MaryAnn Weis Selected Research

cyclophilin B

6/2014	Abnormal type I collagen post-translational modification and crosslinking in a cyclophilin B KO mouse model of recessive osteogenesis imperfecta.
5/2010	Generalized connective tissue disease in Crtap-/- mouse.
2/2010	Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding.

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MaryAnn Weis Research Topics

Disease

15	Osteogenesis Imperfecta (Lobstein Disease) 03/2021 - 12/2006
3	Contracture 01/2021 - 09/2014
2	Ehlers-Danlos Syndrome (Syndrome, Ehlers-Danlos) 01/2018 - 06/2008
1	Congenital Abnormalities (Deformity) 01/2021
1	Developmental Bone Diseases (Bone Dysplasia) 01/2020
1	Neoplasms (Cancer) 01/2019
1	Fibrosis (Cirrhosis) 01/2019
1	Hypoxia (Hypoxemia) 01/2019
1	Ehlers-Danlos syndrome type 6 01/2017
1	Musculoskeletal Abnormalities 11/2016
1	type VIII Osteogenesis imperfecta 01/2016
1	Lathyrism 06/2015
1	Myopia 03/2015
1	Multiple Abnormalities 05/2010
1	Segmental glomerulosclerosis 05/2010
1	Bone Diseases (Bone Disease) 03/2007
1	Osteoporosis 12/2006

Drug/Important Bio-Agent (IBA)

12	CollagenIBA 03/2021 - 12/2006
11	Collagen Type I (Type I Collagen)IBA 01/2020 - 12/2006
9	Proteins (Proteins, Gene)FDA Link 01/2020 - 12/2006
3	Tacrolimus Binding Proteins (FKBP)IBA 01/2021 - 09/2014
3	2-oxoglutarate 3-dioxygenase prolineIBA 01/2020 - 03/2007
3	cyclophilin BIBA 06/2014 - 02/2010
2	Procollagen Type IIBA 01/2019 - 01/2018
2	Mixed Function Oxygenases (Monooxygenases)IBA 05/2010 - 02/2010
1	Transcription Factors (Transcription Factor)IBA 01/2019
1	Lysine (L-Lysine)FDA Link 01/2017
1	CationsIBA 01/2016
1	CalciumIBA 01/2016
1	EnzymesIBA 03/2012
1	zinc-binding protein (zinc binding protein)IBA 06/2008