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Hypertension (Dallas, Tex. : 1979)|March 22, 2021
Reference Intervals for Brachial Artery Flow-Mediated Dilation and the Relation With Cardiovascular Risk FactorsSophie M Holder, Rosa Maria Bruno, Daria A Shkredova, et al.
Cancer Research Communications|October 3, 2022
BRCA1-associated RING domain-1 (BARD1) loss and GBP1 expression enhance sensitivity to DNA damage in Ewing sarcomaLisa M Maurer, Jessica D Daley, Elina Mukherjee, et al.
The Journal of Experimental Medicine|August 15, 2012
Whole-genome sequencing identifies recurrent somatic NOTCH2 mutations in splenic marginal zone lymphomaMark J Kiel, Thirunavukkarasu Velusamy, Bryan L Betz, et al.
Nature Communications|September 30, 2015
Genomic analyses reveal recurrent mutations in epigenetic modifiers and the JAK-STAT pathway in Sézary syndromeMark J Kiel, Anagh A Sahasrabuddhe, Delphine C M Rolland, et al.
Blood|May 15, 2014
Integrated genomic sequencing reveals mutational landscape of T-cell prolymphocytic leukemiaMark J Kiel, Thirunavukkarasu Velusamy, Delphine Rolland, et al.
Blood|October 29, 2014
A novel recurrent NPM1-TYK2 gene fusion in cutaneous CD30-positive lymphoproliferative disordersThirunavukkarasu Velusamy, Mark J Kiel, Anagh A Sahasrabuddhe, et al.
Cancers|December 16, 2020
Widespread Aberrant Alternative Splicing despite Molecular Remission in Chronic Myeloid Leukaemia PatientsUlf Schmitz, Jaynish S Shah, Bijay P Dhungel, et al.
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