19 results on '"van der Maarel S"'
Search Results
2. FSHD
3. FSHD / OPMD / MYOTONIC DYSTROPHY
4. FSHD / OPMD / MYOTONIC DYSTROPHY
5. P.48The role of Dnmt3b in DUX4 repression in transgenic mice
6. P.40Ophthalmological findings in facioscapulohumeral dystrophy
7. NEW GENES, FUNCTIONS AND BIOMARKERS
8. Adding quantitative muscle MRI to the FSHD clinical trial toolbox
9. Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model
10. Monosomy 18p: Risks for developing FSHD
11. Gene variants in SMCHD1 and DNMT3B modify the risk for FSHD
12. Changes in sarcomeric contractile function influence force generation in facioscapulohumeral muscular dystrophy
13. Why are FSHD muscles weak? A novel role for sarcomeric proteins
14. Disease modifying factors in facioscapulohumeral muscular dystrophy: Protocol of the FSHD-FOCUS study
15. Actualités physiopathologiques dans la dystrophie musculaire facio-scapulo-humerale : rôle majeur de la clinique dans les avancées de la recherche
16. T.P.1.09 Oculopharyngeal muscular dystrophy (OPMD): Physiopathological mechanisms and gene therapy approaches
17. G.O.1 Specific sequence variations associated with FSHD
18. G.P.7.13 Gene expression profiling in a skeletal muscle cell model of oculopharyngeal muscular dystrophy reveals an extracellular matrix defect
19. DXS6673E Encodes a Predominantly Nuclear Protein, and Its Mouse Ortholog DXHXS6673E Is Alternatively Spliced in a Developmental- and Tissue-Specific Manner
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