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Untargeted Metabolomic and Lipidomic Profiling Reveals Distinct Biochemical Patterns in Treated Biotinidase Deficiency. [PDF]
Ünlü Torlak E +12 more
europepmc +1 more source
Stimulation of High-Conductivity Points in Human Skin Reduces Biotin Levels to Modulate Intracellular Metabolism and Local Energy Production. [PDF]
Takagaki K +6 more
europepmc +1 more source
Recent Advances in Proximity Labeling-Based Subcellular Proteomic Mapping. [PDF]
Wang G +5 more
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Cold Spring Harbor Protocols, 2021
Biotin is a water-soluble vitamin that can be attached to a variety of proteins and nucleic acids, often without altering their properties. Its use in molecular biology is introduced here.
Michael R, Green, Joseph, Sambrook
openaire +3 more sources
Biotin is a water-soluble vitamin that can be attached to a variety of proteins and nucleic acids, often without altering their properties. Its use in molecular biology is introduced here.
Michael R, Green, Joseph, Sambrook
openaire +3 more sources
International Journal of Toxicology, 2023
The Expert Panel for Cosmetic Ingredient Safety reviewed updated information that has become available since their original assessment from 2001, along with updated information regarding product types, and frequency and concentrations of use, and reaffirmed their original conclusion that Biotin is safe as a cosmetic ingredient in the practices of use ...
Monice, Fiume +10 more
openaire +2 more sources
The Expert Panel for Cosmetic Ingredient Safety reviewed updated information that has become available since their original assessment from 2001, along with updated information regarding product types, and frequency and concentrations of use, and reaffirmed their original conclusion that Biotin is safe as a cosmetic ingredient in the practices of use ...
Monice, Fiume +10 more
openaire +2 more sources
2006
Two inherited defects in biotin metabolism are known: holocarboxylase synthetase (HCS) deficiency and biotinidase deficiency. Both lead to deficiency of all biotindependent carboxylases, i.e. to multiple carboxylase deficiency (MCD). In HCS deficiency, the binding of biotin to apocarboxylases is impaired.
Baumgartner, Matthias R, Suormala, T
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Two inherited defects in biotin metabolism are known: holocarboxylase synthetase (HCS) deficiency and biotinidase deficiency. Both lead to deficiency of all biotindependent carboxylases, i.e. to multiple carboxylase deficiency (MCD). In HCS deficiency, the binding of biotin to apocarboxylases is impaired.
Baumgartner, Matthias R, Suormala, T
openaire +3 more sources
Biotin Deficiency and Biotin Supply
Annals of the New York Academy of Sciences, 1985R, Bitsch, A, Tôth-Dersi, D, Hoetzel
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