Ultimate NEET PG Biochemistry Study Materials

Brief Introduction to Hartnup DiseaseHartnup disorder was named after the first family that was diagnosed with the disease.It belongs to the cate...

Mastering the INI-CET demands a strategic approach to preparation, with an emphasis on high-yield topics proving to be a successful tactic. This

IntroductionMucopolysaccharidosis, also known as glycosaminoglycans.They are long, straight, unbranched chains containing repetitive uronic acid

Heme is a metal containing protoporphyrin ring. There are 4 pyrrole rings with metal in the center. That metal is mainly iron in hemoglobin and m...

Glycogen storage diseases are inherited conditions in which there is an inability of the body to store and metabolize glycogen efficiently leadin...

Fanconi anemia is an autosomal recessive disease ( Inheritance) characterized by bone marrow failure leading to pancytopenia. It is one of the ca...

PKU, sometimes called phenylketonuria, is a rare genetic disorder that causes the body to accumulate the amino acid phenylalanine. PKU is caused

Medium chain acyl-coenzyme Your body cannot turn certain fats into energy due to a genetic disorder known as a dehydrogenase (MCAD) deficiency. M...

Gaucher disease can result from an accumulation of particular fatty substances in particular organs, primarily the liver and spleen. This causes

Metabolism of PhenylanilinePhenylalanine is converted to tyrosine (hydroxylated phenylalanine) catalyzed by phenylalanine hydroxylase.All hydroxy...

A metabolic route and anaerobic energy source known as glycolysis has evolved in almost all sorts of organisms. The Embden-Meyerhof pathway is an...

In the human body, fatty acids are oxidized in a variety of cell structures, including the mitochondria, where only beta-oxidation takes place, t...