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Caspase-dependent pathway can be further divided based on the initiator caspases into the extrinsic pathway or intrinsic pathway.
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The responder, aware of the initiator's IP address based on the initial request, sends a challenge message back to the initiator via unicast, allowing the initiator to associate the responder's HIT to its IP address.
A control of the degree of polymerization (DP, measured by NMR) can be achieved in the range between 6 and 24 for HA-PCB and HA-PCV, based on the initial monomer/initiator ratio.
Based on the classical initiation-promotion model, we have used N-[4- 5-nitro-2-furyl -2-thiazolyl]formamide N-[4- 5-nitro-2-furyl -2-thiazolyl]formamide N-[4- 5-nitro-2-furyl -2-thiazolyl]formamide N-[4- 5-nitro-2-furyl -2-thiazolyl]formamide N-[4- 5-nitro-2-furyl -2-thiazolyl]formamide N-[4- 5-nitro-2-furyl -2-thiazolyl]formamide N-[4- 5-nitro-2-furyl -2-thiazolyl]formamide N-[4- 5-nitro-2-furyl -2-thiazolyl]formamide
As shown in Fig. 3, approaches are categorized based on the type of project initiator (i.e. public vs. private) and the type of collected funds (i.e. purely from the crowd vs. partially from the crowd with matched funds from the government).
We developed a simple protein patterning protocol based on the deposition of an initiator monolayer (thiol for gold and silane for glass or silicon) using micro-contact printing and the adsorption of a protein of interest from solution (Fig. 2).
Based on the N-terminal prodomain, the initiators can be divided further into two categories: one class containing a caspase recruitment domain (CARD), such as caspase-2 and -9 in mammals and DRONC in fruit flies, and the other possessing a death effector domain (DED), such as caspase-8 and -10 in mammals.
In UniProtKB/Swiss-Prot, COL1A1 variants, as well as all other sequence features, are always numbered based on the canonical sequence, starting at the initiator methionine.
Our previous TSS prediction for ALMS1 was based on the presence of a potential initiator element close to the most extreme 5' cDNA sequence obtained by RT-PCR (Hearn et al., 2002; our unpublished observations).
The explosion temperature of the initiator is determined based on the "double-line atomic emission spectroscopy of a copper element" with the fundamental principle described in this literature [18, 19].
We could have used a measure of cumulative dose instead but, based on the small number of NPH initiators and the potential for time-varying confounding, opted to focus on the duration of treatment irrespective of dose analysis.
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