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Furthermore, mapping of hα-syn throughout the rat brain revealed its absence in the SNc.
The experimental studies in the rat brain revealed a deranged neurotransmitter proflle during septic encephalopathy.
In vivo analysis of pig WJ-MSC injected into damaged rat brain revealed successful engraftment, proliferation, and differentiation into tyrosine hydroxylase positive neuronal cells without requiring immune suppression [ 89].
ELISA analysis on different days after transplantation of cells into rat brain revealed that the BDNF protein expressed in brain tissues was detectable on day 1, peaked on day 7, and persisted for two weeks.
FAK transcripts cloned from rat brain revealed several 5'-leader sequences containing various combinations of five sequences termed boxes A-E [ 39] (sequence E was later shown likely to be a cloning artifact, Studler and Girault unpublished observations).
Interestingly an N-terminal-truncated form of PYK2, named PRNK (PYK2-related non kinase), has also been reported [ 38]. Cloning FAK transcripts from rat brain revealed the existence of various 5'-leader sequences, and alternative splice variants predicting changes in the amino acid sequence of FAK [ 39, 40].
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Ex vivo autoradiograms of [18F]FMDAA1106 and [18F]FEDAA1106 binding sites in the rat brains revealed that a high radioactivity was present in the olfactory bulb, the highest PBR density region in the brain.
Radioligand binding studies on α7* and α4β2* nAChRs (rat brain homogenate) revealed one compound (7) with a 2-fold higher affinity for the α4β2*-subtype, and four compounds (11, 13, 14 and 16) with at least 3-fold higher affinity for α7* nAChR.
Similarly, in situ hybridization of synArfGEF mRNA (Accesion # AB057643) on adult rat brain sections revealed labeling only in the cell bodies of CA1 pyramidal cells in the hippocampus [40].
Immunoblot analysis of rat brain membranes revealed a single band with a molecular weight of 67 72 kDa (Arvidsson et al. 1995).
The 3D-reconstructions of frog neuromuscular junction and rat brain synaptosomes revealed readily-releasable-pool (RRP) organization and identified protein-linkages (Fernandez-Busnadiego et al. 2010; Harlow et al. 2001; Rizzoli and Betz 2004) that could presumably dock SVs in proximity to Ca2+-channels Ca2+-channels
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