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searching for Melanocortin 1 receptor 16 found (108 total)

alternate case: melanocortin 1 receptor

Rock pocket mouse (509 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 (1,672 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 (2,266 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 (1,018 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
Light skin (6,974 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
Discrimination against people with red hair (3,294 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
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
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
Porphyria (6,616 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 anatomy (4,131 words) [view diff] exact match in snippet view article find links to article
Stäubert C, Catalano G, Hughes D, et al. (November 2007). "A melanocortin 1 receptor allele suggests varying pigmentation among Neanderthals". Science
Common raccoon dog (5,963 words) [view diff] no match in snippet view article find links to article
Hyun; Jeung, Eui-Bae; Na, Ki-Jeong (2012). "Altered expression of melanocortin1 receptor (MC1R) in a yellow‐coloured wild raccoon dog (Nyctereutes procyonoides)"
Dark skin (8,450 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 (12,460 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
Recent human evolution (12,002 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
Neanderthal (35,808 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
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