Exact(2)
Interference with either arm of this pathway should allow highly targeted pharmacological intervention, provided that compounds with sufficient selectivity can be identified (Refs 3, 4, 5, 6, 7, 8, 9) (Fig. 1).
Cytosolic proteins that specifically recognise and bind IREs (IRP1 and IRP2) were later identified (Refs 11, 12), and subsequently the identification of five IRE motifs in the 3′ UTR of the mRNA for transferrin receptor 1 (TfR1) (approved gene symbol TFRC) (Ref. 13), which controls cellular iron uptake, indicated that IRPs might be the common regulators of genes involved in iron homeostasis.
Similar(57)
Several major effect resistance genes have been mapped [4], but only one of these has been identified (ref(2 P; see above).
The resulting N-acetylglucosaminylinositol phosphate [1- O- 2-acetamido-2-deoxy-α- d-glucO- 2-acetamido-2-deoxy-α-tO- 2-acetamido-2-deoxy-α-ephO- 2-acetamido-2-deoxy-α-s gene has nO- 2-acetamido-2-deoxy-α-Ref. 81) and deacetylated by MshB (Ref. 82).
For example "wvn60.23/ray" refers to the 60th chronological post in which the "wvn" (identifying ref to be supplied) thread was embedded, and the 23rd post deemed to have maintained that topic.
Corresponding ELISA and multiplex approaches primarily identified VEGF (Refs 86, 87, 88), hepatocyte growth factor (HGF) (Refs 82, 89) and insulin-like growth factor-1 (IGF-1) (Refs 77, 90) as factors that are responsible for the described intercellular communication.
This region was selected to encompass the 1 2 Mb highly differentiated interval defined by F ST identified by refs [ 12, 13].
They could be the states at ≈0.8 eV below the CBM that were identified in refs. 9, 10, which may then be compensated by the hydrogen donor species.
We have started from a manual superposition of the likely Na+-binding ligands of KR2, identified in refs. [ 16, 38, 40, 41, 51], and the Na+-binding ligands of Na+-bound δ-opioid receptor (hereafter δ-OR, PDB: 4N6H) [ 26].
The molecular mechanisms of the interaction of P. falciparum with platelets are not fully understood; however, three platelet receptors for clumping have been identified: CD36 (Ref. 13), globular C1q receptor (gC1qR/HABP1/p32) (Ref. 107) and P-selectin (Ref. 141).
Reference categories for each variable are identified with (ref).
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