1993
DOI: 10.1016/0925-4773(93)90016-q
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Characterization and developmental expression of Tlx-1, the murine homolog of HOX11

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Cited by 81 publications
(76 citation statements)
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“…16,[22][23][24][25] All three Hox11 family members exhibit a restricted pattern of expression, since they are expressed essentially in neural tissues during development and also in liver and pancreas of adult mice. [26][27][28][29][30] The corresponding knock-out models indicated a very specific role of these proteins during normal embryogenesis. Hox11 is a central player in controlling spleen formation, perhaps through regulating cell survival, 31,32 and the two other genes appear important for specific neuronal functions.…”
Section: Leukemiamentioning
confidence: 99%
“…16,[22][23][24][25] All three Hox11 family members exhibit a restricted pattern of expression, since they are expressed essentially in neural tissues during development and also in liver and pancreas of adult mice. [26][27][28][29][30] The corresponding knock-out models indicated a very specific role of these proteins during normal embryogenesis. Hox11 is a central player in controlling spleen formation, perhaps through regulating cell survival, 31,32 and the two other genes appear important for specific neuronal functions.…”
Section: Leukemiamentioning
confidence: 99%
“…Similar to other HOX genes, HOX11 plays an important role in embryonic development, and functions as a master transcriptional regulator necessary for the genesis of the spleen (Roberts et al, 1994;Dear et al, 1995). In the mouse embryo, Hox11 expression can be detected in the branchial arches, restricted areas of the hindbrain and the splenic primordium (Raju et al, 1993;Roberts et al, 1995), where it is required for the survival of early splenic progenitors (Dear et al, 1995). The proposed function of HOX11 as a transcriptional regulator is supported by the presence of both a 61-amino acid, helix-turn-helix DNA-binding domain (or homeodomain) and by the localization of the HOX11 protein in the cell nucleus (Neale et al, 1995).…”
Section: Aberrant Protein Expression In T-cell Acute Lymphoblastic Lementioning
confidence: 99%
“…SPE, serine, proline and glutamine acid-rich nine amino acid repeats; PHD, PHD ®ngers; ARD, acidic-rich domain; PolyQ, polyglutamine-rich region; ZNF, potential Zn ®ngers; ATA1 and ATA2, regions of homology unique to the three proteins; SET, SET domain. The two ALR proteins are encoded by alternatively spliced transcripts expression pattern in the branchial arches and trigerminal ganglia (Raju et al, 1993;Bulfone et al, 1993).…”
Section: Embryonic Expressionmentioning
confidence: 99%