Kefeng F. Shen
1095 Jiefang Avenue, Qiaokou District
Wuhan, 430030, China
Wuhan, 430030, China
Last Updated: 09/26/2026
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Found 23 publications
TET2 germline mutation in a patient with sequential lymphoid malignancies: a novel case report.
Journal: Annals of hematology
Published: July 05, 2025
TNFRSF13B Variant-Induced TACI Dysregulation Underlies CAEBV Pathogenesis.
Journal: Journal of clinical immunology
Published: February 09, 2025
Improving CAR-T cell function through a targeted cytokine delivery system utilizing car target-modified extracellular vesicles.
Journal: Experimental hematology & oncology
Published: December 05, 2024
TET2 mutation in acute myeloid leukemia: biology, clinical significance, and therapeutic insights.
Journal: Clinical epigenetics
Published: October 05, 2024
MYH9-related inherited thrombocytopenia: the genetic spectrum, underlying mechanisms, clinical phenotypes, diagnosis, and management approaches.
Journal: Research and practice in thrombosis and haemostasis
Published: July 08, 2024
A case of Hb M-Iwate combined with diffuse large B-cell lymphoma
Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi
Published: September 25, 2023
Case report: Differential diagnosis of highly amplified anti-CD5 CAR T cells and relapsed lymphoma cells in a patient with refractory ALK positive anaplastic large cell lymphoma.
Journal: Frontiers in immunology
Published: August 19, 2023
Novel heterozygous mutations of TNFRSF13B in EBV-associated T/NK lymphoproliferative diseases (EBV-T/NK-LPDs).
Journal: Blood science (Baltimore, Md.)
Published: July 19, 2023
Transformation to diffuse large B-cell lymphoma and its impact on survival in patients with marginal zone lymphoma: A population-based study.
Journal: International journal of cancer
Published: July 12, 2023
Case report: Application of targeted NGS for the detection of non-canonical driver variants in MPN.
Journal: Frontiers in genetics
Published: April 02, 2023
Case report: Germline RECQL mutation potentially involved in hereditary predisposition to acute leukemia.
Journal: Frontiers in oncology
Published: October 10, 2022
CD137 deficiency because of two novel biallelic TNFRSF9 mutations in a patient presenting with severe EBV-associated lymphoproliferative disease.
Journal: Clinical & translational immunology
Published: October 01, 2022
Last Updated: 09/26/2026