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Sarah J Rice

Showing results (11-20 of 32) with videos related to

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Human Molecular Genetics|July 17, 2018
Identification of a novel, methylation-dependent, RUNX2 regulatory region associated with osteoarthritis riskSarah J Rice, Guillaume Aubourg, Antony K Sorial, et al.
Arthritis Research & Therapy|April 3, 2024
Specific isoforms of the ubiquitin ligase gene WWP2 are targets of osteoarthritis genetic risk via a differentially methylated DNA sequenceJack B Roberts, Olivia L G Boldvig, Guillaume Aubourg, et al.
Frontiers in Genetics|December 17, 2021
Case Report: A Novel In-Frame Deletion of <i>GLIS2</i> Leading to Nephronophthisis and Early Onset Kidney FailureIntisar Al Alawi, Laura Powell, Sarah J Rice, et al.
Human Molecular Genetics|October 9, 2022
Genetic risk of osteoarthritis operates during human skeletogenesisSarah J Rice, Abby Brumwell, Julia Falk, et al.
Osteoarthritis and Cartilage Open|October 10, 2025
A proteomics investigation of primary human articular chondrocyte isolationAbby Brumwell, Simran Raheja, William Cawley, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|February 8, 2019
Prioritization of PLEC and GRINA as Osteoarthritis Risk Genes Through the Identification and Characterization of Novel Methylation Quantitative Trait LociSarah J Rice, Maria Tselepi, Antony K Sorial, et al.
Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Epigenetic mechanisms of osteoarthritis risk in human skeletal developmentEuan McDonnell, Sarah E Orr, Matthew J Barter, et al.
American Journal of Human Genetics|November 23, 2024
The methylomic landscape of human articular cartilage development contains epigenetic signatures of osteoarthritis riskEuan McDonnell, Sarah E Orr, Matthew J Barter, et al.
Physiological Reports|June 21, 2018
Clinical, biochemical, and pathophysiological analysis of SLC34A1 mutationsAmy Fearn, Benjamin Allison, Sarah J Rice, et al.
Clinical Kidney Journal|February 26, 2015
A novel LMX1B mutation in a family with end-stage renal disease of 'unknown cause'Noel Edwards, Sarah J Rice, Shreya Raman, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|July 17, 2018
Identification of a novel, methylation-dependent, RUNX2 regulatory region associated with osteoarthritis riskSarah J Rice, Guillaume Aubourg, Antony K Sorial, et al.
Arthritis Research & Therapy|April 3, 2024
Specific isoforms of the ubiquitin ligase gene WWP2 are targets of osteoarthritis genetic risk via a differentially methylated DNA sequenceJack B Roberts, Olivia L G Boldvig, Guillaume Aubourg, et al.
Frontiers in Genetics|December 17, 2021
Case Report: A Novel In-Frame Deletion of <i>GLIS2</i> Leading to Nephronophthisis and Early Onset Kidney FailureIntisar Al Alawi, Laura Powell, Sarah J Rice, et al.
Human Molecular Genetics|October 9, 2022
Genetic risk of osteoarthritis operates during human skeletogenesisSarah J Rice, Abby Brumwell, Julia Falk, et al.
Osteoarthritis and Cartilage Open|October 10, 2025
A proteomics investigation of primary human articular chondrocyte isolationAbby Brumwell, Simran Raheja, William Cawley, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|February 8, 2019
Prioritization of PLEC and GRINA as Osteoarthritis Risk Genes Through the Identification and Characterization of Novel Methylation Quantitative Trait LociSarah J Rice, Maria Tselepi, Antony K Sorial, et al.
Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Epigenetic mechanisms of osteoarthritis risk in human skeletal developmentEuan McDonnell, Sarah E Orr, Matthew J Barter, et al.
American Journal of Human Genetics|November 23, 2024
The methylomic landscape of human articular cartilage development contains epigenetic signatures of osteoarthritis riskEuan McDonnell, Sarah E Orr, Matthew J Barter, et al.
Physiological Reports|June 21, 2018
Clinical, biochemical, and pathophysiological analysis of SLC34A1 mutationsAmy Fearn, Benjamin Allison, Sarah J Rice, et al.
Clinical Kidney Journal|February 26, 2015
A novel LMX1B mutation in a family with end-stage renal disease of 'unknown cause'Noel Edwards, Sarah J Rice, Shreya Raman, et al.
Pageof 4