de Melo, 2021 - Google Patents
The impact of Lama2-deficiency on cell cycle regulation and survivalde Melo, 2021
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- 5756837202842567555
- Author
- de Melo C
- Publication year
- Publication venue
- PQDT-Global
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Laminin α2 chain-deficient congenital muscular dystrophy (LAMA2-CMD) is caused by recessive mutations in the LAMA2 gene. This neuromuscular disease is diagnosed at birth or within the first few months of life and is characterized by hypotonia and severe muscle …
- 230000004083 survival 0 title abstract description 24
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- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4702—Regulators; Modulating activity
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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