Rebecca D. Burdine - Publications

Molecular Biology Princeton University, Princeton, NJ 
Molecular Biology, Human Development

73 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Willgoss T, Cassater D, Connor S, Krishnan ML, Miller MT, Dias-Barbosa C, Phillips D, McCormack J, Bird LM, Burdine RD, Claridge S, Bichell TJ. Measuring What Matters to Individuals with Angelman Syndrome and Their Families: Development of a Patient-Centered Disease Concept Model. Child Psychiatry and Human Development. PMID 32880036 DOI: 10.1007/s10578-020-01051-z  0.04
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  1
2019 Gripp KW, Schill L, Schoyer L, Stronach B, Bennett AM, Blaser S, Brown A, Burdine R, Burkitt-Wright E, Castel P, Darilek S, Dias A, Dyer T, Ellis M, Erickson G, et al. The sixth international RASopathies symposium: Precision medicine-From promise to practice. American Journal of Medical Genetics. Part A. PMID 31825160 DOI: 10.1002/ajmg.a.61434  1
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  1
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  1
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  1
2018 Kolevzon A, Bird LM, Burdine RD, During M, Grieco J, Visootsak J, Thibert RL. 3.1 Topline Results From a Phase 2 Adult and Adolescent Angelman Syndrome Clinical Trial: A Randomized, Double-Blind, Safety and Efficacy Study of Gaboxadol (Ov101) Journal of the American Academy of Child & Adolescent Psychiatry. 57: S182. DOI: 10.1016/j.jaac.2018.09.159  0.01
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  1
2017 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, et al. Guidelines for morpholino use in zebrafish. Plos Genetics. 13: e1007000. PMID 29049395 DOI: 10.1371/journal.pgen.1007000  1
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  1
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  1
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  1
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  1
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  1
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  0.01
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  0.01
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2013 Burdine RD, Caspary T. Left-right asymmetry: lessons from Cancún. Development (Cambridge, England). 140: 4465-70. PMID 24194469 DOI: 10.1242/dev.097907  1
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  1
2013 Park CY, Wong AK, Greene CS, Rowland J, Guan Y, Bongo LA, Burdine RD, Troyanskaya OG. Functional knowledge transfer for high-accuracy prediction of under-studied biological processes. Plos Computational Biology. 9: e1002957. PMID 23516347 DOI: 10.1371/journal.pcbi.1002957  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  0.01
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  0.01
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  0.01
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  1
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  0.01
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  0.01
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  0.01
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  0.04
2008 Schötz EM, Burdine RD, Jülicher F, Steinberg MS, Heisenberg CP, Foty RA. Quantitative differences in tissue surface tension influence zebrafish germ layer positioning. Hfsp Journal. 2: 42-56. PMID 19404452 DOI: 10.2976/1.2834817  1
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: 10.1002/dvdy.21730  1
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  1
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  1
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  1
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  0.01
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  0.04
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  0.01
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  0.01
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  1
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  1
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  0.01
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  0.01
2006 Okabe N, Burdine RD. KUPFFER'S vesicle in zebrafish Developmental Biology. 295: 441-442. DOI: 10.1016/j.ydbio.2006.04.358  0.01
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  1
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  1
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  0.01
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  1
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  1
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  1
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  1
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  1
2000 Burdine RD, Schier AF. Conserved and divergent mechanisms in left-right axis formation. Genes & Development. 14: 763-76. PMID 10766733  1
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  1
1998 Burdine RD, Branda CS, Stern MJ. EGL-17(FGF) expression coordinates the attraction of the migrating sex myoblasts with vulval induction in C. elegans. Development (Cambridge, England). 125: 1083-93. PMID 9463355  1
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  1
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