Zobrazeno 1 - 10
of 184
pro vyhledávání: '"Xinting Liu"'
Autor:
Jing Zhang, Gang Zhu, Yan Liang, Lin Wan, Xinting Liu, Huimin Yan, Guoyin Liu, Bo Zhang, Guang Yang
Publikováno v:
Pediatric Investigation, Vol 8, Iss 3, Pp 171-176 (2024)
Externí odkaz:
https://doaj.org/article/983354af6d0641a09da9468538edf4b1
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract To evaluate the repeatability of a novel automated technique called Smart ERA (Smart Endometrial Receptivity Analysis) for the automated segmentation and volume calculation of the endometrium in patients with normal uteri,, and to compare th
Externí odkaz:
https://doaj.org/article/b360dc66da564b97a410d79837be4504
Autor:
Xinting Liu, Danyang Zou, Yizhu Wang, Yutong Zhuang, Yang Liu, Yanyu Li, Zhenzhu Sun, Chaoxia Ye
Publikováno v:
Animal Nutrition, Vol 17, Iss , Pp 447-462 (2024)
This study aimed to investigate the application of cottonseed protein concentrate (CPC) in Chinese mitten crabs (Eriocheir sinensis). First, the apparent digestibility coefficient (ADC) of CPC, fish meal and soybean meal were compared in crabs (21.72
Externí odkaz:
https://doaj.org/article/e12829b5da964ceca077e78d8b0b1b73
Autor:
Lin Wan, Huan Wang, Yan Liang, Xun Zhang, Xinyun Yao, Gang Zhu, Jun Cai, Guoyin Liu, Xinting Liu, Qianqian Niu, Siwen Li, Bo Zhang, Jing Gao, Jing Wang, Xiuyu Shi, Linyan Hu, Xiaoyan Liu, Zhiyong Zou, Guang Yang
Publikováno v:
Clinical and Translational Medicine, Vol 14, Iss 9, Pp n/a-n/a (2024)
Externí odkaz:
https://doaj.org/article/211f2b88562842bcb1c0681ef810bbe3
Publikováno v:
iEnergy, Vol 2, Iss 4, Pp 314-322 (2023)
Electric field measurement holds immense significance in various domains. The power supply and signal acquisition units of the sensor may be coupled with ground wire interference, which could result in reduced measurement accuracy. Moreover, this pro
Externí odkaz:
https://doaj.org/article/6ef8538990ee4572b6ba3235db0d6033
Publikováno v:
Brain and Behavior, Vol 14, Iss 5, Pp n/a-n/a (2024)
Abstract Background Several biallelic truncating and missense variants of the gem nuclear organelle–associated protein 5 (GEMIN5) gene have been reported to cause neurodevelopmental disorders characterized by cerebellar atrophy, intellectual disabi
Externí odkaz:
https://doaj.org/article/5c14682b5e004721b44781e419b2c3bb
Autor:
Jiefang Wang, Xinting Liu, Jing Huang, Ruoyun Deng, Sijun Zhao, Yulei Chen, Zhaohe Chen, Yanli Wang, Yu Rong, Qian Liu, Jia Qu, Xinjie Mao
Publikováno v:
Frontiers in Neuroscience, Vol 18 (2024)
PurposeTo investigate the contrast sensitivity function (CSF) changes in simple high myopia (SHM) and evaluate the correlations between these changes with the early changes in the retinal microstructure.MethodsThis prospective study comprised 81 subj
Externí odkaz:
https://doaj.org/article/29ccefcff255451bb15c39f96bdbea99
Autor:
Lin Wan, Dan Yu, Zhichao Li, Xinting Liu, Yan Liang, Huimin Yan, Gang Zhu, Bo Zhang, Guang Yang
Publikováno v:
Epilepsia Open, Vol 8, Iss 3, Pp 867-876 (2023)
Abstract Objective Biallelic variants of RARS1, a gene that encodes the cytoplasmic tRNA synthetase for arginine (ArgRS), are associated with central nervous system (CNS) manifestations, such as hypomyelinating leukodystrophy‐9 and developmental an
Externí odkaz:
https://doaj.org/article/819c303f24a841f5b0b9f3f8cd0d91c1
Publikováno v:
Frontiers in Neurology, Vol 14 (2024)
ObjectiveTo the literature, variants in the ATP6AP2 gene may cause abnormal nervous system development and associated neurological symptoms.MethodsWe report a patient with developmental and epileptic encephalopathy (DEE) carrying an ATP6AP2 c.858G >
Externí odkaz:
https://doaj.org/article/65a13c522a774adabccce43ee60cc55f
Autor:
Xinting Liu, Chen Chen, Lin Wan, Gang Zhu, Yan Zhao, Lizhu Hu, Yan Liang, Jing Gao, Jing Wang, Guang Yang
Publikováno v:
Brain and Behavior, Vol 13, Iss 12, Pp n/a-n/a (2023)
Abstract Introduction Sotos syndrome (SS) is an overgrowth disease characterized by distinctive facial features, advanced bone age, macrocephaly, and developmental delay is associated with alterations in the NSD1 gene. Here, we report a case of a 4
Externí odkaz:
https://doaj.org/article/427b802c2acc486fb19db3b6e9245530