Pages that link to "Q24596814"
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The following pages link to The homeodomain protein vax1 is required for axon guidance and major tract formation in the developing forebrain (Q24596814):
Displaying 50 items.
- Ventral anterior homeobox 1 (Q21989692) (← links)
- Complex trait analysis of the mouse striatum: independent QTLs modulate volume and neuron number (Q24797749) (← links)
- Molecular basis of cleft palates in mice (Q26795762) (← links)
- The role of homeobox genes in retinal development and disease (Q27021998) (← links)
- Expression profiling during ocular development identifies 2 Nlz genes with a critical role in optic fissure closure (Q28312171) (← links)
- Hedgehog-regulated localization of Vax2 controls eye development (Q28509927) (← links)
- Complementary Gli activity mediates early patterning of the mouse visual system (Q28511181) (← links)
- Defective postnatal neurogenesis and disorganization of the rostral migratory stream in absence of the Vax1 homeobox gene (Q28512515) (← links)
- The temporal requirement for vitamin A in the developing eye: mechanism of action in optic fissure closure and new roles for the vitamin in regulating cell proliferation and adhesion in the embryonic retina (Q28581420) (← links)
- Vax genes ventralize the embryonic eye (Q28588805) (← links)
- A novel mechanism for the transcriptional regulation of Wnt signaling in development (Q28591721) (← links)
- Ocular abnormalities in mice lacking the immunoglobulin superfamily member Cdo (Q28591959) (← links)
- A POU domain transcription factor-dependent program regulates axon pathfinding in the vertebrate visual system (Q28593839) (← links)
- Deletion of Vax1 from Gonadotropin-Releasing Hormone (GnRH) Neurons Abolishes GnRH Expression and Leads to Hypogonadism and Infertility. (Q30356438) (← links)
- Heterozygous deletion of ventral anterior homeobox (vax1) causes subfertility in mice (Q30370622) (← links)
- Perturbations of microRNA function in mouse dicer mutants produce retinal defects and lead to aberrant axon pathfinding at the optic chiasm (Q33553406) (← links)
- COUP-TFs regulate eye development by controlling factors essential for optic vesicle morphogenesis (Q33684591) (← links)
- Interoperability of time series cytometric data: a cross platform approach for modeling tumor heterogeneity. (Q33825540) (← links)
- Retinal ganglion cell axon guidance in the mouse optic chiasm: expression and function of robos and slits. (Q33906731) (← links)
- Regulation of retinal axon growth by secreted Vax1 homeodomain protein (Q34437491) (← links)
- Connecting the retina to the brain (Q34453720) (← links)
- Patterning the neural retina (Q34542013) (← links)
- Lack of the ventral anterior homeodomain transcription factor VAX1 leads to induction of a second pituitary (Q34558020) (← links)
- Disruption of SoxB1-dependent Sonic hedgehog expression in the hypothalamus causes septo-optic dysplasia (Q34636655) (← links)
- Vax1/2 genes counteract Mitf-induced respecification of the retinal pigment epithelium (Q34648878) (← links)
- Smad4 is required predominantly in the developmental processes dependent on the BMP branch of the TGF-β signaling system in the embryonic mouse retina (Q35027463) (← links)
- Regulation of axial patterning of the retina and its topographic mapping in the brain. (Q35068992) (← links)
- The visual system of zebrafish and its use to model human ocular diseases (Q35449573) (← links)
- A role for VAX2 in correct retinal function revealed by a novel genomic deletion at 2p13.3 causing distal Renal Tubular Acidosis: case report. (Q35661887) (← links)
- Roles of cell-extrinsic growth factors in vertebrate eye pattern formation and retinogenesis (Q35703376) (← links)
- VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humans (Q36107483) (← links)
- Mechanisms of axon guidance in the developing nervous system. (Q36294315) (← links)
- The retinal ganglion cell axon's journey: insights into molecular mechanisms of axon guidance (Q36846033) (← links)
- Zebrafish blowout provides genetic evidence for Patched1-mediated negative regulation of Hedgehog signaling within the proximal optic vesicle of the vertebrate eye. (Q36862083) (← links)
- Bcl6a function is required during optic cup formation to prevent p53-dependent apoptosis and colobomata (Q37078872) (← links)
- Homeoprotein signaling in the developing and adult nervous system. (Q37272428) (← links)
- Loss of Tbx2 delays optic vesicle invagination leading to small optic cups. (Q37327635) (← links)
- The PAX258 gene subfamily: a comparative perspective (Q37635066) (← links)
- Disrupting hedgehog and WNT signaling interactions promotes cleft lip pathogenesis (Q37679924) (← links)
- Compartmentalization of vertebrate optic neuroephithelium: external cues and transcription factors (Q37997316) (← links)
- Retinal stem cells and regeneration of vision system (Q38167719) (← links)
- Genetic regulation of vertebrate eye development (Q38244962) (← links)
- Differential expression and methylation of brain developmental genes define location-specific subsets of pilocytic astrocytoma (Q38315617) (← links)
- From Bench to Bedside and Back: Improving Diagnosis and Treatment of Craniofacial Malformations Utilizing Animal Models (Q38641260) (← links)
- Retinal axon guidance at the midline: Chiasmatic misrouting and consequences (Q39025983) (← links)
- The Transcription Factor Foxg1 Promotes Optic Fissure Closure in the Mouse by Suppressing Wnt8b in the Nasal Optic Stalk (Q41438489) (← links)
- Slit inhibition of retinal axon growth and its role in retinal axon pathfinding and innervation patterns in the diencephalon. (Q41743029) (← links)
- Stefano Bertuzzi: science first. Interview by Caitlin Sedwick (Q42388765) (← links)
- Vax1 Plays an Indirect Role in the Etiology of Murine Cleft Palate (Q42513214) (← links)
- Temporal and spatial effects of Sonic hedgehog signaling in chick eye morphogenesis (Q45042027) (← links)