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1 rt striking reciprocal phenotypic effects on androgenetic (AG: two paternal genomes) and parthenogene
2 the mother (gynogenetic [GG]) or the father (androgenetic [AG]) are unique models for studying genomi
3 [95% confidence intervals]) in patients with androgenetic alopecia (37.3 128.4, 46.1]) and alopecia a
11 Dermal papilla cells (DPCs) taken from male androgenetic alopecia (AGA) patients undergo premature s
15 s is used in established scoring systems for androgenetic alopecia (AGA), central centrifugal cicatri
16 l variants implicated in the pathobiology of androgenetic alopecia (AGA), eczema and other complex tr
17 lative efficacy of 3 commonly used drugs for androgenetic alopecia (AGA), namely, minoxidil and the t
19 ed patients with telogen effluvium (n = 30), androgenetic alopecia (n = 52), alopecia areata (n = 17)
21 ison, skin biopsies from alopecia areata and androgenetic alopecia affected humans were also collecte
22 in the miniaturization of hair follicles of androgenetic alopecia by interfering with the dermal pap
27 d occipital region in males with and without androgenetic alopecia revealed that next to the androgen
28 zed by premature entry into catagen, such as androgenetic alopecia, alopecia areata, and telogen effl
31 therapy-induced alopecia, telogen effluvium, androgenetic alopecia, cicatricial alopecia, graying).
32 reatment of benign prostatic hyperplasia and androgenetic alopecia, reduced self-administration of mu
33 eptor degraders, both in clinical trials for androgenetic alopecia, with GT20029 also evaluated for a
42 etic ova), and in individual gynogenetic and androgenetic blastomeres, both maternal and paternal Igf
43 ion were also present in parthenogenetic and androgenetic cells and in tissues from animals maternall
44 is phenotypically indistinguishable from an androgenetic complete hydatidiform mole, in which abnorm
45 Both maternal (gynogenetic) and paternal (androgenetic) derived cells conveyed long-term, multilin
46 -modified paternal pronucleus should support androgenetic development (i.e., from the paternal pronuc
47 ans by generating exclusively paternal human androgenetic embryonic stem cells (aESCs) and comparing
48 pressed in differentiated cells derived from androgenetic embryonic stem cells and normal embryos but
50 s a difference in developmental potential of androgenetic embryos produced with eggs from females of
54 We developed a meiotic mapping panel of 94 androgenetic haploid embryos that were scored for geneti
56 ge is the strongest risk factor for sporadic androgenetic HM, which affects 1 in every 600 pregnancie
57 H5, SYCP2, MEIOB, and HFM1, in patients with androgenetic HMs, including a familial case of 3 affecte
58 enome in sporadic hydatidiform moles (purely androgenetic in complete hydatidiform moles and diandric
61 enetic material from other species may allow androgenetic lineages of Corbicula to mitigate the effec
64 ntire genome is either exclusively paternal (androgenetic) or maternal (parthenogenetic), exhibit dra
66 ion mechanisms: in individual blastomeres of androgenetic ova, both paternal Snrpn alleles were activ
67 normal ova were unchanged in gynogenetic and androgenetic ova; the latter contain two maternal and tw
68 lopment that are particularly evident in the androgenetic phenotype, uniparental cells of both parent
69 ions in Drosophila melanogaster that produce androgenetic progeny, we demonstrate that the Wolbachia-
70 al and nuclear loci from multiple sexual and androgenetic species across the global distribution of C
73 arthenogenetic (two maternal chromosomes) or androgenetic (two paternal chromosomes) cells displaying
74 ferences in X-linked gene expression between androgenetic (two paternal genomes), gynogenetic (two ma