Year |
Citation |
Score |
2023 |
Hua K, Ferland RJ. Fixation methods and immunolabeling for cilia proteins in ciliary and extraciliary locations. Methods in Cell Biology. 176: 43-57. PMID 37164542 DOI: 10.1016/bs.mcb.2023.01.002 |
0.616 |
|
2021 |
Hsiao YC, Muñoz-Estrada J, Tuz K, Ferland RJ. The transition zone protein AHI1 regulates neuronal ciliary trafficking of MCHR1 and its downstream signaling pathway. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 33741721 DOI: 10.1523/JNEUROSCI.2993-20.2021 |
0.77 |
|
2019 |
Muñoz-Estrada J, Ferland RJ. Ahi1 promotes Arl13b ciliary recruitment, regulates Arl13b stability and is required for normal cell migration. Journal of Cell Science. PMID 31391239 DOI: 10.1242/Jcs.230680 |
0.779 |
|
2019 |
Bourgeois JR, Ferland RJ. Loss of the neurodevelopmental Joubert syndrome causing protein, Ahi1, causes motor and muscle development delays independent of central nervous system involvement. Developmental Biology. PMID 30695685 DOI: 10.1016/J.Ydbio.2019.01.014 |
0.61 |
|
2018 |
Hua K, Ferland RJ. Primary Cilia Reconsidered in the Context of Ciliopathies: Extraciliary and Ciliary Functions of Cilia Proteins Converge on a Polarity theme? Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. e1700132. PMID 29882973 DOI: 10.1002/Bies.201700132 |
0.634 |
|
2018 |
Kaskow BJ, Buttrick TS, Klein HU, White C, Bourgeois JR, Ferland RJ, Patsopoulos N, Bradshaw EM, De Jager PL, Elyaman W. MS AHI1 genetic risk promotes IFNγ+ CD4+ T cells. Neurology(R) Neuroimmunology & Neuroinflammation. 5: e414. PMID 29379820 DOI: 10.1212/Nxi.0000000000000414 |
0.563 |
|
2018 |
Hua K, Ferland RJ. Primary cilia proteins: ciliary and extraciliary sites and functions. Cellular and Molecular Life Sciences : Cmls. PMID 29305615 DOI: 10.1007/S00018-017-2740-5 |
0.654 |
|
2017 |
Srinivasan A, Muñoz-Estrada J, Bourgeois JR, Nalwalk JW, Pumiglia KM, Sheen VL, Ferland RJ. BranchAnalysis2D/3D Automates Morphometry Analyses of Branching Structures. Journal of Neuroscience Methods. PMID 29061345 DOI: 10.1016/J.Jneumeth.2017.10.017 |
0.738 |
|
2017 |
Kadiyala SB, Ferland RJ. Dissociation of spontaneous seizures and brainstem seizure thresholds in mice exposed to eight flurothyl-induced generalized seizures. Epilepsia Open. 2: 48-58. PMID 28825051 DOI: 10.1002/epi4.12031 |
0.697 |
|
2017 |
Löscher W, Ferland RJ, Ferraro TN. The relevance of inter- and intrastrain differences in mice and rats and their implications for models of seizures and epilepsy. Epilepsy & Behavior : E&B. 73: 214-235. PMID 28651171 DOI: 10.1016/J.Yebeh.2017.05.040 |
0.423 |
|
2017 |
Ferland RJ, Smith J, Papandrea D, Gracias J, Hains L, Kadiyala SB, O'Brien B, Kang EY, Beyer BS, Herron BJ. Multidimensional Genetic Analysis of Repeated Seizures in the Hybrid Mouse Diversity Panel Reveals a Novel Epileptogenesis Susceptibility Locus. G3 (Bethesda, Md.). PMID 28620084 DOI: 10.1534/G3.117.042234 |
0.795 |
|
2017 |
Hua K, Ferland RJ. Fixation methods can differentially affect ciliary protein immunolabeling. Cilia. 6: 5. PMID 28352462 DOI: 10.1186/S13630-017-0045-9 |
0.641 |
|
2016 |
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. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 7485-96. PMID 27413158 DOI: 10.1523/Jneurosci.3232-14.2016 |
0.786 |
|
2015 |
Kadiyala SB, Papandrea D, Tuz K, Anderson TM, Jayakumar S, Herron BJ, Ferland RJ. 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 Research. 109: 183-96. PMID 25524858 DOI: 10.1016/J.Eplepsyres.2014.11.009 |
0.777 |
|
2014 |
Hu J, Lu J, Lian G, Ferland RJ, Dettenhofer M, Sheen VL. Formin 1 and filamin B physically interact to coordinate chondrocyte proliferation and differentiation in the growth plate. Human Molecular Genetics. 23: 4663-73. PMID 24760772 DOI: 10.1093/Hmg/Ddu186 |
0.377 |
|
2014 |
Kadiyala SB, Papandrea D, Herron BJ, Ferland RJ. Segregation of seizure traits in C57 black mouse substrains using the repeated-flurothyl model. Plos One. 9: e90506. PMID 24594686 DOI: 10.1371/Journal.Pone.0090506 |
0.792 |
|
2014 |
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, ... ... Ferland RJ, et al. Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy. American Journal of Human Genetics. 94: 62-72. PMID 24360808 DOI: 10.1016/J.Ajhg.2013.11.019 |
0.781 |
|
2014 |
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, ... ... Ferland RJ, et al. Erratum: Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without jeune asphyxiating thoracic dystrophy (American Journal of Human Genetics (2014) 94 (62-72)) American Journal of Human Genetics. 94. DOI: 10.1016/J.Ajhg.2014.01.003 |
0.777 |
|
2013 |
Tuz K, Hsiao YC, Juárez 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. The Journal of Biological Chemistry. 288: 13676-94. PMID 23532844 DOI: 10.1074/Jbc.M112.420786 |
0.768 |
|
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. Neurological Research. 35: 79-89. PMID 23317802 DOI: 10.1179/1743132812Y.0000000117 |
0.348 |
|
2012 |
Hsiao YC, Tuz K, Ferland RJ. Trafficking in and to the primary cilium. Cilia. 1: 4. PMID 23351793 DOI: 10.1186/2046-2530-1-4 |
0.759 |
|
2012 |
Zhang J, Neal J, Lian G, Shi B, Ferland RJ, Sheen V. Brefeldin A-inhibited guanine exchange factor 2 regulates filamin A phosphorylation and neuronal migration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 12619-29. PMID 22956851 DOI: 10.1523/Jneurosci.1063-12.2012 |
0.786 |
|
2012 |
Lian G, Lu J, Hu J, Zhang J, Cross SH, Ferland RJ, Sheen VL. Filamin a regulates neural progenitor proliferation and cortical size through Wee1-dependent Cdk1 phosphorylation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 7672-84. PMID 22649246 DOI: 10.1523/Jneurosci.0894-12.2012 |
0.353 |
|
2010 |
Westfall JE, Hoyt C, Liu Q, Hsiao YC, 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. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 8759-68. PMID 20592197 DOI: 10.1523/Jneurosci.5229-09.2010 |
0.54 |
|
2010 |
Ault J, Tuz K, Shi B, Walsh J, Andreas A, Shimakawa E, Ferland R. Imaging Dynabeads with the Scanning Electron Microscope Microscopy and Microanalysis. 16: 630-631. DOI: 10.1017/S1431927610054383 |
0.73 |
|
2010 |
Ferland RJ, Walsh CA. Joubert Syndrome Encyclopedia of Neuroscience. 249-256. DOI: 10.1016/B978-008045046-9.01487-X |
0.379 |
|
2009 |
Yu F, Keinan A, Chen H, Ferland RJ, Hill RS, Mignault AA, Walsh CA, Reich D. Detecting natural selection by empirical comparison to random regions of the genome. Human Molecular Genetics. 18: 4853-67. PMID 19783549 DOI: 10.1093/Hmg/Ddp457 |
0.467 |
|
2009 |
Papandrea D, Kukol WS, Anderson TM, Herron BJ, Ferland RJ. Analysis of flurothyl-induced myoclonus in inbred strains of mice. Epilepsy Research. 87: 130-6. PMID 19744831 DOI: 10.1016/J.Eplepsyres.2009.08.003 |
0.792 |
|
2009 |
Ferland RJ, Guerrini R. Nodular heterotopia is built upon layers. Neurology. 73: 742-3. PMID 19625704 DOI: 10.1212/Wnl.0B013E3181B529B1 |
0.413 |
|
2009 |
Hsiao YC, Tong ZJ, Westfall JE, Ault JG, Page-McCaw PS, Ferland RJ. Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking. Human Molecular Genetics. 18: 3926-41. PMID 19625297 DOI: 10.1093/Hmg/Ddp335 |
0.56 |
|
2009 |
Ferland RJ, Batiz LF, Neal J, Lian G, Bundock E, Lu J, Hsiao YC, Diamond R, Mei D, Banham AH, Brown PJ, Vanderburg CR, Joseph J, Hecht JL, Folkerth R, et al. Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia. Human Molecular Genetics. 18: 497-516. PMID 18996916 DOI: 10.1093/Hmg/Ddn377 |
0.78 |
|
2009 |
Papandrea D, Anderson TM, Herron BJ, Ferland RJ. Dissociation of seizure traits in inbred strains of mice using the flurothyl kindling model of epileptogenesis. Experimental Neurology. 215: 60-8. PMID 18950623 DOI: 10.1016/J.Expneurol.2008.09.016 |
0.798 |
|
2008 |
Doering JE, Kane K, Hsiao YC, Yao C, Shi B, Slowik AD, Dhagat B, Scott DD, Ault JG, Page-McCaw PS, Ferland RJ. Species differences in the expression of Ahi1, a protein implicated in the neurodevelopmental disorder Joubert syndrome, with preferential accumulation to stigmoid bodies. The Journal of Comparative Neurology. 511: 238-56. PMID 18785627 DOI: 10.1002/Cne.21824 |
0.721 |
|
2008 |
Morrow EM, Yoo SY, Flavell SW, Kim TK, Lin Y, Hill RS, Mukaddes NM, Balkhy S, Gascon G, Hashmi A, Al-Saad S, Ware J, Joseph RM, Greenblatt R, Gleason D, ... ... Ferland RJ, et al. Identifying autism loci and genes by tracing recent shared ancestry. Science (New York, N.Y.). 321: 218-23. PMID 18621663 DOI: 10.1126/Science.1157657 |
0.711 |
|
2007 |
Yu F, Hill RS, Schaffner SF, Sabeti PC, Wang ET, Mignault AA, Ferland RJ, Moyzis RK, Walsh CA, Reich D. Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens". Science (New York, N.Y.). 316: 370. PMID 17446375 DOI: 10.1126/Science.1137568 |
0.44 |
|
2006 |
Ferland RJ, Gaitanis JN, Apse K, Tantravahi U, Walsh CA, Sheen VL. Periventricular nodular heterotopia and Williams syndrome. American Journal of Medical Genetics. Part A. 140: 1305-11. PMID 16691586 DOI: 10.1002/Ajmg.A.31259 |
0.486 |
|
2006 |
Sheen VL, Ferland RJ, Harney M, Hill RS, Neal J, Banham AH, Brown P, Chenn A, Corbo J, Hecht J, Folkerth R, Walsh CA. Impaired proliferation and migration in human Miller-Dieker neural precursors. Annals of Neurology. 60: 137-44. PMID 16642511 DOI: 10.1002/Ana.20843 |
0.788 |
|
2006 |
Sheen VL, Ferland RJ, Neal J, Harney M, Hill RS, Banham A, Brown P, Chenn A, Corbo J, Hecht J, Folkerth R, Walsh CA. Neocortical neuronal arrangement in Miller Dieker syndrome. Acta Neuropathologica. 111: 489-96. PMID 16456669 DOI: 10.1007/S00401-005-0010-3 |
0.78 |
|
2006 |
Basel-Vanagaite L, Attia R, Yahav M, Ferland RJ, Anteki L, Walsh CA, Olender T, Straussberg R, Magal N, Taub E, Drasinover V, Alkelai A, Bercovich D, Rechavi G, Simon AJ, et al. The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation. Journal of Medical Genetics. 43: 203-10. PMID 16033914 DOI: 10.1136/Jmg.2005.035709 |
0.503 |
|
2005 |
Ferland RJ, Li X, Buhlmann JE, Bu X, Walsh CA, Lim B. Characterization of Rho-GDIgamma and Rho-GDIalpha mRNA in the developing and mature brain with an analysis of mice with targeted deletions of Rho-GDIgamma. Brain Research. 1054: 9-21. PMID 16054116 DOI: 10.1016/J.Brainres.2005.04.088 |
0.518 |
|
2004 |
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, Walsh CA. Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome. Nature Genetics. 36: 1008-13. PMID 15322546 DOI: 10.1038/Ng1419 |
0.515 |
|
2004 |
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, Walsh CA. Erratum: Corrigendum: Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome Nature Genetics. 36: 1126-1126. DOI: 10.1038/Ng1004-1126B |
0.486 |
|
2003 |
Ferland RJ, Cherry TJ, Preware PO, Morrisey EE, Walsh CA. Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. The Journal of Comparative Neurology. 460: 266-79. PMID 12687690 DOI: 10.1002/Cne.10654 |
0.529 |
|
2003 |
Ferland RJ, Williams JP, Gross RA, Applegate CD. The effects of brain-irradiation-induced decreases in hippocampal mitotic activity on flurothyl-induced epileptogenesis in adult C57BL/6J mice. Experimental Neurology. 179: 71-82. PMID 12504869 DOI: 10.1006/Exnr.2002.8051 |
0.718 |
|
2002 |
Ferland RJ, Gross RA, Applegate CD. Increased mitotic activity in the dentate gyrus of the hippocampus of adult C57BL/6J mice exposed to the flurothyl kindling model of epileptogenesis. Neuroscience. 115: 669-83. PMID 12435406 DOI: 10.1016/S0306-4522(02)00514-6 |
0.725 |
|
2002 |
Ferland RJ, Gross RA, Applegate CD. Differences in hippocampal mitotic activity within the dorsal and ventral hippocampus following flurothyl seizures in mice. Neuroscience Letters. 332: 131-5. PMID 12384228 DOI: 10.1016/S0304-3940(02)00808-X |
0.698 |
|
1999 |
Ferland RJ, Applegate CD. Bidirectional transfer between electrical and flurothyl kindling in mice: evidence for common processes in epileptogenesis. Epilepsia. 40: 144-52. PMID 9952259 DOI: 10.1111/J.1528-1157.1999.Tb02067.X |
0.665 |
|
1998 |
Ferland RJ, Applegate CD. The role of the ventromedial nucleus of the hypothalamus in epileptogenesis. Neuroreport. 9: 3623-9. PMID 9858370 DOI: 10.1097/00001756-199811160-00013 |
0.668 |
|
1998 |
Ferland RJ, Nierenberg J, Applegate CD. A role for the bilateral involvement of perirhinal cortex in generalized kindled seizure expression. Experimental Neurology. 151: 124-37. PMID 9582260 DOI: 10.1006/Exnr.1998.6794 |
0.667 |
|
1998 |
Ferland RJ, Applegate CD. Decreased brainstem seizure thresholds and facilitated seizure propagation in mice exposed to repeated flurothyl-induced generalized forebrain seizures. Epilepsy Research. 30: 49-62. PMID 9551844 DOI: 10.1016/S0920-1211(97)00093-4 |
0.676 |
|
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