Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Jia-Yu Shi"'
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-18 (2024)
Abstract Background Zingiber officinale Roscoe, colloquially known as ginger, is a crop of significant medicinal and culinary value that frequently encounters adversity stemming from inhospitable environmental conditions. The MYB transcription factor
Externí odkaz:
https://doaj.org/article/cc45805aaeb54067a6cdfec4fe443b1f
Autor:
Yong Li, Chao Wang, Zheng-Wei He, Awang Danzeng, Fu-Bin Liu, Jia-Yu Shi, Pingcuo Ciren, Xiao-Yin Yuan, Cheng-Xian Wu, Run-hu Lan, Bin-Hao Zhang
Publikováno v:
BMJ Open, Vol 13, Iss 9 (2023)
Objectives This meta-analysis aims to evaluate the effect of n-3 polyunsaturated fatty acids (PUFAs) as a part of parenteral nutrition in patients undergoing liver surgery.Design Systematic review and meta-analysis.Data sources PubMed, the Cochrane C
Externí odkaz:
https://doaj.org/article/912c091f852e41c1b1823f3e37ddd36c
Autor:
Xiao-hang Liu, Jia-yu Shi, Ding-ding Zhang, Fu-wei Jia, Xue Lin, Yan-lin Zhu, Jun-ling Zhuang, Li-gang Fang, Wei Chen
Publikováno v:
BMC Cardiovascular Disorders, Vol 22, Iss 1, Pp 1-11 (2022)
Abstract Background Light-chain amyloidosis is a plasma cell disorder associated with poor outcomes, especially when the heart is involved. The characteristics of left atrial (LA) function and its prognostic implications in cardiac amyloidosis (CA) h
Externí odkaz:
https://doaj.org/article/c22c6e6ab7764c63afe1c9bfe352f3dc
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Rs560426 at 1p22 was proved to be associated with NSCL/P (non-syndromic cleft lip with or without the palate) in several populations, including Han Chinese population. Here, we conducted a deep sequencing around rs560426 to locate more susceptibility
Externí odkaz:
https://doaj.org/article/97c64797560a468bb23744105266a35b
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
rs7590268 present on the 2p21 locus was identified to be associated with non-syndromic cleft lip with or without cleft palate (NSCL/P) in several populations, including the Chinese Han population, indicating that 2p21 was a susceptibility locus for N
Externí odkaz:
https://doaj.org/article/d5e31f33991f4586bd568eeb4c2fb0c0
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 19, Iss 6, Pp 452-457 (2019)
DOI: 10.3969/j.issn.1672-6731.2019.06.014
Externí odkaz:
https://doaj.org/article/3f67badea84748868ac0c17d9e0577fd
Autor:
Marco Rossi, Ghada Badawy, Zhi‐Yuan Zhang, Guang Yang, Guo‐An Li, Jia‐Yu Shi, Roy L. M. Op het Veld, Sasa Gazibegovic, Lu Li, Jie Shen, Marcel A. Verheijen, Erik P. A. M. Bakkers
Publikováno v:
Advanced Functional Materials, 33(17):2212029. Wiley-VCH Verlag
Indium Antimonide (InSb) is a semiconductor material with unique properties, that are suitable for studying new quantum phenomena in hybrid semiconductor-superconductor devices. The realization of such devices with defect-free InSb thin films is chal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9885e7a39b3207b353cef941a42100e
https://research.tue.nl/nl/publications/99d9f92a-7b03-4468-b99e-a545e3e75cf4
https://research.tue.nl/nl/publications/99d9f92a-7b03-4468-b99e-a545e3e75cf4
Autor:
Bin, Yin, Yu-Ya, Pang, Jia-Yu, Shi, Yan-Song, Lin, Jia-Lin, Sun, Qian, Zheng, Bing, Shi, Zhong-Lin, Jia
Publikováno v:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.
The purpose of this study is to analyze the clinical characteristics of a Treacher Collins syndrome (TCS) patient carrying a de novo variant ofA Chinese pedigree with TCS containing 8 members was enrolled. Phenotype of the proband was evaluated by a
Publikováno v:
Cardiovascular Toxicology. 21:759-771
Pathological cardiac hypertrophy is the leading cause of heart failure, and miRNAs have been recognized as key factors in cardiac hypertrophy. This study aimed to elucidate whether miR-17-5p affects cardiac hypertrophy by targeting the mitochondrial
Publikováno v:
The Cleft Palate Craniofacial Journal. :105566562311575
The purpose of this study is to analyze the clinical characteristics of patients with Van der Woude syndrome (VWS) and to detect variations in each patient. Finally, the combination of genotype and phenotype can make a clear diagnosis of VWS patients