Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mianmian Zhu"'
Autor:
Yujing Gong, Weijian Zhu, Mianmian Zhu, Dan Chen, Sunke Wu, Sisi Hu, Yi Luo, Yiyi Jiang, Ting Zhu, Dan Wang
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
BackgroundStickler syndrome type I (STL1) is an autosomal dominant disorder characterized by ocular, auditory, orofacial, and skeletal anomalies. The main causes of STL1 are variants in the COL2A1 gene, which encodes a type II collagen precursor prot
Externí odkaz:
https://doaj.org/article/63e3e3f513d44b9d9db7c02a73571eca
Publikováno v:
Frontiers in Bioengineering and Biotechnology, Vol 9 (2021)
Microalgal heterotrophic cultivation is an emerging technology that can enable producing high cell-density algal cell cultures, which can be coupled with photoautotrophic cultivation for valuable chemicals such as lipids manufacturing. However, how t
Externí odkaz:
https://doaj.org/article/a8ff1a607de54ccc90a9c7d953e07d3b
Autor:
Ting Zhu, Lijie Guan, Yi Luo, Mianmian Zhu, Rongyue Sun, Jiamin Shi, Qiu Wang, Yuan Chen, Yihong Wang, Hongwei Wang, Zhongqiu Lu, Dan Wang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f48adb0a3881ad31dd305171c2b35fdb
https://doi.org/10.2139/ssrn.4356060
https://doi.org/10.2139/ssrn.4356060
Autor:
Miaohua Ruan, Hongwei Wang, Mianmian Zhu, Rongyue Sun, Jiamin Shi, Qiu Wang, Yuan Chen, Yihong Wang, Dan Wang
Publikováno v:
Journal of Clinical Laboratory Analysis. 36
CWF19L1 is responsible for spinocerebellar ataxia, autosomal recessive 17, which presents with cerebellar ataxia, and atrophy. Here, we report novel compound heterozygous variants of CWF19L1 in a Chinese family with progressive ataxia and mental reta
Autor:
Yuan, Chen, Jiamin, Shi, Xiaoxia, Huang, Anqun, Sheng, Chaosheng, Lu, Mianmian, Zhu, Qiu, Wang, Mingshan, Wang, Dan, Wang
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 39(11)
To explore the molecular pathogenesis of a Chinese pedigree affected with inherited protein C (PC) deficiency.The protein C activity (PC:A) and protein C antigen (PC:Ag) of the proband and his family members were determined by a chromogenic substrate
Autor:
Mianmian Zhu, Yihong Wang, Lijie Guan, Chaosheng Lu, Rongyue Sun, Yuan Chen, Jiamin Shi, Yanying Zhu, Dan Wang
Publikováno v:
Journal of Clinical Laboratory Analysis. 36
Terminal or interstitial deletion of chromosome 2q is rarely reported but clinically significant, which can result in developmental malformations and psychomotor retardation in humans. In the present study, we analyzed this deletion to comprehensivel
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 39(7)
To explore the genetic basis for a proband with Shprintzen-Goldberg syndrome (SGS).Whole exome sequencing was carried out to detect potential variants associated with the relevant phenotypes. Candidate variants were verified by Sanger sequencing of t
Publikováno v:
Forum Mathematicum. 33:743-755
In this paper, we construct a class of new modules for the quantum group U q ( s l 2 ) U_{q}(\mathfrak{sl}_{2}) which are free of rank 1 when restricted to C [ K ± 1 ] \mathbb{C}[K^{\pm 1}] . The irreducibility of these modules and submo
Autor:
Hailong Yan, Bahareh Nahidian, Qiang Hu, Yanhua Li, Danxiang Han, Liang Zhao, Mianmian Zhu, Juan Lin
Publikováno v:
Environmental microbiologyReferences. 23(9)
Fungi can parasitize microalgae, exerting profound impacts on both the aquatic ecosystems and microalgal mass cultures. In this study, the unicellular green alga Haematococcus pluvialis and the blastocladialean fungus Paraphysoderma sedebokerense wer