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Aggregation of Ribosomal Protein S6 at Nucleolus Is Cell Cycle-Controlled and Its Function in Pre-rRNA Processing Is Phosphorylation Dependent

Journal of cellular biochemistry, 2016-07, Vol.117 (7), p.1649-1657

2016

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Diagnostic Accuracies of the TUNEL, SCD, and Comet Based Sperm DNA Fragmentation Assays for Male Infertility: a Meta-analysis Study

Clinical laboratory (Heidelberg), 2015, Vol.61 (5-6), p.525

2015

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Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study

Biology of reproduction, 2022-01, Vol.106 (1), p.108-117

2022

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Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study

Biology of reproduction, 2022-01, Vol.106 (1), p.227-227

2022

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Pathogenesis of acephalic spermatozoa syndrome caused by SUN5 variant

Molecular human reproduction, 2021-05, Vol.27 (5)

2021

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Splicing of exon 9a in FMR1 transcripts results in a truncated FMRP with altered subcellular distribution

Gene, 2020-03, Vol.731, p.144359-144359, Article 144359

2020

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Further identification of a 140bp sequence from amid intron 9 of human FMR1 gene as a new exon

BMC genetics, 2020-06, Vol.21 (1), p.63, Article 63

2020

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Bioinformatics analysis of gene expression profiles of dermatomyositis

Molecular medicine reports, 2016-10, Vol.14 (4), p.3785-3790

2016

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Increased expression of hLRH-1 in human gastric cancer and its implication in tumorigenesis

Molecular and cellular biochemistry, 2008, Vol.308 (1-2), p.93-100

2008

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Isothiafludine, a novel non-nucleoside compound, inhibits hepatitis B virus replication through blocking pregenomic RNA encapsidation

Acta pharmacologica Sinica, 2014-03, Vol.35 (3), p.410-418

2014

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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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Progress in molecular diagnosis of fragile X syndrome

Zhonghua yi xue yi chuan xue za zhi, 2012-06, Vol.29 (3), p.296

2012

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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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Mutation analysis of SMN gene in a patient and his family with spinal muscular atrophy

Zhonghua yi xue yi chuan xue za zhi, 2009-04, Vol.26 (2), p.139

2009

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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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Advances in the studies of spermatogonial stem cells in primate mammals

Zhonghua nan ke xue, 2016-04, Vol.22 (4), p.347

2016

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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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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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Aggregation of Ribosomal Protein S6 at Nucleolus Is Cell Cycle-Controlled and Its Function in Pre-rRNA Processing Is Phosphorylation Dependent

Diagnostic Accuracies of the TUNEL, SCD, and Comet Based Sperm DNA Fragmentation Assays for Male Infertility: a Meta-analysis Study

Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study

Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study

Pathogenesis of acephalic spermatozoa syndrome caused by SUN5 variant

Splicing of exon 9a in FMR1 transcripts results in a truncated FMRP with altered subcellular distribution

Further identification of a 140bp sequence from amid intron 9 of human FMR1 gene as a new exon

Bioinformatics analysis of gene expression profiles of dermatomyositis

Increased expression of hLRH-1 in human gastric cancer and its implication in tumorigenesis

Isothiafludine, a novel non-nucleoside compound, inhibits hepatitis B virus replication through blocking pregenomic RNA encapsidation

Molecular diagnosis and prenatal diagnosis in a hereditary multiple osteochondromas family

Progress in molecular diagnosis of fragile X syndrome

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

Mutation analysis of SMN gene in a patient and his family with spinal muscular atrophy

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

Advances in the studies of spermatogonial stem cells in primate mammals

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

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

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