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

Year Number of Results
1977 1
1986 1
1991 1
1992 1
1997 2
1998 1
1999 1
2000 2
2001 6
2002 2
2003 2
2004 6
2005 4
2006 6
2007 4
2008 2
2009 9
2010 6
2011 5
2012 4
2013 9
2014 6
2015 11
2016 3
2017 8
2018 9
2019 5
2020 5
2021 8
2022 3
2024 0

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Similar articles for PMID: 11389161

122 results

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Page 1
GATA3 abnormalities and the phenotypic spectrum of HDR syndrome.
Muroya K, Hasegawa T, Ito Y, Nagai T, Isotani H, Iwata Y, Yamamoto K, Fujimoto S, Seishu S, Fukushima Y, Hasegawa Y, Ogata T. Muroya K, et al. J Med Genet. 2001 Jun;38(6):374-80. doi: 10.1136/jmg.38.6.374. J Med Genet. 2001. PMID: 11389161 Free PMC article.
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor.
Ali A, Christie PT, Grigorieva IV, Harding B, Van Esch H, Ahmed SF, Bitner-Glindzicz M, Blind E, Bloch C, Christin P, Clayton P, Gecz J, Gilbert-Dussardier B, Guillen-Navarro E, Hackett A, Halac I, Hendy GN, Lalloo F, Mache CJ, Mughal Z, Ong AC, Rinat C, Shaw N, Smithson SF, Tolmie J, Weill J, Nesbit MA, Thakker RV. Ali A, et al. Hum Mol Genet. 2007 Feb 1;16(3):265-75. doi: 10.1093/hmg/ddl454. Epub 2007 Jan 8. Hum Mol Genet. 2007. PMID: 17210674
GATA3 haplo-insufficiency causes human HDR syndrome.
Van Esch H, Groenen P, Nesbit MA, Schuffenhauer S, Lichtner P, Vanderlinden G, Harding B, Beetz R, Bilous RW, Holdaway I, Shaw NJ, Fryns JP, Van de Ven W, Thakker RV, Devriendt K. Van Esch H, et al. Nature. 2000 Jul 27;406(6794):419-22. doi: 10.1038/35019088. Nature. 2000. PMID: 10935639
122 results