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1 atinocyte nuclei, including nuclear envelope lobulation and decreased nuclear circularity not present
2  Lbr in EML-ic/ic cells rescued both nuclear lobulation and growth arrest in cholesterol starvation c
3                                              Lobulation and internal septation, which appear to refle
4                            Severe defects in lobulation and severe lung hypoplasia were observed when
5 gakaryopoiesis with abnormalities of nuclear lobulation and size.
6 ation showed severe distortion with multiple lobulations and irregular extensions.
7                             The induction of lobulations and the clustering of centromeres originate
8 ys are required for branching morphogenesis, lobulation, and formation of the peripheral lung parench
9                                              Lobulation, atrophy, and hypertrophy were subclassified
10 erogeneity, extrahepatic metastases, surface lobulation, calcification, and isoattenuation with liver
11 cient expression disrupts neutrophil nuclear lobulation characteristic of Pelger-Huet anomaly.
12 ated at 7 weeks of age resulted in excessive lobulation, indicating that adipocytes are critically in
13 loid lineage vacuolization, abnormal nuclear lobulation of both erythroid and myeloid precursors, nuc
14  and have cerebellar hypoplasia and abnormal lobulation of the cerebellum.
15                The morphologic findings were lobulation of the liver contour, atrophy of the lateral
16 nificant changes in nuclear shape, including lobulation of the nuclear envelope, thickening of the nu
17 rimary tumors, tumors invading the gland, or lobulations of the enlarged gland from the body of the g
18 his method was not adequate for detection of lobulation or size of aneurysm.
19  scale (texture, border definition, contour, lobulation, spiculation, and concavity).
20 connections correlated well with the nuclear lobulation, suggesting a relationship with cleavage furr
21 givae were lobulated, and the surface of the lobulations was pebbly and granular.

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