Protein O‐glycosylation in the Bacteroidota phylum
Species of the Bacteroidota phylum exhibit a unique O‐glycosylation system. It modifies noncytoplasmic proteins on a specific amino acid motif with a shared glycan core but a species‐specific outer glycan. A locus of multiple glycosyltransferases responsible for the synthesis of the outer glycan has been identified.
Lonneke Hoffmanns+2 more
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Patients with anorexia nervosa have an increased burden of rare, damaging mutations in the BBOX1 gene. [PDF]
Lutter M.
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Long non‐coding RNAs (lncRNAs) occupy an abundant fraction of the eukaryotic transcriptome and an emerging area in cancer research. Regulation by lncRNAs is based on their subcellular localization in HNSCC. This cartoon shows the various functions of lncRNAs in HNSCC discussed in this review.
Ellen T. Tran+3 more
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The clinical utility and prognostic value of next-generation sequencing for measurable residual disease assessment in acute myeloid leukemia. [PDF]
Liu Y, Cheng H, Sun M, Gong T, Ma J.
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Gut alterations in a chronic kidney disease rat model with diet‐induced vascular calcification
Chronic kidney disease (CKD) patients often suffer from intestinal and/or mineral and bone disorders. Using a rat model, we showed that uremic vascular calcification is associated with gut barrier alterations (decreased gut mucus production and Nlrp6 gene expression, increased gut inflammation), and plasma retention of gut‐origin uremic toxins (indoxyl
Piotr Bartochowski+13 more
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High-resolution map of the Plasmodium falciparum genome reveals MORC/ApiAP2-mediated links between distant, functionally related genes. [PDF]
Singh P+9 more
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Positive selection on rare variants of IGF1R and BRD4 underlying the cold adaptation of wild boar. [PDF]
Chen J+16 more
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Identification of Monogenic Causes of Arterial Ischemic Stroke in Children with Arteriopathies by Next-Generation Sequencing. [PDF]
Balcerzyk-Matić A+4 more
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Clinical relevance of the somatic mutational landscaping in predicting outcome of bladder cancer patients. [PDF]
Nedjadi T+6 more
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The global prevalence and genetic spectrum of primary carnitine deficiency. [PDF]
Sun L, Yao K, Wu HJ.
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