Results 161 to 170 of about 43,668 (265)

The Covalent Structure of Sheep-Heart Myoglobin [PDF]

open access: bronze, 1972
Kia‐Ki Han   +4 more
openalex   +1 more source

Optimization of Nutritional and Sensory Properties of Unleavened Flatbread Developed From Maize‐Boiled Rhizome of Water Lily—Fish

open access: yesFood Science &Nutrition, Volume 13, Issue 4, April 2025.
Our study revealed that the blending ratio containing 62.62% of maize flour, 29.92% of boiled rhizome of water lily flour, and 7.45% of fish flour had the best formulation with a desirability function value of 0.516, with enhanced protein, gross energy value, potassium, iron, zinc, and overall sensory acceptability of flatbreads.
Alemu Lema Abelti   +2 more
wiley   +1 more source

Comparison of Myoglobins from Harbor Seal, Porpoise, and Sperm Whale

open access: hybrid, 1971
Dan A. Ver Ploeg   +2 more
openalex   +2 more sources

Reversible Disruption by Cupric Ions of Myoglobin and Its Carboxamidomethyl Derivative

open access: hybrid, 1967
Charles R. Hartzell   +3 more
openalex   +1 more source

IL-6/GATA2/SERPINE1 pathway is implicated in regulating cellular senescence after acute kidney injury. [PDF]

open access: yesFront Mol Biosci
Su H   +11 more
europepmc   +1 more source

An X‐Linked Ataxia Syndrome in a Family with Hearing Loss Associated with a Novel Variant in the BCAP31 Gene

open access: yesMovement Disorders, Volume 40, Issue 4, Page 672-682, April 2025.
Abstract Objective Pathogenic variants in B‐cell receptor‐associated protein (BCAP31) are associated with X‐linked, deafness, dystonia and cerebral hypomyelination (DDCH) syndrome. DDCH is congenital and non‐progressive, featuring severe intellectual disability (ID), variable dysmorphism, and sometimes associated with shortened survival. BCAP31 encodes
Martin Paucar   +10 more
wiley   +1 more source

Data Mining of the FDA Adverse Event Reporting System and Animal Experiments for Assessment of Rhabdomyolysis Risk Associated with Lipid-lowering Drugs. [PDF]

open access: yesInt J Med Sci
Kobuchi S   +10 more
europepmc   +1 more source

Identification of Compound Heterozygous Variants in OBSCN Gene Associated With Rhabdomyolysis: A Case Report

open access: yesMolecular Genetics &Genomic Medicine, Volume 13, Issue 4, April 2025.
The OBSCN gene encodes a structural protein crucial for myocyte stability and Ca2+ signaling. We identified compound heterozygous OBSCN variants in a patient with exercise‐induced rhabdomyolysis, expanding the OBSCN‐associated disease spectrum and highlighting its relevance for genetic counseling and early diagnosis of similar cases.
Xiaolan Sun   +5 more
wiley   +1 more source

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