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Summary Expression Gene Literature (133) GO Terms (17) Nucleotides (402) Proteins (61) Interactants (1238) Wiki
XB--1018553

Papers associated with fgfr1 (and Disease Ontology)

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A YWHAZ Variant Associated With Cardiofaciocutaneous Syndrome Activates the RAF-ERK Pathway., Popov IK, Hiatt SM, Whalen S, Keren B, Ruivenkamp C, van Haeringen A, Chen MJ, Cooper GM, Korf BR, Chang C., Front Physiol. January 1, 2019; 10 388.                  


A molecular atlas of the developing ectoderm defines neural, neural crest, placode, and nonneural progenitor identity in vertebrates., Plouhinec JL, Medina-Ruiz S, Borday C, Bernard E, Vert JP, Eisen MB, Harland RM, Monsoro-Burq AH., PLoS Biol. October 1, 2017; 15 (10): e2004045.                                              


Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus., Roberts NA, Woolf AS, Stuart HM, Thuret R, McKenzie EA, Newman WG, Hilton EN., Hum Mol Genet. August 15, 2014; 23 (16): 4302-14.                


Identification of a novel gene, FGFR1OP2, fused to FGFR1 in 8p11 myeloproliferative syndrome., Grand EK, Grand FH, Chase AJ, Ross FM, Corcoran MM, Oscier DG, Cross NC., Genes Chromosomes Cancer. May 1, 2004; 40 (1): 78-83.

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