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1  and shape of the hair produced in the mouse pelage.
2 production, metabolism, immune function, and pelage.
3 e saliva of mice and then transferred to the pelage after grooming and subsequently to the environmen
4 engal genome that harbor candidate genes for pelage and color pattern and that are associated with do
5                               The variegated pelage and social complexity of the African wild dog (Ly
6                  Complete elimination of all pelage and tail follicles occurs after two to three hair
7 n, the complex visual features of real zebra pelage and the natural range of stripe widths have been
8 how that when skin from the sites of primary pelage and whisker follicle development is exposed to in
9 , breed standard phenotypes such as stature, pelage, and craniofacial structure are analyzed through
10 populations with variation for darker winter pelage are predicted to adapt rapidly, providing a trait
11                 Moreover, analysis of mosaic pelage, as well as cultured whisker follicles provided e
12            First, we quantified variation in pelage color (n=107 mice) and habitat color (n=51 rocks)
13  showed that there was a correlation between pelage color and habitat color across 14 sampled populat
14 s of positive selection in genes involved in pelage coloration and immune functions, as well as skele
15 riation and mtDNA phylogeny, suggesting that pelage coloration has evolved rapidly.
16        Survival was positively influenced by pelage coloration, likely as a form of camouflage from p
17                                              Pelage coloration, which serves numerous functions, is c
18 escent protein (GFP), large numbers of fresh pelage DP cells were isolated from newborn transgenic sk
19 proximal-distal axis of the mouse coat hair (pelage) follicle provides a historical record of all epi
20 1(Deltagt/Deltagt)) have a reduced number of pelage follicles and lack vibrissae follicles postnatall
21 e field is whether the bulb region of anagen pelage follicles contains multipotential progenitors and
22 gene is expressed in dermal papilla cells of pelage follicles during catagen but not in anagen or tel
23  human scalp follicles in culture and rodent pelage follicles in vivo, mirroring eyelash behavior, an
24                      The resident nude-mouse pelage follicles targeted by jumping whisker HAP stem ce
25 b and other areas of the resident nude mouse pelage follicles where they differentiated to keratinocy
26  a timely anagen-catagen transition in mouse pelage follicles, and that its ablation partially rescue
27  as a dermal papilla signature gene in mouse pelage follicles.
28 ft proteomics to the study of such diseases, pelage from AKR/J and two other mouse strains without th
29 It is expressed in the dermal papilla of all pelage hair follicle types from the earliest stages of t
30 ary (tylotrich) and secondary (nontylotrich) pelage hair follicles had already occurred, thus allowin
31 tal survival, but had defects in whisker and pelage hair formation.
32 lp follicle organ culture and advanced mouse pelage hair regrowth in vivo compared to vehicle alone.
33                                 The distinct pelage hair types are lost.
34 appaB suppression in the epithelium revealed pelage hair-type-dependent functions of NF-kappaB in cyc
35 phenotypes of curly whiskers and wavy, sheen pelage hair.
36 ferents that innervate primary and secondary pelage hairs.
37  hair density and the production of abnormal pelage hairs.
38 re required for the growth and patterning of pelage hairs.
39 in mice inhabiting sandy beaches; this light pelage has evolved independently on Florida's Gulf and A
40      We show that light versus dark seasonal pelage in white-tailed jackrabbits (Lepus townsendii) tr
41 ga angustirostris), whose excreta and molted pelage, in turn, constitute a source of environmental Me
42  exhibits such typical mammalian features as pelage, mane, pinna, and a variety of skin structures: k
43  only IGL-intact hamsters exhibited seasonal pelage molt.
44 oncentrations in seawater, and HgT in molted pelage of M. angustirostris, at the Ano Nuevo State Rese
45 e, is responsible for the obesity and yellow pelage of the Yellow mouse (A(y)).
46 he results of a morphometric analysis of the pelages of 57 clouded leopards sampled throughout the sp
47   Changing from summer-brown to winter-white pelage or plumage is a crucial adaptation to seasonal sn
48 ajus apella, based on phylogenetic analyses, pelage pattern and geographic provenance.
49 laterally asymmetrical left- and right-sided pelage patterns using a Bayesian spatial partial identit
50 verse regulation of Agouti and Corin renders pelage pigmentation sensitive to changes in beta-catenin
51 catenin activity in the DP that do not alter pelage structure.
52  with extraordinary preservation of skin and pelage that extends the record of key mammalian integume
53 iage and snow when present, and intermediate pelage tones match rocks and ground.
54 genome are thought to account for the unique pelage traits and ornate color patterns of the Bengal br
55 n the skin, no differences in either skin or pelage were observed, demonstrating that FGF22 is dispen
56 4-Agouti transgenic lines, with light-yellow pelage, were analyzed for obesity and hyperglycemia.
57 ted mice, pigment loss did not expand to the pelage, whereas mice in the ampicillin group were approx