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SPINK2 Protein Expression Is an Independent Adverse Prognostic Marker in AML and Is Potentially Implicated in the Regulation of Ferroptosis and Immune Response

International journal of molecular sciences, 2023-06, Vol.24 (11), p.9696

2023

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DNA of Erythroid Origin Is Present in Human Plasma and Informs the Types of Anemia

Clinical chemistry (Baltimore, Md.), 2017-10, Vol.63 (10), p.1614-1623

2017

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Deep genomic characterization highlights complexities and prognostic markers of pediatric acute myeloid leukemia

Communications biology, 2023-03, Vol.6 (1), p.356-356, Article 356

2023

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Minimal residual disease-based risk stratification in Chinese childhood acute lymphoblastic leukemia by flow cytometry and plasma DNA quantitative polymerase chain reaction

PloS one, 2013-07, Vol.8 (7), p.e69467-e69467

2013

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RUNX1 upregulation via disruption of long-range transcriptional control by a novel t(5;21)(q13;q22) translocation in acute myeloid leukemia

Molecular cancer, 2018-08, Vol.17 (1), p.133-6, Article 133

2018

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Helicase-like transcription factor is a RUNX1 target whose downregulation promotes genomic instability and correlates with complex cytogenetic features in acute myeloid leukemia

Haematologica (Roma), 2016-04, Vol.101 (4), p.448

2016

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Initial Treatment of Immune Thrombocytopenic Purpura with High-Dose Dexamethasone

The New England journal of medicine, 2003-08, Vol.349 (9), p.831-836

2003

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Secreted-frizzled related protein 1 is a transcriptional repression target of the t(8;21) fusion protein in acute myeloid leukemia

Blood, 2011-12, Vol.118 (25), p.6638-6648

2011

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Distinctive regional-specific PROS1 mutation spectrum in Southern China

Journal of thrombosis and thrombolysis, 2018-07, Vol.46 (1), p.120-124

2018

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Mutational spectrum and prognosis in Chinese patients with prefibrotic primary myelofibrosis

EJHaem, 2022-02, Vol.3 (1), p.184-190

2022

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A polymorphism in the 3′-untranslated region of the NPM1 gene causes illegitimate regulation by microRNA-337-5p and correlates with adverse outcome in acute myeloid leukemia

Haematologica (Roma), 2013-06, Vol.98 (6), p.913-917

2013

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Transcriptional repression of the RUNX3/AML2 gene by the t(8;21) and inv(16) fusion proteins in acute myeloid leukemia

Blood, 2008-10, Vol.112 (8), p.3391-3402

2008

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FNDC3B is another novel partner fused to RARA in the t(3;17)(q26;q21) variant of acute promyelocytic leukemia

Blood, 2017-05, Vol.129 (19), p.2705-2709

2017

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4q loss is potentially an important genetic event in MM tumorigenesis: identification of a tumor suppressor gene regulated by promoter methylation at 4q13.3, platelet factor 4

Blood, 2007-03, Vol.109 (5), p.2089-2099

2007

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An Evaluation for the Causes of Reduced Hb A2 and the Molecular Characterization of HBD Variants in Hong Kong

Hemoglobin, 2021-11, Vol.45 (6), p.387-391

2021

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An Evaluation for the Causes of Reduced Hb A 2 and the Molecular Characterization of HBD Variants in Hong Kong

Hemoglobin, 2021-11, Vol.45 (6), p.387-391

2021

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Bone marrow xanthomas associated with hypertriglyceridemia

American journal of hematology, 2017-12, Vol.92 (12), p.1400-1401

2017

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Platelet factor 4 induces cell apoptosis by inhibition of STAT3 via up-regulation of SOCS3 expression in multiple myeloma

Haematologica (Roma), 2013-02, Vol.98 (2), p.288-295

2013

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t(1;22)(p13;q13) Acute Megakaryoblastic Leukemia Complicated by Hepatic Fibrosis: Antifibrosis Therapy?

Journal of pediatric hematology/oncology, 2021-11, Vol.43 (8), p.e1164

2021

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A novel NUP98-JADE2 fusion in a patient with acute myeloid leukemia resembling acute promyelocytic leukemia

Blood advances, 2022-01, Vol.6 (2), p.410-415

2022

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Prevalence and Clinicopathologic Significance of BRAF V600E Mutation in Chinese Multiple Myeloma Patients

Clinical lymphoma, myeloma and leukemia, 2018-07, Vol.18 (7), p.e315-e325

2018

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Alterations of RAS signalling in Chinese multiple myeloma patients: absent BRAF and rare RAS mutations, but frequent inactivation of RASSF1A by transcriptional silencing or expression of a non‐functional variant transcript

British journal of haematology, 2003-11, Vol.123 (4), p.637-645

2003

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Outcomes of adolescents with acute lymphoblastic leukaemia

Hong Kong medical journal = Xianggang yi xue za zhi, 2022-06, Vol.28 (3), p.204-214

2022

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A Multi-locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese β-thalassemia Carriers

Hemoglobin, 2016-11, Vol.40 (6), p.400-404

2016

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First Report of Hb Kent [β37(C3)Trp→Cys (TGG>TGC) HBB: c.114G>C] in a Chinese Family

Hemoglobin, 2017-11, Vol.41 (4-6), p.283-285

2017

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SPINK2 Protein Expression Is an Independent Adverse Prognostic Marker in AML and Is Potentially Implicated in the Regulation of Ferroptosis and Immune Response

DNA of Erythroid Origin Is Present in Human Plasma and Informs the Types of Anemia

Deep genomic characterization highlights complexities and prognostic markers of pediatric acute myeloid leukemia

Minimal residual disease-based risk stratification in Chinese childhood acute lymphoblastic leukemia by flow cytometry and plasma DNA quantitative polymerase chain reaction

RUNX1 upregulation via disruption of long-range transcriptional control by a novel t(5;21)(q13;q22) translocation in acute myeloid leukemia

Helicase-like transcription factor is a RUNX1 target whose downregulation promotes genomic instability and correlates with complex cytogenetic features in acute myeloid leukemia

Initial Treatment of Immune Thrombocytopenic Purpura with High-Dose Dexamethasone

Secreted-frizzled related protein 1 is a transcriptional repression target of the t(8;21) fusion protein in acute myeloid leukemia

Distinctive regional-specific PROS1 mutation spectrum in Southern China

Mutational spectrum and prognosis in Chinese patients with prefibrotic primary myelofibrosis

A polymorphism in the 3′-untranslated region of the NPM1 gene causes illegitimate regulation by microRNA-337-5p and correlates with adverse outcome in acute myeloid leukemia

Transcriptional repression of the RUNX3/AML2 gene by the t(8;21) and inv(16) fusion proteins in acute myeloid leukemia

FNDC3B is another novel partner fused to RARA in the t(3;17)(q26;q21) variant of acute promyelocytic leukemia

4q loss is potentially an important genetic event in MM tumorigenesis: identification of a tumor suppressor gene regulated by promoter methylation at 4q13.3, platelet factor 4

An Evaluation for the Causes of Reduced Hb A2 and the Molecular Characterization of HBD Variants in Hong Kong

An Evaluation for the Causes of Reduced Hb A 2 and the Molecular Characterization of HBD Variants in Hong Kong

Bone marrow xanthomas associated with hypertriglyceridemia

Platelet factor 4 induces cell apoptosis by inhibition of STAT3 via up-regulation of SOCS3 expression in multiple myeloma

t(1;22)(p13;q13) Acute Megakaryoblastic Leukemia Complicated by Hepatic Fibrosis: Antifibrosis Therapy?

A novel NUP98-JADE2 fusion in a patient with acute myeloid leukemia resembling acute promyelocytic leukemia

Prevalence and Clinicopathologic Significance of BRAF V600E Mutation in Chinese Multiple Myeloma Patients

Alterations of RAS signalling in Chinese multiple myeloma patients: absent BRAF and rare RAS mutations, but frequent inactivation of RASSF1A by transcriptional silencing or expression of a non‐functional variant transcript

Outcomes of adolescents with acute lymphoblastic leukaemia

A Multi-locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese β-thalassemia Carriers

First Report of Hb Kent [β37(C3)Trp→Cys (TGG>TGC) HBB: c.114G>C] in a Chinese Family

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