Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Frontiers in Medicine|January 30, 2023
Stromal cells support the survival of human primary chronic lymphocytic leukemia (CLL) cells through Lyn-driven extracellular vesiclesThaís Dolzany de Oliveira, Alexander Vom Stein, Rocio Rebollido-Rios, et al.
The Journal of Allergy and Clinical Immunology|August 12, 2019
Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formationXiaolei Ding, Sebastian Willenborg, Wilhelm Bloch, et al.
Communications Biology|May 27, 2020
The ubiquitin-conjugating enzyme UBE2K determines neurogenic potential through histone H3 in human embryonic stem cellsAzra Fatima, Dilber Irmak, Alireza Noormohammadi, et al.
Human Molecular Genetics|November 20, 2018
Mechanism suppressing H3K9 trimethylation in pluripotent stem cells and its demise by polyQ-expanded huntingtin mutationsDilber Irmak, Azra Fatima, Ricardo Gutiérrez-Garcia, et al.
Cancers|November 27, 2019
JAK/STAT-Activating Genomic Alterations Are a Hallmark of T-PLLLinus Wahnschaffe, Till Braun, Sanna Timonen, et al.
Journal of Translational Medicine|June 21, 2019
Unilateral L4-dorsal root ganglion stimulation evokes pain relief in chronic neuropathic postsurgical knee pain and changes of inflammatory markers: part II whole transcriptome profilingThomas M Kinfe, Maria Asif, Krishnan V Chakravarthy, et al.
Nature Aging|October 2, 2023
In planta expression of human polyQ-expanded huntingtin fragment reveals mechanisms to prevent disease-related protein aggregationErnesto Llamas, Seda Koyuncu, Hyun Ju Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 18, 2022
Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signalingWilliam Dufour, Salem Alawbathani, Anne-Sophie Jourdain, et al.
HGG Advances|May 16, 2022
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathwayMaria Asif, Emrah Kaygusuz, Marwan Shinawi, et al.
Blood|April 6, 2023
Oncogenic role and target properties of the lysine-specific demethylase KDM1A in chronic lymphocytic leukemiaQu Jiang, Johanna Stachelscheid, Johannes Bloehdorn, et al.
Pageof 2