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Structural and ultrastructural analyses revealed that the engineered mucosa had a well-organized stratified epithelium on the surface of the fibroblast-populated lamina propria tissue.
Ultrastructural analyses revealed a granular OB with irregular form and size containing single rod-shaped nucleocapsid.
Ultrastructural analyses revealed inclusions in axonal processes in the spinal cord, sciatic nerve and brain, but no excess of multivesicular bodies.
Ultrastructural analyses revealed large amounts of storage material in the kidney proximal and distal tubular epithelia cells (Fig. 8A C), while mesangial cells appeared normal.
Ultrastructural analyses revealed that axonal and neuronal processes contained electron-dense complex membrane whirl inclusions in saposin C−/− mice at 18 months (Fig. 8).
Histological and ultrastructural analyses revealed vasodilation of both peripheral arteries and veins of notch3 mutants, indicating that notch3, which is expressed in the walls of both vessel types, has an essential role in limiting vasodilation.
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Ultrastructural analyses have revealed that the grana of Chl1 and Chl9 mutants are poorly stacked, resulting in the underdevelopment of chloroplasts (Zhang et al. 2006).
Ultrastructural analyses have revealed that most D-cells in the gastric corpus and antrum are open type (14), allowing them to make direct contact with, and potentially sense the composition of, the luminal contents.
Electron microscopic analyses revealed unique ultrastructural features of lanceolate complexes that are proposed to underlie mechanotransduction.
Importantly, ultrastructural imaging and subsequent detailed lysosomal activity analyses revealed reduced basal autophagic degradation and the accumulation of defective mitochondria in DJ-1 KO cells, that was linked with decreased levels of phospho-activated ERK2.
In line with ultrastructural analyses that reveal defective outer dynein arms in most patients, autosomal recessive mutations have been described in genes encoding components of the outer dynein arms, radial spokes, and cytoplasmic pre-assembly factors of axonemal dyneins.
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