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1 n critical for the formation of a functional theca.
2 e murine sperm perforatorium and perinuclear theca.
3 with a characteristic echinoderm-like plated theca, a muscular stalk reminiscent of the hemichordates
4 s are often polyovulatory and have disrupted theca and granulosa cell layers.
5 lands was compared to mRNA levels in ovarian theca and granulosa cells using real-time quantitative p
6 l activity in DF-1, LMH, LMH/2A, and primary theca and granulosa cells.
7 expressed in testis Leydig cells and ovarian theca and luteal cells.
8 2-weighted images, which corresponded to the theca and stromal reaction around the cyst.
9 nsulin-like 3 (INSL3) transcripts in ovarian theca and testicular Leydig cells.
10 as highly expressed in follicular granulosa, theca, and endothelial cells; NTSR1 and NTSR2 were expre
11 vealed distinct gene activities for oocytes, theca, and granulosa cells.
12 ociated membrane protein and the perinuclear theca, and the exclusion of the nuclear mitotic apparatu
13    These data contributed panels of oocyte-, theca-, and granulosa-specific genes, thus expanding the
14 omponent of the calyx within the perinuclear theca at the posterior part of mature sperm nuclei.
15 h the granulosa cell layer and sometimes the theca, but rarely with the stroma.
16              A hallmark of PCOS is excessive theca cell androgen secretion, which is directly linked
17 osa cells, reach preantral stages containing theca cell layers by 2 weeks.
18 mutant stromal cells consist of a luteinized theca cell lineage at various differentiation stages inc
19 in impaired granulosa cell proliferation and theca cell recruitment as well as fewer primordial folli
20 r development by antagonizing the actions of theca cell-derived BMPs.
21 overexpressing steroidogenic enzyme CYP17, a theca cell-specific marker.
22 is showing that treatment of cultured bovine theca cells (TC) with BMP6 significantly (>twofold; P <
23 strong mRNA labeling for BMP-4 and -7 in the theca cells and BMP receptor types IA, IB, and II in the
24                Oocyte growth is supported by theca cells and granulosa cells, which establish dynamic
25 he first genetic evidence for the origins of theca cells and reveal a multicellular interaction criti
26 n and insulin resistance persist in cultured theca cells and skin fibroblasts, respectively, from wom
27 g in the development and function of ovarian theca cells and the pathophysiologic effects of hyperins
28 l interactions between ovarian granulosa and theca cells as an approach to cHRT.
29                            Here we show that theca cells derive from two sources: Wt1(+) cells indige
30               Only mural granulosa cells and theca cells express large numbers of LH receptors, and L
31                         In this environment, theca cells form, oestrogen is produced and germ cells a
32       Our previous studies demonstrated that theca cells from PCOS ovaries maintained in long term cu
33              Our analysis revealed that PCOS theca cells have a gene expression profile that is disti
34 ved in excess androgen synthesis by the PCOS theca cells in order to identify candidate PCOS genes.
35                                        Using theca cells isolated and propagated from normal cycling
36 lls, the identification of mutant luteinized theca cells may add crucial evidence in understanding th
37                                        Thus, theca cells may contribute significantly to the inhibin
38 in expression to Leydig cells of the testis, theca cells of the ovary, and cells of the adrenal corte
39 ocytes and interstitial cells of the testis, theca cells of the ovary, cerebral cortical neurons, and
40 results suggest that GT198 mutant luteinized theca cells overexpressing CYP17 are common in ovarian c
41             Knock-down of DENND1A.V2 in PCOS theca cells reduced androgen biosynthesis and CYP17A1 an
42 orced overexpression of DENND1A.V2 in normal theca cells resulted in a PCOS phenotype of augmented CY
43 we report the unexpected finding that bovine theca cells show abundant INHA expression and 'free' inh
44  activated medullary follicles recruit fetal theca cells to establish a two-cell system for sex-stero
45  genes with increased mRNA abundance in PCOS theca cells were aldehyde dehydrogenase 6 and retinol de
46 , turn over most granulosa cells, but retain theca cells which expand in number together with interst
47 defined a stable molecular phenotype of PCOS theca cells, 2) suggested new mechanisms for excess andr
48 anisms for excess androgen synthesis by PCOS theca cells, and 3) identified new candidate genes that
49 subfamily C member 3) were identified in GC, theca cells, and oocyte.
50 omatic cell types, including follicle cells, theca cells, and ovarian stromal cells.
51 ciated with the persistence of steroidogenic theca cells, but this connection is poorly understood.
52 ocated in the cytoplasm as well as nuclei of theca cells, suggesting a possible role in gene regulati
53 tly greater amounts of androgens than normal theca cells, suggesting an intrinsic abnormality.
54                Reelin, which is expressed in theca cells, triggers a signal in granulosa cells via ap
55                          Human granulosa and theca cells, which express endogenous SF-1, contained mo
56 rian surface epithelium, granulosa cells and theca cells.
57 NA when added to the medium of cultured PCOS theca cells.
58 rotein and mRNA levels are increased in PCOS theca cells.
59 pression and intrinsic abnormalities in PCOS theca cells.
60 ression profile that is distinct from normal theca cells.
61  expression, although both theca interna and theca externa were also positive, interna greater than e
62                 After stamen initiation, two theca form at the tip, and each forms an adaxial and aba
63 erplasia and hypervascularity of the ovarian theca interna and stroma are also prominent features of
64 e found strong expression of EG-VEGF mRNA in theca interna and stroma in most of the specimens examin
65 howed the greatest expression, although both theca interna and theca externa were also positive, inte
66  Sertoli and Leidig cells of the testes; (i) theca interna cells in the ovary; and (j) adrenal cortex
67 titial gland, and in the granulosa cells and theca interna of small to medium-sized antral follicles,
68 sulin receptor (IR) gene specifically in the theca-interstitial (TI) cells of the ovaries (Cyp17IRKO)
69 anulosa) and steroidogenic cells (Leydig and theca-interstitium) are two major somatic cell types in
70 . subclathratus is moved to Indonaia, and T. theca is transferred to Lamellidens.
71              Ovaries lacking Dhh/Ihh exhibit theca layer loss, blunted steroid production, arrested f
72 en, including ovarian follicle granulosa and theca layers.
73                    These progenitors acquire theca lineage marker Gli1 in response to paracrine signa
74 either membrane tethering to the perinuclear theca nor the fatty acid composition of sperm.
75 ich resembles tissue dendritic cells, in the theca of antral follicles.
76 c CD8alpha(+) cells were able to home to the theca of follicles in the recipients.
77 cells of veins, either in the inner layer of theca of ovulating follicles during ovulation, or surrou
78 NND1A immunostaining was more intense in the theca of PCOS ovaries.
79  granulosa cells are known, the origin(s) of theca progenitor cells have not been definitively identi
80 n the mesenchyme, cotreatment with AMH halts theca progenitor differentiation and reduces apoptotic g
81 x molecular interactions between perinuclear theca proteins required during spermiogenesis.
82                              The perinuclear theca (PT) is a unique cytoskeletal structure whose ante
83 posure and solubilization of the perinuclear theca (PT), as evidenced by transmission electron micros
84 ated ovarian steroidogenic cells (granulosa, theca, small luteal, and large luteal), and isolated lut
85  single-cell RNA sequencing of granulosa and theca/stroma cell fractions.
86 s of follicle maturation, with granulosa and theca/stroma cells also displaying molecular hallmarks o
87 tivation and being stored in the perinuclear theca, the sperm compartment whose content is first rele
88  be expressed in adult ovarian granulosa and theca tissues.
89 or a single origin of the group's cellulosic theca, which we show coincided with a radiation of cellu