The Amino Acid Sequence of Wheat Germ Cytochrome c
Frits C. Stevens+2 more
openalex +1 more source
The Possibility of Common Amino Acid Sequences in High-Sulphur Protein Fractions from Wool [PDF]
RL Darskus, JM Gillespie, H. Lindley
openalex +1 more source
ABSTRACT Objective Paroxysmal kinesigenic dyskinesia (PKD) is the most common hereditary paroxysmal movement disorder. The PRRT2 gene is the first identified causative gene and accounts for the majority of PKD. In this study, we investigated the pathogenicity of PRRT2 variants in the splice regions. Methods Patients with clinically suspected PKD and no
Jiao‐Jiao Xu+5 more
wiley +1 more source
Comparative analysis of amino acid sequence level in plant GATA transcription factors. [PDF]
Kim M.
europepmc +1 more source
Amino acid sequence homology between thyroid autoantigens and central nervous system proteins: Implications for the steroid-responsive encephalopathy associated with autoimmune thyroiditis. [PDF]
Benvenga S+5 more
europepmc +1 more source
Crystalline Leghemoglobin. XI. The Amino Acid Sequences of two Histidine-containing Tryptic Peptides of the Slow Component. [PDF]
Nils Ellfolk+5 more
openalex +1 more source
ABSTRACT Objective Epilepsy is increasingly associated with immune dysregulation and inflammation. The T cell receptor (TCR), a key mediator of adaptive immunity, shows repertoire alterations in various immune‐mediated diseases. The unique TCR sequence serves as a molecular barcode for T cells, and clonal expansion accompanied by reduced overall TCR ...
Yong‐Won Shin+12 more
wiley +1 more source
Amino acid sequence encodes protein abundance shaped by protein stability at reduced synthesis cost. [PDF]
Buric F+9 more
europepmc +1 more source
The Amino Acid Sequence of Cytochrome b5
Juris Ozols, Philipp Strittmatter
openalex +1 more source
INF2‐Related Charcot–Marie–Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights
ABSTRACT Background INF2 mutations cause focal segmental glomerulosclerosis (FSGS) and Charcot–Marie–Tooth disease (CMT). Accurate genetic diagnosis is critical, as INF2‐related FSGS is typically resistant to immunotherapy yet rarely recurs after transplantation, and its associated neuropathy can mimic treatable immune‐mediated disorders such as ...
Chikashi Yano+27 more
wiley +1 more source