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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1991 | 1 |
2006 | 1 |
2012 | 2 |
2014 | 3 |
2024 | 0 |
PubMed (cited) for id: 300835
7 results
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Page 1
Altered translation of GATA1 in Diamond-Blackfan anemia.
Nat Med. 2014 Jul;20(7):748-53. doi: 10.1038/nm.3557. Epub 2014 Jun 22.
Nat Med. 2014.
PMID: 24952648
Free PMC article.
Recurrent GATA1 mutations in Diamond-Blackfan anaemia.
Klar J, Khalfallah A, Arzoo PS, Gazda HT, Dahl N.
Klar J, et al.
Br J Haematol. 2014 Sep;166(6):949-51. doi: 10.1111/bjh.12919. Epub 2014 Apr 28.
Br J Haematol. 2014.
PMID: 24766296
Free article.
No abstract available.
Item in Clipboard
Loss of GATA-1 full length as a cause of Diamond-Blackfan anemia phenotype.
Parrella S, Aspesi A, Quarello P, Garelli E, Pavesi E, Carando A, Nardi M, Ellis SR, Ramenghi U, Dianzani I.
Parrella S, et al.
Pediatr Blood Cancer. 2014 Jul;61(7):1319-21. doi: 10.1002/pbc.24944. Epub 2014 Jan 22.
Pediatr Blood Cancer. 2014.
PMID: 24453067
Free PMC article.
Clinical Trial.
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Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia.
Sankaran VG, Ghazvinian R, Do R, Thiru P, Vergilio JA, Beggs AH, Sieff CA, Orkin SH, Nathan DG, Lander ES, Gazda HT.
Sankaran VG, et al.
J Clin Invest. 2012 Jul;122(7):2439-43. doi: 10.1172/JCI63597. Epub 2012 Jun 18.
J Clin Invest. 2012.
PMID: 22706301
Free PMC article.
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What's in a name?
Weiss MJ, Mason PJ, Bessler M.
Weiss MJ, et al.
J Clin Invest. 2012 Jul;122(7):2346-9. doi: 10.1172/JCI63989. Epub 2012 Jun 18.
J Clin Invest. 2012.
PMID: 22706300
Free PMC article.
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An inherited mutation leading to production of only the short isoform of GATA-1 is associated with impaired erythropoiesis.
Hollanda LM, Lima CS, Cunha AF, Albuquerque DM, Vassallo J, Ozelo MC, Joazeiro PP, Saad ST, Costa FF.
Hollanda LM, et al.
Nat Genet. 2006 Jul;38(7):807-12. doi: 10.1038/ng1825. Epub 2006 Jun 18.
Nat Genet. 2006.
PMID: 16783379
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Mapping the gene encoding the human erythroid transcriptional factor NFE1-GF1 to Xp11.23.
Caiulo A, Nicolis S, Bianchi P, Zuffardi O, Bardoni B, Maraschio P, Ottolenghi S, Camerino G, Giglioni B.
Caiulo A, et al.
Hum Genet. 1991 Feb;86(4):388-90. doi: 10.1007/BF00201840.
Hum Genet. 1991.
PMID: 1999341
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