminal luminal loop of the ryanodine receptor is important for skeletal muscle excitation contraction coupling. In vivo RyR1 reduction in muscle triggers a core-like myopathy https://hal.archives-ouvertes.fr/hal-04789694#id Role of triadin in the organization of reticulum membrane at the muscle triad. Cardiomyocyte overexpression of neuronal nitric oxide synthase delays transition toward heart failure in response to pressure overload by preserving calcium cycling. Kinetics of nucleotide transport in rat heart mitochondria studied by a rapid filtration technique Altered expression of triadin 95 causes parallel changes in localized Ca2+ release events and global Ca2+ signals in skeletal muscle cells in culture.

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