Deborah Krakow
16PUBLICATIONS
55CO-AUTHORS
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Publications (16)
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|May 04, 2024
Clinical utility of comprehensive gene panel testing for common and rare causes of skeletal dysplasia and other skeletal disorders: Results from the largest cohort to date.Gretchen MacCarrick, Swaroop Aradhya, Mitch Bailey
|Feb 13, 2023
Nosology of genetic skeletal disorders: 2023 revision.Sheila Unger, Carlos R Ferreira, Geert R Mortier
|Jan 08, 2022
4-PBA Treatment Improves Bone Phenotypes in the Aga2 Mouse Model of Osteogenesis Imperfecta.Ivan Duran, Jennifer Zieba, Fabiana Csukasi
|Jun 23, 2021
Localized chondro-ossification underlies joint dysfunction and motor deficits in the Fkbp10 mouse model of osteogenesis imperfecta.Joohyun Lim, Caressa Lietman, Matthew W Grol
|May 06, 2021
An RNA aptamer restores defective bone growth in FGFR3-related skeletal dysplasia in mice.Takeshi Kimura, Michaela Bosakova, Yosuke Nonaka
|Nov 17, 2020
Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling.Michaela Bosakova, Sara P Abraham, Alexandru Nita
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Frequent Collaborators
4 joint publications
Michaela Kunova Bosakova
3 joint publications
Ivan Duran
2 joint publications
Stephen P Robertson
2 joint publications
Daniel H Cohn
2 joint publications
Bohumil Fafilek
2 joint publications
Tomas Gregor
2 joint publications
Pavel Krejci
2 joint publications
Greggory R DeVore
1 joint publications
Lukas Balek
1 joint publications
Miroslav Varecha
