Discovery of ultrafast myosin, its amino acid sequence, and structural features. [PDF]
Proc Natl Acad Sci U S A, 2022 Haraguchi T +9 more
europepmc +1 more source
Neuropeptide Y: complete amino acid sequence of the brain peptide.
Proceedings of the National Academy of Sciences of the United States of America, 1982 K. Tatemoto
semanticscholar +1 more source
Evaluating the involvement of autolysosomes in the nuclear translocation of fluorescent proteins
FEBS Open Bio, EarlyView.Endogenously expressed fluorescent proteins can be degraded by autophagy and transported to cell nuclei via the nuclear pore complex. But in some cell lines, for example, HeLa cells which are positive for immunoreactivity of a receptor ligand, such as UCN I, in cell nuclei, fusion of autolysosome with the nuclear envelope is involved in the nuclear ...
Keiichi Ikeda
wiley +1 more source
Calling the amino acid sequence of a protein/peptide from the nanospectrum produced by a sub-nanometer diameter pore. [PDF]
Sci Rep, 2022 Liu X, Dong Z, Timp G.
europepmc +1 more source
Aging Is a Key Driver for Adult Acute Myeloid Leukemia
Aging and Cancer, EarlyView.Acute myeloid leukemia (AML) is a classical age‐related hematologic malignancy, and a key driver of AML is aging, which profoundly regulates intrinsic factors such as genomic instability, epigenetic reprogramming, and metabolic dysregulation, and alters bone marrow microenvironment.
Rong Yin, Haojian Zhang
wiley +1 more source
Targeted modulation of protein liquid-liquid phase separation by evolution of amino-acid sequence. [PDF]
PLoS Comput Biol, 2021 Lichtinger SM +3 more
europepmc +1 more source
A method for the determination of amino acid sequence in peptides.
Archives of biochemistry, 1949 P. Edman +3 more
semanticscholar +1 more source
Mutant NPM1 in Acute Myeloid Leukemia Initiation and Maintenance
Aging and Cancer, EarlyView.NPM1 mutations drive acute myeloid leukemia by acting as neomorphic transcriptional regulators that cooperate with Menin–MLL and XPO1 to sustain HOX/MEIS1 expression and block differentiation. Targeting these mutant‐specific transcriptional dependencies provides a rational therapeutic strategy for NPM1‐mutated AML.
Yanan Jiang +3 more
wiley +1 more source
Taxonomy of Mitochondrial Cytochrome B Proteins of the Same Amino Acid Sequence Length. [PDF]
ScientificWorldJournal, 2021 Zamyatnin AA +2 more
europepmc +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi +2 more
wiley +1 more source