Determinación de la frecuencia alélica del SNP 19 del gen Calpaína 10 (CAP10) y factores de riesgo de diabetes 2 en población peruana

Paredes Anaya, Mónica; Lizaraso Soto, Frank; Rodríguez Zárate, Eduardo; Lissón Abanto, Rosa; Rodriguez, Elba G; Calderón, Jorge R; Fujita Alarcón, Ricardo.
Horiz. méd. (Impresa) ; 5(1): 13-16, jun. 2005. graf
Artículo en Español | LILACS, LIPECS | ID: lil-676651

Documentos relacionados

  1. Membrane to cytosol redistribution of αII-spectrin drives extracellular vesicle biogenesis in malignant breast cells.
  2. Compound heterozygous c.598_612del and c.1746-20C > G CAPN3 genotype cause autosomal recessive limb-girdle muscular dystrophy-1: a case report.
  3. CAPN3 c.1746-20C>G variant is hypomorphic for LGMD R1 calpain 3-related.
  4. Experiences in the molecular genetic and histopathological evaluation of calpainopathies.
  5. DNA polymerase η is a substrate for calpain: a possible mechanism for pol η retention in UV-induced replication foci.
  6. Acute endoplasmic reticulum stress-induced mitochondria respiratory chain damage: The role of activated calpains.
  7. Fam20c regulates the calpain proteolysis system through phosphorylating Calpasatatin to maintain cell homeostasis.
  8. An easy-to-use FRET protein substrate to detect calpain cleavage in vitro and in vivo.
  9. Therapeutic use of calpeptin in COVID-19 infection.
  10. Cardiopulmonary involvement in limb girdle muscular dystrophy 2A.