Sentence examples for distinctive defects from inspiring English sources

Exact(5)

Some fake paintings are so good that they contain the artist's distinctive defects.

In previous empirical data processing methods, the data grouping and distribution fitting were excessively coarse and contained distinctive defects.

Perturbations in mitochondrial fusion, fission, motility and turnover can lead to distinctive defects in neurons (Fig.  1).

Loss of HIF-1α in all cartilaginous elements using the Cre/loxP-technology of conditional tissue knock-out led to distinctive defects in the center of most long bone growth-plates reaching from the articular cap to the hypertrophic zone.

The core components regulating elongation are expressed in all cells and recruited to numerous genes; however, disruption of their function in vivo leads to distinctive defects revealing that promoter proximal pausing must be influenced by contextual transcription factors.

Similar(54)

One of the distinctive developmental defects of JMJD6-knockout mice is the thinning of the retinal layer [ 3].

Mst1/2 pancreas-specific knockout (Mst1/2-Pdx-Cre) mice were born with no distinctive pancreatic defects at birth, however, in contrast to Mst1/2 liver-specific knockout mice with the hepatomegaly phenotype, Mst1/2-Pdx-Cre mice have a significantly decrease in pancreas mass relative to that of wild-type littermate controls at adult age [ 59, 60].

A null mutation in the fax-1 gene causes a distinctive movement defect.

Homozygous dcl1-7 and dcl1-8 plants containing the L1 GUS transgene were identified by their distinctive recessive phenotypic defects [53].

http://dx.doi.org/10.1016/j.coph.2012.09.003 Glaucoma is a family of multifactorial optical neuropathies characterized by loss of retinal ganglion cells (RGCs) leading to typical optic nerve head (ONH) damage and distinctive visual field defects.

BRCAness is defined as the spectrum of phenotypes that some sporadic tumors share with BRCA mutated cancers, reflecting the underlying distinctive DNA repair defects arising from loss of HR; for example, by epigenomic down regulation of BRCA1 and FANCF [ 17].

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