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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Hazel Sutherland

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Genes & Diseases|June 10, 2022

Metabolomic studies in the inborn error of metabolism alkaptonuria reveal new biotransformations in tyrosine metabolismBrendan P Norman, Andrew S Davison, Juliette H Hughes, et al.

Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|February 25, 2026

Repeated Disuse Atrophy Imprints a Molecular Memory in Skeletal Muscle: Transcriptional Resilience in Young Adults and Susceptibility in Aged MuscleDaniel C Turner, Truls Raastad, Max Ullrich, et al.

Journal of Inherited Metabolic Disease|February 22, 2020

Nitisinone causes acquired tyrosinosis in alkaptonuriaMilad Khedr, Maggie S Cooper, Andrew T Hughes, et al.

The Journal of Physiology|May 17, 2019

UBR5 is a novel E3 ubiquitin ligase involved in skeletal muscle hypertrophy and recovery from atrophyRobert A Seaborne, David C Hughes, Daniel C Turner, et al.

Bone Research|January 26, 2025

Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulationMohammad Alhashmi, Abdulrahman M E Gremida, Santosh K Maharana, et al.

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Search research articles

Showing results (31-40 of 35) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 35 results.

Genes & Diseases|June 10, 2022

Metabolomic studies in the inborn error of metabolism alkaptonuria reveal new biotransformations in tyrosine metabolismBrendan P Norman, Andrew S Davison, Juliette H Hughes, et al.

Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|February 25, 2026

Repeated Disuse Atrophy Imprints a Molecular Memory in Skeletal Muscle: Transcriptional Resilience in Young Adults and Susceptibility in Aged MuscleDaniel C Turner, Truls Raastad, Max Ullrich, et al.

Journal of Inherited Metabolic Disease|February 22, 2020

Nitisinone causes acquired tyrosinosis in alkaptonuriaMilad Khedr, Maggie S Cooper, Andrew T Hughes, et al.

The Journal of Physiology|May 17, 2019

UBR5 is a novel E3 ubiquitin ligase involved in skeletal muscle hypertrophy and recovery from atrophyRobert A Seaborne, David C Hughes, Daniel C Turner, et al.

Bone Research|January 26, 2025

Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulationMohammad Alhashmi, Abdulrahman M E Gremida, Santosh K Maharana, et al.

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