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CRIPSR-Cas9: Une stratégie thérapeutique pour les laminopathies ?
- Published in:
- Médecine Sciences, 2023, v. 39, p. 65, doi. 10.1051/medsci/2023139
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- Article
À la recherche de facteurs génétiques modificateurs dans les cardiomyopathies.
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- Médecine Sciences, 2021, v. 37, p. 49, doi. 10.1051/medsci/2021195
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- Article
Preclinical Advances of Therapies for Laminopathies.
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- Journal of Clinical Medicine, 2021, v. 10, n. 21, p. 4834, doi. 10.3390/jcm10214834
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- Article
Cellular and Genomic Features of Muscle Differentiation from Isogenic Fibroblasts and Myoblasts.
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- Cells (2073-4409), 2023, v. 12, n. 15, p. 1995, doi. 10.3390/cells12151995
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- Article
Lamin A/C Assembly Defects in LMNA-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery–Dreifuss Muscular Dystrophy.
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- Cells (2073-4409), 2020, v. 9, n. 4, p. 844, doi. 10.3390/cells9040844
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- Article
Atypical antipsychotics and effects on feeding: from mice to men.
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- Psychopharmacology, 2016, v. 233, n. 14, p. 2629, doi. 10.1007/s00213-016-4324-8
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- Article
Quantifying the Genetic Basis of Marfan Syndrome Clinical Variability.
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- Genes, 2020, v. 11, n. 5, p. 574, doi. 10.3390/genes11050574
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- Article
Reference Expression Profile of Three FBN1 Transcript Isoforms and Their Association with Clinical Variability in Marfan Syndrome.
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- Genes, 2019, v. 10, n. 2, p. 128, doi. 10.3390/genes10020128
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- Article
Marfan Syndrome Variability: Investigation of the Roles of Sarcolipin and Calcium as Potential Transregulator of FBN1 Expression.
- Published in:
- Genes, 2018, v. 9, n. 9, p. 421, doi. 10.3390/genes9090421
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- Article