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Tracking Down Rare Hereditary Diseases

Tracking Down Rare Hereditary Diseases
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United statesFrankfurt am mainSchara safarianMax planck institute of biophysicsFraunhofer institute for translational medicineElla maru studioMax planck instituteFraunhofer instituteTranslational medicineClinical pharmacologyGoethe university frankfurt

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 mainSchara safarianFraunhofer institute for translational medicineMax planck institute of biophysicsMax planck instituteFraunhofer instituteTranslational medicineClinical pharmacologyGoethe university frankfurt

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 zealandAhmadr mehdipourHelenk opelSonja welschHartmut michelIan stewartKurt krauseGregorym cookMichele krauseSchara safarianMelanie radloffGerhard hummerGreg cookRoyal society of new zealand catalyst fundingResearch fellow dr kiel hardsNature communications