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Transverse section of head of chick embryo of forty-eight hours’ incubation Transverse section of head of chick embryo of fifty-two hours’ incubation, showing the lens and the optic cup. Eye formation in the human embryo begins at approximately three weeks into embryonic development and continues through the tenth week. [1]
During embryonic development of the eye, the outer wall of the bulb of the optic vesicles becomes thickened and invaginated, and the bulb is thus converted into a cup, the optic cup (or ophthalmic cup), consisting of two strata of cells.
Human embryonic development covers the first eight weeks of development, which have 23 stages, called Carnegie stages. At the beginning of the ninth week, the embryo is termed a fetus (spelled "foetus" in British English). In comparison to the embryo, the fetus has more recognizable external features and a more complete set of developing organs.
The ectoderm generates the outer layer of the embryo, and it forms from the embryo's epiblast. [13] The ectoderm develops into the surface ectoderm, neural crest, and the neural tube. [14] The surface ectoderm develops into: epidermis, hair, nails, lens of the eye, sebaceous glands, cornea, tooth enamel, the epithelium of the mouth and nose.
The notochord plays an integral role in the development of the neural tube. Prior to neurulation, during the migration of epiblastic endoderm cells towards the hypoblastic endoderm, the notochordal process opens into an arch termed the notochordal plate and attaches overlying neuroepithelium of the neural plate.
Morphogenesis also describes the development of unicellular life forms that do not have an embryonic stage in their life cycle. Morphogenesis is essential for the evolution of new forms. Morphogenesis is a mechanical process involving forces that generate mechanical stress, strain, and movement of cells, [ 1 ] and can be induced by genetic ...
Pax6 is a transcription factor that is essential to the development of the lens placode. More specifically, it is needed for the surface ectoderm to fully develop. Pax6 has been identified as a necessary transcription factor for the thickness of the lens placode. [3] SOX2 is a transcription factor that works alongside Pax6 to develop the lens ...
The current research indicates fibroblast growth factor receptors (FGFR) FGFR2 and FGFR3 as the leading factors in causing the autosomal dominant Crouzon syndrome. [7] [8] These two transmembrane proteins are two of four fibroblast growth factor receptors involved in osteoblast differentiation during embryonic development; mutations amongst these receptors are involved in several genetic ...