Works by Zhu, Baosheng
Results: 31
LOVD–DASH: A comprehensive LOVD database coupled with diagnosis and an at‐risk assessment system for hemoglobinopathies.
- Published in:
- Human Mutation, 2019, v. 40, n. 12, p. 2221, doi. 10.1002/humu.23863
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- Article
Low-density lipoprotein cholesterol and the risk of hyperemesis gravidarum: a Mendelian randomization study.
- Published in:
- Journal of Maternal-Fetal & Neonatal Medicine, 2024, v. 37, n. 1, p. 1, doi. 10.1080/14767058.2024.2397722
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- Article
Genotyping of clinical varicella-zoster virus isolates collected from Yunnan in Southwestern China.
- Published in:
- Biomedical Reports, 2016, v. 4, n. 2, p. 209, doi. 10.3892/br.2015.562
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- Article
A case report of a novel HIST1H1E mutation and a review of the bibliography to evaluate the genotype–phenotype correlations.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 12, p. 1, doi. 10.1002/mgg3.2273
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- Article
Five novel globin gene mutations identified in five Chinese families by next‐generation sequencing.
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- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 12, p. 1, doi. 10.1002/mgg3.1835
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- Article
Targeted next‐generation sequencing of deaf patients from Southwestern China.
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- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 4, p. 1, doi. 10.1002/mgg3.1660
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- Article
Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 6, p. N.PAG, doi. 10.1002/mgg3.706
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- Article
Molecular epidemiology, pathogenicity, and structural analysis of haemoglobin variants in the Yunnan province population of Southwestern China.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-44793-0
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- Article
Prevalence of hemoglobin E in Yunnan Province of Southwest China.
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- Hematology, 2016, v. 21, n. 1, p. 54, doi. 10.1179/1607845415Y.0000000044
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- Article
Experience of Low-Pass Whole-Genome Sequencing-Based Copy Number Variant Analysis: A Survey of Chinese Tertiary Hospitals.
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- Diagnostics (2075-4418), 2022, v. 12, n. 5, p. N.PAG, doi. 10.3390/diagnostics12051098
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- Article
Protective effect of metformin on a rat model of lipopolysaccharide‐induced preeclampsia.
- Published in:
- Fundamental & Clinical Pharmacology, 2019, v. 33, n. 6, p. 649, doi. 10.1111/fcp.12501
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- Article
First-trimester maternal serum alpha-fetoprotein is not a good predictor for adverse pregnancy outcomes: a retrospective study of 3325 cases.
- Published in:
- 2020
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- Publication type:
- journal article
A rat model of placental inflammation explains the unexplained elevated maternal serum alpha‐fetoprotein associated with adverse pregnancy outcomes.
- Published in:
- Journal of Obstetrics & Gynaecology Research, 2019, v. 45, n. 10, p. 1980, doi. 10.1111/jog.14085
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- Article
Clinical and genetic characterization of six cases with complete androgen insensitivity syndrome in China.
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- Journal of Genetics, 2017, v. 96, n. 4, p. 695, doi. 10.1007/s12041-017-0809-4
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- Article
The relationship of maternal polymorphisms of genes related to meiosis and DNA damage repair with fetal chromosomal stability.
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- Journal of Perinatal Medicine, 2023, v. 51, n. 8, p. 1082, doi. 10.1515/jpm-2022-0613
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- Article
In Vitro and In Vivo Supplementation with Curcumin Promotes Hippocampal Neuronal Synapses Development in Rats by Inhibiting GSK-3β and Activating β-catenin.
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- Molecular Neurobiology, 2024, v. 61, n. 4, p. 2390, doi. 10.1007/s12035-023-03665-5
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- Article
Factors associated with fetal karyotype in spontaneous abortion: a case-case study.
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- 2022
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- Publication type:
- journal article
Evaluation of the deficiency status of 25‐hydroxyvitamin D and associated factors in Southwest China: A hospital‐based retrospective cross‐sectional analysis of a low‐latitude, high‐altitude, multiracial region.
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- Nutrition Bulletin, 2023, v. 48, n. 4, p. 535, doi. 10.1111/nbu.12645
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- Article
Influence of TP53 Codon 72 Polymorphism Alone or in Combination with HDM2 SNP309 on Human Infertility and IVF Outcome.
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- PLoS ONE, 2016, v. 11, n. 11, p. 1, doi. 10.1371/journal.pone.0167147
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- Article
Association of TP53 rs1042522 G > C, MDM2 rs2279744 T > G, and miR-34b/c rs4938723 T > C polymorphisms with aneuploidy pregnancy susceptibility.
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- BMC Pregnancy & Childbirth, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12884-023-05945-3
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- Article
Ultrasonographic classification of 26 cases of fetal umbilical-portal-systemic venous shunts and the correlations with fetal chromosomal abnormalities.
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- BMC Pregnancy & Childbirth, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12884-023-05525-5
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- Article
Construction of restored model of fractured femurs based on anatomic features.
- Published in:
- Biotechnology & Biotechnological Equipment, 2019, v. 33, n. 1, p. 988, doi. 10.1080/13102818.2019.1637277
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- Publication type:
- Article
Acute myeloid leukemia with DNMT3A mutations.
- Published in:
- Leukemia & Lymphoma, 2014, v. 55, n. 9, p. 2002, doi. 10.3109/10428194.2013.869802
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- Article
Newborn Genetic Screening Improves the Screening Efficiency for Congenital Hypothyroidism: A Prospective Multicenter Study in China.
- Published in:
- International Journal of Neonatal Screening (IJNS), 2024, v. 10, n. 4, p. 78, doi. 10.3390/ijns10040078
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- Publication type:
- Article
Newborn Screening for Inborn Errors of Metabolism by Next-Generation Sequencing Combined with Tandem Mass Spectrometry.
- Published in:
- International Journal of Neonatal Screening (IJNS), 2024, v. 10, n. 2, p. 28, doi. 10.3390/ijns10020028
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- Article
Maternal genetic polymorphisms in the major mitotic checkpoint genes MAD1L1 and MAD2L1 associated with the risk of survival in abnormal chromosomal fetuses.
- Published in:
- Frontiers in Genetics, 2023, v. 14, p. 1, doi. 10.3389/fgene.2023.1105184
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- Article
Identification of Zygosaccharomyces mellis strains in stored honey and their stress tolerance.
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- Food Science & Biotechnology, 2016, v. 25, n. 6, p. 1645, doi. 10.1007/s10068-016-0253-x
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- Article
Pyrethroid pesticide exposure during early pregnancy and birth outcomes in southwest China: a birth cohort study.
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- Journal of Toxicological Sciences, 2020, v. 45, n. 5, p. 281, doi. 10.2131/jts.45.281
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- Article
Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis.
- Published in:
- 2021
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- Publication type:
- journal article
ESTABLISHMENT OF FEEDER-FREE CULTURE SYSTEM OF HUMAN PARTHENOGENETIC EMBRYONIC STEM CELLS.
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- Chinese Journal of Reparative & Reconstructive Surgery, 2013, v. 27, n. 5, p. 559, doi. 10.7507/1002-1892.20130124
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- Article
Genotypes and phenotypes of a family with a deaf child carrying combined heterozygous mutations in SLC26A4 and GJB3 genes.
- Published in:
- Molecular Medicine Reports, 2016, v. 14, n. 1, p. 319, doi. 10.3892/mmr.2016.5280
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- Article