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Dual roles for the Dab2 adaptor protein in embryonic development and kidney transport
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The impact of Dab2 deletion on cardiac development is not notable.
“though impact of Dab2 deletion on cardiac development is not notable (Morris et al., 2002b; Moore et al., 2013).”
From Endocytosis and Physiology: Insights from Disabled-2 Deficient Mice (2016) · cites this paper as Morris et al., 2002b
The rescue section (page unavailable) reports that mice with Dab2 deleted from the embryo proper appeared normal, were born and survived, supporting no obvious developmental defect under that condition. It does not assess cardiac development specifically; complete Dab2 deletion instead caused early embryonic lethality, as reported in the targeting section (page unavailable). (LLM, conf=0.82)
Experimental — accuracy not yet measuredDab2 is linked to megalin endocytosis in the kidney in vivo.
“This links Dab2 to megalin endocytosis in the kidney in vivo.”
From Disabled‐2 exhibits the properties of a cargo‐selective endocytic clathrin adaptor (2002) · cites this paper as Morris et al., 2002b
No increased tumor incidence was reported in the characterization of a Dab2 conditional knockout line using Meox2-Cre.
“though no increased tumor incidence was reported in the characterization of a Dab2 conditional knockout line (using Meox2-Cre; Morris et al., 2002b).”
From Endocytosis and Physiology: Insights from Disabled-2 Deficient Mice (2016) · cites this paper as Morris et al., 2002b
Conventional dab2 gene deletion in mice results in early embryonic death.
“Conventional dab2 gene deletion in mice results in early embryonic death”
From Endocytic adaptors Arh and Dab2 control homeostasis of circulatory cholesterol (2016) · cites this paper as [27]
The phenotype of Dab2 nullizygous mice supports a role for Dab2 in endocytosis.
“The phenotype of Dab2 nullizygous mice also supports a role for Dab2 in endocytosis.”
From Disabled‐2 exhibits the properties of a cargo‐selective endocytic clathrin adaptor (2002) · cites this paper as Morris et al., 2002b
Dab2 is essential for mouse embryonic development; gene deletion causes early embryonic lethality prior to gastrulation.
“Dab2 is essential for mouse embryonic development and gene deletion in mice causes early embryonic lethality at a stage prior to gastrulation (Morris et al., 2002b; Yang et al., 2002a, 2007).”
From Endocytosis and Physiology: Insights from Disabled-2 Deficient Mice (2016) · cites this paper as Morris et al., 2002b
Dab2 null mice show failed cell sorting in blastocysts/primitive and extraembryonic endoderm early embryos.
“Blastocysts/primitive and extraembryonic endoderm early embryos | Failed cell sorting”
From Endocytosis and Physiology: Insights from Disabled-2 Deficient Mice (2016) · cites this paper as Morris et al., 2002b
Dab2 null mice show mild proteinuria.
“Kidney/proximal convoluted tubule epithelia | Mild proteinuria”
From Endocytosis and Physiology: Insights from Disabled-2 Deficient Mice (2016) · cites this paper as Morris et al., 2002b
Dab2 is involved in cell positioning and formation of the visceral endoderm during mouse embryogenesis.
“Dab2, one of two mammalian orthologs of Drosophila Disabled, has been shown to be involved in cell positioning and formation of visceral endoderm during mouse embryogenesis, but its role in neuronal development is not yet fully understood.”
From Dynamic expression of Dab2 in the mouse embryonic central nervous system (2008) · cites this paper as [19]
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Metadata
- Authors
- Morris, S. M., Tallquist, M. D., Rock, C. O., & Cooper, J. A.
- Venue
- The EMBO Journal
- Published
- 2002-04-01
- Volume
- 21
- Issue
- 7
- Pages
- 1555-1564
- ISSN
- 0261-4189
- 1460-2075
- Cited by
- 186
- References
- 0
- Language
- en
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