D’Apice et al., 2020 - Google Patents
Cutaneous and metabolic defects associated with nuclear abnormalities in a transgenic mouse model expressing R527H lamin A mutation causing mandibuloacral …D’Apice et al., 2020
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- 6400591590255623657
- Author
- D’Apice M
- De Dominicis A
- Murdocca M
- Amati F
- Botta A
- Sangiuolo F
- Lattanzi G
- Federici M
- Novelli G
- Publication year
- Publication venue
- Acta Myologica
External Links
Snippet
LMNA gene encodes for lamin A/C, attractive proteins linked to nuclear structure and functions. When mutated, it causes different rare diseases called laminopathies. In particular, an Arginine change in Histidine in position 527 (p. Arg527His) falling in the C …
- 102100011754 LMNA 0 title abstract description 115
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- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
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