ライフサイエンスコーパス: labyrinthine

1 h the core of cytochrome bc complexes can be labyrinthine.

2 MVS is ideal for prolonged labyrinthine activation because it mimics constant head

3 es, hexagonally packed cylinders, spots, and labyrinthine and lamellar patterns.

4 ly, Arnt(-/-) placentas show greatly reduced labyrinthine and spongiotrophoblast layers, and increase

5 he ultrastructural organization of the blood labyrinthine barrier (BLB) was investigated in the human

6 Fractones consisted of labyrinthine BL projecting from SEL blood vessels to ter

7 ental defects included significantly reduced labyrinthine branching morphogenesis, widespread penetra

8 ts, having flattened twisting processes with labyrinthine cavities communicating with the extracellul

9 While labyrinthine cells are present in the mutant Tfeb placen

10 calize to the ND at the entry point into the labyrinthine channels and, like their vertebrate counter

11 and to reduced passage of proteins into the labyrinthine channels for uptake by endocytosis, suggest

12 gh an SD-like nephrocyte diaphragm (ND) into labyrinthine channels that are active sites of endocytos

13 Twelve bilateral labyrinthine-defective (LD) subjects and twelve normal h

14 These defects include the failure of labyrinthine development, the dilation of maternal blood

15 spongiotrophoblast layers, and a decrease in labyrinthine development.

16 uch as stroke may masquerade as a peripheral labyrinthine disorder and conversely benign conditions s

17 trate this approach by imaging ferrimagnetic labyrinthine domains in a Gd/Fe multilayer with perpendi

18 (26):11676-11681, where the two enantiomeric labyrinthine domains of the gyroid are connected to the

19 m, with the minority components also forming labyrinthine domains whose geometry and topology changes

20 nd naturally occurring ionic currents in the labyrinthine endolymph fluid.

21 y the role of Igf2 in the development of the labyrinthine exchange membrane and its functional conseq

22 Patients lacking labyrinthine function did not.

23 ycosylated and subsequently localized to the labyrinthine ingrowths of the transfer cell walls.

24 In addition to labyrinthine inputs, the majority of neurons in this reg

25 Thus, cross-labyrinthine interactions appear to play important roles

26 inol/quinone (Q/QH2) transfer emphasizes the labyrinthine internal structure of the complex, includin

27 ignificant reduction in the thickness of the labyrinthine layer of the placenta is observed in LBP-1a

28 eads to a failure to correctly elaborate the labyrinthine layer of the placenta.

29 s restricted to the pituitary and hCS to the labyrinthine layer of the placenta.

30 l structural improvement was observed in the labyrinthine layer that was disrupted in the SOCS3-defic

31 Defects in the morphogenesis of the labyrinthine layer were observed as early as 11.5 dpc.

32 ormation, and the formation of the placental labyrinthine layer.

33 al defects that alter the development of the labyrinthine layer.

34 rophoblast marker Mash2 and decreases in the labyrinthine markers Tfeb and Gcm1.

35 interface, (ii) a discoid shape, and (iii) a labyrinthine maternofetal interdigitation.

36 of an acoustic metasurface based on tapered labyrinthine metamaterials.

37 ithelial sheet of ectoderm gives rise to the labyrinthine network of cells that constitutes the funct

38 d inhibitor morphogens for stripe, spot, and labyrinthine patterns and confirm the model predictions

39 Striking circular, labyrinthine, polygonal, and striped patterns of stones

40 n and the remaining mutants did not have the labyrinthine portion of the placenta.

41 ef review we discuss new insights into these labyrinthine relationships.

42 l (suprainiac and nuchal torus) and temporal labyrinthine (semicircular canal) morphology with the Ne

43 of the placenta to vascularize and form the labyrinthine spongiotrophoblast.

44 the form of complex stackable cisternae and labyrinthine structures adjoining the PM at junctional c

45 on by combining the hybrid metastuctures and labyrinthine structures.

46 nta without affecting differentiation of the labyrinthine syncytiotrophoblasts.

47 The mature striatum is divided into a labyrinthine system of striosomes embedded in a surround

48 zed exclusively to the apical surface of the labyrinthine trophoblast around maternal blood sinuses,

49 h their physiological inhibitor HAI-1 to the labyrinthine trophoblast cells in proximity to basement

50 vels in the embryo but at high levels in the labyrinthine trophoblast cells of the placenta.

51 ), a transcription factor critical for mouse labyrinthine trophoblast development.

52 cells and chorionic plate, and later in the labyrinthine trophoblast of the chorioallantoic placenta

53 ctoderm of the chorion, and subsequently the labyrinthine trophoblast of the chorioallantoic placenta

54 gene expression occurred specifically in the labyrinthine trophoblast of the mouse placenta, which co

55 ranscript (P0) specifically expressed in the labyrinthine trophoblast of the placenta leads to reduce

56 dpc in ectoplacental cone, giant cells, and labyrinthine trophoblasts.

57 ctional zone, and decreased proliferation of labyrinthine trophoblasts.

58 at the BL located at the pial surface formed labyrinthine tube-like structures enclosing numerous fib

59 scribe the proposed metamaterial with hybrid labyrinthine units, which reveals the mechanism of coexi

60 nfers placental insufficiency with decreased labyrinthine vascularization, yielding no viable offspri

61 sruption of the maternal allele in mice, the labyrinthine volume was increased in a manner consistent

62 centomegaly with specific defects within the labyrinthine zone involved in maternal-fetal nutrient tr

63 The labyrinthine zone of the placenta is diminished in Plk2(

64 th an increase in the volume fraction of the labyrinthine zone responsible for nutrient exchange, whe

65 , as were the volume and surface area of the labyrinthine zone responsible for placental nutrient tra