ライフサイエンスコーパス: fibrillar collagen

1 d emerging microscopy techniques to quantify fibrillar collagen.

2 0/G1 arrest of human melanoma cells grown on fibrillar collagen.

3 isrupt cell proliferation in the presence of fibrillar collagen.

4 n attenuates platelet adhesion to soluble or fibrillar collagen.

5 tor was responsible for cell cycle arrest on fibrillar collagen.

6 ary evidence for the expression of a B-clade fibrillar collagen.

7 ith extracellular matrix proteins, including fibrillar collagen.

8 collagens, as well as impaired migration on fibrillar collagen.

9 been shown to be activated mainly by soluble fibrillar collagen.

10 h type IV collagen and gelatin prepared from fibrillar collagen.

11 cellular layers and a diminished content of fibrillar collagen.

12 mesenchymal tissues, the ligand of which is fibrillar collagen.

13 which appears restricted in the presence of fibrillar collagen.

14 independent platelet adhesion to immobilized fibrillar collagen.

15 t zones, enriched either in proteoglycans or fibrillar collagen.

16 anism for tension-dependent stabilization of fibrillar collagen.

17 lation may regulate cross-link maturation in fibrillar collagen.

18 r thermal stability is comparable to that of fibrillar collagen.

19 fibrosis and changes in the organization of fibrillar collagen.

20 mary epithelial cells on stiff matrices like fibrillar collagen.

21 ed to the protostome/deuterostome A clade of fibrillar collagens.

22 the -Gly-X-Y- repeating pattern found in non-fibrillar collagens.

23 t are uniquely able to cleave triple helical fibrillar collagens.

24 tients harboring mutations in genes encoding fibrillar collagens.

25 ase collagen receptors that are activated by fibrillar collagens.

26 der resulting from altered metabolism of the fibrillar collagens.

27 may be common aggregation motifs for the non-fibrillar collagens.

28 uration of extracellular matrices containing fibrillar collagens.

29 educed deposition of both elastic fibers and fibrillar collagens.

30 s different than that caused by mutations in fibrillar collagens.

31 ential for the processing of procollagens to fibrillar collagens.

32 lization of TIMP-2 with type IV collagen and fibrillar collagens.

33 s and marked depletion of elastic fibers and fibrillar collagens.

34 expression of EMT/myofibroblast markers and fibrillar collagens.

35 ed to the formation and further expansion of fibrillar collagens.

36 he cross-striated banding pattern typical of fibrillar collagens.

37 d fibroblasts and pathological deposition of fibrillar collagens.

38 capable of initiating degradation of native fibrillar collagens.

39 An increase in fibrillar collagens 1 and 5 was detected.

40 cells (6/14 [43%] vs 0/14 [0%]; P = .05) and fibrillar collagen (13/14 [93%] vs 2/14 [14%]; P < .0001

41 collagen, indicative of a limbal annulus of fibrillar collagen 2.2 mm in diameter, was identified in

42 diac fibrosis, and morphological evidence of fibrillar collagen accumulation at the infarcted and non

43 M2 macrophages, IL-4, IL-13, fibrillar collagen accumulation, and proteolysis of coll

44 m Aggregatibacter actinomycetemcomitans is a fibrillar collagen adhesin belonging to the family of tr

45 oviding a physical barrier against invasion, fibrillar collagen also restricts cell proliferation.

46 Fibrillar collagen, an essential structural component of

47 een cloned including a basement membrane and fibrillar collagen and an A and B chain of laminin.

48 accompanied by proteolytic modifications of fibrillar collagen and an influx of host proteins, the r

49 combinant human CTRP-1 specifically bound to fibrillar collagen and blocked collagen-induced platelet

50 es depend on changes in extracellular matrix fibrillar collagen and cardiomyocyte titin.

51 ome a principal method for studying decidual fibrillar collagen and characterizing mouse models assoc

52 In culture, tumor cells are invasive in a fibrillar collagen and COX-2-dependent manner.

53 aft model and highlight the critical role of fibrillar collagen and DDRs in supporting the growth of

54 -induced alterations in extracellular matrix fibrillar collagen and diastolic function.

55 efficient induction of invadopodia on dense fibrillar collagen and for local degradation of collagen

56 primary mouse megakaryocytes in response to fibrillar collagen and in response to cross-linking of t

57 th PyMT(mgko) tumors is stiffer and has more fibrillar collagen and increased expression of the colla

58 dysfunction and immune evasion by remodeling fibrillar collagen and inhibiting T cell autophagic flux

59 cantly different, and the average content of fibrillar collagen and macrophages in the lesions was si

60 tilage and bone cells to cleave high-density fibrillar collagen and modulate their resident matrix to

61 nization, including density and alignment of fibrillar collagen and myofibroblasts.

62 t1 expression also leads to dysregulation of fibrillar collagen and periostin expression, as well as

63 High levels of perivascular fibrillar collagen and pulmonary interleukin-6 overexpre

64 atrix proteins have been reported to bind to fibrillar collagen and regulate the diameter of collagen

65 tially, this fibroblast response reorganized fibrillar collagen and stiffened the myocardium, albeit

66 antive reduction in cardiac fibroblasts, but fibrillar collagen and the ECM proteome were not overtly

67 al in vivo degradation of the self-assembled fibrillar collagen and the majority of implants experien

68 iple sites on the triple helical portions of fibrillar collagens and also capable of competing for su

69 d Glu40 as essential residues for binding to fibrillar collagens and collagen-related peptides (CRPs)

70 wn to catalyze the covalent cross-linking of fibrillar collagens and elastin at peptidyl lysine resid

71 he catalysis of lysyl-derived cross-links in fibrillar collagens and elastin in the extracellular mat

72 s unique structural features of invertebrate fibrillar collagens and is expressed predominantly in bo

73 Cardiac extracellular matrix (ECM) contains fibrillar collagens and proteoglycans, important for mai

74 secreted by lung fibroblasts was retained on fibrillar collagen, and ACLP-deficient lung fibroblasts

75 iological stimulus for MT1-MMP expression is fibrillar collagen, and it has been shown that it up-reg

76 igitation of rete ridges, abundant organized fibrillar collagen, and plentiful arrays of elastic fibe

77 e growth regulatory signals originating from fibrillar collagen, and the proteolytic degradation of f

78 chemicals (e.g., triolein, elastin, keratin, fibrillar collagen, and type IV collagen) associated wit

79 occurrence of related motifs in other human fibrillar collagens, and located a conserved array of no

80 include MMP-1, which preferentially degrades fibrillar collagens, and MMP-3, which can initiate a loc

81 found in the triple-helix domains of all non-fibrillar collagens, and perturbations to the triple-hel

82 We conclude that autoantibodies to fibrillar collagen antigens are present frequently in lu

83 ephrotic syndrome and glomerular deposits of fibrillar collagen are associated with multiple exostose

84 The thermal transitions of fibrillar collagen are investigated with second-harmonic

85 Thrombin and fibrillar collagen are potent activators of platelets at

86 ges reveal that the C-terminal prodomains of fibrillar collagens are partially uncleaved in PDAC ECM,

87 Fibrillar collagens are present in a wide variety of ani

88 Non-fibrillar collagens are structurally more variable and r

89 Type I and III fibrillar collagens are the major structural proteins of

90 crosirius red-positive streaks," enriched in fibrillar collagens, are a hallmark of adipose tissue su

91 ages in cell culture, suggesting proteolyzed fibrillar collagen as a candidate ECM mediator of macrop

92 atrix (ECM) is a complex mixture composed of fibrillar collagens as well as additional protein and ca

93 ontaneous Ca(2+) oscillations in MSCs during fibrillar collagen assembly, and hypothesized that the t

94 hough sulfate and divalent phosphate bind to fibrillar collagen at physiological concentrations, our

95 MMPs, which have a unique ability to degrade fibrillar collagens at neutral pH.

96 Fibrillar collagen, being highly noncentrosymmetric, pos

97 ECM and was inhibited by laminin and type-1 fibrillar collagen but increased by fibronectin.

98 s is critically dependent on the cleavage of fibrillar collagen by a previously unidentified intersti

99 the progressive accumulation of disorganized fibrillar collagen by airway fibroblasts.

100 nic fluid, characteristic of the cleavage of fibrillar collagen by interstitial collagenase.

101 proteinase-14 is required for degradation of fibrillar collagen by mesenchymal cells.

102 xtracellular matrix components, particularly fibrillar collagens, by PRDM5 is a key molecular mechani

103 Additionally, we demonstrate that fibrillar collagen can also arrest cells at the G2 phase

104 Thus, fibrillar collagen can be a formidable barrier to viral

105 one position in the triple-helical domain of fibrillar collagen chains, and its biological significan

106 ions (PTMs) than do similar domains of other fibrillar collagen chains, PTMs consisting of hydroxylat

107 These results indicate that fibrillar collagen cleavage at collagenase-specific site

108 damts14, and of the genes encoding the major fibrillar collagens, Col1a1, Col2a1 and Col3a1, during m

109 to vertebrates, possess an ancestral clade A fibrillar collagen (ColA) gene that is expressed in the

110 hesis by SoxE and SoxD regulation of clade A fibrillar collagen (ColA) genes--suggesting that the cho

111 ing Mg++-independent adhesion to immobilized fibrillar collagen, collagen-induced platelet aggregatio

112 ined more collagen with greater alignment of fibrillar collagen compared with wild-type fibroblast-de

113 Cre tumors was enriched with stromal-derived fibrillar collagen, compared with wild-type or Hras-driv

114 Type V collagen is a quantitatively minor fibrillar collagen comprised of different chain composit

115 Aortic wall morphometry and fibrillar collagen content (a measure of fibrosis) was q

116 activity accompanied by an increase in total fibrillar collagen content and an increase in myocardial

117 changes in total MMP activity and myocardial fibrillar collagen content were related to a time- depen

118 addition, in SPARC-null mice, TAC increased fibrillar collagen content, albeit significantly less th

119 oad causes myocardial hypertrophy, increased fibrillar collagen content, and abnormal diastolic funct

120 expression, myocardial diastolic stiffness, fibrillar collagen content, and soluble and insoluble co

121 that was accompanied by an increase in total fibrillar collagen content.

122 rresponded to a decrease in total myocardial fibrillar collagen content.

123 esponded with a decrease in total myocardial fibrillar collagen content.

124 Exposure of platelets to fibrillar collagen converts the surface-bound proMMP-1 z

125 t while DDR1b clusters co-localized with non-fibrillar collagen, DDR1b/DDR2 filamentous structures as

126 metalloproteinase-1 (MMP-1), which initiates fibrillar collagen degradation.

127 idinoline (HP), a specific marker for mature fibrillar collagen degradation.

128 s important in cell cycle arrest mediated by fibrillar collagen, demonstrate the complexity of cell c

129 The tensile strength of fibrillar collagens depends on stable intermolecular cro

130 ugh BMP1, as a secreted proteinase, promotes fibrillar collagen deposition from both cancer cells and

131 50 Pa and increased to 1-6 kPa in areas near fibrillar collagen deposition in fibrotic livers.

132 Microarchitectural cues drive aligned fibrillar collagen deposition in vivo and in biomaterial

133 On the other hand, fibrillar collagen deposition was significantly increase

134 ding high matrix metalloproteinase activity, fibrillar collagen deposition, and release of bioactive

135 , organ atrophy was accompanied by increased fibrillar collagen deposition, suggesting a compensatory

136 ls mediate M migration and mechanosensing in fibrillar collagen ECM.

137 inal cord parenchyma do not normally contain fibrillar collagens, except in disease states.

138 Fibrillar collagen expression and content were increased

139 tigated the role of CRT in the regulation of fibrillar collagen expression, secretion, processing, an

140 A-3D mouse immortal keratinocytes growing on fibrillar collagen failed to activate FiRE and subsequen

141 , third clade (type C) within the vertebrate fibrillar collagen family.

142 eptides from procollagens, a crucial step in fibrillar collagen fiber formation.

143 cross-linking collagen I and III to form the fibrillar collagen fibers.

144 Collagen XV (COLXV) is a secreted non-fibrillar collagen found within basement membrane (BM) z

145 each antibody inhibited platelet adhesion to fibrillar collagen from 70 to 85%, especially during the

146 Although other fibrillar collagen-gene mutations that lead to allele in

147 port the characterization of a further three fibrillar collagen genes (Hcol2, Hcol3, and Hcol5) and t

148 mice revealed a significant upregulation of fibrillar collagen genes at mRNA level, as well as incre

149 Phylogenetic analyses reveal that the hydra fibrillar collagen genes form a distinct clade that appe

150 Mutations in the major fibrillar collagen genes lead to osteogenesis imperfecta

151 Fibrillar collagen genes were increased in CLAD, indicat

152 ely to carry disruptive rare variants within fibrillar collagen genes.

153 p27(KIP1) in cells plated in the presence of fibrillar collagen has led to the assumption that this k

154 Fibrillar collagens have an absolute requirement for Gly

155 We report that a novel high-density fibrillar collagen (HDFC) matrix is a potent inducer of

156 ge tumors that are characterized by abundant fibrillar collagen, high cyclooxygenase-2 (COX-2) expres

157 -/-) MEFs) have reduced transcript levels of fibrillar collagen I and III and less soluble collagen a

158 wn of collagen IV in the basal lamina and of fibrillar collagen I in the adjacent interstitium in the

159 We found that fibrillar collagen I induced linear F-actin structures,

160 This study demonstrates that fibrillar collagen I is the physiological inducer of a n

161 r invadosomes upon contact of the cells with fibrillar collagen I.

162 proteinase activity that processes the major fibrillar collagens I-III.

163 roblasts are deficient in their packaging of fibrillar collagen-I and express less decorin, important

164 ure in the pathogenesis of liver fibrosis is fibrillar Collagen-I deposition; yet, mediators that cou

165 Mapping integrin-binding sites within the fibrillar collagens identified GFOGER as a high affinity

166 proteinase 8 (MMP8), an enzyme that degrades fibrillar collagens imparting strength to the fetal memb

167 es new blood vessel growth into well-defined fibrillar collagen implants.

168 s emerged as a powerful modality for imaging fibrillar collagen in a diverse range of tissues.

169 The mesothelial niche was enriched with fibrillar collagen in human and murine omental metastase

170 Fibrillar collagen in its native form inhibits cell prol

171 in the human melanoma Mu89 is limited by the fibrillar collagen in the extracellular matrix.

172 Biosynthesis of fibrillar collagen in the skin is precisely regulated to

173 show that it is possible to optically image fibrillar collagen in tumors growing in mice using secon

174 d-order nonlinear polarization properties of fibrillar collagen in various rat tissues (vertebrae, ti

175 increasing awareness of the critical role of fibrillar collagens in breast cancer biology, tumor-perm

176 d that OSCAR binds to specific motifs within fibrillar collagens in the ECM that become revealed on n

177 issue to resist stress is mainly imparted by fibrillar collagens in the extracellular matrix, changes

178 ation of extracellular matrix (ECM), namely, fibrillar collagens in the hepatic stellate cells (HSCs)

179 llagen fiber architecture in tissues rich in fibrillar collagen, including bone, tendon, and skin.

180 ere shown by immunohistochemistry to contain fibrillar collagens, including type I collagen.

181 ts and enhanced expression and deposition of fibrillar collagens) increased progressively.

182 n the presence of Mg2+, platelet adhesion to fibrillar collagen induced activation of the GP IIb-IIIa

183 In unchallenged endothelial cells, fibrillar collagen induced robust capillary morphogenesi

184 e I collagen and a delayed onset to low dose fibrillar collagen-induced aggregation, results consiste

185 e was an increase in intimal and medial mean fibrillar collagen intensity from 22 11 a.u. pre-LVAD to

186 ablish a general approach to investigate MMP-fibrillar collagen interactions.

187 mong other requirements, cross-links between fibrillar collagens, introduced by tissue transglutamina

188 Glomerular deposition of fibrillar collagen is a characteristic finding of geneti

189 Highly resistant to proteolysis, fibrillar collagen is degraded by specific matrix metall

190 A hierarchical organizational model of fibrillar collagen is developed to interpret the second-

191 Efficient removal of fibrillar collagen is essential for adaptive subcutaneou

192 o experiments.Measurements and Main Results: Fibrillar collagen is not only increased but also highly

193 y Tnap ectopic expression in cells producing fibrillar collagen is sufficient to induce pathological

194 Type I fibrillar collagen is the most abundant protein in the h

195 sumed that the growth regulatory activity of fibrillar collagen is the result of an indirect restrict

196 A defining feature of fibrillar collagens is a 67-nm periodic banding along th

197 The mechanical strength of fibrillar collagens is highly dependent on the formation

198 Degradation of fibrillar collagens is important in many physiological a

199 density on top of or within 100-microm-thick fibrillar collagen lattices.

200 Fibrillar collagen levels and proteolysis increased dram

201 al cultures from cKO mice expressed elevated fibrillar collagen levels, providing further evidence th

202 pattern recognition collectins that contain fibrillar collagen-like regions and globular carbohydrat

203 amily of innate immune proteins that contain fibrillar collagen-like regions and globular carbohydrat

204 le blood over a 250-mum long patch of type I fibrillar collagen/lipidated tissue factor (TF; approxim

205 s in mouse (termed SMKO) resulted in altered fibrillar collagen localization with larger, poorly orga

206 On polymerized fibrillar collagen, M24met cells are growth arrested at

207 sence of a gap of transparency in scattering fibrillar collagen matrices within a narrow range of con

208 human corneal fibroblasts were plated inside fibrillar collagen matrices.

209 g fibroblasts generate deformation fields in fibrillar collagen matrix that provide far-reaching phys

210 asement membrane components and disorganized fibrillar collagen matrix, independently of classical in

211 oinformatic analysis provides insight on how fibrillar collagens might have arisen from the duplicati

212 Three fibrillar collagen mRNAs, alpha1(I), alpha2(I), and alph

213 gth of the heart is provided by a continuous fibrillar collagen network embracing individual myocytes

214 III, can be categorized into five subgroups: fibrillar collagens, network-forming collagens, fibril-a

215 the hypothesis that the microarchitecture of fibrillar collagen networks mechanically regulates myofi

216 A GVMGFO motif in fibrillar collagens (O denotes 4-hydroxyproline) binds 3

217 r, and collagen type I constitutes the major fibrillar collagen of bone.

218 Type V collagen is a fibrillar collagen of low abundance that is incorporated

219 man atherosclerotic lesions by digesting the fibrillar collagens of the neointimal ECM.

220 e evidence for a direct inhibitory effect of fibrillar collagen on proliferation of human melanoma an

221 rombin, but not saturating concentrations of fibrillar collagen or adenosine 5'-diphosphate, uniquely

222 -Danlos syndrome gene that does not encode a fibrillar collagen or collagen-modifying enzyme, we sugg

223 ts failed to aggregate in response to type I fibrillar collagen or convulxin, a snake venom protein a

224 hese sites, together with an accumulation of fibrillar collagen, or fibrosis, as evidenced by a signi

225 We measured the local fibrillar collagen order using X-ray diffraction methods

226 Both golgins were required for fibrillar collagen organization and glycosaminoglycan sy

227 After release from the fibrillar collagen, PDE1C expression is induced and asso

228 l components of extracellular matrices (ECM) fibrillar collagens play a critical role, and single ami

229 Defective fibrillar collagen polymerization in primary tumors has

230 differences are shown in ability to process fibrillar collagen precursors and to cleave Chordin, the

231 An annulus of fibrillar collagen probably exists near the limbus of th

232 er SLP-76(+/-) or SLP-76(-/-) platelets, but fibrillar collagen produced a 1.9-fold increase in proco

233 ceptor tyrosine kinase in that its ligand is fibrillar collagen rather than a growth factor-like pept

234 In this study, we show that the fibrillar collagen receptor, Discoidin Domain Receptor 2

235 rom mice bearing these mutations showed less fibrillar collagen, reduced axial stiffness, and lower r

236 Type XI collagen is a quantitatively minor fibrillar collagen related to type V collagen and associ

237 -1(-/-) LDLR(-/-) plaques were enriched with fibrillar collagens relative to LDLR(-/-), which also co

238 Over the past two decades, fibrillar collagen reorganization parameters such as the

239 eterotypic fibrils composed of two different fibrillar collagens represents a general mechanism regul

240 direct mechanism by which cell contact with fibrillar collagen restricts proliferation.

241 OM) and texture analysis algorithms to image fibrillar collagen (second harmonic generation) and elas

242 le helices (FACITs) must differ from that of fibrillar collagens, since they lack the characteristic

243 opy of the pellet cultures revealed abundant fibrillar collagen, some of which was aligned in paralle

244 Thus, fibrillar collagen specifically regulates early integrin

245 Fibrillar collagens store, transmit and dissipate elasti

246 cks, powder, and HA/TCP powder-type I bovine fibrillar collagen strips, and bone was maintained for a

247 /TCP powder, the HA/TCP powder-type I bovine fibrillar collagen strips, and HA/TCP powder held togeth

248 The mechanism by which fibrillar collagen structures form from liquid crystalli

249 te limiting in remodeling of tissues rich in fibrillar collagen such as the skin and lungs.

250 normally in the triple helix domains of non-fibrillar collagens, such as type IV collagen in basemen

251 es P3H1 specifically to tissues that express fibrillar collagens, suggesting that other P3H family me

252 negative microvessels embedded in bundles of fibrillar collagen surrounded by F4/80-positive MC/Mph.

253 that the 5' stem-loop specifically regulates fibrillar collagen synthesis and represents a novel targ

254 selective transcriptional downregulation of fibrillar collagen synthesis.

255 exhibited higher stiffness and expression of fibrillar collagens than control fibroblasts, concomitan

256 ino acid sequence of type VI collagen, a non-fibrillar collagen that forms antiparallel dimers.

257 le in amnion fibroblasts, which lay down the fibrillar collagen that gives tensile strength to the am

258 I collagen gene codes for a novel vertebrate fibrillar collagen that is highly conserved in man, mous

259 high-density breast contains more oriented, fibrillar collagen that is stiffer and correlates with h

260 triple helices (FACITs) differs from that of fibrillar collagens that have special C-propeptides.

261 Fibrillar collagens, the most abundant proteins in the v

262 h a small collagenous region, interacts with fibrillar collagens through its C-terminal region.

263 that is missing in many structural models of fibrillar collagen to date.

264 Exposure of the aortic rings embedded in 3D fibrillar collagen to recombinant endorepellin for 2-4 h

265 efines the composition and chain register of fibrillar collagen trimers.

266 MIF arises mainly because of alterations in fibrillar collagen turnover leading to collagen fiber ac

267 is an association between IOP regulation and fibrillar collagen turnover.

268 -) fibroblasts lost their ability to process fibrillar collagen type I and to activate proMMP-2.

269 entric thickening of the perivascular space (fibrillar collagen type I deposition) and affected almos

270 t endothelial cell adhesion and migration on fibrillar collagen type I.

271 ed human SMCs made quiescent by attaching to fibrillar collagen type I.

272 and an X chromosome that disrupts the minor fibrillar collagen type V gene COL5A1 in a patient with

273 The low abundance fibrillar collagen type V is incorporated into and regul

274 The low abundance fibrillar collagen type V is widely distributed in tissu

275 Mutations in the genes encoding the major fibrillar collagen types I and III have been demonstrate

276 VWF) mediates adhesion of blood platelets to fibrillar collagen types I, II, and III, which is essent

277 The fibrillar collagen types I, II, and V/XI have recently b

278 rent genes, the majority of which encode the fibrillar collagen types I, III and V, modifying or proc

279 1) and alpha(2) (alpha(1)I and alpha(2)I) to fibrillar collagen types I-III and showed that each I do

280 apy, mean serum levels of antibodies binding fibrillar collagen types I-III and V were significantly

281 llagen C-proteinase that processes the major fibrillar collagen types I-III, and it may process proly

282 However, compared with other vertebrate fibrillar collagens (types I, II, III, V, and XI), type

283 esion to immobilized monomeric and polymeric fibrillar collagen under static conditions in the presen

284 Degradation of fibrillar collagen underlies processes including tissue

285 on-chip platelet thrombosis assay on type 1 fibrillar collagen, using whole blood.

286 the alpha2-I domain (alpha2-I), which binds fibrillar collagen via Mg(2+)-bridged interactions.

287 l area was increased with selective MMPi but fibrillar collagen volume fraction remained unchanged re

288 usceptibility to CatK-mediated hydrolysis of fibrillar collagen was observed following mineralization

289 The fibrillar collagen weave in MHCmTNF mice with concentric

290 and increased collagen content, whereas the fibrillar collagen weave in the MHCsTNF2 mice with LV di

291 independent conditions, platelets adhered to fibrillar collagen were able to secrete contents of both

292 Cells plated in the presence of fibrillar collagen were growth arrested in the G0/G1 pha

293 oid potential immunogenicity associated with fibrillar collagens, were fabricated with and without ch

294 Types I, II, III, V, and XI constitute the fibrillar collagens, whereas types IV, VI to X, and XII

295 on of lysine residues in the telopeptides of fibrillar collagens, which leads to the formation of sta

296 least partly, via biosynthetic processing of fibrillar collagens, while TLD affects dorsal-ventral pa

297 h encodes the alpha chain of an atypical non-fibrillar collagen with a single transmembrane domain.

298 Mineralization of fibrillar collagen with biomimetic process-directing age

299 of A2058 human melanoma cells cocultured in fibrillar collagen with HS-68 primary human fibroblasts.

300 s to enter the cell cycle in the presence of fibrillar collagen without a requirement for spreading a