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  3. Research By Disease

Disease: Ermine phenotype

  • Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism
  • Functional flexibility as a prelude to signal diversity?: Role of a fatty acyl reductase in moth pheromone evolution
  • Genomic diversity and signatures of selection in meat and fancy rabbit breeds based on high-density marker data
  • Long-Term Motor Deficit and Diffuse Cortical Atrophy Following Focal Cortical Ischemia in Athymic Rats
  • Microsatellite markers for American mink (Mustela vison) and ermine (Mustela erminea)
  • Modelling the dopamine and noradrenergic cell loss that occurs in Parkinson's disease and the impact on hippocampal neurogenesis
  • Nepal after the disaster. Insider points of view for the future of critical care medicine
  • Phenotypic and microscopic description of a new case of Ermine phenotype
  • Population genomic structures and signatures of selection define the genetic uniqueness of several fancy and meat rabbit breeds
  • The ermine phenotype: pigmentary-hearing loss heterogeneity
  • Understanding the Influence of Target Acquisition on Survival, Integration, and Phenotypic Maturation of Dopamine Neurons within Stem Cell-Derived Neural Grafts in a Parkinson's Disease Model
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About CheckOrphan

CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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