Sentence examples for defective development of the from inspiring English sources

Exact(22)

The overlap is most pronounced in the limb developmental defects, which likely originate in defective development of the apical ectodermal ridge or maintenance of stem cells of this specialized epithelium.

The congenital, but not hereditary, T-cell deficiency disease called DiGeorge syndrome arises from a developmental defect occurring in the fetus that results in the defective development of the thymus.

A hernia may be present at birth as the result of defective development of the abdominal wall, or it may occur later in life as the result of an injury.

Open image in new window Figure 5 The Mesp1/Mesp2 double-knockout embryos exhibited defective development of the embryonic mesoderm.

It has been also reported that the mutation in VEGFR results in the defective development of the central nervous system of Drosophila embryos [34].

However, previous results were obtained after chronic FIAU treatments, which did not allow identifying the immediate consequences of oligodendrocyte ablation that lead to the defective development of the cerebellar cortex.

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Similar(38)

sll1 mutants display extremely incurved leaves due to the defective development of sclerenchymatous cells on the abaxial side of the leaf; moreover, the overexpression of SLL1 also resulted in leaf rolling by stimulating phloem development on the abaxial side and suppressing bulliform cell and sclerenchyma development on the adaxial side (Zhang et al. 2009).

SHALLOT-LIKE 1 (SLL1) encodes a SHAQKYF class MYB family transcription factor which belongs to the KANADI family and sll1 mutant displays extremely incurved leaves because of the defective development of sclerenchymatous cells on the abaxial side.

ROLLED LEAF9 (RL9)/ SHALLOT-LIKE1 (SLL1) encodes a KANADI transcription factor, and rl9/sll1 mutants display extremely incurved leaves due to the defective development of sclerenchymatous cells on the abaxial side [ 1, 15].

To determine if loss of Akt expression contributes to the defective development of runt-1 morphants we asked whether the latter could be rescued by akt mRNA overexpression.

Moreover, mutations in the genes encoding homeobox transcription factors are responsible for the defective development of outer ears [ 17].

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