Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Haixia Miao"'
Autor:
Ting Zhang, Shasha Zhu, Haixia Miao, Jianbin Yang, Yezhen Shi, Yuwei Yue, Yu Zhang, Rulai Yang, Benqing Wu, Xinwen Huang
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2022)
Introduction: Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) is a pan-ethnic complicated inborn error of metabolism but the specific mechanism is not fully understood.Methods: A total of 169 patients with NICCD who have biallel
Externí odkaz:
https://doaj.org/article/41db918405e2496cb499eeb0cf52e4d5
Autor:
Duo Zhou, Yi Cheng, Xiaoshan Yin, Haixia Miao, Zhenzhen Hu, Jianbin Yang, Yu Zhang, Benqing Wu, Xinwen Huang
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Disorders of mitochondrial carnitine–acylcarnitine cycle is a heterogeneous group of hereditary diseases of mitochondrial β-oxidation of fatty acids tested in NBS program in Zhejiang province, China. Large-scale studies reporting disor
Externí odkaz:
https://doaj.org/article/bf7b1dcd87214c73b32aa898d07e73a6
Publikováno v:
Journal of Stomatology, Oral and Maxillofacial Surgery. 123:663-665
Autor:
Yu Zhang, Haixia Miao, Rulai Yang, Dingwen Wu, Rongqing Chen, Ting Zhang, Kexin Fang, Yezhen Shi, Xinwen Huang
Publikováno v:
Zhejiang Da Xue Xue Bao Yi Xue Ban
OBJECTIVE: To evaluate the performance of genetic screening processor (GSP analyzer) in neonatal screening for glucose-6-phosphate dehydrogenase (G6PD)deficiency. METHODS: The accuracy and precision of GSP analyzer was evaluated with the control mate
Publikováno v:
Journal of Biomaterials and Tissue Engineering. 11:937-942
Alveolar bone-derived mesenchymal stem cells (AB-BMSCs) have a biological morphology and antigen phenotype similar to those of BMSCs. However, the intrinsic characteristics of AB-BMSCs and their underlying mechanisms, in which the involvement of micr
Autor:
Yiming Lin, Xiaochun Zhu, Chao Zhang, Xiaoshan Yin, Haixia Miao, Zhenzhen Hu, Jianbin Yang, Benqing Wu, Xinwen Huang
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 530
Glutaric acidemia type 1 (GA1) is a treatable neurometabolic disorder caused by biallelic variants in the glutaryl-CoA dehydrogenase (GCDH) gene. There are few large-scale reports describing newborn screening (NBS) for GA1 in China. We report the NBS
Publikováno v:
Clinica Chimica Acta. 542:117266
Publikováno v:
Journal of Biomaterials and Tissue Engineering. 8:391-396
Publikováno v:
Catalysis Communications. 78:68-70
A microspherical mesostructured zeolite (MMZ-5) with MFI-topological frameworks is employed. In-situ FT-IR spectra of pyridine and 2, 6-di-tert-butylpyridine have indicated that almost all of the acid sites are located on the zeolitic external surfac
Publikováno v:
Journal of Alloys and Compounds. 613:18-24
It is a generally accepted method to synthesize the monodisperse NaYF4:Yb3+, Er3+ with uniform size and shape by using oleic acid (OA) as surfactant or solvent. However, the obtained oleate-capped up-conversion nanoparticles NaYF4:Yb3+, Er3+ (Ln-UCNP