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Recombinant DNA Technology
There are various parts of DNA recombinant technology. In this blog, we will read about them in detail. This is a very important topic in biochem...
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Aug 22 2024
Recombinant DNA Technology
Properties of Genetic Code Mutation
Properties of Genetic CodeWe often call the genetic code a degenerate codon. Four choices of nucleotides (A, U, G, C). 3 combinations of nucleoti...
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Aug 21 2024
Properties of Genetic Code Mutation
Hartnup Disease and Glycine Metabolic Effects
Brief Introduction to Hartnup DiseaseHartnup disorder was named after the first family that was diagnosed with the disease.It belongs to the cate...
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Jul 15 2024
Hartnup Disease and Glycine Metabolic Effects
INI-CET High Yield Questions For Biochemistry
Mastering the INI-CET demands a strategic approach to preparation, with an emphasis on high-yield topics proving to be a successful tactic. This
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Jul 05 2024
INI-CET High Yield Questions For Biochemistry
Mucopolysaccharides : Exceptions, Important Facts
IntroductionMucopolysaccharidosis, also known as glycosaminoglycans.They are long, straight, unbranched chains containing repetitive uronic acid
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Jun 25 2024
Mucopolysaccharides : Exceptions, Important Facts
Heme Synthesis Disorders
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...
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May 22 2024
Heme Synthesis Disorders
Glycogen Storage Diseases
Glycogen storage diseases are inherited conditions in which there is an inability of the body to store and metabolize glycogen efficiently leadin...
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Apr 16 2024
Glycogen Storage Diseases
Fanconi Anemia: Symptoms, Causes and Treatment
Fanconi anemia is an autosomal recessive disease ( Inheritance) characterized by bone marrow failure leading to pancytopenia. It is one of the ca...
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Mar 29 2024
Fanconi Anemia: Symptoms, Causes and Treatment
Phenylketonuria: Symptoms, Causes and Treatment
PKU, sometimes called phenylketonuria, is a rare genetic disorder that causes the body to accumulate the amino acid phenylalanine. PKU is caused
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Mar 20 2024
Phenylketonuria: Symptoms, Causes and Treatment
MCAD Deficiency: Causes, Symptoms, Risk Factors, Diagnosis, Treatment and Complications
Medium chain acyl-coenzyme Your body cannot turn certain fats into energy due to a genetic disorder known as a dehydrogenase (MCAD) deficiency. M...
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Jan 08 2024
MCAD Deficiency: Causes, Symptoms, Risk Factors, Diagnosis, Treatment and Complications
Gaucher Disease: Causes, Symptoms, Risk Factors, Diagnosis, Treatment and Complications
Gaucher disease can result from an accumulation of particular fatty substances in particular organs, primarily the liver and spleen. This causes
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Dec 26 2023
Gaucher Disease: Causes, Symptoms, Risk Factors, Diagnosis, Treatment and Complications
Phenylalanine And Tyrosine Metabolism, Urine Odors
Metabolism of PhenylanilinePhenylalanine is converted to tyrosine (hydroxylated phenylalanine) catalyzed by phenylalanine hydroxylase.All hydroxy...
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May 22 2023
Phenylalanine And Tyrosine Metabolism, Urine Odors
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