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Dan Yang
Government of the United States of America - Translational Vascular Medicine Branch
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SCHOLARLY PAPERS
1
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Scholarly Papers (1)
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1.
Generation of Myeloid Lineage Cells from Induced Pluripotent Stems Cells (iPSCs) as Powerful Platform to Study Patients with CCR5Δ32 Mutation
Number of pages: 36
Posted: 04 May 2023
Guibin Chen
,
Francesca Calcaterra
,
Yuchi Ma
,
Xianfeng Ping
,
Elena Pontarini
, Dan Yang,
Ferdinando Oriolo
,
Zhen Yu
,
Assunta Cancellara
,
Joanna Mikulak
,
Yuting Huang
,
Silvia Della Bella
,
Yangtengyu Liu
,
Rebecca L. Harper
,
Clifton L. Dalgard
,
Manfred Boehm
and
Domenico Mavilio
Government of the United States of America - Translational Vascular Medicine Branch, University of Milan - Department of Medical Biotechnology and Translational Medicine, Government of the United States of America - Translational Vascular Medicine Branch, Government of the United States of America - Translational Vascular Medicine Branch, University of Milan - Department of Medical Biotechnology and Translational Medicine, Government of the United States of America - Translational Vascular Medicine Branch, University of Milan - Department of Medical Biotechnology and Translational Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC) - State Key Laboratory of Experimental Hematology, University of Milan - Department of Medical Biotechnology and Translational Medicine, IRCCS Humanitas Research Hospital, Government of the United States of America - Translational Vascular Medicine Branch, University of Milan - Department of Medical Biotechnology and Translational Medicine, Central South University - Department of Rheumatology, Government of the United States of America - Translational Vascular Medicine Branch, Uniformed Services University of the Health Sciences - Department of Anatomy, Physiology and Genetics, Government of the United States of America - Translational Vascular Medicine Branch and University of Milan - Department of Medical Biotechnology and Translational Medicine
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Abstract:
iPSC, CCR5, Monocyte, Macrophage, CCR5Δ32 mutation
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