Results 181 to 190 of about 1,616,704 (331)

Taxonomy of Mitochondrial Cytochrome B Proteins of the Same Amino Acid Sequence Length. [PDF]

open access: yesScientificWorldJournal, 2021
Zamyatnin AA   +2 more
europepmc   +1 more source

Pathway Analyses of Inherited Neuropathies Identify Putative Common Mechanisms of Axon Degeneration

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Inherited neuropathies (IN) are associated with over 100 different genetic mutations presenting with a variety of phenotypes. This complexity suggests multiple pathways may converge onto a limited number of downstream pathways to effect axonal injury.
Christopher R. Cashman   +2 more
wiley   +1 more source

Cloning and mRNA tissue distribution of rabbit cholesteryl ester transfer protein.

open access: yesJournal of Lipid Research, 1988
The amino acid sequence of rabbit cholesteryl ester transfer protein (CETP) has been obtained from cloned cDNA and genomic sequences. The 496 amino acid rabbit CETP has an overall sequence homology of 81% compared to the 476 amino acid human CETP, with ...
M Nagashima, J W McLean, R M Lawn
doaj  

Targeted modulation of protein liquid-liquid phase separation by evolution of amino-acid sequence. [PDF]

open access: yesPLoS Comput Biol, 2021
Lichtinger SM   +3 more
europepmc   +1 more source

Amino Acid Sequence Studies on Fibrinopeptides from Several Species. [PDF]

open access: bronze, 1963
Birger Blombäck   +4 more
openalex   +1 more source

Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large‐Scale Exome Sequencing

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Dystonia is one of the most prevalent movement disorders, characterized by significant clinical and etiological heterogeneity. Despite considerable heritability (~25%), the etiology in most patients remains elusive. Moreover, understanding correlations between clinical manifestations and genetic variants has become increasingly ...
Mirja Thomsen   +47 more
wiley   +1 more source

Investigating the Cellular Effects of GALC Dosing in Enzyme Replacement Therapy for Krabbe Disease Supports the Role of Nanomedicine

open access: yesAdvanced Biology, EarlyView.
A detailed workflow for recombinant GALC production and characterization is presented to support enzyme replacement therapy for Krabbe disease. In vitro assays demonstrate that physiological GALC doses restore enzymatic activity and autophagic flux without affecting cell viability, whereas higher doses impair autophagy and reduce viability.
Ambra Del Grosso   +5 more
wiley   +1 more source

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