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In eye-specific somatic clones, homozygous mutation of dOpa1 causes rough (mispatterning) and glossy (decreased lens deposition) eye phenotypes in adult Drosophila.
In the eye-specific somatic clones, homozygous mutation of dOpa1 caused rough (mispatterning) and glossy (decreased lens deposition) eye phenotypes in adult Drosophila and is associated with increased ROS production [18].
In the eye-specific somatic clones, the somatic homozygous mutation of dOpa1 in the eyes caused rough (mispatterning) and glossy (decreased lens and pigment deposition) eye phenotypes in adult Drosophila.
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He et al. observed an increase in mature collagen type I deposition in eyes that have suffered acute symptomatic episodes of angle closure, along with their contralateral fellow eyes [ 14].
Expression of the w+ gene, which is necessary for pigment deposition in the eye, is modulated clonally by the state of this nearby chromatin.
Eye deposition of amyloid may occur from 4-5 yeafterfthe the liver transplantation [ 14].
Also, membrane-bound regulatory proteins in the eye block deposition of C3b (deposition involved in opsonophagocytosis of gram-positive bacteria) so that the complement pathway will not destroy self-tissue of the eye.
We believe that this is because the b g8 mutation suppresses melanin deposition in the eyes less severely than the i-3 mutation.
Mice that were sensitized by immunization with CEP-adducted proteins display complement deposition in the eyes and develop signs of AMD [114].
It was understandable that the b g8 and i-3 mutations reduced viability because these mutations suppress melanin deposition in the eyes (and skin), causing a typical phenotype known as albino.
A re-examination of posterior corneal surface did not reveal Krukenberg's spindle or any other pigment deposition patterns in either eye.
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