Results 61 to 70 of about 508,657 (349)

Posttranslational modifications of GLUT4 affect its subcellular localization and translocation [PDF]

open access: yes, 2013
The facilitative glucose transporter type 4 (GLUT4) is expressed in adipose and muscle and plays a vital role in whole body glucose homeostasis. In the absence of insulin, only ~1% of cellular GLUT4 is present at the plasma membrane, with the vast ...
Bayer   +64 more
core   +3 more sources

Novel biochemistry: post-translational protein splicing and other lessons from the school of antigen processing [PDF]

open access: yesJournal of Molecular Medicine, 2005
In the past 15 years, the molecular identification of antigens that can mediate the killing of tumor cells by T cells has been vigorously pursued. Molecular identification of tumor-associated antigens not only provided the means to activate or monitor anti-tumor immunity, but also gave insights into new and unexpected biochemical processes that are ...
Ken-ichi, Hanada, James C, Yang
openaire   +2 more sources

How can platelet proteomics best be used to interrogate disease?

open access: yesPlatelets, 2023
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

Glycosylation and S-palmitoylation regulate SARS-CoV-2 spike protein intracellular trafficking

open access: yesiScience, 2022
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

Molecular medicine of microRNAs: structure, function and implications for diabetes [PDF]

open access: yes, 2008
MicroRNAs (miRNAs) are a family of endogenous small noncoding RNA molecules, of 19–28 nucleotides in length. In humans, up to 3% of all genes are estimated to encode these evolutionarily conserved sequences.
Duncan   +5 more
core   +1 more source

Nonsynonymous Mutations in Intellectual Disability and Autism Spectrum Disorder Gene PTCHD1 Disrupt N-Glycosylation and Reduce Protein Stability

open access: yesCells
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

STAT3 as a mediator of oncogenic cellular metabolism: Pathogenic and therapeutic implications

open access: yesNeoplasia: An International Journal for Oncology Research, 2021
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

Post-translational glycosylation and proteolytic processing of a lysyl oxidase precursor.

open access: yesJournal of Biological Chemistry, 1992
The synthesis and post-translational processing of a lysyl oxidase precursor protein predicted by the cDNA sequence of rat aorta lysyl oxidase were investigated.
Philip   +5 more
semanticscholar   +1 more source

Mass spectrometry quantification of clusterin in the human brain

open access: yesMolecular Neurodegeneration, 2012
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

The role of the Amyloid Precursor Protein mutations and PERK-dependent signaling pathways in the pathogenesis of Alzheimer’s disease [PDF]

open access: yes, 2016
Alzheimer’s disease (AD) is a highly complex, progressive, age-related neurodegenerative human disease entity. The genetic basis of AD is strictly connected with occurrence of mutations in Amyloid Precursor (APP) gene on chromosome 21.
Diehl, J. Alan   +5 more
core   +2 more sources

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