Spatial and temporal homogeneity of driver mutations in diffuse intrinsic pontine glioma.

Nikbakht, Hamid; Panditharatna, Eshini; Mikael, Leonie G; Li, Rui; Gayden, Tenzin; Osmond, Matthew; Ho, Cheng-Ying; Kambhampati, Madhuri; Hwang, Eugene I; Faury, Damien; Siu, Alan; Papillon-Cavanagh, Simon; Bechet, Denise; Ligon, Keith L; Ellezam, Benjamin; Ingram, Wendy J; Stinson, Caedyn; Moore, Andrew S; Warren, Katherine E; Karamchandani, Jason; Packer, Roger J; Jabado, Nada; Majewski, Jacek; Nazarian, Javad

Nikbakht, Hamid; Panditharatna, Eshini; Mikael, Leonie G; Li, Rui; Gayden, Tenzin; Osmond, Matthew; Ho, Cheng-Ying; Kambhampati, Madhuri; Hwang, Eugene I; Faury, Damien; Siu, Alan; Papillon-Cavanagh, Simon; Bechet, Denise; Ligon, Keith L; Ellezam, Benjamin; Ingram, Wendy J; Stinson, Caedyn; Moore, Andrew S; Warren, Katherine E; Karamchandani, Jason; Packer, Roger J; Jabado, Nada; Majewski, Jacek; Nazarian, Javad.

Afiliación

Nikbakht H; Department of Human Genetics, McGill University, Montreal, Québec, Canada H3A 1B1.
Panditharatna E; McGill University and Génome Québec Innovation Centre, Montreal, Québec, Canada H3A 0G1.
Mikael LG; Research Center for Genetic Medicine, Children's National Health System, Washington, District Of Columbia 20010, USA.
Li R; Institute for Biomedical Sciences, George Washington University School of Medicine and Health Sciences, Washington, District Of Columbia 20052, USA.
Gayden T; Department of Pediatrics, McGill University and McGill University Heath Centre Research Institute, Montreal, Québec, Canada H4A 3J1.
Osmond M; Department of Human Genetics, McGill University, Montreal, Québec, Canada H3A 1B1.
Ho CY; McGill University and Génome Québec Innovation Centre, Montreal, Québec, Canada H3A 0G1.
Kambhampati M; Department of Human Genetics, McGill University, Montreal, Québec, Canada H3A 1B1.
Hwang EI; Department of Human Genetics, McGill University, Montreal, Québec, Canada H3A 1B1.
Faury D; McGill University and Génome Québec Innovation Centre, Montreal, Québec, Canada H3A 0G1.
Siu A; Division of Pathology, Children's National Health System, Washington, District Of Columbia 20010, USA.
Papillon-Cavanagh S; Research Center for Genetic Medicine, Children's National Health System, Washington, District Of Columbia 20010, USA.
Bechet D; Center for Cancer and Blood Disorders, Children's National Health System, Washington, District Of Columbia 20010, USA.
Ligon KL; Department of Pediatrics, McGill University and McGill University Heath Centre Research Institute, Montreal, Québec, Canada H4A 3J1.
Ellezam B; The Department of Neurological Surgery, George Washington University School of Medicine and Health Sciences, Washington, District Of Columbia 20052, USA.
Ingram WJ; Department of Human Genetics, McGill University, Montreal, Québec, Canada H3A 1B1.
Stinson C; McGill University and Génome Québec Innovation Centre, Montreal, Québec, Canada H3A 0G1.
Moore AS; Department of Human Genetics, McGill University, Montreal, Québec, Canada H3A 1B1.
Warren KE; Center for Molecular Oncologic Pathology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusett 02115, USA.
Karamchandani J; Department of Pathology, CHU Ste-Justine, Université de Montréal, Montreal, Québec, Canada H3T 1C5.
Packer RJ; UQ Child Health Research Centre, The University of Queensland, Brisbane, Queensland 4101, Australia.
Jabado N; University of Queensland Diamantina Institute, The University of Queensland, Brisbane, Queensland 4102, Australia.
Majewski J; UQ Child Health Research Centre, The University of Queensland, Brisbane, Queensland 4101, Australia.
Nazarian J; University of Queensland Diamantina Institute, The University of Queensland, Brisbane, Queensland 4102, Australia.

Nat Commun ; 7: 11185, 2016 Apr 06.

Article en En | MEDLINE | ID: mdl-27048880

Asunto(s)

Neoplasias del Tronco Encefálico/genética; Carcinogénesis/genética; Regulación Neoplásica de la Expresión Génica; Glioma/genética; Histonas/genética; Mutación; Receptores de Activinas Tipo I/genética; Receptores de Activinas Tipo I/metabolismo; Autopsia; Mapeo Encefálico; Tronco Encefálico/metabolismo; Tronco Encefálico/patología; Neoplasias del Tronco Encefálico/metabolismo; Neoplasias del Tronco Encefálico/patología; Carcinogénesis/metabolismo; Carcinogénesis/patología; Cerebro/metabolismo; Cerebro/patología; Niño; Fosfatidilinositol 3-Quinasa Clase Ia; Evolución Clonal; Glioma/metabolismo; Glioma/patología; Histonas/metabolismo; Humanos; Fosfatidilinositol 3-Quinasas/genética; Fosfatidilinositol 3-Quinasas/metabolismo; Fosfoproteínas Fosfatasas/genética; Fosfoproteínas Fosfatasas/metabolismo; Proteína Fosfatasa 2C; Transducción de Señal; Técnicas Estereotáxicas; Factores de Tiempo; Proteína p53 Supresora de Tumor/genética; Proteína p53 Supresora de Tumor/metabolismo

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_brain_nervous_system_cancer Asunto principal: Histonas / Regulación Neoplásica de la Expresión Génica / Neoplasias del Tronco Encefálico / Carcinogénesis / Glioma / Mutación Límite: Child / Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2016 Tipo del documento: Article

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