Latest Breaking News On - ஒர்கனிஸ்மால் ஆய்வுகள் - Page 1 : vimarsana.com

Heidelberg researchers replicate rare genetic defect in fish model A rare genetic defect that affects the so-called ALG2 gene can cause serious metabolic diseases in humans. It does so through the defective formation of proteins and sugar molecules. Until now, its rareness and complexity made it difficult to study this congenital glycosylation disorder. A research team led by Prof. Dr Joachim Wittbrodt and Dr Thomas Thumberger from the Centre for Organismal Studies (COS) of Heidelberg University has finally succeeded in introducing the underlying mutation in the ALG2 gene in a fish model, thus allowing the causes of these complex diseases to be studied at the molecular level.

Joachim wittbrodtThomas thumbergerEmily hendersonCentre for organismal studiesHeidelberg universityOrganismal studiesஜேயொவாகிம் விட்திப்ரொடட்எமிலி ஹென்டர்சன்மையம் க்கு ஒர்கனிஸ்மால் ஆய்வுகள்ஹைடெல்பெர்க் பல்கலைக்கழகம்ஒர்கனிஸ்மால் ஆய்வுகள்