Pages that link to "Q72213941"
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The following pages link to Facioscapulohumeral muscular dystrophy in the Dutch population (Q72213941):
Displaying 50 items.
- Facioscapulohumeral dystrophy: the path to consensus on pathophysiology (Q21195884) (← links)
- Facioscapulohumeral muscular dystrophy: consequences of chromatin relaxation (Q26998289) (← links)
- Population-based incidence and prevalence of facioscapulohumeral dystrophy (Q28245908) (← links)
- SORBS2 transcription is activated by telomere position effect-over long distance upon telomere shortening in muscle cells from patients with facioscapulohumeral dystrophy (Q30009101) (← links)
- Clinical trial preparedness in facioscapulohumeral muscular dystrophy: Clinical, tissue, and imaging outcome measures 29-30 May 2015, Rochester, New York (Q30201978) (← links)
- Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population (Q33685609) (← links)
- Mechanism and timing of mitotic rearrangements in the subtelomeric D4Z4 repeat involved in facioscapulohumeral muscular dystrophy (Q33909967) (← links)
- Expression profiling of FSHD-1 and FSHD-2 cells during myogenic differentiation evidences common and distinctive gene dysregulation patterns (Q33939411) (← links)
- De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10. (Q34146154) (← links)
- Muscular dystrophy candidate gene FRG1 is critical for muscle development (Q34244856) (← links)
- Facioscapulohumeral Muscular Dystrophy: More Complex than it Appears (Q34685919) (← links)
- Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study (Q35061314) (← links)
- Multiplex Screen of Serum Biomarkers in Facioscapulohumeral Muscular Dystrophy (Q35094699) (← links)
- FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1). (Q35103393) (← links)
- FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients (Q35444098) (← links)
- Muscle Quantitative MR Imaging and Clustering Analysis in Patients with Facioscapulohumeral Muscular Dystrophy Type 1 (Q35693421) (← links)
- Muscle pathology grade for facioscapulohumeral muscular dystrophy biopsies (Q35988817) (← links)
- Immunohistochemical Characterization of Facioscapulohumeral Muscular Dystrophy Muscle Biopsies (Q36028441) (← links)
- Conditional over-expression of PITX1 causes skeletal muscle dystrophy in mice (Q36364517) (← links)
- Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry (Q36472254) (← links)
- miR-411 is up-regulated in FSHD myoblasts and suppresses myogenic factors (Q36797876) (← links)
- Telomere position effect regulates DUX4 in human facioscapulohumeral muscular dystrophy (Q37013579) (← links)
- Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers. (Q37147175) (← links)
- FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy (Q37175879) (← links)
- DUX4 induces a transcriptome more characteristic of a less-differentiated cell state and inhibits myogenesis (Q37381271) (← links)
- Facioscapulohumeral dystrophy and scapuloperoneal syndromes (Q37865706) (← links)
- Recommendations for the management of facioscapulohumeral muscular dystrophy in 2011. (Q38007039) (← links)
- Upper extremity function and activity in facioscapulohumeral dystrophy and limb-girdle muscular dystrophies: a systematic review (Q38237456) (← links)
- What's in a name? The clinical features of facioscapulohumeral muscular dystrophy (Q38728144) (← links)
- Long-term regulation of gene expression in muscle cells by systemically delivered siRNA. (Q39272515) (← links)
- Are Antioxidants a Potential Therapy for FSHD? A Review of the Literature (Q39424672) (← links)
- Facioscapulohumeral muscular dystrophy: a prospective study of weakness and functional impairment (Q39887707) (← links)
- Electrical impedance myography in facioscapulohumeral muscular dystrophy (Q41654042) (← links)
- Mutation spectrum and phenotypic manifestation in FSHD Greek patients (Q44357279) (← links)
- Upper extremity kinematics and muscle activation patterns in subjects with facioscapulohumeral dystrophy (Q45796069) (← links)
- [Clinical and molecular diagnosis of facioscapulohumeral dystrophy type 1 (FSHD1) in 2012]. (Q45979333) (← links)
- Upper limb function and activity in people with facioscapulohumeral muscular dystrophy: a web-based survey (Q47865945) (← links)
- Modifications of brain tissue volumes in facioscapulohumeral dystrophy (Q48484402) (← links)
- Risk of functional impairment in Facioscapulohumeral muscular dystrophy (Q50356822) (← links)
- Facioscapulohumeral muscular dystrophy can be a cause of isolated childhood cognitive dysfunction (Q50462676) (← links)
- Evaluation of muscle oxygenation by near infrared spectroscopy in patients with facioscapulohumeral muscular dystrophy. (Q51570682) (← links)
- Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy. (Q51828623) (← links)
- A family-based study into penetrance in facioscapulohumeral muscular dystrophy type 1 (Q57174014) (← links)
- Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy (Q58036360) (← links)
- Facioscapulohumeral Muscular Dystrophy Type 1A in Northwestern Tuscany: A Molecular Genetics-based Epidemiological and Genotype–Phenotype Study (Q59690751) (← links)
- Early-Onset Facioscapulohumeral Muscular Dystrophy Type 1 With Some Atypical Features (Q60297054) (← links)
- Facioscapulohumeral muscular dystrophy (Q60297061) (← links)
- Somatic mosaicism in FSHD often goes undetected (Q60297067) (← links)
- Genotype-phenotype correlations in FSHD (Q64096947) (← links)
- Histone Modifications and the Maintenance of Telomere Integrity (Q64104141) (← links)