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1 ding plasma, nuclear, peripheral, single and multipass.
2 on were prospectively enrolled and underwent multipass [(18)F]FDG PET/CT with direct Patlak reconstru
3                         To assess adherence, multipass 24-h dietary recalls were administered at base
4 no acids) were obtained from 4 standardized, multipass, 24-hour dietary recalls and 2 timed 24-hour u
5 re designed as an acoustic resonator and for multipass absorption enhancement, respectively.
6 ass enhanced photoacoustic (MPPA) and direct multipass absorption spectroscopy with a mid-infrared qu
7                                              Multipass analysis is proposed as a method for DESI surf
8 sirable, this study points to the value of a multipass APMF approach to generate AMT tag databases, w
9 converted to CCS values by deconvoluting the multipass arrival times into accurate single-pass values
10 d was validated using transmission FT-IR and multipass ATR-FT-IR as referee methods.
11                                The optimized multipass beam reflection structure enhances the effecti
12                    For each sequence variant Multipass calculates the likelihood and nucleotide seque
13 attributed to the challenges associated with multipass calibration methods, which require both calibr
14 lysis of the immunoglobulin VDJ region where Multipass can be combined with a model for the known rec
15 y using a Stirling-cooled segmented circular multipass cell (SC-MPC).
16                                  A 76 m-long multipass cell provides a detection limit of 1 ng m(-3)
17                                            A multipass cell was used to provide sufficient measuremen
18  arrangement, comprising a single-pass and a multipass cell, provides a dynamic range of six decades
19 ocessing strategy capable of better handling multipass cIM data.
20           Interestingly, use of one-pass and multipass cIM routines produced unique peptide populatio
21                           Using one-pass and multipass cIM routines, we use the recently commercializ
22        We first assessed the extent to which multipass cIM-MS experiments could improve the separatio
23 ness the high mobility resolution offered by multipass cIMS analyses without compromising the accurac
24 ce a novel calibration strategy designed for multipass cIMS analyses, directly targeting the root cau
25                                         This multipass data enables analysis of the rising and fallin
26 on both considerably longer path lengths and multipass designs.
27 tem is developed based on the combination of multipass enhanced photoacoustic (MPPA) and direct multi
28 y consisted of: (1) using mobile phones with multipass excitation and emission filters on the flash a
29 ring drift times measured during single- and multipass experiments and extrapolating the number of pa
30                                              Multipass experiments of a narrow m/z range (m/z 870-920
31  its 13 m separation path length, allows for multipass experiments to be performed for increased reso
32  from a malaria virulence gene family, where Multipass generates 20 % more error-free sequences than
33 oundation for extremely long path length and multipass IM separations in SLIM providing greatly enhan
34 th racetrack geometry that enables scalable, multipass IM separations.
35 Linear encoders also enable the alignment of multipass images that increase image homogeneity and sig
36 new basecalling method described here, named Multipass, implements a probabilistic framework for work
37   However, determining the CCS of an ion for multipass IMS systems, such as in cyclic ion mobility-ma
38 priori method to calibrate cyclic (including multipass) IMS developed here may be broadly useful.
39             Sample ionization is assisted by multipass infrared laser beam in the interface.
40     HER-1 inhibits the function of TRA-2A, a multipass integral membrane protein thought to serve as
41 egulatory element binding protein, is also a multipass integral membrane protein which cleaves within
42 functional splicing of a pre-mRNA encoding a multipass integral membrane protein.
43 ) genes encode a broadly conserved family of multipass integral membrane proteins in animals.
44                                           As multipass integral membrane proteins, Rh30 and Rh50 are
45 ng beta-barrel and alpha-helical (single and multipass) integral membrane proteins and membrane-assoc
46                                 SERINC5 is a multipass intrinsic membrane protein that suppresses HIV
47                       This system allows for multipass ion separations and for pre-, intra-, and post
48                Finally, ultrahigh-resolution multipass (long path length) SLIM TWIMS separations demo
49  we demonstrate that CCS values derived from multipass measurements closely align with those obtained
50                                          The multipass membrane protein APH-1, found in the gamma-sec
51 ghts into the poorly understood processes of multipass membrane protein biogenesis and multi-subunit
52 ne chaperone and suggest a new framework for multipass membrane protein biogenesis at the endoplasmic
53 and assembly of a translocon specialized for multipass membrane protein biogenesis(3).
54 ave identified a previously uncharacterized, multipass membrane protein called PrsW (annotated YpdC)
55 ivated by binding of Hedgehog protein to the multipass membrane protein Patched (Ptc).
56                                          The multipass membrane protein Prm1 is the only known compon
57 ses in Drosophila have demonstrated that the multipass membrane protein Smoothened (Smo) is essential
58 his pair thus serves as a model for studying multipass membrane protein targeting.
59       In this issue, Ji et al.(1) show how a multipass membrane protein that initially inserts into t
60                             Ferroportin is a multipass membrane protein that serves as an iron export
61 subunits of the TIM23 complex, the essential multipass membrane protein Tim23, together with the evol
62 ses disease phenotypes through dysfunctional multipass membrane protein topogenesis.
63          ACCELERATED CELL DEATH6 (ACD6) is a multipass membrane protein with an ankyrin domain that a
64                          Here, we identify a multipass membrane protein, ICM1, with homology to trans
65                     This effort identified a multipass membrane protein, OR14I1, as a receptor for HC
66 w that mammalian APH-1 (mAPH-1), a conserved multipass membrane protein, physically associates with n
67                                Previously, a multipass membrane protein, PRM1, was characterized and
68 he dispatched gene, which encodes a putative multipass membrane protein, was initially identified in
69 redicted to encode a novel, highly conserved multipass membrane protein.
70                                              Multipass membrane proteins have a myriad of functions,
71 of both intracellularly localized termini of multipass membrane proteins in the sorting pathway sugge
72                                              Multipass membrane proteins play numerous roles in biolo
73                                              Multipass membrane proteins span the membrane multiple t
74 identified in Drosophila, defines a class of multipass membrane proteins that control cell fate and c
75 AN9 is a member of the tetraspanin family of multipass membrane proteins, but its cellular function i
76 ling is controlled by the interaction of two multipass membrane proteins, patched (Ptc) and smoothene
77 ss of insertion competence, particularly for multipass membrane proteins, resulting in their impaired
78  compared to the observations made for other multipass membrane proteins.
79                      MAL encodes an integral multipass membrane proteolipid, myelin and lymphocyte pr
80 screens to identify the poorly characterized multipass membrane transporter MFSD6 as a host entry fac
81 , revealing a topological pattern supporting multipass membrane transporter models.
82 en gene of Drosophila melanogaster encodes a multipass membrane-spanning protein that negatively regu
83                                          The multipass membrane-spanning proteins Patched (Ptc) [2-4]
84  drug discovery strategies using recombinant multipass MPs, and outline methods to successfully expre
85     To overcome this challenge, we propose a multipass NF process with brine recirculation to achieve
86 ving optical feedback from a retroreflecting multipass optical cavity, effectively creating an extern
87 ts Caenorhabditis elegans homolog PAQR-2 are multipass plasma membrane proteins that protect cells ag
88  structural analysis of intermediates during multipass protein biogenesis showed that the nascent cha
89                      As gamma-secretase is a multipass protein complex with 19 transmembrane domains,
90  cells lacking these components show reduced multipass protein stability.
91 ts that each transmembrane domain (TMD) of a multipass protein successively passes into the lipid bil
92 ively bind the ribosome-Sec61 complex during multipass protein synthesis: the GET- and EMC-like (GEL)
93                                          How multipass proteins are co-translationally inserted and f
94 ir emergence from the ribosome suggests that multipass proteins insert and fold behind Sec61.
95 lts establish the mechanism by which nascent multipass proteins selectively recruit the multipass tra
96 ng Asterix and CCDC47, engages early TMDs of multipass proteins to promote their biogenesis by an unk
97           Accordingly, biogenesis of several multipass proteins was unimpeded by inhibitors of the Se
98 rse tail-anchored (TA), signal-anchored, and multipass proteins, but not outer membrane beta-barrel p
99 r trace hydrocarbons was investigated with a multipass Raman analyzer.
100                                        Using multipass separation and targeted ion slicing, we resolv
101 bility peak resolution for ADH improved with multipass separations (up to 24-m path length).
102                    In addition to single and multipass separations around the cIM, providing selectab
103                    For apo-transferrin, 40-m multipass separations were performed allowing for comple
104                                          For multipass separations, the ATDs were converted to CCS va
105 applied to any IMS-MS platform that utilizes multipass separations.
106                                   Such SLIM "multipass" separations provide unprecedentedly high ion
107 ased ion switch to achieve higher resolution multipass serpentine ultralong path with extended routin
108                             Here, we present multipass SLIM separations for gas-phase proteins in the
109 ion library, we identified the transmembrane multipass sodium-dependent phosphate transporter 1 PiT1/
110 ns the positively charged soluble domains of multipass substrates in the cytosol, thereby ensuring th
111                                          The multipass SUPER IM-MS provided resolution approximately
112 h-resolution mass analyzer based on a planar multipass time-of-flight mass spectrometer with periodic
113 ls how features of the nascent chain trigger multipass translocon assembly.
114 econstitution studies demonstrate a role for multipass translocon components in protein topogenesis,
115 ec61, where the PAT complex contributes to a multipass translocon surrounding a semi-enclosed, lipid-
116 t multipass proteins selectively recruit the multipass translocon to facilitate their biogenesis.
117                                        This 'multipass translocon' is distinguished by three componen
118  model for coordination between the EMC, the multipass translocon, and Sec61 for the biogenesis of di
119 k of Sec61 (BOS) complex, a component of the multipass translocon, was a physical and genetic interac
120  peptide peptidase gene (Spp) that encodes a multipass transmembrane aspartyl protease.
121 ition, the predicted Ags1 protein contains a multipass transmembrane domain that might contribute to
122         Hedgehog acyltransferase (Hhat) is a multipass transmembrane enzyme that mediates the covalen
123                We show that CALHM1 encodes a multipass transmembrane glycoprotein that controls cytos
124                        Only tetraspanin-7, a multipass transmembrane glycoprotein with neuroendocrine
125 ned by covalently linking Cy5 to single- and multipass transmembrane helical proteins.
126                   The thermosensor DesK is a multipass transmembrane histidine-kinase that allows the
127   Here, we show that the ank locus encodes a multipass transmembrane protein (ANK) that is expressed
128  endoproteolytically processed in vivo, is a multipass transmembrane protein and is a functional homo
129 xport of inorganic pyrophosphate through the multipass transmembrane protein ANK and generation of eP
130                         sing encodes a small multipass transmembrane protein containing a MARVEL doma
131 d Bartscherer et al. identify Wntless/Evi, a multipass transmembrane protein in the secretory pathway
132 nt families and in isolated cases, in ANK, a multipass transmembrane protein involved in the transpor
133                                  The encoded multipass transmembrane protein is required for choleste
134                                     The NPC1 multipass transmembrane protein is resident in late endo
135                                   UNC93B1, a multipass transmembrane protein required for TLR3, TLR7,
136 lecular analysis reveals that rasp encodes a multipass transmembrane protein that has homology to a f
137  Serine Incorporator 5 (SERINC5), a cellular multipass transmembrane protein that is involved in sphi
138                              gem-1 encodes a multipass transmembrane protein that is similar to SLC16
139                                      It is a multipass transmembrane protein that regulates the trans
140    Autophagy-related gene 9 (Atg9) encodes a multipass transmembrane protein thought to act as a memb
141                        The NPC1 protein is a multipass transmembrane protein whose deficiency causes
142 ne protein, (2) type-2 membrane protein, (3) multipass transmembrane protein, (4) lipid chain-anchore
143           This protein - PiT1/SLC20A1 - is a multipass transmembrane protein, also known as the recep
144                           A newly identified multipass transmembrane protein, ANK, appears to functio
145                           Gpr177, encoding a multipass transmembrane protein, regulates Wnt sorting a
146  identified spinster (spin), which encodes a multipass transmembrane protein.
147                                     RFC is a multipass transmembrane protein.
148 TMEM208-mediated ER translocation to include multipass transmembrane proteins and suggest that TRPC6
149 ll interfering RNAs (siRNAs) targeting 2,726 multipass transmembrane proteins for strain-induced memb
150 eptor by the FeLV Env backbone suggests that multipass transmembrane proteins may be particularly sui
151 olycystic kidney disease (ADPKD), encode the multipass transmembrane proteins polycystin-1 (PC1) and
152                              Rhomboid family multipass transmembrane proteins regulate diverse cellul
153 nd glycoGag prevent the incorporation of the multipass transmembrane proteins serine incorporator 3 (
154 ining Protein S-Acyl Transferases (PATs) are multipass transmembrane proteins that catalyze S-acylati
155 1 and related Piezo2 (Fam38B) are vertebrate multipass transmembrane proteins with homologs in invert
156 evealed two genes, aph-1 and pen-2, encoding multipass transmembrane proteins, that interact strongly
157  novel gene family that encodes over a dozen multipass transmembrane proteins.
158 e protein; 2), type II membrane protein; 3), multipass transmembrane proteins; 4), lipid chain-anchor
159 estigations of protein ion stability using a multipass traveling wave (TW) cyclic IM (cIM) device.
160 en participants were imaged with PET using a multipass whole-body continuous-bed-motion acquisition,

 
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