A joint study conducted by several health professionals has concluded that mutated genes found in New Delhi are to be blamed for the high triglyceride levels..
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Most of the porphyrias are inherited conditions. The genes for all the enzymes in the heme pathway have been identified. Some forms of porphyria result from inheriting one altered..
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A Personalized Plan May Be in Your Future You may be one of the many people who take vitamin and mineral supplements as a kind of insurance plan, to make sure your body’s getting enough..
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Diabetes is most often feared because of the latent damages it is associated with. Apart from raising blood sugar levels, which leads to chronic fatigue and associated symptoms, major organs..
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Insomnia is a common problem and it can affect anyone. Read to know more on who is affected by insomnia. Insomnia can affect any age group be it adults, elderly and even children...
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Scientists in USA and Finland have discovered a gene linked to premature births. They hope to eventually develop tests that could confirm the risk of early delivery in women. According to BBC,..
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Mutations in the SLC26A2 and COL2A1 genes cause achondrogenesis types 1B and 2, respectively. The genetic cause of achondrogenesis type 1A is unknown. Achondrogenesis..
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Mutations in the SLC3A1 and SLC7A9 genes cause cystinuria. The SLC3A1 and SLC7A9 genes provide instructions for making the two parts (subunits) of a transporter..
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The human red blood cells are disc-like and roughly concave in shape. When a person starts to suffer from sickle cell disease, the cells become shaped like a sickle. This has the effect of reducing..
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British researchers of the Oxford BioMedica firm are claiming that they have developed a revolutionary injection of genes that will reduce the symptoms of Parkinson’s disease...
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