Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Chiyan Zhou"'
Autor:
Huling Jiang, Zepeng Ping, Jianguo Wang, Xiaodan Liu, Yuxia Jin, Suping Li, Chiyan Zhou, Pinghua Huang, Yi Jin, Ling Ai, Jie Chen
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-4 (2021)
Abstract Background Molecular genetic testing for the 11p15-associated imprinting disorder Beckwith-Wiedemann syndrome (BWS) is challenging because of the molecular heterogeneity and complexity of the affected imprinted regions. An integrated molecul
Externí odkaz:
https://doaj.org/article/4007fde2d25f4241872ee3f3c37140c8
Autor:
Suping Li, Yuxia Jin, Jing Yang, Li Yang, Ping Tang, Chiyan Zhou, Liping Wu, Jinhua Dong, Jie Chen, Huaxiang Shen
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-6 (2020)
Abstract Background 22q11.2 deletion syndrome (22q11.2DS) and 22q11.2 duplication syndrome (22q11.2DupS) are the most common copy number variations in humans. The clinical phenotypes of these two syndromes are variable, and there are no large sample
Externí odkaz:
https://doaj.org/article/60c1ac97bf5c48788c3e82fd3cfffc7e
Publikováno v:
Agriculture, Vol 12, Iss 6, p 779 (2022)
The vascular bundle plays a vital role in photoassimilates transportation in rice. However, the vascular bundle characteristics of basal internode and its relationship with stem assimilates allocation and yield remain unclear. In this study, experime
Externí odkaz:
https://doaj.org/article/5f25facab6d64fd2b16376b4fcd5f3e2
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 40(1)
To explore the incidence of azoospermia factor c (AZFc) microdeletion among patients with azoospermia or severe oligospermia, its association with sex hormone/chromosomal karyotype, and its effect on the outcome of pregnancy following intracytoplasmi
Publikováno v:
Plantcell physiology. 63(7)
The grain filling of rice depends on photoassimilates from leaves and stems. Phloem loading is the first crucial step for the transportation of sucrose to grains. However, phloem loading mechanisms in rice leaves and stems and their response to nitro
Autor:
Ren Yan, Yingfeng Lu, Deyin Chen, Yida Yang, Jiajie Qian, Xiaoling Su, Lanjuan Li, Chiyan Zhou, Huan Cai, Jiangshan Lian, Jiong Yu
Publikováno v:
Journal of pharmaceutical and biomedical analysis. 206
Chronic hepatitis B (CHB) remains a major public health problem globally. HBeAg seroconversion is a vital hallmark for the improvement of CHB. The plasma metabolic profile has not been clear in CHB patients and searching metabolic candidates to repre
Autor:
Huling Jiang, Zepeng Ping, Jianguo Wang, Xiaodan Liu, Yuxia Jin, Suping Li, Chiyan Zhou, Pinghua Huang, Yi Jin, Ling Ai, Jie Chen
BackgroundMolecular genetic testing for the 11p15-associated imprinting disorder Beckwith-Wiedemann syndrome(BWS) is challenging because of the molecular heterogeneity and complexity of the affected imprinted regions. An accurate diagnosis of BWS req
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2692c52c74e4f9cf98c8c8dbd13166d
https://doi.org/10.21203/rs.3.rs-116725/v1
https://doi.org/10.21203/rs.3.rs-116725/v1
Autor:
Yi Jin, Suping Li, Xiaodan Liu, Yuxia Jin, Jie Chen, Jianguo Wang, Zepeng Ping, Pinghua Huang, Huling Jiang, Ling Ai, Chiyan Zhou
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-4 (2021)
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-4 (2021)
Background Molecular genetic testing for the 11p15-associated imprinting disorder Beckwith-Wiedemann syndrome (BWS) is challenging because of the molecular heterogeneity and complexity of the affected imprinted regions. An integrated molecular approa
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 37(10)
To assess the value of non-invasive prenatal testing (NIPT) for the screening of fetal chromosomal abnormalities.For 12 085 pregnant women, the results of NIPT and invasive prenatal diagnosis were compared.The test was successful in 12 067 cases and
Autor:
Li Yang, Jinhua Dong, Jing Yang, Suping Li, Yuxia Jin, Jie Chen, Chiyan Zhou, Ping Tang, Liping Wu, Huaxiang Shen
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-6 (2020)
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-6 (2020)
Background 22q11.2 deletion syndrome (22q11.2DS) and 22q11.2 duplication syndrome (22q11.2DupS) are the most common copy number variations in humans. The clinical phenotypes of these two syndromes are variable, and there are no large sample data on t