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M Shore

Showing results (381-390 of 422) with videos related to

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Journal of Neurology|June 28, 2012
CNS demyelination in fibrodysplasia ossificans progressivaLixin Kan, Joseph A Kitterman, Daniele Procissi, et al.
American Journal of Human Genetics|January 13, 2000
Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 31, 2016
Cellular Hypoxia Promotes Heterotopic Ossification by Amplifying BMP SignalingHaitao Wang, Carter Lindborg, Vitali Lounev, et al.
Biomolecules|July 29, 2023
Polypeptide Substrate Accessibility Hypothesis: Gain-of-Function R206H Mutation Allosterically Affects Activin Receptor-like Protein Kinase ActivityJay C Groppe, Guorong Lu, Mary R Tandang-Silvas, et al.
Science Immunology|March 3, 2023
CD19 CAR antigen engagement mechanisms and affinity tuningChanghao He, Jorge Mansilla-Soto, Nandish Khanra, et al.
Calcified Tissue International|August 14, 1998
The human bone morphogenetic protein 4 (BMP-4) gene: molecular structure and transcriptional regulationE M Shore, M Xu, P B Shah, et al.
Nature Communications|October 18, 2022
Suppression of heterotopic ossification in fibrodysplasia ossificans progressiva using AAV gene deliveryYeon-Suk Yang, Jung-Min Kim, Jun Xie, et al.
OTJR : Occupation, Participation and Health|November 5, 2025
Engagement to Identify Health Priorities of People With Intellectual and/or Developmental DisabilityTeal W Benevides, Hoangmai H Pham, May-Lynn Andresen, et al.
Clinical Genetics|November 15, 2000
Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)M Q Xu, G Feldman, M Le Merrer, et al.
Pediatric Radiology|February 18, 2016
The etiology and significance of fractures in infants and young children: a critical multidisciplinary reviewSabah Servaes, Stephen D Brown, Arabinda K Choudhary, et al.
Pageof 43

Showing results (381-390 of 422) with videos related to

Sort By:
Pageof 43
Journal of Neurology|June 28, 2012
CNS demyelination in fibrodysplasia ossificans progressivaLixin Kan, Joseph A Kitterman, Daniele Procissi, et al.
American Journal of Human Genetics|January 13, 2000
Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 31, 2016
Cellular Hypoxia Promotes Heterotopic Ossification by Amplifying BMP SignalingHaitao Wang, Carter Lindborg, Vitali Lounev, et al.
Biomolecules|July 29, 2023
Polypeptide Substrate Accessibility Hypothesis: Gain-of-Function R206H Mutation Allosterically Affects Activin Receptor-like Protein Kinase ActivityJay C Groppe, Guorong Lu, Mary R Tandang-Silvas, et al.
Science Immunology|March 3, 2023
CD19 CAR antigen engagement mechanisms and affinity tuningChanghao He, Jorge Mansilla-Soto, Nandish Khanra, et al.
Calcified Tissue International|August 14, 1998
The human bone morphogenetic protein 4 (BMP-4) gene: molecular structure and transcriptional regulationE M Shore, M Xu, P B Shah, et al.
Nature Communications|October 18, 2022
Suppression of heterotopic ossification in fibrodysplasia ossificans progressiva using AAV gene deliveryYeon-Suk Yang, Jung-Min Kim, Jun Xie, et al.
OTJR : Occupation, Participation and Health|November 5, 2025
Engagement to Identify Health Priorities of People With Intellectual and/or Developmental DisabilityTeal W Benevides, Hoangmai H Pham, May-Lynn Andresen, et al.
Clinical Genetics|November 15, 2000
Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)M Q Xu, G Feldman, M Le Merrer, et al.
Pediatric Radiology|February 18, 2016
The etiology and significance of fractures in infants and young children: a critical multidisciplinary reviewSabah Servaes, Stephen D Brown, Arabinda K Choudhary, et al.
Pageof 43