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Tracking Down Rare Hereditary Diseases

Tracking Down Rare Hereditary Diseases
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Singapore
United-states
Frankfurt-am-main
Hessen
Germany
Frankfurt
Brandenburg
Schara-safarian
Max-planck-institute-of-biophysics
Fraunhofer-institute-for-translational-medicine
Ella-maru-studio
Max-planck-institute

Researchers reveal dynamic structure of FLVCR proteins and their function in nutrient transport

It is known that malfunctions of the proteins FLVCR1 and FLVCR2 lead to rare hereditary diseases in humans that cause motor, sensory and neurological disorders. However, the biochemical mechanisms behind this and the physiological functions of the FLVCR proteins have been unclear to date.

Frankfurt-am-main
Hessen
Germany
Frankfurt
Brandenburg
Singapore
Schara-safarian
Fraunhofer-institute-for-translational-medicine
Max-planck-institute-of-biophysics
Max-planck-institute
Fraunhofer-institute
Translational-medicine

TB research will make 'enormous global health impact'

The Otago research team, from left: Assistant Research Fellow Helen Opel-Reading, Professor Kurt Krause, Professor Greg Cook and Research Fellow Dr

New-zealand
Otago
Ahmadr-mehdipour
Helenk-opel
Sonja-welsch
Hartmut-michel
Ian-stewart
Kurt-krause
Gregorym-cook
Michele-krause
Schara-safarian
Melanie-radloff

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