Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
Current Opinion in Pediatrics|April 1, 2026
Treatment advances for Duchenne muscular dystrophyAlexander Zygmunt, Cuixia Tian
Blood|November 2, 2002
The function of the bcl-x promoter in erythroid progenitor cellsCuixia Tian, Paul Gregoli, Maurice Bondurant
Journal of Clinical Neuromuscular Disease|February 26, 2025
RNA Sequencing Confirms the Pathogenicity of a Novel FHL1 Deletion in a Kinship With Emery-Dreifuss Muscular DystrophyChinmayee B Nagaraj, Cuixia Tian, Hani Kushlaf
Pediatric Neurology|April 22, 2019
White Matter Lesions Detected by Magnetic Resonance Imaging in Neonates and Children With Congenital Myotonic DystrophyLindsay M Peglar, Usha D Nagaraj, Cuixia Tian, et al.
Molecular Genetics & Genomic Medicine|November 25, 2022
Identification of Biallelic dystrophin gene variants during maternal carrier testing for Becker muscular dystrophy and review of the DMD exon 49-51 deletion phenotypeElizabeth A Ulm, Chinmayee B Nagaraj, Cuixia Tian, et al.
The Journal of Nutritional Biochemistry|January 31, 2026
SIRT3 ameliorates hepatic inflammation, oxidative stress, and fibrosis in HFD- or MCD diet-fed miceHuifang Lv, Wenyue Sun, Cuixia Tian, et al.
Neurology. Genetics|July 22, 2024
Compound Heterozygous Variants of <i>GOSR2</i> Associated With Congenital Muscular Dystrophy and Progressive Myoclonus Epilepsy: A Case ReportMonica S Arroyo, Christine Fuller, Elizabeth K Schorry, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 30, 2026
The burden of bone disease in Duchenne muscular dystrophy: age-specific prevalence of osteoporosis and low bone densityNat Nasomyont, Cuixia Tian, Lindsey Hornung, et al.
Pageof 7