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1 filaments of rod-shaped cells that failed to septate.
2 enlarged regions are convoluted or partially septated.
3 ant that produces a larger LAM becomes multi-septated.
4 ates toward the caudal midline as the cloaca septates.
5 h failing at nuclear division, these mutants septate and divide.
6 sted by the inability of plo1 Delta cells to septate and the prolific septation following plo1(+) ove
7 ogs of the BBB are occlusive (pleated-sheet) septate and tight junctions between perineurial cells, g
8 nd ZO-1, which are arranged symmetrically at septate and tight junctions, respectively.
9        Microscopically, hyphae were hyaline, septate, and branched and remained totally devoid of con
10                                Patients with septated ascites and intraperitoneal adhesions are at po
11 H resulted in a viable strain that failed to septate at any temperature.
12 ls formed a misshapen actin ring, but rarely septated at 36 degrees C.
13  the cells are arrested in the cell cycle as septated, binucleated cells with highly condensed chroma
14  tissue from lungs and brain showed hyaline, septate, branched hyphae with clamp connections.
15           Microscopically, their hyphae were septate, branched, and phaeoid and bore lateral and term
16       Histopathological examination revealed septate branching hyphae, suggesting a diagnosis of inva
17 arance of abnormal medial ring structures in septated cells that lack imp2.
18                                              Septating cells are attacked more readily than nonseptat
19 oskeleton shows the lack of a medial ring in septating cells that overexpress imp2, and the appearanc
20 (iii) a medial band in a small percentage of septating cells.
21 ineered mutants of HDC1 had smaller and less septate conidia and exhibited an approximately 50% reduc
22 haeoid and bore lateral and terminal, erect, septate conidiophores.
23                           Fifty patients had septated cysts; seven of these patients had borderline n
24  is in place before the machinery to degrade septated daughter cells is enabled.
25 tomy and excisional biopsy by observation of septate, dematiaceous hyphal elements 2 to 3 microm in w
26 rongly and consistently associated with dark septate endophyte colonization than with mycorrhizal col
27                         RAF taxa in the dark septate endophyte, ERM, and ECM guilds strongly correlat
28 ad, a range of ascomycete fungi, termed dark septate endophytes (DSEs), frequently colonise the roots
29                    Root colonization by dark septate endophytes also has a consistent negative associ
30 but also that the hitherto less studied dark septate endophytes are likely to be central players in t
31  Helotiales, a group that includes many dark septate endophytes known to associate positively with ro
32 ycorrhizal, arbuscular mycorrhizal, and dark septate endophytic fungi also shapes tree-associated mic
33                 Vitreous biopsy smear showed septate fungal filaments, and culture yielded significan
34 amine silver stains showed numerous hyaline, septate, fungal hyphae of various lengths, many broken i
35 ted germination-structures and then produced septate germlings at a water-activity of just 0.585 ( id
36 of differentiated germination-structures and septate germlings, and subsequent development of myceliu
37                                    Branched, septate hyphae and moniliform hyphae consisting of chain
38             A black velvety mould with brown septate hyphae and tapered annellides was isolated from
39 fections due to molds characterized by thin, septate hyphae branching at acute angles, voriconazole s
40 eg lesion also noted on day 67 p.t. revealed septate hyphae consistent with Aspergillus species, and
41 olar lavage (BAL) fluid in order to identify septate hyphae noted by Gomori methenamine silver (GMS)
42                      At the time of autopsy, septate hyphae were present in heart, thyroid, and lung
43                   Filamentous fungi with non-septate hyphae were presumptively identified as agents o
44 stinal wall showed infiltration by branching septate hyphae.
45 yogranulomatous inflammation with branching, septate hyphae.
46 ori's methenamine silver strains showed many septate hyphal elements of various lengths, some exhibit
47  outflow tract (OFT) of the developing heart septates into the base of the pulmonary artery and aorta
48  Von Meyenberg complexes, usually present as septated intrahepatic cystic lesions.
49 t the Drosophila Na,K-ATPase is required for septate junction (SJ) formation and that of the three be
50       We also show that vari is an essential septate junction (SJ) gene encoding a membrane associate
51 pecific requirement for Shrub in maintaining septate junction (SJ) integrity by transporting the clau
52 pericardial cell adhesion also relies on the septate junction (SJ) proteins Neurexin-IV (Nrx-IV), Sin
53 elia, whereas in invertebrate epithelia, the septate junction (SJ) provides this function.
54 ar junction that is rare in vertebrates, the septate junction (SJ).
55  is localized on the cytoplasmic face of the septate junction and is required for the maintenance of
56 e initiation site (AMIS) when they reach the septate junction between the enterocytes.
57 inantly required for correct localization of septate junction components, while Sinuous is predominan
58                      Finally, the enterocyte septate junction disassembles and the enteroblast/pre-en
59 nd the transmembrane protein Neurexin to the septate junction display an interdependent relationship,
60 ng that Kune-kune has a more central role in septate junction formation than either Sinuous or Megatr
61 ed for tracheal tube size control, including septate junction formation, deposition of a lumenal/apic
62 equirements for these claudins in epithelial septate junction formation.
63  of the Na+/K+ ATPase play a crucial role in septate junction function and that septate junctions hav
64 sinuous functions in the same pathway as the septate junction genes neurexin and scribble, but that n
65 ted that Coracle protein is localized to the septate junction in epithelial cells and is required for
66  is localized to the cytoplasmic face of the septate junction in epithelial cells.
67 tion in epithelial cells and is required for septate junction integrity.
68  is both necessary and sufficient for proper septate junction localization in transgenic embryos.
69 ion of production of their respective smooth septate junction membrane proteins located within the in
70 tegrity by regulating cell-cell adhesion and septate junction molecules such as Ed and Cora.
71 zes to septate junctions and is required for septate junction organization and paracellular barrier f
72 ture septate junctions, and we find that the septate junction protein neurexin IV does not participat
73 SF2, of the apical determinant Crumbs, or of septate junction protein Varicose.
74 ells become irregular in size and shape, and septate junction proteins are mislocalized to a more api
75 ly required for maintaining normal levels of septate junction proteins.
76 e is a necessary structural component of the septate junction required for the maintenance of the tra
77 markedly reduced gut acidification, atypical septate junction structure, depressed gut motility, and
78 sential membrane-organizing functions at the septate junction, and that these functions are carried o
79 ateral domain of epithelia, particularly the septate junction, functions in restricting apical membra
80         Scrib is localized to the epithelial septate junction, the analogue of the vertebrate tight j
81  Fas2, and Fas3 are components of the insect septate junction, the functional equivalent of the verte
82  Drosophila, this barrier is provided by the septate junction, which, despite being ultrastructurally
83  we report that the Drosophila transmembrane septate junction-specific protein Neurexin IV (Nrx IV) f
84  required for restricting the protein to the septate junction.
85 h one another at the cytoplasmic face of the septate junction.
86 s into an apical domain below the enterocyte septate junction.
87 he electron microscopic observations of the "septate" junction conform to a honeycomb structure, with
88                    We imaged a member of the septate-junction complex that was used to outline the th
89  of the Drosophila cardiac system depends on septate-junction proteins even though the heart lacks di
90 es and destabilization of paranodal axoglial septate junctions (AGSJs) as early as postnatal day 30.
91 elia where tight junctions in vertebrates or septate junctions (SJ) in invertebrates from three cells
92 tion by glial cells and the establishment of septate junctions (SJs) between glial cell membranes.
93 incipally tight junctions in vertebrates and septate junctions (SJs) in invertebrates.
94  notum, alteration of the bi- or tricellular septate junctions (SJs) triggers a mechanism with two pr
95                          Here we report that septate junctions (SJs), the vertebrate analogs of TJs,
96 the tight junctions analogous structure, the septate junctions (SJs).
97 ode membrane proteins associated with smooth septate junctions (SSJ) which are required for intestina
98                   Immature Diptera have such septate junctions (without tight junctions) while both j
99 ophila discs large (dlg) disrupts epithelial septate junctions and causes overgrowth of imaginal disc
100 , abnormally enhanced Mmp1 activity disrupts septate junctions and glial ensheathment of peripheral m
101 ophila claudin, Kune-kune, that localizes to septate junctions and is required for junction organizat
102 e Dlg protein is a critical component of the septate junctions and is required for maintaining apicob
103  sinuous encodes a claudin that localizes to septate junctions and is required for septate junction o
104  regulation of the transport pathway through septate junctions and the reversible assembly of proton
105 he paracellular barriers formed by arthropod septate junctions and vertebrate tight junctions have a
106 nents identified at the vertebrate axo-glial septate junctions are also present at the Drosophila sep
107 now provide genetic evidence that Drosophila septate junctions are part of the gut immune barrier, a
108          Collectively, our data suggest that septate junctions are required to maintain the subtle ba
109 s gene, the Dlg protein, is localized at the septate junctions between epithelial cells, and that mut
110 te a new apical domain and break through the septate junctions between neighbouring enterocytes, whil
111 eripheral nervous system where pleated-sheet septate junctions bond cells of the nascent (embryonic)
112                           Mutations in known septate junctions genes cause the same tracheal tube-siz
113                      In the tracheal system, septate junctions have a barrier-independent function th
114 ATPalpha and nrv2 mutations, indicating that septate junctions have a previously unidentified role in
115  addition, new roles for axo-glial paranodal septate junctions have emerged, which suggest that the p
116 l role in septate junction function and that septate junctions have multiple distinct functions that
117 ing vertebrate tight junctions and arthropod septate junctions in epithelia.
118 ed at and required for the formation of both septate junctions in epithelial cells and synaptic junct
119 t analyses suggest that tube-size control by septate junctions is mediated by at least two discernabl
120 tion of SPG polyploidy caused rupture of the septate junctions necessary for the blood-brain barrier.
121 ch in turn is necessary for the formation of septate junctions of sufficient length to achieve proper
122 ates, it has recently been demonstrated that septate junctions play an essential role in axonal insul
123  localization of Coracle, a component of the septate junctions that is required for the late-larval i
124                                          New septate junctions then form laterally with the enterocyt
125 liferating follicle cells do not have mature septate junctions, and we find that the septate junction
126 exin IV, a molecular component of Drosophila septate junctions, has been shown to be essential for ax
127 a midgut, BBG is present at the level of the septate junctions, on the apical side of the enterocytes
128               The mutant mice lack paranodal septate junctions, resulting in the diffusion of Caspr a
129 2 mutations also disrupt stable formation of septate junctions, structures with some functional and m
130 target an epitope-tagged Dlg to pre-existing septate junctions.
131 ateralisation at a stage before formation of septate junctions.
132 eins even though the heart lacks discernable septate junctions.
133 sium-rich hemolymph by forming intercellular septate junctions.
134 junctions are also present at the Drosophila septate junctions.
135 nd Malpighian tubules have junctions of the "septate" kind.
136 actin enables the formation of the paranodal septate-like axo-glial junctions in myelinated periphera
137                  Our results indicate that a septate-like junction provides structural support to cal
138  out in mice lacking the core protein of the septate-like junction) conclusively demonstrates that ty
139 med paranodin--has been shown to localize to septate-like junctional structures.These vertebrate junc
140  deletion of Nfasc155 results in the loss of septate-like junctions and in conduction slowing.
141 component Dumbfounded accumulates at ectopic septate-like junctions between abnormally aggregated nep
142 are not clustered in md spinal cords, and no septate-like junctions between oligodendrocyte processes
143 myelin loops, and focal absence of paranodal septate-like junctions between the terminal loops and ax
144  At the ultrastructural level, the paranodal septate-like junctions immediately adjacent to the node
145 ell adhesion molecule expressed in paranodal septate-like junctions of peripheral and central myelina
146 odes, but the glial and axonal components of septate-like junctions remain colocalized.
147  demonstrated that Caspr is localized to the septate-like junctions that form between axons and the p
148 al cells closely appose and form specialized septate-like junctions with axons.
149 sis of the junctions showed intact paranodal septate-like junctions.
150                         All three had large, septate low-attenuation areas at computed tomography con
151  mycological examination identified numerous septate mycelial filaments.
152 d, namely tight (occludin) and pleated-sheet septate (neurexin IV).
153 the mutants had smooth colony morphology and septated normally, but all were lysozyme sensitive.
154 xtensive screen for this novel class of sns (septated, not in S-phase) mutants.
155         The lack of Ltbp1L in the ECM of the septating OFT and associated vessels results in altered
156  leading to premature abscission and a multi-septated phenotype.
157  of an extensive network of brown-pigmented, septate, profusely branched hyphae.
158 planate divided bicellular forms or multiply septated sclerotic bodies in post-log phase, when the G1
159  cells and insufficient mesenchymal cells to septate the cardiac outflow tract.
160 hyme and hypoplastic cushions that failed to septate the ventricular inlet.
161 erian duct anomaly which is characterised by septate uterus with obstruction of a one-sided cavity an
162 ngle ventricular chamber or two incompletely septated ventricles?

 
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