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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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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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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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Therapeutic effects of DZ2002, a reversible SAHH inhibitor, on lupus-prone NZBxNZW F1 mice via interference with TLR-mediated APC response

中国药理学报：英文版, 2014-02 (2), p.219-229

Shi-jun HE Ze-min LIN Yan-wei WU Bing-xin BAI Xiao-qian YANG Pei-lan HE Feng-hua ZHU Wei TANG Jian-ping ZUO

2014

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Experimental Study on the Suppression of Human Nuclear Receptor hLRH-1 via a Vector-based RNA Interference

Yíchuán xuébào, 2006, Vol.33 (1), p.26-31

2006

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Two novel multiple mutations in chinese patients with adrenoleukodystrophy

Neuropediatrics, 2010-06, Vol.41 (3), p.151-153

2010

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Microarray Analysis of Gene-Expression Profile in Hepatocellular Carcinoma Cell, BEL-7402, with Stable Suppression of hLRH-1 via a DNA Vector-based RNA Interference

Yíchuán xuébào, 2006-10, Vol.33 (10), p.881-891

2006

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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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A Mutation of Testis-specific Lactate Dehydrogenase Gene Found in Male Patients With Unexplained Infertility: A Mutation of Testis-specific Lactate Dehydrogenase Gene Found in Male Patients With Unexplained Infertility

Shēngwù huàxué yŭ shēngwù wùlĭ jìnzhán, 2010-04, Vol.37 (4), p.445-450

2010

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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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Exome sequencing discovered a novel splice donor mutation in dystrophin gene: Exome sequencing discovered a novel splice donor mutation in dystrophin gene

Di er jun yi da xue xue bao, 2013-11, Vol.33 (5), p.493-497

2013

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A compound heterozygote in the NADH-cytochrome b5 reductase gene from a Chinese patient with hereditary methemoglobinemia type I

International journal of hematology, 2000-07, Vol.72 (1), p.34-36

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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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

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

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

Therapeutic effects of DZ2002, a reversible SAHH inhibitor, on lupus-prone NZBxNZW F1 mice via interference with TLR-mediated APC response

Experimental Study on the Suppression of Human Nuclear Receptor hLRH-1 via a Vector-based RNA Interference

Two novel multiple mutations in chinese patients with adrenoleukodystrophy

Microarray Analysis of Gene-Expression Profile in Hepatocellular Carcinoma Cell, BEL-7402, with Stable Suppression of hLRH-1 via a DNA Vector-based RNA Interference

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

A Mutation of Testis-specific Lactate Dehydrogenase Gene Found in Male Patients With Unexplained Infertility: A Mutation of Testis-specific Lactate Dehydrogenase Gene Found in Male Patients With Unexplained Infertility

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

Exome sequencing discovered a novel splice donor mutation in dystrophin gene: Exome sequencing discovered a novel splice donor mutation in dystrophin gene

A compound heterozygote in the NADH-cytochrome b5 reductase gene from a Chinese patient with hereditary methemoglobinemia type I

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

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