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hematopoietic stem cells

Cytovia and Cellectis Expand Their TALEN® Gene-Edited iNK Partnership to Enable Broader Collaboration in China

[Cytovia Therapeutics, Inc. (GlobeNewswire, Inc.)] Cytovia Therapeutics, Inc. and Cellectis announced that they have expanded their collaboration of TALEN® gene-edited iPSC-derived natural killer (NK) and chimeric antigen receptor (CAR)-NK cells to include new CAR target and development in China by Cytovia’s joint venture entity, CytoLynx Therapeutics.

Implementing a Functional Precision Medicine Tumor Board for Acute Myeloid Leukemia

[Cancer Discovery] Scientists generated ex vivo drug response and multi-omics profiling data for a prospective series of 252 samples from 186 acute myeloid leukemia patients. Functional precision medicine tumor board integrated clinical, molecular and functional data for application in clinical treatment decisions.

Differentiation of Fetal Hematopoietic Stem Cells Requires ARID4B to Restrict Autocrine KITLG/KIT-Src Signaling

[Cell Reports] Investigators showed that AT-rich interaction domain 4B (ARID4B) interfered with KITLG/KIT signaling, consequently allowing HSC differentiation. Conditional Arid4b knockout in mouse hematopoietic cells blocked fetal HSC differentiation, preventing hematopoiesis.

IL-18R-Mediated HSC Quiescence and MLKL-Dependent Cell Death Limit Hematopoiesis during Infection-Induced Shock

[Stem Cell Reports] Using Ixodes ovatus Ehrlichia, a tick-borne pathogen that causes severe shock-like illness and bone marrow aplasia, type I and II interferons promoted the loss of hematopoietic stem progenitor cells via increased cell death and enforced quiescence.

Toward Platelet Transcriptomics in Cancer Diagnosis, Prognosis and Therapy

[British Journal of Cancer] The authors present a few actionable steps for basic, translational and clinical research communities in advancing the utility of the platelet transcriptome as a highly sensitive biomarker in cancer and collectively enable efforts toward clinical translation and patient benefit.

Graphite Bio Enrolls First Patient in Phase I/II Clinical Trial of GPH101 for Sickle Cell Disease

[Graphite Bio, Inc.] Graphite Bio, Inc. announced that the first patient has been enrolled in the company’s Phase I/II clinical trial of GPH101, an investigational gene-edited autologous hematopoietic stem cell therapy designed to directly correct the genetic mutation that causes sickle cell disease.

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