User profiles for Mahlon A. Collins

Mahlon A. Collins

Researcher, University of Minnesota
Verified email at umn.edu
Cited by 562

Label-free LC–MS/MS proteomic analysis of cerebrospinal fluid identifies protein/pathway alterations and candidate biomarkers for amyotrophic lateral sclerosis

MA Collins, J An, BL Hood, TP Conrads… - Journal of proteome …, 2015 - ACS Publications
Analysis of the cerebrospinal fluid (CSF) proteome has proven valuable to the study of
neurodegenerative disorders. To identify new protein/pathway alterations and candidate …

[HTML][HTML] Total protein is an effective loading control for cerebrospinal fluid western blots

MA Collins, J An, D Peller, R Bowser - Journal of neuroscience methods, 2015 - Elsevier
Background Cerebrospinal fluid (CSF) has been used to identify biomarkers of neurological
disease. CSF protein biomarkers identified by high-throughput methods, however, require …

[PDF][PDF] The Story of Mahlon Day Collins

HE Collins - The Iowa Journal of History and Politics, 1930 - pubs.lib.uiowa.edu
Mahlon Collins was to furnish this and did so as long as he was with them. Each mo1'ning
he started on foot as the expedition broke camp, g·oj11g ahead along· a line agreed ltpon for …

[HTML][HTML] Substrate-specific effects of natural genetic variation on proteasome activity

MA Collins, R Avery, FW Albert - PLoS genetics, 2023 - journals.plos.org
Protein degradation is an essential biological process that regulates protein abundance
and removes misfolded and damaged proteins from cells. In eukaryotes, most protein …

Variation in ubiquitin system genes creates substrate-specific effects on proteasomal protein degradation

MA Collins, G Mekonnen, FW Albert - Elife, 2022 - elifesciences.org
Precise control of protein degradation is critical for life, yet how natural genetic variation
affects this essential process is largely unknown. Here, we developed a statistically powerful …

Identification of amyotrophic lateral sclerosis disease mechanisms by cerebrospinal fluid proteomic profiling

MA Collins - 2016 - search.proquest.com
Amyotrophic lateral sclerosis (ALS) is the most common form of adult-onset motor neuron
disease. Heterogeneity in clinical, genetic, and pathological features of ALS suggest the …

[HTML][HTML] The RNA-binding motif 45 (RBM45) protein accumulates in inclusion bodies in amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration with …

M Collins, D Riascos, T Kovalik, J An, K Krupa… - Acta …, 2012 - Springer
RNA-binding protein pathology now represents one of the best characterized pathologic
features of amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration patients …

[HTML][HTML] Immunoprecipitation and mass spectrometry defines an extensive RBM45 protein–protein interaction network

Y Li, M Collins, J An, R Geiser, T Tegeler, K Tsantilas… - Brain research, 2016 - Elsevier
The pathological accumulation of RNA-binding proteins (RBPs) within inclusion bodies is a
hallmark of amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD…

[PDF][PDF] Substrate-Specific Effects of Natural Genetic Variation on Proteasome

MA Collins, RR Avery, FW Albert - scholar.archive.org
The bulk of targeted cellular protein degradation is performed by the proteasome, a multi-subunit
11 complex consisting of the 19S regulatory particle, which binds, unfolds, and …

[PDF][PDF] Genetic Basis of Variation in Ubiquitin-Proteasome System

MA Collins, G Mekonnen, FW Albert, MA Collins… - scholar.archive.org
Protein degradation by the ubiquitin-proteasome system (UPS) is an essential biological
process 32 that regulates the abundance of cellular proteins and removes damaged and …