Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Linjie, Pu"'
Publikováno v:
SAGE Open, Vol 14 (2024)
Previous studies suggest that learning experience influences students’ academic engagement and self-efficacy mediates the association between them, and the sub-types of self-efficacy are distinct and play different roles. However, the different rol
Externí odkaz:
https://doaj.org/article/b40953d8740447e7888680dbe42f3949
Publikováno v:
SAGE Open, Vol 14 (2024)
Previous research has indicated that students’ academic engagement is related to their emotional support from teachers. However, there is scarce evidence on how teacher emotional support relates to students’ academic engagement. Given the potenti
Externí odkaz:
https://doaj.org/article/bdf619f3877f4c4b9ba38d55c55d20f5
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Background Variants in the DEPDC5 have been proved to be main cause of not only various dominant familial focal epilepsies, but also sporadic focal epilepsies. In the present study, a novel variant in DEPDC5 was detected in the patient with
Externí odkaz:
https://doaj.org/article/e6660956ec24496f986017119887fa9e
Autor:
Yan Liu, Liang Dong, Xiufang Zhi, Yang Liu, Linsheng Zhao, Xiaowei Xu, Lu Wang, Jie Zheng, Linjie Pu, Chunyu Gu, Jianbo Shu, Chunquan Cai
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 1, Pp n/a-n/a (2023)
Abstract Background To screen the single nucleotide polymorphisms (SNPs) in the coding regions of VANGL and FZD family members related to the plane cell polarity (PCP) signaling pathway in neural tube defects (NTDs) patients, so as to provide theoret
Externí odkaz:
https://doaj.org/article/43fdc44bfdfd48658c413f6a54420ef6
Autor:
Xiaofang Chen, Jia Fu, Ying Qian, Xiufang Zhi, Linjie Pu, Chunyu Gu, Jianbo Shu, Ling Lv, Chunquan Cai
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Low vitamin D levels may play a role in type 1 diabetes (T1D) susceptibility. Since 25(OH)D synthesis is genetically regulated, single nucleotide polymorphisms (SNPs) of important genes have also been shown to modulate the risk of T1D, so this study
Externí odkaz:
https://doaj.org/article/9e9070d633f44b1283f66b066777f41d
Publikováno v:
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-6 (2020)
Abstract Background Spinal muscular atrophy (SMA) is an autosomal recessive hereditary disease associated with severe muscle atrophy and weakness in the limbs and trunk. The discovery of mutated genes is helpful in diagnosis and treatment for SMA. Me
Externí odkaz:
https://doaj.org/article/43135657b4674b8f86285a2633e747b9
Autor:
Yuping Yu, Jinyue Huang, Xiaofang Chen, Jia Fu, Xinhui Wang, Linjie Pu, Chunyu Gu, Chunquan Cai
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
ObjectiveAutism Spectrum Disorder is a neurodevelopmental disorder, with a rapid increase in recognition over the past decade. Interest in alternative therapies is growing annually, such as dietary therapies including gluten-free and/or casein-free d
Externí odkaz:
https://doaj.org/article/20122cd3cd484b5fa6e0da72f0f108a9
Autor:
Yan Liu, Liang Dong, Xiufang Zhi, Yang Liu, Linsheng Zhao, Xiaowei Xu, Lu Wang, Jie Zheng, Linjie Pu, Chunyu Gu, Jianbo Shu, Chunquan Cai
Publikováno v:
Molecular Genetics & Genomic Medicine. 11
To screen the single nucleotide polymorphisms (SNPs) in the coding regions of VANGL and FZD family members related to the plane cell polarity (PCP) signaling pathway in neural tube defects (NTDs) patients, so as to provide theoretical and experimenta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7955cc2dece729a39c16844b050615ea
https://doi.org/10.1002/mgg3.2094
https://doi.org/10.1002/mgg3.2094
Publikováno v:
Pediatric Surgery International. 38:169-181
Asymmetric conjoined twining (ACT) is a form of conjoined twining which is a rare malformation of monochorionic monoamniotic twin pregnancy. Most publications were single case reports. We reported a cohort of five cases with ACT from a single tertiar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd8b3d79741c81f171bc9ed3498f5a56
https://doi.org/10.1007/s00383-021-05006-w
https://doi.org/10.1007/s00383-021-05006-w
Autor:
Na Li, Linjie Pu, Jianbo Shu, Xiufang Zhi, Yulian Fang, Chunquan Cai, Jie Zheng, Chunyu Gu, Yang Liu
Publikováno v:
Neurological Sciences. 42:1827-1833
Spinal muscular atrophy (SMA) is a type of autosomal recessive genetic disease, which seriously threatens the health and lives of children and adolescents. We attempted to find some genes and mutations related to the onset of SMA. Eighty-three whole-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e320425f37524e00042d1ecead36aa7
https://doi.org/10.1007/s10072-020-04697-8
https://doi.org/10.1007/s10072-020-04697-8