Literature DB >> 27261779

Short-term serum deprivation causes no significant mitochondrial DNA mutation in vascular smooth muscle cells revealed by a new next generation sequencing technology.

Xiangqi Li1, Lianyong Liu2, Qian Xi3, Xuemei Zhao3, Mingshuang Fang3, Junhua Ma3, Zhaohui Zhu3, Xing Wang3, Chao Shi3, Jingnan Wang3, Hongling Zhu3, Jichen Zhang3, Chaobao Zhang4, Shuanggang Hu5, Minjie Ni4, Mingjun Gu1.   

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Year:  2016        PMID： 27261779     DOI： 10.1093/abbs/gmw059

Source DB:  PubMed          Journal:  Acta Biochim Biophys Sin (Shanghai)        ISSN： 1672-9145            Impact factor:   3.848


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  2 in total

1.  Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panel.

Authors:  Yu Dai; Chenghui Wang; Zhipeng Nie; Jiamin Han; Ting Chen; Xiaoxu Zhao; Cheng Ai; Yanchun Ji; Tao Gao; Pingping Jiang
Journal:  Biomed Rep       Date:  2017-11-08

2.  Next-generation sequencing identifies novel mitochondrial variants in pituitary adenomas.

Authors:  K Németh; O Darvasi; I Likó; N Szücs; S Czirják; L Reiniger; B Szabó; P A Kurucz; L Krokker; P Igaz; A Patócs; H Butz
Journal:  J Endocrinol Invest       Date:  2019-01-25       Impact factor: 4.256
  2 in total

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