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1 rt striking reciprocal phenotypic effects on androgenetic (AG: two paternal genomes) and parthenogene
2 [95% confidence intervals]) in patients with androgenetic alopecia (37.3 128.4, 46.1]) and alopecia a
6 Dermal papilla cells (DPCs) taken from male androgenetic alopecia (AGA) patients undergo premature s
9 ed patients with telogen effluvium (n = 30), androgenetic alopecia (n = 52), alopecia areata (n = 17)
11 ison, skin biopsies from alopecia areata and androgenetic alopecia affected humans were also collecte
15 zed by premature entry into catagen, such as androgenetic alopecia, alopecia areata, and telogen effl
21 etic ova), and in individual gynogenetic and androgenetic blastomeres, both maternal and paternal Igf
22 ion were also present in parthenogenetic and androgenetic cells and in tissues from animals maternall
23 is phenotypically indistinguishable from an androgenetic complete hydatidiform mole, in which abnorm
24 Both maternal (gynogenetic) and paternal (androgenetic) derived cells conveyed long-term, multilin
25 -modified paternal pronucleus should support androgenetic development (i.e., from the paternal pronuc
26 pressed in differentiated cells derived from androgenetic embryonic stem cells and normal embryos but
28 s a difference in developmental potential of androgenetic embryos produced with eggs from females of
31 We developed a meiotic mapping panel of 94 androgenetic haploid embryos that were scored for geneti
32 enome in sporadic hydatidiform moles (purely androgenetic in complete hydatidiform moles and diandric
35 enetic material from other species may allow androgenetic lineages of Corbicula to mitigate the effec
38 ntire genome is either exclusively paternal (androgenetic) or maternal (parthenogenetic), exhibit dra
40 ion mechanisms: in individual blastomeres of androgenetic ova, both paternal Snrpn alleles were activ
41 normal ova were unchanged in gynogenetic and androgenetic ova; the latter contain two maternal and tw
42 lopment that are particularly evident in the androgenetic phenotype, uniparental cells of both parent
43 ions in Drosophila melanogaster that produce androgenetic progeny, we demonstrate that the Wolbachia-
44 al and nuclear loci from multiple sexual and androgenetic species across the global distribution of C
46 arthenogenetic (two maternal chromosomes) or androgenetic (two paternal chromosomes) cells displaying
47 ferences in X-linked gene expression between androgenetic (two paternal genomes), gynogenetic (two ma
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