DDR1 Deficiency in Mice: A Spontaneous Model of Bronchopulmonary Dysplasia-associated Pulmonary Hypertension?

Am J Respir Cell Mol Biol. 2022 Nov;67(5):518-519. doi: 10.1165/rcmb.2022-0312ED.
No abstract available

Publication types

  • Editorial
  • Research Support, N.I.H., Extramural
  • Comment

MeSH terms

  • Animals
  • Bronchopulmonary Dysplasia* / physiopathology
  • Discoidin Domain Receptor 1
  • Humans
  • Hypertension, Pulmonary* / physiopathology
  • Infant, Newborn
  • Infant, Premature
  • Mice
  • Pulmonary Arterial Hypertension*

Substances

  • DDR1 protein, human
  • Discoidin Domain Receptor 1