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The most studied terminal kinases of these pathways: extracellular signal regulated protein kinases (ERK), c-Jun NH2-terminal kinases (JNK), and p38, activate transcription factors that ultimately affect gene expression [ 10].
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Endostatin is a polypeptide of 184 amino acids, corresponding to the globular domain found at the C-terminal of type XVIII collagen, and it is the most studied of the endogenous angiogenesis inhibitors.
These fusions were most frequently studied in two terminal taxa of the minutoides group (MOTU 26 - musculoides and MOTU 27 - minutoides), but they were also observed in M. goundae and M. oubangui (very probably belonging to the sorella group) and in M. triton (MOTU 4) [ 9].
Up to now, most studies conducted in barley focused on effects of terminal drought stress whereas drought in juvenile stages is less well documented [ 10].
A 3'-terminal dideoxynucleotide has been utilized in most studies [ 34, 35].
Of note, expression in nerve terminals is typically not detected in most studies as they represent only a minor fraction of the overall expression.
In Pseudomonas resinovorans CA10, the most intensively studied pseudomonad, CARDO consists of a terminal oxygenase, a ferredoxin, and a ferredoxin reductase, encoded by carAa, carAc, and carAd, respectively.
Most studies of RPA post-translational modifications have focused on hyperphosphorylation of the 40-amino-acid (aa) N-terminal region of human RPA2 in response to DNA damage.
While most studies focused on general dialysis populations, two PD studies [ 58, 60] and one HD study [ 63] examined HC in special dialysis populations that had severe disability, terminal illness or complex comorbid conditions.
In the most extensively studied diaphanous formin, mDia1, and the interaction of the N-terminal DID domain with the C-terminal diaphanous activating domain (DAD) inhibit mDia1 function.
The most extensively studied collagen-derived markers in liver fibrosis are the N-terminal propeptide of type III procollagen (PIIINP) and type IV collagen [ 8- 11].
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