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Showing results (241-250 of 348) with videos related to

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Scientific Reports|January 20, 2018
The ten-year evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusionAnna Burford, Alan Mackay, Sergey Popov, et al.
Neuropathology and Applied Neurobiology|July 10, 2024
Decision making for health-related research outcomes that alter diagnosis: A model from paediatric brain tumoursJessica C Pickles, Kristian Aquilina, Jane Chalker, et al.
Neoplasia (New York, N.Y.)|August 2, 2008
Genomic deletions correlate with underexpression of novel candidate genes at six loci in pediatric pilocytic astrocytomaNicola Potter, Aikaterini Karakoula, Kim P Phipps, et al.
Neurology. Genetics|July 9, 2020
Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma geneYing Hong, Annette Keylock, Barbara Jensen, et al.
Biorxiv : the Preprint Server for Biology|September 15, 2025
Structure, dynamics, and processing of 8oxoG:A in the nucleosomeAbigayle F Vito, Justin A Ling, Julia C Ferrara, et al.
Plos One|January 7, 2016
A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial DiseaseSanjeev Rajakulendran, Robert D S Pitceathly, Jan-Willem Taanman, et al.
Brain : a Journal of Neurology|July 1, 2015
Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fissionRojeen Shahni, Catherine M Cale, Glenn Anderson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutationsOmar Hikmat, Charalampos Tzoulis, Wui K Chong, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 24, 2016
Muscle Biopsy Findings in Combination With Myositis-Specific Autoantibodies Aid Prediction of Outcomes in Juvenile DermatomyositisClaire T Deakin, Shireena A Yasin, Stefania Simou, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 20, 2018
Correction: The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutationsOmar Hikmat, Charalampos Tzoulis, Wui K Chong, et al.
Pageof 35

Showing results (241-250 of 348) with videos related to

Sort By:
Pageof 35
Scientific Reports|January 20, 2018
The ten-year evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusionAnna Burford, Alan Mackay, Sergey Popov, et al.
Neuropathology and Applied Neurobiology|July 10, 2024
Decision making for health-related research outcomes that alter diagnosis: A model from paediatric brain tumoursJessica C Pickles, Kristian Aquilina, Jane Chalker, et al.
Neoplasia (New York, N.Y.)|August 2, 2008
Genomic deletions correlate with underexpression of novel candidate genes at six loci in pediatric pilocytic astrocytomaNicola Potter, Aikaterini Karakoula, Kim P Phipps, et al.
Neurology. Genetics|July 9, 2020
Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma geneYing Hong, Annette Keylock, Barbara Jensen, et al.
Biorxiv : the Preprint Server for Biology|September 15, 2025
Structure, dynamics, and processing of 8oxoG:A in the nucleosomeAbigayle F Vito, Justin A Ling, Julia C Ferrara, et al.
Plos One|January 7, 2016
A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial DiseaseSanjeev Rajakulendran, Robert D S Pitceathly, Jan-Willem Taanman, et al.
Brain : a Journal of Neurology|July 1, 2015
Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fissionRojeen Shahni, Catherine M Cale, Glenn Anderson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutationsOmar Hikmat, Charalampos Tzoulis, Wui K Chong, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 24, 2016
Muscle Biopsy Findings in Combination With Myositis-Specific Autoantibodies Aid Prediction of Outcomes in Juvenile DermatomyositisClaire T Deakin, Shireena A Yasin, Stefania Simou, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 20, 2018
Correction: The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutationsOmar Hikmat, Charalampos Tzoulis, Wui K Chong, et al.
Pageof 35