A recent joint investigation identified uncommon mutations in the YKT6 gene as the source of a novel neurological illness characterised by developmental delays, severe progressive liver disease, and a risk…

A Covid-19 diagnosis is no longer as frightening as it used to…
Scientists at the DZD partner German Institute of Human Nutrition Potsdam-Rehbrucke (DIfE)…
The waist-to-height ratio predicts the incidence of heart failure, according to data…
When obese children receive weight-loss treatment, the effects last throughout their lives,…

Researchers discovered that early puberty or childbirth doubles women's risk…

The Government e-Marketplace (GeM) has enabled cumulative procurement of over…

The Government e-Marketplace (GeM) has enabled cumulative procurement of over…

The Government e-Marketplace (GeM) has enabled cumulative procurement of over…

The Indian Council of Medical Research (ICMR), through its Regional…

The Indian Council of Medical Research (ICMR), through its Regional…

The Indian Council of Medical Research (ICMR), through its Regional…

The Indian Council of Medical Research (ICMR), through its Regional…

The Indian Council of Medical Research (ICMR), through its Regional…

Gene editing technologies, such as those used in agriculture and…
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