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Benjamin A Alman

Showing results (121-130 of 130) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|November 18, 2021
CRISPR-SID: Identifying EZH2 as a druggable target for desmoid tumors via in vivo dependency mappingThomas Naert, Dieter Tulkens, Tom Van Nieuwenhuysen, et al.
Cell Reports|June 2, 2023
Mutant IDH regulates glycogen metabolism from early cartilage development to malignant chondrosarcoma formationSinthu Pathmanapan, Raymond Poon, Tomasa Barrientos De Renshaw, et al.
Cell|April 10, 2012
A mechanism for gene-environment interaction in the etiology of congenital scoliosisDuncan B Sparrow, Gavin Chapman, Allanceson J Smith, et al.
The Lancet. Neurology|February 4, 2018
Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic managementDavid J Birnkrant, Katharine Bushby, Carla M Bann, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|February 4, 2025
Impact of Lumbar Degenerative Changes on Vertebral Bone Strength: A Finite Element AnalysisSoji Tani, Koji Ishikawa, Erika Chiapparelli, et al.
Nature Communications|December 7, 2018
Macrophage cells secrete factors including LRP1 that orchestrate the rejuvenation of bone repair in miceLinda Vi, Gurpreet S Baht, Erik J Soderblom, et al.
Cell Reports|September 12, 2019
Tracing Tumor Evolution in Sarcoma Reveals Clonal Origin of Advanced MetastasisYuning J Tang, Jianguo Huang, Hidetoshi Tsushima, et al.
Nature Materials|August 16, 2016
Mechanism of hard-nanomaterial clearance by the liverKim M Tsoi, Sonya A MacParland, Xue-Zhong Ma, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2015
Mutant IDH is sufficient to initiate enchondromatosis in miceMakoto Hirata, Masato Sasaki, Rob A Cairns, et al.
American Journal of Human Genetics|December 7, 2015
Mutations Preventing Regulated Exon Skipping in MET Cause Osteofibrous DysplasiaMary J Gray, Peter Kannu, Swarkar Sharma, et al.
Pageof 13

Showing results (121-130 of 130) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 130 results.
Proceedings of the National Academy of Sciences of the United States of America|November 18, 2021
CRISPR-SID: Identifying EZH2 as a druggable target for desmoid tumors via in vivo dependency mappingThomas Naert, Dieter Tulkens, Tom Van Nieuwenhuysen, et al.
Cell Reports|June 2, 2023
Mutant IDH regulates glycogen metabolism from early cartilage development to malignant chondrosarcoma formationSinthu Pathmanapan, Raymond Poon, Tomasa Barrientos De Renshaw, et al.
Cell|April 10, 2012
A mechanism for gene-environment interaction in the etiology of congenital scoliosisDuncan B Sparrow, Gavin Chapman, Allanceson J Smith, et al.
The Lancet. Neurology|February 4, 2018
Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic managementDavid J Birnkrant, Katharine Bushby, Carla M Bann, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|February 4, 2025
Impact of Lumbar Degenerative Changes on Vertebral Bone Strength: A Finite Element AnalysisSoji Tani, Koji Ishikawa, Erika Chiapparelli, et al.
Nature Communications|December 7, 2018
Macrophage cells secrete factors including LRP1 that orchestrate the rejuvenation of bone repair in miceLinda Vi, Gurpreet S Baht, Erik J Soderblom, et al.
Cell Reports|September 12, 2019
Tracing Tumor Evolution in Sarcoma Reveals Clonal Origin of Advanced MetastasisYuning J Tang, Jianguo Huang, Hidetoshi Tsushima, et al.
Nature Materials|August 16, 2016
Mechanism of hard-nanomaterial clearance by the liverKim M Tsoi, Sonya A MacParland, Xue-Zhong Ma, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2015
Mutant IDH is sufficient to initiate enchondromatosis in miceMakoto Hirata, Masato Sasaki, Rob A Cairns, et al.
American Journal of Human Genetics|December 7, 2015
Mutations Preventing Regulated Exon Skipping in MET Cause Osteofibrous DysplasiaMary J Gray, Peter Kannu, Swarkar Sharma, et al.
Pageof 13