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Neuropathology and Applied Neurobiology
|
July 13, 2026
Utility of Optical Genome Mapping in the Characterisation of the Global Genomic Architecture of Paediatric Central Nervous System Tumours: A Pilot Study
Viola Alesi, Silvia Genovese, Serena Russo, et al.
Gut
|
April 9, 2017
CHK1-targeted therapy to deplete DNA replication-stressed, p53-deficient, hyperdiploid colorectal cancer stem cells
Gwenola Manic, Michele Signore, Antonella Sistigu, et al.
Pigment Cell & Melanoma Research
|
January 6, 2026
Melanomas and Mesenchymal Tumors Arising in Giant Congenital Melanocytic Nevi: Clinico-Pathological and Molecular Characterization of a Case Series
Sabrina Rossi, Sabina Barresi, Isabella Giovannoni, et al.
Haematologica
|
May 9, 2020
CD28.OX40 co-stimulatory combination is associated with long in vivo persistence and high activity of CAR.CD30 T-cells
Marika Guercio, Domenico Orlando, Stefano Di Cecca, et al.
Cancer Letters
|
February 29, 2024
Clinicopathological and molecular landscape of 5-year IDH-wild-type glioblastoma survivors: A multicentric retrospective study
Evelina Miele, Elena Anghileri, Chiara Calatozzolo, et al.
Cell Reports
|
March 5, 2020
The Interplay between CD27<sup>dull</sup> and CD27<sup>bright</sup> B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory
Ola Grimsholm, Eva Piano Mortari, Alexey N Davydov, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
November 25, 2023
PATZ1-Rearranged Tumors of the Central Nervous System: Characterization of a Pediatric Series of Seven Cases
Sabrina Rossi, Sabina Barresi, Giovanna Stefania Colafati, et al.
American Journal of Human Genetics
|
December 20, 2023
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome
Vincenzo Salpietro, Reza Maroofian, Maha S Zaki, et al.
Nature Communications
|
February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
Holger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
Science Advances
|
December 3, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patients
Laura Bryant, Dong Li, Samuel G Cox, et al.
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Search research articles
Search
Showing results (81-90 of 90) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 90 results.
Neuropathology and Applied Neurobiology
|
July 13, 2026
Utility of Optical Genome Mapping in the Characterisation of the Global Genomic Architecture of Paediatric Central Nervous System Tumours: A Pilot Study
Viola Alesi, Silvia Genovese, Serena Russo, et al.
Gut
|
April 9, 2017
CHK1-targeted therapy to deplete DNA replication-stressed, p53-deficient, hyperdiploid colorectal cancer stem cells
Gwenola Manic, Michele Signore, Antonella Sistigu, et al.
Pigment Cell & Melanoma Research
|
January 6, 2026
Melanomas and Mesenchymal Tumors Arising in Giant Congenital Melanocytic Nevi: Clinico-Pathological and Molecular Characterization of a Case Series
Sabrina Rossi, Sabina Barresi, Isabella Giovannoni, et al.
Haematologica
|
May 9, 2020
CD28.OX40 co-stimulatory combination is associated with long in vivo persistence and high activity of CAR.CD30 T-cells
Marika Guercio, Domenico Orlando, Stefano Di Cecca, et al.
Cancer Letters
|
February 29, 2024
Clinicopathological and molecular landscape of 5-year IDH-wild-type glioblastoma survivors: A multicentric retrospective study
Evelina Miele, Elena Anghileri, Chiara Calatozzolo, et al.
Cell Reports
|
March 5, 2020
The Interplay between CD27<sup>dull</sup> and CD27<sup>bright</sup> B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory
Ola Grimsholm, Eva Piano Mortari, Alexey N Davydov, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
November 25, 2023
PATZ1-Rearranged Tumors of the Central Nervous System: Characterization of a Pediatric Series of Seven Cases
Sabrina Rossi, Sabina Barresi, Giovanna Stefania Colafati, et al.
American Journal of Human Genetics
|
December 20, 2023
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome
Vincenzo Salpietro, Reza Maroofian, Maha S Zaki, et al.
Nature Communications
|
February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
Holger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
Science Advances
|
December 3, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patients
Laura Bryant, Dong Li, Samuel G Cox, et al.
Page
of 9