"complete defect" is correct and usable in written English.
It is primarily used to refer to something that is totally deficient or malfunctioning. For example, "The plane experienced a complete defect of its engine and had to be grounded immediately."
A complete defect size estimation algorithm is proposed that is more accurate and less biased by shaft speed when compared with existing methods.
Cleavage of the Mlh1 linker arm in vitro resulted in a defect in Mlh1 Pms1 DNA binding activity, and in vivo proteolytic cleavage resulted in a complete defect in MMR.
Mesp1 and Mesp2 double-knockout embryo showed a complete defect of mesodermal migration and heart formation which confirmed the compensation effect of Mesp2 for Mesp1 (Kitajima et al., 2000).
That is, a cross between the male (pollen) from an MTD1/mtd1 1 heterozygous plant and the female (ovary) of the WT shows a complete defect (0/35) in gene-transfer through the male gametophyte.
Cases presenting with an ISH and IMSH do not show a complete defect in the mesosigmoid; therefore, laparoscopic detachment of peritoneal adhesions to enable sigmoid colon mobilization is often possible and sufficient.
Treatment of meniscal full size defects with this scaffold seeded with autologous mesenchymal stem cells after resection of the pars intermedia of the medial meniscus in a rabbit model resulted in a complete defect filling after 3 months in vivo.
Also, the diagnosis of complete defects (grade IV lesions) in general did not appear to present any problems.
Importantly, the Hck / Fgr / Lyn /–, Syk /–, PLCγ2 /–, and Vav1 / Vav2 / Vav3 /– mutations all caused complete defects in leucocyte recruitment to the site of inflammation and the overall phenotype strongly resembled that of CD18 /– mice lacking all β2-integrins.
Partial or complete defects of this type have been shown to induce resistance to apoptosis in yeast (Harris et al, 2000) and mammalian cells (Tomiyama et al, 2006), and Jass has suggested that evasion of apoptosis may be the pathogenic mechanism that gives rise to the glandular serrated phenotype (Higuchi & Jass, 2004).
Additionally, when a different mtDNA is placed on this background, (sm21); Aatm Ore, bristle length is completely restored, demonstrating that both mutations are required for the complete bristle defect.
During the eight weeks observation period the application of a hollow chamber design resulted in almost complete cranial defect healing, whereby the copolymer composition had no effect on the amount or the morphology of the regenerate.
