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1 nternal architecture of multiple 'grapelike' lobulations.
2 atinocyte nuclei, including nuclear envelope lobulation and decreased nuclear circularity not present
3 Lbr in EML-ic/ic cells rescued both nuclear lobulation and growth arrest in cholesterol starvation c
9 These patients display cleft palate, tongue lobulations and polydactyly, phenotypes characteristic o
11 ys are required for branching morphogenesis, lobulation, and formation of the peripheral lung parench
12 intermediate T2 signal, well-defined margin, lobulation, and hypointense rim, were detected in a high
13 intermediate T2 signal, well-defined margin, lobulation, and/or hypointense rim, together with restri
15 vity following VRK1 knockdown caused nuclear lobulation, blebbing, and micronucleation, which subsequ
16 erogeneity, extrahepatic metastases, surface lobulation, calcification, and isoattenuation with liver
18 ated at 7 weeks of age resulted in excessive lobulation, indicating that adipocytes are critically in
19 loid lineage vacuolization, abnormal nuclear lobulation of both erythroid and myeloid precursors, nuc
22 nificant changes in nuclear shape, including lobulation of the nuclear envelope, thickening of the nu
23 rimary tumors, tumors invading the gland, or lobulations of the enlarged gland from the body of the g
24 reveals changes such as abnormal granulocyte lobulation or granularity and altered red blood cell (RB
27 connections correlated well with the nuclear lobulation, suggesting a relationship with cleavage furr