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1 r the enhancer variant responsible for light eye color.
2 sun tanning responses, ethnicity, hair, and eye color.
3 integrants simply by the loss of mini-white eye color.
4 enetic system in which many mutations affect eye color.
5 omere region can be identified by changes in eye color.
6 function mutations at eight loci that affect eye color.
7 an effect on the OAER due to photophobia or eye color.
8 lting in heritable epigenetic differences in eye color.
9 indicating a role for these pigments beyond eye color.
10 ons and evolutionary drivers of variation in eye color.
11 pean Americans in the replication stage (for eye color, 3871 males in the discovery stage and 2496 ma
12 butable to genetic effects: 7% associated to eye color, 6% to hair color, and 1% to reported skin typ
17 ed host phenotypes (such as pigmentation and eye color) and tested them for association with UM risk.
18 ous knowledge and expectations, highlighting eye color as a genetically highly complex human trait.
20 ue, intermediate (including green) and brown eye colors as co-dominant outcomes, we identified the SN
24 nstrate that the genetic complexity of human eye color considerably exceeds previous knowledge and ex
26 aracterized by defective platelets, coat and eye color dilution, lysosomal abnormalities, inner ear d
29 e of Drosophila melanogaster result in prune eye color due to reductions in red pigment accumulation.
30 cally relevant SNPs associated with hair and eye color, facial morphology, and myopia, imply strong g
31 of RNAi is effective for both the white (w) eye color gene and green fluorescent protein (GFP), indi
32 modifiers of gene expression with the white eye color gene as a target, a third chromosomal P-elemen
34 pendent trans-acting regulators of the white eye color gene in combinations to understand their inter
37 tested whether variegated expression of the eye-color gene brown in Drosophila is influenced by its
39 lar identification of two classic Drosophila eye-color genes required for pigment granule biogenesis,
40 The Tribolium orthologs of the Drosophila eye-color genes vermilion (tryptophan oxygenase) and cin
41 dels adjusted for age, sex, medical history, eye color, hair color, and likeliness of tanning versus
42 ecessive mutations at several loci affecting eye color imply that our EMS treatment was equivalent to
45 6/Hps6 double mutant mice mimic, in coat and eye colors, in melanosome ultrastructure, and in levels
46 d skin color; notably, 50% of variability in eye color is associated with variation in the SNP rs1291
50 exogenous DNA yielded a frequency of somatic eye-color mosaicism of approximately 10% and a frequency
52 These results provide direct evidence that eye color mutations of the granule group also disrupt ve
54 rs12913832 (HERC2), which is related to blue eye color, not only is a genetic factor related to the r
55 nome-wide association studies on hair color, eye color, number of sunburns, tanning ability and numbe
57 while longer arrays increase the background eye color or increase the number of spots sufficiently t
58 nburns (OR, 2.59 [95% CI, 1.31-5.10]), light eye color (OR, 2.47 [95% CI, 1.30-4.67]), and less of an
60 age of a Drosophila strain with a variegated eye color phenotype that is sensitive to heterochromatin
65 on cassettes results in flies with different eye color phenotypes due to position effects at the site
68 g a mini-white construct can exhibit various eye colors ranging from pale orange to intense red, depe
69 ps between qAF and age, sex, race/ethnicity, eye color, refraction/axial length, and smoking status w
72 of rs12913832 (HERC2), which codes for blue eye color showed a worse prognosis (P = 0.017) and more
74 hat solicited information on skin, hair, and eye color; skin cancer family history; and sun exposure
75 ts with UM and performed sequencing, using 6 eye color SNPs from the HIrisPlex-S assay (Erasmus MC, W
77 he largest genome-wide association study for eye color to date, involving up to 192,986 European part
79 (95% confidence interval, 45.4 to 61.0%) of eye color variation using common single-nucleotide polym
81 The transgene-mediated complementation of eye color was observed to segregate in a Mendelian manne
82 cts, using smartphone cameras with different eye colors, was also collected to demonstrate the method
84 sociated with common traits such as hair and eye color, while others are associated with susceptibili
85 e those coding for lactase persistence, blue eye color, Y chromosome R1b haplotypes, and the hemochro