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A cohort autopsy study defines COVID-19 systemic pathogenesis

Cell research, 2021-08, Vol.31 (8), p.836-846

2021

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Relationship of serum vitamin D levels with diabetic microvascular complications in patients with type 2 diabetes mellitus

Chinese medical journal, 2021-04, Vol.134 (7), p.814-820

2021

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Extraction of Extracelluar Vesicles Derived from Mycobacterium tuberculosis and Their Effect on the Production of Reactive Oxygen Species and Expression of Inflammatory Factors in Mouse Bone Marrow-Derived Dendritic Cells

Sichuan da xue xue bao. Journal of Sichuan University. Yi xue ban, 2023-01, Vol.54 (1), p.122-127

2023

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Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome

PloS one, 2017-05, Vol.12 (5), p.e0177685-e0177685

2017

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Epidemiological investigation and proteomic profiling of typical TCM syndrome in HIV/AIDS immunological nonresponders

Anatomical record (Hoboken, N.J. : 2007), 2023-12, Vol.306 (12), p.3106-3119

2023

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A novel p. Gly630Ser mutation of COL2A1 in a Chinese family with presentations of Legg-Calvé-Perthes disease or avascular necrosis of the femoral head

PloS one, 2014-06, Vol.9 (6), p.e100505-e100505

2014

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Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria

PloS one, 2013-11, Vol.8 (11), p.e79808-e79808

2013

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Successful recovery of COVID-19-associated recurrent diarrhea and gastrointestinal hemorrhage using convalescent plasma

Military medical research, 2020-09, Vol.7 (1), p.1-45, Article 45

2020

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Detection of RASSF1A promoter hypermethylation in serum from gastric and colorectal adenocarcinoma patients

World journal of gastroenterology : WJG, 2008-05, Vol.14 (19), p.3074-3080

2008

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A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese family

BMC ophthalmology, 2014-09, Vol.14 (1), p.108-108, Article 108

2014

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Association between ubiquitin-specific protease USP26 polymorphism and male infertility in Chinese men

Clinica chimica acta, 2011-03, Vol.412 (7), p.545-549

2011

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Clinical and cytogenetic characterization of a boy with a de novo pure partial trisomy 16q24.1q24.3 and complex chromosome rearrangement

American journal of medical genetics. Part A, 2013-04, Vol.161A (4), p.897-900

2013

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Effects of Graded Hypothermia on Hypoxic-ischemic Brain Damage in the Neonatal Rat

Chinese medical sciences journal, 2011-03, Vol.26 (1), p.49-53

2011

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Proteomic investigation and biomarker identification of lung and spleen deficiency syndrome in HIV/AIDS immunological nonresponders

Journal of thoracic disease, 2023-03, Vol.15 (3), p.1460-1472

2023

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The COL4A3 and COL4A4 Digenic Mutations in cis Result in Benign Familial Hematuria in a Large Chinese Family

Cytogenetic and genome research, 2018-01, Vol.154 (3), p.132-136

2018

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Three Novel Heterozygous COL4A4 Mutations Result in Three Different Collagen Type IV Kidney Disease Phenotypes

Cytogenetic and genome research, 2018-01, Vol.154 (1), p.30-36

2018

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Target gene panel method versus whole-exome sequencing in detection of idiopathic hypogonadotropic hypogonadism in males

Zhonghua nan ke xue, 2021-10, Vol.27 (10), p.899

2021

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Mutation analysis of NF2 gene and clinical investigation in a Chinese family with neurofibromatosis type II

Zhonghua yi xue yi chuan xue za zhi, 2010-12, Vol.27 (6), p.688

2010

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Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive

BMC urology, 2014-08, Vol.14 (1), p.70-70, Article 70

2014

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An infertile male with apparent 45,X turned out to have 45,X,der(Y)t(Y;13)(q11.2;q12),-13: clinicopathologic and cytogenomic studies

Fertility and sterility, 2007-12, Vol.88 (6), p.1676.e7-1676.e11

2007

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A girl with distinctive features of borderline high blood pressure, short stature, characteristic brachydactyly, and 11.47 Mb deletion in 12p11.21-12p12.2 by oligonucleotide array CGH

American journal of medical genetics. Part A, 2009-10, Vol.149A (10), p.2321-2323

2009

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Changes of Nerve Growth Factor in Amniotic Fluid and Correlation with Ventriculomegaly

Chinese medical sciences journal, 2011-06, Vol.26 (2), p.109-112

2011

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Correlation between microRNA-34b/c single nucleotide polymorphism rs4938723 and male infertility

Zhonghua nan ke xue, 2020-09, Vol.26 (9), p.807

2020

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Polymorphisms in estrogen receptors predict the risk of male infertility: a meta-analysis

Reproductive biology and endocrinology, 2014-08, Vol.12 (1), p.79-79, Article 79

2014

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Detection of DPY19L2 gene mutation in 2 cases of globozoospermia

Zhonghua nan ke xue, 2020-07, Vol.26 (7), p.620

2020

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A cohort autopsy study defines COVID-19 systemic pathogenesis

Relationship of serum vitamin D levels with diabetic microvascular complications in patients with type 2 diabetes mellitus

Extraction of Extracelluar Vesicles Derived from Mycobacterium tuberculosis and Their Effect on the Production of Reactive Oxygen Species and Expression of Inflammatory Factors in Mouse Bone Marrow-Derived Dendritic Cells

Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome

Epidemiological investigation and proteomic profiling of typical TCM syndrome in HIV/AIDS immunological nonresponders

A novel p. Gly630Ser mutation of COL2A1 in a Chinese family with presentations of Legg-Calvé-Perthes disease or avascular necrosis of the femoral head

Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria

Successful recovery of COVID-19-associated recurrent diarrhea and gastrointestinal hemorrhage using convalescent plasma

Detection of RASSF1A promoter hypermethylation in serum from gastric and colorectal adenocarcinoma patients

A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese family

Association between ubiquitin-specific protease USP26 polymorphism and male infertility in Chinese men

Clinical and cytogenetic characterization of a boy with a de novo pure partial trisomy 16q24.1q24.3 and complex chromosome rearrangement

Effects of Graded Hypothermia on Hypoxic-ischemic Brain Damage in the Neonatal Rat

Proteomic investigation and biomarker identification of lung and spleen deficiency syndrome in HIV/AIDS immunological nonresponders

The COL4A3 and COL4A4 Digenic Mutations in cis Result in Benign Familial Hematuria in a Large Chinese Family

Three Novel Heterozygous COL4A4 Mutations Result in Three Different Collagen Type IV Kidney Disease Phenotypes

Target gene panel method versus whole-exome sequencing in detection of idiopathic hypogonadotropic hypogonadism in males

Mutation analysis of NF2 gene and clinical investigation in a Chinese family with neurofibromatosis type II

Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive

An infertile male with apparent 45,X turned out to have 45,X,der(Y)t(Y;13)(q11.2;q12),-13: clinicopathologic and cytogenomic studies

A girl with distinctive features of borderline high blood pressure, short stature, characteristic brachydactyly, and 11.47 Mb deletion in 12p11.21-12p12.2 by oligonucleotide array CGH

Changes of Nerve Growth Factor in Amniotic Fluid and Correlation with Ventriculomegaly

Correlation between microRNA-34b/c single nucleotide polymorphism rs4938723 and male infertility

Polymorphisms in estrogen receptors predict the risk of male infertility: a meta-analysis

Detection of DPY19L2 gene mutation in 2 cases of globozoospermia

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