Xiaohui Cai - Publications

A novel prognostic model of methylation-associated genes in acute myeloid leukemia.

Journal: Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico

Published: September 08, 2022

Frequency and clinical impact of WT1 mutations in the context of CEBPA-mutated acute myeloid leukemia.

Journal: Hematology (Amsterdam, Netherlands)

Published: September 06, 2022

Clinical features and prognostic significance of DNMT3A, FLT3, and NPM1 mutations in de novo acute myeloid leukemia patients.

Journal: International journal of laboratory hematology

Published: July 08, 2022

Molecular genetic and clinical characterization of acute myeloid leukemia with trisomy 8 as the sole chromosome abnormality.

Journal: Hematology (Amsterdam, Netherlands)

Published: May 13, 2022

Comprehensive Mutation Profile in Acute Myeloid Leukemia Patients with RUNX1-RUNX1T1 or CBFB-MYH11 Fusions

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: April 21, 2022

Companion gene mutations and their clinical significance in AML with double or single mutant CEBPA.

Journal: International journal of hematology

Published: September 08, 2021

Molecular genetic characterization of acute myeloid leukemia with isolated trisomy of chromosomes 4, 11, and 21.

Journal: International journal of laboratory hematology

Published: August 14, 2021

Mutational landscape of chronic myelomonocytic leukemia and its potential clinical significance.

Journal: International journal of hematology

Published: April 23, 2021

Myeloid/lymphoid neoplasm with CEP110-FGFR1 fusion: An analysis of 16 cases show common features and poor prognosis.

Journal: Hematology (Amsterdam, Netherlands)

Published: January 25, 2021

Combination of Gemcitabine and Thymosin alpha 1 exhibit a better anti-tumor effect on nasal natural killer/T-cell lymphoma.

Journal: International immunopharmacology

Published: January 08, 2021

Adult Acute Myeloid Leukemia with the KMT2A-Mixed Lineage Leukemia T10 Fusion: An Analysis of 10 Cases Showed Common Features and Frequent Mutations in the RAS Signaling Pathway.

Journal: Acta haematologica

Published: December 24, 2020

Mutational landscape of patients with acute myeloid leukemia or myelodysplastic syndromes in the context of RUNX1 mutation.

Journal: Hematology (Amsterdam, Netherlands)

Published: June 02, 2020