Associated Papers
Large scale clinical exome sequencing uncovers the scope and severity of skin disorders associated with MC1R genetic variants.
Moore BS et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
34326492 (PubMed )
Supplement: NIHMS1754145-supplement-Supplemental_Table_2.xlsx › Sheet1
A 1-bp deletion in Mc1r in a Norway rat (Rattus norvegicus) from Sado Island, Japan gives rise to a yellowish color variant: an insight into mammalian MC1R variants.
Tsunoi T et al.
Genes & Genetic Systems, 2021
Mouse Hair Significantly Lightened Through Replacement of the Cysteine Residue in the N-Terminal Domain of Mc1r Using the CRISPR/Cas9 System.
Suzuki H et al.
The Journal of Heredity, 2020
Characterization of patients at high risk of melanoma in Austria.
Müller C et al.
The British Journal of Dermatology, 2016
Independent nonframeshift deletions in the MC1R gene are not associated with melanistic coat coloration in three mustelid lineages.
Hosoda T et al.
The Journal of Heredity, 0
Select a paper to view details