Pages that link to "Q37175879"
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The following pages link to FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy (Q37175879):
Displaying 29 items.
- DUX4c is up-regulated in FSHD. It induces the MYF5 protein and human myoblast proliferation (Q21091176) (← links)
- Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD (Q21563357) (← links)
- Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD) (Q27318439) (← links)
- Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD) (Q28513387) (← links)
- Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites (Q33748620) (← links)
- Testing the effects of FSHD candidate gene expression in vertebrate muscle development (Q33861089) (← links)
- BAC TG-EMBED: one-step method for high-level, copy-number-dependent, position-independent transgene expression (Q33922474) (← links)
- Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein (Q34539583) (← links)
- Determining the role of sarcomeric proteins in facioscapulohumeral muscular dystrophy: a study protocol (Q35015983) (← links)
- FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1). (Q35103393) (← links)
- Facioscapulohumeral muscular dystrophy region gene 1 is a dynamic RNA-associated and actin-bundling protein (Q35127142) (← links)
- AAV6-mediated systemic shRNA delivery reverses disease in a mouse model of facioscapulohumeral muscular dystrophy (Q35568525) (← links)
- Combined treatment with intravitreal bevacizumab and laser photocoagulation for exudative maculopathy in facioscapulohumeral muscular dystrophy (Q36259503) (← links)
- Alternative splicing and muscular dystrophy. (Q36599506) (← links)
- The cell biology of disease: FSHD: copy number variations on the theme of muscular dystrophy (Q37819663) (← links)
- Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled? (Q37943770) (← links)
- In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy. (Q37961725) (← links)
- Deciphering transcription dysregulation in FSH muscular dystrophy. (Q38020380) (← links)
- Prospect for pharmacological therapies to treat skeletal muscle dysfunction (Q38264369) (← links)
- Current status and future prospect of FSHD region gene 1. (Q38676318) (← links)
- Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) expression and possible function in mouse tooth germ development (Q38767967) (← links)
- Direct interplay between two candidate genes in FSHD muscular dystrophy. (Q38946853) (← links)
- RNA interference improves myopathic phenotypes in mice over-expressing FSHD region gene 1 (FRG1). (Q39319041) (← links)
- FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis. (Q45290619) (← links)
- Increased FSHD region gene1 expression reduces in vitro cell migration, invasion, and angiogenesis, ex vivo supported by reduced expression in tumors. (Q47119855) (← links)
- Facioscapulohumeral Muscular Dystrophy. (Q52506936) (← links)
- Rapid and convergent evolution in the glioblastoma multiforme genome. (Q53641003) (← links)
- Reduced FRG1 expression promotes prostate cancer progression and affects prostate cancer cell migration and invasion (Q64053310) (← links)
- Ophthalmological findings in facioscapulohumeral dystrophy (Q99585314) (← links)