Sentence examples for liver bat from inspiring English sources

Quagliarini et al. showed comparable Angptl8 expression levels in liver, BAT and WAT, and also in the adrenal gland [ 19].

In addition, Western blot analysis of total membranes from heart, liver, BAT, and pancreas of hadh+/+ and hadh−/− mice demonstrated the absence of the SCHAD protein in knockout mice (Fig. 1C).

Cross-linked membranes of liver, BAT and muscle samples were hybridised overnight at 42°C using 5′ digoxigenin end-labelled oligonucleotides (Eurogentec) for liver [IGF1 (5′-GATAGGGACGGGGACTTCTGAGTCTTGGGC-3′)], BAT [UCP1 (5′-CGGACTTTGGCGGTGTCCAGCGGGAAGGTGAT-3′)] and muscle [UCP3 (5′-CCCTGACTCCTTCCTCCCTGGCGATGGTTCTG-3′)] mRNA.

Approximately 100 mg of the following tissues were collected and homogenized in 1 mL of Trizol LS (Invitrogen, Carlsbad, CA): liver (bat id:BAT7, BAT17), lung (BAT05, BAT15), heart (BAT03, BAT13), kidney (BAT04, BAT14), brain (BAT02, BAT12), axillary lymph nodes (bilateral, pooled) (BAT06, BAT16), spleen (BAT10, BAT19), bone marrow (BAT01, BAT11), and gonad (BAT08, BAT20).

This GCK-mediated liver-to-BAT neuronal relay system provides a novel mechanism in modulating obesity predisposition in mice.

We also sampled 31 desert pipistrelle bats (Pipistrellus deserti) and detected an HKU9-like betacoronavirus (β-CoV) in the liver of 1 bat (prevalence 3.2%).

Different from BAT, liver mitochondria were coupled after the single addition of respiratory substrate (Fig 10. inset), synthesized a considerable amount of ATP but produced only a small amount of heat (Table 2).

Virus was not detected in the liver of either bat.

In this study, we found PPARα upregulation at both mRNA and protein levels in bat liver during torpor, providing clear evidence of PPARα in adaptation to mammalian hibernation.

When the ABVV-positive bat liver cDNA was used as a control, the nested PCR yielded an amplicon of 704 bases, and its sequence was confirmed by cloning and Sanger sequencing.

The transcription factor FOXO1, like PGC-1α, is a classical mediator of gluconeogenesis in species ranging from worms to mammals, and Foxo1 and its upstream regulator Creb1 [ 24] are expressed at a higher level in the Brandt's bat liver (Supplemental Table 3).