Ronald Conlon - Publications

Affiliations: 
Case Western Reserve University, Cleveland Heights, OH, United States 

22 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
2006 Atit R, Sgaier SK, Mohamed OA, Taketo MM, Dufort D, Joyner AL, Niswander L, Conlon RA. Beta-catenin activation is necessary and sufficient to specify the dorsal dermal fate in the mouse. Developmental Biology. 296: 164-76. PMID 16730693 DOI: 10.1016/J.Ydbio.2006.04.449  0.388
2005 Woda JM, Calzonetti T, Hilditch-Maguire P, Duyao MP, Conlon RA, MacDonald ME. Inactivation of the Huntington's disease gene (Hdh) impairs anterior streak formation and early patterning of the mouse embryo. Bmc Developmental Biology. 5: 17. PMID 16109169 DOI: 10.1186/1471-213X-5-17  0.445
2004 Hadland BK, Huppert SS, Kanungo J, Xue Y, Jiang R, Gridley T, Conlon RA, Cheng AM, Kopan R, Longmore GD. A requirement for Notch1 distinguishes 2 phases of definitive hematopoiesis during development. Blood. 104: 3097-105. PMID 15251982 DOI: 10.1182/Blood-2004-03-1224  0.324
2003 Atit R, Conlon RA, Niswander L. EGF signaling patterns the feather array by promoting the interbud fate. Developmental Cell. 4: 231-40. PMID 12586066 DOI: 10.1016/S1534-5807(03)00021-2  0.345
2003 McCallion AS, Stames E, Conlon RA, Chakravarti A. Phenotype variation in two-locus mouse models of Hirschsprung disease: tissue-specific interaction between Ret and Ednrb. Proceedings of the National Academy of Sciences of the United States of America. 100: 1826-31. PMID 12574515 DOI: 10.1073/Pnas.0337540100  0.306
2002 Dunwoodie SL, Clements M, Sparrow DB, Sa X, Conlon RA, Beddington RS. Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm. Development (Cambridge, England). 129: 1795-806. PMID 11923214  0.337
2001 Correia KM, Conlon RA. Whole-mount in situ hybridization to mouse embryos. Methods (San Diego, Calif.). 23: 335-8. PMID 11316434 DOI: 10.1006/meth.2000.1145  0.333
2000 Correia KM, Conlon RA. Surface ectoderm is necessary for the morphogenesis of somites. Mechanisms of Development. 91: 19-30. PMID 10704827 DOI: 10.1016/S0925-4773(99)00260-9  0.353
1999 Barrantes IB, Elia AJ, Wünsch K, Hrabe de Angelis MH, Mak TW, Rossant J, Conlon RA, Gossler A, de la Pompa JL. Interaction between Notch signalling and Lunatic fringe during somite boundary formation in the mouse. Current Biology : Cb. 9: 470-80. PMID 10330372 DOI: 10.1016/S0960-9822(99)80212-7  0.552
1998 Hoang BH, Thomas JT, Abdul-Karim FW, Correia KM, Conlon RA, Luyten FP, Ballock RT. Expression pattern of two Frizzled-related genes, Frzb-1 and Sfrp-1, during mouse embryogenesis suggests a role for modulating action of Wnt family members. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 212: 364-72. PMID 9671940 DOI: 10.1002/(SICI)1097-0177(199807)212:3<364::AID-AJA4>3.0.CO;2-F  0.428
1997 de la Pompa JL, Wakeham A, Correia KM, Samper E, Brown S, Aguilera RJ, Nakano T, Honjo T, Mak TW, Rossant J, Conlon RA. Conservation of the Notch signalling pathway in mammalian neurogenesis. Development (Cambridge, England). 124: 1139-48. PMID 9102301  0.559
1995 Conlon RA. Retinoic acid and pattern formation in vertebrates. Trends in Genetics : Tig. 11: 314-9. PMID 8585129 DOI: 10.1016/S0168-9525(00)89089-7  0.318
1995 Luo J, Pasceri P, Conlon RA, Rossant J, Giguère V. Mice lacking all isoforms of retinoic acid receptor beta develop normally and are susceptible to the teratogenic effects of retinoic acid. Mechanisms of Development. 53: 61-71. PMID 8555112 DOI: 10.1016/0925-4773(95)00424-6  0.455
1995 Conlon RA, Reaume AG, Rossant J. Notch1 is required for the coordinate segmentation of somites. Development (Cambridge, England). 121: 1533-45. PMID 7789282  0.525
1994 Ang SL, Conlon RA, Jin O, Rossant J. Positive and negative signals from mesoderm regulate the expression of mouse Otx2 in ectoderm explants. Development (Cambridge, England). 120: 2979-89. PMID 7607086  0.535
1993 Yamaguchi TP, Dumont DJ, Conlon RA, Breitman ML, Rossant J. flk-1, an flt-related receptor tyrosine kinase is an early marker for endothelial cell precursors. Development (Cambridge, England). 118: 489-98. PMID 8223275  0.53
1992 Dumont DJ, Yamaguchi TP, Conlon RA, Rossant J, Breitman ML. tek, a novel tyrosine kinase gene located on mouse chromosome 4, is expressed in endothelial cells and their presumptive precursors. Oncogene. 7: 1471-80. PMID 1630810  0.479
1992 Moens CB, Auerbach AB, Conlon RA, Joyner AL, Rossant J. A targeted mutation reveals a role for N-myc in branching morphogenesis in the embryonic mouse lung. Genes & Development. 6: 691-704. PMID 1577267 DOI: 10.1101/Gad.6.5.691  0.568
1992 Reaume AG, Conlon RA, Zirngibl R, Yamaguchi TP, Rossant J. Expression analysis of a Notch homologue in the mouse embryo. Developmental Biology. 154: 377-87. PMID 1426644 DOI: 10.1016/0012-1606(92)90076-S  0.557
1992 Conlon RA, Rossant J. Exogenous retinoic acid rapidly induces anterior ectopic expression of murine Hox-2 genes in vivo. Development (Cambridge, England). 116: 357-68. PMID 1363087  0.502
1992 Yamaguchi TP, Conlon RA, Rossant J. Expression of the fibroblast growth factor receptor FGFR-1/flg during gastrulation and segmentation in the mouse embryo. Developmental Biology. 152: 75-88. PMID 1321062 DOI: 10.1016/0012-1606(92)90157-C  0.53
1987 Conlon RA, Tufaro F, Brandhorst BP. Post-transcriptional restriction of gene expression in sea urchin interspecies hybrid embryos. Genes & Development. 1: 337-46. PMID 3678826 DOI: 10.1101/Gad.1.4.337  0.321
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