About: Lucie Carrier

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Lucie Carrier Goto Sponge NotDistinct Permalink

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

Attributes	Values
type	Person
sameAs	Carrier, Lucie (19..-.... ; biologiste) Carrier, Lucie (19..-.... ; biologiste) Carrier, Lucie (19..-.... ; biologiste)
Life Event	http://www.idref.fr/083020063/birth
preferred label	Carrier, Lucie (19..-.... ; biologiste)
name	Lucie Carrier
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	0000000432632942
Given name	Lucie
familyName	Carrier
has biographical i...tion (Deprecated)	Chercheur INSERM U 582, Institut de myologie, Hôpital Salpetriere, Paris 13, 2004 Professeur de génomique fonctionnelle des cardiomyopathies. En poste au Centre médical universitaire de Hambourg-Eppendorf, Allemagne (en 2022) Auteure d'une thèse de doctorat en biologie (Grenoble 1, 1989)
gender	female
ORCID iD	0000-0001-8776-5820
Scopus ID	55199727100
is sameAs of	Carrier, Lucie (19..-.... ; biologiste) Carrier, Lucie (19..-.... ; biologiste)
is Thesis advisor of	http://www.sudoc.fr/060062339/id http://www.sudoc.fr/246580860/id Anomalies génétiques de la cardiomyopathie hypertrophique familiale, de leur identification à l'analyse de leurs conséquences ex vivo et in vitro
is Publisher of	http://www.sudoc.fr/060585617/id
is Author of	http://www.sudoc.fr/007020341/id Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience FHL2 expression and variants in hypertrophic cardiomyopathy Proteomic and Functional Studies Reveal Detyrosinated Tubulin as Treatment Target in Sarcomere Mutation-Induced Hypertrophic Cardiomyopathy Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice Biomolecular interactions between human recombinant β-MyHC and cMyBP-Cs implicated in familial hypertrophic cardiomyopathy Expression of cardiac myosin-binding protein-C (cMyBP-C) in Drosophila as a model for the study of human cardiomyopathies Cardiovascular magnetic resonance detects microvascular dysfunction in a mouse model of hypertrophic cardiomyopathy Distinction Between Two Populations of Islet-1-Positive Cells in Hearts of Different Murine Strains http://www.sudoc.fr/245461124/id First description of germline mosaicism in familial hypertrophic cardiomyopathy DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death. Protein kinase D increases maximal Ca 2+ -activated tension of cardiomyocyte contraction by phosphorylation of cMyBP-C-Ser 315 Length and protein kinase A modulations of myocytes in cardiac myosin binding protein C-deficient mice Depletion of Vasohibin 1 Speeds Contraction and Relaxation in Failing Human Cardiomyocytes Anomalie de la libération de calcium dans les fibres musculaires squelettiques de porc atteints d'hyperthermie maligne Relation between QT duration and maximal wall thickness in familial hypertrophic cardiomyopathy Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity. Expression of cardiac myosin-binding protein-C (cMyBP-C) in Drosophila as a model for the study of human cardiomyopathies Impairment of the ubiquitin-proteasome system by truncated cardiac myosin binding protein C mutants https://serval.unil.ch/notice/serval:BIB_CDE4D50474A1#id https://serval.unil.ch/notice/serval:BIB_DCB435FBAB69#id https://serval.unil.ch/notice/serval:BIB_C3E520FB4004#id https://serval.unil.ch/notice/serval:BIB_B4DB7BF07223#id Rescue of cardiomyopathy through U7snRNA-mediated exon skipping in Mybpc3 -targeted knock-in mice https://serval.unil.ch/notice/serval:BIB_34E8E01E9EFA#id Targeted therapies in genetic dilated and hypertrophic cardiomyopathies: from molecular mechanisms to therapeutic targets. A position paper from the Heart Failure Association (HFA) and the Working Group on Myocardial Function of the European Society of Cardiology (ESC) Repair of Mybpc3 mRNA by 5′-trans-splicing in a Mouse Model of Hypertrophic Cardiomyopathy
is primary topic of	http://www.idref.fr/083020063
is Opponent of	http://www.sudoc.fr/24939751X/id http://www.sudoc.fr/254677770/id De la caractérisation de la cardiomyopathie dilatée à la modulation à visée thérapeutique des voies de signalisation impliquées dans le phénotype cardiaque de myopathies d'origine génétique. http://www.sudoc.fr/280682689/id
is Thesis referee of	http://www.sudoc.fr/192215582/id http://www.sudoc.fr/176383581/id http://www.sudoc.fr/196916399/id http://www.sudoc.fr/260500062/id http://www.sudoc.fr/244941483/id

Faceted Search & Find service v1.13.91 as of Aug 16 2018

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3229 as of May 14 2019, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (70 GB total memory)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software