全部文献期刊会议图书|学者科研项目
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作者:... Shu Chen , Qi Zhang , Baosheng Zhu
来源:[J].Journal of Genetics(IF 0.876), 2017, Vol.96 (4), pp.695-700
摘要:The mutations of androgen receptor ( AR ) gene are the most common cause for complete androgen insensitivity syndrome (CAIS). We aimed to characterize the six cases enrolled in our hospital (the First People’s Hospital of Yunnan, China) and explore the molecular mechanism of...
作者:... Chao Ding , Fangqing Yu , Baosheng Zhu
来源:[J].International Journal of Pediatric Otorhinolaryngology(IF 1.35), 2019, Vol.120, pp.166-172
摘要:Abstract(#br)Introduction(#br)MYO7A gene has been shown to be associated with Usher syndrome 1B and nonsyndromic deafness. Although a lot of mutations have been reported in MYO7A gene, novel MYO7A mutations are continuously to be identified.(#br)Methods(#br)Targeted next generati...
作者:Baosheng Zhu , Zhijian Mao
来源:[J].Biotechnology & Biotechnological Equipment(IF 0.622), 2019, Vol.33 (1), pp.988-999
摘要:To facilitate the construction of intact model of fractured bone and satisfy the representation of fracture information, a novel approach of constructing a restored model of fractured femur (RMFF) based on anatomic feature is put forward. First, the fracture mesh model is divided...
作者:... Hong Chen , Jie Su , Baosheng Zhu
来源:[J].Scientific Reports(IF 2.927), 2019, Vol.9 (1), pp.1-8
摘要:Abstract Abnormal haemoglobin (Hb) variants result in the most commonly inherited disorders in humans worldwide. In this study, we investigated the molecular epidemiology characteristics of Hb variants, along with associated structural and functional predictions in the Yunna...
作者:Baosheng Zhu , Hongguo Jiang ...
来源:[J].PLoS ONE(IF 3.73), 2017, Vol.11 (11)
摘要:To evaluate the association of the TP53 codon 72 (rs 1042522) alone or in combination with HDM2 SNP309 (rs 2279744) polymorphisms with human infertility and IVF outcome, we collected 1450 infertility women undergoing their first controlled ovarian stimulation for IVF treatment an...
作者:Baosheng Zhu , Jie Su ...
来源:[J].International Journal of Pediatric Otorhinolaryngology(IF 1.35), 2016, Vol.91, pp.1-5
摘要:Abstract(#br)Large vestibular aqueduct syndrome (LVAS) is a type of hearing loss characterized by an autosomal recessive inheritance. LVAS has been shown to be associated with mutations in SLC26A4 gene. In the present study, we report the clinical, genetic and molecular character...
作者:Baosheng Zhu , Hua Wang ...
来源:[J].Taiwanese Journal of Obstetrics & Gynecology(IF 1.418), 2016, Vol.55 (3), pp.379-384
摘要:Abstract(#br)Objective(#br)This study aimed to determine the rates of different fetal chromosomal abnormalities among women of advanced maternal age in China and to discuss the possible misdiagnosis risks of newer molecular techniques, for selection of appropriate prenatal s...
作者:Baosheng Zhu , Zhijian Mao
来源:[J].Biotechnology & Biotechnological Equipment(IF 0.622), 2019, Vol.33 (1), pp.988-999
摘要:Abstract(#br)To facilitate the construction of intact model of fractured bone and satisfy the representation of fracture information, a novel approach of constructing a restored model of fractured femur (RMFF) based on anatomic feature is put forward. First, the fracture mesh mod...
作者:... Jian Pu , Chanchan Jin , Baosheng Zhu
来源:[J].Hematology(IF 1.393), 2016, Vol.21 (1), pp.54-59
摘要:Objective(#br): The aim of this study was to investigate the prevalence of hemoglobin E (Hb E) as well as the hematological and the phenotypic features of Hb E-related disorders in Yunnan Province of Southwest China.(#br)Methods(#br): A total of 30 908 individuals from more ...

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