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Circulating MicroRNAs in Cancer: Potential and Challenge

Frontiers in genetics, 2019-07, Vol.10, p.626-626

2019

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Saracatinib prompts hemin-induced K562 erythroid differentiation but suppresses erythropoiesis of hematopoietic stem cells

Human cell : official journal of Human Cell Research Society, 2024-05, Vol.37 (3), p.648-665

2024

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MiR-6875-3p promotes the proliferation, invasion and metastasis of hepatocellular carcinoma via BTG2/FAK/Akt pathway

Journal of experimental & clinical cancer research, 2019-01, Vol.38 (1), p.7-7, Article 7

2019

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The connection between innervation and metabolic rearrangements in pancreatic cancer through serine

Frontiers in oncology, 2022-12, Vol.12, p.992927-992927

2022

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Immunotherapy for Hepatocellular Carcinoma: Current Advances and Future Expectations

Journal of Immunology Research, 2018-01, Vol.2018, p.8740976-8

2018

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Different culture method changing CD105 expression in amniotic fluid MSCs without affecting differentiation ability or immune function

Journal of cellular and molecular medicine, 2020-04, Vol.24 (7), p.4212-4222

2020

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A universal KOH-free strategy towards nitrogen-doped carbon nanosheets for high-rate and high-energy storage devices

Journal of materials chemistry. A, Materials for energy and sustainability, 2019, Vol.7 (46), p.26469-26478

2019

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RS12574989 and haplotype associated with α/β-chain imbalance and population HbA2 reduction

BMC medical genomics, 2022-08, Vol.15 (1), p.1-179, Article 179

2022

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Application of MFI-5 in severe complications and unfavorable outcomes after radical resection of colorectal cancer

World journal of surgical oncology, 2023-09, Vol.21 (1), p.1-307, Article 307

2023

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The use of high-resolution SNP arrays to detect congenital cardiac defects

The journal of maternal-fetal & neonatal medicine, 2024-12, Vol.37 (1), p.2301831-2301831

2024

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MSCs derived from amniotic fluid and umbilical cord require different administration schemes and exert different curative effects on different tissues in rats with CLP-induced sepsis

Stem cell research & therapy, 2021-03, Vol.12 (1), p.164-164, Article 164

2021

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A de novo PAK1 likely pathogenic variant and a de novo terminal 1q microdeletion in a Chinese girl with global developmental delay, severe intellectual disability, and seizures

BMC medical genomics, 2023-01, Vol.16 (1), p.3-3, Article 3

2023

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Generation of two induced pluripotent stem cell lines, GZHMCi009-A and GZHMCi010-A, derived from peripheral blood mononuclear cells of two SCA3 patients with 14/74 CAG repeats of the ATXN3 mutation

Stem cell research, 2022-05, Vol.61, p.102782-102782, Article 102782

2022

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A retrospective analysis of MS/MS screening for IEM in high-risk areas

BMC medical genomics, 2023-03, Vol.16 (1), p.57-57, Article 57

2023

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Molecular Characterization Analysis of Thalassemia and Hemoglobinopathy in Quanzhou, Southeast China: A Large-Scale Retrospective Study

Frontiers in genetics, 2021-09, Vol.12, p.727233-727233

2021

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Extracellular Vesicles of Mesenchymal Stem Cells Are More Effectively Accessed through Polyethylene Glycol-Based Precipitation than by Ultracentrifugation

Stem cells international, 2022-09, Vol.2022, p.1-12

2022

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A Tumor Microenvironment Responsive Nanotheranostics Agent for Magnetic Resonance Imaging and Synergistic Photodynamic Therapy/Photothermal Therapy of Liver Cancer

Frontiers in chemistry, 2021-04, Vol.9, p.650899-650899

2021

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Complex Chromosomal Rearrangement Causes Male Azoospermia: A Case Report and Literature Review

Frontiers in genetics, 2022-02, Vol.13, p.792539-792539

2022

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Prenatal diagnosis of dent disease type I with a nonsense pathogenic variant in CLCN5: a case study

BMC medical genomics, 2024-01, Vol.17 (1), p.34-34, Article 34

2024

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Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication

Frontiers in genetics, 2022-07, Vol.13

2022

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Generation of induced pluripotent stem cell GZLSL-i001-A derived from urine-derived cells of Hemophilia A patient with Inv22 mutation

Stem cell research, 2020-12, Vol.49, p.102053-102053, Article 102053

2020

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Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing

Frontiers in genetics, 2022-03, Vol.13, p.829613

2022

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The safety and effectiveness of genetically corrected iPSCs derived from β-thalassaemia patients in nonmyeloablative β-thalassaemic mice

Stem cell research & therapy, 2020-07, Vol.11 (1), p.1-288, Article 288

2020

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Chromosomal Uniparental Disomy 16 and Fetal Intrauterine Growth Restriction

European journal of obstetrics & gynecology and reproductive biology, 2017-04, Vol.211, p.1-7

2017

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CRISPR/Cas9 gene correction of HbH-CS thalassemia-induced pluripotent stem cells

Annals of hematology, 2019-12, Vol.98 (12), p.2661-2671

2019

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Circulating MicroRNAs in Cancer: Potential and Challenge

Saracatinib prompts hemin-induced K562 erythroid differentiation but suppresses erythropoiesis of hematopoietic stem cells

MiR-6875-3p promotes the proliferation, invasion and metastasis of hepatocellular carcinoma via BTG2/FAK/Akt pathway

The connection between innervation and metabolic rearrangements in pancreatic cancer through serine

Immunotherapy for Hepatocellular Carcinoma: Current Advances and Future Expectations

Different culture method changing CD105 expression in amniotic fluid MSCs without affecting differentiation ability or immune function

A universal KOH-free strategy towards nitrogen-doped carbon nanosheets for high-rate and high-energy storage devices

RS12574989 and haplotype associated with α/β-chain imbalance and population HbA2 reduction

Application of MFI-5 in severe complications and unfavorable outcomes after radical resection of colorectal cancer

The use of high-resolution SNP arrays to detect congenital cardiac defects

MSCs derived from amniotic fluid and umbilical cord require different administration schemes and exert different curative effects on different tissues in rats with CLP-induced sepsis

A de novo PAK1 likely pathogenic variant and a de novo terminal 1q microdeletion in a Chinese girl with global developmental delay, severe intellectual disability, and seizures

Generation of two induced pluripotent stem cell lines, GZHMCi009-A and GZHMCi010-A, derived from peripheral blood mononuclear cells of two SCA3 patients with 14/74 CAG repeats of the ATXN3 mutation

A retrospective analysis of MS/MS screening for IEM in high-risk areas

Molecular Characterization Analysis of Thalassemia and Hemoglobinopathy in Quanzhou, Southeast China: A Large-Scale Retrospective Study

Extracellular Vesicles of Mesenchymal Stem Cells Are More Effectively Accessed through Polyethylene Glycol-Based Precipitation than by Ultracentrifugation

A Tumor Microenvironment Responsive Nanotheranostics Agent for Magnetic Resonance Imaging and Synergistic Photodynamic Therapy/Photothermal Therapy of Liver Cancer

Complex Chromosomal Rearrangement Causes Male Azoospermia: A Case Report and Literature Review

Prenatal diagnosis of dent disease type I with a nonsense pathogenic variant in CLCN5: a case study

Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication

Generation of induced pluripotent stem cell GZLSL-i001-A derived from urine-derived cells of Hemophilia A patient with Inv22 mutation

Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing

The safety and effectiveness of genetically corrected iPSCs derived from β-thalassaemia patients in nonmyeloablative β-thalassaemic mice

Chromosomal Uniparental Disomy 16 and Fetal Intrauterine Growth Restriction

CRISPR/Cas9 gene correction of HbH-CS thalassemia-induced pluripotent stem cells

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