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Multistage Self-Assembled Nanomaterials for Cancer Immunotherapy

Molecules (Basel, Switzerland), 2023-11, Vol.28 (23), p.7750

2023

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Conductive biomaterials for cardiac repair: A review

Acta biomaterialia, 2022-02, Vol.139, p.157-178

2022

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KRAS mutation: from undruggable to druggable in cancer

Signal transduction and targeted therapy, 2021-11, Vol.6 (1), p.386-20, Article 386

2021

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MiR-652-5p elevated glycolysis level by targeting TIGAR in T-cell acute lymphoblastic leukemia

Cell death & disease, 2022-02, Vol.13 (2), p.148-148, Article 148

2022

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Association of systemic inflammatory response index with ST segment elevation myocardial infarction and degree of coronary stenosis: a cross-sectional study

BMC cardiovascular disorders, 2024-02, Vol.24 (1), p.98-98, Article 98

2024

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Whole exome sequencing for non-selective pediatric patients with hyperlipidemia

Gene, 2021-02, Vol.768, p.145310-145310, Article 145310

2021

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Identification of a GNE homozygous mutation in a Han‐Chinese family with GNE myopathy

Journal of cellular and molecular medicine, 2018-11, Vol.22 (11), p.5533-5538

2018

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Identification of novel pathogenic ABCA4 variants in a Han Chinese family with Stargardt disease

Bioscience reports, 2019-01, Vol.39 (1)

2019

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Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma

Cellular physiology and biochemistry, 2018-01, Vol.46 (5), p.1919-1929

2018

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Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly

PloS one, 2016-05, Vol.11 (5), p.e0155180-e0155180

2016

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Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing

PloS one, 2016-05, Vol.11 (5), p.e0155908-e0155908

2016

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COL1A2 p.Gly1066Val variant identified in a Han Chinese family with osteogenesis imperfecta type I

Molecular genetics & genomic medicine, 2019-05, Vol.7 (5), p.e619-n/a

2019

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Co-transplantation of mesenchymal stromal cells and cord blood cells in treatment of diabetes

Cytotherapy (Oxford, England), 2013-11, Vol.15 (11), p.1374-1384

2013

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Identification of MET exon14 skipping by targeted DNA- and RNA-based next-generation sequencing in pulmonary sarcomatoid carcinomas

Lung cancer (Amsterdam, Netherlands), 2018-08, Vol.122, p.113-119

2018

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Novel CLCN7 mutation identified in a Han Chinese family with autosomal dominant osteopetrosis-2

Molecular pain, 2016, Vol.12, p.174480691665262

2016

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Identification of a novel EVC variant in a Han‐Chinese family with Ellis‐van Creveld syndrome

Molecular genetics & genomic medicine, 2019-09, Vol.7 (9), p.e885-n/a

2019

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Genetic analysis of the S100B gene in Chinese patients with Parkinson disease

Neuroscience letters, 2013-10, Vol.555, p.134-136

2013

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Identification of a novel GJA3 mutation in congenital nuclear cataract

Optometry and vision science, 2015-03, Vol.92 (3), p.337

2015

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A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorder

Molecular medicine reports, 2017-10, Vol.16 (4), p.4241-4246

2017

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Characterization of a novel human UDP-GalNAc transferase, pp-GalNAc-T15

FEBS letters, 2004-05, Vol.566 (1), p.17-24

2004

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S1P-S1PR3-RAS promotes the progression of S1PR3 hi TAL1 + T-cell acute lymphoblastic leukemia that can be effectively inhibited by an S1PR3 antagonist

Leukemia, 2023-10, Vol.37 (10), p.1982

2023

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Cloning and characterization of a novel UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, pp-GalNAc-T14

Biochemical and biophysical research communications, 2003-01, Vol.300 (3), p.738-744

2003

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Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing

Molecular biology reports, 2014-06, Vol.41 (6), p.3631-3635

2014

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Molecular cloning and characterization of a novel member of the UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase family, pp-GalNAc-T12

FEBS letters, 2002-07, Vol.524 (1), p.211-218

2002

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Identification of a GJA3 mutation in a Chinese family with congenital nuclear cataract using exome sequencing

Indian journal of biochemistry & biophysics, 2013-08, Vol.50 (4), p.253-258

2013

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Multistage Self-Assembled Nanomaterials for Cancer Immunotherapy

Conductive biomaterials for cardiac repair: A review

KRAS mutation: from undruggable to druggable in cancer

MiR-652-5p elevated glycolysis level by targeting TIGAR in T-cell acute lymphoblastic leukemia

Association of systemic inflammatory response index with ST segment elevation myocardial infarction and degree of coronary stenosis: a cross-sectional study

Whole exome sequencing for non-selective pediatric patients with hyperlipidemia

Identification of a GNE homozygous mutation in a Han‐Chinese family with GNE myopathy

Identification of novel pathogenic ABCA4 variants in a Han Chinese family with Stargardt disease

Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma

Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly

Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing

COL1A2 p.Gly1066Val variant identified in a Han Chinese family with osteogenesis imperfecta type I

Co-transplantation of mesenchymal stromal cells and cord blood cells in treatment of diabetes

Identification of MET exon14 skipping by targeted DNA- and RNA-based next-generation sequencing in pulmonary sarcomatoid carcinomas

Novel CLCN7 mutation identified in a Han Chinese family with autosomal dominant osteopetrosis-2

Identification of a novel EVC variant in a Han‐Chinese family with Ellis‐van Creveld syndrome

Genetic analysis of the S100B gene in Chinese patients with Parkinson disease

Identification of a novel GJA3 mutation in congenital nuclear cataract

A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorder

Characterization of a novel human UDP-GalNAc transferase, pp-GalNAc-T15

S1P-S1PR3-RAS promotes the progression of S1PR3 hi TAL1 + T-cell acute lymphoblastic leukemia that can be effectively inhibited by an S1PR3 antagonist

Cloning and characterization of a novel UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, pp-GalNAc-T14

Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing

Molecular cloning and characterization of a novel member of the UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase family, pp-GalNAc-T12

Identification of a GJA3 mutation in a Chinese family with congenital nuclear cataract using exome sequencing

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