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Year | Number of Results |
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2002 | 1 |
2003 | 1 |
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The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.
J Clin Invest. 2014 Aug;124(8):3551-65. doi: 10.1172/JCI75334. Epub 2014 Jun 24.
J Clin Invest. 2014.
PMID: 24960165
Free PMC article.
Growth retardation and skin abnormalities of the Recql4-deficient mouse.
Hoki Y, Araki R, Fujimori A, Ohhata T, Koseki H, Fukumura R, Nakamura M, Takahashi H, Noda Y, Kito S, Abe M.
Hoki Y, et al.
Hum Mol Genet. 2003 Sep 15;12(18):2293-9. doi: 10.1093/hmg/ddg254. Epub 2003 Jul 29.
Hum Mol Genet. 2003.
PMID: 12915449
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Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome.
Mann MB, Hodges CA, Barnes E, Vogel H, Hassold TJ, Luo G.
Mann MB, et al.
Hum Mol Genet. 2005 Mar 15;14(6):813-25. doi: 10.1093/hmg/ddi075. Epub 2005 Feb 9.
Hum Mol Genet. 2005.
PMID: 15703196
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[Preparation of the gene targeted knockout mice for human premature aging diseases, Werner syndrome, and Rothmund-Thomson syndrome caused by the mutation of DNA helicases].
Ichikawa K, Noda T, Furuichi Y.
Ichikawa K, et al.
Nihon Yakurigaku Zasshi. 2002 Apr;119(4):219-26. doi: 10.1254/fpj.119.219.
Nihon Yakurigaku Zasshi. 2002.
PMID: 11979727
Review.
Japanese.
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