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1 e murine sperm perforatorium and perinuclear theca.
2 n critical for the formation of a functional theca.
4 lands was compared to mRNA levels in ovarian theca and granulosa cells using real-time quantitative p
9 ociated membrane protein and the perinuclear theca, and the exclusion of the nuclear mitotic apparatu
12 mutant stromal cells consist of a luteinized theca cell lineage at various differentiation stages inc
13 in impaired granulosa cell proliferation and theca cell recruitment as well as fewer primordial folli
16 is showing that treatment of cultured bovine theca cells (TC) with BMP6 significantly (>twofold; P <
17 strong mRNA labeling for BMP-4 and -7 in the theca cells and BMP receptor types IA, IB, and II in the
19 he first genetic evidence for the origins of theca cells and reveal a multicellular interaction criti
20 n and insulin resistance persist in cultured theca cells and skin fibroblasts, respectively, from wom
21 g in the development and function of ovarian theca cells and the pathophysiologic effects of hyperins
27 ved in excess androgen synthesis by the PCOS theca cells in order to identify candidate PCOS genes.
29 lls, the identification of mutant luteinized theca cells may add crucial evidence in understanding th
30 in expression to Leydig cells of the testis, theca cells of the ovary, and cells of the adrenal corte
31 ocytes and interstitial cells of the testis, theca cells of the ovary, cerebral cortical neurons, and
32 results suggest that GT198 mutant luteinized theca cells overexpressing CYP17 are common in ovarian c
34 orced overexpression of DENND1A.V2 in normal theca cells resulted in a PCOS phenotype of augmented CY
35 genes with increased mRNA abundance in PCOS theca cells were aldehyde dehydrogenase 6 and retinol de
36 defined a stable molecular phenotype of PCOS theca cells, 2) suggested new mechanisms for excess andr
37 anisms for excess androgen synthesis by PCOS theca cells, and 3) identified new candidate genes that
38 ocated in the cytoplasm as well as nuclei of theca cells, suggesting a possible role in gene regulati
47 expression, although both theca interna and theca externa were also positive, interna greater than e
48 erplasia and hypervascularity of the ovarian theca interna and stroma are also prominent features of
49 e found strong expression of EG-VEGF mRNA in theca interna and stroma in most of the specimens examin
50 howed the greatest expression, although both theca interna and theca externa were also positive, inte
51 Sertoli and Leidig cells of the testes; (i) theca interna cells in the ovary; and (j) adrenal cortex
52 titial gland, and in the granulosa cells and theca interna of small to medium-sized antral follicles,
53 sulin receptor (IR) gene specifically in the theca-interstitial (TI) cells of the ovaries (Cyp17IRKO)
54 anulosa) and steroidogenic cells (Leydig and theca-interstitium) are two major somatic cell types in
61 cells of veins, either in the inner layer of theca of ovulating follicles during ovulation, or surrou
63 granulosa cells are known, the origin(s) of theca progenitor cells have not been definitively identi
65 posure and solubilization of the perinuclear theca (PT), as evidenced by transmission electron micros
66 tivation and being stored in the perinuclear theca, the sperm compartment whose content is first rele
68 or a single origin of the group's cellulosic theca, which we show coincided with a radiation of cellu
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