Results 1 to 10 of about 233,151 (265)
Consequences of Disease-causing Mutations on Lubricin Protein Synthesis, Secretion, and Post-translational Processing [PDF]
Lubricin, a protein product of the gene PRG4, is a secreted mucin-like proteoglycan that is a major lubricant in articulating joints. Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
David K, Rhee +8 more
openaire +2 more sources
Controlling the activation of the NLRP3 inflammasome by post-translational modifications (PTMs) of critical protein subunits has emerged as a key determinant in inflammatory processes as well as in pathophysiology. In this review, we put into context the
Zhu Liang +3 more
doaj +1 more source
Poly ADP-ribosylation of proteins. Processivity of a post-translational modification.
The nuclear enzyme poly(ADP-ribose) polymerase (EC 2.4.2.30) participates in DNA excision repair by post-translational selfmodification ("automodification") and the modification of other chromatin proteins ("heteromodification") with ADP-ribose polymers.
H, Naegeli, P, Loetscher, F R, Althaus
openaire +2 more sources
How can platelet proteomics best be used to interrogate disease?
Various modifications of proteins and the resulting proteoforms of a protein can associate with many diseases and are also significantly involved in the rapid regulation of hemostasis and thrombosis.
Maria Zellner
doaj +1 more source
STAT3 as a mediator of oncogenic cellular metabolism: Pathogenic and therapeutic implications
The oncogenic transcription factor signal transducer and activator of transcription 3 (STAT3) is activated constitutively in a wide array of human cancers. It is an appealing molecular target for novel therapy as it directly regulates expression of genes
Isidora Tošić, David A. Frank
doaj +1 more source
PTCHD1 has been implicated in Autism Spectrum Disorders (ASDs) and/or intellectual disability, where copy-number-variant losses or loss-of-function coding mutations segregate with disease in an X-linked recessive fashion. Missense variants of PTCHD1 have
Connie T. Y. Xie +4 more
doaj +1 more source
Mass spectrometry quantification of clusterin in the human brain
Background The multifunctional glycoprotein clusterin has been associated with late-onset Alzheimer’s disease (AD). Further investigation to define the role of clusterin in AD phenotypes would be aided by the development of techniques to quantify level ...
Chen Junjun +2 more
doaj +1 more source
Glycosylation and S-palmitoylation regulate SARS-CoV-2 spike protein intracellular trafficking
Summary: Post-translational modifications (PTMs), such as glycosylation and palmitoylation, are critical to protein folding, stability, intracellular trafficking, and function.
Chih-Feng Tien +13 more
doaj +1 more source
New mechanism for post-translational processing during assembly of a cytoplasmic membrane protein? [PDF]
Insertion of nitrate reductase into the Escherichia coli cytoplasmic membrane was examined by following the fate of pulse-labeled enzyme in both the membrane and cytoplasm during various times after the addition of an unlabeled chase. The polypeptide composition of this labeled enzyme was determined by autoradiography of immunoprecipitated material ...
C H, MacGregor, G E, McElhaney
openaire +2 more sources
Rescue of Heart Failure by Mitochondrial Recovery [PDF]
Heart failure (HF) is a multifactorial disease brought about by numerous, and oftentimes complex, etiological mechanisms. Although well studied, HF continues to affect millions of people worldwide and current treatments can only prevent further ...
Jubert Marquez +3 more
doaj +1 more source

