264) (A)-associated elongation checkpoint of a protein-coding gene model. |
265) extra copy of β-amyloid-(Aβ)-precursor-protein gene. |
266) ndent kinase 1 (CDK1), mitogen-associated protein kinases (MAPKs), and protein kinas |
267) though endogenous ouabain stimulates both protein kinases and NKA endocytosis, digit |
268) ndent activation of the mitogen-activated protein kinases, ERK1/2, in human airway e |
269) athways relayed by distinct intracellular protein/lipid kinases, and endocytosis cha |
270) We leverage Bisbee's prediction of protein level effects as a benchmark of it |
271) e impact of GRK1 missense variants at the protein level were then predicted using a |
272) Here, we found that FTO protein levels, but not RNA levels, were d |
273) lated (r = 0.87, P < 0.001) with AADAC protein levels, suggesting that the enzyme |
274) GNIFICANCE STATEMENT: New developments in protein mass spectrometry are facilitating |
275) argely unknown until the advent of modern protein mass spectrometry techniques that |
276) tations, indicating mutations in the same protein may cause neuropathy through diffe |
277) Thus, the Sars-Cov-2 E protein may initially suppress the host NL |
278) These predicted protein networks can inform future researc |
279) investigate gene ontologies and predicted protein-interaction networks. |
280) actors in cancer, particularly microsomal protein per gram of liver (MPPGL) and cyto |
281) scalars, namely microsomal and cytosolic protein per gram of liver, is not known in |
282) Label-free protein quantification allowed insights in |
283) proteomic methods are currently used for protein quantification in tissues and in v |
284) reticulum (ER) lumen triggers an unfolded protein response (UPR) for stress adaptati |
285) The unfolded protein response (UPR) is an intracellular |
286) Many of these metabolic responses to protein restriction are secondary to trans |
287) the kidney.NEW & NOTEWORTHY Long-term protein restriction is not advantageous fo |
288) ous effect of SHANK1 p.(Gly126Arg) on the protein structure and the related function |
289) analyses to evaluate how their impact on protein structure could lead to pathogenic |
290) ex- and tissue-specific effects of Rap on protein synthesis, adding Met yielded more |
291) ult of increased AR gene transcription or protein synthesis, nor is it fully abrogat |
292) monstrate that the noncovalent capture of protein targets on EM grids modified with |
293) research in cancer is largely focused on protein targets that are encoded by about |
294) desirable to verify experimentally that a protein used for hit optimization in vitro |
295) system group, although the type of plasma protein used in in vitro assays may requir |
296) translation initiation factor 4E-binding protein (4E-BP) 1 in the translational com |
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