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Russell Ferland的大头照

Russ Ferland, Ph.D.

Professor

COM生物医学科学系主席

Location

Stella Maris Hall 331
Biddeford Campus

The combined long-term objectives of our research are to better understand the molecular, genetic, 以及导致神经发育和神经紊乱的细胞机制. Overall, my research interests lie primarily in the study of disorders of brain development and neurological disease, 具体涉及以下调查领域:

1) functional analyses of AHI1 and CSPP1, two novel genes which we mapped and cloned in individuals with Joubert syndrome (Hsiao et al., J. Neurosci., 2021; Munoz and Ferland, J. Cell Sci., 2019; Bourgeois and Ferland, Dev. Biol., 2019; Tuz et al., Am. J. Hum. Genet., 2014; Tuz et al., J. Biol. Chem., 2013; Westfall et al., J. Neurosci., 2010; Hsiao et al., Hum. Mol. Genet., 2009; Doering et al., J. Comp. Neurol., 2008; Ferland et al., Nature Genetics, 2004),

2) formation and function of the primary non-motile cilia in development and disease (Hua and Ferland, Methods Cell Bio., 2023; Hsiao et al., J. Neurosci., 2021; Munoz and Ferland, J. Cell Sci., 2019; Munoz and Ferland, J. Cell Sci., 2019; Bourgeois and Ferland, Dev. Biol., 2019; Hua and Ferland, Bioessays, 2018; Hua and Feland, Cell. Mol. Life Sci., 2018; Hua and Ferland, Cilia, 2017; Tuz et al., Am. J. Hum. Genet., 2014; Tuz et al., J. Biol. Chem., 2013; Hsiao et al., Cilia, 2012; Westfall et al., J. Neurosci., 2010; Hsiao et al., Hum. Mol. Genet., 2009), 

3)癫痫阈值的遗传和神经解剖学机制, seizure propagation, epileptogenesis, 和癫痫猝死(SUDEP)(威尔逊, et al., FASEB J., 2021; Ferland et al., G3 Genes, Genom. Genet, 2017; Ferland, 2017; Loscher, Ferland, and Ferraro, Epilepsy and Behavior, 2017; Kadiyala et al., J. Neurosci., 2016; Kadiyala et al., Epil. Res., 2015; Kadiyala et al., PLoS ONE, 2014; Papandrea et al., Exp. Neurol., 2009; Papandrea et al., Epil. Res., 2009; Ferland et al, 1998a,b,c, 1999, 2002a,b, 2003).

Credentials

Education

MS, Neuroscience
罗切斯特大学医学院
1998
PhD, Neuroscience
罗切斯特大学医学院
2000

Post-Doctoral Training

博士后培训,神经遗传学/神经发育
Harvard Medical School & 霍华德休斯医学研究所(波士顿,马萨诸塞州)

Research

Selected publications

Hua K, Ferland RJ. Fixation methods and immunolabeling for cilia proteins in ciliary and extraciliary locations. (Invited submission). Methods Cell Biol., 176:43-57, 2023.

Wilson CS, Dohare P, Orbeta S, Nalwalk JW, Huang Y, Ferland RJ, Sah R, Scimemi A, Mongin AA. Late adolescence mortality in mice with brain-specific deletion of the volume-regulated anion channel subunit LRRC8A. FASEB J., 35(10):e21869, 2021.

肖玉成,Muñoz-Estrada J,杜志强,陈志强. The transition zone protein AHI1 regulates neuronal ciliary trafficking of MCHR1 and its downstream signaling pathway. J. Neurosci., 41(17):3932-3943, 2021.

Srinivasan A, Srinivasan A, Ferland RJ. AutoSholl允许独立于用户跟踪的Sholl分析自动化. 中华神经科学杂志,2016,31 (1):1-6. Source code & 编译版本的算法是可用的 at: http://github.com/ferlandlab/AutoSholl

Muñoz-Estrada J和Ferland RJ. Ahi1促进Arl13b纤毛招募, 调节Arl13b的稳定性,是正常细胞迁移所必需的. 中国生物医学工程学报,32(6):1145 - 1145.

Bourgeois JR and Ferland RJ.  失去神经发育的Joubert综合症导致的蛋白质, Ahi1, causes motor and muscle development delays independent of central nervous system involvement. 中国生物医学工程学报,2016,36 (1):444 - 444.

Hua K and Ferland RJ. Primary cilia reconsidered in the context of ciliopathies: Extraciliary and ciliary functions of cilia proteins converge on a polarity theme? 中国生物工程学报,2016,31 (2):481 - 481,2018.

Hua K and Ferland RJ. 初级纤毛蛋白:纤毛和纤毛外的位置和功能. Mol. Life Sci., 75:1521–1540, 2018.

Kaskow BJ, Buttrick TS, Klein H-U, White C, Bourgeois JR, Ferland RJ, Patsopoulos N, Bradshaw EM, De Jager PL, Elyaman W. 多发性硬化症AHI1遗传风险促进IFNγ+ CD4+ T细胞. Neurology: Neuroimmunology & 中华神经科学杂志,2018,35 (1):1-10 (e414).

Srinivasan A, Muñoz-Estrada J, Bourgeois JR, Nalwalk J, Pumiglia K, Sheen V, Ferland RJ. BranchAnalysis2D/3D自动分析分支结构的形态. 中华神经科学杂志,2018,29 (4):1-6. Source code & 该算法的编译版本可在以下网址下载: http://github.com/ferlandlab/BranchAnalysis2D-3D

Ferland RJ. 小鼠氟醚反复发作模型. Invited submission.  中国生物医学工程学报,2017,37 (11):1104 - 1104.  DOI:10.21769/BioProtoc.2309.

Löscher W,费兰RJ,费拉罗TN. The relevance of inter- and intrastrain differences in mice and rats and their implications for models of seizures and epilepsy. Epilepsy Behav., 73: 214-235, 2017.

Ferland RJ, Smith J, Papandrea D, Gracias J, Haines L, Kadiyala SB, O'Brien B, Kang EY, Beyer B, Herron BJ. Multidimensional genetic analysis of repeated seizures in the hybrid mouse diversity panel reveals a novel epileptogenesis susceptibility locus. G3 Genes Genom. Genet., 7(8): 2545-2558, 2017.

Hua K and Ferland RJ. 固定方法对纤毛蛋白免疫标记的影响不同. Cilia, 6;5: pp. 1-17, 2017. 

Kadiyala SB and Ferland RJ. Dissociation of spontaneous seizures and brainstem seizure thresholds in mice exposed to eight flurothyl-induced generalized seizures. 癫痫病杂志,2(1):48-58,2017.

Kadiyala SB, Yannix JQ, Nalwalk JW, Papandrea D, Beyer BS, Herron BJ, Ferland RJ. Eight flurothyl-induced generalized seizures lead to the rapid evolution of spontaneous seizures in mice: a model of epileptogenesis with seizure remission. J. Neurosci., 36(28): 7485-7496, 2016.

李建军,李建军,李建军,李建军,李建军,李建军. Spatiotemporal differences in the c-fos pathway between C57BL/6J and DBA/2J mice following flurothyl-induced seizures: A dissociation of hippocampal Fos from seizure activity. Epilepsy Res., 109:183-196, 2015.

胡军,陆军,连刚,Ferland RJ, Dettenhofer M, Sheen VL. Formin 1 and Filamin B physically interact to coordinate chondrocyte proliferation and differentiation in the growth plate. Hum. Mol. Genet., 23(17):4663-4673, 2014.

刘建军,刘建军,刘建军. Segregation of seizure traits in C57 Black mouse substrains using the repeated-flurothyl model. 科学通报,2014,37 (3):391 - 391.

Tuz K, Bachmann-Gagescu R, O'Day DR, Hua K, Isabella CR, Phelps IG, Stolarski AE, O'Roak BJ, Dempsey JC, Lourenco C, Alswaid A, Bönnemann CG, Medne L, Nampoothiri S, Stark Z, Leventer RJ, Topçu M, Cansu A, Jagadeesh S, Done S, Ishak GE, Glass IA, Shendure J, Neuhauss SC, Haldeman-Englert CR, Doherty D, Ferland RJ. Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy. Am. J. Hum. Genet., 94(1): 62–72, 2014.

Tuz K, Hsiao YC, Juarez O, Shi B, Harmon EY, Phelps IG, Lennartz MR, Glass IA, Doherty D, Ferland RJ. The Joubert syndrome associated missense mutation (V443D) in the Abelson-helper integration site 1 (AHI1) protein alters its localization and protein-protein interactions. J. Biol. Chem., 288(19):13676-94, 2013.

Bhoiwala DL, Koleilat I, Qian J, Beyer B, Hushmendy SF, Mathew A, Bhoiwala DL, Ferland RJ, Crawford DR. Overexpression of RCAN1 isoform 4 in mouse neurons leads to a moderate behavioral impairment. Neurol. Res., 35(1):79-89, 2013.

张军,Neal J,连刚,石斌,Ferland RJ, Sheen VL. Brefeldin A-inhibited guanine exchange factor 2 regulates Filamin A phosphorylation and neuronal migration. J. Neurosci., 32(36):12619-12629, 2012.

连刚,卢军,胡军,张军,克罗斯,费兰荣军,辛维林. Filamin A Regulates Neural Progenitor Proliferation and Brain Size through Wee1-Dependent Cdk1 Phosphorylation. J. Neurosci., 32(22):7672-84, 2012.

肖玉春,张建军,张建军,等。主要纤毛的贩卖与贩卖. Cilia, 1:4 (1-13), 2012

Westfall (Doering) JE, Hoyt C, Liu Q, Hsiao Y-C, Pierce EA, Page-McCaw PS, Ferland RJ. Retinal degeneration and failure of photoreceptor outer segment formation in mice with targeted deletion of the Joubert syndrome gene, Ahi1. J. Neurosci., 30(26):8759-8768, 2010.

刘建军,刘建军,刘建军,刘建军. 小鼠近交系氟基诱导的肌阵挛分析. Epil. Res., 87:130-136, 2009.

肖永昌,童志军,Westfall (Doering) JE, Ault JG, Page-McCaw PS, Ferland RJ. Ahi1, 他的人类同源基因在朱伯特综合症中发生了突变, 是Rab8a正确定位所必需的, ciliogenesis, and vesicular trafficking. Hum. Mol. Genet., 18(20):3926-3941, 2009.

Ferland RJ, Batiz LF, Neal J, Lian G, Bundock E, Lu J, Hsiao Y-C, Diamond R, Mei D, Banham A, Brown PJ, Vanderburg CR, Joseph J, Hecht JL, Folkerth R, Guerrini R, Walsh CA, Rodriguez EM, Sheen VL. Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia. Hum. Mol. Genet., 18(3):497-516, 2009.

刘建军,刘建军,刘建军,等. Genetic dissociation of seizure traits in inbred strains of mice using the flurothyl model of epileptogenesis. Exp. Neurol., 215:60-68, 2009.

Morrow EM, Yoo S-Y, Flavell SW, Kim T-K, Lin Y, Hill RS, Mukaddes NM, Balkhy S, Gascon G, Hashmi A, Al-Saad S, Ware J, Joseph RM, Greenblatt R, Gleason D, Ertelt JA, Apse KA, Bodell A, Partlow JN, Barry B, Yao H, Markianos K, Ferland RJ, Greenberg ME, Walsh CA. 通过追踪最近的共同祖先来识别自闭症位点和基因. Science, 321:218-223, 2008.

Doering JE, Kane K, Hsiao Y-C, Yao C, Shi B, Slowik A, Dhagat B, Scott D, Ault JG, Page-McCaw PS, Ferland RJ. AHI1表达的物种差异, 一种与神经发育障碍朱伯特综合症有关的蛋白质, 优先向柱状体积累. J. Comp. Neurol., 511:238-256, 2008.

Ferland RJ, Eyaid W, Collura RV, Tully LD, Hill RS, Al-Nouri D, Al-Rumayyan A, Topcu M, Gascon G, Bodell A, Shugart YY, Ruvolo M, and Walsh CA. Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert Syndrome. Nature Genet., 36:1008-1013, 2004.

Other scholarly activity

Book Chapters:

Löscher W,费兰RJ,费拉罗TN. 应变对癫痫发作和癫痫表达的影响. In: Models of Seizure and Epilepsy, 2nd edition, Cambridge: Academic Press (2017) pp. 21-38.  ISBN 9780128040669

华坤,陈文杰,陈文杰. Joubert syndrome. In: Reference Module in Neuroscience and Biobehavioral Psychology, Elsevier (2017) pp. 1-8.   ISBN 9780128093245

Ferland RJ, Walsh CA. The genetics of Joubert syndrome: Insights into the development of the posterior midline of the brain.  In: Squire, LR (Ed.神经科学百科全书.  圣地亚哥:学术出版社(2009)pp. 249-256.

陈志强,陈志强,陈志强.   鼻脑神经网络在点火后期的作用.  见:Corcoran, M和Moshe, S(主编).) Kindling 5.  纽约:Raven出版社(1998)pp. 151-165.

Invited Editorials:

Ferland RJ and Guerrini R.  结节性异位是建立在层次上的. 中国生物医学工程学报,30 (3):742-743,2009.

Ferland R and Hua K. Referee Report For: Murine Cep290 phenotypes are modified by genetic backgrounds and provide an impetus for investigating disease modifier alleles [version 1; referees: 2 approved] F1000Research 2015, 4:590 (doi: 10.5256/f1000research.7495.r10185)

Hua K and Ferland RJ. Primary cilia: the story of the hair-like organelle that signals just became more complicated. Atlas of science, 2019. http://atlasofscience.org/primary-cilia-the-story-of-the-hair-like-organelle-that-signals-just-became-more-complicated/

Research topics

Biosignaling
Brain
COM Faculty Research
Development
Developmental Biology
Gene Expression
Neural Stem Cell
Neuroscience