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Science Translational Medicine
|
September 4, 2015
ACVR1R206H receptor mutation causes fibrodysplasia ossificans progressiva by imparting responsiveness to activin A
Sarah J Hatsell, Vincent Idone, Dana M Alessi Wolken, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 8, 2017
The Expansion of Heterotopic Bone in Fibrodysplasia Ossificans Progressiva Is Activin A-Dependent
Jaymin Upadhyay, LiQin Xie, Lily Huang, et al.
Elife
|
December 13, 2024
Genetic inactivation of zinc transporter SLC39A5 improves liver function and hyperglycemia in obesogenic settings
Shek Man Chim, Kristen Howell, John Dronzek, et al.
Molecular Psychiatry
|
February 15, 2022
Regulation of sensorimotor gating via Disc1/Huntingtin-mediated Bdnf transport in the cortico-striatal circuit
Hanna Jaaro-Peled, Sunil Kumar, Dalton Hughes, et al.
Human Molecular Genetics
|
October 26, 2020
NMIHBA results from hypomorphic PRUNE1 variants that lack short-chain exopolyphosphatase activity
Harikiran Nistala, John Dronzek, Claudia Gonzaga-Jauregui, et al.
Nature Biotechnology
|
May 6, 2003
High-throughput engineering of the mouse genome coupled with high-resolution expression analysis
David M Valenzuela, Andrew J Murphy, David Frendewey, et al.
Molecular Therapy. Methods & Clinical Development
|
October 2, 2025
Functional, sustained recovery of hearing in Otoferlin-deficient mice using DB-OTO, a hair-cell-specific AAV-based gene therapy
Yoojin Chung, Seth D Koehler, Sarah Cancelarich, et al.
Nature Genetics
|
August 9, 2023
Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis
Sirui Zhou, Olukayode A Sosina, Jonas Bovijn, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 7, 2013
Conditionals by inversion provide a universal method for the generation of conditional alleles
Aris N Economides, David Frendewey, Peter Yang, et al.
JCI Insight
|
June 23, 2025
A TMPRSS6-inhibiting mAb improves disease in a β-thalassemia mouse model and reduces iron in healthy humans
Heinrich E Lob, Nikhil Singh, Kusha Mohammadi, et al.
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of 10
Search research articles
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Showing results (81-90 of 96) with videos related to
Sort By:
Page
of 10
Science Translational Medicine
|
September 4, 2015
ACVR1R206H receptor mutation causes fibrodysplasia ossificans progressiva by imparting responsiveness to activin A
Sarah J Hatsell, Vincent Idone, Dana M Alessi Wolken, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 8, 2017
The Expansion of Heterotopic Bone in Fibrodysplasia Ossificans Progressiva Is Activin A-Dependent
Jaymin Upadhyay, LiQin Xie, Lily Huang, et al.
Elife
|
December 13, 2024
Genetic inactivation of zinc transporter SLC39A5 improves liver function and hyperglycemia in obesogenic settings
Shek Man Chim, Kristen Howell, John Dronzek, et al.
Molecular Psychiatry
|
February 15, 2022
Regulation of sensorimotor gating via Disc1/Huntingtin-mediated Bdnf transport in the cortico-striatal circuit
Hanna Jaaro-Peled, Sunil Kumar, Dalton Hughes, et al.
Human Molecular Genetics
|
October 26, 2020
NMIHBA results from hypomorphic PRUNE1 variants that lack short-chain exopolyphosphatase activity
Harikiran Nistala, John Dronzek, Claudia Gonzaga-Jauregui, et al.
Nature Biotechnology
|
May 6, 2003
High-throughput engineering of the mouse genome coupled with high-resolution expression analysis
David M Valenzuela, Andrew J Murphy, David Frendewey, et al.
Molecular Therapy. Methods & Clinical Development
|
October 2, 2025
Functional, sustained recovery of hearing in Otoferlin-deficient mice using DB-OTO, a hair-cell-specific AAV-based gene therapy
Yoojin Chung, Seth D Koehler, Sarah Cancelarich, et al.
Nature Genetics
|
August 9, 2023
Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis
Sirui Zhou, Olukayode A Sosina, Jonas Bovijn, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 7, 2013
Conditionals by inversion provide a universal method for the generation of conditional alleles
Aris N Economides, David Frendewey, Peter Yang, et al.
JCI Insight
|
June 23, 2025
A TMPRSS6-inhibiting mAb improves disease in a β-thalassemia mouse model and reduces iron in healthy humans
Heinrich E Lob, Nikhil Singh, Kusha Mohammadi, et al.
Page
of 10