Zobrazeno 1 - 10
of 396
pro vyhledávání: '"Causative gene"'
Autor:
Hao Zheng, San-ya Xiong, Shi-jun Xiao, Ze-kai Zhang, Jin-min Tu, Deng-shuai Cui, Nai-biao Yu, Zhi-yong Huang, Long-yun Li, Yuan-mei Guo
Publikováno v:
BMC Genomic Data, Vol 24, Iss 1, Pp 1-10 (2023)
Abstract Background Coat color, as a distinct phenotypic characteristic of pigs, is often subject to preference and selection, such as in the breeding process of new breed. Shanxia long black pig was derived from an intercross between Berkshire boars
Externí odkaz:
https://doaj.org/article/932811b8255b4dafa91b25c575442485
Akademický článek
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Autor:
Duan, Ran a, c, #, Li, Hong-Ming b, c, #, Hu, Wen-Bao f, Hong, Chun-Gu c, Chen, Meng-Lu a, c, Cao, Jia c, Wang, Zhen-Xing c, Chen, Chun-Yuan a, c, Yin, Fei i, Hu, Zhong-Hua f, Li, Jia-Da g, Xie, Hui a, b, c, d, e, h, ⁎, Liu, Zheng-Zhao a, b, c, d, ⁎
Publikováno v:
In Progress in Neurobiology September 2022 216
Autor:
Tsunenori Saito, Naoko Saito Sato, Kosuke Mozawa, Akiko Adachi, Yoshihiro Sasaki, Kotoka Nakamura, Eiichiro Oka, Toshiaki Otsuka, Eitaro Kodani, Kuniya Asai, Kyoichi Mizuno, Wataru Shimizu, Roberta A. Gottlieb
Publikováno v:
ESC Heart Failure, Vol 8, Iss 6, Pp 5178-5191 (2021)
Abstract Aims The aim of the present study was to consider whether the ultrastructural features of cardiomyocytes in dilated cardiomyopathy can be used to guide genetic testing. Methods and results Endomyocardial biopsy and whole‐exome sequencing w
Externí odkaz:
https://doaj.org/article/2bae72efb5c54cd899bb402878691bd3
Autor:
Cheng, Hao-Ling a, b, 1, Dong, Hai-Lin a, 1, Liu, De-Shan a, Ni, Wang a, Ma, Yin a, Yang, Lu a, Du, Yi-Chu a, Chen, Dian-Fu a, Dong, Yi a, ⁎, Wu, Zhi-Ying a, ⁎
Publikováno v:
In Gene 5 May 2021 779
Autor:
Dai, Can 1, Hu, Liang 1, 2, 3, 4, Gong, Fei 1, 2, 3, Tan, Yueqiu 1, 2, 3, Cai, Sufen 1, 2, Zhang, Shuoping 1, 2, Dai, Jing 1, 2, Lu, Changfu 1, 2, 3, Chen, Jing 2, Chen, Yongzhe 2, Lu, Guangxiu 1, 3, 4, Du, Juan 1, 2, 3, Lin, Ge 1, 2, 3, 4
Publikováno v:
In Genetics in Medicine February 2019 21(2):431-440
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Bone mineral density (BMD) is a complex and highly hereditary trait that can lead to osteoporotic fractures. It is estimated that BMD is mainly affected by genetic factors (about 85%). BMD has been reported to be associated with both common and rare
Externí odkaz:
https://doaj.org/article/cbe38c7ced9f44a8be03b0c2ab1e31e3
Autor:
Vandersmissen, I. a, Biancalana, V. b, c, d, e, f, Servais, L. g, j, Dowling, J.J. h, Vander Stichele, G. a, Van Rooijen, S. i, Thielemans, L. i, ⁎
Publikováno v:
In Neuromuscular Disorders September 2018 28(9):766-777
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
Cardiomyopathies are a highly heterogeneous group of heart muscle disorders. More than 100 causative genes have been linked to various cardiomyopathies, which explain about half of familial cardiomyopathy cases. More than a dozen candidate therapeuti
Externí odkaz:
https://doaj.org/article/deafcd06f7f348f98f2691da45b3cbaa
Autor:
Giuseppe Crisafulli, Tommaso Aversa, Giuseppina Zirilli, Filippo De Luca, Romina Gallizzi, Malgorzata Wasniewska
Publikováno v:
Italian Journal of Pediatrics, Vol 44, Iss 1, Pp 1-4 (2018)
Abstract Aim of this commentary is to analyze the relationships between genotypic bases and phenotypic expression of congenital “multiple pituitary hormone deficiency” (MPHD) syndrome and to indicate some reliable criteria for selecting the patie
Externí odkaz:
https://doaj.org/article/17493d9bd814427091be4093f2875848