Mei Li-Bin相关文献与解析，生知库 | 链接生命科学的每一步

Congenital Short-Bowel Syndrome Is Associated With a Novel Deletion Mutation in the CLMP Gene: Mutations in CLMP Caused CSBS

先天性短肠综合征与CLMP基因中的一种新型缺失突变相关：CLMP基因突变导致先天性短肠综合征

期刊:Frontiers in Pediatrics

影响因子:2

doi:10.3389/fped.2021.778859

Ou, Fen-Fen; Li, Ming-Jie; Mei, Li-Bin; Lin, Xin-Zhu; Wu, Yan-An

发表日期：2021

文献求助收藏

DEPDC5 Variants Associated Malformations of Cortical Development and Focal Epilepsy With Febrile Seizure Plus/Febrile Seizures: The Role of Molecular Sub-Regional Effect

DEPDC5变异与皮质发育畸形和伴有热性惊厥/热性惊厥的局灶性癫痫相关：分子亚区域效应的作用

期刊:Frontiers in Neuroscience

影响因子:3.2

doi:10.3389/fnins.2020.00821

Liu, Liu; Chen, Zi-Rong; Xu, Hai-Qing; Liu, De-Tian; Mao, Yong; Liu, Han-Kui; Liu, Xiao-Rong; Zhou, Peng; Lin, Si-Mei; Li, Bin; He, Na; Su, Tao; Zhai, Qiong-Xiang; Meng, Heng; Liao, Wei-Ping; Yi, Yong-Hong

Novel IFT140 variants cause spermatogenic dysfunction in humans.

新型 IFT140 变异体导致人类精子发生功能障碍

期刊:Molecular Genetics & Genomic Medicine

影响因子:1.6

doi:10.1002/mgg3.920

Wang Xiong, Sha Yan-Wei, Wang Wen-Ting, Cui Yuan-Qing, Chen Jie, Yan Wei, Hou Xiao-Tao, Mei Li-Bin, Yu Cui-Cui, Wang Jiahui

发育与干细胞

发表日期：2019

文献求助收藏

Globozoospermic infertility associated with balanced DPY19L2 translocation/gene deletion at the chromosomal breakpoint

与染色体断点处平衡的DPY19L2易位/基因缺失相关的圆头精子症不育

期刊:Asian Journal of Andrology

影响因子:2.7

doi:10.4103/1008-682X.196314

Sha, Yan-Wei; Mei, Li-Bin; Zheng, Liang-Kai; Tian, Rui-Hua; Ding, Lu; Ji, Zhi-Yong; Zhang, Qing; Li, Ping

发表日期：2018

文献求助收藏

Sperm-egg fusion disorder in a Chinese male patient was associated with a rare ADAM20 variant

中国一名男性患者的精卵融合障碍与一种罕见的ADAM20变异相关

期刊:Oncotarget

影响因子:

doi:10.18632/oncotarget.23331

Sha, Yan-Wei; Xu, Xiaohui; Ji, Zhi-Yong; Mei, Li-Bin; Qiu, Ping-Ping; Ji, Hong; Li, Ping; Li, Lin; Liu, Wei-Wu

Clinical and molecular characteristics of emerging hypervirulent Klebsiella pneumoniae bloodstream infections in mainland China

中国大陆新出现的高毒力肺炎克雷伯菌血流感染的临床和分子特征

期刊:Antimicrobial Agents and Chemotherapy

影响因子:4.5

doi:10.1128/AAC.02523-14

Liu, Ying Mei; Li, Bin Bin; Zhang, Yu Yu; Zhang, Wu; Shen, Hong; Li, Hui; Cao, Bin

Characterization of nucleosides and nucleobases in natural Cordyceps by HILIC-ESI/TOF/MS and HILIC-ESI/MS

通过 HILIC-ESI/TOF/MS 和 HILIC-ESI/MS 表征天然冬虫夏草中的核苷和核碱基

期刊:Molecules

影响因子:4.2

doi:10.3390/molecules18089755

Heng-Qiang Zhao, Xiao Wang, Hong-Mei Li, Bin Yang, Hong-Jun Yang, Luqi Huang

信号转导

发表日期：2013

文献求助收藏

SheepInst: A High-Performance Instance Segmentation of Sheep Images Based on Deep Learning

SheepInst：一种基于深度学习的高性能绵羊图像实例分割方法

Congenital Short-Bowel Syndrome Is Associated With a Novel Deletion Mutation in the CLMP Gene: Mutations in CLMP Caused CSBS

先天性短肠综合征与CLMP基因中的一种新型缺失突变相关：CLMP基因突变导致先天性短肠综合征

DEPDC5 Variants Associated Malformations of Cortical Development and Focal Epilepsy With Febrile Seizure Plus/Febrile Seizures: The Role of Molecular Sub-Regional Effect

DEPDC5变异与皮质发育畸形和伴有热性惊厥/热性惊厥的局灶性癫痫相关：分子亚区域效应的作用

Novel IFT140 variants cause spermatogenic dysfunction in humans.

新型 IFT140 变异体导致人类精子发生功能障碍

Globozoospermic infertility associated with balanced DPY19L2 translocation/gene deletion at the chromosomal breakpoint

与染色体断点处平衡的DPY19L2易位/基因缺失相关的圆头精子症不育

Sperm-egg fusion disorder in a Chinese male patient was associated with a rare ADAM20 variant

中国一名男性患者的精卵融合障碍与一种罕见的ADAM20变异相关

Clinical and molecular characteristics of emerging hypervirulent Klebsiella pneumoniae bloodstream infections in mainland China

中国大陆新出现的高毒力肺炎克雷伯菌血流感染的临床和分子特征

Characterization of nucleosides and nucleobases in natural Cordyceps by HILIC-ESI/TOF/MS and HILIC-ESI/MS

通过 HILIC-ESI/TOF/MS 和 HILIC-ESI/MS 表征天然冬虫夏草中的核苷和核碱基