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Year | Number of Results |
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1992 | 1 |
2005 | 1 |
2009 | 1 |
2010 | 1 |
2024 | 0 |
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Homeosis in the mouse induced by a null mutation in the Hox-3.1 gene.
Cell. 1992 Apr 17;69(2):251-64. doi: 10.1016/0092-8674(92)90406-3.
Cell. 1992.
PMID: 1348969
Retinaldehyde dehydrogenase 2 and Hoxc8 are required in the murine brachial spinal cord for the specification of Lim1+ motoneurons and the correct distribution of Islet1+ motoneurons.
Vermot J, Schuhbaur B, Le Mouellic H, McCaffery P, Garnier JM, Hentsch D, Brûlet P, Niederreither K, Chambon P, Dollé P, Le Roux I.
Vermot J, et al.
Development. 2005 Apr;132(7):1611-21. doi: 10.1242/dev.01718.
Development. 2005.
PMID: 15753214
Free article.
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Generation of conditional Hoxc8 loss-of-function and Hoxc8-->Hoxc9 replacement alleles in mice.
Blackburn J, Rich M, Ghitani N, Liu JP.
Blackburn J, et al.
Genesis. 2009 Oct;47(10):680-7. doi: 10.1002/dvg.20547.
Genesis. 2009.
PMID: 19621436
Free PMC article.
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Hematopoietic origin of pathological grooming in Hoxb8 mutant mice.
Chen SK, Tvrdik P, Peden E, Cho S, Wu S, Spangrude G, Capecchi MR.
Chen SK, et al.
Cell. 2010 May 28;141(5):775-85. doi: 10.1016/j.cell.2010.03.055.
Cell. 2010.
PMID: 20510925
Free PMC article.
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