Hasten et al., 2019 - Google Patents
Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11. 2 deletion syndromeHasten et al., 2019
View HTML- Document ID
- 2455616561322251315
- Author
- Hasten E
- Morrow B
- Publication year
- Publication venue
- PLoS genetics
External Links
Snippet
We investigated whether Tbx1, the gene for 22q11. 2 deletion syndrome (22q11. 2DS) and Foxi3, both required for segmentation of the pharyngeal apparatus (PA) to individual arches, genetically interact. We found that all Tbx1+/-; Foxi3+/-double heterozygous mouse embryos …
- 101700022528 TBX1 0 title abstract description 243
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
- G01N33/502—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Hasten et al. | Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11. 2 deletion syndrome | |
Linton et al. | The ECM protein nephronectin promotes kidney development via integrinα8β1-mediated stimulation of Gdnf expression | |
Yu et al. | Frizzled 2 and frizzled 7 function redundantly in convergent extension and closure of the ventricular septum and palate: evidence for a network of interacting genes | |
Chizhikov et al. | Cilia proteins control cerebellar morphogenesis by promoting expansion of the granule progenitor pool | |
Hadrys et al. | Nkx5-1 controls semicircular canal formation in the mouse inner ear | |
May-Simera et al. | Ciliary proteins Bbs8 and Ift20 promote planar cell polarity in the cochlea | |
Yanagihara et al. | Current models of pulmonary fibrosis for future drug discovery efforts | |
De Langhe et al. | Formation and differentiation of multiple mesenchymal lineages during lung development is regulated by β-catenin signaling | |
Klar et al. | Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage | |
Bangs et al. | Generation of mice with functional inactivation of talpid3, a gene first identified in chicken | |
Chan et al. | Fukutin-related protein is essential for mouse muscle, brain and eye development and mutation recapitulates the wide clinical spectrums of dystroglycanopathies | |
Briggs et al. | Expression of the BMP receptor Alk3 in the second heart field is essential for development of the dorsal mesenchymal protrusion and atrioventricular septation | |
Jain | The many faces of RET dysfunction in kidney | |
Metzis et al. | Patched1 is required in neural crest cells for the prevention of orofacial clefts | |
Yu et al. | VGLL4 plays a critical role in heart valve development and homeostasis | |
Rana et al. | Targeted deletion of the novel cytoplasmic dynein mD2LIC disrupts the embryonic organiser, formation of the body axes and specification of ventral cell fates | |
Escot et al. | Disruption of CXCR4 signaling in pharyngeal neural crest cells causes DiGeorge syndrome-like malformations | |
Burns et al. | The dorsal mesenchymal protrusion and the pathogenesis of atrioventricular septal defects | |
Nagy et al. | HACE1 deficiency leads to structural and functional neurodevelopmental defects | |
Chan et al. | Cardiac neural crest of the mouse embryo: axial level of origin, migratory pathway and cell autonomy of the splotch (Sp2H) mutant effect | |
Schock et al. | A tissue-specific role for intraflagellar transport genes during craniofacial development | |
Serrano et al. | Inhibition of Notch signaling rescues cardiovascular development in Kabuki Syndrome | |
Qian et al. | Stage specific requirement of platelet-derived growth factor receptor-α in embryonic development | |
Tornini et al. | Live fate-mapping of joint-associated fibroblasts visualizes expansion of cell contributions during zebrafish fin regeneration | |
Deng et al. | LMO4 functions as a negative regulator of sensory organ formation in the mammalian cochlea |