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Milena Dimori

Showing results (1-10 of 14) with videos related to

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Physiological Reports|April 19, 2022
Haploinsufficiency of Col5a1 causes intrinsic lung and respiratory changes in a mouse model of classical Ehlers-Danlos syndromeJordan Fett, Milena Dimori, John L Carroll, et al.
JBMR Plus|August 3, 2019
The Osteocyte Transcriptome Is Extensively Dysregulated in Mouse Models of Osteogenesis ImperfectaSarah M Zimmerman, Milena Dimori, Melissa E Heard-Lipsmeyer, et al.
The Journal of Physiology|October 26, 2022
Distinct type I collagen alterations cause intrinsic lung and respiratory defects of variable severity in mouse models of osteogenesis imperfectaMilena Dimori, Jordan Fett, Sergey Leikin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 24, 2026
Dissecting primary versus secondary effects of osteogenesis imperfecta on abnormal lung development and functionMilena Dimori, Mahtab Toulany, Shafina Jahan, et al.
Scientific Reports|February 25, 2022
Loss of chaperone-mediated autophagy is associated with low vertebral cancellous bone massNisreen Akel, Ryan S MacLeod, Stuart B Berryhill, et al.
The Journal of Biological Chemistry|January 25, 2017
P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIADavid M Hudson, MaryAnn Weis, Jyoti Rai, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|February 6, 2020
Respiratory defects in the <i>Crtap</i>KO mouse model of osteogenesis imperfectaMilena Dimori, Melissa E Heard-Lipsmeyer, Stephanie D Byrum, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 20, 2024
A new Col1a1 conditional knock-in mouse model to study osteogenesis imperfectaMilena Dimori, Mahtab Toulany, Lira Samia Sultana, et al.
Bone Reports|August 15, 2018
Loss of RANKL in osteocytes dramatically increases cancellous bone mass in the osteogenesis imperfecta mouse (oim)Sarah M Zimmerman, Melissa E Heard-Lipsmeyer, Milena Dimori, et al.
Frontiers in Genetics|June 26, 2023
A <i>Rab33b</i> missense mouse model for Smith-McCort dysplasia shows bone resorption defects and altered protein glycosylationMilena Dimori, Irina D Pokrovskaya, Shijie Liu, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Physiological Reports|April 19, 2022
Haploinsufficiency of Col5a1 causes intrinsic lung and respiratory changes in a mouse model of classical Ehlers-Danlos syndromeJordan Fett, Milena Dimori, John L Carroll, et al.
JBMR Plus|August 3, 2019
The Osteocyte Transcriptome Is Extensively Dysregulated in Mouse Models of Osteogenesis ImperfectaSarah M Zimmerman, Milena Dimori, Melissa E Heard-Lipsmeyer, et al.
The Journal of Physiology|October 26, 2022
Distinct type I collagen alterations cause intrinsic lung and respiratory defects of variable severity in mouse models of osteogenesis imperfectaMilena Dimori, Jordan Fett, Sergey Leikin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 24, 2026
Dissecting primary versus secondary effects of osteogenesis imperfecta on abnormal lung development and functionMilena Dimori, Mahtab Toulany, Shafina Jahan, et al.
Scientific Reports|February 25, 2022
Loss of chaperone-mediated autophagy is associated with low vertebral cancellous bone massNisreen Akel, Ryan S MacLeod, Stuart B Berryhill, et al.
The Journal of Biological Chemistry|January 25, 2017
P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIADavid M Hudson, MaryAnn Weis, Jyoti Rai, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|February 6, 2020
Respiratory defects in the <i>Crtap</i>KO mouse model of osteogenesis imperfectaMilena Dimori, Melissa E Heard-Lipsmeyer, Stephanie D Byrum, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 20, 2024
A new Col1a1 conditional knock-in mouse model to study osteogenesis imperfectaMilena Dimori, Mahtab Toulany, Lira Samia Sultana, et al.
Bone Reports|August 15, 2018
Loss of RANKL in osteocytes dramatically increases cancellous bone mass in the osteogenesis imperfecta mouse (oim)Sarah M Zimmerman, Melissa E Heard-Lipsmeyer, Milena Dimori, et al.
Frontiers in Genetics|June 26, 2023
A <i>Rab33b</i> missense mouse model for Smith-McCort dysplasia shows bone resorption defects and altered protein glycosylationMilena Dimori, Irina D Pokrovskaya, Shijie Liu, et al.
Pageof 2