Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Jianqiang, Tan"'
Publikováno v:
Animals, Vol 13, Iss 18, p 2881 (2023)
This study investigated the effect of dietary protein levels on Litopenaeus vannamei. Five isolipid diets with protein levels of 32%, 36%, 40%, 44% and 48% were prepared using C. sorokiniana as the main protein source. L. vannamei (initial body weigh
Externí odkaz:
https://doaj.org/article/12243265651b4598923d8041211e3596
Autor:
Dejian Yuan, Tizhen Yan, Shiqiang Luo, Jun Huang, Jianqiang Tan, Jianping Zhang, Victor Wei Zhang, Yueyuan Lan, Taobo Hu, Jing Guo, Mingwei Huang, Dingyuan Zeng
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
ARR3 has been associated with X-linked, female-limited, high myopia. However, using exome sequencing (ES), we identified the first high myopia case with hemizygous ARR3-related mutation in a male patient in a Southern Chinese family. This novel trunc
Externí odkaz:
https://doaj.org/article/23c904e13f4e46448a4b1e2fb757cabd
Autor:
Jianqiang Tan, Dayu Chen, Rongni Chang, Lizhen Pan, Jinling Yang, Dejian Yuan, Lihua Huang, Tizhen Yan, Haiping Ning, Jiangyan Wei, Ren Cai
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Inborn errors of metabolism (IEMs) often causing progressive and irreversible neurological damage, physical and intellectual development lag or even death, and serious harm to the family and society. The screening of neonatal IEMs by tandem mass spec
Externí odkaz:
https://doaj.org/article/5a50ef295c5a44debd4713dc7e6eb224
Autor:
Yinhui Li, Jianqiang Tan, Kun Liang, Yong Li, Jiaojiao Sun, Hulin Zhang, Cuixian Luo, Pengwei Li, Jianle Xu, Huabei Jiang, Kaiying Wang
Publikováno v:
Journal of Materials Science: Materials in Electronics. 33:4291-4304
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f7fe519d3b2e20d752cdc2b72af8d19
https://doi.org/10.1007/s10854-021-07622-7
https://doi.org/10.1007/s10854-021-07622-7
Autor:
Jianqiang, Tan, Min, Zheng, Ren, Cai, Ting, Zeng, Biao, Yin, Jinling, Yang, Ba, Wei, Ronni, Chang, Yongjiang, Jiang, Dejian, Yuan, Lizhen, Pan, Lihua, Huang, Haiping, Ning, Jiangyan, Wei, Dayu, Chen
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 39(12)
To detect variants of IVD gene among 4 neonates with suspected isovalerate acidemia in order to provide a guidance for clinical treatment.111 986 newborns and 7461 hospitalized children with suspected metabolic disorders were screened for acyl carnit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::02f34cb41d825a12ba4ac0b27d445ca4
https://pubmed.ncbi.nlm.nih.gov/36453955
https://pubmed.ncbi.nlm.nih.gov/36453955
Autor:
Xuran Li, Yinhui Li, Yong Li, Jianqiang Tan, Jin Zhang, Hulin Zhang, Jianguo Liang, Tingyu Li, Yaodong Liu, Huabei Jiang, Pengwei Li
Publikováno v:
ACS applied materialsinterfaces. 14(41)
Self-powered wearable electronics to convert mechanical and thermal energy into electrical energy are important for biomedical monitoring, which highly require good flexibility, comfortability, signal sensitivity, and accuracy. In this work, composit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5f395ed91643ffa53ecd849872a7b0c
https://pubmed.ncbi.nlm.nih.gov/36194663
https://pubmed.ncbi.nlm.nih.gov/36194663
Autor:
Xinyang Zhang, Xinhu Yang, Zhanming Shi, Rui Xu, Jianqiang Tan, Jianwen Yang, Xiong Huang, Xingbing Huang, Wei Zheng
Publikováno v:
Journal of Personalized Medicine. 13:485
Objective: Neurocognitive dysfunction is thought to be one of the core clinical features of schizophrenia, and older adults with schizophrenia exhibited greater overall cognitive deficits than younger adults. The aim of this systematic review was to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4701b6972e37bf19e7c1b2016cb991de
https://doi.org/10.3390/jpm13030485
https://doi.org/10.3390/jpm13030485
Autor:
Jinling Yang, Dejian Yuan, Xiaohui Tan, Yexi Zeng, Ning Tang, Dayu Chen, Jianqiang Tan, Ren Cai, Jun Huang, Tizhen Yan
Publikováno v:
Molecular Medicine Reports
Mitochondrial trifunctional protein (MTP) deficiency (MTPD; MIM 609015) is a metabolic disease of fatty acid oxidation. MTPD is an autosomal recessive disorder caused by mutations in the HADHA gene, encoding the α-subunit of a trifunctional protease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d1771b945840137f59940e4f19cebd3
http://europepmc.org/articles/PMC8674702
http://europepmc.org/articles/PMC8674702
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 37(1)
To identify potential variant in a child diagnosed as infantile neuroaxonal dystrophy.Genomic DNA was extracted from peripheral blood samples from the patient and his parents and subjected to next generation sequencing. Suspected variant was verified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aedbe5d8dd1e1faf0e09089efe6c86b8
https://pubmed.ncbi.nlm.nih.gov/31922589
https://pubmed.ncbi.nlm.nih.gov/31922589
Autor:
Jianqiang, Tan, Lizhen, Pan, Jun, Huang, Wugao, Li, Zhetao, Li, Rongni, Chang, Jingwen, Li, Tizhen, Yan, Jiwei, Huang, Dejian, Yuan, Ren, Cai
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 36(12)
To analyze variations of TYR and P genes among 14 patients with clinically diagnosed oculocutaneous albinism.Potential variations of the TYR and P genes were detected by Sanger sequencing. Novel variations were predicted with bioinformatics software
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5408f1b968e3556eccef94c123647f6d
https://pubmed.ncbi.nlm.nih.gov/31813138
https://pubmed.ncbi.nlm.nih.gov/31813138