Bijun Zhang
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Explore the profile of Bijun Zhang including associated specialties, affiliations and a list of published articles.
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41
Citations
226
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Recent Articles
1.
Zhang B, Zhang D, Sun F, Si X, Luan M, He R
Orphanet J Rare Dis
. 2025 Mar;
20(1):121.
PMID: 40075430
Background: Multiple acyl-coenzyme A (CoA) dehydrogenase deficiency (MADD) is an autosomal recessive disorder resulting from mutations in the ETFDH gene. It is characterized by a wide spectrum of clinical symptoms,...
2.
Luan M, Zhang B, Wei Y, Liu F, Zhao Y, Yu Y, et al.
Chem Biol Interact
. 2024 Jun;
399:111116.
PMID: 38908812
Enhanced drug resistance poses a significant challenge in treating ovarian cancer (OC). Phenylethyl isothiocyanate (PEITC) is involved in drug resistance in OC, but the mechanism remains unclear. In this study,...
3.
Du Y, Jiang P, Yang J, Zhao M, Wu L, Hui Y, et al.
Clin Lab
. 2024 Apr;
70(4).
PMID: 38623669
Background: We aimed to evaluate the diagnostic capabilities of Chinese laboratories for inherited metabolic disorders (IMDs) using gas chromatography-mass spectrometry (GC-MS) on urine samples. Meanwhile, based on the result of...
4.
Liang X, Liu X, Li W, Zhang L, Zhang B, Lai G, et al.
Arch Biochem Biophys
. 2023 May;
742:109619.
PMID: 37142076
Fructose-1,6-bisphosphatase (FBPase) deficiency is an autosomal recessive disorder characterized by impaired gluconeogenesis caused by mutations in the fructose-1,6-bisphosphatase 1 (FBP1) gene. The molecular mechanisms underlying FBPase deficiency caused by FBP1...
5.
Zhang B, Fan T
Front Genet
. 2022 Sep;
13:951939.
PMID: 36081985
Deep learning technology has been widely used in genetic research because of its characteristics of computability, statistical analysis, and predictability. Herein, we aimed to summarize standardized knowledge and potentially innovative...
6.
Zhang L, Liu X, Zhao Y, Wang Q, Zhang Y, Gao H, et al.
Ital J Pediatr
. 2022 Jul;
48(1):121.
PMID: 35870983
Background: Prader-Willi syndrome (PWS) is a complex disorder caused by impaired paternally expressed genes on chromosome 15q11-q13. Variable findings have been reported about the phenotypic differences among PWS genetic subtypes....
7.
Liu X, Zhang L, Zhang H, Liang X, Zhang B, Tu J, et al.
Front Mol Neurosci
. 2022 Jul;
15:919718.
PMID: 35832397
Neural precursor cell expressed developmentally downregulated gene 4-like (NEDD4-2) is an epilepsy-associated gene encoding an E3 ligase that ubiquitinates neuroactive substrates. An involvement of NEDD4-2 in endoplasmic reticulum (ER) stress...
8.
Zou Z, Zhang B, Nie X, Cheng Y, Hu Z, Liao M, et al.
RSC Adv
. 2022 May;
10(65):39722-39730.
PMID: 35515393
Interpenetrating polymer network (IPN) hydrogels are crosslinked by two or more polymer networks, providing free volume space in the three-dimensional network structure, and providing conditions for the sustained and controlled...
9.
Zhang B, Zhao Y
Clin Chim Acta
. 2022 Mar;
530:104-112.
PMID: 35314173
Multiple acyl-CoA dehydrogenase deficiency (MADD) is a rare autosomal recessive metabolic disease. Patients present with metabolic decompensation, muscle weakness, respiratory failure, and cardiomyopathy. Late-onset MADD is primarily caused by mutations...
10.
Zhang Y, Liu X, Gao H, Cui W, Zhang B, Zhao Y
Mol Cytogenet
. 2021 Dec;
14(1):57.
PMID: 34922566
Chromosome 15q24 microdeletion is a rare genetic disorder characterized by development delay, facial dysmorphism, congenital malformations, and occasional autism spectrum disorder (ASD). In this study, we identified five cases of...