Pages that link to "Q28737558"
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The following pages link to Melanocortin 1 receptor variants in an Irish population (Q28737558):
Displaying 50 items.
- Evidence for variable selective pressures at MC1R (Q22066136) (← links)
- Aberrant trafficking of human melanocortin 1 receptor variants associated with red hair and skin cancer: Steady-state retention of mutant forms in the proximal golgi (Q24311916) (← links)
- The genetics of sun sensitivity in humans (Q24534055) (← links)
- Melanocortin 1 Receptor: Structure, Function, and Regulation (Q26745953) (← links)
- Skin Pigmentation and Pigmentary Disorders: Focus on Epidermal/Dermal Cross-Talk (Q26747625) (← links)
- Understanding the Evolution of Human Pigmentation: Recent Contributions from Population Genetics (Q27008258) (← links)
- The Genetics of Human Pigmentary Disorders (Q27008379) (← links)
- Significance of the Melanocortin 1 and Endothelin B Receptors in Melanocyte Homeostasis and Prevention of Sun-Induced Genotoxicity (Q28079461) (← links)
- Genetics of Hair and Skin Color (Q28184398) (← links)
- Distinct pigmentary and melanocortin 1 receptor-dependent components of cutaneous defense against ultraviolet radiation (Q33269159) (← links)
- Nucleotide diversity and population differentiation of the melanocortin 1 receptor gene, MC1R. (Q33327597) (← links)
- Detecting the Genetic Signature of Natural Selection in Human Populations: Models, Methods, and Data (Q33630381) (← links)
- Genome-wide scans for footprints of natural selection (Q33743128) (← links)
- Melanocortin-1 receptor gene variants in four Chinese ethnic populations (Q33942625) (← links)
- Genetic predisposition in cutaneous melanoma (Q33997130) (← links)
- MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations (Q34020538) (← links)
- Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma. (Q34020543) (← links)
- Human pigmentation genes: identification, structure and consequences of polymorphic variation (Q34095282) (← links)
- Melanocortin-1 receptor gene variants determine the risk of nonmelanoma skin cancer independently of fair skin and red hair (Q34114660) (← links)
- Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype? (Q34146111) (← links)
- Skin pigmentation, biogeographical ancestry and admixture mapping (Q34176523) (← links)
- Sequences associated with human iris pigmentation. (Q34287539) (← links)
- Melanocortin-1 receptor, skin cancer and phenotypic characteristics (M-SKIP) project: study design and methods for pooling results of genetic epidemiological studies (Q34365732) (← links)
- Single-nucleotide polymorphisms in pigment genes and nonmelanoma skin cancer predisposition: a systematic review. (Q34443721) (← links)
- Melanocyte function and its control by melanocortin peptides (Q34499612) (← links)
- Melanocortin-1 receptor structure and functional regulation. (Q34562487) (← links)
- Stepping up melanocytes to the challenge of UV exposure (Q34616432) (← links)
- MC1R, eumelanin and pheomelanin: their role in determining the susceptibility to skin cancer (Q34988063) (← links)
- The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes. (Q35129937) (← links)
- Ultraviolet radiation and cutaneous malignant melanoma (Q35146567) (← links)
- The genetics of malignant melanoma: lessons from mouse and man. (Q35190150) (← links)
- Cutaneous photobiology. The melanocyte vs. the sun: who will win the final round? (Q35209745) (← links)
- Pharmacogenetic candidate genes for melanoma (Q35574952) (← links)
- Melanocortin 1 receptor genotype: an important determinant of the damage response of melanocytes to ultraviolet radiation. (Q35588847) (← links)
- Is there more than one road to melanoma? (Q35684000) (← links)
- Crucial role of the melanocortin receptor MC1R in experimental colitis (Q35760868) (← links)
- Host Phenotype Characteristics and MC1R in Relation to Early-Onset Basal Cell Carcinoma (Q35834723) (← links)
- MC1R gene variants and non-melanoma skin cancer: a pooled-analysis from the M-SKIP project (Q35863179) (← links)
- Melanocortin 1 receptor variants, pigmentation, and skin cancer susceptibility. (Q38633108) (← links)
- An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W). (Q36095344) (← links)
- Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development (Q36098992) (← links)
- Red hair--a desirable mutation? (Q36674178) (← links)
- Genetic mutations involved in melanoma: a summary of our current understanding (Q37045209) (← links)
- The melanocortin 1 receptor and the UV response of human melanocytes--a shift in paradigm (Q37087448) (← links)
- The melanocortin-1 receptor gene polymorphism and association with human skin cancer. (Q37726402) (← links)
- Melanocortin 1 receptor and risk of cutaneous melanoma: a meta-analysis and estimates of population burden (Q37815455) (← links)
- Melanocortin 1 Receptor Variants: Functional Role and Pigmentary Associations (Q37900332) (← links)
- Sun-induced freckling: ephelides and solar lentigines (Q38187201) (← links)
- MC1R, the cAMP pathway, and the response to solar UV: extending the horizon beyond pigmentation (Q38210121) (← links)
- Human melanocortin 1 receptor (MC1R) gene variants alter melanoma cell growth and adhesion to extracellular matrix (Q38360797) (← links)