Suchergebnisse - "Zheng, Fuze"

PubPharm (7)

1

CGG repeat expansion in LOC642361/NUTM2B-AS1 typically presents as oculopharyngodistal myopathy

enthalten in: Journal of genetics and genomics = Yi chuan xue bao | 2024

von Shi, Y. | Cao, C. | Zeng, Y. | +16

2

An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 1

enthalten in: Brain : a journal of neurology | 2023

von Zheng, F. | Qiu, L. | Chen, L. | +8

CommentOn: Brain. 2023 Apr 19;146(4):1388-1402. - PMID 36100962

3

Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy

enthalten in: Neurology | 2023

von Zheng, F. | Qiu, L. | Chen, L. | +15

CommentIn: Neurology. 2023 Jul 18;101(3):97-98. - PMID 37277202

4

The China facioscapulohumeral muscular dystrophy type 1 (FSHD1) registry: rationale for and description of a nationwide, observational cohort study

enthalten in: ResearchSquare.com | 2022

von Qiu, L. | Chen, L. | Zheng, F. | +11

5

Wheelchair use in genetically confirmed FSHD1 from a large cohort study in Chinese population

enthalten in: Brain : a journal of neurology | 2022

von Qiu, L. | Chen, L. | Zheng, F. | +5

CommentIn: Brain. 2022 Jun 30;145(6):e55-e56. - PMID 35302588

6

Reprogramming of adult human peripheral blood mononuclear cells into hiPSCs from two patients with facioscapulohumeral muscular dystrophy type 1

enthalten in: Stem cell research | 2022

von Zheng, F. | Chen, L. | Qiu, L. | +7

7

Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020 : a nationwide population-based study

enthalten in: The Lancet regional health. Western Pacific | 2022

von Wang, Z. | Qiu, L. | Lin, M. | +14

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