Works matching IS 02614189 AND DT 2022 AND VI 41 AND IP 2
Results: 11
Cytosolic GDH1 degradation restricts protein synthesis to sustain tumor cell survival following amino acid deprivation.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
The circadian clock ticks in organoids.
- Published in:
- EMBO Journal, 2022, v. 41, n. 2, p. 1, doi. 10.15252/embj.2021110157
- By:
- Publication type:
- Article
Genetic control of the pluripotency epigenome determines differentiation bias in mouse embryonic stem cells.
- Published in:
- EMBO Journal, 2022, v. 41, n. 2, p. 1, doi. 10.15252/embj.2021109445
- By:
- Publication type:
- Article
Deciphering functional tumor states at single‐cell resolution.
- Published in:
- 2022
- By:
- Publication type:
- Literature Review
A viral protein disrupts vacuolar acidification to facilitate virus infection in plants.
- Published in:
- EMBO Journal, 2022, v. 41, n. 2, p. 1, doi. 10.15252/embj.2021108713
- By:
- Publication type:
- Article
BCL‐2‐family protein tBID can act as a BAX‐like effector of apoptosis.
- Published in:
- EMBO Journal, 2022, v. 41, n. 2, p. 1, doi. 10.15252/embj.2021108690
- By:
- Publication type:
- Article
Heterotypic Amyloid β interactions facilitate amyloid assembly and modify amyloid structure.
- Published in:
- EMBO Journal, 2022, v. 41, n. 2, p. 1, doi. 10.15252/embj.2021108591
- By:
- Publication type:
- Article
NKG2D discriminates diverse ligands through selectively mechano‐regulated ligand conformational changes.
- Published in:
- EMBO Journal, 2022, v. 41, n. 2, p. 1, doi. 10.15252/embj.2021107739
- By:
- Publication type:
- Article
Ontogeny and function of the circadian clock in intestinal organoids.
- Published in:
- EMBO Journal, 2022, v. 41, n. 2, p. 1, doi. 10.15252/embj.2020106973
- By:
- Publication type:
- Article
Molecular species selectivity of lipid transport creates a mitochondrial sink for di‐unsaturated phospholipids.
- Published in:
- EMBO Journal, 2022, v. 41, n. 2, p. 1, doi. 10.15252/embj.2020106837
- By:
- Publication type:
- Article
Mutation in protein disulfide isomerase A3 causes neurodevelopmental defects by disturbing endoplasmic reticulum proteostasis.
- Published in:
- EMBO Journal, 2022, v. 41, n. 2, p. 1, doi. 10.15252/embj.2020105531
- By:
- Publication type:
- Article