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Wyszukujesz frazę ""Delattre, O."" wg kryterium: Wszystkie pola


Tytuł :
ART-DeCo: easy tool for detection and characterization of cross-contamination of DNA samples in diagnostic next-generation sequencing analysis.
Autorzy :
Fiévet A; Department of Genetics, Institut Curie, 75005, Paris, France. .; Institut Curie, PSL Research University, INSERM U830, Institut de recherche, F-75005, Paris, France. .
Bernard V; Institut Curie Genomics of Excellence (ICGex) platform, Institut Curie Research Center, Paris, France.
Tenreiro H; Department of Genetics, Institut Curie, 75005, Paris, France.
Dehainault C; Department of Genetics, Institut Curie, 75005, Paris, France.
Girard E; Institut Curie, 26 rue d'Ulm, F-75005, Paris, France.; PSL Research University, F-75005, Paris, France.; Inserm, U900, F-75005, Paris, France.; Mines Paris Tech, F-77305, cedex Fontainebleau, France.
Deshaies V; Institut Curie, 26 rue d'Ulm, F-75005, Paris, France.; PSL Research University, F-75005, Paris, France.; Inserm, U900, F-75005, Paris, France.; Mines Paris Tech, F-77305, cedex Fontainebleau, France.
Hupe P; Institut Curie, 26 rue d'Ulm, F-75005, Paris, France.; PSL Research University, F-75005, Paris, France.; Inserm, U900, F-75005, Paris, France.; Mines Paris Tech, F-77305, cedex Fontainebleau, France.
Delattre O; Department of Genetics, Institut Curie, 75005, Paris, France.; Institut Curie, PSL Research University, INSERM U830, Institut de recherche, F-75005, Paris, France.
Stern MH; Department of Genetics, Institut Curie, 75005, Paris, France.; Institut Curie, PSL Research University, INSERM U830, Institut de recherche, F-75005, Paris, France.
Stoppa-Lyonnet D; Department of Genetics, Institut Curie, 75005, Paris, France.; Institut Curie, PSL Research University, INSERM U830, Institut de recherche, F-75005, Paris, France.; University Paris Descartes, Sorbonne Paris Cité, France.
Golmard L; Department of Genetics, Institut Curie, 75005, Paris, France.
Houdayer C; Department of Genetics, Institut Curie, 75005, Paris, France.; Institut Curie, PSL Research University, INSERM U830, Institut de recherche, F-75005, Paris, France.; University Paris Descartes, Sorbonne Paris Cité, France.; Department of Genetics, F76000 and Normandy Univ, UNIROUEN, Inserm U1245, Normandy Centre for Genomic and Personalized Medicine, Rouen University Hospital, Rouen, France.
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Źródło :
European journal of human genetics : EJHG [Eur J Hum Genet] 2019 May; Vol. 27 (5), pp. 792-800. Date of Electronic Publication: 2019 Jan 25.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
DNA Contamination*
High-Throughput Nucleotide Sequencing*
Molecular Diagnostic Techniques*
DNA/*analysis
Alleles ; Genotype ; Humans ; Polymorphism, Single Nucleotide/genetics
Czasopismo naukowe
Tytuł :
SHH medulloblastoma in a young adult with a TCF4 germline pathogenic variation.
Autorzy :
Blanluet M; Unité de Génétique Somatique, Institut Curie, Paris, France.
Masliah-Planchon J; Unité de Génétique Somatique, Institut Curie, Paris, France.; Pediatric Oncology Department, SIREDO Oncology Centre (Care, Innovation, Research in Pediatric, Adolescent and Young Adults Oncology), Institut Curie, 26, rue d'Ulm, 75248, Paris Cedex 05, France.
Giurgea I; UF de Génétique Moléculaire, Hôpital Armand Trousseau, APHP, Paris, France.; Sorbonne Université, INSERM, UMR S933, Paris, France.
Bielle F; Departement de Neuropathologie, Groupe Hospitalier Pitié-Salpêtrière, AP-HP, Paris, France.
Girard E; INSERM U900, Institut Curie, Paris, France.
Andrianteranagna M; Pediatric Oncology Department, SIREDO Oncology Centre (Care, Innovation, Research in Pediatric, Adolescent and Young Adults Oncology), Institut Curie, 26, rue d'Ulm, 75248, Paris Cedex 05, France.
Clemenceau S; Neurochirurgie, GH Pitie-Salpêtrière-Charles Foix, APHP, Paris, France.
Bourneix C; Unité de Génétique Somatique, Institut Curie, Paris, France.
Burglen L; Centre de Référence Maladies Rares 'Malformations et Maladies Congénitales du Cervelet', et Département de Génétique, Hôpital Armand Trousseau, GHUEP, APHP, Paris, France.
Doummar D; Département de Neuropédiatrie, Hôpital Armand Trousseau, APHP, Paris, France.
Rapinat A; Translational Research Department, Genomics Platform, Institut Curie, PSL Research University, Paris, 75248, France.
Oumoussa BM; Sorbonne Université, Inserm, UMS Omique, Plateforme Post-Génomique de la Pitié-Salpêtrière, P3S, 75013, Paris, France.
Ayrault O; Université Paris Sud, Université Paris-Saclay, CNRS, UMR 3347, INSERM U1021, Orsay, France.; Institut Curie, PSL Research University, CNRS UMR, INSERM, Orsay, France.
Pouponnot C; Université Paris Sud, Université Paris-Saclay, CNRS, UMR 3347, INSERM U1021, Orsay, France.; Institut Curie, PSL Research University, CNRS UMR, INSERM, Orsay, France.
Gentien D; Translational Research Department, Genomics Platform, Institut Curie, PSL Research University, Paris, 75248, France.
Pierron G; Unité de Génétique Somatique, Institut Curie, Paris, France.; Pediatric Oncology Department, SIREDO Oncology Centre (Care, Innovation, Research in Pediatric, Adolescent and Young Adults Oncology), Institut Curie, 26, rue d'Ulm, 75248, Paris Cedex 05, France.
Delattre O; Unité de Génétique Somatique, Institut Curie, Paris, France.; Pediatric Oncology Department, SIREDO Oncology Centre (Care, Innovation, Research in Pediatric, Adolescent and Young Adults Oncology), Institut Curie, 26, rue d'Ulm, 75248, Paris Cedex 05, France.; Inserm U830, PSL Université, Institut Curie, Paris, France.
Doz F; Pediatric Oncology Department, SIREDO Oncology Centre (Care, Innovation, Research in Pediatric, Adolescent and Young Adults Oncology), Institut Curie, 26, rue d'Ulm, 75248, Paris Cedex 05, France.; Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
Bourdeaut F; Pediatric Oncology Department, SIREDO Oncology Centre (Care, Innovation, Research in Pediatric, Adolescent and Young Adults Oncology), Institut Curie, 26, rue d'Ulm, 75248, Paris Cedex 05, France. .; Inserm U830, PSL Université, Institut Curie, Paris, France. .
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Źródło :
Acta neuropathologica [Acta Neuropathol] 2019 Apr; Vol. 137 (4), pp. 675-678. Date of Electronic Publication: 2019 Mar 08.
Typ publikacji :
Case Reports; Letter
MeSH Terms :
Brain Stem Neoplasms/*genetics
Hyperventilation/*genetics
Intellectual Disability/*genetics
Medulloblastoma/*genetics
Adult ; Brain Stem Neoplasms/pathology ; Facies ; Female ; Humans ; Hyperventilation/pathology ; Intellectual Disability/pathology ; Medulloblastoma/pathology
SCR Disease Name :
Pitt-Hopkins syndrome
Raport
Tytuł :
Circulating tumor DNA analysis enables molecular characterization of pediatric renal tumors at diagnosis.
Autorzy :
Jiménez I; SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Institut Curie, Paris, France.; INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, Institut Curie, Paris, France.; SiRIC RTOP « Recherche Translationelle en Oncologie Pédiatrique », Institut Curie, Paris, France.; PSL Research University, Paris, France.
Chicard M; SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Institut Curie, Paris, France.; INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, Institut Curie, Paris, France.; SiRIC RTOP « Recherche Translationelle en Oncologie Pédiatrique », Institut Curie, Paris, France.; PSL Research University, Paris, France.
Colmet-Daage L; SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Institut Curie, Paris, France.; INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, Institut Curie, Paris, France.; SiRIC RTOP « Recherche Translationelle en Oncologie Pédiatrique », Institut Curie, Paris, France.; PSL Research University, Paris, France.
Clément N; SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Institut Curie, Paris, France.; SiRIC RTOP « Recherche Translationelle en Oncologie Pédiatrique », Institut Curie, Paris, France.; PSL Research University, Paris, France.
Danzon A; SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Institut Curie, Paris, France.; INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, Institut Curie, Paris, France.; SiRIC RTOP « Recherche Translationelle en Oncologie Pédiatrique », Institut Curie, Paris, France.; PSL Research University, Paris, France.
Lapouble E; Somatic Genetics Unit, Institut Curie, Paris, France.
Pierron G; Somatic Genetics Unit, Institut Curie, Paris, France.
Bohec M; Research Center, Institut Curie, Institut Curie Genomics of Excellence (ICGex) Platform, Paris, France.
Baulande S; Research Center, Institut Curie, Institut Curie Genomics of Excellence (ICGex) Platform, Paris, France.
Berrebi D; Service de Pathologie, Hôpital Robert Debré, APHP, Paris, France.
Fréneaux P; PSL Research University, Paris, France.; Service de Pathologie, Hospital Group, Institut Curie, Paris, France.
Coulomb A; Service de Pathologie, Hôpital Armand Trousseau, APHP, Paris, France.; Université Pierre et Marie Curie, Paris, France.
Galmiche-Rolland L; Service de Pathologie, Hôpital Necker, APHP, Paris, France.
Sarnacki S; Département de Chirurgie Pédiatrique, Hôpital Necker, APHP, Paris, France.; Université Paris Descartes, Paris, France.
Audry G; Université Pierre et Marie Curie, Paris, France.; Département de Chirurgie Pédiatrique, Hôpital Armand Trousseau, APHP, Paris, France.
Philippe-Chomette P; Département de Chirurgie Pédiatrique, Hôpital Robert Debré, APHP, Paris, France.
Brisse HJ; PSL Research University, Paris, France.; Département d'Imagerie, Hospital Group, Institut Curie, Paris, France.
Doz F; SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Institut Curie, Paris, France.; PSL Research University, Paris, France.; Université Paris Descartes, Paris, France.
Michon J; SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Institut Curie, Paris, France.; PSL Research University, Paris, France.
Delattre O; SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Institut Curie, Paris, France.; INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, Institut Curie, Paris, France.; PSL Research University, Paris, France.
Schleiermacher G; SIREDO Oncology Center (Care, Innovation and research for children and AYA with cancer), Institut Curie, Paris, France.; INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Research Center, Institut Curie, Paris, France.; SiRIC RTOP « Recherche Translationelle en Oncologie Pédiatrique », Institut Curie, Paris, France.; PSL Research University, Paris, France.
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Źródło :
International journal of cancer [Int J Cancer] 2019 Jan 01; Vol. 144 (1), pp. 68-79. Date of Electronic Publication: 2018 Oct 26.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Biomarkers, Tumor/*genetics
Circulating Tumor DNA/*genetics
Kidney Neoplasms/*genetics
Wilms Tumor/*genetics
Biomarkers, Tumor/blood ; Child ; Child, Preschool ; Circulating Tumor DNA/blood ; DNA Copy Number Variations ; Female ; Humans ; Infant ; Kidney Neoplasms/diagnosis ; Kidney Neoplasms/therapy ; Male ; Neoadjuvant Therapy ; Nephrectomy ; Retrospective Studies ; Sensitivity and Specificity ; Whole Genome Sequencing/methods ; Wilms Tumor/diagnosis ; Wilms Tumor/therapy
Czasopismo naukowe

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