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首都師范大學(xué)李夏璐博士實(shí)驗(yàn)室2016年招收碩士調(diào)劑生

高校名稱 首都師范大學(xué) 所在省市 北京
調(diào)劑專業(yè) 生物化學(xué)和細(xì)胞生物學(xué) 是否有公費(fèi)名額 未知
發(fā)布時(shí)間 2016-03-20 截止時(shí)間 未注明

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首都師范大學(xué)李夏璐博士實(shí)驗(yàn)室招收碩士調(diào)劑生(若干):

1. 招生類型:2016年碩士調(diào)劑生,科研型

2. 招收學(xué)校(單位)名稱:首都師范大學(xué), 生命科學(xué)學(xué)院

3. 學(xué)制以及何種專業(yè):三年制碩士,生物化學(xué)和細(xì)胞生物學(xué)方向

4. 學(xué)校或單位地點(diǎn):北京市海淀區(qū)

5. 導(dǎo)師(課題組)介紹:李夏璐博士1995年畢業(yè)于復(fù)旦大學(xué)生物化學(xué)系,獲學(xué)士學(xué)位;2000年從中國(guó)科學(xué)院上海生物化學(xué)研究所獲博士學(xué)位;同年11月赴美工作,在哥倫比亞大學(xué)生物系從事5年博士后研究,2006年回國(guó)在北京生命科學(xué)研究所建立獨(dú)立研究團(tuán)隊(duì),2013年起受聘為首都師范大學(xué)生命科學(xué)學(xué)院特聘教授。李博士長(zhǎng)期開(kāi)展生物化學(xué)和細(xì)胞生物學(xué)研究,相應(yīng)研究工作已在Cell、Genes & Development和PNAS等國(guó)際一流學(xué)術(shù)期刊上發(fā)表,多項(xiàng)研究成果被Faculty 1000 of Biology推薦。曾主持完成國(guó)家高技術(shù)研究發(fā)展計(jì)劃(863)和國(guó)家重點(diǎn)基礎(chǔ)研究發(fā)展計(jì)劃(973)課題各一項(xiàng)。目前在研國(guó)家自然科學(xué)基金委面上項(xiàng)目和國(guó)家重大研究計(jì)劃(973課題負(fù)責(zé)人)資助各一項(xiàng)。實(shí)驗(yàn)室主要研究興趣在于運(yùn)用遺傳學(xué),分子生物學(xué),生物化學(xué)和生物信息學(xué)等方法,理解哺乳動(dòng)物細(xì)胞是如何應(yīng)對(duì)在生長(zhǎng)和增殖過(guò)程中必然會(huì)面對(duì)的RNA轉(zhuǎn)錄、DNA復(fù)制和基因組穩(wěn)定性維護(hù)三者間的沖突;并探索這一沖突形成后可能產(chǎn)生的病理后果。希望實(shí)驗(yàn)室研究工作有助于加深對(duì)于腫瘤等重大疾病發(fā)病機(jī)理的理解,從而為癌癥的診斷、治療和藥物的開(kāi)發(fā)提供新的理論基礎(chǔ)。

發(fā)表文章(*責(zé)任作者)

Bing Liang, Peng Peng, She Chen, Lin Li, Meijun Zhang, Dongyan Cao, Jiaxin Yang, Haixia Li, Ting Gui, Xialu Li* and Keng Shen*, Characterization and proteomic analysis of ovarian cancer-derived exosomes, Journal of Proteomics, vol.80, p171-182, 2013

Wenxing Jin, Zhaoyang Niu, Dan Xu and Xialu Li*, RBM5 promotes exon 4 skipping of AID pre-mRNA by competing with the binding of U2AF65 to the polypyrimidine tract, FEBS Lett, vol. 586,p3852-3857, 2012.

Zhaoyang Niu, Wenxing Jin, Libo Zhang, Xialu Li*, Tumor suppressor RBM5 directly interacts with the DExD/H-box protein DHX15 and stimulates its helicase activity, FEBS Lett, vol. 586, p977-983, 2012.

Yuichi Kanehiro, Kagefumi Todo, Misaki Negishi, Junji Fukuoka, Wenjian Gan, Takuya Hikasa, Yoshiaki Kaga, Masayuki Takemoto, Masaki Magari, Xialu Li, James L.Manley, Hitoshi Ohmori, Naoki Kanayama, Activation-induced cytidine deaminase (AID)-dependent somatic hypermutation requires a splice isoform of the serine/arginine-rich (SR) protein SRSF1, Proc Natl Acad Sci USA, vol.109, pp1216-1221, 2012 (Selected by faculty 1000 of biology)

Wenjian Gan, Zhishuang Guan, Jie Liu, Ting Gui, Keng Shen, James.L. Manley, Xialu Li*, R-loop-mediated genomic instability is caused by impairment of replication fork progression, Genes & Development, vol. 25, pp2041-2056, 2011 (Selected by faculty 1000 of biology)

Xialu Li and James L. Manley, 2009, The Role of Alternative Splicing During the Cell Cycle and Programmed Cell Death. In Ralph A. Bradshaw and Edward A. Dennis, editors: Handbook of Cell Signaling 2nd edition, Oxford:Academic Press, pp. 2329-2334. (invited book chapter)

Xialu Li*, Tianhui Niu., and James L Manley. 2007. The RNA binding protein RNPS1 alleviates ASF/SF2 depletion-induced genomic instability. RNA 13(12): 2108-2115

Xialu Li and James L Manley, 2006, Co-transcriptional processes and their influence on genome stability. Genes & Development, 2006; 20(14):1838-1847.
Xialu Li and James L Manley. 2006. Alternative Splicing and Control of Apoptotic DNA Fragmentation. Cell Cycle 5(12).1286-1288

Xialu Li and James L. Manley, 2005, New talents for an old acquaintance: the SR protein splicing factor ASF/SF2 functions in the maintenance of genome stability. Cell cycle, 4(12): 1706-1708.

Xialu Li, Jin Wang and James L Manley, 2005, Loss of splicing factor ASF/SF2 induces G2 cell-cycle arrest and apoptosis, but inhibits internucleosomal DNA fragmentation, Genes & Development, 19(22):2705-2714.

Xialu Li and James L Manley, 2005, Inactivation of the SR protein splicing factor ASF/SF2 results in genomic instability. Cell, 122 (3), p365-378. (Selected by faculty 1000 of biology)

Boliang Li, Xialu Li et al., 1999, Human acyl-CoA:Cholesterol acyltransferase-1 (ACAT-1) gene organization and evidence that the 4.3-kilobase ACAT-1 mRNA is produced from two different chromosomes., J Biol Chem, 274 (16): p11060-11071

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