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PhDDay2024 Booklet
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Loss-of-function mutations protective against human disease provide in vivo validation of therapeutic targets, but none have yet been described for type 2 diabetes (T2D). Through sequencing or genotyping of ∼150,000 individuals across 5 ancestry groups, we identified 12 rare protein-truncating variants in SLC30A8, which encodes an islet zinc transporter (ZnT8) and harbors a common variant (p.Trp32
Diagram Alla Grupper 1968-2021
Ledningsgruppsprotokoll2017-4
Ledningsgruppsprotokoll2018-1
Våning 2
https://www.ehuset.lth.se/vaning-2 - 2026-07-23
CS-lunchrum
https://www.ehuset.lth.se/cs-lunchrum - 2026-07-23
Våning 0
https://www.ehuset.lth.se/vaning-0 - 2026-07-23
Edekvata
https://www.ehuset.lth.se/edekvata - 2026-07-23
Elg
https://www.ehuset.lth.se/elg - 2026-07-23
Elgkalv
https://www.ehuset.lth.se/elgkalv - 2026-07-23
Falk
https://www.ehuset.lth.se/falk - 2026-07-23
iDet
https://www.ehuset.lth.se/idet - 2026-07-23
Våning 1
https://www.ehuset.lth.se/vaning-1 - 2026-07-23
