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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
3                                              Androgenetic alopecia (AGA) is a common heritable and an
4                                        Early androgenetic alopecia (AGA) is patterned hair loss occur
5                                  Presence of androgenetic alopecia (AGA) might be such a predictor.
6  Dermal papilla cells (DPCs) taken from male androgenetic alopecia (AGA) patients undergo premature s
7                                              Androgenetic alopecia (AGA), a hereditary disorder that
8                                              Androgenetic alopecia (AGA), also known as common baldne
9 ed patients with telogen effluvium (n = 30), androgenetic alopecia (n = 52), alopecia areata (n = 17)
10 nt follicular cycling in the scalp including androgenetic alopecia (pattern hair loss).
11 ison, skin biopsies from alopecia areata and androgenetic alopecia affected humans were also collecte
12               Male pattern baldness (MPB) or androgenetic alopecia is one of the most common conditio
13                                              Androgenetic alopecia may begin in adolescence, and topi
14 c skin disorders such as acne, hirsutism, or androgenetic alopecia remains to be established.
15 zed by premature entry into catagen, such as androgenetic alopecia, alopecia areata, and telogen effl
16 opecia in adolescence are telogen effluvium, androgenetic alopecia, and alopecia areata.
17 ntagonist for sebum control and treatment of androgenetic alopecia.
18 us-to-terminal and terminal-to-vellus during androgenetic alopecia.
19 aking finasteride over the past 3 months for androgenetic alopecia.
20 al (already demethylated) paternal genome in androgenetic and triploid diandric embryos.
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
27 f the coding sequence in parthenogenetic and androgenetic embryonic stem cells.
28 s a difference in developmental potential of androgenetic embryos produced with eggs from females of
29 licated in the periimplantation lethality of androgenetic embryos.
30                                        Mouse androgenetic haploid embryonic stem cells (AG-haESCs) ca
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
33                Although most complete HM are androgenetic in origin, a rare, frequently familial, bip
34 ise to a 46,XX genotype and is thought to be androgenetic in origin.
35 enetic material from other species may allow androgenetic lineages of Corbicula to mitigate the effec
36 NA from other species occur within otherwise androgenetic lineages of Corbicula.
37 of which are indistinguishable from those in androgenetic or gynogenetic embryos.
38 ntire genome is either exclusively paternal (androgenetic) or maternal (parthenogenetic), exhibit dra
39 HM, identical to that seen in complete HM of androgenetic origin (AnCHM).
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
45 the hypothesis of long-term clonality of the androgenetic species.
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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