The genetic deletion and protein expression of PRDM1 and its clinical implications in diffuse large B cell lymphoma: A retrospective cohort study in China

Lin Nong(Peking University), Ting Li(Shaanxi Normal University), Dong Li(Children's Hospital of Philadelphia), Yalin Zheng(University of Liverpool), Liang Li(Peking University First Hospital), Wei Wang(Peking University), Xin Li(Obstetrics and Gynecology Hospital of Fudan University)
Pathology - Research and Practice
March 28, 2022
10.1016/j.prp.2022.153860
Cited by 6

Related Papers

SCF-mediated mast cell infiltration and activation exacerbate the inflammation and immunosuppression in tumor microenvironment
|Blood|2008|345
Mutations in PDGFRB Cause Autosomal-Dominant Infantile Myofibromatosis
|The American Journal of Human Genetics|2013|206
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers
|The American Journal of Human Genetics|2016|183
Autism-Associated Mutations in ProSAP2/Shank3 Impair Synaptic Transmission and Neurexin–Neuroligin-Mediated Transsynaptic Signaling
|Journal of Neuroscience|2012|180
Human papillomavirus infection and cervical intraepithelial neoplasia progression are associated with increased vaginal microbiome diversity in a Chinese cohort
|BMC Infectious Diseases|2020|177