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1. A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism. Issue 10 (7th August 2019)

5. Biallelic mutation of human SLC6A6 encoding the taurine transporter TAUT is linked to early retinal degeneration. Issue 10 (25th July 2019)

6. BRD4 inhibition regulates MAPK, NF‐κB signals, and autophagy to suppress MMP‐13 expression in diabetic intervertebral disc degeneration. Issue 10 (22nd July 2019)

7. C5a receptors C5aR1 and C5aR2 mediate opposing pathologies in a mouse model of melanoma. Issue 10 (12th July 2019)

9. Circulating levels of butyrate are inversely related to portal hypertension, endotoxemia, and systemic inflammation in patients with cirrhosis. Issue 10 (25th July 2019)

10. Constitutive TNF‐α signaling in neonates is essential for the development of tissue‐resident leukocyte profiles at barrier sites. Issue 10 (29th June 2019)