| Year |
Citation |
Score |
| 2023 |
Patterson V, Ullah F, Bryant L, Griffin JN, Sidhu A, Saliganan S, Blaile M, Saenz MS, Smith R, Ellingwood S, Grange DK, Hu X, Mireguli M, Luo Y, Shen Y, ... ... Burdine R, et al. Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish. Science Advances. 9: eade0631. PMID 37126546 DOI: 10.1126/sciadv.ade0631 |
0.792 |
|
| 2021 |
Maerker M, Getwan M, Dowdle ME, McSheene JC, Gonzalez V, Pelliccia JL, Hamilton DS, Yartseva V, Vejnar C, Tingler M, Minegishi K, Vick P, Giraldez AJ, Hamada H, Burdine RD, et al. Bicc1 and Dicer regulate left-right patterning through post-transcriptional control of the Nodal inhibitor Dand5. Nature Communications. 12: 5482. PMID 34531379 DOI: 10.1038/s41467-021-25464-z |
0.764 |
|
| 2020 |
Patterson VL, Burdine RD. Swimming toward solutions: Using fish and frogs as models for understanding RASopathies. Birth Defects Research. PMID 32506834 DOI: 10.1002/Bdr2.1707 |
0.811 |
|
| 2019 |
Patel AL, Yeung E, McGuire SE, Wu AY, Toettcher JE, Burdine RD, Shvartsman SY. Optimizing photoswitchable MEK. Proceedings of the National Academy of Sciences of the United States of America. PMID 31796593 DOI: 10.1073/Pnas.1912320116 |
0.789 |
|
| 2019 |
Grimes DT, Patterson VL, Luna-Arvizu G, Schottenfeld-Roames J, Irons ZH, Burdine RD. Left-right asymmetric heart jogging increases the robustness of dextral heart looping in zebrafish. Developmental Biology. PMID 31758943 DOI: 10.1016/J.Ydbio.2019.11.012 |
0.798 |
|
| 2018 |
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, et al. ZNRF3 functions in mammalian sex determination by inhibiting canonical WNT signaling. Proceedings of the National Academy of Sciences of the United States of America. PMID 29735715 DOI: 10.1073/Pnas.1801223115 |
0.746 |
|
| 2017 |
Pelliccia JL, Jindal GA, Burdine RD. Gdf3 is required for robust Nodal signaling during germ layer formation and left-right patterning. Elife. 6. PMID 29140250 DOI: 10.7554/Elife.28635 |
0.799 |
|
| 2017 |
Jindal GA, Goyal Y, Humphreys JM, Yeung E, Tian K, Patterson VL, He H, Burdine RD, Shvartsman SY, Goldsmith EJ. How activating mutations affect MEK1 regulation and function. The Journal of Biological Chemistry. PMID 29018093 DOI: 10.1074/Jbc.C117.806067 |
0.786 |
|
| 2017 |
Grimes DT, Burdine RD. Left-Right Patterning: Breaking Symmetry to Asymmetric Morphogenesis. Trends in Genetics : Tig. PMID 28720483 DOI: 10.1016/J.Tig.2017.06.004 |
0.753 |
|
| 2017 |
Grant MG, Patterson VL, Grimes DT, Burdine RD. Modeling Syndromic Congenital Heart Defects in Zebrafish. Current Topics in Developmental Biology. 124: 1-40. PMID 28335857 DOI: 10.1016/Bs.Ctdb.2016.11.010 |
0.764 |
|
| 2017 |
Goyal Y, Jindal GA, Pelliccia JL, Yamaya K, Yeung E, Futran AS, Burdine RD, Schüpbach T, Shvartsman SY. Divergent effects of intrinsically active MEK variants on developmental Ras signaling. Nature Genetics. PMID 28166211 DOI: 10.1038/Ng.3780 |
0.791 |
|
| 2017 |
Jindal GA, Goyal Y, Yamaya K, Futran AS, Kountouridis I, Balgobin CA, Schüpbach T, Burdine RD, Shvartsman SY. In vivo severity ranking of Ras pathway mutations associated with developmental disorders. Proceedings of the National Academy of Sciences of the United States of America. PMID 28049852 DOI: 10.1073/Pnas.1615651114 |
0.809 |
|
| 2017 |
Pelliccia JL, Jindal GA, Burdine RD. Author response: Gdf3 is required for robust Nodal signaling during germ layer formation and left-right patterning Elife. DOI: 10.7554/Elife.28635.025 |
0.784 |
|
| 2017 |
Morante NFC, Grimes DT, Burdine R. Forward and Reverse Genetics to Probe Motile Cilia Defects in Zebrafish Development Mechanisms of Development. 145: S67. DOI: 10.1016/J.Mod.2017.04.150 |
0.739 |
|
| 2017 |
Grimes D, Boswell C, Morante N, Henkelman M, Ciruna B, Burdine R. Linking cilia motility and cerebrospinal fluid flow to the etiopathogenesis of idiopathic scoliosis Mechanisms of Development. 145: S30. DOI: 10.1016/J.Mod.2017.04.026 |
0.755 |
|
| 2016 |
Burdine RD, Grimes DT. Antagonistic interactions in the zebrafish midline prior to the emergence of asymmetric gene expression are important for left-right patterning. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 371. PMID 27821532 DOI: 10.1098/Rstb.2015.0402 |
0.753 |
|
| 2016 |
Grimes DT, Boswell CW, Morante NF, Henkelman RM, Burdine RD, Ciruna B. Zebrafish models of idiopathic scoliosis link cerebrospinal fluid flow defects to spine curvature. Science (New York, N.Y.). 352: 1341-4. PMID 27284198 DOI: 10.1126/Science.Aaf6419 |
0.794 |
|
| 2016 |
Jaffe KM, Grimes DT, Schottenfeld-Roames J, Werner ME, Ku TJ, Kim SK, Pelliccia JL, Morante NF, Mitchell BJ, Burdine RD. c21orf59/kurly Controls Both Cilia Motility and Polarization. Cell Reports. PMID 26904945 DOI: 10.1016/J.Celrep.2016.01.069 |
0.765 |
|
| 2015 |
Jindal GA, Goyal Y, Burdine RD, Rauen KA, Shvartsman SY. RASopathies: unraveling mechanisms with animal models. Disease Models & Mechanisms. 8: 1167. PMID 26398161 DOI: 10.1242/Dmm.022442 |
0.757 |
|
| 2015 |
Jindal GA, Goyal Y, Burdine RD, Rauen KA, Shvartsman SY. RASopathies: unraveling mechanisms with animal models. Disease Models & Mechanisms. 8: 769-82. PMID 26203125 DOI: 10.1242/Dmm.020339 |
0.804 |
|
| 2015 |
Onoufriadis A, Hjeij R, 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, ... ... Burdine RD, et al. Gene discovery for motile cilia disorders: mutation spectrum in primary ciliary dyskinesia and discovery of mutations in CCDC151 Cilia. 4: 30. DOI: 10.1186/2046-2530-4-S1-P30 |
0.812 |
|
| 2014 |
Kim CK, Miri A, Leung LC, Berndt A, Mourrain P, Tank DW, Burdine RD. Prolonged, brain-wide expression of nuclear-localized GCaMP3 for functional circuit mapping. Frontiers in Neural Circuits. 8: 138. PMID 25505384 DOI: 10.3389/Fncir.2014.00138 |
0.71 |
|
| 2014 |
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, ... ... Burdine RD, et al. CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation. American Journal of Human Genetics. 95: 257-74. PMID 25192045 DOI: 10.1016/J.Ajhg.2014.08.005 |
0.799 |
|
| 2013 |
Burdine RD, Caspary T. Left-right asymmetry: lessons from Cancún. Development (Cambridge, England). 140: 4465-70. PMID 24194469 DOI: 10.1242/Dev.097907 |
0.324 |
|
| 2013 |
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, ... ... Burdine RD, et al. DYX1C1 is required for axonemal dynein assembly and ciliary motility. Nature Genetics. 45: 995-1003. PMID 23872636 DOI: 10.1038/Ng.2707 |
0.806 |
|
| 2013 |
Lenhart KF, Holtzman NG, Williams JR, Burdine RD. Integration of nodal and BMP signals in the heart requires FoxH1 to create left-right differences in cell migration rates that direct cardiac asymmetry. Plos Genetics. 9: e1003109. PMID 23358434 DOI: 10.1371/Journal.Pgen.1003109 |
0.802 |
|
| 2012 |
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, ... ... Burdine RD, et al. CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms. Nature Genetics. 44: 714-9. PMID 22581229 DOI: 10.1038/Ng.2277 |
0.816 |
|
| 2012 |
Burdine R, Slagle C. Loss of outer arm dynein components produce specific and separable phenotypes in zebrafish Cilia. 1: 1-1. DOI: 10.1186/2046-2530-1-S1-O17 |
0.823 |
|
| 2011 |
Daily JL, Nash K, Jinwal U, Golde T, Rogers J, Peters MM, Burdine RD, Dickey C, Banko JL, Weeber EJ. Adeno-associated virus-mediated rescue of the cognitive defects in a mouse model for Angelman syndrome. Plos One. 6: e27221. PMID 22174738 DOI: 10.1371/Journal.Pone.0027221 |
0.32 |
|
| 2011 |
Lenhart KF, Lin SY, Titus TA, Postlethwait JH, Burdine RD. Two additional midline barriers function with midline lefty1 expression to maintain asymmetric Nodal signaling during left-right axis specification in zebrafish. Development (Cambridge, England). 138: 4405-10. PMID 21937597 DOI: 10.1242/Dev.071092 |
0.8 |
|
| 2011 |
McSheene JC, Burdine RD. Examining the establishment of cellular axes using intrinsic chirality. Proceedings of the National Academy of Sciences of the United States of America. 108: 12191-2. PMID 21768357 DOI: 10.1073/Pnas.1109367108 |
0.798 |
|
| 2011 |
Slagle CE, Aoki T, Burdine RD. Nodal-dependent mesendoderm specification requires the combinatorial activities of FoxH1 and Eomesodermin. Plos Genetics. 7: e1002072. PMID 21637786 DOI: 10.1371/Journal.Pgen.1002072 |
0.814 |
|
| 2011 |
Fogelgren B, Lin SY, Zuo X, Jaffe KM, Park KM, Reichert RJ, Bell PD, Burdine RD, Lipschutz JH. The exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypes. Plos Genetics. 7: e1001361. PMID 21490950 DOI: 10.1371/Journal.Pgen.1001361 |
0.797 |
|
| 2011 |
Sullivan-Brown J, Bisher ME, Burdine RD. Embedding, serial sectioning and staining of zebrafish embryos using JB-4 resin. Nature Protocols. 6: 46-55. PMID 21212782 DOI: 10.1038/Nprot.2010.165 |
0.752 |
|
| 2011 |
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, ... ... Burdine RD, et al. The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation. Nature Genetics. 43: 79-84. PMID 21131974 DOI: 10.1038/Ng.727 |
0.801 |
|
| 2011 |
Miri A, Daie K, Burdine RD, Aksay E, Tank DW. Regression-based identification of behavior-encoding neurons during large-scale optical imaging of neural activity at cellular resolution. Journal of Neurophysiology. 105: 964-80. PMID 21084686 DOI: 10.1152/Jn.00702.2010 |
0.679 |
|
| 2010 |
Xu B, Feng X, Burdine RD. Categorical data analysis in experimental biology. Developmental Biology. 348: 3-11. PMID 20826130 DOI: 10.1016/J.Ydbio.2010.08.018 |
0.324 |
|
| 2010 |
Jaffe KM, Thiberge SY, Bisher ME, Burdine RD. Imaging cilia in zebrafish. Methods in Cell Biology. 97: 415-35. PMID 20719283 DOI: 10.1016/S0091-679X(10)97022-2 |
0.638 |
|
| 2010 |
Jaffe KM, Burdine RD. More than maintenance? A role for IFT genes in planar cell polarity. Journal of the American Society of Nephrology : Jasn. 21: 1240-1. PMID 20651164 DOI: 10.1681/Asn.2010060665 |
0.636 |
|
| 2010 |
McSheene J, Burdine R. The role of pkd2 in zebrafish embryonic nodal patterning Developmental Biology. 344: 476. DOI: 10.1016/J.Ydbio.2010.05.251 |
0.787 |
|
| 2010 |
Rowland JR, Baker K, Burdine RD. Identifying mechanisms which control asymmetric development of the zebrafish heart Developmental Biology. 344: 448-449. DOI: 10.1016/J.Ydbio.2010.05.148 |
0.313 |
|
| 2010 |
Burdine RD, Xu B. Establishment of left–right asymmetry in zebrafish: Surprising predictions from a modeling approach Developmental Biology. 344: 426. DOI: 10.1016/J.Ydbio.2010.05.070 |
0.354 |
|
| 2009 |
Serluca FC, Xu B, Okabe N, Baker K, Lin SY, Sullivan-Brown J, Konieczkowski DJ, Jaffe KM, Bradner JM, Fishman MC, Burdine RD. 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. Development (Cambridge, England). 136: 1621-31. PMID 19395640 DOI: 10.1242/Dev.020735 |
0.819 |
|
| 2009 |
Baker KF, Burdine RD. Investigating the role of TGFbeta signaling in asymmetric morphogenesis of the zebrafish heart Developmental Biology. 331: 493. DOI: 10.1016/J.Ydbio.2009.05.402 |
0.348 |
|
| 2009 |
Xu B, Serluca FC, Okabe N, Baker K, Lin S, Sullivan-Brown J, Konieczkowski DJ, Jaffe KM, Fishman MC, Burdine RD. Mutations in the cilia motility gene seahorse, result in pronephric cysts, but have variable effects on left–-right patterning Developmental Biology. 331: 426. DOI: 10.1016/J.Ydbio.2009.05.141 |
0.785 |
|
| 2009 |
Jaffe KM, Burdine RD. Investigating the role of a novel mutation during zebrafish left–right patterning Developmental Biology. 331: 424. DOI: 10.1016/J.Ydbio.2009.05.135 |
0.672 |
|
| 2009 |
Lin S, Carter SB, Burdine RD. Investigating the genetic basis of left–right asymmetry in the zebrafish Developmental Biology. 331: 424. DOI: 10.1016/J.Ydbio.2009.05.133 |
0.632 |
|
| 2008 |
Okabe N, Xu B, Burdine RD. Fluid dynamics in zebrafish Kupffer's vesicle. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 3602-12. PMID 18924242 DOI: 10.1016/J.Ydbio.2008.05.398 |
0.784 |
|
| 2008 |
Baker K, Holtzman NG, Burdine RD. Direct and indirect roles for Nodal signaling in two axis conversions during asymmetric morphogenesis of the zebrafish heart. Proceedings of the National Academy of Sciences of the United States of America. 105: 13924-9. PMID 18784369 DOI: 10.1073/Pnas.0802159105 |
0.391 |
|
| 2008 |
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, ... ... Burdine RD, et al. SIX2 and BMP4 mutations associate with anomalous kidney development. Journal of the American Society of Nephrology : Jasn. 19: 891-903. PMID 18305125 DOI: 10.1681/Asn.2006111282 |
0.796 |
|
| 2008 |
Sullivan-Brown J, Schottenfeld J, Okabe N, Hostetter CL, Serluca FC, Thiberge SY, Burdine RD. Zebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants. Developmental Biology. 314: 261-75. PMID 18178183 DOI: 10.1016/J.Ydbio.2007.11.025 |
0.804 |
|
| 2008 |
Baker K, Holtzman NG, Burdine RD. Nodal dependent and independent axis conversions during asymmetric morphogenesis of the zebrafish heart Developmental Biology. 319: 602-603. DOI: 10.1016/J.Ydbio.2008.05.438 |
0.314 |
|
| 2008 |
Lin S, Burdine R. Investigating the role of schnitter during zebrafish brain development Developmental Biology. 319: 581-582. DOI: 10.1016/J.Ydbio.2008.05.406 |
0.619 |
|
| 2008 |
Xu B, Burdine RD. Systematic modeling analysis of one-eyed pinhead involved Nodal signaling in zebrafish development Developmental Biology. 319: 581. DOI: 10.1016/J.Ydbio.2008.05.405 |
0.426 |
|
| 2008 |
Schottenfeld J, Burdine RD. A role for kurly in left-right patterning, kidney cysts, and cilia Developmental Biology. 319: 483-484. DOI: 10.1016/J.Ydbio.2008.05.064 |
0.794 |
|
| 2007 |
Fan X, Hagos EG, Xu B, Sias C, Kawakami K, Burdine RD, Dougan ST. Nodal signals mediate interactions between the extra-embryonic and embryonic tissues in zebrafish. Developmental Biology. 310: 363-78. PMID 17850782 DOI: 10.1016/J.Ydbio.2007.08.008 |
0.463 |
|
| 2007 |
Schottenfeld J, Sullivan-Brown J, Burdine RD. Zebrafish curly up encodes a Pkd2 ortholog that restricts left-side-specific expression of southpaw. Development (Cambridge, England). 134: 1605-15. PMID 17360770 DOI: 10.1242/Dev.02827 |
0.815 |
|
| 2006 |
Sullivan-Brown J, Burdine RD. Using zebrafish to study the cellular and molecular defects in renal cystic disease Developmental Biology. 295: 458-459. DOI: 10.1016/J.Ydbio.2006.04.412 |
0.762 |
|
| 2006 |
Schottenfeld J, Burdine RD. New insights into left–right patterning: The role of pkd2 in the zebrafish Developmental Biology. 295: 442. DOI: 10.1016/J.Ydbio.2006.04.362 |
0.783 |
|
| 2006 |
Okabe N, Burdine RD. KUPFFER'S vesicle in zebrafish Developmental Biology. 295: 441-442. DOI: 10.1016/J.Ydbio.2006.04.358 |
0.751 |
|
| 2005 |
Lin SY, Burdine RD. Brain asymmetry: switching from left to right. Current Biology : Cb. 15: R343-5. PMID 15886094 DOI: 10.1016/J.Cub.2005.04.026 |
0.645 |
|
| 2005 |
Dutta S, Dietrich JE, Aspöck G, Burdine RD, Schier A, Westerfield M, Varga ZM. pitx3 defines an equivalence domain for lens and anterior pituitary placode. Development (Cambridge, England). 132: 1579-90. PMID 15728669 DOI: 10.1242/Dev.01723 |
0.563 |
|
| 2005 |
Bisher M, Sullivan-Brown J, Rosen J, Burdine R. Morphological Analysis of Zebrafish Embryos Using JB-4 Resin Microscopy and Microanalysis. 11. DOI: 10.1017/S1431927605507979 |
0.766 |
|
| 2003 |
Hostetter CL, Sullivan-Brown JL, Burdine RD. Zebrafish pronephros: a model for understanding cystic kidney disease. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 228: 514-22. PMID 14579389 DOI: 10.1002/Dvdy.10371 |
0.787 |
|
| 2003 |
Goodman SJ, Branda CS, Robinson MK, Burdine RD, Stern MJ. Alternative splicing affecting a novel domain in the C. elegans EGL-15 FGF receptor confers functional specificity. Development (Cambridge, England). 130: 3757-66. PMID 12835392 DOI: 10.1242/Dev.00604 |
0.589 |
|
| 2002 |
de la Cruz JM, Bamford RN, Burdine RD, Roessler E, Barkovich AJ, Donnai D, Schier AF, Muenke M. A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects. Human Genetics. 110: 422-8. PMID 12073012 DOI: 10.1007/S00439-002-0709-3 |
0.623 |
|
| 2000 |
Concha ML, Burdine RD, Russell C, Schier AF, Wilson SW. A nodal signaling pathway regulates the laterality of neuroanatomical asymmetries in the zebrafish forebrain. Neuron. 28: 399-409. PMID 11144351 DOI: 10.1016/S0896-6273(00)00120-3 |
0.6 |
|
| 2000 |
Bamford RN, Roessler E, Burdine RD, SaplakoÄŸlu U, dela Cruz J, Splitt M, Goodship JA, Towbin J, Bowers P, Ferrero GB, Marino B, Schier AF, Shen MM, Muenke M, Casey B. Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects. Nature Genetics. 26: 365-9. PMID 11062482 DOI: 10.1038/81695 |
0.628 |
|
| 2000 |
Burdine RD, Schier AF. Conserved and divergent mechanisms in left-right axis formation. Genes & Development. 14: 763-76. PMID 10766733 DOI: 10.1101/Gad.14.7.763 |
0.553 |
|
| 1999 |
Yan YT, Gritsman K, Ding J, Burdine RD, Corrales JD, Price SM, Talbot WS, Schier AF, Shen MM. Conserved requirement for EGF-CFC genes in vertebrate left-right axis formation. Genes & Development. 13: 2527-37. PMID 10521397 DOI: 10.1101/Gad.13.19.2527 |
0.738 |
|
| 1997 |
Burdine RD, Chen EB, Kwok SF, Stern MJ. egl-17 encodes an invertebrate fibroblast growth factor family member required specifically for sex myoblast migration in Caenorhabditis elegans. Proceedings of the National Academy of Sciences of the United States of America. 94: 2433-7. PMID 9122212 DOI: 10.1073/Pnas.94.6.2433 |
0.634 |
|
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