Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 57

1.

AutoSholl allows for automation of Sholl analysis independent of user tracing.

Srinivasan A, Srinivasan A, Ferland RJ.

J Neurosci Methods. 2020 Feb 1;331:108529. doi: 10.1016/j.jneumeth.2019.108529. Epub 2019 Nov 21.

PMID:
31760060
2.

Ahi1 promotes Arl13b ciliary recruitment, regulates Arl13b stability and is required for normal cell migration.

Muñoz-Estrada J, Ferland RJ.

J Cell Sci. 2019 Sep 4;132(17). pii: jcs230680. doi: 10.1242/jcs.230680.

PMID:
31391239
3.

Loss of the neurodevelopmental Joubert syndrome causing protein, Ahi1, causes motor and muscle development delays independent of central nervous system involvement.

Bourgeois JR, Ferland RJ.

Dev Biol. 2019 Apr 1;448(1):36-47. doi: 10.1016/j.ydbio.2019.01.014. Epub 2019 Jan 26.

PMID:
30695685
4.

Primary Cilia Reconsidered in the Context of Ciliopathies: Extraciliary and Ciliary Functions of Cilia Proteins Converge on a Polarity theme?

Hua K, Ferland RJ.

Bioessays. 2018 Aug;40(8):e1700132. doi: 10.1002/bies.201700132. Epub 2018 Jun 8. Review.

5.

MS AHI1 genetic risk promotes IFNγ+ CD4+ T cells.

Kaskow BJ, Buttrick TS, Klein HU, White C, Bourgeois JR, Ferland RJ, Patsopoulos N, Bradshaw EM, De Jager PL, Elyaman W.

Neurol Neuroimmunol Neuroinflamm. 2017 Dec 8;5(1):e414. doi: 10.1212/NXI.0000000000000414. eCollection 2018 Jan.

6.

Primary cilia proteins: ciliary and extraciliary sites and functions.

Hua K, Ferland RJ.

Cell Mol Life Sci. 2018 May;75(9):1521-1540. doi: 10.1007/s00018-017-2740-5. Epub 2018 Jan 5. Review.

7.

BranchAnalysis2D/3D automates morphometry analyses of branching structures.

Srinivasan A, Muñoz-Estrada J, Bourgeois JR, Nalwalk JW, Pumiglia KM, Sheen VL, Ferland RJ.

J Neurosci Methods. 2018 Jan 15;294:1-6. doi: 10.1016/j.jneumeth.2017.10.017. Epub 2017 Oct 20.

8.

Dissociation of spontaneous seizures and brainstem seizure thresholds in mice exposed to eight flurothyl-induced generalized seizures.

Kadiyala SB, Ferland RJ.

Epilepsia Open. 2017 Mar;2(1):48-58. doi: 10.1002/epi4.12031. Epub 2016 Dec 19.

9.

The Repeated Flurothyl Seizure Model in Mice.

Ferland RJ.

Bio Protoc. 2017 Jun 5;7(11). pii: e2309. doi: 10.21769/BioProtoc.2309.

10.

The relevance of inter- and intrastrain differences in mice and rats and their implications for models of seizures and epilepsy.

Löscher W, Ferland RJ, Ferraro TN.

Epilepsy Behav. 2017 Aug;73:214-235. doi: 10.1016/j.yebeh.2017.05.040. Epub 2017 Jun 23. Review.

11.

Multidimensional Genetic Analysis of Repeated Seizures in the Hybrid Mouse Diversity Panel Reveals a Novel Epileptogenesis Susceptibility Locus.

Ferland RJ, Smith J, Papandrea D, Gracias J, Hains L, Kadiyala SB, O'Brien B, Kang EY, Beyer BS, Herron BJ.

G3 (Bethesda). 2017 Aug 7;7(8):2545-2558. doi: 10.1534/g3.117.042234.

12.

Fixation methods can differentially affect ciliary protein immunolabeling.

Hua K, Ferland RJ.

Cilia. 2017 Mar 24;6:5. doi: 10.1186/s13630-017-0045-9. eCollection 2017.

13.

Eight Flurothyl-Induced Generalized Seizures Lead to the Rapid Evolution of Spontaneous Seizures in Mice: A Model of Epileptogenesis with Seizure Remission.

Kadiyala SB, Yannix JQ, Nalwalk JW, Papandrea D, Beyer BS, Herron BJ, Ferland RJ.

J Neurosci. 2016 Jul 13;36(28):7485-96. doi: 10.1523/JNEUROSCI.3232-14.2016.

14.

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.

Kadiyala SB, Papandrea D, Tuz K, Anderson TM, Jayakumar S, Herron BJ, Ferland RJ.

Epilepsy Res. 2015 Jan;109:183-96. doi: 10.1016/j.eplepsyres.2014.11.009. Epub 2014 Nov 22.

15.

Formin 1 and filamin B physically interact to coordinate chondrocyte proliferation and differentiation in the growth plate.

Hu J, Lu J, Lian G, Ferland RJ, Dettenhofer M, Sheen VL.

Hum Mol Genet. 2014 Sep 1;23(17):4663-73. doi: 10.1093/hmg/ddu186. Epub 2014 Apr 23.

16.

Segregation of seizure traits in C57 black mouse substrains using the repeated-flurothyl model.

Kadiyala SB, Papandrea D, Herron BJ, Ferland RJ.

PLoS One. 2014 Mar 3;9(3):e90506. doi: 10.1371/journal.pone.0090506. eCollection 2014.

17.

Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy.

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.

Am J Hum Genet. 2014 Jan 2;94(1):62-72. doi: 10.1016/j.ajhg.2013.11.019. Epub 2013 Dec 19. Erratum in: Am J Hum Genet. 2014 Feb 6;94(2):310.

18.

The Joubert syndrome-associated missense mutation (V443D) in the Abelson-helper integration site 1 (AHI1) protein alters its localization and protein-protein interactions.

Tuz K, Hsiao YC, Juárez O, Shi B, Harmon EY, Phelps IG, Lennartz MR, Glass IA, Doherty D, Ferland RJ.

J Biol Chem. 2013 May 10;288(19):13676-94. doi: 10.1074/jbc.M112.420786. Epub 2013 Mar 26.

19.

Trafficking in and to the primary cilium.

Hsiao YC, Tuz K, Ferland RJ.

Cilia. 2012 Apr 25;1(1):4. doi: 10.1186/2046-2530-1-4.

20.

Overexpression of RCAN1 isoform 4 in mouse neurons leads to a moderate behavioral impairment.

Bhoiwala DL, Koleilat I, Qian J, Beyer B, Hushmendy SF, Mathew A, Bhoiwala DL, Ferland RJ, Crawford DR.

Neurol Res. 2013 Jan;35(1):79-89. doi: 10.1179/1743132812Y.0000000117.

PMID:
23317802
21.

Brefeldin A-inhibited guanine exchange factor 2 regulates filamin A phosphorylation and neuronal migration.

Zhang J, Neal J, Lian G, Shi B, Ferland RJ, Sheen V.

J Neurosci. 2012 Sep 5;32(36):12619-29. doi: 10.1523/JNEUROSCI.1063-12.2012.

22.

Filamin a regulates neural progenitor proliferation and cortical size through Wee1-dependent Cdk1 phosphorylation.

Lian G, Lu J, Hu J, Zhang J, Cross SH, Ferland RJ, Sheen VL.

J Neurosci. 2012 May 30;32(22):7672-84. doi: 10.1523/JNEUROSCI.0894-12.2012.

23.

Retinal degeneration and failure of photoreceptor outer segment formation in mice with targeted deletion of the Joubert syndrome gene, Ahi1.

Westfall JE, Hoyt C, Liu Q, Hsiao YC, Pierce EA, Page-McCaw PS, Ferland RJ.

J Neurosci. 2010 Jun 30;30(26):8759-68. doi: 10.1523/JNEUROSCI.5229-09.2010.

24.

Detecting natural selection by empirical comparison to random regions of the genome.

Yu F, Keinan A, Chen H, Ferland RJ, Hill RS, Mignault AA, Walsh CA, Reich D.

Hum Mol Genet. 2009 Dec 15;18(24):4853-67. doi: 10.1093/hmg/ddp457. Epub 2009 Sep 25.

25.

Analysis of flurothyl-induced myoclonus in inbred strains of mice.

Papandrea D, Kukol WS, Anderson TM, Herron BJ, Ferland RJ.

Epilepsy Res. 2009 Dec;87(2-3):130-6. doi: 10.1016/j.eplepsyres.2009.08.003. Epub 2009 Sep 9.

26.

Nodular heterotopia is built upon layers.

Ferland RJ, Guerrini R.

Neurology. 2009 Sep 8;73(10):742-3. doi: 10.1212/WNL.0b013e3181b529b1. Epub 2009 Jul 22. No abstract available. Erratum in: Neurology. 2009 Dec 1;73(22):1935.

PMID:
19625704
27.

Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking.

Hsiao YC, Tong ZJ, Westfall JE, Ault JG, Page-McCaw PS, Ferland RJ.

Hum Mol Genet. 2009 Oct 15;18(20):3926-41. doi: 10.1093/hmg/ddp335. Epub 2009 Jul 22.

28.

Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia.

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, Guerrini R, Walsh CA, Rodriguez EM, Sheen VL.

Hum Mol Genet. 2009 Feb 1;18(3):497-516. doi: 10.1093/hmg/ddn377. Epub 2008 Nov 7.

29.

Dissociation of seizure traits in inbred strains of mice using the flurothyl kindling model of epileptogenesis.

Papandrea D, Anderson TM, Herron BJ, Ferland RJ.

Exp Neurol. 2009 Jan;215(1):60-8. doi: 10.1016/j.expneurol.2008.09.016. Epub 2008 Oct 7.

30.

Species differences in the expression of Ahi1, a protein implicated in the neurodevelopmental disorder Joubert syndrome, with preferential accumulation to stigmoid bodies.

Doering JE, Kane K, Hsiao YC, Yao C, Shi B, Slowik AD, Dhagat B, Scott DD, Ault JG, Page-McCaw PS, Ferland RJ.

J Comp Neurol. 2008 Nov 10;511(2):238-56. doi: 10.1002/cne.21824.

31.

Identifying autism loci and genes by tracing recent shared ancestry.

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, Ertelt JA, Apse KA, Bodell A, Partlow JN, Barry B, Yao H, Markianos K, Ferland RJ, Greenberg ME, Walsh CA.

Science. 2008 Jul 11;321(5886):218-23. doi: 10.1126/science.1157657. Erratum in: Science. 2010 Dec 24;330(6012):1746.

32.

Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens".

Yu F, Hill RS, Schaffner SF, Sabeti PC, Wang ET, Mignault AA, Ferland RJ, Moyzis RK, Walsh CA, Reich D.

Science. 2007 Apr 20;316(5823):370.

33.

Periventricular nodular heterotopia and Williams syndrome.

Ferland RJ, Gaitanis JN, Apse K, Tantravahi U, Walsh CA, Sheen VL.

Am J Med Genet A. 2006 Jun 15;140(12):1305-11.

PMID:
16691586
34.

Impaired proliferation and migration in human Miller-Dieker neural precursors.

Sheen VL, Ferland RJ, Harney M, Hill RS, Neal J, Banham AH, Brown P, Chenn A, Corbo J, Hecht J, Folkerth R, Walsh CA.

Ann Neurol. 2006 Jul;60(1):137-44.

PMID:
16642511
35.

Neocortical neuronal arrangement in Miller Dieker syndrome.

Sheen VL, Ferland RJ, Neal J, Harney M, Hill RS, Banham A, Brown P, Chenn A, Corbo J, Hecht J, Folkerth R, Walsh CA.

Acta Neuropathol. 2006 May;111(5):489-96. Epub 2006 Feb 3.

PMID:
16456669
36.
37.

The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation.

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, Shohat M.

J Med Genet. 2006 Mar;43(3):203-10. Epub 2005 Jul 20.

38.

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.

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.

Nat Genet. 2004 Sep;36(9):1008-13. Epub 2004 Aug 22. Erratum in: Nat Genet. 2004 Oct;36(10):1126.

PMID:
15322546
39.

Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain.

Ferland RJ, Cherry TJ, Preware PO, Morrisey EE, Walsh CA.

J Comp Neurol. 2003 May 26;460(2):266-79.

PMID:
12687690
40.
42.
43.

Patient satisfaction with laparoscopic Burch retropubic urethropexy.

Myers DL, Peipert JF, Rosenblatt PL, Ferland RJ, Jackson ND; George Anderson Outcomes Measurement Unit.

J Reprod Med. 2000 Nov;45(11):939-43.

PMID:
11127109
44.

The emerging role of uterine artery embolization in the management of symptomatic uterine fibroids.

Dubel GJ, Ferland RJ, Murphy TP, Frishman G.

Med Health R I. 2000 Oct;83(10):305-11. Review. No abstract available.

PMID:
11070680
46.

The role of the ventromedial nucleus of the hypothalamus in epileptogenesis.

Ferland RJ, Applegate CD.

Neuroreport. 1998 Nov 16;9(16):3623-9. Erratum in: Neuroreport 2000 Mar 20;11(4):inside back cover, 899.

PMID:
9858370
47.

A role for the bilateral involvement of perirhinal cortex in generalized kindled seizure expression.

Ferland RJ, Nierenberg J, Applegate CD.

Exp Neurol. 1998 May;151(1):124-37.

PMID:
9582260
49.

Analysis of the importance of controllable versus uncontrollable stress on subsequent behavioral and physiological functioning.

Drugan RC, Basile AS, Ha JH, Healy D, Ferland RJ.

Brain Res Brain Res Protoc. 1997 Dec 1;2(1):69-74.

PMID:
9438074
50.

Laparoscopic-assisted vaginal hysterectomy using the laparosonic coagulating shears.

Robbins ML, Ferland RJ.

J Am Assoc Gynecol Laparosc. 1995 May;2(3):339-43.

PMID:
9050581

Supplemental Content

Loading ...
Support Center