| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/FEBS.13622 |
| P698 | PubMed publication ID | 26662366 |
| P50 | author | Moisés Mallo | Q37619605 |
| P2860 | cites work | Retinoic acid controls body axis extension by directly repressing Fgf8 transcription | Q34341664 |
| FGF4 and FGF8 comprise the wavefront activity that controls somitogenesis. | Q34652756 | ||
| Retinoic Acid Activity in Undifferentiated Neural Progenitors Is Sufficient to Fulfill Its Role in Restricting Fgf8 Expression for Somitogenesis | Q35774500 | ||
| Segmentation in vertebrates: clock and gradient finally joined | Q35876942 | ||
| Stem cells, signals and vertebrate body axis extension | Q37460556 | ||
| Opposing FGF and retinoid pathways control ventral neural pattern, neuronal differentiation, and segmentation during body axis extension | Q44607276 | ||
| Retinoic acid signalling links left-right asymmetric patterning and bilaterally symmetric somitogenesis in the zebrafish embryo | Q46486381 | ||
| A complex oscillating network of signaling genes underlies the mouse segmentation clock. | Q51929054 | ||
| Wnt3a/beta-catenin signaling controls posterior body development by coordinating mesoderm formation and segmentation. | Q51971087 | ||
| FGF signaling acts upstream of the NOTCH and WNT signaling pathways to control segmentation clock oscillations in mouse somitogenesis. | Q51974022 | ||
| FGF signaling controls somite boundary position and regulates segmentation clock control of spatiotemporal Hox gene activation. | Q52130820 | ||
| fgf8 mRNA decay establishes a gradient that couples axial elongation to patterning in the vertebrate embryo. | Q54731950 | ||
| Mechanisms of retinoic acid signalling and its roles in organ and limb development | Q27014957 | ||
| Signaling by FGF4 and FGF8 is required for axial elongation of the mouse embryo | Q28274409 | ||
| Targeted disruption of Fgf8 causes failure of cell migration in the gastrulating mouse embryo | Q28584770 | ||
| Inactivation of FGF8 in early mesoderm reveals an essential role in kidney development | Q28585034 | ||
| RDH10 is essential for synthesis of embryonic retinoic acid and is required for limb, craniofacial, and organ development | Q28587012 | ||
| Wnt3a plays a major role in the segmentation clock controlling somitogenesis | Q28587356 | ||
| Dynamic expression and essential functions of Hes7 in somite segmentation | Q28593057 | ||
| Wnt-regulated dynamics of positional information in zebrafish somitogenesis | Q30573415 | ||
| Retinoic-acid signalling in node ectoderm and posterior neural plate directs left-right patterning of somitic mesoderm | Q33586341 | ||
| Signaling gradients during paraxial mesoderm development | Q33687019 | ||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | somitogenesis | Q3489847 |
| P304 | page(s) | 1430-1437 | |
| P577 | publication date | 2015-12-10 | |
| P1433 | published in | FEBS Journal | Q1388041 |
| P1476 | title | Revisiting the involvement of signaling gradients in somitogenesis | |
| P478 | volume | 283 |
| Q91188390 | A sense of place, many times over - pattern formation and evolution of repetitive morphological structures |
| Q28069407 | Delta-Notch signalling in segmentation |
| Q55638745 | Location, Location, Location: Signals in Muscle Specification. |
| Q41639915 | Nuclear receptor corepressors Ncor1 and Ncor2 (Smrt) are required for retinoic acid-dependent repression of Fgf8 during somitogenesis |
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