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C1GALT1 polymorphisms are associated with Henoch–Schönlein purpura nephritis

Pediatric nephrology (Berlin, West), 2012-09, Vol.27 (9), p.1505-1509

2012

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MEFV E148Q polymorphism is associated with Henoch–Schönlein purpura in Chinese children

Pediatric nephrology (Berlin, West), 2010-10, Vol.25 (10), p.2077-2082

2010

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Analysis of the distribution of chemical elements in Adelie penguin bone using synchrotron radiation X-ray fluorescence

Polar biology, 2003-03, Vol.26 (3), p.171-177

2003

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A prototype study of the POLAR front-end electronics

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 2011-12, Vol.659 (1), p.322-327

2011

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Serum Amyloid A Levels Associated with Gastrointestinal Manifestations in Henoch-Schönlein Purpura

Inflammation, 2012-08, Vol.35 (4), p.1251-1255

2012

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Interior temperature monitoring of NaI(Tl) crystal in space environment by pulse width measurement

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 2010-04, Vol.615 (3), p.272-276

2010

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The CD18 AvaII polymorphic site not associated with Henoch-Schönlein purpura

Clinical and experimental rheumatology, 2011-01, Vol.29 (1 Suppl 64), p.S117

2011

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Oxcarbazepine-Related Thrombocytopenic Purpura

Journal of clinical psychopharmacology, 2011-02, Vol.31 (1), p.137-138

2011

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Conceptual design of a synchrotron radiation source dedicated to X-ray lithography

Il Nuovo cimento, A, 1991-12, Vol.104 (12), p.1725-1733

1991

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X-ray mask copying based on negative resist RAY-PN

Microelectronic engineering, 1994, Vol.23 (1), p.231-234

1994

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Oxcarbazepine-related thrombocytopenic purpura

Journal of clinical psychopharmacology, 2011, Vol.31 (1), p.137-138

2011

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Genetic Analysis of a Case of Sotos Syndrome with Suspected Germinal Mosaicism in Mother

Applied biochemistry and biotechnology, 2023-10, Vol.195 (10), p.5792-5801

2023

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Cbx4 governs HIF-1α to involve in Th9 cell differentiation promoting asthma by its SUMO E3 ligase activity

Biochimica et biophysica acta. Molecular cell research, 2023-10, Vol.1870 (7), p.119524-119524, Article 119524

2023

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Impacts of mixed ferrous sulfate-biochar additives on humification and bacterial community during electric field-assisted aerobic composting

Bioresource technology, 2024-07, Vol.404, p.130901, Article 130901

2024

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A novel de novo synonymous variant in GREB1L impacts the mRNA splicing associated with aplasia of the urogenital system

American journal of medical genetics. Part A, 2024-08, p.e63823

2024

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Case Report: Twin Pregnancy Gives Birth to a Girl with Partial Trisomy 21 Mosaicism after in vitro Fertilization and Embryo Transfer

Frontiers in genetics, 2022-02, Vol.12, p.740415

2022

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心衰住院患者焦虑抑郁共病及其相关因素的研究

四川大学学报：医学版, 2017, Vol.48 (3), p.435-440

史秀莉亢玉陈晨张庆

2017

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Construction and evaluation of a novel set of 90 microhaplotypes for forensic applications using NGS technology

Forensic science international, 2023-12, Vol.353, p.111848-111848, Article 111848

2023

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HNRNPC mediated m6A methylation of 5-methyltetrahydrofolate-homocysteine methyltransferase and involved in the occurrence of RSA

Journal of reproductive immunology, 2023-12, Vol.160, p.104160-104160, Article 104160

2023

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Evaluation of the genetic parameters and mutation analysis of 22 STR loci in the central Chinese Han population

International Journal of Legal Medicine, 2017, Vol.131 (1), p.103-105

2017

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Genetic analysis and prenatal diagnosis of a Chinese pedigree affected with Usher syndrome due to novel compound heterozygous variants of PCDH15 gene

Zhonghua yi xue yi chuan xue za zhi, 2022-03, Vol.39 (3), p.305

2022

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Clinical predictive value of pre-pregnancy tests for unexplained recurrent spontaneous abortion: a retrospective study

Frontiers in medicine, 2024-08, Vol.11

2024

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Application of whole exome sequencing for the inferential analysis of recessive genetic disease carrier status for couples with a child died of Primary immunodeficiency

Zhonghua yi xue yi chuan xue za zhi, 2024-02, Vol.41 (2), p.134

2024

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Analysis of a Chinese pedigree affected with dyschromatosis symmetrica hereditaria due to a novel variant of ADAR gene

Zhonghua yi xue yi chuan xue za zhi, 2022-01, Vol.39 (1), p.64

2022

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HNRNPC mediated m 6 A methylation of 5-methyltetrahydrofolate-homocysteine methyltransferase and involved in the occurrence of RSA

Journal of reproductive immunology, 2023-12, Vol.160, p.104160

2023

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