Biography and Research Information
OverviewAI-generated summary
Jordan Fett investigates the role of type I collagen in genetic disorders affecting lung and respiratory function. Fett's research has explored mouse models of osteogenesis imperfecta, examining how distinct alterations in type I collagen contribute to varying degrees of lung and respiratory defects. Additionally, Fett has studied haploinsufficiency of the COL5A1 gene, a cause of classical Ehlers-Danlos syndrome, and its impact on intrinsic lung and respiratory changes in a mouse model. Fett's work also includes clinical case reports, such as a neonate with cyanosis and crying, and a case of Eikenella Corrodens exacerbating cystic fibrosis. Fett has collaborated with researchers including John L. Carroll, Roy Morello, Milena Dimori, and Markus S. Renno at the University of Arkansas for Medical Sciences.
Metrics
- h-index: 3
- Publications: 5
- Citations: 30
Selected Publications
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Distinct type I collagen alterations cause intrinsic lung and respiratory defects of variable severity in mouse models of osteogenesis imperfecta (2022)
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Haploinsufficiency of <i>Col5a1</i> causes intrinsic lung and respiratory changes in a mouse model of classical Ehlers‐Danlos syndrome (2022)
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A term neonate with cyanosis with crying (2021)
Collaboration Network
Top Collaborators
- Distinct type I collagen alterations cause intrinsic lung and respiratory defects of variable severity in mouse models of osteogenesis imperfecta
- Haploinsufficiency of <i>Col5a1</i> causes intrinsic lung and respiratory changes in a mouse model of classical Ehlers‐Danlos syndrome
- Distinct type I collagen alterations cause intrinsic lung and respiratory defects of variable severity in mouse models of osteogenesis imperfecta
- Haploinsufficiency of <i>Col5a1</i> causes intrinsic lung and respiratory changes in a mouse model of classical Ehlers‐Danlos syndrome
- Distinct type I collagen alterations cause intrinsic lung and respiratory defects of variable severity in mouse models of osteogenesis imperfecta
- Haploinsufficiency of <i>Col5a1</i> causes intrinsic lung and respiratory changes in a mouse model of classical Ehlers‐Danlos syndrome
- A term neonate with cyanosis with crying
- A term neonate with cyanosis with crying
- A term neonate with cyanosis with crying
- A term neonate with cyanosis with crying
- A term neonate with cyanosis with crying
- A Case of Eikenella Corrodens Causing Cystic Fibrosis Exacerbation
- A Case of Eikenella Corrodens Causing Cystic Fibrosis Exacerbation
- Distinct type I collagen alterations cause intrinsic lung and respiratory defects of variable severity in mouse models of osteogenesis imperfecta
- Distinct type I collagen alterations cause intrinsic lung and respiratory defects of variable severity in mouse models of osteogenesis imperfecta
- Distinct type I collagen alterations cause intrinsic lung and respiratory defects of variable severity in mouse models of osteogenesis imperfecta
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