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Autologous peripheral blood hematopoietic stem cell transplantation in the treatment of type 1 diabetic mellitus: a report of 16 cases

Zhong hua yi xue za zhi, 2011-07, Vol.91 (28), p.1966-1969

2011

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Pediatric burns due to hot water from water dispenser： a neglected issue that should be highly concerned

Chinese medical journal, 2012-06, Vol.125 (11), p.2053-2056

2012

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Unplanned decannulation of tracheotomy tube in massive burn patients： a retrospective case series study

Chinese medical journal, 2011-10, Vol.124 (20), p.3309-3313

2011

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Pharmacological modulation of the voltage-gated neuronal Kv7/KCNQ/M-channel alters the intrinsic excitability and synaptic responses of pyramidal neurons in rat prefrontal cortex slices

Acta pharmacologica Sinica, 2017-09, Vol.38 (9), p.1248-1256

2017

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Comparative Analysis of the Multi-Frequency Bio-impedance and Dual-energy X-ray Absorptiometry on Body Composition in Obese Subjects

Biomedical and environmental sciences, 2018, Vol.31 (1), p.72-75

2018

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Two novel TMEM67 variations in a Chinese family with recurrent pregnancy loss: a case report

BMC medical genomics, 2024-06, Vol.17 (1), p.156-7

2024

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Integrated CNV-seq, karyotyping and SNP-array analyses for effective prenatal diagnosis of chromosomal mosaicism

BMC medical genomics, 2021-02, Vol.14 (1), p.56-12, Article 56

2021

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Antioxidant catalase rescues against high fat diet-induced cardiac dysfunction via an IKKβ-AMPK-dependent regulation of autophagy

Biochimica et biophysica acta, 2015-02, Vol.1852 (2), p.343-352

2015

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Stem Cell Factor Combined with Matrix Proteins Regulates the Attachment and Migration of Melanocyte Precursors of Human Hair Follicles in Vitro

Biological and Pharmaceutical Bulletin, 2013/08/01, Vol.36(8), pp.1317-1325

2013

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Overexpression of EIF-5A2 is associated with metastasis of human colorectal carcinoma

Human pathology, 2008, Vol.39 (1), p.80-86

2008

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Clinical and genetic analysis of classical Ehlers‐Danlos syndrome patient caused by synonymous mutation in COL5A2

Molecular genetics & genomic medicine, 2021-05, Vol.9 (5), p.e1632-n/a

2021

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Clinical and molecular characterization of 12 prenatal cases of Cri‐du‐chat syndrome

Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1312-n/a

2020

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Compound heterozygous variants in MAN2B2 identified in a Chinese child with congenital disorders of glycosylation

European journal of human genetics : EJHG, 2023-12, Vol.31 (12), p.1455-1457

2023

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Whole exome sequencing reveals two novel mutations in GREB1L in two Chinese families with renal agenesis

QJM : An International Journal of Medicine, 2024-06, Vol.117 (6), p.462-464

2024

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Autotransfusion in the management of cardiac tamponade occurring during catheter ablation of atrial fibrillation

Chinese medical journal, 2010-04, Vol.123 (7), p.961-963

2010

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Gene mutation analysis of a Chinese family of congenital long Q-T syndrome type three

Zhonghua er ke za zhi, 2009-12, Vol.47 (12), p.926

2009

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Linkage analysis and gene mapping of one Chinese family with benign familial infantile convulsions

Zhongguo dang dai er ke za zhi, 2010-02, Vol.12 (2), p.89

2010

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Hyperbaric oxygen improves long-term learning-memory deficits and brain injury in neonatal rat with hypoxia-ischemia brain damage

Sichuan da xue xue bao. Journal of Sichuan University. Yi xue ban, 2007-01, Vol.38 (1), p.73

2007

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CD8+ cell noncytotoxic antiviral response (CNAR) to HIV in nosocomial HIV-infected individuals

Zhonghua shi yan he lin chuang bing du xue za ji, 2008-06, Vol.22 (3), p.195

2008

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A novel mutation in KCNQ2 gene causes benign familial infantile convulsions (BFIC) in a Chinese family

Zhonghua er ke za zhi, 2006-07, Vol.44 (7), p.487

2006

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Genetic analysis of a child with mental retardation and hypospadia

Zhonghua yi xue yi chuan xue za zhi, 2019-12, Vol.36 (12), p.1199

2019

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Efficacy of catheter ablation of atrial fibrillation beyond HATCH score

Chinese medical journal, 2012-10, Vol.125 (19), p.3425-3429

2012

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Colostomy is a simple and effective procedure for severe chronic radiation proctitis

World journal of gastroenterology : WJG, 2016-06, Vol.22 (24), p.5598-5608

2016

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DNA methyltransferase3a expression is an independent poor prognostic indicator in gastric cancer

World journal of gastroenterology : WJG, 2014-07, Vol.20 (25), p.8201-8208

2014

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Impact of different termination modes on atrial fibrillation termination in catheter ablation of persistent atrial fibrillation

Chinese medical journal, 2012-06, Vol.125 (11), p.1877-1883

2012

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Autologous peripheral blood hematopoietic stem cell transplantation in the treatment of type 1 diabetic mellitus: a report of 16 cases

Pediatric burns due to hot water from water dispenser： a neglected issue that should be highly concerned

Unplanned decannulation of tracheotomy tube in massive burn patients： a retrospective case series study

Pharmacological modulation of the voltage-gated neuronal Kv7/KCNQ/M-channel alters the intrinsic excitability and synaptic responses of pyramidal neurons in rat prefrontal cortex slices

Comparative Analysis of the Multi-Frequency Bio-impedance and Dual-energy X-ray Absorptiometry on Body Composition in Obese Subjects

Two novel TMEM67 variations in a Chinese family with recurrent pregnancy loss: a case report

Integrated CNV-seq, karyotyping and SNP-array analyses for effective prenatal diagnosis of chromosomal mosaicism

Antioxidant catalase rescues against high fat diet-induced cardiac dysfunction via an IKKβ-AMPK-dependent regulation of autophagy

Stem Cell Factor Combined with Matrix Proteins Regulates the Attachment and Migration of Melanocyte Precursors of Human Hair Follicles in Vitro

Overexpression of EIF-5A2 is associated with metastasis of human colorectal carcinoma

Clinical and genetic analysis of classical Ehlers‐Danlos syndrome patient caused by synonymous mutation in COL5A2

Clinical and molecular characterization of 12 prenatal cases of Cri‐du‐chat syndrome

Compound heterozygous variants in MAN2B2 identified in a Chinese child with congenital disorders of glycosylation

Whole exome sequencing reveals two novel mutations in GREB1L in two Chinese families with renal agenesis

Autotransfusion in the management of cardiac tamponade occurring during catheter ablation of atrial fibrillation

Gene mutation analysis of a Chinese family of congenital long Q-T syndrome type three

Linkage analysis and gene mapping of one Chinese family with benign familial infantile convulsions

Hyperbaric oxygen improves long-term learning-memory deficits and brain injury in neonatal rat with hypoxia-ischemia brain damage

CD8+ cell noncytotoxic antiviral response (CNAR) to HIV in nosocomial HIV-infected individuals

A novel mutation in KCNQ2 gene causes benign familial infantile convulsions (BFIC) in a Chinese family

Genetic analysis of a child with mental retardation and hypospadia

Efficacy of catheter ablation of atrial fibrillation beyond HATCH score

Colostomy is a simple and effective procedure for severe chronic radiation proctitis

DNA methyltransferase3a expression is an independent poor prognostic indicator in gastric cancer

Impact of different termination modes on atrial fibrillation termination in catheter ablation of persistent atrial fibrillation

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