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1 ory protein (StAR) is required for efficient adrenal cortical and gonadal but not trophoblast steroid
9 and cholesterol to the culture medium of Y-1 adrenal cortical cells greatly increased the storage of
11 epitope-tagged perilipins in transfected Y-1 adrenal cortical cells was regulated by lipid similarly
12 n-proliferating cells like cardiac myocytes, adrenal cortical cells, and neurons, suggesting an addit
13 chemistry revealed high ACSVL3 expression in adrenal cortical cells, spermatocytes and interstitial c
14 ll types in the intestine, and in kidney and adrenal cortical cells, whereas ACAT2 is present only in
16 eta-HSD II promoter was examined using human adrenal cortical (H295R; steroidogenic) and cervical (He
17 hic chondrocytes; renal medullary dysplasia; adrenal cortical hyperplasia and cytomegaly; and lens ce
18 of the kidneys, aldosteronism resulting from adrenal cortical hyperplasia, and persistently normal bl
19 Fetal development and fractal dimensions of adrenal cortical mosaic patches are consistent with an a
20 Focal pancreatic acinar necrosis and spotty adrenal cortical necrosis were seen transiently between
21 staining was extremely robust in fetal sheep adrenal cortical neurofibers and cells while weak in fib
24 We have demonstrated the purification of adrenal cortical progenitor cells from digestions of mur
27 t NGF and bFGF represent a link by which the adrenal cortical system can exert trophic action on the
28 3 months of age, adrenal size, the ratio of adrenal cortical to medullary area and stimulated cortis
29 her tumors, including gastrinoma, carcinoid, adrenal cortical tumors, angiofibroma, collagenoma, and
31 oplet (LD) organelles in steroidogenic mouse adrenal cortical (Y-1) cells with CARS microscopy in rea
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