Loss of evolutionary conserved GM-CSF-dependent signature in pulmonary macrophages in COVID-19 provides a rationale for inhaled GM-CSF treatment (microarray)

Loss of GM-CSF-dependent instruction of alveolar macrophages in COVID-19 provides a rationale for inhaled GM-CSF treatment

Innovative mouse models for the tumor suppressor activity of Protocadherin-10 isoforms

Spatial proteogenomics reveals distinct and evolutionarily-conserved hepatic macrophage niches (single cells)

Spatial proteogenomics reveals distinct and evolutionarily-conserved hepatic macrophage niches (spatial)

Spatial proteogenomics reveals distinct and evolutionarily-conserved hepatic macrophage niches

A20 deficiency in myeloid cells protects mice from diet-induced obesity and insulin resistance due to increased fatty acid metabolism

Osteopontin expression identifies a subset of recruited macrophages distinct from Kupffer cells in the fatty liver. [Bulk RNA Seq]

Osteopontin expression identifies a subset of recruited macrophages distinct from Kupffer cells in the fatty liver. [Single cell RNA Seq]

Osteopontin expression identifies a subset of recruited macrophages distinct from Kupffer cells in the fatty liver.

Inflammatory Type 2 cDCs Acquire Features of cDC1s and Macrophages to Orchestrate Immunity to Respiratory Virus Infection (scRNA-Seq)

Inflammatory Type 2 cDCs Acquire Features of cDC1s and Macrophages to Orchestrate Immunity to Respiratory Virus Infection (microarray)

Inflammatory Type 2 cDCs Acquire Features of cDC1s and Macrophages to Orchestrate Immunity to Respiratory Virus Infection

Distinct signature, origin and dynamics of macrophages in the peripheral and central nervous system (microarray)

Distinct signature, origin and dynamics of macrophages in the peripheral and central nervous system (bulk)

Distinct signature, origin and dynamics of macrophages in the peripheral and central nervous system (single cells)

Distinct signature, origin and dynamics of macrophages in the peripheral and central nervous system

Epithelial HMGB1 delays skin wound healing and drives tumor initiation by priming neutrophils for NET formation

Stellate cells, hepatocytes and endothelial cells imprint the Kupffer cell identity on monocytes colonizing the liver macrophage niche (microarray)

Stellate cells, hepatocytes and endothelial cells imprint the Kupffer cell identity on monocytes colonizing the liver macrophage niche (RNA-Seq)