溫州醫(yī)科大學(xué)檢驗(yàn)醫(yī)學(xué)與生命科學(xué)學(xué)院2014年考研調(diào)劑信息

24考研復(fù)試面試模擬體驗(yàn)包（1次）

2024考研復(fù)試特訓(xùn)班[1V1材料修改+面試模擬+聽口糾音]

一、錄取要求：

1.本實(shí)驗(yàn)室擬招收生物學(xué)或臨床檢驗(yàn)診斷學(xué)專業(yè)碩士研究生6名；

2.總分?jǐn)?shù)、單科須過(guò)國(guó)家A類分?jǐn)?shù)線；

3.來(lái)自“985”、“211”等高校的優(yōu)秀考生，同等條件下優(yōu)先錄�。�

4.通過(guò)國(guó)家英語(yǔ)六級(jí)的優(yōu)秀考生，同等條件下優(yōu)先調(diào)劑。

二、待遇

1.除學(xué)校提供的生活補(bǔ)貼外，導(dǎo)師根據(jù)學(xué)生表現(xiàn)每月提供額外的勞務(wù)補(bǔ)貼。

2.為研究生提供良好的生活條件，國(guó)家和本校通過(guò)設(shè)立獎(jiǎng)學(xué)金、助學(xué)金、助學(xué)貸款、三助崗位、綠色通道等制度，建立多元獎(jiǎng)助體系。目前已設(shè)的獎(jiǎng)學(xué)金如下：

國(guó)家獎(jiǎng)學(xué)金：20000元。

臺(tái)灣光華教育基金會(huì)設(shè)立的光華獎(jiǎng)學(xué)金：我校是浙江省屬院校中唯一設(shè)立該獎(jiǎng)學(xué)金的學(xué)校。

中國(guó)科學(xué)院毛江森院士在我校設(shè)立的毛江森獎(jiǎng)學(xué)金和助學(xué)金:特等獎(jiǎng)學(xué)金2萬(wàn)元,獎(jiǎng)學(xué)金5000元，助學(xué)金2000元。

生物藥械豪森藥業(yè)獎(jiǎng)學(xué)金和助學(xué)金：特等獎(jiǎng)5000元，一等獎(jiǎng)2000元，二等獎(jiǎng)1000元，三等獎(jiǎng)500元。

康泉獎(jiǎng)學(xué)金：特等獎(jiǎng)5000元。

東甌獎(jiǎng)學(xué)金、迪安獎(jiǎng)學(xué)金等。

三、實(shí)驗(yàn)室基本情況

本實(shí)驗(yàn)室近20年來(lái)致力于線粒體分子遺傳學(xué)和母性遺傳病致病機(jī)制的研究,主要方向有耳聾遺傳、Leber遺傳性視神經(jīng)病變、原發(fā)性高血壓,tRNA堿基修飾機(jī)制及其在線粒體疾病發(fā)病中的作用等。課題組已在國(guó)內(nèi)外著名刊物上發(fā)表論文100多篇，SCI收錄論文80余篇，累計(jì)影響因子300余分。導(dǎo)師管敏鑫教授作為國(guó)際線粒體分子遺傳學(xué)和母性遺傳病領(lǐng)域知名專家，國(guó)際該領(lǐng)域領(lǐng)軍人物之一，目前主持及參與國(guó)家“973”計(jì)劃項(xiàng)目，十二五支撐項(xiàng)目，國(guó)家自然科學(xué)基金重點(diǎn)項(xiàng)目等。熱誠(chéng)歡迎對(duì)線粒體生物醫(yī)學(xué)研究感興趣的研究生加入我們的研究團(tuán)隊(duì)！

四、導(dǎo)師簡(jiǎn)介：

管敏鑫教授:

（一）基本信息：

1962年生于浙江省樂(lè)清市

1979.9-1983.7杭州大學(xué)（現(xiàn)浙江大學(xué)）生物系本科

1983.8-1989.9浙江圖書館館員

1989.9-1993.7澳大利亞國(guó)立大學(xué)（ANU）生物化學(xué)與分子生物學(xué)博士研究生

1993.8-1996.7加州理工學(xué)院（Caltech）人類分子遺傳學(xué)ResearchFellow

1996.8-1999.7加州理工學(xué)院生物系SeniorResearchFellow

1999.8-2011.9辛辛那提大學(xué)兒童醫(yī)院醫(yī)學(xué)中心人類遺傳學(xué)助理教授、副教授、教授

2011.1-2013.11浙江大學(xué)生命科學(xué)學(xué)院院長(zhǎng)

2011.1-至今浙江大學(xué)生命科學(xué)學(xué)院教授、博導(dǎo)

（二）學(xué)術(shù)兼職

溫州醫(yī)學(xué)院生命科學(xué)學(xué)院院長(zhǎng),教授(2004-2010)

中國(guó)人民解放軍總醫(yī)院/軍醫(yī)進(jìn)修學(xué)院客座教授（2002-至今）

美國(guó)辛辛那提大學(xué)兒童醫(yī)院醫(yī)學(xué)中心客座教授(2011.10-至今)

浙江省高等學(xué)校特聘教授(2006-2009)

浙江省醫(yī)學(xué)遺傳學(xué)重點(diǎn)實(shí)驗(yàn)室學(xué)術(shù)委員會(huì)主任（2005-至今）

第四屆亞洲線粒體研究與醫(yī)學(xué)學(xué)會(huì)（ASMRM）主席（2011-至今）

（三）獎(jiǎng)勵(lì)榮譽(yù)

國(guó)家“千人計(jì)劃”入選者(2012)

浙江省特聘專家(2010)

國(guó)務(wù)院政府特殊津貼(2010)

浙江省有突出貢獻(xiàn)中青年專家（2009）

浙江省優(yōu)秀留學(xué)回國(guó)人員（2008）

首批浙江省衛(wèi)生高層次創(chuàng)新人才（2007）

浙江省高等學(xué)校特聘教授（2006年）

浙江省“新世紀(jì)151人才工程”第一層次培養(yǎng)人員（2006）

國(guó)家自然科學(xué)基金海外及港澳學(xué)者合作研究基金(2006)

（四）主持項(xiàng)目

1.國(guó)家重點(diǎn)基礎(chǔ)研究發(fā)展計(jì)劃（973計(jì)劃）:單基因遺傳性聾病的分子機(jī)制研究,2014.1-2018.12

2.國(guó)家自然科學(xué)基金重點(diǎn)項(xiàng)目：核修飾基因調(diào)控母系遺傳性耳聾發(fā)病機(jī)制及聽覺功能重建的策略研究,2014.1-2017.12

3.十二五支撐項(xiàng)目：Leber遺傳性視神經(jīng)病變的分子診斷和治療研究,2012.1-2015.12

（五）研究成果

2009年度《母系遺傳藥物性耳聾致病機(jī)制研究及干預(yù)》中華醫(yī)學(xué)科技獎(jiǎng),二等獎(jiǎng)

2009年度《母系遺傳藥物性耳聾致病機(jī)制的研究》浙江省科學(xué)技術(shù)獎(jiǎng),一等獎(jiǎng)

2008年度《聾病發(fā)生的分子機(jī)制與防控預(yù)警的系統(tǒng)研究》國(guó)家科技進(jìn)步獎(jiǎng),二等獎(jiǎng)

2007年度《Leber氏遺傳性視神經(jīng)萎縮遺傳性狀研究》，國(guó)家科技進(jìn)步獎(jiǎng),二等獎(jiǎng)

（六）代表性論文
耳聾遺傳
Guan, M.X., Fischel-Ghodsian,N. and Attardi,G. (1996) Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation.Hum. Mol. Genet. 5:963-972.
Guan, M.X.,Enriquez,J.A., Fischel-Ghodsian, N., Puranam, R., Lin, C.P., Marion, M.A. and Attardi,G. (1998) The Deafness-associated mtDNA 7445 mutation, which affects tRNAprecursor processing, has long-range effects on NADH dehydrogenase ND6 subunit gene expression.Mol. Cell. Biol.18:5868-5879.
Guan, M.X,Fischel-Ghodsian, N. and Attardi,G. (2000) A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity.Hum. Mol. Genet. 9: 1787-1793.
Guan, M.X.,Fischel-Ghodsian, N. and Attardi,G. (2001) Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation.Hum. Mol. Genet.10: 573-580.
Li, X., Fischel-Ghodsian,N., Schwartz, F., Yan, Q., Friedman,R.A. and*Guan,M.X.(2004) Biochemical characterization of the mitochondrial tRNAT7511C mutation associated with nonsyndromic deafness.Nucleic Acids Res.32: 867-877.
Zhao, H., Li, R., Wang, Q., Yan, Q., Deng, J.H., Han, D., Bai, Y., Young, W.Y. and*Guan, M.X. (2004) Maternally inherited aminoglycoside-induced and non-syndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family.Am. J. Hum. Genet.74:139-152.
Li, R., Greinwald, J.H., Yang, L., Choo, D.I., Wenstrup, R.J. and*Guan, M.X.(2004) Molecular analysis of mitochondrial 12S rRNA and tRNAgenes in pediatric subjects with nonsyndromic hearing loss.J. Med. Genet. 41:615-620.
Li, Z., Li, R., Chen, J., Liao, Z.,Zhu,Y., Qian,Y., Xiong,S., Heman-Ackah,S., Wu, J., Choo, D.I., and*Guan, M.-X.(2005)Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside induced and non-syndromic hearing loss.Hum. Genet.117:9-15.
Zhao, H., Young, W.Y., Yan, Q., Li, R., Cao, J., Wang, Q., Li, X., Peters, J.L., Han, D., and*Guan, M.X.(2005) Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and nonsyndromic hearing loss.Nucleic Acid Res.33:1132-1139.
*Guan, M.X,Yan, Q., Li, X., Bykhovskaya, Y., J. Gallo-Teran, P. Hajek, N. Umeda, H. Zhao, G. Garrido, E. Mengesha, T.Suzuki, I.del Castillo, J.L. Peters, R. Li, Qian, Y., Wang, X., Ballana, E., M. Shohat, Lu, J., X. Estivill,K. Watanabe, & Fischel-Ghodsian, N. (2006) Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations.Am. J. Hum. Genet.79:291-302.
Qian Y,*Guan MX.(2009) Interaction of aminoglycosides with human mitochondrial 12S rRNA carrying the deafness-associated mutation.Antimicrob Agents Chemother. 53:4612-4618.
Guan, MX.(2011) Mitochondrial 12S rRNA Mutations associated with aminoglycoside ototoxicity.Mitochondrion11: 237-245.
Yan X, Wang X, Wang Z, Sun S, Chen G, He Y, Mo JQ, Li R, Jiang P, Lin Q, Sun M, Li W, Bai Y, Zhang J, Zhu Y, Lu J, Yan Q, Li H,Guan MX. (2011)Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAgene. J Med Genet. 48:682-90.
Raimundo N, Song, L, Shutt TE, McKay SE, Cotney J,Guan MX, Gilliland TC, Hohuan, D, Santos-Sacchi S, Shadel GS. (2012) Mitochondrial Stress Engages E2F1Apoptotic Signaling to Cause Deafness. Cell. 148, 716-726.
Chen H, Zheng J, Xue L, Meng Y, Wang Y, Zheng B, Fang F, Shi S, Qiu Q, Jiang P, Lu Z, Mo JQ, Lu J,Guan MX. (2012)The 12S rRNA A1555G mutation in the mitochondrial haplogroup D5a is responsible for maternally inherited hypertension and hearing loss in two Chinese pedigrees.Eur J Hum Genet.20(6):607-12.
Zheng J, Ji Y, Guan MX (2012)Mitochondrial tRNA mutations associated with deafness.Mitochondrion. 2012 May;12(3):406-13.
Leber遺傳性視神經(jīng)病變

Qu,J., Li,R., Tong,Y., Zhou,X., Lu,F., Qian,Y., Hu,Y., Mo, J.Q., West, C.E.,*Guan, M.X.(2006) The novel A4435G mutation in the mitochondrial tRNAmay modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation in a Chinese family.Invest. Ophth. Vis. Sci.47:475-83.

Qu, J., Zhou, X., Zhang, J., Zhao, F., Sun, Y.H., Yong, Y., Wei, Q.P., Cai, W., West, C.E. and*Guan, M.X. (2009) Extremely low penetrance of Leber’s hereditary optic neuropathy in eight Han Chinese families carrying the ND4 G11778A mutation.Ophthalmology16:558-564.

Qu J, Wang Y, Tong Y, Zhou X, Zhao F, Yang L, Zhang S, Zhang J, West CE,*Guan MX.(2010)Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families.Invest Ophthalmol Vis Sci. 51:4906-4912.

Liu XL, Zhou T, Zhou J, Zhao F, Zhang J, Li C, Ji Y, Zhang Y, Wei QP,Sun YH, Yang L, Lin B, Yuan Y, Li Y, Qu J,*Guan MX.(2011) Leber’s hereditary optic neuropathy is associated with the novel T12338C mutation in mitochondrial ND5 gene in six Han Chinese families.Ophthalmology118:.978-985.

原發(fā)性高血壓

Liu, Y., Li, R., Li, Z., Wang, X., Yang, L., Wang, S.,Guan, M.X.(2009).The mitochondrial tRNA4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree.Hypertension.53:1083-1090.

Li, R., Liu, Y., Li, Z., Yang, L., Wang, S.,Guan, M.X. (2009) Failures in mitochondrial tRNAand tRNAmetabolism caused by the novel 4401A>G mutation are involved in essential hypertension in a Han Chinese family.Hypertension54:329-337.

Wang SW,Li RH, Fettermann A, Li ZB, Qian YP, Liu YQ, Wang XJ, Zhou A, Mo JQ, Yang L, Jiang PP, Taschner A, Rossmanith W,andGuanMX.. (2011) Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAgene in a large Han Chinese family.Circ. Res.108:862-70.

Lu Z, Chen H, Meng Y, Wang Y, Xue L, Zhi S, Qiu Q, Yang L, Mo JQ,*Guan MX. (2011) The tRNA4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree.Eur J Hum Genet. 19(11):1181-6
Qiu Q, Li R, Jiang P, Xue L, Lu Y, Song Y, Han J, Lu Z, Zhi S, Mo JQ, Guan MX. (2012)Mitochondrial tRNA mutations are associated with maternally inherited hypertension in two Han Chinese pedigrees.Hum Mutat. 2012 May 1. doi: 10.1002/humu.22109. [Epub ahead of print]

線粒體tRNA堿基修飾機(jī)制

Li, X., Li,R., Lin,X. and*Guan,M.X.(2002) Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12S rRNA A1555G mutation.J. Biol. Chem.277:27256-27264.

Li, X.,*Guan,M.X.(2002) A human mitochondrial GTP binding protein related to tRNA modification may modulate the phenotypic expression of the deafness-associated mitochondrial 12S rRNA mutation.Mol. Cell. Biol.22:7701-7711.

Yan, Q., Li, X., Faye, G. and *Guan, M.X. (2005) Mutations in MTO2 related to tRNA modification impair mitochondrial gene expression and protein synthesis in the presence of a paromomycin resistance mutation in mitochondrial 15S rRNA.J. Biol. Chem. 280: 29151-29157.

Guan, M.X,Yan, Q., Li, X., Bykhovskaya, Y., J. Gallo-Teran, P. Hajek, N. Umeda, H. Zhao, G. Garrido, E. Mengesha, T.Suzuki, I.del Castillo, J.L. Peters, R. Li, Qian, Y., Wang, X., Ballana, E., M. Shohat, Lu, J., X. Estivill,K. Watanabe, & Fischel-Ghodsian, N. (2006) Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations.Am. J. Hum. Genet.79:291-302.

Wang X, Yan Q,*Guan MX.(2010) Combination of the loss of cmnm5U34 with the lack of s2U34 modifications of tRNA, tRNA, and tRNAaltered mitochondrial biogenesis and respiration.J Mol Biol.395:1038-1048.

Li R,*Guan MX. (2010) Human mitochondrial leucyl-tRNA synthetase correctes mitochondrial dysfunctions due to the MELAS and diabetes associated tRNAA3243G mutation.Mol Cell Biol. 30:2147-54.

五、聯(lián)系方式

有意者，請(qǐng)聯(lián)系鄭老師，郵箱：148271673@qq.com

24考研復(fù)試面試模擬體驗(yàn)包（1次）

2024考研復(fù)試特訓(xùn)班[1V1材料修改+面試模擬+聽口糾音]

2024考研復(fù)試標(biāo)準(zhǔn)班【復(fù)試指導(dǎo)+中英文面試模擬+復(fù)試資料】