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3 during branching morphogenesis are lined by cuboidal and squamous cells that facilitate gas exchange
7 g a molecular basis for the retention of the cuboidal cell shape observed in the Wt1KO epicardium.
9 tions only, there were areas of hyperplastic cuboidal cells adjacent to normal pseudostratified colum
10 al cells, known as adaxial cells, are large, cuboidal cells adjacent to the notochord that express my
11 WDR1 mRNA was detected in homogene cells and cuboidal cells by embryonic day 7, in the undifferentiat
13 splatin effect is reduction in the number of cuboidal cells of the glomerular capsule, a change we te
16 r epithelial type II (ATII) cells are small, cuboidal cells that constitute approximately 60% of the
18 praja1 demonstrated cytoplasmic staining of cuboidal cells that have hepatocyte morphology and organ
19 e peripodial epithelium (PE); and a strip of cuboidal cells that joins the other two cellular sheets
20 re greatly expanded and some contained large cuboidal cells that were positive for cytokeratin and ot
21 ; the transition from a roughly 4x5 array of cuboidal cells to a 1x20 stack of elongated cells, prior
22 detected in hair cells, homogene cells, and cuboidal cells, all of which contain high levels of F-ac
24 derm-like phenotype and dedifferentiate into cuboidal cells, reminiscent of the basal epithelial cell
27 ulosum opposes Nrp1 and PlxnA1 in the future cuboidal cells; the abutment of ligand and receptors in
28 ed in pituitary anterior lobes were lined by cuboidal, ciliated epithelial cells, focally immunoposit
29 introduction by rational design of a [Fe4S4] cuboidal cluster into the hydrophobic core of Escherichi
30 anes (EBDCs), P(N)-type clusters, and double-cuboidal clusters, have been devised using the concept o
33 helium transitions between simple geometries-cuboidal, columnar and squamous-and redistributes cell p
35 requency EPR spectroscopy of a Mn(IV)(4)O(4) cuboidal complex as a spectroscopic model of the S(3) st
37 the previously reported Mn(III)Mn(IV)(3)O(4) cuboidal complex to the Mn(IV)(4)O(4) complex described
38 gnetic interactions have been modeled in the cuboidal compound Co(4)(DPM)(4)(CH(3)O)(4)(CH(3)OH)(4) (
39 limit of accuracy of the two refinements the cuboidal core is differently distorted in the two protei
43 such pore architectures through face-shared cuboidal, cuboctahedral, and rhombicuboctahedral cages.
44 ctin ligands displayed at the surface of the cuboidal endothelial cells lining the post-capillary ven
46 ially elicited benign lung tumors comprising cuboidal epithelial cells expressing markers of alveolar
47 vertebrate lens has a distinct polarity with cuboidal epithelial cells on the anterior side and diffe
48 sists of a single layer of undifferentiated, cuboidal epithelial cells that stratifies to produce an
49 rols this morphogenesis from randomly packed cuboidal epithelial cells to highly organized hexagonal
50 orphologically, tumors were characterized as cuboidal epithelial cells with a type II cell phenotype,
51 amatic, cytoskeletal response in these tall, cuboidal epithelial cells; and why junctional buttressin
52 s epithelia from vagina and skin, as well as cuboidal epithelium from lung, stomach, and salivary gla
53 howed a multiloculated mass lined by flat or cuboidal epithelium leading to the diagnosis of BMPM.
54 ands, which are replaced by a GLUT2-positive cuboidal epithelium resembling the bile duct lining.
56 tumor displayed a premedullary monolayer of cuboidal epithelium that was S100(+), NeuN(-), and CRX(-
57 luminal coverage by respiratory or flattened cuboidal epithelium, and extent and density of peritrach
61 the P cluster in the P(N) state in which two cuboidal Fe(3)S(3) units are connected by a mu(6)-S atom
62 The most ubiquitous metalloclusters are the cuboidal Fe-S clusters, which are comprised of Fe sites
63 he synthesis and characterization of an open-cuboidal [Fe(3)S(4)] cluster in both biologically releva
64 logy-diamond-core [Fe(2)S(2)] clusters, open-cuboidal [Fe(3)S(4)] clusters, and cuboidal [Fe(4)S(4)]
66 es, and (ii) metal atom incorporation into a cuboidal [Fe(3)S(4)](0) cluster with a M(0) reactant in
68 ers, open-cuboidal [Fe(3)S(4)] clusters, and cuboidal [Fe(4)S(4)] clusters-have been reported in each
70 al changes of pre-GCs from a squamous into a cuboidal form, though it did not influence oocyte activa
71 of 7 is built of two (Tp)MoFe(3)(mu(3)-S)(3) cuboidal fragments bridged by two mu(2)-S atoms and one
72 y a mixed-ligand approach, each possessing a cuboidal framework made of 160 metal ions and a nanosize
76 s consist of a stalk ectodomain supporting a cuboidal head; physiological oligomers consist of non-co
78 However, the cells of mutants are round or cuboidal in all of the tissues with mutant phenotypes, c
80 affects occlusion body shape, but the large cuboidal inclusions formed by granulin indicate that the
81 PV) yielded a few very large (2 to 5 micron) cuboidal inclusions in the cytoplasm and nucleus of infe
82 us and resulted in more structurally uniform cuboidal inclusions in which no virions were observed.
84 aP cells formed multicellular spheroids with cuboidal-like epithelial morphology, whereas MT1-GFP-exp
85 ession of GATA3 in MDA-MB-231 cells led to a cuboidal-like epithelial phenotype and reduced cell inva
87 f the preceding S(2) state, which contains a cuboidal Mn(3)O(4)Ca unit tethered to an external, 5-coo
88 or the oxygen-evolving complex involving the cuboidal Mn4Ca structure in photosystem II (PSII) has re
89 aortae from the LKLF-/- animals displayed a cuboidal morphology and failed to organize into a compac
90 vivo and in vitro resulted in the absence of cuboidal morphology and pigmentation, and in concomitant
91 our keratinocytes that lack the polarity and cuboidal morphology of basal keratinocytes in tissue.
95 t of CVC for 3 days induced osteoblast-like "cuboidal" morphology, inhibited proliferation, and enhan
96 ytes are located in large bile ducts and the cuboidal non-mucin-producing cholangiocytes are located
101 nuclei; conjunctival epithelium: stratified cuboidal or polygonal cells, hyperreflective cytoplasm,
103 re we demonstrate self-assembly to nanoscale cuboidal particles with a bicontinuous cubic structure b
105 ates the conversion of epithelial cells to a cuboidal phenotype capable of apical endocytosis; theref
107 epithelium (RPE) consists of a monolayer of cuboidal, pigmented cells that is located between the re
108 helium of the Drosophila melanogaster ovary, cuboidal precursor cells transform into a squamous epith
109 development, including undilated airspaces, cuboidal respiratory epithelium, thickened mesenchyme, a
116 model supports predictions of two coexisting cuboidal structures and provides precise values for the
117 s structural and spectroscopic models of the cuboidal subunit of the oxygen-evolving complex (OEC).
119 results provide insight into the squamous to cuboidal to columnar epithelial transitions seen in comp
123 atic transformation in cell morphology, from cuboidal to the eponymous stellate shape, during metamor
124 cells in different imaginal discs undergo a cuboidal-to-squamous cell shape change at distinct larva
125 ation, primordial germ cell positioning, and cuboidal-to-squamous cell shape transitions in the extra
126 Our findings indicate the importance of the cuboidal-to-squamous transition in epicardial maturation
127 rganizes Fe(2+/3+) and sulfide/selenide into cuboidal [(Tp*)WFe(2)S(3)] or cubane [(Tp*)WFe(3)S(3)Q]
129 imately 95% of the gas-exchange surface, and cuboidal type II cells, which secrete surfactants and mo
130 ficient mice contained highly differentiated cuboidal type II epithelial cells that are normally rest
131 e links the outer Mn to the Mn(3)O(3)Ca open-cuboidal unit (O4 and O5 in the Umena et al. structure).
132 (1-), FeCl(2), and Na(2)Se yields the double-cuboidal [W(2)Fe(4)S(6)Se(3)](2+/0) core with mu(2)-Se a
133 the nanoscale precipitates from spherical to cuboidal while simultaneously tailoring the phase bounda