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searching for Melanocortin 1 receptor 16 found (108 total)

Rock pocket mouse (512 words) [view diff] no match in snippet view article find links to article

discovered a perfect association between different versions of the Melanocortin-1 receptor (Mc41r6) gene and coat colour. Subsequent studies demonstrated

Chromosome 16 (1,677 words) [view diff] exact match in snippet view article find links to article

Luc7-like 1 LYPLA3: encoding enzyme Group XV phospholipase A2 MC1R: melanocortin 1 receptor MCOPCT1: Microphthalmia with cataract 1 METRN: encoding protein

Melanocyte (2,278 words) [view diff] no match in snippet view article find links to article

Im S, Lamoreux L, Ito S, Barsh G, Hearing VJ (2000-01-01). "The melanocortin-1 receptor is a key regulator of human cutaneous pigmentation". Pigment Cell

Rhinelander rabbit (1,014 words) [view diff] exact match in snippet view article find links to article

Oulmouden, Ahmad (2010). "A composite six bp in-frame deletion in the melanocortin 1 receptor (MC1R) gene is associated with the Japanese brindling coat colour

Introduction to genetics (3,014 words) [view diff] case mismatch in snippet view article find links to article

from the original on 10 February 2008. Retrieved 24 January 2008. Melanocortin 1 Receptor, Accessed 27 November 2010 Multifactorial Inheritance Health Library

Light skin (9,015 words) [view diff] exact match in snippet view article find links to article

This phenotype is caused by a loss-of-function mutation in the melanocortin 1 receptor (MC1R) gene. However, variations in the MC1R gene sequence only

Patricia G. Parker (3,155 words) [view diff] no match in snippet view article find links to article

the Plumage Polymorphism in Red-Footed Boobies (Sula sula): A Melanocortin-1 Receptor (MC1R) Analysis". Journal of Heredity. 98 (4): 287–292. doi:10

Discrimination against people with red hair (3,743 words) [view diff] exact match in snippet view article find links to article

hair is one potential manifestation of a gene mutation in the melanocortin 1 receptor (MC1R). While red hair most frequently occurs among European peoples

Porphyria (6,585 words) [view diff] exact match in snippet view article find links to article

phase 2 trial, dersimelagon, an orally administered, selective melanocortin 1 receptor agonist that increases levels of skin eumelanin, was reported to

Neanderthal (11,543 words) [view diff] exact match in snippet view article find links to article

Lalueza-Fox, C.; Rompler, H.; Caramelli, D.; et al. (2007). "A melanocortin 1 receptor allele suggests varying pigmentation among Neanderthals". Science

Common raccoon dog (5,827 words) [view diff] no match in snippet view article find links to article

Hyun; Jeung, Eui-Bae; Na, Ki-Jeong (2012). "Altered expression of melanocortin-1 receptor (MC1R) in a yellow-coloured wild raccoon dog (Nyctereutes procyonoides)"

Dark skin (8,506 words) [view diff] exact match in snippet view article find links to article

; Jorde, L. B. (1 April 1999). "High polymorphism at the human melanocortin 1 receptor locus". Genetics. 151 (4): 1547–1557. doi:10.1093/genetics/151

Early modern human (12,602 words) [view diff] no match in snippet view article find links to article

Schöneberg, T; Bertranpetit, J; Hofreiter, M; et al. (2007). "A melanocortin-1 receptor allele suggests varying pigmentation among Neanderthals". Science

Neanderthal anatomy (7,221 words) [view diff] exact match in snippet view article find links to article

Lalueza-Fox, C.; Rompler, H.; Caramelli, D.; et al. (2007). "A melanocortin 1 receptor allele suggests varying pigmentation among Neanderthals". Science

Recent human evolution (11,903 words) [view diff] case mismatch in snippet view article find links to article

Schoneberg, T.; Bertranpetit, J.; Hofreiter, M. (November 30, 2007). "A Melanocortin 1 Receptor Allele Suggests Varying Pigmentation Among Neanderthals". Science

Outcomes Research Consortium (5,459 words) [view diff] no match in snippet view article find links to article

with other hair colors. Red hair results from a mutation of the melanocortin-1 receptor. The Consortium's results thus indicate that something about this