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1     Composed of a gecko-inspired elastomeric microfibrillar adhesive membrane supported by a pressure
2                            Large collagen VI microfibrillar aggregates were present at the top of the
3 ermis of photoaged forearm skin, with sparse microfibrillar apparatus and interstitial collagen.
4 nd III, collagen VII, and the fibrillin-rich microfibrillar apparatus in this area.
5 ignificant increases in the abundance of the microfibrillar apparatus was observed proximal to the de
6 finding was the association of myocilin with microfibrillar architecture in sheath-derived plaques wh
7 thermore, high-resolution measurement of the microfibrillar architecture of cell walls suggests that
8 imarily from reversible alterations in supra-microfibrillar arrangements rather than from intrinsic e
9 ation is due primarily to the failure by the microfibrillar array of the adventitia to sustain physio
10 t the importance of Ca2+ to microfibrils and microfibrillar arrays in vivo.
11 lyses of isolated Ca2+-containing, staggered microfibrillar arrays were used to interpret the effects
12 n the gross organization and distribution of microfibrillar arrays.
13  to sustain hemodynamic stress by disrupting microfibrillar assembly, by impairing the homeostasis of
14 d exert a strong dominant negative effect on microfibrillar assembly, leading to a loss of normal loc
15 ed a dominant-negative effect on collagen VI microfibrillar assembly.
16 nt fibrillin-1 can participate in productive microfibrillar assembly.
17 rotein, as the primary determinant of failed microfibrillar assembly.
18 r triple-helix formation but is critical for microfibrillar assembly.
19 -2 and suggest that MAGP-2 may help regulate microfibrillar assembly.
20 clude elastic fibre maturation by disrupting microfibrillar assembly.
21                         MFAP5, also known as microfibrillar-associated glycoprotein-2 (MAGP2), may in
22                             The glycoprotein microfibrillar-associated protein 4 (MFAP4) is an integr
23                                       MFAP4 (microfibrillar-associated protein 4) is an extracellular
24       We further show that the proangiogenic microfibrillar-associated protein 5 (MFAP5) is a direct
25 ovarian tumour samples and find that stromal microfibrillar-associated protein 5 (MFAP5) is a prognos
26 alcium-dependent signaling pathway involving microfibrillar-associated protein 5 (MFAP5), focal adhes
27                                              Microfibrillar-associated protein-1/2 was found with ela
28  elastin-associated proteins fibrillin-1 and microfibrillar-associated protein-1/2 were identified wi
29 antibodies against elastin, fibrillin-1, and microfibrillar-associated protein-1/2.
30 ed to control the position of self-assembled microfibrillar bundles of cyclic peptide nanotubes in wa
31 e packing degree and the spatial position of microfibrillar bundles of cyclic peptide nanotubes.
32 ly available hemicelluloses and pectins, and microfibrillar cellulose isolated form apple parenchyma
33 y form membrane complexes in vivo or produce microfibrillar cellulose.
34  B-d-glucan) showed the ability to adsorb to microfibrillar cellulose.
35 he distribution and quantity of collagen VI, microfibrillar collagen that forms an open network with
36 lar weight components of the fibrillin-based microfibrillar complex.
37   In mice, Fbn1 and Fbn2, encoding the major microfibrillar components, are strongly expressed during
38 at may influence its associations with other microfibrillar components.
39 missense mutation (C1039G) revealed impaired microfibrillar deposition, skeletal deformity, and progr
40 rs a spontaneous internal duplication in the microfibrillar glycoprotein fibrillin-1, might show whet
41                                          The microfibrillar glycoprotein gene, fibrillin 1 (FBN1), on
42 ng electron microscopy of up to six distinct microfibrillar lamellae.
43 suggesting that Wnts contribute to increased microfibrillar matrices in Tsk skin.
44  to an altered LTBP1 loosely anchored in the microfibrillar network and cause increased ECM depositio
45 se studies highlight that the fibrillin-rich microfibrillar network associated with the upper dermis
46 al non-collagenous regions, forms a distinct microfibrillar network in most connective tissues.
47 icroscopy revealed that the papillary dermal microfibrillar network was truncated and depleted in pho
48 rotein interacts with elastin fibers and the microfibrillar network.
49 ibute to the biomechanical properties of the microfibrillar network.
50                                Extracellular microfibrillar networks composed of fibrillins and their
51 ular microenvironments composed of intricate microfibrillar networks influence cell fate decisions in
52          Whether fibrillins form independent microfibrillar networks or can co-polymerize, forming a
53 oteins and their assembly into extracellular microfibrillar networks with focal aggregation of microf
54                           To investigate the microfibrillar organization and structural properties of
55 N2 gene, which encodes an elastin-associated microfibrillar protein called fibrillin-2.
56 N1 gene, which encodes the connective-tissue microfibrillar protein fibrillin 1.
57 onnective tissue, caused by mutations of the microfibrillar protein fibrillin-1, that predisposes aff
58 inhibition of sulfation was shown to prevent microfibrillar protein incorporation into the extracellu
59                                  The related microfibrillar protein MAGP-1 was also found to interact
60 VI is a ubiquitously expressed extracellular microfibrillar protein.
61 n fibrosis via its interface with associated microfibrillar proteins and type I collagen; in particul
62 d decorin secretion, suggesting that the two microfibrillar proteins can associate in the absence of
63                                          The microfibrillar proteins include, among others, the fibri
64                    Little is known about how microfibrillar proteins interact to support fiber assemb
65 ults demonstrate for the first time that the microfibrillar proteins MAGP-1 and MAGP-2 can function o
66                                              Microfibrillar proteins mainly include fibrillins and mi
67 olecular basis of its interaction with other microfibrillar proteins, deletion constructs of MAGP1 we
68 onstrated that amino-terminal domains of two microfibrillar proteins, fibrillin-1 and fibrillin-2, in
69 Wnt3a markedly stimulated matrix assembly of microfibrillar proteins, including Fbn-1, by cultured fi
70      Six of 13 positive clones encoded known microfibrillar proteins, including fibrillin-1 and -2.
71 acilitating the deposition of elastin onto a microfibrillar scaffold via direct molecular interaction
72  indicated that 1a and 1b self-organize into microfibrillar species, whereas 1c and 1d do not.
73                               The effects of microfibrillar stiffening factors k(1) and k(2), the cel
74 om model structures of the axially projected microfibrillar structure and the observed X-ray diffract
75 on, thereby retaining the essentially native microfibrillar structure.
76  membrane where they are integrated into the microfibrillar structure.
77 change in either molecular or macromolecular microfibrillar structure.
78        Muscle-driven actuation of biomimetic microfibrillar structures is achieved using integrative
79 plain the difficulty in isolating individual microfibrillar structures.
80          These morphologically heterogeneous microfibrillar systems are found in many vertebrate tiss