Tiejun Qin
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View article: The prognostic impact of chromosome 7 with both arms loss [der(7)del(7p)del(7q)] in myelodysplastic syndrome/neoplasm
The prognostic impact of chromosome 7 with both arms loss [der(7)del(7p)del(7q)] in myelodysplastic syndrome/neoplasm Open
Der(7) defines a distinct high-risk subgroup with a unique molecular profile and poor prognosis comparable to -7.
View article: A correlation of ineffective erythropoiesis and dysregulated signaling pathways in myelodysplastic syndromes/neoplasms
A correlation of ineffective erythropoiesis and dysregulated signaling pathways in myelodysplastic syndromes/neoplasms Open
View article: Molecular characteristics and clinical implications of TP53 mutations in therapy-related myelodysplastic syndromes
Molecular characteristics and clinical implications of TP53 mutations in therapy-related myelodysplastic syndromes Open
View article: Comprehensive genomic characterization of programmed cell death-related genes to predict drug resistance and prognosis for patients with multiple myeloma
Comprehensive genomic characterization of programmed cell death-related genes to predict drug resistance and prognosis for patients with multiple myeloma Open
A 12-gene Risk score model developed with PCD-related genes can accurately predict the survival for MM patients. Our study provided potential targets and strategies for individualized treatment of MM.
View article: Targeting CD38 effectively prevents myelofibrosis in myeloproliferative neoplasms
Targeting CD38 effectively prevents myelofibrosis in myeloproliferative neoplasms Open
Proinflammatory signaling is a hallmark of myeloproliferative neoplasms (MPNs). Several studies have shown that monocytes are a major source of proinflammatory cytokines and monocyte-derived fibrocytes play a pivotal role in the pathogenes…
View article: Impact of <scp><i>ASXL1</i></scp> Gene Alterations on Myelodysplastic Syndrome With Isolated 20q Deletion
Impact of <span><i>ASXL1</i></span> Gene Alterations on Myelodysplastic Syndrome With Isolated 20q Deletion Open
Background Isolated 20q deletion [del(20q)] is a recurrent favorable abnormality in myelodysplastic syndrome (MDS) and may cause deletion of the ASXL1 gene. Meanwhile, ASXL1 mutations are also common in individuals with MDS. This study aim…
View article: The Molecular Features of Chronic Eosinophilic Leukemia, Not Otherwise Specified
The Molecular Features of Chronic Eosinophilic Leukemia, Not Otherwise Specified Open
View article: GATA1 insufficiencies in dysmegakaryopoiesis of myelodysplastic syndromes
GATA1 insufficiencies in dysmegakaryopoiesis of myelodysplastic syndromes Open
GATA1 is one of critical transcription factors for megakaryopoiesis and platelet production. Our study aimed to explore the correlations between GATA1 expression and dysmegakaryopoiesis in myelodysplastic syndromes (MDS). Data of blood cel…
View article: Predicting survival in patients with myelodysplastic/myeloproliferative neoplasms with SF3B1 mutation and thrombocytosis
Predicting survival in patients with myelodysplastic/myeloproliferative neoplasms with SF3B1 mutation and thrombocytosis Open
We investigated data from 180 consecutive patients with myelodysplastic/myeloproliferative neoplasms with SF3B1 mutation and thrombocytosis (MDS/MPN- SF3B1 -T) who were diagnosed according to the 2022 World Health Organization (WHO) classi…
View article: Combination therapy with venetoclax and azacitidine for the treatment of myelodysplastic syndromes with <i>DDX41</i> mutations
Combination therapy with venetoclax and azacitidine for the treatment of myelodysplastic syndromes with <i>DDX41</i> mutations Open
Myelodysplastic syndromes (MDS) patients with DEAD-box helicase 41 (DDX41) mutations have been reported to be treated effectively with lenalidomide; however, there are no randomized studies to prove it. Venetoclax and azacitidine ar…
View article: Gadd45g insufficiency drives the pathogenesis of myeloproliferative neoplasms
Gadd45g insufficiency drives the pathogenesis of myeloproliferative neoplasms Open
View article: Predicting survival in myelodysplastic/myeloproliferative neoplasms with SF3B1 mutation and thrombocytosis
Predicting survival in myelodysplastic/myeloproliferative neoplasms with SF3B1 mutation and thrombocytosis Open
We interrogated data from 180 consecutive subjects with myelodysplastic/myeloproliferative neoplasm with SF3B1 mutation and thrombocytosis (MDS/MPN-SF3B1-T) diagnosed according to the 2022 World Health Organization (WHO) classification of …
View article: Micheliolide exerts effects in myeloproliferative neoplasms through inhibiting STAT3/5 phosphorylation via covalent binding to STAT3/5 proteins
Micheliolide exerts effects in myeloproliferative neoplasms through inhibiting STAT3/5 phosphorylation via covalent binding to STAT3/5 proteins Open
Ruxolitinib is a cornerstone of management for some subsets of myeloproliferative neoplasms (MPNs); however, a considerable number of patients respond suboptimally. Here, we evaluated the efficacy of micheliolide (MCL), a natural guaianoli…
View article: Olverembatinib for myeloid/lymphoid neoplasm associated with eosinophilia and <i>FGFR1</i> rearrangement
Olverembatinib for myeloid/lymphoid neoplasm associated with eosinophilia and <i>FGFR1</i> rearrangement Open
View article: <i>ASXL1</i> mutations accelerate bone marrow fibrosis via EGR1-TNFA axis-mediated neoplastic fibrocyte generation in myeloproliferative neoplasms.
<i>ASXL1</i> mutations accelerate bone marrow fibrosis via EGR1-TNFA axis-mediated neoplastic fibrocyte generation in myeloproliferative neoplasms. Open
Apart from the central role of the activated JAK/STAT signaling pathway, ASXL1 mutations are the most recurrent additional mutations in myeloproliferative neoplasms and occur much more commonly in myelofibrosis than in essential thrombocyt…
View article: Non-driver mutations landscape in different stages of primary myelofibrosis determined ASXL1 mutations play a critical role in disease progression
Non-driver mutations landscape in different stages of primary myelofibrosis determined ASXL1 mutations play a critical role in disease progression Open
View article: Case of cryptic TNIP1::PDGFRB rearrangement presenting with myelodysplastic syndrome achieved hematologic and cytogenetic remission with low-dose imatinib plus decitabine therapy
Case of cryptic TNIP1::PDGFRB rearrangement presenting with myelodysplastic syndrome achieved hematologic and cytogenetic remission with low-dose imatinib plus decitabine therapy Open
View article: IPSS-M has greater survival predictive accuracy compared with IPSS-R in persons ≥ 60 years with myelodysplastic syndromes
IPSS-M has greater survival predictive accuracy compared with IPSS-R in persons ≥ 60 years with myelodysplastic syndromes Open
View article: Comparison of the revised 4th (2016) and 5th (2022) editions of the World Health Organization classification of myelodysplastic neoplasms
Comparison of the revised 4th (2016) and 5th (2022) editions of the World Health Organization classification of myelodysplastic neoplasms Open
View article: IPSS-M has greater survival predictive accuracy compared with IPSS-R in persons ≥ 60 years with myelodysplastic syndromes
IPSS-M has greater survival predictive accuracy compared with IPSS-R in persons ≥ 60 years with myelodysplastic syndromes Open
There are considerable new data on mutation topography in persons with myelodysplastic syndromes (MDS). These data have been used to update conventional risk models such as the Revised International Prognostic Scoring System (IPSS-R). Whet…
View article: <i>ASXL1</i> mutations accelerate bone marrow fibrosis via EGR1-TNFA axis-mediated neoplastic fibrocyte generation in myeloproliferative neoplasms
<i>ASXL1</i> mutations accelerate bone marrow fibrosis via EGR1-TNFA axis-mediated neoplastic fibrocyte generation in myeloproliferative neoplasms Open
Apart from the central role of the activated JAK/STAT signaling pathway, ASXL1 mutations are the most recurrent additional mutations in myeloproliferative neoplasms and occur much more commonly in myelofibrosis than in essential thrombocyt…
View article: Myelodysplastic syndromes are multiclonal diseases derived from hematopoietic stem and progenitor cells
Myelodysplastic syndromes are multiclonal diseases derived from hematopoietic stem and progenitor cells Open
Myelodysplastic syndromes (MDS) are generally considered as a group of clonal diseases derived from hematopoietic stem cells, but a number of studies have suggested that they are derived from myeloid progenitor cells. We aimed to identify …
View article: Conventional interferon-α 2b versus hydroxyurea for newly-diagnosed patients with polycythemia vera in a real world setting: a retrospective study based on 286 patients from a single center
Conventional interferon-α 2b versus hydroxyurea for newly-diagnosed patients with polycythemia vera in a real world setting: a retrospective study based on 286 patients from a single center Open
Conventional interferon-a 2b versus hydroxyurea for newly-diagnosed patients with polycythemia vera in a real world setting: a retrospective study based on 286 patients from a single center Data are presented as median (interquartile range…
View article: ASXL2 mutated myelodysplastic syndrome in a novel germline G6b variant
ASXL2 mutated myelodysplastic syndrome in a novel germline G6b variant Open
View article: Iron deficiency in JAK2 exon12 and JAK2-V617F mutated polycythemia vera
Iron deficiency in JAK2 exon12 and JAK2-V617F mutated polycythemia vera Open
View article: RBC distribution width predicts thrombosis risk in polycythemia vera
RBC distribution width predicts thrombosis risk in polycythemia vera Open
View article: Author response for "Is race important in genomic classification of hematological neoplasms?"
Author response for "Is race important in genomic classification of hematological neoplasms?" Open
View article: Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization for detecting chromosome abnormalities in myelodysplastic syndromes
Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization for detecting chromosome abnormalities in myelodysplastic syndromes Open
This study aimed to compare interphase fluorescence in situ hybridization (iFISH) and multiplex ligation dependent probe amplification (MLPA) for identifying genetic changes in myelodysplastic syndromes (MDS). The frequencies of cytogeneti…
View article: VEXAS syndrome in myelodysplastic syndrome with autoimmune disorder
VEXAS syndrome in myelodysplastic syndrome with autoimmune disorder Open
View article: Evaluation of Reduced-Dose Decitabine and Azacitidine for Treating Myelodysplastic Syndromes: A Retrospective Study
Evaluation of Reduced-Dose Decitabine and Azacitidine for Treating Myelodysplastic Syndromes: A Retrospective Study Open
BACKGROUND Hypomethylating agents (HMA) are considered the first-line therapy for high-risk myelodysplastic syndromes (MDS). However, as the efficacy and safety of rational dosing regimens are lacking, we evaluated the effectiveness and sa…