Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Xu-Yang Liu"'
Autor:
Xiao-qian SHA, Hong-hui GUAN, Yu-qian ZHOU, Er-hu SU, Jian GUO, Yong-xiang LI, Deng-feng ZHANG, Xu-yang LIU, Guan-hua HE, Yu LI, Tian-yu WANG, Hua-wen ZOU, Chun-hui LI
Publikováno v:
Journal of Integrative Agriculture, Vol 22, Iss 11, Pp 3394-3407 (2023)
The crown root system is the most important root component in maize at both the vegetative and reproductive stages. However, the genetic basis of maize crown root traits (CRT) is still unclear, and the relationship between CRT and aboveground agronom
Externí odkaz:
https://doaj.org/article/5b5005c173124521b6e0631c252394ad
Publikováno v:
Guoji Yanke Zazhi, Vol 23, Iss 11, Pp 1930-1934 (2023)
AIM: To investigate the clinical features and genetic background of autosomal recessive Wolfram syndrome caused by WFS1 gene mutation.METHODS: A pedigree with autosomal recessive Wolfram syndrome was studied by clinical examination, gene analysis and
Externí odkaz:
https://doaj.org/article/b63f8a17a25c4e1a8397e8459297e5f9
Autor:
Jun-Kai Tan, Ying Xiao, Guo Liu, Long-Xiang Huang, Wen-Hao Ma, Yan Xia, Xi-Zhen Wang, Xian-Jun Zhu, Su-Ping Cai, Xiao-Bing Wu, Yun Wang, Xu-Yang Liu
Publikováno v:
International Journal of Ophthalmology, Vol 16, Iss 8, Pp 1196-1209 (2023)
AIM: To evaluate the potential of two trabecular meshwork (TM)-specific promoters, Chitinase 3-like 1 (Ch3L1) and matrix gla protein (MGP), for improving specificity and safety in glaucoma gene therapy based on self-complementary AAV2 (scAAV2) vector
Externí odkaz:
https://doaj.org/article/8772af439d924f33b47576524ad993af
Publikováno v:
International Journal of Ophthalmology, Vol 16, Iss 5, Pp 694-699 (2023)
AIM: To explore the phenotype and genotype of Weill-Marchesani syndrome (WMS) in a Chinese family and review related literature. METHODS: Three WMS patients and other unaffected individuals in this family with a history of consanguineous marriage wer
Externí odkaz:
https://doaj.org/article/8937dd5885874c8f8cc23b6fe814566c
Autor:
Su-Ping Cai, Lan Lu, Xi-Zhen Wang, Yun Wang, Fen He, Ning Fan, Jing-Ning Weng, Jun-Hua Zhang, Xu-Yang Liu
Publikováno v:
International Journal of Ophthalmology, Vol 14, Iss 6, Pp 800-804 (2021)
AIM: To investigate the causal gene mutation and clinical characteristics for two Chinese families with autosomal dominant congenital coralliform cataract. METHODS: Two Chinese pedigrees with congenital cataract were investigated. Routine ophthalmic
Externí odkaz:
https://doaj.org/article/f332b8c733884a41bb7059ddd2d2f521
Autor:
Lu-yang HAO, Xu-yang LIU, Xiao-jing ZHANG, Bao-cheng SUN, Cheng LIU, Deng-feng ZHANG, Huai-jun TANG, Chun-hui LI, Yong-xiang LI, Yun-su SHI, Xiao-qing XIE, Yan-chun SONG, Tian-yu WANG, Yu LI
Publikováno v:
Journal of Integrative Agriculture, Vol 19, Iss 2, Pp 449-464 (2020)
Drought is one of the most important abiotic stresses affecting maize growth and development and therefore resulting in yield loss. Thus it is essential to understand molecular mechanisms of drought stress responses in maize for drought tolerance imp
Externí odkaz:
https://doaj.org/article/8cb9f98761d24b8bb952bdc6e68f4d45
Autor:
Deng-feng ZHANG, Ting-ru ZENG, Xu-yang LIU, Chen-xi GAO, Yong-xiang LI, Chun-hui LI, Yan-chun SONG, Yun-su SHI, Tian-yu WANG, Yu LI
Publikováno v:
Journal of Integrative Agriculture, Vol 18, Iss 9, Pp 1980-1995 (2019)
Drought stress affects the growth and productivity of crop plants including sorghum. To study the molecular basis of drought tolerance in sorghum, we conducted the transcriptomic profiling of sorghum leaves and roots under drought stress using RNA-Se
Externí odkaz:
https://doaj.org/article/e546f2b3444b47fcb9a84bb010d37eba
Publikováno v:
Guoji Yanke Zazhi, Vol 17, Iss 8, Pp 1461-1464 (2017)
Avellino corneal dystrophy(ACD)is an autosomal dominant eye disorder caused by mutation of R124H in the transforming growth factor-beta induced gene(TGFBI)on chromosome 5, which was responsible for accumulating of abnormal TGFBI. Although the underly
Externí odkaz:
https://doaj.org/article/6e8f650a762b4f088abffac0a2d56d6c
Publikováno v:
Guoji Yanke Zazhi, Vol 15, Iss 8, Pp 1375-1377 (2015)
AIM: To study a large glaucoma family by screening the disease-causing genes in order to understand the pathogenesis mechanism of glaucoma.METHODS: The diagnosis of glaucoma family was made by ophthalmological examination; peripheral blood was collec
Externí odkaz:
https://doaj.org/article/f70639fcf4bf478fa317a0a438820b06
Autor:
Su-Ping Cai, Wen-Han Yu, Yun Wang, Hong-Bo Cheng, Xiao-Hong Li, Ning Fan, Yan Yin, Xiao-Min Zhou, Xu-Yang Liu
Publikováno v:
International Journal of Ophthalmology, Vol 6, Iss 3, Pp 264-268 (2013)
AIM: To detect the mutations in two candidate genes, myocilin (MYOC) and cytochrome P450 1B1 (CYP1B1), in a Chinese family with primary open angle glaucoma (POAG).METHODS: The family was composed of three members, the parents and a daughter. All memb
Externí odkaz:
https://doaj.org/article/490fca243e1040fc827fb187b0d16cd4