| Year |
Citation |
Score |
| 2008 |
Park EJ, Watanabe Y, Smyth G, Miyagawa-Tomita S, Meyers E, Klingensmith J, Camenisch T, Buckingham M, Moon AM. An FGF autocrine loop initiated in second heart field mesoderm regulates morphogenesis at the arterial pole of the heart. Development (Cambridge, England). 135: 3599-610. PMID 18832392 DOI: 10.1242/Dev.025437 |
0.635 |
|
| 2008 |
Goddeeris MM, Rho S, Petiet A, Davenport CL, Johnson GA, Meyers EN, Klingensmith J. Intracardiac septation requires hedgehog-dependent cellular contributions from outside the heart. Development (Cambridge, England). 135: 1887-95. PMID 18441277 DOI: 10.1242/Dev.016147 |
0.742 |
|
| 2007 |
Goddeeris MM, Schwartz R, Klingensmith J, Meyers EN. Independent requirements for Hedgehog signaling by both the anterior heart field and neural crest cells for outflow tract development. Development (Cambridge, England). 134: 1593-604. PMID 17344228 DOI: 10.1242/Dev.02824 |
0.763 |
|
| 2007 |
Choi M, Stottmann RW, Yang YP, Meyers EN, Klingensmith J. The bone morphogenetic protein antagonist noggin regulates mammalian cardiac morphogenesis. Circulation Research. 100: 220-8. PMID 17218603 DOI: 10.1161/01.Res.0000257780.60484.6A |
0.61 |
|
| 2006 |
Ilagan R, Abu-Issa R, Brown D, Yang YP, Jiao K, Schwartz RJ, Klingensmith J, Meyers EN. Fgf8 is required for anterior heart field development. Development (Cambridge, England). 133: 2435-45. PMID 16720880 DOI: 10.1242/Dev.02408 |
0.699 |
|
| 2005 |
Grieshammer U, Cebrián C, Ilagan R, Meyers E, Herzlinger D, Martin GR. FGF8 is required for cell survival at distinct stages of nephrogenesis and for regulation of gene expression in nascent nephrons. Development (Cambridge, England). 132: 3847-57. PMID 16049112 DOI: 10.1242/Dev.01944 |
0.667 |
|
| 2005 |
Byrd NA, Meyers EN. Loss of Gbx2 results in neural crest cell patterning and pharyngeal arch artery defects in the mouse embryo. Developmental Biology. 284: 233-45. PMID 15996652 DOI: 10.1016/J.Ydbio.2005.05.023 |
0.503 |
|
| 2005 |
Washington Smoak I, Byrd NA, Abu-Issa R, Goddeeris MM, Anderson R, Morris J, Yamamura K, Klingensmith J, Meyers EN. Sonic hedgehog is required for cardiac outflow tract and neural crest cell development. Developmental Biology. 283: 357-72. PMID 15936751 DOI: 10.1016/J.Ydbio.2005.04.029 |
0.752 |
|
| 2004 |
Stumpo DJ, Byrd NA, Phillips RS, Ghosh S, Maronpot RR, Castranio T, Meyers EN, Mishina Y, Blackshear PJ. Chorioallantoic fusion defects and embryonic lethality resulting from disruption of Zfp36L1, a gene encoding a CCCH tandem zinc finger protein of the Tristetraprolin family. Molecular and Cellular Biology. 24: 6445-55. PMID 15226444 DOI: 10.1128/Mcb.24.14.6445-6455.2004 |
0.424 |
|
| 2004 |
Stottmann RW, Choi M, Mishina Y, Meyers EN, Klingensmith J. BMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardium. Development (Cambridge, England). 131: 2205-18. PMID 15073157 DOI: 10.1242/Dev.01086 |
0.607 |
|
| 2004 |
Brown CB, Wenning JM, Lu MM, Epstein DJ, Meyers EN, Epstein JA. Cre-mediated excision of Fgf8 in the Tbx1 expression domain reveals a critical role for Fgf8 in cardiovascular development in the mouse. Developmental Biology. 267: 190-202. PMID 14975726 DOI: 10.1016/J.Ydbio.2003.10.024 |
0.504 |
|
| 2004 |
Brown CB, Wenning JM, Lu MM, Epstein DJ, Meyers EN, Epstein JA. Corrigendum to “Cre-mediated excision of Fgf8 in the Tbx1 expression domain reveals a critical role for Fgf8 in cardiovascular development in the mouse” [Dev. Biol. 267 (2004) 190–202] Developmental Biology. 271: 223. DOI: 10.1016/J.Ydbio.2004.04.002 |
0.432 |
|
| 2003 |
Yamagishi H, Maeda J, Hu T, McAnally J, Conway SJ, Kume T, Meyers EN, Yamagishi C, Srivastava D. Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer. Genes & Development. 17: 269-81. PMID 12533514 DOI: 10.1101/Gad.1048903 |
0.434 |
|
| 2002 |
Abu-Issa R, Smyth G, Smoak I, Yamamura K, Meyers EN. Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse. Development (Cambridge, England). 129: 4613-25. PMID 12223417 |
0.548 |
|
| 2000 |
Sun X, Lewandoski M, Meyers EN, Liu YH, Maxson RE, Martin GR. Conditional inactivation of Fgf4 reveals complexity of signalling during limb bud development. Nature Genetics. 25: 83-6. PMID 10802662 DOI: 10.1038/75644 |
0.514 |
|
| 1999 |
Sun X, Meyers EN, Lewandoski M, Martin GR. Targeted disruption of Fgf8 causes failure of cell migration in the gastrulating mouse embryo. Genes & Development. 13: 1834-46. PMID 10421635 DOI: 10.1101/Gad.13.14.1834 |
0.608 |
|
| 1999 |
Meyers EN, Martin GR. Differences in left-right axis pathways in mouse and chick: functions of FGF8 and SHH. Science (New York, N.Y.). 285: 403-6. PMID 10411502 DOI: 10.1126/Science.285.5426.403 |
0.439 |
|
| 1999 |
Meyers EN, Martin GR. Fgf8 Is Required for Specification of the Left-Right Axis and for Normal Cardiac Development in Mice Pediatric Research. 45: 57A-57A. DOI: 10.1203/00006450-199904020-00343 |
0.458 |
|
| 1998 |
Meyers EN, Lewandoski M, Martin GR. An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination. Nature Genetics. 18: 136-41. PMID 9462741 DOI: 10.1038/Ng0298-136 |
0.415 |
|
| 1998 |
Meyers EN, Lewandoski M, Martin GR. Generation and Analysis of Mice Carrying an Allelic Series of Mutations at the Fgf8 Locus Demonstrate Requirements for FGF8 During Gastrulation, Limb, Craniofacial, Cardiac and CNS Development • 286 Pediatric Research. 43: 51-51. DOI: 10.1203/00006450-199804001-00307 |
0.456 |
|
| 1997 |
Lewandoski M, Meyers EN, Martin GR. Analysis of Fgf8 Gene Function in Vertebrate Development Cold Spring Harbor Symposia On Quantitative Biology. 62: 159-168. DOI: 10.1101/Sqb.1997.062.01.021 |
0.381 |
|
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