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American Journal of Hematology|February 26, 2024
CALR-mutated patients with low allele burden represent a specific subtype of essential thrombocythemia: A study on behalf of FIM and GBMHMLaura Aubin, Rúben Vilas Boas, Rafael Daltro De Oliveira, et al.
Nature Genetics|February 17, 2025
The Marchantia polymorpha pangenome reveals ancient mechanisms of plant adaptation to the environmentChloé Beaulieu, Cyril Libourel, Duchesse Lacourt Mbadinga Zamar, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA|November 10, 2021
Integrate mechanistic evidence from new approach methodologies (NAMs) into a read-across assessment to characterise trends in shared mode of actionSylvia E Escher, Alejandro Aguayo-Orozco, Emilio Benfenati, et al.
The Lancet. Oncology|June 12, 2009
Predicting outcomes for children with neuroblastoma using a multigene-expression signature: a retrospective SIOPEN/COG/GPOH studyJoëlle Vermeulen, Katleen De Preter, Arlene Naranjo, et al.
The Journal of Clinical Investigation|August 12, 2020
Type 2 diabetes risk gene Dusp8 regulates hypothalamic Jnk signaling and insulin sensitivitySonja C Schriever, Dhiraj G Kabra, Katrin Pfuhlmann, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|April 5, 2016
Metastatic neuroblastoma in infants: are survival rates excellent only within the stringent framework of clinical trials?A Di Cataldo, A Agodi, J Balaguer, et al.
JCI Insight|June 1, 2023
Mucosal transcriptomics highlight lncRNAs implicated in ulcerative colitis, Crohn's disease, and celiac diseaseTzipi Braun, Katya E Sosnovski, Amnon Amir, et al.
European Journal of Human Genetics : EJHG|August 30, 2020
Successful application of genome sequencing in a diagnostic setting: 1007 index cases from a clinically heterogeneous cohortAida M Bertoli-Avella, Christian Beetz, Najim Ameziane, et al.
Acta Neuropathologica|November 19, 2016
The current consensus on the clinical management of intracranial ependymoma and its distinct molecular variantsKristian W Pajtler, Stephen C Mack, Vijay Ramaswamy, et al.
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