Ontology highlight
ABSTRACT:
INSTRUMENT(S): TripleTOF 5600
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Lung
DISEASE(S): Pulmonary Alveolar Microlithiasis
SUBMITTER: ken greis
LAB HEAD: Kenneth D. Greis
PROVIDER: PXD039280 | Pride | 2023-03-11
REPOSITORIES: Pride
Items per page: 1 - 5 of 6 |
Nature communications 20230302 1
Pulmonary alveolar microlithiasis is an autosomal recessive lung disease caused by a deficiency in the pulmonary epithelial Npt2b sodium-phosphate co-transporter that results in accumulation of phosphate and formation of hydroxyapatite microliths in the alveolar space. The single cell transcriptomic analysis of a pulmonary alveolar microlithiasis lung explant showing a robust osteoclast gene signature in alveolar monocytes and the finding that calcium phosphate microliths contain a rich protein ...[more]