Zobrazeno 1 - 10
of 275
pro vyhledávání: '"Yuying Jiang"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Hemoglobin (Hb) Lepore is a rare deletional δβ-thalassemia caused by the fusion between delta-beta genes, and cannot be identified by traditional thaltassemia gene testing technology. The aim of this study was to conduct molecular diagnosi
Externí odkaz:
https://doaj.org/article/cdf33d28c58940f4ae9513fdd204a17c
Autor:
Rui Gao, Guanghui Li, Pingxiang Liu, Lei Gao, Jingxiu Bi, Yuying Jiang, Honglei Liu, Yutao Wang
Publikováno v:
Food Science & Nutrition, Vol 12, Iss 4, Pp 2908-2916 (2024)
Abstract Asparagus, a vital economic contributor, is a well‐liked vegetable grown around the globe, and some secondary metabolites in its spear are beneficial to human health. Asparagus spears possess a significant quantity of nutrients and phytoch
Externí odkaz:
https://doaj.org/article/11575a0828284a9bafc0ae03f6c9388e
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Few existing reports have investigated the copy number variants (CNVs) in fetuses with central nervous system (CNS) anomalies. To gain further insights into the genotype–phenotype relationship, we conducted chromosomal microarray analysis
Externí odkaz:
https://doaj.org/article/c18921ddb65e4034ab4ecf1752332f22
Autor:
Chunmei Ma, Jiajia Huang, Yuying Jiang, Lu Liu, Na Wang, Shaoqiong Huang, Honghui Li, Xiangyu Zhang, Shuang Wen, Bingwei Wang, Shuo Yang
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 2, Pp 361-385 (2024)
Abstract Inflammation in the testes induced by infection and autoimmunity contributes significantly to male infertility, a public health issue. Current therapies using antibiotics and broad-spectrum anti-inflammatory drugs are ineffective against non
Externí odkaz:
https://doaj.org/article/2f913822d8e2453f8e7a5d4257329bcd
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 4, Pp n/a-n/a (2024)
Abstract Background Limited research has been conducted regarding the elucidation of genotype–phenotype correlations within the 20q13.33 region. The genotype–phenotype association of 20q13.33 microdeletion remains inadequately understood. In the
Externí odkaz:
https://doaj.org/article/ce51793ffaff4c2fb1e50ec987e5c2a9
Publikováno v:
Molecular Cytogenetics, Vol 16, Iss 1, Pp 1-6 (2023)
Abstract Background Isolated terminal 4q35.2 microdeletion is an extremely rare copy number variant affecting people all over the world. To date, researchers still have controversial opinions and results on its pathogenicity. Here, we aim to present
Externí odkaz:
https://doaj.org/article/211f274424fa4140b4c7a7e7e172c5c2
Autor:
Yuying Jiang, Xiaorong Bao
Publikováno v:
PLoS ONE, Vol 19, Iss 4, p e0302073 (2024)
BackgroundThe purpose of this study was to look at the relationship between the Systemic Immune Inflammatory Index (SII) and bone mineral density (BMD) in the pelvis, left upper and lower limbs, lumbar spine, thoracic spine, and trunk in a chronic ki
Externí odkaz:
https://doaj.org/article/0e4ec455da28472a9a7d3d8d270c9dba
Autor:
Yiling Jiao, Shuozhen Zhang, Haitao Jin, Yuwen Wang, Yamin Jia, Hua Zhang, Yuying Jiang, Wenqiang Liao, Li-Song Chen, Jiuxin Guo
Publikováno v:
Frontiers in Plant Science, Vol 14 (2023)
IntroductionCitrus fruit is considered a superfood due to its multiple nutritional functions and health benefits. Quantitative analysis of the numerous quality characteristics of citrus fruit is required to promote its sustainable production and indu
Externí odkaz:
https://doaj.org/article/6b6333ebd5374dbcbddcb37b0f4959e8
Publikováno v:
Applied Sciences, Vol 14, Iss 4, p 1398 (2024)
With the strengthening of worldwide counter-terrorism initiatives, it is increasingly important to detect contrabands such as controlled knives and flammable materials hidden in clothes and bags. Terahertz (THz) imaging technology is widely used in t
Externí odkaz:
https://doaj.org/article/7d3edcc7181649cb9ca6dbe9f2070a41
Autor:
Jianlong Zhuang, Shufen Liu, Junyu Wang, Yu'e Chen, Hegan Zhang, Yuying Jiang, Gaoxiong Wang, Chunnuan Chen
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 10, Pp n/a-n/a (2023)
Abstract Background Pathogenic mutations in EVC or EVC2 gene can lead to Ellis‐van Creveld (EvC) syndrome, which is a rare autosomal recessive skeletal dysplasia disorder. This study aimed to determine pathogenic gene variations associated with EvC
Externí odkaz:
https://doaj.org/article/a1d314ae38544097b1dc78ac76fa0c6d