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Discovery of novel gene solves mystery of scar formation
medicalxpress.com
Discovery of novel gene solves mystery of scar ... Sébastien Küry, Gasnat Shaboodien, Darren T. Houniet, Nonhlanhla P. Khumalo, Chantal Bou-Hanna, Nathalie
Interests
Delineation of the infrequent mosaicism of KRAS mutational status in...
jcp.bmj.com
Sébastien Küry, Philippe Jamet, Hélène Senellart, Fabrice Airaud, Jean-François Ramée, Stéphane Bézieau, Tamara Matysiak-Budnik, Christian L Laboisse,
Business Profiles
Researchgate: Sébastien Küry
Nantes, France
Education
Team Identifies New Neurodevelopmental Syndrome | Columbia University...
www.cuimc.columbia.edu
Columbia University researchers discover a new neurodevelopmental syndrome and the genetic mutation that causes it.
Books & Literature
Genome-wide search for gene-gene interactions in colorectal cancer. –...
doaj.org
Information about the open-access article 'Genome-wide search for gene-gene interactions in colorectal cancer.' in DOAJ. DOAJ is an online directory that...
SpringerCitations - Search Results
citations.springernature.com
... Hermann Brenner, Bernd Frank, Stéphane Bézieau, Sébastien Küry, Martha L. Slattery, John L. Hopper, Mark A. Jenkins, Loic Marchand,
AACR Proceedings: Abstracts American Association for...
books.google.co.uk
The AACR Annual Meeting highlights the best cancer science and medicine from institutions all over the world. Attendees are invited to stretch their...
Related Documents
(PPT) Mutations in FAM111B Cause Hereditary Fibrosing Poikiloderma...
pdfslide.net
Slide 1Mutations in FAM111B Cause Hereditary Fibrosing Poikiloderma with Tendon Contracture, Myopathy, and Pulmonary Fibrosis Sandra Mercier, Sébastien Küry,...
Identification of a Novel Mutation in the SLC39A4 Gene in a ...www.medicaljournals.se › acta › content
www.medicaljournals.se
... SLC39A4 Gene in a Case of Acrodermatitis Enteropathica. Rüdiger Panzer, Sébastien Küry, Sébastien Schmitt, Regina Fölster-Holst DOI:
Scientific Publications
Laboratory of Molecular Genetics (Pr. Bezieau's lab ...www.ncbi.nlm.nih.gov › clinvar › submitters
www.ncbi.nlm.nih.gov
; Sebastien KURY, Contact Phone: ; Sébastien Küry, Contact
Low-penetrance alleles predisposing to sporadic colorectal cancers: a...
bmccancer.biomedcentral.com
... Sébastien Küry † Equal contributors; Author Affiliations. 1 Service de Génétique Médicale, Pôle de
Publications
Low-penetrance alleles predisposing to sporadic colorectal cancers: a...
link.springer.com
Sébastien Küry (1) Bruno Buecher (2) Sébastien Robiou-du-Pont (3) Catherine Scoul (3) Hélène Colman (3) Tanguy Le Neel (4) Claire Le Houérou (5) Roger Faroux (6)
Meta-analysis of new genome-wide association studies of colorectal...
link.springer.com
Meta-analysis of new genome-wide association studies of colorectal cancer risk ... Sébastien Küry (31) Martha L. Slattery (32) John L. Hopper (33) Mark A. Jenkins (33)
theses.fr – Sébastien Küry , Recherche et mise en évidence d'une base...
www.theses.fr
L'acrodermatite entéropathique est un syndrome héréditaire rare, transmis de manière autosomique récessive, dont la cause est une malabsorption intestinale du...
Reports & Statements
Clinical utility gene card for: acrodermatitis enteropathica – update...
www.nature.com
Clinical utility gene card for: acrodermatitis enteropathica – update Sébastien Küry ,; Monia Kharfi ...
Clinical utility gene card for: acrodermatitis enteropathica |...
www.nature.com
Clinical Utility Gene Card
Miscellaneous
sg:person Springer Nature SciGraph
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Go. You are here: Home · Persons; http://scigraph.springernature.com/person Sébastien Küry. Ontology type: schema:Person.
Sébastien Küry | Centre hospitalier universitaire de Nantes -...
chu-nantes.academia.edu
Academia.edu is a place to share and follow research.
Joint Diseases: Küry, Sébastien - Expertscape.com
www.expertscape.com
Medical and scientific articles about Joint Diseases, written by Sébastien Küry
Sébastien Küry - Rennes, Coulaines, Le Mans, Neuville-sur-Sarthe
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Retrouve avec Trombi.com - retrouveur d'amis - tes anciens camarades de classe, tes collègues, tes camarades de promotions, tes premiers amours et tes amis perdus de
Bases moléculaires de l’acrodermatite entéropathi… – M/S : médecine...
www.erudit.org
Bases moléculaires de l'acrodermatite entéropathiqueMolecular bases of acrodermatitis enteropathica. Sébastien Küry. Laboratoire d'étude du polymorphisme ...
Bases moléculaires de l'acrodermatite entéropathi… – M/S ...www.erudit.org › v1-n1-ms837
www.erudit.org
Sébastien Küry,; Stéphane Bézieau and; Jean-Paul Moisan …more information. Sébastien Küry Laboratoire d'étude du polymorphisme de l'ADN, Faculté de ...
Combinations of cytochrome P450 gene polymorphisms enhancing the risk...
hal.archives-ouvertes.fr
Sébastien Küry, Bruno Buecher, Sébastien Robiou-Du-Pont, Catherine Scoul, Véronique Sébille, et al.. Combinations of cytochrome P450 gene polymorphisms ...
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause...
www.hal.inserm.fr
Sébastien Küry 1, * Geeske van Woerden 2, 3 Thomas Besnard 1 Martina Onori 2, 3 Xénia Latypova 1 Meghan Towne 4, 5 Megan Cho 6 Trine Prescott
Myopathie : découverte d'un nouveau gène au CHU de Nantes -...
www.allodocteurs.fr
Un nouveau gène, FAM111B, vient d'être identifié par l'équipe du service de génétique médicale du CHU de Nantes. Ce gène est responsable d'un syndrome rare, la...
De Novo and inherited loss-of-function variants in TLK2: Clinical and...
eprints.soton.ac.uk
Author: Sébastien Küry. Author: Eduardo Calpena. Author: Nils Koelling. Author: Simon J. Mcgowan. Author: Stephen R.F. Twigg. Author: Irene ...
Genome-Wide Search for Gene-Gene Interactions in Colorectal Cancer |...
journals.plos.org
Sébastien Küry, Affiliation: Service de Génétique Médicale, CHU Nantes, Nantes, France X. Loic Le Marchand, Affiliation
JCP -- Electronic Letters submission
jcp.bmjjournals.com
Delineation of the infrequent mosaicism of KRAS mutational status in metastatic colorectal adenocarcinomas. Céline Bossard,; Sébastien Küry,; Philippe Jamet, ...
All variants in the SLC39A4 gene - Global Variome shared LOVD
databases.lovd.nl
2002, OMIM:var0003, -, Germline (inherited), yes, -, -, 0, -, Sébastien Küry. +?/+?
Full data view for gene SLC39A4 - Global Variome shared LOVD
databases.lovd.nl
Curator: Sébastien Küry · SLC39A4 homepage · View transcripts · View variants · View individuals · View diseases · View screenings · Submit new data · LOVD ...
Mutations in FAM111B Cause Hereditary Fibrosing Poikiloderma with...
www.infona.pl
Congenital poikiloderma is characterized by a combination of mottled pigmentation, telangiectasia, and epidermal atrophy in the first few months of life. We...
Genetic variant predictors of gene expression provide new insight...
pure.au.dk
... Heidelberg, University of Virginia Medical School; ,; Sébastien Küry, Centre Hospitalier Universitaire Hotel-Dieu, CHU Nantes, University of ...
Germline de Novo Mutations in GNB1 Cause Severe Neurodevelopmental...
experts.umn.edu
Slavé Petrovski, Sébastien Küry, Candace T. Myers, Kwame Anyane-Yeboa, Benjamin Cogné, Martin Bialer, Fan Xia, Parisa Hemati, James ...
Catalogue SUDOC
www.sudoc.abes.fr
Sébastien Robiou du Pont ; sous la direction de Stéphane Bézieau, Sébastien Küry.
Locus Specific Database list
grenada.lumc.nl
Global Variome shared LOVD https://databases.lovd.nl/shared/genes/FAM111B, Sébastien Küry CHU de Nantes, -, -, LOVD 3.X, ClinVar at NCBI
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