A PERTURBATION CELL ATLAS OF HUMAN INDUCED PLURIPOTENT STEM CELLS. Read more about A PERTURBATION CELL ATLAS OF HUMAN INDUCED PLURIPOTENT STEM CELLS.
CRISPR screens in iPSC-derived neurons reveal principles of tau proteostasis. Read more about CRISPR screens in iPSC-derived neurons reveal principles of tau proteostasis.
Automated segmentation of soft X-ray tomography: native cellular structure with sub-micron resolution at high throughput for whole-cell quantitative imaging in yeast. Read more about Automated segmentation of soft X-ray tomography: native cellular structure with sub-micron resolution at high throughput for whole-cell quantitative imaging in yeast.
Human GM-CSF/IL-3 enhance tumor immune infiltration in humanized HCC patient-derived xenografts. Read more about Human GM-CSF/IL-3 enhance tumor immune infiltration in humanized HCC patient-derived xenografts.
A multi-subunit autophagic capture complex facilitates degradation of ER stalled MHC-I in pancreatic cancer. Read more about A multi-subunit autophagic capture complex facilitates degradation of ER stalled MHC-I in pancreatic cancer.
Combinatorial effector targeting (COMET) for transcriptional modulation and locus-specific biochemistry. Read more about Combinatorial effector targeting (COMET) for transcriptional modulation and locus-specific biochemistry.
Comprehensive structure-function analysis reveals gain- and loss-of-function mechanisms impacting oncogenic KRAS activity. Read more about Comprehensive structure-function analysis reveals gain- and loss-of-function mechanisms impacting oncogenic KRAS activity.
Expansion of a bacterial operon during cancer treatment ameliorates drug toxicity. Read more about Expansion of a bacterial operon during cancer treatment ameliorates drug toxicity.
Liver CYP4A autophagic-lysosomal degradation (ALD): A major role for the autophagic receptor SQSTM1/p62 through an uncommon target interaction site. Read more about Liver CYP4A autophagic-lysosomal degradation (ALD): A major role for the autophagic receptor SQSTM1/p62 through an uncommon target interaction site.
Fetal Liver-like Organoids Recapitulate Blood-Liver Niche Development and Multipotent Hematopoiesis from Human Pluripotent Stem Cells. Read more about Fetal Liver-like Organoids Recapitulate Blood-Liver Niche Development and Multipotent Hematopoiesis from Human Pluripotent Stem Cells.