| 2020 |
Mumm S, Gottesman GS, Wenkert D, Campeau PM, Nenninger A, Huskey M, Bijanki VN, Veis DJ, Barnes AM, Marini JC, Stolina M, Zhang F, McAlister WH, Whyte MP. Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation. Bone. January 2020;130:115047. |
2 |
0 |
| 2022 |
Hedjazi G, Guterman-Ram G, Blouin S, Schemenz V, Wagermaier W, Fratzl P, Hartmann MA, Zwerina J, Fratzl-Zelman N, Marini JC. Alterations of bone material properties in growing Ifitm5/BRIL p.s42 knock-in mice, a new model for atypical type vi osteogenesis imperfecta. Bone. September 2022;162:116451. |
1 |
0 |
| 2004 |
Kozloff KM, Carden A, Bergwitz C, Forlino A, Uveges TE, Morris MD, Marini JC, Goldstein SA. Brittle IV mouse model for osteogenesis imperfecta IV demonstrates postpubertal adaptations to improve whole bone strength. J Bone Miner Res. April 2004;19(4):614-622. |
30 |
18 |
| 2022 |
Kang H, Aryal AC S, Barnes AM, Martin A, David V, Crawford SE, Marini JC. Antagonism between PEDF and TGF-β contributes to type VI osteogenesis imperfecta bone and vascular pathogenesis. J Bone Miner Res. May 2022;37(5):925-937. |
1 |
0 |
| 2016 |
Forlino A, Marini JC. Osteogenesis imperfecta. Lancet. April 16, 2016;387(10028):1657-1671. |
43 |
42 |