Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 50

1.

ZNRF3 functions in mammalian sex determination by inhibiting canonical WNT signaling.

Harris A, Siggers P, Corrochano S, Warr N, Sagar D, Grimes DT, Suzuki M, Burdine RD, Cong F, Koo BK, Clevers H, Stévant I, Nef S, Wells S, Brauner R, Ben Rhouma B, Belguith N, Eozenou C, Bignon-Topalovic J, Bashamboo A, McElreavey K, Greenfield A.

Proc Natl Acad Sci U S A. 2018 May 22;115(21):5474-5479. doi: 10.1073/pnas.1801223115. Epub 2018 May 7.

2.

Gdf3 is required for robust Nodal signaling during germ layer formation and left-right patterning.

Pelliccia JL, Jindal GA, Burdine RD.

Elife. 2017 Nov 15;6. pii: e28635. doi: 10.7554/eLife.28635.

3.

Guidelines for morpholino use in zebrafish.

Stainier DYR, Raz E, Lawson ND, Ekker SC, Burdine RD, Eisen JS, Ingham PW, Schulte-Merker S, Yelon D, Weinstein BM, Mullins MC, Wilson SW, Ramakrishnan L, Amacher SL, Neuhauss SCF, Meng A, Mochizuki N, Panula P, Moens CB.

PLoS Genet. 2017 Oct 19;13(10):e1007000. doi: 10.1371/journal.pgen.1007000. eCollection 2017 Oct. No abstract available.

4.

How activating mutations affect MEK1 regulation and function.

Jindal GA, Goyal Y, Humphreys JM, Yeung E, Tian K, Patterson VL, He H, Burdine RD, Goldsmith EJ, Shvartsman SY.

J Biol Chem. 2017 Nov 17;292(46):18814-18820. doi: 10.1074/jbc.C117.806067. Epub 2017 Oct 10.

5.

Left-Right Patterning: Breaking Symmetry to Asymmetric Morphogenesis.

Grimes DT, Burdine RD.

Trends Genet. 2017 Sep;33(9):616-628. doi: 10.1016/j.tig.2017.06.004. Epub 2017 Jul 15. Review.

6.

Modeling Syndromic Congenital Heart Defects in Zebrafish.

Grant MG, Patterson VL, Grimes DT, Burdine RD.

Curr Top Dev Biol. 2017;124:1-40. doi: 10.1016/bs.ctdb.2016.11.010. Epub 2017 Jan 24. Review.

PMID:
28335857
7.

Divergent effects of intrinsically active MEK variants on developmental Ras signaling.

Goyal Y, Jindal GA, Pelliccia JL, Yamaya K, Yeung E, Futran AS, Burdine RD, Schüpbach T, Shvartsman SY.

Nat Genet. 2017 Mar;49(3):465-469. doi: 10.1038/ng.3780. Epub 2017 Feb 6.

8.

In vivo severity ranking of Ras pathway mutations associated with developmental disorders.

Jindal GA, Goyal Y, Yamaya K, Futran AS, Kountouridis I, Balgobin CA, Schüpbach T, Burdine RD, Shvartsman SY.

Proc Natl Acad Sci U S A. 2017 Jan 17;114(3):510-515. doi: 10.1073/pnas.1615651114. Epub 2017 Jan 3.

9.
10.

Zebrafish models of idiopathic scoliosis link cerebrospinal fluid flow defects to spine curvature.

Grimes DT, Boswell CW, Morante NF, Henkelman RM, Burdine RD, Ciruna B.

Science. 2016 Jun 10;352(6291):1341-4. doi: 10.1126/science.aaf6419.

11.

c21orf59/kurly Controls Both Cilia Motility and Polarization.

Jaffe KM, Grimes DT, Schottenfeld-Roames J, Werner ME, Ku TS, Kim SK, Pelliccia JL, Morante NF, Mitchell BJ, Burdine RD.

Cell Rep. 2016 Mar 1;14(8):1841-9. doi: 10.1016/j.celrep.2016.01.069. Epub 2016 Feb 18.

12.

RASopathies: unraveling mechanisms with animal models.

Jindal GA, Goyal Y, Burdine RD, Rauen KA, Shvartsman SY.

Dis Model Mech. 2015 Sep;8(9):1167. doi: 10.1242/dmm.022442. No abstract available.

13.

RASopathies: unraveling mechanisms with animal models.

Jindal GA, Goyal Y, Burdine RD, Rauen KA, Shvartsman SY.

Dis Model Mech. 2015 Aug 1;8(8):769-82. doi: 10.1242/dmm.020339. Review. Erratum in: Dis Model Mech. 2015 Sep;8(9):1167.

14.

Prolonged, brain-wide expression of nuclear-localized GCaMP3 for functional circuit mapping.

Kim CK, Miri A, Leung LC, Berndt A, Mourrain P, Tank DW, Burdine RD.

Front Neural Circuits. 2014 Nov 26;8:138. doi: 10.3389/fncir.2014.00138. eCollection 2014.

15.

CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation.

Hjeij R, Onoufriadis A, Watson CM, Slagle CE, Klena NT, Dougherty GW, Kurkowiak M, Loges NT, Diggle CP, Morante NF, Gabriel GC, Lemke KL, Li Y, Pennekamp P, Menchen T, Konert F, Marthin JK, Mans DA, Letteboer SJ, Werner C, Burgoyne T, Westermann C, Rutman A, Carr IM, O'Callaghan C, Moya E, Chung EM; UK10K Consortium, Sheridan E, Nielsen KG, Roepman R, Bartscherer K, Burdine RD, Lo CW, Omran H, Mitchison HM.

Am J Hum Genet. 2014 Sep 4;95(3):257-74. doi: 10.1016/j.ajhg.2014.08.005.

16.

Left-right asymmetry: lessons from Cancún.

Burdine RD, Caspary T.

Development. 2013 Nov;140(22):4465-70. doi: 10.1242/dev.097907.

17.

DYX1C1 is required for axonemal dynein assembly and ciliary motility.

Tarkar A, Loges NT, Slagle CE, Francis R, Dougherty GW, Tamayo JV, Shook B, Cantino M, Schwartz D, Jahnke C, Olbrich H, Werner C, Raidt J, Pennekamp P, Abouhamed M, Hjeij R, Köhler G, Griese M, Li Y, Lemke K, Klena N, Liu X, Gabriel G, Tobita K, Jaspers M, Morgan LC, Shapiro AJ, Letteboer SJ, Mans DA, Carson JL, Leigh MW, Wolf WE, Chen S, Lucas JS, Onoufriadis A, Plagnol V, Schmidts M, Boldt K; UK10K, Roepman R, Zariwala MA, Lo CW, Mitchison HM, Knowles MR, Burdine RD, Loturco JJ, Omran H.

Nat Genet. 2013 Sep;45(9):995-1003. doi: 10.1038/ng.2707. Epub 2013 Jul 21.

18.

Functional knowledge transfer for high-accuracy prediction of under-studied biological processes.

Park CY, Wong AK, Greene CS, Rowland J, Guan Y, Bongo LA, Burdine RD, Troyanskaya OG.

PLoS Comput Biol. 2013;9(3):e1002957. doi: 10.1371/journal.pcbi.1002957. Epub 2013 Mar 14.

19.

Integration of nodal and BMP signals in the heart requires FoxH1 to create left-right differences in cell migration rates that direct cardiac asymmetry.

Lenhart KF, Holtzman NG, Williams JR, Burdine RD.

PLoS Genet. 2013;9(1):e1003109. doi: 10.1371/journal.pgen.1003109. Epub 2013 Jan 24.

20.

CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms.

Panizzi JR, Becker-Heck A, Castleman VH, Al-Mutairi DA, Liu Y, Loges NT, Pathak N, Austin-Tse C, Sheridan E, Schmidts M, Olbrich H, Werner C, Häffner K, Hellman N, Chodhari R, Gupta A, Kramer-Zucker A, Olale F, Burdine RD, Schier AF, O'Callaghan C, Chung EM, Reinhardt R, Mitchison HM, King SM, Omran H, Drummond IA.

Nat Genet. 2012 May 13;44(6):714-9. doi: 10.1038/ng.2277.

21.

Adeno-associated virus-mediated rescue of the cognitive defects in a mouse model for Angelman syndrome.

Daily JL, Nash K, Jinwal U, Golde T, Rogers J, Peters MM, Burdine RD, Dickey C, Banko JL, Weeber EJ.

PLoS One. 2011;6(12):e27221. doi: 10.1371/journal.pone.0027221. Epub 2011 Dec 9.

22.

Two additional midline barriers function with midline lefty1 expression to maintain asymmetric Nodal signaling during left-right axis specification in zebrafish.

Lenhart KF, Lin SY, Titus TA, Postlethwait JH, Burdine RD.

Development. 2011 Oct;138(20):4405-10. doi: 10.1242/dev.071092.

23.

Examining the establishment of cellular axes using intrinsic chirality.

McSheene JC, Burdine RD.

Proc Natl Acad Sci U S A. 2011 Jul 26;108(30):12191-2. doi: 10.1073/pnas.1109367108. Epub 2011 Jul 18. No abstract available.

24.

Nodal-dependent mesendoderm specification requires the combinatorial activities of FoxH1 and Eomesodermin.

Slagle CE, Aoki T, Burdine RD.

PLoS Genet. 2011 May;7(5):e1002072. doi: 10.1371/journal.pgen.1002072. Epub 2011 May 26.

25.

The exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypes.

Fogelgren B, Lin SY, Zuo X, Jaffe KM, Park KM, Reichert RJ, Bell PD, Burdine RD, Lipschutz JH.

PLoS Genet. 2011 Apr;7(4):e1001361. doi: 10.1371/journal.pgen.1001361. Epub 2011 Apr 7.

26.

Embedding, serial sectioning and staining of zebrafish embryos using JB-4 resin.

Sullivan-Brown J, Bisher ME, Burdine RD.

Nat Protoc. 2011 Jan;6(1):46-55. doi: 10.1038/nprot.2010.165. Epub 2010 Dec 16.

27.

The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation.

Becker-Heck A, Zohn IE, Okabe N, Pollock A, Lenhart KB, Sullivan-Brown J, McSheene J, Loges NT, Olbrich H, Haeffner K, Fliegauf M, Horvath J, Reinhardt R, Nielsen KG, Marthin JK, Baktai G, Anderson KV, Geisler R, Niswander L, Omran H, Burdine RD.

Nat Genet. 2011 Jan;43(1):79-84. doi: 10.1038/ng.727. Epub 2010 Dec 5.

28.

Regression-based identification of behavior-encoding neurons during large-scale optical imaging of neural activity at cellular resolution.

Miri A, Daie K, Burdine RD, Aksay E, Tank DW.

J Neurophysiol. 2011 Feb;105(2):964-80. doi: 10.1152/jn.00702.2010. Epub 2010 Nov 17.

29.

Categorical data analysis in experimental biology.

Xu B, Feng X, Burdine RD.

Dev Biol. 2010 Dec 1;348(1):3-11. doi: 10.1016/j.ydbio.2010.08.018. Epub 2010 Sep 6. Review.

30.

Imaging cilia in zebrafish.

Jaffe KM, Thiberge SY, Bisher ME, Burdine RD.

Methods Cell Biol. 2010;97:415-35. doi: 10.1016/S0091-679X(10)97022-2. Review.

PMID:
20719283
31.

More than maintenance? A role for IFT genes in planar cell polarity.

Jaffe KM, Burdine RD.

J Am Soc Nephrol. 2010 Aug;21(8):1240-1. doi: 10.1681/ASN.2010060665. Epub 2010 Jul 22. No abstract available.

32.

Mutations in zebrafish leucine-rich repeat-containing six-like affect cilia motility and result in pronephric cysts, but have variable effects on left-right patterning.

Serluca FC, Xu B, Okabe N, Baker K, Lin SY, Sullivan-Brown J, Konieczkowski DJ, Jaffe KM, Bradner JM, Fishman MC, Burdine RD.

Development. 2009 May;136(10):1621-31. doi: 10.1242/dev.020735.

33.

Fluid dynamics in zebrafish Kupffer's vesicle.

Okabe N, Xu B, Burdine RD.

Dev Dyn. 2008 Dec;237(12):3602-12. doi: 10.1002/dvdy.21730.

34.

Direct and indirect roles for Nodal signaling in two axis conversions during asymmetric morphogenesis of the zebrafish heart.

Baker K, Holtzman NG, Burdine RD.

Proc Natl Acad Sci U S A. 2008 Sep 16;105(37):13924-9. doi: 10.1073/pnas.0802159105. Epub 2008 Sep 10.

35.

SIX2 and BMP4 mutations associate with anomalous kidney development.

Weber S, Taylor JC, Winyard P, Baker KF, Sullivan-Brown J, Schild R, Knüppel T, Zurowska AM, Caldas-Alfonso A, Litwin M, Emre S, Ghiggeri GM, Bakkaloglu A, Mehls O, Antignac C, Network E, Schaefer F, Burdine RD.

J Am Soc Nephrol. 2008 May;19(5):891-903. doi: 10.1681/ASN.2006111282. Epub 2008 Feb 27.

36.

Quantitative differences in tissue surface tension influence zebrafish germ layer positioning.

Schötz EM, Burdine RD, Jülicher F, Steinberg MS, Heisenberg CP, Foty RA.

HFSP J. 2008 Feb;2(1):42-56. doi: 10.2976/1.2834817. Epub 2008 Jan 25.

37.

Zebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants.

Sullivan-Brown J, Schottenfeld J, Okabe N, Hostetter CL, Serluca FC, Thiberge SY, Burdine RD.

Dev Biol. 2008 Feb 15;314(2):261-75. doi: 10.1016/j.ydbio.2007.11.025. Epub 2007 Dec 3.

38.

Nodal signals mediate interactions between the extra-embryonic and embryonic tissues in zebrafish.

Fan X, Hagos EG, Xu B, Sias C, Kawakami K, Burdine RD, Dougan ST.

Dev Biol. 2007 Oct 15;310(2):363-78. Epub 2007 Aug 10.

39.

Zebrafish curly up encodes a Pkd2 ortholog that restricts left-side-specific expression of southpaw.

Schottenfeld J, Sullivan-Brown J, Burdine RD.

Development. 2007 Apr;134(8):1605-15. Epub 2007 Mar 14.

40.

Brain asymmetry: switching from left to right.

Lin SY, Burdine RD.

Curr Biol. 2005 May 10;15(9):R343-5. Review.

41.

pitx3 defines an equivalence domain for lens and anterior pituitary placode.

Dutta S, Dietrich JE, Aspöck G, Burdine RD, Schier A, Westerfield M, Varga ZM.

Development. 2005 Apr;132(7):1579-90. Epub 2005 Feb 23.

42.

Zebrafish pronephros: a model for understanding cystic kidney disease.

Hostetter CL, Sullivan-Brown JL, Burdine RD.

Dev Dyn. 2003 Nov;228(3):514-22.

43.

Alternative splicing affecting a novel domain in the C. elegans EGL-15 FGF receptor confers functional specificity.

Goodman SJ, Branda CS, Robinson MK, Burdine RD, Stern MJ.

Development. 2003 Aug;130(16):3757-66.

44.

A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.

de la Cruz JM, Bamford RN, Burdine RD, Roessler E, Barkovich AJ, Donnai D, Schier AF, Muenke M.

Hum Genet. 2002 May;110(5):422-8. Epub 2002 Apr 10.

PMID:
12073012
45.

A nodal signaling pathway regulates the laterality of neuroanatomical asymmetries in the zebrafish forebrain.

Concha ML, Burdine RD, Russell C, Schier AF, Wilson SW.

Neuron. 2000 Nov;28(2):399-409.

46.

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects.

Bamford RN, Roessler E, Burdine RD, Saplakoğlu U, dela Cruz J, Splitt M, Goodship JA, Towbin J, Bowers P, Ferrero GB, Marino B, Schier AF, Shen MM, Muenke M, Casey B.

Nat Genet. 2000 Nov;26(3):365-9. Erratum in: Nat Genet 2000 Dec;26(4):501.

PMID:
11062482
47.

Conserved and divergent mechanisms in left-right axis formation.

Burdine RD, Schier AF.

Genes Dev. 2000 Apr 1;14(7):763-76. Review. No abstract available.

48.

Conserved requirement for EGF-CFC genes in vertebrate left-right axis formation.

Yan YT, Gritsman K, Ding J, Burdine RD, Corrales JD, Price SM, Talbot WS, Schier AF, Shen MM.

Genes Dev. 1999 Oct 1;13(19):2527-37.

49.
50.

Supplemental Content

Loading ...
Support Center