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This cannot be modeled without knowledge of the rates of synthase enzyme insertion at the exocyst and endocytosis at the actin cortical patches, the diffusion constant of synthase within the membrane, and the rate of lipid insertion into the membrane.
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Objective: Our purpose was to investigate the contribution of angiotensin-converting enzyme insertion-deletion polymorphism in the development of obstetric complications.
Study Design: In a retrospective case-control study, angiotensin-converting enzyme insertion-deletion polymorphism was investigated in a control group of healthy women (n = 115) and in a group of women diagnosed with preeclampsia (n = 133) and obstetric cholestasis (n = 57).
Some ALDH genes harbored more than two TEs; for example, OsALDH18B2, which encodes a P5CS enzyme, contained insertions of a helitron (I02744) and a MITE (OS1) (Figure 2A), and the OsALDH7B6 gene contained three TEs, including a mutator-like element and a nested MITE block (Figure 2B).
The underlined nucleotide sequences indicate the sites of the restriction enzymes for insertion into multiple cloning sites of a plasmid.
The association of Angiotensin Converting Enzyme (ACE) insertion-deletion (I/D) polymorphism with Type 2 Diabetes Mellitus (T2DM) and hypertension has been extensively studied throughout various ethnic populations but largely with inconsistent findings.
In addition, in these 17 Mpl enzymes, several insertions (residues 141 152, 161 171, 262 285 and 444 450, Figure 2, yellow bars) are found only in Psychrobacter Mpl enzymes (n.b. only residues corresponding to 161 171 are also found in the NmMpl).
With enzyme sites, the insertion sequences were as follows: oligo1: 5′-CACCGCCATCTTTCTCGCGTTACC-3′, oligo2: 5′-AAACGGTAACGCGAGAAAGAT GGC-3′.
This iron-dependent enzyme catalyzes the insertion of a cis double bond at the Δ9 position of fatty acyl-CoAs with NADPH as a cofactor [13].
This increased susceptibility to proteolysis could be due to local conformational changes or to a destabilisation of the enzyme upon the insertion of the exogenous polypeptide.
The first PCR based characterisation method based on restriction enzyme analysis of insertion sequence 1311 ISS 1311 PCR-REA) and Heat shock protein 65 gene, used limited amounts of DNA but could not distinguish between most isolates [ 8, 9].
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