Exact(2)
Indeed, one of our major findings was that despite many subjects of the autism group (41.3%) displaying absence of behavioral pain reactivity to the venepuncture, individuals with autism showed a robust physiological response with a significant reactional tachycardia to the venepuncture.
Also, liver metastasis was studied, displaying absence of metastatic nodules (10/11 mice injected with A33- E1adenovirusus) and strongly reduced metastatic areas (1/11).
Similar(58)
Pax3 mutant mice display absence of muscular diaphragm.
However, in a separate project, numerous genes encoding putative flagellum and basal body proteins were silenced (our unpublished data) and one mutant displayed absence of flagellar connection (Fig. 5).
Based on those criteria 293 (76.3%) and 91 (23.7%) tumours out of the 384 that were assessable, displayed absence or presence of nuclear Snail staining respectively (Table 2).
KO mice displayed absence of ATG7, decreased pre-autophagosome-associated ATG5-ATG12 levels, LC3-I andumulossof and loss of autophagosome-bound LC3-II in BAT and SKM (EDL, extensor digitorum longus; Fig 1A) without modifying those in epididymal (e) WAT or heart (Fin 1BAT and SKM
The BIO14.6 hamster displays absence of delta-sarcoglycan from the muscle membrane, followed by the deficiency of alpha, beta and gamma sarcoglycan, reproducing the human LGMD2F phenotype [4].
Mice null for Isl1 display absence of SHF derived structures (OFT and right ventricle) and have severely reduced atrial tissue (Cai et al., 2003; Lin et al., 2007); they experience developmental arrest by ∼E9.5 and lethality around E10.5.
This may be the case of ankyloblepharon, a characteristic defect of AEC syndrome, not found in Fgfr2b −/− mice, which on the contrary display absence of eyelids (De Moerlooze et al, 2000; Revest et al, 2001).
The Sgca-null and Sgca-; Sgce-null mice displayed the absence of α-SG, while we observed the absence of ɛ-SG only in the Sgca-; Sgce-null mice.
These UV-free engineered melanomas have also displayed an absence of transcriptomic signatures of repair processes [ 51], a fact consistent with the absence of a detectable defective mismatch repair (MMR) mechanism involving the hMLH1 and MSH2 proteins in our series.
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