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hypaxial sentence in Hindi

"hypaxial" meaning in Hindihypaxial in a sentence
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  • The SIX1 gene plays a critical role in hypaxial muscle differentiation in myogenesis.
  • In mice lacking this gene, severe muscle hypoplasia affected most of the body muscles, specifically hypaxial muscles.
  • Therefore, variability in AGR within the hypaxial musculature of the Siren lacertian counteracts varying mesolateral fiber distances and optimizes performance.
  • Its trigeminal canals contain separate hypaxial electric organ, extending along the entire ventral margin of the fish's body.
  • In addition, some segmented muscle groups, such the lateral hypaxial musculature in the salamander are oriented at an angle to the longitudinal direction.
  • Azizi " et al . " found that longitudinal contractions of the constant volume hypaxial muscles were compensated by an increase in the dorsoventral dimensions.
  • The limb myogenic precursors ( derived from the hypaxial myotome ) do not begin expressing Myf5 or any MRFs, in fact, until after migration to the limb buds.
  • Bulging was accompanied by fiber rotation as well as an increase in both ? hypaxial fiber trajectory and architectural gear ratio ( AGR ), a phenomenon also seen in pennate muscle contractions.
  • Specifically, it is first seen in the dorsomedial portion of the dermomyotome, which develops into the epaxial myotome . it is instead directly activated by the transcription factor Pax3 in hypaxial cells.
  • Specifically, while Myf5 plays a large role in the initiation of epaxial development, MyoD directs the initiation of hypaxial development, and these separate lineages can compensate for the absence of one or the other.
  • In fishes, salamanders, caecilians, and reptiles, the body musculature remains segmented as in the embryo, though it often becomes folded and overlapping, with epaxial and hypaxial masses divided into several distinct muscle groups.
  • The exception is " Trichosurus ", which remarkably among marsupials has shifted the hypaxial muscles from the epipubic to the pelvis, exploying a more placental-like breathing, having lost the benefits of the epipubic in regards to lung ventilation.
  • PAX3 is generally expressed at its highest levels during embryonic development and is expressed at a lesser degree during the fetal stages; it is expressed in migrating hypaxial cells and dermomyotome cells, but is not expressed at all during the development of facial muscle.
  • Azizi " et al . " constructed a mathematical model to predict the final hypaxial fiber angle, AGR and dorsoventral height, where : ?x = longitudinal extension ratio of the segment ( portortion of final longitudinal length after contraction to initial longitudinal length ), ? = final fiber angle, ? = initial fiber angle, f = initial fiber length, and ?x and ?f = longitudinal and fiber strain respectively.
  • Only placentals, and possibly the early mammaliformes " Megazostrodon " and " Erythrotherium ", lack them; in thylacines and sparassodonts, they appear to have become primarily cartilaginous and the osseous element has become strongly reduced or even absent . " Trichosurus " mimicked placentals in shifting hypaxial muscles attachment sites from the epipubic to the pelvis, losing the respiratory benefits ( see below ), but otherwise retains large epipubics.
  • Via this equation, we see that z is directly proportional to ?; the strain experienced by the EO exceeds that of the IO . Azizi " et al . " discovered that the initial hypaxial fiber ? trajectory in the EO is greater than that of the IO . Because initial ? trajectory is proportional to the AGR, the EO contracts with a greater AGR than the IO . The resulting velocity amplification allows both layers of muscles to operate at similar strains and shortening velocities; this enables the EO and IO to function on comparable portions of the length-tension and force-velocity curves.

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