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Hence, it is justified to view sexual selection as one of the prime candidates for explaining any strong morphological differentiation that is not readily explained by ecological niche differentiation.
Paracoccidioides dimorphism can be triggered by 37°C temperatures in hosts or in culture, and the morphological differentiation that takes place during the mycelial-to-yeast transition is considered to be vital to the pathogenesis of PCM [ 43, 44].
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It is important to note that the fact that puna individuals appear as partially distinct only in the second set of PLS axes is not necessarily unusual because PLS axes are not expected to capture the main axis of morphological differentiation given that they do not maximize the within block variance [ 47, 48].
They undergo a complex process of morphological and physiological differentiation that leads to the production of exospores and specialised metabolites [ 1] with a wide range of biological activities.
Taken together, these observations suggest that efavirenz induces morphological differentiation in a manner that is dependent upon on the particular cell type.
Identification in alveolar epithelial cells has led to the implication of RAGE in important developmental processes such as morphological differentiation and increased adherence that characterize the transitioning of cuboidal surfactant-secreting ATII cells to squamous ATI cells (Buckley and Ehrhardt 2010).
Under the assumption that morphological differentiation among modern humans during the Final Pleistocene and the Holocene was mainly a result of neutral microevolutionary processes [14] [17], the observed rates of morphological differentiation favor the idea that Early and Late American samples included in this study shared a last common ancestor outside the New World.
Our data suggest that morphological differentiation may occur rapidly in Polygonia, once speciation has occurred.
Accordingly, it has been reported that morphological differentiation of neuroblastoma cells upon treatment with RA is accompanied by an increase of expression of a number of HOX genes.
Since αVβ1 and α6β1 are the only β1 integrins expressed on oligodendrocytes, and because RGD peptides would be expected to block αVβ1, we conclude that morphological differentiation leading to myelin sheet formation by oligodendrocytes on laminin-2 is α6β1-dependent.
Given the apparent lack of differentiation in chloroplast genes, yet recognized morphological differentiation, it appears be that nuclear genome markers (e.g., expressed sequence tags [ESTs] and/or microsatellites) sampled from multiple populations combined with coalescent-based analysis and detailed morphological measurement would be useful for studying the relationships of these taxa.
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