44 results on '"Simeone, Antonio"'
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2. Loss of the Otx2-Binding Site in the Nanog Promoter Affects the Integrity of Embryonic Stem Cell Subtypes and Specification of Inner Cell Mass-Derived Epiblast
3. Mitochondrial Protection by Exogenous Otx2 in Mouse Retinal Neurons
4. A WNT1-regulated developmental gene cascade prevents dopaminergic neurodegeneration in adult En1 mice
5. Sox6 and Otx2 Control the Specification of Substantia Nigra and Ventral Tegmental Area Dopamine Neurons
6. Reorganization of Enhancer Patterns in Transition from Naive to Primed Pluripotency
7. Otx2 selectively controls the neurogenesis of specific neuronal subtypes of the ventral tegmental area and compensates En1-dependent neuronal loss and MPTP vulnerability
8. The H3K27 Demethylase JMJD3 Is Required for Maintenance of the Embryonic Respiratory Neuronal Network, Neonatal Breathing, and Survival
9. Fgf15-mediated control of neurogenic and proneural gene expression regulates dorsal midbrain neurogenesis
10. Bmp5/7 in concert with the mid-hindbrain organizer control development of noradrenergic locus coeruleus neurons
11. Expression of the Brain Transcription Factor OTX1 Occurs in a Subset of Normal Germinal-Center B Cells and in Aggressive Non-Hodgkin Lymphoma
12. Selective inactivation of Otx2 mRNA isoforms reveals isoform-specific requirement for visceral endoderm anteriorization and head morphogenesis and highlights cell diversity in the visceral endoderm
13. Orthopedia Homeodomain Protein Is Essential for Diencephalic Dopaminergic Neuron Development
14. Orthopedia Homeodomain Protein Is Essential for Diencephalic Dopaminergic Neuron Development
15. Altered dopaminergic innervation and amphetamine response in adult Otx2 conditional mutant mice
16. Otx genes in the evolution of the vertebrate brain
17. Genetic control of dopaminergic neuron differentiation
18. OTX1 compensates for OTX2 requirement in regionalisation of anterior neuroectoderm
19. The Otx family
20. The paired-type homeobox gene Dmbx1 marks the midbrain and pretectum
21. Towards the comprehension of genetic mechanisms controlling brain morphogenesis
22. Otx genes in brain morphogenesis
23. Differential patterns of expression of Eps15 and Eps15R during mouse embryogenesis
24. Positioning the isthmic organizer
25. Genetic and molecular roles of Otx homeodomain proteins in head development
26. Conserved usage of gap and homeotic genes in patterning the CNS
27. The TINS Lecture
28. OtxGenes and the Genetic Control of Brain Morphogenesis
29. Cloning of the Human Interferon-Related Developmental Regulator (IFRD1) Gene Coding for the PC4 Protein, a Member of a Novel Family of Developmentally Regulated Genes
30. Identification and Characterization of a Novel RING-Finger Gene (RNF4) Mapping at 4p16.3
31. Xrxl, a novel Xenopus homeobox gene expressed during eye and pineal gland development
32. Uncoupling of Grb2 from the Met Receptor In Vivo Reveals Complex Roles in Muscle Development
33. Retinoic Acid Induces Stage-Specific Repatterning of the Rostral Central Nervous System
34. Retinoic acid induces stage-specific antero-posterior transformation of rostral central nervous system
35. Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and drosophila
36. Chromosome Locations of Human EMX and OTX Genes
37. HOX gene activation by retinoic acid
38. EVX2, a human homeobox gene homologous to the even-skipped segmentation gene, is localized at the 5′ end of HOX4 locus on chromosome 2
39. Differential regulation by retinoic acid of the homeobox genes of the four HOX loci in human embryonal carcinoma cells
40. Expression of HOX homeogenes in human neuroblastoma cell culture lines
41. Human HOX genes are differentially activated by retinoic acid in embryonal carcinoma cells according to their position within the four loci
42. Differential expression of human HOX-2 genes along the anterior-posterior axis in embryonic central nervous system
43. Activation of four homeobox gene clusters in human embryonal carcinoma cells induced to differentiate by retinoic acid
44. Molecular analysis of the heterogeneity region of the human ribosomal spacer
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