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The silk proteins , sericin and fibroin in silkworm , Bombyx mori
- M. Mondal
- 1 April 2007
The domesticated silkworm, Bombyx mori Linn., a lepidopteran molecular model and an important economic insect that are emerging as an ideal molecular genetic resource for solving a broad range of… Expand
Molecular basis of albinism in India: evaluation of seven potential candidate genes and some new findings.
Albinism represents a group of genetic disorders with a broad spectrum of hypopigmentary phenotypes dependent on the genetic background of the patients. Oculocutaneous albinism (OCA) patients have… Expand
Comprehensive analysis of the molecular basis of oculocutaneous albinism in Indian patients lacking a mutation in the tyrosinase gene
Background Oculocutaneous albinism (OCA) refers to a group of inherited disorders where the patients have little or no pigment in the eyes, skin and hair. Mutations in genes regulating multi‐step… Expand
Functional assessment of tyrosinase variants identified in individuals with albinism is essential for unequivocal determination of genotype‐to‐phenotype correlation
Oculocutaneous albinism type 1 (OCA1), caused by pathogenic variations in the tyrosinase gene (TYR), is the most frequent and severe form of hypopigmentary disorder worldwide. While OCA1A manifests… Expand