Works by Bingbing Wu
Results: 112
Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome.
- Published in:
- 2015
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- Publication type:
- journal article
Analysis of β-Catenin Expression and Exon 3 Mutations in Pediatric Sporadic Aggressive Fibromatosis.
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- Pediatric & Developmental Pathology, 2012, v. 15, n. 3, p. 173, doi. 10.2350/10-07-0866-OA.1
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- Publication type:
- Article
Predictive Prenatal Diagnosis for Infantile-onset Inflammatory Bowel Disease Because of Interleukin-10 Signalling Defects.
- Published in:
- 2021
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- Publication type:
- journal article
Key technical solutions and standardization progress of high-speed optical modules.
- Published in:
- Telecommunications Science, 2022, v. 38, n. 9, p. 105, doi. 10.11959/j.issn.1000--0801.2022249
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- Publication type:
- Article
Analysis on the progress of all-optical network standardization and technology development.
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- Telecommunications Science, 2019, v. 35, n. 4, p. 1, doi. 10.11959/j.issn.1000-0801.2019067
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- Publication type:
- Article
Genetic spectrums and clinical profiles of critically ill neonates with congenital auricular deformity in the China Neonatal Genomes Project.
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- Human Genetics, 2023, v. 142, n. 12, p. 1737, doi. 10.1007/s00439-023-02612-7
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- Publication type:
- Article
Optimized trio genome sequencing (OTGS) as a first-tier genetic test in critically ill infants: practice in China.
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- Human Genetics, 2020, v. 139, n. 4, p. 473, doi. 10.1007/s00439-019-02103-8
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- Publication type:
- Article
NKCC1 involvement in the epithelial-to- mesenchymal transition is a prognostic biomarker in gliomas.
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- PeerJ, 2020, p. 1, doi. 10.7717/peerj.8787
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- Publication type:
- Article
The TRIM37 variants in Mulibrey nanism patients paralyze follicular helper T cell differentiation.
- Published in:
- Cell Discovery, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41421-023-00561-z
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- Publication type:
- Article
A tissue specific-infection mouse model of SARS-CoV-2.
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- Cell Discovery, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41421-023-00536-0
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- Publication type:
- Article
SFRP4<sup>+</sup> stromal cell subpopulation with IGF1 signaling in human endometrial regeneration.
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- Cell Discovery, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41421-022-00438-7
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- Publication type:
- Article
Fructose-1,6-bisphosphatase deficiency: estimation of prevalence in the Chinese population and analysis of genotype-phenotype association.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1296797
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- Publication type:
- Article
Mass cytometry and transcriptomic profiling reveal body‐wide pathology induced by Loxl1 deficiency.
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- Cell Proliferation, 2021, v. 54, n. 7, p. 1, doi. 10.1111/cpr.13077
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- Publication type:
- Article
Does Hazy Weather Influence Earnings Management of Heavy-Polluting Enterprises? A Chinese Empirical Study from the Perspective of Negative Social Concerns.
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- Sustainability (2071-1050), 2017, v. 9, n. 12, p. 2296, doi. 10.3390/su9122296
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- Publication type:
- Article
Engagement/Disengagement Characteristics of Pull-Type Diaphragm Spring Clutch for Heavy-Duty Commercial Vehicles.
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- Chinese Journal of Mechanical Engineering, 2024, v. 37, n. 1, p. 1, doi. 10.1186/s10033-024-01115-4
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- Publication type:
- Article
Diagnostic biomolecules and combination therapy for pre-eclampsia.
- Published in:
- 2022
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- Publication type:
- Literature Review
Ulva pertusa lectin 1 delivery through adenovirus vector affects multiple signaling pathways in cancer cells.
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- Glycoconjugate Journal, 2017, v. 34, n. 4, p. 489, doi. 10.1007/s10719-017-9767-6
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- Publication type:
- Article
Effect of immunization with a recombinant cholera toxin B subunit/somatostatin fusion protein on immune response and growth hormone levels in mice.
- Published in:
- Biotechnology Letters, 2012, v. 34, n. 12, p. 2199, doi. 10.1007/s10529-012-1027-z
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- Publication type:
- Article
Comparison of Genetic Profiles of Neonates in Intensive Care Units Conceived With or Without Assisted Reproductive Technology.
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- JAMA Network Open, 2023, v. 6, n. 4, p. e236537, doi. 10.1001/jamanetworkopen.2023.6537
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- Publication type:
- Article
Association Between Expanded Genomic Sequencing Combined With Hearing Screening and Detection of Hearing Loss Among Newborns in a Neonatal Intensive Care Unit.
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- JAMA Network Open, 2022, v. 5, n. 7, p. e2220986, doi. 10.1001/jamanetworkopen.2022.20986
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- Publication type:
- Article
Hyaline fibromatosis syndrome with a novel 4.41‐kb deletion in ANTXR2 gene: A case report and literature review.
- Published in:
- 2022
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- Publication type:
- Case Study
Intron retention by a novel intronic mutation in DKC1 gene caused recurrent still birth and early death in a Chinese family.
- Published in:
- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 6, p. 1, doi. 10.1002/mgg3.1934
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- Publication type:
- Article
Cover.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1458
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- Publication type:
- Article
COQ8B nephropathy: Early detection and optimal treatment.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1360
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- Publication type:
- Article
First maternal uniparental disomy for chromosome 2 with PREPL novel frameshift mutation of congenital myasthenic syndrome 22 in an infant.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 3, p. 1, doi. 10.1002/mgg3.1144
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- Publication type:
- Article
Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 12, p. N.PAG, doi. 10.1002/mgg3.1009
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- Publication type:
- Article
Diagnosis of mixed infection and a primary immunodeficiency disease using next-generation sequencing: a case report.
- Published in:
- Frontiers in Cellular & Infection Microbiology, 2023, p. 1, doi. 10.3389/fcimb.2023.1179090
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- Publication type:
- Article
China and New Middle East.
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- Journal of Balkan & Near Eastern Studies, 2021, v. 23, n. 3, p. 443, doi. 10.1080/19448953.2021.1888248
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- Publication type:
- Article
A Chinese girl of Blau syndrome with renal arteritis and a literature review.
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- Pediatric Rheumatology, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12969-023-00804-z
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- Publication type:
- Article
A novel deletion of IGF1 in a patient with idiopathic short stature provides insight Into IGF1 haploinsufficiency.
- Published in:
- 2014
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- Publication type:
- journal article
Possible physiological mechanism of exogenous vitamin E influencing shelf life, physicochemical quality, and microorganism of fresh‐cut water chestnuts.
- Published in:
- Journal of Food Processing & Preservation, 2022, v. 46, n. 3, p. 1, doi. 10.1111/jfpp.16372
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- Publication type:
- Article
New respirator performance monitor (RePM) for powered air-purifying respirators.
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- Journal of Occupational & Environmental Hygiene, 2020, v. 17, n. 11/12, p. 538, doi. 10.1080/15459624.2020.1814491
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- Publication type:
- Article
A technique to measure respirator protection factors against aerosol particles in simulated workplace settings using portable instruments.
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- Journal of Occupational & Environmental Hygiene, 2020, v. 17, n. 5, p. 231, doi. 10.1080/15459624.2020.1735640
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- Publication type:
- Article
Performance of a novel real-time respirator seal integrity monitor on firefighters: Simulated workplace pilot study.
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- Journal of Occupational & Environmental Hygiene, 2018, v. 15, n. 8, p. 607, doi. 10.1080/15459624.2018.1479065
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- Publication type:
- Article
Targeted Directed Evolution of an α-L-Rhamnosidase on Hesperidin Through Six-Codon Combinatorial Mutagenesis.
- Published in:
- Catalysts (2073-4344), 2024, v. 14, n. 12, p. 935, doi. 10.3390/catal14120935
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- Publication type:
- Article
Improving Rutin Biotransformation Efficiency of α-L-Rhamnosidase from Bacteroides thetaiotaomicron VPI-5482 via Targeted Mutagenesis Focused on General Acid Motif.
- Published in:
- Catalysts (2073-4344), 2024, v. 14, n. 8, p. 501, doi. 10.3390/catal14080501
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- Publication type:
- Article
The missing linker between SUN5 and PMFBP1 in sperm head-tail coupling apparatus.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-25227-w
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- Publication type:
- Article
Novel Variants of PPP2R1A in Catalytic Subunit Binding Domain and Genotype–Phenotype Analysis in Neurodevelopmentally Delayed Patients.
- Published in:
- Genes, 2023, v. 14, n. 9, p. 1750, doi. 10.3390/genes14091750
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- Publication type:
- Article
An Analysis of Phenotype and Genotype in a Large Cohort of Chinese Children with Angelman Syndrome.
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- Genes, 2022, v. 13, n. 8, p. 1447, doi. 10.3390/genes13081447
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- Publication type:
- Article
Clinical Targeted Panel Sequencing Analysis in Clinical Evaluation of Children with Autism Spectrum Disorder in China.
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- Genes, 2022, v. 13, n. 6, p. 1010, doi. 10.3390/genes13061010
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- Publication type:
- Article
BANCR Regulates The Cell Invasion And Migration In Esophageal Squamous Cell Carcinoma Through Wnt/β-Catenin Signaling Pathway.
- Published in:
- OncoTargets & Therapy, 2019, v. 12, p. 9319, doi. 10.2147/OTT.S227220
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- Publication type:
- Article
Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohort.
- Published in:
- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01102-x
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- Publication type:
- Article
Identification of Pathogenic Variants in RPGRIP1L with Meckel Syndrome and Preimplantation Genetic Testing in a Chinese Family.
- Published in:
- Reproductive Sciences, 2022, v. 29, n. 8, p. 2200, doi. 10.1007/s43032-022-00898-y
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- Publication type:
- Article
Clinical and genetic risk factors associated with neonatal severe hyperbilirubinemia: a case-control study based on the China Neonatal Genomes Project.
- Published in:
- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2023.1292921
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- Publication type:
- Article
The Clinical and Genetic Features of Co-occurring Epilepsy and Autism Spectrum Disorder in Chinese Children.
- Published in:
- Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2019.00505
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- Publication type:
- Article
Effect of birth ball abdominal core training on pregnancy fatigue, waist pain and delivery outcomes.
- Published in:
- International Journal of Gynecology & Obstetrics, 2022, v. 158, n. 3, p. 613, doi. 10.1002/ijgo.14045
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- Publication type:
- Article
Clinical severity prediction in children with osteogenesis imperfecta caused by COL1A1/2 defects.
- Published in:
- Osteoporosis International, 2022, v. 33, n. 6, p. 1373, doi. 10.1007/s00198-021-06263-0
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- Publication type:
- Article
Autophagy mediated tubulobulbar complex components degradation is required for spermiation.
- Published in:
- Fundamental Research, 2024, v. 4, n. 6, p. 1557, doi. 10.1016/j.fmre.2022.10.006
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- Publication type:
- Article
Bi-potential hPSC-derived Müllerian duct-like cells for full-thickness and functional endometrium regeneration.
- Published in:
- NPJ Regenerative Medicine, 2022, v. 7, n. 1, p. 1, doi. 10.1038/s41536-022-00263-2
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- Publication type:
- Article
Laboratory Evaluation of a Novel Real-Time Respirator Seal Integrity Monitor.
- Published in:
- Annals of Work Exposures & Health, 2018, v. 62, n. 6, p. 742, doi. 10.1093/annweh/wxy026
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- Publication type:
- Article