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1 nase (LOX), or the 5-LOX-activating protein (FLAP).
2 ase (5-LO) aided by 5-LO-activating protein (FLAP).
3 n overpower the strength of the nasal lining flap.
4 l placement of tumors and wounds or ischemic flap.
5 followed by tongue reconstruction with free flap.
6 Rossmann fold connected to a protruding beta-flap.
7 al tunnel underneath the superficial scleral flap.
8 4) molecules of cPLA(2) were associated with FLAP.
9 tical incision with an interdental tunneling flap.
10 en implicated in processing Okazaki fragment flaps.
11 , in the treatment of infected ischemic skin flaps.
12 parating the strands of duplex DNA, creating flaps.
13 is protein functions at DNA ends to generate flaps.
14 eaved, unthreaded, and partially threaded 5' flaps.
15 /-44 deg) and C(2v)-symmetric triplet (omega(flap) = 0 deg) stem from nonclassical electron delocaliz
16 es between the C(s)-symmetric singlet (omega(flap) = +/-44 deg) and C(2v)-symmetric triplet (omega(fl
17 in MHRD surgery could stabilize inverted ILM flaps, achieve good anatomical results and improve posto
19 urrent study evaluated the status of the ILM flap after MH surgery with superior wide-base ILM flap t
21 cellular dermal matrix, collagen matrix, and flap alone showed a similar tendency for gingival recess
24 mutants, lacking a C-terminal autoregulatory flap, also promote strand exchange in a 5'-to-3' polarit
27 nderwent AV loop placement with delayed free flap anastomosis for microsurgical reconstructions of lo
29 econstruction with a vascularized myofascial flap and 2-year follow-up was in good health with no res
30 elevate inflammatory leukotriene levels, 2) FLAP and 5-LOX inhibitors reduce leukotrienes in M1 but
31 s, patients reconstructed with a soft tissue flap and bridging plate (odds ratio (OR) 3.997; 95% conf
34 uctive number of the infection (R0) for both FLAPS and randomized configurations, we investigated how
35 ion-dependent close associations of cPLA(2), FLAP, and 5-LO in higher order assemblies on the nuclear
37 , in combination with an apically positioned flap [APF]), resulted in significantly more KT than trea
39 aft (CTG) when combined with a buccal single flap approach (SFA) in the regenerative treatment of int
42 Our data strongly support the idea that 3' flaps are generated as replication fork complexes fuse.
47 g a semicircular single-layered ILM inverted flap assisted by a sub-perfluorocarbon liquid injection
48 l wing kinematics; their long, slender wings flap at remarkably high frequencies for their size (>800
50 plexus with a chimeric compound skin paddle flap based on the subclavian vessels was transplanted fr
53 lly as robust on cytologic analysis and open-flap biopsy specimens of ciliary epithelial and iris epi
60 e surgically treated with coronally advanced flap (CAF) associated with SCTG harvested by: double bla
62 ve tissue grafts (SCTG) + coronally advanced flap (CAF) compared to guided tissue regeneration with r
63 impact on the outcomes of coronally advanced flap (CAF) for treating multiple adjacent gingival reces
64 MD) in combination with a coronally advanced flap (CAF) on CDH, esthetics, and oral health-related qu
65 for root coverage (RC) by coronally advanced flap (CAF) procedures in localized gingival recessions.
66 positioned flap (LPF) and coronally advanced flap (CAF) techniques in the treatment of localized maxi
67 assigned to four groups: coronally advanced flap (CAF); CAF + CM; CAF + EMD; and CAF + CM + EMD (spl
69 Immobilized DNA nanorobots with a switchable flap can then be actuated by a specific target DNA prese
70 e of 3' exonucleases, such as ExoI, these 3' flaps can be converted into 5' flaps, which are degraded
73 ranslocation of Dna2 on ssDNA facilitates 5' flap cleavage near a single-strand-double strand junctio
75 act of a second fibula flap or a soft tissue flap combined with bridging plate for a repeated segment
77 human blood from females, and bioactive 5-LO/FLAP complexes were formed in female, but not male, huma
78 ey's K to quantify clustering, we found that FLAPS configurations were substantially more clustered a
80 the plasmepsin inhibitors that bind in open flap conformation have led to several inhibitor classes
81 that leads to inhibitor binding to the open flap conformation, summarizes known nonpeptidomimetic pl
83 rconversion between closed and open protease flap conformations facilitates the formation of a transi
86 estimate such impact on the outcome of open flap debridement (OFD) for the management of chronic per
91 ochemical parameters, and (b) following open flap debridement most of the values returned to baseline
92 , implant placement, soft tissue graft, open flap debridement or surgical removal of impacted teeth w
96 to investigate the impact of tooth location, flap design, and flap extension on the outcomes of MAGRs
100 surgery time were reduced markedly, as were flap dislocation and pterygium recurrence with Tisseel f
102 eviates the inhibitory effect of RAD51 on 3'-flap DNA cleavage by MUS81-EME1 through its RAD51 filame
103 ed that Pif1 drives the formation of long 5'-flaps during Okazaki fragment maturation, and that the e
106 combined activities of polymerase B (PolB), flap endonuclease (Fen1), and DNA ligase are required to
107 he enzymes DNA polymerase delta (Pol delta), flap endonuclease 1 (FEN1) and DNA ligase I (LigI) that
113 cates the lagging strand and cooperates with flap endonuclease 1 (FEN1) to process the Okazaki fragme
116 rocessive 5'-3' exonuclease and secondary 5'-flap endonuclease activities participate in various DNA
117 ermore, BRCA2-deficient cells require the 5' flap endonuclease but not the 5'-3' exonuclease activity
121 ctional enzyme composed of an N-terminal DNA flap endonuclease/5' exonuclease domain (FEN/EXO) and a
123 e impact of tooth location, flap design, and flap extension on the outcomes of MAGRs following CAF wi
124 cid is generated by cPLA(2) in apposition to FLAP, facilitating its transfer to 5-LO to initiate LT s
126 ntrast, Montagu's harriers predominantly use flapping flight during their migrations; this adult male
129 avialan Archaeopteryx was capable of active flapping flight or only passive gliding is still unresol
131 s were the first vertebrates to achieve true flapping flight, but in the absence of living representa
133 exonuclease, indicating Cas9 exposes the 3' flap for potential interaction with the DNA repair machi
134 ze inverted internal limiting membrane (ILM) flap for the treatment of macular hole retinal detachmen
141 tics were comparable, but the mobile intimal flap group showed a lower re-intervention rate (3 vs. 8p
142 rated complete coverage of the MH by the ILM flap in 14 eyes (82%), partial coverage in 1 eye (6%), a
147 whether higher order assemblies of 5-LO and FLAP included cytosolic phospholipase A(2) (cPLA(2)) and
149 have been discontinued and the link between FLAP inhibition and outcome in inflammatory diseases rem
150 olution-initiating SPM biosynthesis, whereas FLAP inhibition increases SPM levels, and 4) that the 15
156 5-Lipoxygenase (5-LO)-activating protein (FLAP) inhibitors have proven to attenuate 5-LO pathway a
157 te strand of a TNR R-loop, creating a double-flap intermediate containing an RNA:DNA hybrid that subs
159 5-LO) and 5-lipoxygenase-activating protein (FLAP) into higher order assemblies on the nuclear envelo
163 er SWIFT, ICG imaging indicates that the ILM flap is intact and in a good position in most cases.
165 , suggests that Archaeopteryx was capable of flapping its wings for cursorial and/or aerial locomotio
166 (VA), IOP, number of sutures in the scleral flap, laser suture lysis, surgeon, and laterality of sur
167 as the origin of the labrum-an anteromedian flap-like structure that overlies the mouth opening in a
168 in the operative time, total hospital stay, flap loss, re-exploration rates, plate exposure rate, or
170 fficacy of single-stage laterally positioned flap (LPF) and coronally advanced flap (CAF) techniques
171 surgical techniques-suturing the vestibular flap margin apically to the base of the recipient bed ve
175 hen performing FSTA surgery when the mucosal flap margin is left free and unsutured when compared wit
179 tive tissue grafting, and coronally advanced flaps may result in regeneration of the intrabony defect
180 roups received the following treatment: open flap mechanical debridement, supracrestal implantoplasty
184 yses, we studied the functional roles of the flap motif by comparing WT hcSHMT with a flap-deleted va
185 understanding of the functional roles of the flap motif in hcSHMT and provide fundamental insight int
187 Eight weeks following SRP, modified Widman flap (MWF) surgery was performed in 40 patients (20 of e
190 t a relatively high energetic penalty in the flap of the 22-bound BACE2 structure may cause a loss in
192 that the conformational dynamics within the flaps of HIV-1 protease that form the lid over the catal
196 cs the pores in human skin, in which pre-cut flaps open to produce pores in Nafion sheets when humidi
197 otease and the substrate, resulting in rapid flap opening and substrate release, thereby allowing pro
200 to investigate the impact of a second fibula flap or a soft tissue flap combined with bridging plate
204 al mammary artery osteomyocutaneous chimeric flap (PIMOC) for salvage head and neck reconstruction.
207 relationship between immediate post-surgical flap position and subsequent probing depth measurements
209 e results indicate that, upon removal of the flap, product release is no longer the rate-limiting ste
211 t just after taking off, the wing motion and flap rate of a large woodpecker may not be the same as i
212 w footage, such as flight path, wing motion, flap rate, behaviors, field marks, and body proportions.
213 hospital market competition both for nonfree flap reconstruction (5.5% increase, 95% CI: 1.1%-10.1%)
214 % increase, 95% CI: 1.1%-10.1%) and for free flap reconstruction (8.2% increase, 95% CI: 1.8%-15.0%).
215 further wide resection with free muscle-skin flap reconstruction followed by adjuvant radiation treat
218 utologous transverse rectus abdominis muscle flap reconstruction with an implant based reconstruction
219 e 6.6% higher (95% CI: 2.8%-10.5%), for free flap reconstruction, and 5.1% higher (95% CI: 2.0%-8.4%)
220 etitive markets, 6.8% (n=857) underwent free flap reconstruction, compared with 13.6% (n=2773) in hig
230 ional functions of Pol1: FEN activity on the flap RNA strand of an RNA:DNA hybrid and reverse transcr
234 unappreciated FEN1 function that enforces 5'-flap specificity and catalysis, preventing genomic insta
235 Gen, like HsGEN1, efficiently cleaves HJs, 5 flaps, splayed arms, and replication fork structures.
238 ctivates MUS81-EME1 for replication fork and flap structure cleavage by relaxing substrate specificit
239 se cleavage takes place in the context of 5' flap structures generated via strand-displacement synthe
240 plex recognizes an abasic analog on a double-flap substrate, which prevents AP endonuclease activity
243 rich fibrin (PRF) combined with conventional flap surgery on growth factor levels in gingival crevicu
244 -2, BD-3, or both BD-2 and BD-3, to increase flap survival in the context of a P. aeruginosa infectio
250 LM peeling (n = 23, Group 1) or inverted ILM flap technique (n = 23, Group 2), between August 2016 an
252 he inverted internal limiting membrane (ILM) flap technique and the complete ILM removal in the treat
253 odified preserved nasal and lacrimal mucosal flap technique in EES-DCR for treating PANDO is simple a
254 odified preserved nasal and lacrimal mucosal flap technique in EES-DCR was applied in all 27 eyes of
255 odified preserved nasal and lacrimal mucosal flap technique in endonasal endoscopic dacryocystorhinos
259 ce, concentric intramural haematoma, intimal flap (the most definite sign), and double lumen of the a
260 ically, the cnidae of Relicanthus has apical flaps, the only existing synapomorphy for sea anemones.
262 ith fewer neighbours than unpaired birds and flapped their wings more slowly, which may result in ene
265 ety, predictability, ocular aberrations, and flap thickness predictability of Visumax femtosecond las
266 In group I, the mean postoperative actual flap thickness was 100.12 +/- 16.1 mum (81 to 122 mum),
267 sidues energetically steer an inverted ss 5'-flap through a gateway over FEN1's active site and shift
268 nds recessed ends at its base and threads 5' flaps through a narrow aperture within its interior.
269 repositioning of the conjunctival autograft (flap time) was significantly shorter in the fibrin glue
270 itution urethroplasty - the use of grafts or flaps to correct the urethral narrowing - remains one of
271 ay also imposed a metabolic cost, with birds flapping toward the end of glides to reach ephemeral the
276 ng outcomes of the coronally advanced tunnel flap (TUN) combined with connective tissue graft (CTG) w
277 ement during lunge feeding: the flippers are flapped using a complex, hydrodynamically active stroke
278 6 sites) as opposed to 50% when the surgical flap was >3 mm away from the alveolar crest (48/96 sites
281 AF alone, no differences were found when the flap was performed with or without vertical releasing in
283 ing depth <=3 mm was 93.5% when the surgical flap was placed within 3 mm of the alveolar crest (286/3
287 es in the cross-sectional area of the lining flap were measured when negative pressure was applied.
289 id on the graft material, the mucoperiosteal flaps were replaced, and the surgical site was sutured.
290 After osseous recontouring was completed, flaps were sutured and compressed, and bone sounding mea
291 ation and Agricultural Production Simulator (FLAPS), which infers location based on features such as
292 xoI, these 3' flaps can be converted into 5' flaps, which are degraded by 5' exonucleases, such as Ex
296 root coverage outcomes of coronally advanced flap with ADM over time, and compare them with their adj
298 the effect of transducing rat ischemic skin flaps with lentiviral vectors encoding human BD-2, BD-3,
299 ve techniques using free vascularised tissue flaps with penile implants are undesirable in this often
300 d27 processes the majority of lagging-strand flaps, with a significant additional contribution from E