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Sarah J Rice

Showing results (21-30 of 32) with videos related to

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Pediatric Nephrology (Berlin, Germany)|May 13, 2019
Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian familiesMohamed H Al-Hamed, Nada Alsahan, Sarah J Rice, et al.
Clinical Journal of the American Society of Nephrology : CJASN|May 13, 2015
Clinical and genetic analysis of patients with cystinuria in the United KingdomHannah L Rhodes, Laura Yarram-Smith, Sarah J Rice, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|August 3, 2024
SERPINA3 is a marker of cartilage differentiation and is essential for the expression of extracellular matrix genes during early chondrogenesisMatthew J Barter, David A Turner, Sarah J Rice, et al.
Osteoarthritis and Cartilage|December 4, 2023
Three decades of advancements in osteoarthritis research: insights from transcriptomic, proteomic, and metabolomic studiesMuhammad Farooq Rai, Kelsey H Collins, Annemarie Lang, et al.
Journal of the American Society of Nephrology : JASN|October 10, 2014
Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosisJan Halbritter, Michelle Baum, Ann Marie Hynes, et al.
Brain Communications|August 23, 2021
Identification of <i>LAMA1</i> mutations ends diagnostic odyssey and has prognostic implications for patients with presumed Joubert syndromeLaura Powell, Eric Olinger, Sarah Wedderburn, et al.
Osteoarthritis and Cartilage|March 1, 2024
Evolution and advancements in genomics and epigenomics in OA research: How far we have comeYolande F M Ramos, Sarah J Rice, Shabana Amanda Ali, et al.
Annals of the Rheumatic Diseases|October 15, 2020
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify <i>WNT9A</i> as novel osteoarthritis geneCindy Germaine Boer, Michelle S Yau, Sarah J Rice, et al.
American Journal of Human Genetics|October 2, 2018
ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein CompositionSumaya Alkanderi, Elisa Molinari, Ranad Shaheen, et al.
Osteoarthritis and Cartilage Open|June 9, 2025
From mechanism to medicine: The progress and potential of epigenetics in osteoarthritisJack B Roberts, Jason S Rockel, Rick Mulders, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Pediatric Nephrology (Berlin, Germany)|May 13, 2019
Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian familiesMohamed H Al-Hamed, Nada Alsahan, Sarah J Rice, et al.
Clinical Journal of the American Society of Nephrology : CJASN|May 13, 2015
Clinical and genetic analysis of patients with cystinuria in the United KingdomHannah L Rhodes, Laura Yarram-Smith, Sarah J Rice, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|August 3, 2024
SERPINA3 is a marker of cartilage differentiation and is essential for the expression of extracellular matrix genes during early chondrogenesisMatthew J Barter, David A Turner, Sarah J Rice, et al.
Osteoarthritis and Cartilage|December 4, 2023
Three decades of advancements in osteoarthritis research: insights from transcriptomic, proteomic, and metabolomic studiesMuhammad Farooq Rai, Kelsey H Collins, Annemarie Lang, et al.
Journal of the American Society of Nephrology : JASN|October 10, 2014
Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosisJan Halbritter, Michelle Baum, Ann Marie Hynes, et al.
Brain Communications|August 23, 2021
Identification of <i>LAMA1</i> mutations ends diagnostic odyssey and has prognostic implications for patients with presumed Joubert syndromeLaura Powell, Eric Olinger, Sarah Wedderburn, et al.
Osteoarthritis and Cartilage|March 1, 2024
Evolution and advancements in genomics and epigenomics in OA research: How far we have comeYolande F M Ramos, Sarah J Rice, Shabana Amanda Ali, et al.
Annals of the Rheumatic Diseases|October 15, 2020
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify <i>WNT9A</i> as novel osteoarthritis geneCindy Germaine Boer, Michelle S Yau, Sarah J Rice, et al.
American Journal of Human Genetics|October 2, 2018
ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein CompositionSumaya Alkanderi, Elisa Molinari, Ranad Shaheen, et al.
Osteoarthritis and Cartilage Open|June 9, 2025
From mechanism to medicine: The progress and potential of epigenetics in osteoarthritisJack B Roberts, Jason S Rockel, Rick Mulders, et al.
Pageof 4