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Akademický článek

Comparison of Talaromyces marneffei Infection in Human Immunodeficiency Virus-positive and Human Immunodeficiency Virus-negative Patients from Fujian, China

Autor: Hong-Ru Li, Shao-Xi Cai, Yu-Sheng Chen, Mei-E Yu, Neng-Luan Xu, Bao-Song Xie, Ming Lin, Xin-Lan Hu

Publikováno v: Chinese Medical Journal, Vol 129, Iss 9, Pp 1059-1065 (2016)

Background: Talaromyces (Penicillium) marneffei (TM) is an emerging dimorphic human pathogenic fungus that is endemic to Southeast Asia. TM mostly occurs as an opportunistic infection in patients with human immunodeficiency virus (HIV). The objective

Externí odkaz: https://doaj.org/article/699005746a114dd9a46f5761023338ce

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Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphology

Publikováno v: Banka, S, Bennington, A, Baker, M J, Clemente, G, Rijckmans, E & Millard, T H 2022, ' Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphology. ', Brain, vol. 145, no. 12, awac049, pp. 4232-4245 . https://doi.org/10.1093/brain/awac049
Banka, Siddharth; Bennington, Abigail; Baker, Martin J; Rijckmans, Ellen; Clemente, Giuliana D; Ansor, Nurhuda Mohamad; Sito, Hilary; Prasad, Pritha; Anyane-Yeboa, Kwame; Badalato, Lauren; Dimitrov, Boyan; Fitzpatrick, David; Hurst, Anna C E; Jansen, Anna C; Kelly, Melissa A; Krantz, Ian; Rieubland, Claudine; Ross, Meredith; Rudy, Natasha L; Sanz, Javier; ... (2022). Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphology. Brain : a journal of neurology, 145(12), pp. 4232-4245. Oxford University Press 10.1093/brain/awac049
Banka, S, Bennington, A, Baker, M J, Rijckmans, E, Clemente, G D, Ansor, N M, Sito, H, Prasad, P, Anyane-Yeboa, K, Badalato, L, Dimitrov, B, Fitzpatrick, D, Hurst, A C E, Jansen, A C, Kelly, M A, Krantz, I, Rieubland, C, Ross, M, Rudy, N L, Sanz, J, Stouffs, K, Xu, Z L, Malliri, A, Kazanietz, M G & Millard, T H 2022, ' Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphology ', Brain . https://doi.org/10.1093/brain/awac049

RAC1 is a highly conserved Rho GTPase critical for many cellular and developmental processes. De novo missense RAC1 variants cause a highly variable neurodevelopmental disorder. Some of these variants have previously been shown to have a dominant neg

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c59ac0233908bd46903a99816ffede10
https://hdl.handle.net/1983/7f3c39a1-5287-457f-ac73-0cedb02ece00

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Development and Internal Validation of a Nomogram Used to Predict Chemotherapy-Induced Neutropenia in Non-Small Cell Lung Cancer Patients: A Retrospective Cohort Study

Autor: Neng-Luan Xu, Wei Zou

Publikováno v: Cancer Management and Research

Wei Zou,1 Neng-Luan Xu2 1Shengli Clinical Medical College of Fujian Medical University, Fujian Medical University, Fuzhou, Fujian, People’s Republic of China; 2Department of Pulmonary and Critical Care Medicine, Fujian Provincial Hospital, Fuzhou,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d70abd35dcdcd0c7ec9fd90fbbdb5b8
https://doi.org/10.2147/cmar.s302722

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Anti-oxidative effect of zinc in human umbilical cord mesenchymal stem cells

Autor: Wang Ruobing, Lu Xiaodan, Fang Yanqiu, Tan Yan, Lin Yifan, Liu Yan, Lin Xiuying, Luan Xu, Wang Zihang, Li Bing, Zhang Qiang, Mi Xuguang, Zhang Xiaofang

Publikováno v: Biophysics Reports. 7:142-151

Human umbilical cord mesenchymal stem cells (HUC-MSCs) are pluripotent and functional in many biological processes, by which releasing secretary factors to promote the self-repairing of damaged tissue or developing into functional cell at local organ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7eff44bd0ee20b77a972ba66fa3b95b8
https://doi.org/10.52601/bpr.2021.200046

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Prenatal presentation and diagnosis of Baraitser‐Winter syndrome using exome sequencing

Autor: Zhuo Luan Xu, Samuel P. Strom, Kelly Usrey, Eleina Cox, Alexis Disilvestro, Kermit S Zhang

Publikováno v: American Journal of Medical Genetics Part A. 182:2124-2128

Baraitser-Winter cerebrofrontofacial syndrome (BWCFF) is a rare autosomal dominant developmental disorder associated with missense mutations in the genes ACTB or ACTG1. The classic presentation of BWCFF is discerned by the combination of unique crani

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7b5f152ccae9da0410fdbffcee90bc4b
https://doi.org/10.1002/ajmg.a.61725

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