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Molecular diagnosis and prenatal diagnosis in a hereditary multiple osteochondromas family

Beijing da xue xue bao. Journal of Peking University. Yi xue ban, 2013-12, Vol.45 (6), p.906

2013

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Identification of a mosaic mutation of NF1 gene in a sporadic case of neurofibromatosis type 1

Zhonghua yi xue yi chuan xue za zhi, 2012-10, Vol.29 (5), p.529

2012

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A novel missense mutation resulting in X-linked adrenoleukodystrophy in female heterozygotes of a Chinese family

Zhonghua yi xue yi chuan xue za zhi, 2010-04, Vol.27 (2), p.144

2010

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Molecular diagnosis of a Chinese pedigree with osteogenesis imperfecta type I

Zhonghua yi xue yi chuan xue za zhi, 2009-02, Vol.26 (1), p.50

2009

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Effect of OA kneepad on apoptosis genes Bcl-2 and p53 expression in articular cartilage cells of experimental knee osteoarthritis

Zhongguo gu shang, 2009-09, Vol.22 (9), p.688

2009

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Avoiding the interference of ABCD1 pseudogenes in the molecular diagnosis of X-linked adrenoleukodystrophy by double amplification refractory mutation system

Zhonghua yi xue yi chuan xue za zhi, 2006-10, Vol.23 (5), p.558

2006

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Prenatal molecular diagnosis of four fetuses at high risk for X-linked adrenoleukodystrophy

Chung-hua fu chʿan kʿo tsa chih, 2008-01, Vol.43 (1), p.25-28

2008

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Prokaryotic expression and characterization of N-terminal truncated glycoprotein gp85 of Epstein-Barr virus

Xi bao yu fen zi mian yi xue za zhi, 2007-02, Vol.23 (2), p.110

2007

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Prenatal diagnosis of 5 fetuses with high risk of developing spinal muscular atrophy

Zhonghua yi xue yi chuan xue za zhi, 2007-08, Vol.24 (4), p.373

2007

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Cyclooxygenase-2 expression is associated with initiation of hepatocellular carcinoma, while prostaglandin receptor-1 expression predicts survival

World journal of gastroenterology : WJG, 2016-10, Vol.22 (39), p.8798-8805

2016

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Prenatal molecular diagnosis of adrenoleukodystrophy

Zhonghua yi xue yi chuan xue za zhi, 2005-12, Vol.22 (6), p.612

2005

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Immunoassay for LMP1 in nasopharyngeal tissue based on surface-enhanced Raman scattering

International journal of nanomedicine, 2012-01, Vol.7 (default), p.73-82

2012

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Antibody-based spot test for NADH–cytochrome b5 reductase activity for the laboratory diagnosis of congenital methemoglobinemia

Clinica chimica acta, 1998-05, Vol.273 (1), p.13-20

1998

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Analysis of small supernumerary marker chromosome 15q11 in four infertile males

Zhonghua yi xue yi chuan xue za zhi, 2013-10, Vol.30 (5), p.539

2013

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Construction of sperm-specific lactate dehydrogenase DNA vaccine and experimental study of its immunocontraceptive effect on mice

Science China. Life sciences, 2008-04, Vol.51 (4), p.308-316

2008

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Study on DNA expression profiles in renal biopsies of patients with IgA nephropathy

Zhonghua bing li xue za zhi, 2009-05, Vol.38 (5), p.342

2009

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Molecular diagnosis of spinal muscular atrophy by multiplex ligation-dependent probe amplification

Zhong hua yi xue za zhi, 2008-12, Vol.88 (46), p.3262-3264

2008

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A novel mutation in the NADH-cytochrome b5 reductase gene of a Chinese patient with recessive congenital methemoglobinemia

Blood, 2000-05, Vol.95 (10), p.3250-3255

2000

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Directed shift of vaginal flora after topical application of sucrose gel in a phase Ⅲ clinical trial： a novel treatment for bacterial vaginosis

Chinese medical journal, 2010-08, Vol.123 (15), p.2051-2057

2010

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Hepatitis B surface antigen levels during natural history of chronic hepatitis B: A Chinese perspective study

World journal of gastroenterology : WJG, 2014-07, Vol.20 (27), p.9178-9184

2014

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Artemisinin analogue SM934 ameliorates DSS-induced mouse ulcerative colitis via suppressing neutrophils and macrophages

Acta pharmacologica Sinica, 2018-10, Vol.39 (10), p.1633-1644

2018

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Population pharmacokinetics of voriconazole and CYP2C19 polymorphisms for optimizing dosing regimens in renal transplant recipients

British journal of clinical pharmacology, 2018-07, Vol.84 (7), p.1587-1597

2018

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Oral administration of artemisinin analog SM934 ameliorates lupus syndromes in MRL/lpr mice by inhibiting Th1 and Th17 cell responses

Arthritis & rheumatology (Hoboken, N.J.), 2011-08, Vol.63 (8), p.2445-2455

2011

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Tumor-associated Lymphatic Endothelial Cells Promote Lymphatic Metastasis By Highly Expressing and Secreting SEMA4C

Clinical cancer research, 2017-01, Vol.23 (1), p.214-224

2017

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Impact of CYP2C19 Genotype and Liver Function on Voriconazole Pharmacokinetics in Renal Transplant Recipients

Therapeutic drug monitoring, 2017-08, Vol.39 (4), p.422-428

2017

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Molecular diagnosis and prenatal diagnosis in a hereditary multiple osteochondromas family

Identification of a mosaic mutation of NF1 gene in a sporadic case of neurofibromatosis type 1

A novel missense mutation resulting in X-linked adrenoleukodystrophy in female heterozygotes of a Chinese family

Molecular diagnosis of a Chinese pedigree with osteogenesis imperfecta type I

Effect of OA kneepad on apoptosis genes Bcl-2 and p53 expression in articular cartilage cells of experimental knee osteoarthritis

Avoiding the interference of ABCD1 pseudogenes in the molecular diagnosis of X-linked adrenoleukodystrophy by double amplification refractory mutation system

Prenatal molecular diagnosis of four fetuses at high risk for X-linked adrenoleukodystrophy

Prokaryotic expression and characterization of N-terminal truncated glycoprotein gp85 of Epstein-Barr virus

Prenatal diagnosis of 5 fetuses with high risk of developing spinal muscular atrophy

Cyclooxygenase-2 expression is associated with initiation of hepatocellular carcinoma, while prostaglandin receptor-1 expression predicts survival

Prenatal molecular diagnosis of adrenoleukodystrophy

Immunoassay for LMP1 in nasopharyngeal tissue based on surface-enhanced Raman scattering

Antibody-based spot test for NADH–cytochrome b5 reductase activity for the laboratory diagnosis of congenital methemoglobinemia

Analysis of small supernumerary marker chromosome 15q11 in four infertile males

Construction of sperm-specific lactate dehydrogenase DNA vaccine and experimental study of its immunocontraceptive effect on mice

Study on DNA expression profiles in renal biopsies of patients with IgA nephropathy

Molecular diagnosis of spinal muscular atrophy by multiplex ligation-dependent probe amplification

A novel mutation in the NADH-cytochrome b5 reductase gene of a Chinese patient with recessive congenital methemoglobinemia

Directed shift of vaginal flora after topical application of sucrose gel in a phase Ⅲ clinical trial： a novel treatment for bacterial vaginosis

Hepatitis B surface antigen levels during natural history of chronic hepatitis B: A Chinese perspective study

Artemisinin analogue SM934 ameliorates DSS-induced mouse ulcerative colitis via suppressing neutrophils and macrophages

Population pharmacokinetics of voriconazole and CYP2C19 polymorphisms for optimizing dosing regimens in renal transplant recipients

Oral administration of artemisinin analog SM934 ameliorates lupus syndromes in MRL/lpr mice by inhibiting Th1 and Th17 cell responses

Tumor-associated Lymphatic Endothelial Cells Promote Lymphatic Metastasis By Highly Expressing and Secreting SEMA4C

Impact of CYP2C19 Genotype and Liver Function on Voriconazole Pharmacokinetics in Renal Transplant Recipients

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