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MSCs derived from unconventional model organisms all present classic fibroblast-like morphology, the expression of MSC-associated cell surface markers such as CD44, CD73, CD90 and CD105 and the absence of CD34 and CD45.
TMAs are commonly used to study tissue morphology, the expression of proteins or genes, and chromosomal aberrations using IHC and in situ hybridization (ISH) [ 11].
These cells are human derived, of non cancerogenous origin and can be differentiated into postmitotic neurons, showing DAergic features, based on morphology, the expression of neuronal and DA specific marker genes, as well as neuron type like electrophysiological properties [ 204].
In accordance with these changes in morphology, the expression of genes associated with adipogenic and osteogenic differentiation, PPARG (peroxisome-proliferator-activated receptor γ) and osteocalcin increased by RT PCR.
The identity of the MSCs was verified by their spindle-shaped morphology, the expression of the MSC markers Sca-1 and CD44 and absence of hematopoietic markers CD45 and CD11b (Supplementary Figure S2), and their abilities to differentiate into adipocytes, osteocytes, and chondrocytes in culture (data not shown) [ 38].
Similar(55)
However, no signs of atrophy were observed in muscle morphology, but the expression of atrophy genes changed during fasting.
The vascular morphology and the expression of profilin-1 in arterial tissues of spontaneously hypertensive rats and Wistar Kyoto rats were assessed.
External magnetic field (EMF) application modulated the swelling, degradation and release of PL-derived growth factors, and impacted both cell morphology and the expression and synthesis of tendon- and bone-like matrix with a more evident effect in co-cultures.
The biologic response was assessed through changes in EC morphology and the expression of fibrinolytic factors tissue plasminogen activator, plasminogen activator inhibitor type 1, profibrinolytic receptor (annexin II), and vasomotor factors endothelial nitric oxide synthase and endothelin 1.
Control and Ras cells were incubated with cytarabine, and differentiation was determined by analyzing cellular morphology and the expression of markers of granulocytic (Gr1) and monocytic differentiation (Mac1).
Of note, mouse EpiSCs exhibit XCI as they are derived from a later stage of mouse embryogenesis and resemble the morphology and the expression patterns of the hESCs [28], [29], [32].
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form the expression
shape the expression
body the expression
pattern the expression
patterns the expression
morphologically the expression
morphology the endocrine
morphology the area
morphology the sonication
morphology the tumor
morphology the yolk
morphology the ductus
morphology the concavity
morphology the inflammatory
morphology the myxosporea
morphology the number
morphology the sorbent
morphology the groundplan
morphology the transcriptome
morphology the roundness
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