Noun:

কথা হইলো মেলামাইন খাইলে,

deamination's Usage Examples:

In the human body, deamination.

It creates mutations in DNA by deamination of cytosine base, which turns it into uracil (which is recognized as.

it is inherently unstable, and can change into uracil (spontaneous deamination).

Transitions can be caused by oxidative deamination and tautomerization.

the breakdown of fat in adipose tissue to fatty acids, and oxidative deamination of neurotransmitters by monoamine oxidase.

protein forms a homotetramer that catalyzes the irreversible hydrolytic deamination of cytidine and deoxycytidine to uridine and deoxyuridine, respectively.

APOBEC3G belongs to the family of cytidine deaminases that catalyze the deamination of cytidine to uridine in the single stranded DNA substrate.

Oxidative deamination is a form of deamination that generates α-keto acids and other oxidized products from amine-containing compounds, and occurs primarily.

It is the keto acid produced by deamination of glutamate, and is an intermediate in the Krebs cycle.

inhibitor of monoamine oxidase A that exhibits selective action on serotonin deamination.

The mechanism of SHM involves deamination of cytosine to uracil in DNA by the enzyme activation-induced cytidine.

"The enzymatic deamination of 6-aminopyrimidine deoxyribonucleotides.

The enzymatic deamination of deoxycytidine 5'-phosphate and.

This pathway is responsible for the deamination of most amino acids.

It can be formed by the deamination of the purine base in deoxyadenosine monophosphate (dAMP).

While spontaneous deamination of cytosine forms uracil, which is recognized and removed by DNA repair enzymes, deamination of 5-methylcytosine forms.

brain, the NAD+/NADH ratio in brain mitochondria encourages oxidative deamination (i.

Lactose non-fermenters may increase the pH by deamination of proteins.

tryptophylquinone-dependent (TTQ-dependent) enzyme that catalyzes the oxidative deamination of a primary amine to an aldehyde and ammonia.