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Profil bibliographique

Xuan Zhang

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

23Publications signalées
178Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Reproductive System and PregnancyPregnancy and preeclampsia studiesMicroRNA in disease regulationEndometriosis Research and TreatmentPreterm Birth and Chorioamnionitis

Les publications récentes

Accès ouvert 2025 conference-abstract OpenAlex

POS0834 AGE-RELATED DIFFERENCES IN CLINICAL AND IMMUNOLOGICAL FEATURES OF PRIMARY SJÖGREN'S SYNDROME: A CROSS-SECTIONAL STUDY

Qian Li, Q. Y. Su, Yulan Duan, Shunying Zhao et autres

Background: Primary Sjögren's syndrome (pSS) is a chronic autoimmune disease characterized by dry mouth and dry eyes, often leading to significant impairment in quality of life [1]. The clinical presentation, disease activity, and immune response can vary between patients with early onset …

cn (code pays fourni par la source)

0 citations Annals of the Rheumatic Diseases
Accès ouvert 2025 review OpenAlex

Analysis of the causes of redo pull-through for recurrent constipation and the risk factors affecting the prognosis of the Hirschsprung’s disease: a single-center retrospective study and systematic review

Jun Xiao, Shimin Yang, Lei Xiang, Bo Qin et autres

BACKGROUND: Hirschsprung's disease (HSCR) is a congenital gastrointestinal disorder. Pull-through (PT) surgery, the primary treatment, often leads to recurrent constipation. The causes of redo pull-through (redo-PT) for recurrent constipation remain unclear, with limited research on follow-up outcomes and prognostic factors. METHODS: We …

cn (code pays fourni par la source)

4 citations BMC Pediatrics
2024 article OpenAlex

Rare and common genetic variants underlying the risk of Hirschsprung’s disease

Jun Xiao, Chenzhao Feng, Tianqi Zhu, Xuan Zhang et autres

Hirschsprung's disease (HSCR) is a congenital enteric neuropathic disorder characterized by high heritability (>80%) and polygenic inheritance (>20 genes). The previous genome-wide association studies (GWAS) identified several common variants associated with HSCR and demonstrated increased predictive performance for HSCR risk in Europeans …

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5 citations Human Molecular Genetics
Accès ouvert 2024 article OpenAlex

Cinchophen induces RPA1 related DNA damage and apoptosis to impair ENS development of zebrafish

Jing Wang, Xinyao Meng, Xuyong Chen, Jun Xiao et autres

Nonsteroidal anti-inflammatory drugs (NSAIDs) have become contaminants widely distributed in the environment due to improper disposal and discharge. Previous study has found several components might involve in impairing enteric nervous system (ENS) development of zebrafish, including NSAIDs cinchophen. Deficient ENS development in …

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4 citations Ecotoxicology and Environmental Safety
Accès ouvert 2023 review OpenAlex

Association of human leukocyte antigen‐G and ‐F with recurrent miscarriage and implantation failure: A systematic review and meta‐analysis

Nana Han, Wanting Xia, Can Zhu, Xuan Zhang et autres

PROBLEM: The immune system plays an essential role in embryonic implantation and pregnancy, but the molecular details remain controversial. In the past four decades, human leukocyte antigen (HLA)-G and -F have garnered significant attention. METHOD OF STUDY: MEDLINE, EMBASE, Web of Science, …

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5 citations American Journal of Reproductive Immunology

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