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Human Molecular Genetics
|
July 17, 2018
Identification of a novel, methylation-dependent, RUNX2 regulatory region associated with osteoarthritis risk
Sarah 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 sequence
Jack 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 Failure
Intisar Al Alawi, Laura Powell, Sarah J Rice, et al.
Human Molecular Genetics
|
October 9, 2022
Genetic risk of osteoarthritis operates during human skeletogenesis
Sarah J Rice, Abby Brumwell, Julia Falk, et al.
Osteoarthritis and Cartilage Open
|
October 10, 2025
A proteomics investigation of primary human articular chondrocyte isolation
Abby 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 Loci
Sarah 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 development
Euan 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 risk
Euan McDonnell, Sarah E Orr, Matthew J Barter, et al.
Physiological Reports
|
June 21, 2018
Clinical, biochemical, and pathophysiological analysis of SLC34A1 mutations
Amy 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.
Page
of 4
Search research articles
Search
Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
Human Molecular Genetics
|
July 17, 2018
Identification of a novel, methylation-dependent, RUNX2 regulatory region associated with osteoarthritis risk
Sarah 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 sequence
Jack 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 Failure
Intisar Al Alawi, Laura Powell, Sarah J Rice, et al.
Human Molecular Genetics
|
October 9, 2022
Genetic risk of osteoarthritis operates during human skeletogenesis
Sarah J Rice, Abby Brumwell, Julia Falk, et al.
Osteoarthritis and Cartilage Open
|
October 10, 2025
A proteomics investigation of primary human articular chondrocyte isolation
Abby 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 Loci
Sarah 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 development
Euan 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 risk
Euan McDonnell, Sarah E Orr, Matthew J Barter, et al.
Physiological Reports
|
June 21, 2018
Clinical, biochemical, and pathophysiological analysis of SLC34A1 mutations
Amy 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.
Page
of 4