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Chinese Scientific Paper Citation & BibTeX Generator

Specially calibrated for Western researchers, graduate students, and R&D teams citing Chinese peer-reviewed journals, CAS preprints, and technological disclosures. Generates perfectly formatted APA 7, BibTeX, MLA 9, Chicago, Harvard, and RIS (Zotero/EndNote) in one click.

Quick Test Samples:
Formatted Academic Citation
Yang, Bingwang, Zhang, Lixin, Liu, Chen, & Wang, Zhiqiang (2025). A Sulfobetaine Polyurethane for Substitutable Meniscus Implant with Excellent Mechanical, Tribological, and Biocompatible Properties. Journal of Central South University (Advanced Materials), 32(3), 108-124. https://doi.org/10.1007/s11771-024-5734-0
Style: APA• Ready for LaTeX, Word, Overleaf & Zotero
Active Paper Details

A Sulfobetaine Polyurethane for Substitutable Meniscus Implant with Excellent Mechanical, Tribological, and Biocompatible Properties

具有优异力学、摩擦学及生物相容性的磺酸基甜菜碱聚氨酯人工半月板假体材料研究

Authors: Yang, Bingwang, Zhang, Lixin, Liu, Chen, Wang, Zhiqiang

Journal: Journal of Central South University (Advanced Materials)

Year: 2025 • Vol. 32, Issue 3

Pages: 108-124

DOI: 10.1007/s11771-024-5734-0

Verified Pinyin Author Matching100% Calibrated

Best Practices for Citing Chinese Scientific Literature

A comprehensive editorial guide compiled by the SinoBioData Bibliographic Standards Committee for authors publishing in Nature, Science, IEEE, Elsevier, and Springer journals.

1Pinyin Author Naming Conventions

Chinese names typically follow the Surname First, Given Name Second structure (e.g. 张伟 $\rightarrow$ Zhang Wei). When publishing in international journals using APA 7 or Chicago styles:

  • Surname first in citation list: Zhang, W. or Zhang, Wei
  • Two-character given names: Should be joined without spaces or hyphenated according to the author's preferred English imprint (e.g. Wang, Xiao-Ming or Wang, Xiaoming).
  • Ambiguous multi-authors: Always retain full romanized given names in the initial BibTeX entry to prevent indexing collisions on Google Scholar.

2Standard Chinese Research Institution Codes

Major Chinese national laboratories have standardized international abbreviations recognized by Thomson Reuters / Clarivate Web of Science:

CAS: Chinese Academy of Sciences (中国科学院)
CASC: China Aerospace Science & Tech (航天科技)
CETC: China Electronics Tech Group (中国电科)
CAEP: China Academy of Engineering Physics (中物院)
IHEP: Institute of High Energy Physics (高能所)

Citing Translated and English-Editions of Chinese Journals

When citing papers translated from Chinese or published in dual-edition journals (such as Acta Metallurgica Sinica (English Letters) or Journal of Central South University), best practice dictates citing the verified English translation while referencing the original DOI or Chinese title in square brackets. This citation tool automatically embeds the canonical DOI and persistent archive link to guarantee digital provenance.

Supported Citation Formats Comparison Table

Citation StylePrimary Target FieldSoftware CompatibilityExport Format
APA 7th EditionPsychology, Social Sciences, Clean EnergyMicrosoft Word, Google Docs, ScrivenerRich Text / Plain Text
BibTeX (.bib)Computer Science, AI, Mathematics, PhysicsOverleaf, TeXmaker, LaTeX, Typst.bib file download
MLA 9th EditionHumanities, Literature, East Asian StudiesWord, Pages, ScrivenerRich Text / Plain Text
Chicago 17thHistory, Economics, Policy, MultidisciplinaryEndNote, Word, ZoteroAuthor-Date / Notes
RIS FormatUniversal Bibliographic Data ExchangeZotero, EndNote, Mendeley, Citavi.ris file download
Open Access Catalog

Explore Peer-Reviewed Chinese Research Papers

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2026 Research Article

Cilta-cel (Carvykti / Legend Biotech) vs. Ide-cel (Abecma): Dual-Epitope BCMA Binding Affinity, Progression-Free Survival (PFS), and CRS Management

Cilta-cel outperforms ide-cel in efficacy: ORR 98% vs 73%, median PFS not reached at 22 months vs 8.8 months in CARTITUDE-4. However, ide-cel shows a safer profile with Grade 3/4 CRS at 4% vs 9% and ICANS at 3% vs 5%. Cilta-cel's dual-epitope VHH design enhances avidity but increases toxicity. Choose based on risk tolerance.

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2026 Research Article

Mesenchymal Stem Cells Alleviate Psoriasis by Regulating the PSPH-PINK1-Parkin-NLRP3 Pathway in HaCaT Keratinocytes via Serine Metabolism

Psoriasis is a chronic inflammatory skin disease affecting 2-3% of the global population. Mesenchymal stem cells (MSCs) have emerged as a potential therapy, but the underlying mechanisms remain unclear. This study investigated the therapeutic effects of adipose-derived MSCs on imiquimod (IMQ)-induced psoriasis in mice and M5-induced psoriatic HaCaT keratinocytes in vitro. MSCs significantly ameliorated skin lesions, reduced inflammatory cytokines (IL-1β, IL-6, IL-8, TNF-α) and chemokines (MCP-1, CCL7, CCL20, CCL27), and restored skin barrier function by upregulating claudin-1. MSCs also normalized keratinocyte differentiation markers (increased KRT1, decreased KRT6). Amino acid metabolomics revealed that MSCs enhanced serine metabolism in mouse skin, upregulating phosphoserine phosphatase (PSPH). Knockdown of PSPH reversed the therapeutic effects of MSCs in vitro. Mechanistically, MSCs activated the PINK1-Parkin mitophagy pathway, as evidenced by increased PINK1, Parkin, p-Parkin, Beclin-1, and LC3B-II/I ratios, and decreased P62. This activation attenuated NLRP3 inflammasome activation and restrained keratinocyte hyperproliferation. The study concludes that MSCs alleviate psoriasis via PSPH-mediated activation of PINK1-Parkin mitophagy, suppressing NLRP3 inflammasome. Limitations include the need to identify specific MSC-secreted factors and lack of clinical validation. These findings provide a rationale for developing PSPH-targeted therapies for psoriasis.

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2026 Research Article

Identifying NOTCH signaling-specialized hematopoietic supportive subpopulation from mesenchymal stem cells

Background: Human umbilical cord mesenchymal stem cells (UC-MSCs) are promising for cellular therapy due to their accessibility, low ethical concerns, and immunomodulatory and tissue repair capacities. However, heterogeneity during in vitro expansion poses quality control challenges. Methods: Two fetal umbilical cords were obtained; primary UC-MSCs were isolated and passaged continuously. Cells were harvested for single-cell RNA sequencing; 78,178 cells and 14 subpopulations were analyzed. Validation used in vitro assays and in vivo studies. Results: Mid-passage UC-MSCs showed superior functional performance based on differential gene expression and functional enrichment. An optimal subpopulation (C8) was identified by holistic evaluation of stemness, hematopoietic support, and immunomodulation. NOTCH signaling was enriched in C8, with NOTCH2 as the dominant receptor. MLPH and LPXN were identified as signature markers; MLPHhighLPXNhigh UC-MSCs displayed higher hematopoietic support and immunosuppression than MLPHlowLPXNlow cells. Conclusions: Mid-passage UC-MSCs are favorable for clinical use. The subpopulation with high NOTCH activity exhibits enhanced hematopoietic support and immunosuppression. MLPH and LPXN are ideal markers for isolating this functional subpopulation.

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