Suchergebnisse - "Chen, Xiang-Jun"

PubPharm (134)

1

Performance assessment of the Bruker Biotyper MALDI-TOF MS for the identification of difficult-to-identify viridans group streptococci

enthalten in: Journal of clinical microbiology | 2023

von Wan, T. | Lee, T. | Chen, X. | +4

2

Applicability of an in-house extraction protocol in a Bruker Biotyper matrix-assisted laser desorption/ionization time-of-flight mass spectrometry system for the identification of Streptococcus agalactiae from broth-enriched vaginal/rectal swab specimens

enthalten in: Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi | 2023

von Chen, X. | Wan, T. | Chao, Q. | +4

3

Autoantibody levels as biomarkers of disease activity in the management of myasthenia gravis

enthalten in: European journal of neurology | 2023

von Li, H. | Gao, F. | Chen, X.

CommentOn: Eur J Neurol. 2023 Jan;30(1):266-282. - PMID 36094738

4

Identification of competing endogenous RNA network in laryngeal squamous cell carcinoma

enthalten in: Oral diseases | 2023

von Cui, X. | Zhang, S. | Wang, W. | +2

5

Fam96b recruits brain-type creatine kinase to fuel mitotic spindle formation

enthalten in: Biochimica et biophysica acta. Molecular cell research | 2023

von Zhang, X. | Chen, X. | Yan, Y.

6

Autoantibody levels as biomarkers of disease activity in the management of myasthenia gravis

enthalten in: European Journal of Neurology | 2023

von Li, H. | Gao, F. | Chen, X.

7

Identification of competing endogenous RNA network in laryngeal squamous cell carcinoma

enthalten in: Oral Diseases | 2023

von Cui, X. | Zhang, S. | Wang, W. | +2

8

Mutation analysis of SUOX in isolated sulfite oxidase deficiency with ectopia lentis as the presenting feature : insights into genotype-phenotype correlation

enthalten in: Orphanet journal of rare diseases | 2022

von Li, J. | Chen, Z. | Chen, X. | +1

9

Mutation analysis of SUOX in isolated sulfite oxidase deficiency with ectopia lentis as the presenting feature: insights into genotype–phenotype correlation

enthalten in: Orphanet journal of rare diseases | 2022

von Li, J. | Chen, Z. | Chen, X. | +1

10

Mutation analysis of SUOX in isolated sulfite oxidase deficiency with ectopia lentis as the presenting feature: insights into genotype–phenotype correlation

enthalten in: Orphanet journal of rare diseases | 2022

von Li, J. | Chen, Z. | Chen, X. | +1

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