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number of genetic mutations in Schizophrenia patients called “rare coding variants.” These mutations change the proteins they produce, but for many of them, we do not yet know the functional consequences
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for place with the projects across the MRC GW4 BioMed3 Doctoral Landscape Award studentships. There are a total of 18 studentships available across the partnership. What if ribosomes carried a code that
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The GW4 BioMed3 Doctoral Landscape Programme is offering up to 18 MRC funded studentships across a range of biomedical disciplines, with a start date of October 2027. These four-year studentships provide funding for fees and stipend at the rate set by the UKRI, as well as other research training...
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Materiales de Aragón (INMA)CountrySpainCityZaragozaGeofield Contact City Zaragoza Website http://www.unizar.es Street c/ Pedro Cerbuna 12 Postal Code 50009 STATUS: EXPIRED X (formerly Twitter) Facebook
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Eindhoven Website http://www.tue.nl/ Street De Rondom 70 Postal Code 5612 AP STATUS: EXPIRED X (formerly Twitter) Facebook LinkedIn Whatsapp More share options E-mail Pocket Viadeo Gmail Weibo Blogger Qzone
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computing? Then join QuBriC, a pan-European doctoral network on quantum error correction, as a PhD candidate at TU/e, designing next-generation codes and decoders for real quantum hardware. Information
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Primary supervisor - Dr Thomas Anthony Haynes Pellet-clad interaction (PCI) is a complicated phenomenon, relatively poorly captured in current commercial fuel performance codes. Models have been
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of Entry – Intake’, code ‘8370F’ in ‘Course Title’, blank in ‘Research Area’. Press ‘Search’, select ‘PhD Population Health Sciences (FT)’, and click ‘Save selection.’ Either upload a document or write
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', ‘Full Time’ in ‘Mode of Study’, ‘2026’ in ‘Year of Entry’, ‘January’ in ‘Month of Entry – Intake’, code ‘8370F’ in ‘Course Title’, blank in ‘Research Area’. Press ‘Search’, select ‘PhD Population Health
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is shaped by microglial genes, particularly the TREM2 signalling axis. The coding mutation TREM2 R47H increases disease risk, while the coding mutation in the downstream signalling molecule PLCG2 P522R