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EcadAb ES cells propagated as a dispersed cell suspension for 15 d maintained expression of pluripotent markers, exhibited a normal karyotype and high viability.
These 14 markers exhibited a wide range of variation in marker genotypes among 10 sequenced lupin cultivars.
In several DH populations derived by androgenesis, we found chromosomes (2B, 3B, 1R, 2R, 4R and 7R) containing regions where markers exhibited a distorted segregation pattern.
All markers exhibited a prognostic value in deceased patients; S100B and MIA were the best predictors for survival time by Cox proportional-hazard regression.
After three passages, the expression of hematopoietic and pluripotency markers decreased, while the expression of mesenchymal stem cell markers exhibited a striking rise.
Although the vast majority of genotyped markers exhibited a picture coherent with their associated scaffolds, a few of them were discordant, pinpointing potential assembly errors.
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Two markers exhibited an underrepresentation of both homozygote classes, yielding a heterozygote excess.
In control retinas, these markers exhibited an organized, parallel and largely colocalized alignment within the OPL (Fig. 7A).
Both apoptotic and necrotic cell death markers exhibited an age‐dependent accumulation and segmental distribution in rat skeletal muscle.
However, these tumor markers exhibit a low sensitivity in detecting ESCC.
Map order was improved by maintaining markers exhibiting a nearest neighbor stress value less than 2 cM.
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