Search research articles
Contact Us
Filters
Showing results (1-10 of 32) with videos related to
Page
of 4
Sort By:
Pediatric Neurosurgery
|
February 6, 2023
Updates in the Management of Central and Peripheral Nervous System Tumors among Patients with Neurofibromatosis Type 1 and Neurofibromatosis Type 2
Chelsea Kotch, Stephanie Nicole Brosius, Thomas De Raedt, et al.
Journal of Visualized Experiments : Jove
|
February 19, 2024
Spheroid Drug Sensitivity Screening in Glioma Stem Cell Lines
Kyra Harvey, Katherine Labella, Angela Liou, et al.
Plos One
|
February 2, 2023
Identification of therapeutic sensitivities in a spheroid drug combination screen of Neurofibromatosis Type I associated High Grade Gliomas
Jacquelyn Dougherty, Kyra Harvey, Angela Liou, et al.
Genomics
|
July 6, 2004
Genomic organization and evolution of the NF1 microdeletion region
Thomas De Raedt, Hilde Brems, Catalina Lopez-Correa, et al.
Pediatric Blood & Cancer
|
August 4, 2005
Therapy-related acute myeloid leukemia in a child with Noonan syndrome and clonal duplication of the germline PTPN11 mutation
Christophe F Chantrain, Priscilla Jijon, Thomas De Raedt, et al.
European Journal of Human Genetics : EJHG
|
January 24, 2008
Copy number variations in the NF1 gene region are infrequent and do not predispose to recurrent type-1 deletions
Katharina Steinmann, Lan Kluwe, David N Cooper, et al.
Gastroenterology
|
November 8, 2006
Intestinal neurofibromatosis is a subtype of familial GIST and results from a dominant activating mutation in PDGFRA
Thomas de Raedt, Jan Cools, Maria Debiec-Rychter, et al.
Cancer Cell
|
September 14, 2013
The RasGAP gene, RASAL2, is a tumor and metastasis suppressor
Sara Koenig McLaughlin, Sarah Naomi Olsen, Benjamin Dake, et al.
Iscience
|
July 27, 2020
Imaging Mass Spectrometry Reveals Tumor Metabolic Heterogeneity
Yang Zhang, Christelle Guillermier, Thomas De Raedt, et al.
Human Mutation
|
August 31, 2006
Comprehensive NF1 screening on cultured Schwann cells from neurofibromas
Ophélia Maertens, Hilde Brems, Jo Vandesompele, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 32) with videos related to
Sort By:
Page
of 4
Pediatric Neurosurgery
|
February 6, 2023
Updates in the Management of Central and Peripheral Nervous System Tumors among Patients with Neurofibromatosis Type 1 and Neurofibromatosis Type 2
Chelsea Kotch, Stephanie Nicole Brosius, Thomas De Raedt, et al.
Journal of Visualized Experiments : Jove
|
February 19, 2024
Spheroid Drug Sensitivity Screening in Glioma Stem Cell Lines
Kyra Harvey, Katherine Labella, Angela Liou, et al.
Plos One
|
February 2, 2023
Identification of therapeutic sensitivities in a spheroid drug combination screen of Neurofibromatosis Type I associated High Grade Gliomas
Jacquelyn Dougherty, Kyra Harvey, Angela Liou, et al.
Genomics
|
July 6, 2004
Genomic organization and evolution of the NF1 microdeletion region
Thomas De Raedt, Hilde Brems, Catalina Lopez-Correa, et al.
Pediatric Blood & Cancer
|
August 4, 2005
Therapy-related acute myeloid leukemia in a child with Noonan syndrome and clonal duplication of the germline PTPN11 mutation
Christophe F Chantrain, Priscilla Jijon, Thomas De Raedt, et al.
European Journal of Human Genetics : EJHG
|
January 24, 2008
Copy number variations in the NF1 gene region are infrequent and do not predispose to recurrent type-1 deletions
Katharina Steinmann, Lan Kluwe, David N Cooper, et al.
Gastroenterology
|
November 8, 2006
Intestinal neurofibromatosis is a subtype of familial GIST and results from a dominant activating mutation in PDGFRA
Thomas de Raedt, Jan Cools, Maria Debiec-Rychter, et al.
Cancer Cell
|
September 14, 2013
The RasGAP gene, RASAL2, is a tumor and metastasis suppressor
Sara Koenig McLaughlin, Sarah Naomi Olsen, Benjamin Dake, et al.
Iscience
|
July 27, 2020
Imaging Mass Spectrometry Reveals Tumor Metabolic Heterogeneity
Yang Zhang, Christelle Guillermier, Thomas De Raedt, et al.
Human Mutation
|
August 31, 2006
Comprehensive NF1 screening on cultured Schwann cells from neurofibromas
Ophélia Maertens, Hilde Brems, Jo Vandesompele, et al.
Page
of 4