Anthony Firulli - Publications

Anatomy & Cell Biology Indiana University, Bloomington, Bloomington, IN, United States 
Genetics, Human Development

67 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
2021 Vincentz JW, Firulli BA, Toolan KP, Osterwalder M, Pennacchio LA, Firulli AB. HAND transcription factors cooperatively specify the aorta and pulmonary trunk. Developmental Biology. 476: 1-10. PMID 33757801 DOI: 10.1016/j.ydbio.2021.03.011  0.84
2020 Vincentz JW, Clouthier DE, Firulli AB. Mis-Expression of a Cranial Neural Crest Cell-Specific Gene Program in Cardiac Neural Crest Cells Modulates HAND Factor Expression, Causing Cardiac Outflow Tract Phenotypes. Journal of Cardiovascular Development and Disease. 7. PMID 32325975 DOI: 10.3390/jcdd7020013  0.84
2019 Vincentz JW, Firulli BA, Toolan KP, Arking DE, Sotoodehnia N, Wan J, Chen PS, de Gier-de Vries C, Christoffels VM, Rubart-von der Lohe M, Firulli AB. Variation in a Left Ventricle-Specific Hand1 Enhancer Impairs GATA Transcription Factor Binding and Disrupts Conduction System Development and Function. Circulation Research. PMID 31366290 DOI: 10.1161/CIRCRESAHA.119.315313  0.84
2019 Firulli BA, Firulli AB. Partially Penetrant Cardiac Neural Crest Defects in Hand1 Phosphomutant Mice: Dimer Choice That Is Not So Critical. Pediatric Cardiology. PMID 31338559 DOI: 10.1007/s00246-019-02162-8  0.72
2019 Firulli BA, George R, Harkin J, Toolan KP, Gao H, Liu Y, Zhang W, Field LJ, Liu Y, Shou W, Payne RM, Rubart-von der Lohe M, Firulli AB. HAND1 loss-of-function within the embryonic myocardium reveals survivable congenital cardiac defects and adult heart failure. Cardiovascular Research. PMID 31286141 DOI: 10.1093/cvr/cvz182  0.72
2017 Firulli BA, Toolan KP, Harkin J, Millar H, Pineda S, Firulli AB. The HAND1 frameshift A126FS mutation does not cause hypoplastic left heart syndrome in mice. Cardiovascular Research. PMID 29016838 DOI: 10.1093/cvr/cvx166  0.72
2017 Vincentz JW, Toolan KP, Zhang W, Firulli AB. Hand factor ablation causes defective left ventricular chamber development and compromised adult cardiac function. Plos Genetics. 13: e1006922. PMID 28732025 DOI: 10.1371/journal.pgen.1006922  0.84
2017 Firulli BA, Milliar H, Toolan KP, Harkin J, Fuchs RK, Robling AG, Firulli AB. Defective Hand1 phosphoregulation uncovers essential roles for Hand1 in limb morphogenesis. Development (Cambridge, England). PMID 28576769 DOI: 10.1242/dev.149963  0.72
2016 Vincentz JW, Casasnovas JJ, Barnes RM, Que J, Clouthier DE, Wang J, Firulli AB. Exclusion of Dlx5/6 expression from the distal-most mandibular arches enables BMP-mediated specification of the distal cap. Proceedings of the National Academy of Sciences of the United States of America. PMID 27335460 DOI: 10.1073/pnas.1603930113  1
2015 Gajula RP, Chettiar ST, Williams RD, Nugent K, Kato Y, Wang H, Malek R, Taparra K, Cades J, Annadanam A, Yoon AR, Fertig E, Firulli BA, Mazzacurati L, Burns TF, ... Firulli AB, et al. Structure-function studies of the bHLH phosphorylation domain of TWIST1 in prostate cancer cells. Neoplasia (New York, N.Y.). 17: 16-31. PMID 25622896 DOI: 10.1016/j.neo.2014.10.009  0.72
2014 Reuter S, Soonpaa MH, Firulli AB, Chang AN, Field LJ. Recombinant neuregulin 1 does not activate cardiomyocyte DNA synthesis in normal or infarcted adult mice. Plos One. 9: e115871. PMID 25545368 DOI: 10.1371/journal.pone.0115871  1
2014 VanDusen NJ, Casanovas J, Vincentz JW, Firulli BA, Osterwalder M, Lopez-Rios J, Zeller R, Zhou B, Grego-Bessa J, De La Pompa JL, Shou W, Firulli AB. Hand2 is an essential regulator for two Notch-dependent functions within the embryonic endocardium. Cell Reports. 9: 2071-83. PMID 25497097 DOI: 10.1016/j.celrep.2014.11.021  1
2014 Firulli BA, Fuchs RK, Vincentz JW, Clouthier DE, Firulli AB. Hand1 phosphoregulation within the distal arch neural crest is essential for craniofacial morphogenesis. Development (Cambridge, England). 141: 3050-61. PMID 25053435 DOI: 10.1242/dev.107680  1
2014 Schindler YL, Garske KM, Wang J, Firulli BA, Firulli AB, Poss KD, Yelon D. Hand2 elevates cardiomyocyte production during zebrafish heart development and regeneration. Development (Cambridge, England). 141: 3112-22. PMID 25038045 DOI: 10.1242/dev.106336  1
2014 VanDusen NJ, Vincentz JW, Firulli BA, Howard MJ, Rubart M, Firulli AB. Loss of Hand2 in a population of Periostin lineage cells results in pronounced bradycardia and neonatal death. Developmental Biology. 388: 149-58. PMID 24565998 DOI: 10.1016/j.ydbio.2014.02.010  1
2014 Vincentz JW, Firulli AB. The Cardiac Neural Crest and Their Role in Development and Disease Neural Crest Cells: Evolution, Development and Disease. 205-229. DOI: 10.1016/B978-0-12-401730-6.00012-0  1
2013 Zhang W, Firulli AB, Shou W. A glimpse of Cre-mediated controversies in epicardial signalling. Cardiovascular Research. 100: 347-9. PMID 24148896 DOI: 10.1093/cvr/cvt241  1
2013 Pham D, Walline CC, Hollister K, Dent AL, Blum JS, Firulli AB, Kaplan MH. The transcription factor Twist1 limits T helper 17 and T follicular helper cell development by repressing the gene encoding the interleukin-6 receptor α chain. The Journal of Biological Chemistry. 288: 27423-33. PMID 23935104 DOI: 10.1074/jbc.M113.497248  1
2013 Chen H, Zhang W, Sun X, Yoshimoto M, Chen Z, Zhu W, Liu J, Shen Y, Yong W, Li D, Zhang J, Lin Y, Li B, VanDusen NJ, Snider P, ... ... Firulli AB, et al. Fkbp1a controls ventricular myocardium trabeculation and compaction by regulating endocardial Notch1 activity. Development (Cambridge, England). 140: 1946-57. PMID 23571217 DOI: 10.1242/dev.089920  1
2013 Vincentz JW, Firulli BA, Lin A, Spicer DB, Howard MJ, Firulli AB. Twist1 controls a cell-specification switch governing cell fate decisions within the cardiac neural crest. Plos Genetics. 9: e1003405. PMID 23555309 DOI: 10.1371/journal.pgen.1003405  1
2012 Pham D, Vincentz JW, Firulli AB, Kaplan MH. Twist1 regulates Ifng expression in Th1 cells by interfering with Runx3 function. Journal of Immunology (Baltimore, Md. : 1950). 189: 832-40. PMID 22685315 DOI: 10.4049/jimmunol.1200854  1
2012 VanDusen NJ, Firulli AB. Twist factor regulation of non-cardiomyocyte cell lineages in the developing heart. Differentiation; Research in Biological Diversity. 84: 79-88. PMID 22516205 DOI: 10.1016/j.diff.2012.03.002  1
2012 Tao W, Soonpaa MH, Field LJ, Chen PS, Firulli AB, Shou W, Rubart M. Functional screening of intracardiac cell transplants using two-photon fluorescence microscopy. Pediatric Cardiology. 33: 929-37. PMID 22481568 DOI: 10.1007/s00246-012-0314-8  1
2012 Vincentz JW, Rubart M, Firulli AB. Ontogeny of cardiac sympathetic innervation and its implications for cardiac disease. Pediatric Cardiology. 33: 923-8. PMID 22395650 DOI: 10.1007/s00246-012-0248-1  1
2012 Vincentz JW, VanDusen NJ, Fleming AB, Rubart M, Firulli BA, Howard MJ, Firulli AB. A Phox2- and Hand2-dependent Hand1 cis-regulatory element reveals a unique gene dosage requirement for Hand2 during sympathetic neurogenesis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 2110-20. PMID 22323723 DOI: 10.1523/JNEUROSCI.3584-11.2012  1
2011 Zook EC, Krishack PA, Zhang S, Zeleznik-Le NJ, Firulli AB, Witte PL, Le PT. Overexpression of Foxn1 attenuates age-associated thymic involution and prevents the expansion of peripheral CD4 memory T cells. Blood. 118: 5723-31. PMID 21908422 DOI: 10.1182/blood-2011-03-342097  1
2011 Vincentz JW, Barnes RM, Firulli AB. Hand factors as regulators of cardiac morphogenesis and implications for congenital heart defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 91: 485-94. PMID 21462297 DOI: 10.1002/bdra.20796  1
2011 Barnes RM, Firulli BA, VanDusen NJ, Morikawa Y, Conway SJ, Cserjesi P, Vincentz JW, Firulli AB. Hand2 loss-of-function in Hand1-expressing cells reveals distinct roles in epicardial and coronary vessel development. Circulation Research. 108: 940-9. PMID 21350214 DOI: 10.1161/CIRCRESAHA.110.233171  1
2010 Barnes RM, Firulli BA, Conway SJ, Vincentz JW, Firulli AB. Analysis of the Hand1 cell lineage reveals novel contributions to cardiovascular, neural crest, extra-embryonic, and lateral mesoderm derivatives. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 239: 3086-97. PMID 20882677 DOI: 10.1002/dvdy.22428  1
2010 Firulli BA, McConville DP, Byers JS, Vincentz JW, Barnes RM, Firulli AB. Analysis of a Hand1 hypomorphic allele reveals a critical threshold for embryonic viability. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 239: 2748-60. PMID 20737509 DOI: 10.1002/dvdy.22402  1
2010 Tang S, Snider P, Firulli AB, Conway SJ. Trigenic neural crest-restricted Smad7 over-expression results in congenital craniofacial and cardiovascular defects. Developmental Biology. 344: 233-47. PMID 20457144 DOI: 10.1016/j.ydbio.2010.05.004  1
2010 Firulli AB, Firulli BA, Wang J, Rogers RH, Conway SJ. Gene replacement strategies to test the functional redundancy of basic helix-loop-helix transcription factor. Pediatric Cardiology. 31: 438-48. PMID 20155416 DOI: 10.1007/s00246-010-9669-x  1
2010 Holler KL, Hendershot TJ, Troy SE, Vincentz JW, Firulli AB, Howard MJ. Targeted deletion of Hand2 in cardiac neural crest-derived cells influences cardiac gene expression and outflow tract development. Developmental Biology. 341: 291-304. PMID 20144608 DOI: 10.1016/j.ydbio.2010.02.001  1
2010 Conway SJ, Firulli B, Firulli AB. A bHLH code for cardiac morphogenesis. Pediatric Cardiology. 31: 318-24. PMID 20033146 DOI: 10.1007/s00246-009-9608-x  1
2009 Barnes RM, Firulli AB. A twist of insight - the role of Twist-family bHLH factors in development. The International Journal of Developmental Biology. 53: 909-24. PMID 19378251 DOI: 10.1387/ijdb.082747rb  1
2008 Vincentz JW, Barnes RM, Firulli BA, Conway SJ, Firulli AB. Cooperative interaction of Nkx2.5 and Mef2c transcription factors during heart development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 3809-19. PMID 19035347 DOI: 10.1002/dvdy.21803  1
2008 Firulli AB, Conway SJ. Phosphoregulation of Twist1 provides a mechanism of cell fate control. Current Medicinal Chemistry. 15: 2641-7. PMID 18855684 DOI: 10.2174/092986708785908987  1
2008 Vincentz JW, Barnes RM, Rodgers R, Firulli BA, Conway SJ, Firulli AB. An absence of Twist1 results in aberrant cardiac neural crest morphogenesis. Developmental Biology. 320: 131-9. PMID 18539270 DOI: 10.1016/j.ydbio.2008.04.037  1
2008 Hendershot TJ, Liu H, Clouthier DE, Shepherd IT, Coppola E, Studer M, Firulli AB, Pittman DL, Howard MJ. Conditional deletion of Hand2 reveals critical functions in neurogenesis and cell type-specific gene expression for development of neural crest-derived noradrenergic sympathetic ganglion neurons. Developmental Biology. 319: 179-91. PMID 18501887 DOI: 10.1016/j.ydbio.2008.03.036  1
2008 Snider P, Hinton RB, Moreno-Rodriguez RA, Wang J, Rogers R, Lindsley A, Li F, Ingram DA, Menick D, Field L, Firulli AB, Molkentin JD, Markwald R, Conway SJ. Periostin is required for maturation and extracellular matrix stabilization of noncardiomyocyte lineages of the heart. Circulation Research. 102: 752-60. PMID 18296617 DOI: 10.1161/CIRCRESAHA.107.159517  1
2007 Firulli BA, Redick BA, Conway SJ, Firulli AB. Mutations within helix I of Twist1 result in distinct limb defects and variation of DNA binding affinities. The Journal of Biological Chemistry. 282: 27536-46. PMID 17652084 DOI: 10.1074/jbc.M702613200  1
2007 Snider P, Olaopa M, Firulli AB, Conway SJ. Cardiovascular development and the colonizing cardiac neural crest lineage. Thescientificworldjournal. 7: 1090-113. PMID 17619792 DOI: 10.1100/tsw.2007.189  1
2007 Lindsley A, Snider P, Zhou H, Rogers R, Wang J, Olaopa M, Kruzynska-Frejtag A, Koushik SV, Lilly B, Burch JB, Firulli AB, Conway SJ. Identification and characterization of a novel Schwann and outflow tract endocardial cushion lineage-restricted periostin enhancer. Developmental Biology. 307: 340-55. PMID 17540359 DOI: 10.1016/j.ydbio.2007.04.041  1
2005 Firulli BA, Krawchuk D, Centonze VE, Vargesson N, Virshup DM, Conway SJ, Cserjesi P, Laufer E, Firulli AB. Altered Twist1 and Hand2 dimerization is associated with Saethre-Chotzen syndrome and limb abnormalities. Nature Genetics. 37: 373-81. PMID 15735646 DOI: 10.1038/ng1525  1
2004 Firulli AB, Conway SJ. Combinatorial transcriptional interaction within the cardiac neural crest: a pair of HANDs in heart formation. Birth Defects Research. Part C, Embryo Today : Reviews. 72: 151-61. PMID 15269889 DOI: 10.1002/bdrc.20009  1
2004 Centonze VE, Firulli BA, Firulli AB. Fluorescence Resonance Energy Transfer (FRET) as a method to calculate the dimerization strength of basic Helix-Loop-Helix (bHLH) proteins. Biological Procedures Online. 6: 78-82. PMID 15188014 DOI: 10.1251/bpo75  1
2004 Firulli BA, Virshup DM, Firulli AB. Phosphopeptide mapping of proteins ectopically expressed in tissue culture cell lines. Biological Procedures Online. 6: 16-22. PMID 15103396 DOI: 10.1251/bpo69  1
2003 Firulli BA, Howard MJ, McDaid JR, McIlreavey L, Dionne KM, Centonze VE, Cserjesi P, Virshup DM, Firulli AB. PKA, PKC, and the protein phosphatase 2A influence HAND factor function: a mechanism for tissue-specific transcriptional regulation. Molecular Cell. 12: 1225-37. PMID 14636580 DOI: 10.1016/S1097-2765(03)00425-8  1
2003 Xu H, Firulli AB, Zhang X, Howard MJ. HAND2 synergistically enhances transcription of dopamine-beta-hydroxylase in the presence of Phox2a. Developmental Biology. 262: 183-93. PMID 14512028 DOI: 10.1016/S0012-1606(03)00361-0  1
2003 Firulli AB. A HANDful of questions: the molecular biology of the heart and neural crest derivatives (HAND)-subclass of basic helix-loop-helix transcription factors. Gene. 312: 27-40. PMID 12909338 DOI: 10.1016/S0378-1119(03)00669-3  1
2002 Thattaliyath BD, Firulli BA, Firulli AB. The basic-helix-loop-helix transcription factor HAND2 directly regulates transcription of the atrial naturetic peptide gene. Journal of Molecular and Cellular Cardiology. 34: 1335-44. PMID 12392994 DOI: 10.1016/S0022-2828(02)92085-7  1
2002 Firulli AB. Another hat for myocardin. Journal of Molecular and Cellular Cardiology. 34: 1293-6. PMID 12392987 DOI: 10.1016/S0022-2828(02)92098-5  1
2002 Thattaliyath BD, Livi CB, Steinhelper ME, Toney GM, Firulli AB. HAND1 and HAND2 are expressed in the adult-rodent heart and are modulated during cardiac hypertrophy. Biochemical and Biophysical Research Communications. 297: 870-5. PMID 12359233 DOI: 10.1016/S0006-291X(02)02297-0  1
2002 Firulli AB, Thattaliyath BD. Transcription factors in cardiogenesis: the combinations that unlock the mysteries of the heart. International Review of Cytology. 214: 1-62. PMID 11893163 DOI: 10.1016/S0074-7696(02)14002-2  1
2000 McFadden DG, Charité J, Richardson JA, Srivastava D, Firulli AB, Olson EN. A GATA-dependent right ventricular enhancer controls dHAND transcription in the developing heart. Development (Cambridge, England). 127: 5331-41. PMID 11076755  1
2000 Firulli BA, Hadzic DB, McDaid JR, Firulli AB. The basic helix-loop-helix transcription factors dHAND and eHAND exhibit dimerization characteristics that suggest complex regulation of function* Journal of Biological Chemistry. 275: 33567-33573. PMID 10924525 DOI: 10.1074/jbc.M005888200  1
1998 Firulli AB. A comparative molecular analysis of four rat smooth muscle cell lines In Vitro Cellular and Developmental Biology - Animal. 34: 217-226. PMID 9557939 DOI: 10.1007/s11626-998-0127-5  1
1998 Firulli AB, McFadden DG, Lin Q, Srivastava D, Olson EN. Heart and extra-embryonic mesodermal defects in mouse embryos lacking the bHLH transcription factor Hand1. Nature Genetics. 18: 266-70. PMID 9500550 DOI: 10.1038/ng0398-266  1
1997 Firulli AB, Olson EN. Modular regulation of muscle gene transcription: A mechanism for muscle cell diversity Trends in Genetics. 13: 364-369. PMID 9287492 DOI: 10.1016/S0168-9525(97)01171-2  1
1996 Molkentin JD, Firulli AB, Black BL, Martin JF, Hustad CM, Copeland N, Jenkins N, Lyons G, Olson EN. MEF2B is a potent transactivator expressed in early myogenic lineages Molecular and Cellular Biology. 16: 3814-3824. PMID 8668199 DOI: 10.1128/MCB.16.7.3814  1
1996 Firulli AB, Miano JM, Bi W, Johnson AD, Casscells W, Olson EN, Schwarz JJ. Myocyte enhancer binding factor-2 expression and activity in vascular smooth muscle cells: Association with the activated phenotype Circulation Research. 78: 196-204. PMID 8575062 DOI: 10.1161/01.RES.78.2.196  1
1996 Miano JM, Firulli AB, Olson EN, Hara P, Giachelli CM, Schwartz SM. Restricted expression of homeobox genes distinguishes fetal from adult human smooth muscle cells Proceedings of the National Academy of Sciences of the United States of America. 93: 900-905. PMID 8570656 DOI: 10.1073/pnas.93.2.900  1
1994 Lilly B, Galewsky S, Firulli AB, Schulz RA, Olson EN. D-MEF2: a MADS box transcription factor expressed in differentiating mesoderm and muscle cell lineages during Drosophila embryogenesis. Proceedings of the National Academy of Sciences of the United States of America. 91: 5662-6. PMID 8202544 DOI: 10.1073/pnas.91.12.5662  1
1994 Firulli AB, Maibenco DC, Kinniburgh AJ. Triplex Forming Ability of a c-myc Promoter Element Predicts Promoter Strength Archives of Biochemistry and Biophysics. 310: 236-242. PMID 8161210 DOI: 10.1006/abbi.1994.1162  1
1994 Kinniburgh AJ, Firulli AB, Kolluri R. DNA triplexes and regulation of the c-myc gene Gene. 149: 93-100. PMID 7958992 DOI: 10.1016/0378-1119(94)90416-2  1
1992 Firulli AB, Maibenco DC, Kinniburgh AJ. The identification of a tandem H-DNA structure in the c-MYC nuclease sensitive promoter element Biochemical and Biophysical Research Communications. 185: 264-270. PMID 1599463 DOI: 10.1016/S0006-291X(05)80985-4  1
1989 Davis TL, Firulli AB, Kinniburgh AJ. Ribonucleoprotein and protein factors bind to an H-DNA-forming c-myc DNA element: Possible regulators of the c-myc gene Proceedings of the National Academy of Sciences of the United States of America. 86: 9682-9686. PMID 2690070 DOI: 10.1073/pnas.86.24.9682  1
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