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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1995 1
2000 1
2001 1
2005 1
2008 1
2009 2
2010 1
2012 1
2017 2
2020 1
2024 0

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PubMed (cited) for id: 600921

13 results

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Page 1
The mole genome reveals regulatory rearrangements associated with adaptive intersexuality.
M Real F, Haas SA, Franchini P, Xiong P, Simakov O, Kuhl H, Schöpflin R, Heller D, Moeinzadeh MH, Heinrich V, Krannich T, Bressin A, Hartmann MF, Wudy SA, Dechmann DKN, Hurtado A, Barrionuevo FJ, Schindler M, Harabula I, Osterwalder M, Hiller M, Wittler L, Visel A, Timmermann B, Meyer A, Vingron M, Jiménez R, Mundlos S, Lupiáñez DG. M Real F, et al. Science. 2020 Oct 9;370(6513):208-214. doi: 10.1126/science.aaz2582. Science. 2020. PMID: 33033216 Free PMC article.
FGF9 mutation causes craniosynostosis along with multiple synostoses.
Rodriguez-Zabala M, Aza-Carmona M, Rivera-Pedroza CI, Belinchón A, Guerrero-Zapata I, Barraza-García J, Vallespin E, Lu M, Del Pozo A, Glucksman MJ, Santos-Simarro F, Heath KE. Rodriguez-Zabala M, et al. Hum Mutat. 2017 Nov;38(11):1471-1476. doi: 10.1002/humu.23292. Epub 2017 Jul 25. Hum Mutat. 2017. PMID: 28730625
FGF9 and FGF20 maintain the stemness of nephron progenitors in mice and man.
Barak H, Huh SH, Chen S, Jeanpierre C, Martinovic J, Parisot M, Bole-Feysot C, Nitschké P, Salomon R, Antignac C, Ornitz DM, Kopan R. Barak H, et al. Dev Cell. 2012 Jun 12;22(6):1191-207. doi: 10.1016/j.devcel.2012.04.018. Dev Cell. 2012. PMID: 22698282 Free PMC article.
Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene.
Wu XL, Gu MM, Huang L, Liu XS, Zhang HX, Ding XY, Xu JQ, Cui B, Wang L, Lu SY, Chen XY, Zhang HG, Huang W, Yuan WT, Yang JM, Gu Q, Fei J, Chen Z, Yuan ZM, Wang ZG. Wu XL, et al. Am J Hum Genet. 2009 Jul;85(1):53-63. doi: 10.1016/j.ajhg.2009.06.007. Am J Hum Genet. 2009. PMID: 19589401 Free PMC article.
FGF9 monomer-dimer equilibrium regulates extracellular matrix affinity and tissue diffusion.
Harada M, Murakami H, Okawa A, Okimoto N, Hiraoka S, Nakahara T, Akasaka R, Shiraishi Y, Futatsugi N, Mizutani-Koseki Y, Kuroiwa A, Shirouzu M, Yokoyama S, Taiji M, Iseki S, Ornitz DM, Koseki H. Harada M, et al. Nat Genet. 2009 Mar;41(3):289-98. doi: 10.1038/ng.316. Epub 2009 Feb 15. Nat Genet. 2009. PMID: 19219044 Free PMC article.
13 results