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Profil bibliographique

Peng Wan

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

63Publications signalées
378Citations signalées
3Affiliations récentes

Les institutions déclarées

Les domaines associés

Opportunistic and Delay-Tolerant NetworksSatellite Communication SystemsWireless Communication Networks ResearchEnergy Harvesting in Wireless NetworksAdvanced Wireless Communication Techniques

Les publications récentes

Accès ouvert 2025 article OpenAlex

Associations of Prenatal Exposures to Fine Particulate Matter and Its Compositions with Preterm Birth Risk in Twins

Yuan Zheng, Xinqi Zhong, Peng Wan, Zhiqing Chen et autres

Twin pregnancies have a higher risk of preterm birth (PTB) than single pregnancies, but studies about prenatal air pollution exposure and PTB in twin pregnancies are still scarce. To explore associations of prenatal fine particulate matter (PM2.5) exposure with PTB in twins, …

cn (code pays fourni par la source)

9 citations Green Health
Accès ouvert 2025 article OpenAlex

Development of the CRISPR/Cas9 system for genome editing in Riemerella anatipestifer

Yi‐Han Chang, Honghao Huang, Ruonan Zhao, Lu Diao et autres

Riemerella anatipestifer (R. anatipestifer) is an important pathogen responsible for high mortality rates and severe economic losses in the poultry industry. Research on R. anatipestifer is constrained by limited genetic manipulation tools, highlighting the need for an effective genome editing toolkit. The …

cn (code pays fourni par la source)

1 citation Poultry Science
Accès ouvert 2025 review OpenAlex

A Complement Factor B Mutation in a Chinese Family with Atypical Hemolytic Uremic Syndrome: A Case Report and Systematic Review

Peng Wan, Xicui Long, Hao-Ran Lei, Fengxiao Bu et autres

Introduction: Atypical hemolytic uremic syndrome (aHUS) is a rare and potentially life-threatening condition, often linked to dysregulation of the complement system. Case Presentation: In this study, a novel heterozygous CFB mutation was identified in both the index patient and her sister, who …

cn (code pays fourni par la source)

0 citations Case Reports in Nephrology and Dialysis
Accès ouvert 2025 article OpenAlex

ALKBH5-mediated NPC2 mRNA m6A demethylation promotes resistance to oxaliplatin in colorectal cancer

Peng Wan, Hongtao Li

Colorectal cancer (CRC) is the third most common cancer globally and a leading cause of cancer-related death. Oxaliplatin, a key platinum-based chemotherapy, significantly improves outcomes in CRC patients. Nevertheless, oxaliplatin resistance often emerges, leading to worse prognosis. Exploring new biomarkers and mechanisms …

cn (code pays fourni par la source)

4 citations Functional & Integrative Genomics
Accès ouvert 2025 article OpenAlex

CLPP Gene Variants Causing Perrault Syndrome Type 3 in Han Chinese Families: A Genotype-Phenotype Study

Xicui Long, Bingqian Yang, Wei Wang, Peng Wan et autres

BACKGROUND: Perrault syndrome is a rare autosomal recessive disorder characterized by sensorineural hearing loss (SNHL) and primary ovarian insufficiency (POI) secondary to ovarian dysgenesis. However, the mutation spectrum of disease-causing genes for Perrault syndrome in the Chinese population remains poorly understood. In …

cn (code pays fourni par la source)

3 citations Human Genomics
Accès ouvert 2025 article OpenAlex

Associations of prenatal exposure to fine particulate matter and its constituents with small for gestational age risk: A twin study in China

Xinqi Zhong, Yuan Zheng, Peng Wan, Yixiang Huang et autres

This study aimed to examine the impact of PM 2.5 and its constituents on small for gestational age (SGA). We collected records of 8082 twin pairs and their mothers from 21 hospitals across China. Concentrations of PM 2.5 and its constituents were …

cn (code pays fourni par la source)

6 citations Ecotoxicology and Environmental Safety
Accès ouvert 2025 article OpenAlex

Genetic variation in patent foramen ovale: a case-control genome-wide association study

Bosi Dong, Yajiao Li, Fandi Ai, Jia Geng et autres

Background Patent foramen ovale (PFO) is a congenital defect between the atria, resulting in abnormal hemodynamics. We conducted a genome-wide association study (GWAS) to identify common genetic variants associated with PFO. Methods We performed a whole genome sequencing in a discovery cohort …

cn (code pays fourni par la source)

2 citations Frontiers in Genetics
2024 article OpenAlex

Analysis of Bacterial Community Composition in Sediments of the Mainstream and Tributaries in the Wanzhou Section of the Three Gorges Reservoir Area, China

Peng Wan, Yu Qin, Zhaoxia Li, Changyue Ouyang et autres

River ecosystems are intricately connected to the biogeochemical processes mediated by sediment bacterial communities. The Three Gorges Reservoir, a critical freshwater resource, has seen limited research on bacterial community composition, particularly in comparative studies between its mainstream and tributaries. High-throughput sequencing was …

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1 citation Geomicrobiology Journal

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