Nucleotides
nucleotides_bioscienceNucleotides is the premium educational podcast that students, researchers and company executives depend on for top notch and accurate bioscience knowledge essential for their career growth and success. Our editorial board consisting of high authorities figures in life science research field are keen in creating scientific content in various research domains ranging from biochemistry, cell and mole... more
| Publishes | Weekly | Episodes | 17 | Founded | a year ago |
|---|---|---|---|---|---|
| Categories | ScienceHealth & FitnessLife SciencesMedicine | ||||
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Latest Episodes
Angiotensin II receptor blockers (ARBs) are a class of antihypertensive medications that act on Angiotensin receptor I on vascular smooth muscles and adrenal glands, there by preventing the binding of Angiotensin II. This leads to a decrease in vasoc... more
ACE inhibitors are a class of medicines used in the treatment of hypertension. They block angiotensin converting enzyme and prevent angiotensin II production, thereby decrease blood pressure. Dry cough, angioedema, hypotension and hyperkalemia are co... more
Friedreich’s ataxia is an autosomal recessive condition caused due to expanded GAA repeats in the FXN gene present on chromosome 9.
Gaucher disease is an autosomal recessive condition wherein there is decreased glucocerebrosidase levels. This results in the build up of glucocerebroside in the lysosomes of macrophages which in turn accumulates in several tissues, causing damage to... more
Albinism is a recessive genetic disorder caused by mutation in the genes of any enzyme or protein taking part in melanin production. This condition causes a decrease or absence of melanin pigment, resulting in decreased skin, hair and eye pigmentatio... more
Von Hippel Lindau disease is an autosomal dominant genetic condition caused by mutation in the VHL gene found on chromosome number 3. This results in increased levels of HIF, platelet-derived and vascular endothelial growth factors, causing tumor dev... more
Tay-Sachs disease is a rare autosomal recessive condition that results from a mutation in HEX-A gene on chromosome 15 that leads to GM2 ganglioside build up within lysosomes in the neurons of CNS resulting in progressive symptoms of CNS degeneration ... more
Fabry disease is a rare genetic disorder that affects the X chromosome. It is caused by mutation in the GLA gene resulting in decreased alpha galactosidase A enzyme or alpha-gal A, leading to the buildup of large glycosphingolipids like Globotriaosyl... more
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| Gender Skew | Engagement Score | Primary Location | |||
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Nucleotides launched a year ago and published 17 episodes to date. You can find more information about this podcast including rankings, audience demographics and engagement in our podcast database.
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