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1                      This regulatory element was localized at -246 to -233 base pairs upstream from t
2 t103 and the Rat1/Rai1 5' --> 3' exonuclease are localized at 3' ends of protein coding genes.
3 suggest that the most frequent region of LOH is localized at 3p24.3.
4 ional sensing by G protein-coupled receptors is localized at a discrete step in the signaling pathway
5                     The m.7551A > G mutation is localized at a highly conserved nucleotide(A37), adja
6                               The NGF target is localized at a postsynaptic site and involves a new T
7 plication were blocked; however, the Z-rings were localized at a subpolar region of the cell.
8 mmunofluorescence analysis shows that PDZD11 is localized at adherens junctions in a PLEKHA7-dependen
9   Both cadherin complex components and L1CAM are localized at all sites of cell-cell contact during g
10 cell-conditioned medium, proliferating cells were localized at ampullae, where a binding receptor for
11                                          Dlg is localized at and required for the formation of both s
12 hird transcriptional unit, designated csk22, was localized at approximately 173 degrees on the chromo
13 we found that in interphase, Sec13 and Nup96 are localized at both sides of the NPC in addition to ot
14  major inhibitory receptors in the brain and are localized at both synaptic and extrasynaptic membran
15               GABA(A) receptors (GABA(A)-Rs) are localized at both synaptic and extrasynaptic sites,
16 ed obscurin, has been described and found to be localized at both the M-lines and Z-discs of striated
17          Moreover, a p95 partner protein has been localized at both focal adhesions and actin-cytoske
18                                 OCT3 protein is localized at both basolateral (blood-facing) and apic
19                                    for3p-GFP is localized at both cell tips in an actin-dependent man
20                         We show that SDCCAG8 is localized at both centrioles and interacts directly w
21       We show that Nasonia otd maternal mRNA is localized at both poles of the embryo, and resulting
22 ssed on both the mRNA and protein levels and is localized at both the apical and basolateral membrane
23                                  Mitofusin 2 is localized at both the outer membrane of mitochondria
24  the capillary in that the TNF-alpha effects were localized at branch points, while the arachidonate
25 s a cell-cycle-related localization pattern, being localized at cell ends during interphase and formi
26                              Moreover, PSGAP is localized at cell periphery in fibroblasts in a pleck
27                   Components of this complex are localized at centrosomes and spindle poles from inte
28         Furthermore, UVRAG was also found to be localized at centrosomes and physically associated wi
29  APC/C activator Fizzy-related (Fzr or Cdh1) is localized at centrosomes in animal cells.
30 taining also reveals that the SAPAP proteins are localized at cholinergic synapses, including neurona
31                                        PRODH is localized at chromosome 22q11 in a region deleted in
32                              The CAPN14 gene is localized at chromosome 2p23.1-p21 and is most homolo
33                                The LOT1 gene is localized at chromosome 6q24-25, a chromosomal region
34 des a protein with 276 amino acids; the gene is localized at chromosome 9q34.
35                            The gene for PrLZ was localized at chromosome 8q21.1, a locus most frequen
36 w that two components of the insulin pathway are localized at CNS synapses, where they are components
37                                         They are localized at constriction sites and impact membrane
38 that dynactin, the dynein-activator complex, is localized at cortical microtubule attachment sites an
39                                        TNFR2 was localized at cortical neurons including parvalbumin-
40 nd the dystrophin-glycoprotein complex (DGC) are localized at costameres and neuromuscular junctions
41 s of the planar cell polarity (PCP) pathway, are localized at developing glutamatergic synapses and i
42  molecules (CAM) neurofascin (NF) and Nr-CAM are localized at developing nodes of Ranvier in peripher
43 gap is smaller and because its HOMO and LUMO are localized at different stations (HOMO exclusively at
44  IPL, suggesting that the two alpha-subunits are localized at different synaptic sites.
45                                     PolC-GFP was localized at discrete intracellular positions, predo
46 binatorial alternative splicing pathways and is localized at diverse intracellular sites including th
47 lK from Bacillus subtilis (WalK(Bsu)), which is localized at division septa, immunofluorescence micro
48 ence microscopy, we have now shown that PBP1 is localized at division sites in vegetative cells of B.
49       The direct interaction of CaM with DR5 is localized at DR5 death domain.
50                Actomyosin-rich purse strings are localized at each of the two leading edges of latera
51 or the fusion of optic fissure margins, FAT1 is localized at earliest cell-cell junctions, consistent
52    Although previous work has shown that Erk is localized at endosomal compartments, no role for Erk
53 ANSPORT I (ESCRT-I) component ELCH (ELC) and is localized at ESCRT-I-positive late endosomes likely t
54                               AMPA receptors are localized at excitatory synapses and are not found o
55           The EphB receptor tyrosine kinases are localized at excitatory synapses where they cluster
56  in the control of junction assembly and has been localized at extrajunctional sites in association w
57 0-76% of connexin-36-immunolabeled particles were localized at focal sites on apposed plasma membrane
58 tem, but it is not known how these receptors are localized at GABA-dependent synapses.
59                           We show that ErbB4 is localized at GABAergic terminals of the prefrontal co
60              Heterochromatin protein 1 (HP1) is localized at heterochromatin sites where it mediates
61 ound that a portion of the active MAP kinase is localized at kinetochores, asters, and the midbody du
62 human katanin antibody and that this protein is localized, at least in part, to the basal body comple
63 on ultrastructural analysis showed that CD44 was localized at mature synapses in the adult brain.
64                       Hence, RIPb appears to be localized at microtubules and is then recruited by ac
65                                     GFP-FtsL was localized at mid-cell in vegetative cells and at the
66 here division proteins such as FtsZ and EzrA are localized at midcell, and the septum formation is in
67 at, like Cdc20, previously has been shown to be localized at mitotic spindle poles and is involved in
68 ron microscopy provide evidence that GABAARs are localized at MNTB axon terminals.
69                            Ca(v)2.2 channels are localized at nerve terminals where they play a criti
70 that phosphatidylinositol signaling pathways are localized at nuclear speckles.
71                    And the spin-up electrons are localized at one edge, the spin-down holes localized
72                                  IcsA, which is localized at one pole of the bacterium, mediates acti
73               Proteins within these pathways are localized at opposite ends of the cell to generate t
74            Moreover, at metaphase, some ATRX is localized at or close to the ribosomal DNA (rDNA) arr
75                           In addition, AP1M2 was localized at or near the trans-Golgi network.
76 ven proximal aphidicolin-induced breakpoints were localized at or near the end of a THE element.
77 result is that electrochemical reactions can be localized at particular locations on the perimeter of
78 (SRIF) receptor subtype, the sst2A receptor, is localized at postsynaptic sites of the principal neur
79 rge proteins that contain two C2-domains and are localized at presynaptic active zones, where neurotr
80 co-culture system to show that P2X receptors are localized at presynaptic sites on DRG neurons; that
81    Immunoelectron microscopy shows that FMRP is localized at presynaptic terminals and in axons withi
82                                SYD-2 protein is localized at presynaptic termini independently of the
83                            We show that Mcm1 is localized at replication origins and plays an importa
84                                    The spins are localized at silicon step edges having the form of g
85 servations, GluN3a subunits in MPP terminals are localized at sites away from the presynaptic release
86                                       VPS13A is localized at sites where the endoplasmic reticulum an
87 mmadelta T cells, but not alphabeta T cells, were localized at sites of DSS-induced epithelial cell d
88 y stable phases of clustered water molecules are localized at some of the defects in zeolite Beta, wh
89       ELG1 protein interacts with PCNAs that are localized at stalled replication forks.
90 ious studies have shown that the M2 receptor is localized at steady state to the apical domain in Mad
91 ed in nonsyndromic progressive hearing loss, is localized at stereocilia tips.
92 bsite -1, even though both Glu180 and Asp309 are localized at subsite 1.
93                           The SAPAP proteins are localized at synapses in a manner consistent with mR
94 ine receptor (AChR) clustering in vitro, and are localized at synapses in vivo.
95 a prevailing assumption that beta1-integrins are localized at synapses, where they contribute to syna
96 Microscopic analysis confirmed that Gs alpha is localized at synapses both pre- and postsynaptically.
97 ted membrane protein) family of proteins and is localized at synapses.
98 tochondria were significantly more likely to be localized at synaptic sites.
99 omo- and heterodimers with TRF1; both dimers were localized at telomeres.
100 sion site by binding to its substrate, which is localized at that place.
101                      Breaks in chromosome 18 are localized at the 3'-UTR of BCL2 gene or downstream a
102 yze the interconversion between SA and MeSA, are localized at the apical region of pollen tubes, indi
103                       ZeExp1 and ZeExp3 mRNA are localized at the apical tip, whereas ZeExp2 mRNA is
104  proteins of Mycobacterium tuberculosis that are localized at the bacterial cell surface or secreted
105 lear matrix, indicating that these sequences are localized at the base of chromatin loops.
106                        Because NHERF1 and -2 are localized at the BB, where they bind NHE3 as well as
107 teropentamers and their ligand binding sites are localized at the beta+ / alpha- interfaces.
108 y through interaction with EI and HPr, which are localized at the cell pole.
109 eria indicates that certain PE_PGRS proteins are localized at the cell surface of BCG and M. tubercul
110 on molecule and the Shaker potassium channel are localized at the Drosophila neuromuscular junction,
111 mechanical insulator whose zero-energy modes are localized at the edge.
112 ne H3 dimethylated at lysine 4 (di-Me H3-K4) are localized at the ends of the active DJ domains of bo
113  mRNA and its zipcode-binding protein, ZBP1, are localized at the growth cone and become asymmetrical
114 moesin family (ERM) of adapter proteins that are localized at the interface between the cell membrane
115 ly the existence of such states: states that are localized at the interface between two topologically
116 recursors, the three reversible redox events are localized at the iron centers distal from the NO lig
117  Mn(+2)-activatable receptors for ATX, which are localized at the leading edge of polarized cells.
118 trates UvrAB introduces changes in DNA which are localized at the lesion and are limited to 1-3 bp.
119  Topological edge modes are excitations that are localized at the materials' edges and yet are charac
120        Within the structure, individual taxa are localized at the micron scale in ways suggestive of
121  the cell but exist as defined clusters that are localized at the mid-cell, or at the 1/4 and 3/4 cel
122 and dimethylated H3R8 (histone 3 arginine 8) are localized at the myogenin promoter in differentiatin
123 g mutant nesprin-1alpha, lamin A/C and SUN2, are localized at the nuclear membrane in this model.
124                                         Both are localized at the pilus tip, and HifE appears to medi
125 ry we show that endogenous Kir2.1 and Kir2.2 are localized at the plasma membrane and T-tubules in ro
126 apparent proportions of DHE and filipin that are localized at the plasma membrane.
127 g cells in Ae. aegypti and Anopheles gambiae are localized at the posterior part of the posterior mid
128 s receptors, ErbB receptor tyrosine kinases, are localized at the postjunctional membrane presumably
129    The eigenstates with the smallest spacing are localized at the saddle point.
130 usively restricted to the interface but also are localized at the Sm-doped CeO2 nanopillars.
131 le-specific ankyrin isoforms, ankB and ankG, are localized at the subsarcolemma level, at which they
132 r the interior whereas for D < 4 nm the ions are localized at the surface, but with much less tendenc
133 ess to CCL21 and CCL19 than do FO cells, and are localized at the T/B cell border in spleen.
134 tron superatoms, where the 8 shell electrons are localized at the two icosahedral halves of the metal
135 tein was found to be expressed in schizonts, be localized at the apical end of the merozoite, and pre
136 rB operon, virB1 and virB2, are predicted to be localized at the bacterial surface, where they could
137 f this machinery, PscN (SctN), is thought to be localized at the base of the secretion apparatus and
138 e protein, CheW, into complexes that tend to be localized at the cell poles.
139 ith confocal microscopy, we found ratAurA to be localized at the centrosome in normal and neoplastic
140    Moreover, a fraction of Crm1 was found to be localized at the centrosomes.
141                            GfsA was found to be localized at the Golgi apparatus based on cellular fr
142 ucleotide sugars and is demonstrated here to be localized at the Golgi apparatus.
143       In solution, the conantokins appear to be localized at the headgroup of vesicles and do not ins
144    Neutron diffraction studies showed VP1 to be localized at the hydrophobic core of model palmitoylo
145 se2 where palmitoylation occurs was found to be localized at the inner leaflet of the plasma membrane
146 e junctional SR, a small number of RyR2s can be localized at the middle of the sarcomere and in the z
147 acetylcholinesterase (A(12)-AChE) appears to be localized at the neuromuscular junction in associatio
148          Additionally, c-di-GMP was found to be localized at the outer boundary of mature colonies in
149 ed to have a membrane-spanning domain and to be localized at the plasma membrane.
150 juxtanuclear compartment and also appears to be localized at the plasma membrane.
151  endogenous Na(V)1.7 revealed the channel to be localized at the soma membrane, axon, axon terminals,
152 ansduction channel of hair cells, thought to be localized at the tips of their stereocilia.
153                                       AR has been localized at the sites of tissue damage, and inhibi
154 mmunoprecipitation assays indicated that BAD is localized at the 12-O-tetradecanoylphorbol-13-acetate
155  the anterior segmentation gene bicoid (bcd) is localized at the anterior pole of the Drosophila egg
156                                       EGL-26 is localized at the apical edge of the vulE cell.
157                                          Nf2 is localized at the apical region of NPCs.
158      Interestingly, the Au plasmon resonance is localized at the Au/vacuum interface, rather than pre
159              The Shaker-type K channel Kv1.1 is localized at the axon arborization preceding the term
160 teins form a complex called the BBSome which is localized at the basal body or ciliary axoneme and re
161                      We also found that Dlg5 is localized at the basal body, where it associates with
162  of these phenotypes, endogenous Cby protein is localized at the base of cilia.
163                         We report that Sept7 is localized at the base of dendritic protrusions and at
164 sicles at the presynaptic active zone, which is localized at the base of the ribbon.
165             In this paper, we show that Dlg1 is localized at the basolateral cell cortex during mitos
166 es uptake of conjugated bile acids (BAs) and is localized at the basolateral membrane of hepatocytes.
167  The epidermal growth factor receptor (EGFR) is localized at the basolateral membrane of most epithel
168                Here, we have shown that Mct8 is localized at the basolateral membrane of thyrocytes a
169 pithelia, the TGFbeta type II receptor (T2R) is localized at the basolateral membranes.
170 e and porcine eyes indicated that bestrophin is localized at the basolateral plasma membrane of RPE c
171 r, termed the isthmic organizer (IsO), which is localized at the boundary between them.
172 er, charge resonance vanishes and the cation is localized at the bridge center (the mixed valence pro
173       The Chk1-interacting region of CK2beta is localized at the C-terminus and the complex between C
174 mes occur at the replication terminus, which is localized at the cell center.
175                                        RGS-7 is localized at the cell cortex, and its effects require
176                           We found that Bud5 is localized at the cell division site and the presumpti
177     Both of these methods revealed that DnaA is localized at the cell membrane, further suggesting th
178           In resting cells, most of the eNOS is localized at the cell membrane.
179 nd cultured neuroendocrine PC12 cells, Glut3 is localized at the cell surface and, also, in a distinc
180 y glycosylated CD39 has apyrase activity and is localized at the cell surface.
181                   A C-terminal Pro-Cys motif is localized at the center of the tetramer and forms rev
182 nd 2) the major contribution to the disorder is localized at the central position of the mixed tetrah
183     Green fluorescent protein-C-terminal Plk is localized at the centrosome and the midbody of transf
184 ds are necessary for activity; and (e) BARD1 is localized at the centrosome throughout the cell cycle
185 The peptide with intermediate affinity (RP2) is localized at the ciliary transition zone as a gate ke
186                                  Fak protein is localized at the cortex of notochord cells and at the
187  sites for the guanosine triphosphatase Ran, is localized at the cytoplasmic periphery of the nuclear
188                           Because iPLA2gamma is localized at the endoplasmic reticulum (ER), this stu
189 with two predicted transmembrane helices and is localized at the endoplasmic reticulum.
190      For the tryptic peptides, fragmentation is localized at the ends of the peptides suggesting that
191                                         GBA2 is localized at the ER and Golgi, which puts GBA2 in a k
192 ve-cell imaging analyses revealed that ORP3a is localized at the ER, and that binding to this organel
193                                        Dasm1 is localized at the excitatory synapses.
194       In swarmer cells, a short form of PodJ is localized at the flagellated pole.
195  that the RAD50-interacting protein, RINT-1, is localized at the Golgi apparatus and the centrosome i
196 ed-coil protein, also known as giantin, that is localized at the Golgi membrane.
197                       Additionally, PITPbeta is localized at the Golgi, and EGF stimulation resulted
198  subunit interaction domain, NAB(HERG), that is localized at the hydrophilic cytoplasmic N terminus a
199 tein Np65, encoded by the Neuroplastin gene, is localized at the IHC presynaptic region.
200 nfocal microscopy analysis showed that IL-15 is localized at the immunologic synapse of LCs and naive
201                        Because activated ERK is localized at the immunological synapse, we investigat
202 itochondrial membrane (OMM), while 3betaHSD2 is localized at the inner mitochondrial space (IMS), whe
203                                  The peptide is localized at the interface between membrane and solve
204  crystal structure of PKCbeta showed that it is localized at the interface between the C2 and catalyt
205 cts: (i) contactin-associated protein-2 that is localized at the juxtaparanodes in myelinated axons;
206 x1), which is up-regulated in breast cancer, is localized at the lamellipodia edges of aggressive bre
207 h is phosphorylated on tyrosine residue 342, is localized at the membrane.
208                  We show that activated RhoA is localized at the mitotic cell cortex, and Rho-associa
209 eorganization contribution to DeltaDeltaH(U) is localized at the mutation site, in contrast to enviro
210          The formation of this ordered phase is localized at the nanometre scale; with increasing wat
211                                          Id3 is localized at the neural plate border during gastrulat
212                                        c-myc is localized at the neural plate border prior to the exp
213 oscopy showed that a portion of Sindbis nsP3 is localized at the nuclear envelope, suggesting a possi
214                                  GFP-cPLA(2) is localized at the nuclear membrane of stably transfect
215                             AtNUP160 protein is localized at the nuclear rim, and poly(A)-mRNA in sit
216                                         Melt is localized at the onset of rapid ice flow in the large
217 the sensing zone of conical-shaped nanopores is localized at the orifice, the translocation of nanopa
218        Electron microscopy showed that Tom22 is localized at the outer mitochondrial membrane (OMM),
219                       The catalytic activity is localized at the perimeter of the Au nanoparticles wh
220 sibility experiments showed that the protein is localized at the periplasmic side of the outer membra
221 ndependent evidence demonstrate that CYBASC1 is localized at the plant tonoplast (TO).
222     In striatal medium spiny neurons, PDE10A is localized at the plasma membrane and in dendritic spi
223 ly overexpressing TSPAN9 to show that TSPAN9 is localized at the plasma membrane and in early and lat
224 ls showed that the majority of hCtr1 protein is localized at the plasma membrane and no significant i
225 psis thaliana FLA4 we show that this protein is localized at the plasma membrane as well as in endoso
226 maging of live cells to demonstrate that Gag is localized at the plasma membrane in a striking puncta
227 ubset of small DRG sensory neurons, where it is localized at the plasma membrane of the soma, axon in
228                        The small GTPase KRAS is localized at the plasma membrane where it functions a
229                                This receptor is localized at the plasma membrane, as well as in intra
230 that TgMTP1::green fluorescent protein (GFP) is localized at the plasma membrane, suggesting that TgM
231         Consistent with such functions, SHK1 is localized at the plasma membrane/cortex, and we show
232 nce protein fusions, we determined that ParC is localized at the poles of the bacteria in rapidly gro
233 at the NF-kappaB inducing IKK kinase complex is localized at the postsynaptic density (PSD) and activ
234                           We show that Bud2p is localized at the presumptive bud site in G(1) cells i
235 urthermore, we find that vertebrate CK1gamma is localized at the primary cilium to promote Smo phosph
236                               The mBD-3 gene is localized at the proximal portion of chromosome 8, th
237                                         Sap1 is localized at the replication origin ori2004 and this
238  We further show that in mouse alpha-catulin is localized at the sarcolemma and neuromuscular junctio
239 ercellular communication, and show that SepJ is localized at the septa.
240 ions for 2 indicate that the cationic charge is localized at the silicon center and depict a LUMO wit
241 ating that the effect of the phosphate group is localized at the ssDNA gap.
242 of an intermediate where the second electron is localized at the superoxo adsorption site.
243 nsisting of an oligomer of the protein FliD, is localized at the tip of the flagellum, and is essenti
244  a newly identified hair bundle protein that is localized at the tips of stereocilia of both cochlear
245    VAC7 encodes a novel 128-kDa protein that is localized at the vacuole membrane.
246                                 Thin protein is localized at the Z-disk in muscle, but l(2)tn mutants
247                           In addition, Fun30 was localized at the 5' and 3' ends of genes and within
248                                        p-ERK was localized at the apical cell surface of bronchiolar
249            Immunostaining revealed that TM14 was localized at the apical pericellular regions of preo
250        In contrast to PSMA/NAALAD1, NAALADL2 was localized at the basal cell surface where it promote
251  The PPI/PI immunodominant epitope LALEGSLQK was localized at the C-peptide/A-chain junction.
252 is PGA59-gLUC fusion (referred to as gLUC59) was localized at the C. albicans cell surface, allowing
253      Confocal imaging revealed that BSEP-YFP was localized at the canalicular membrane and in tubulo-
254 uorescence microscopy demonstrated that VASP was localized at the cell cortex in round cells and redi
255 ocal immunomicroscopy revealed that cyclin E was localized at the centrosome.
256                                         RhoA was localized at the cleavage furrow or at the necks of
257 hat in the presence of B-lineage cells, CD28 was localized at the contact interface between B cell pr
258 fate-polyacrylamide gel electrophoresis, and was localized at the cytoplasm and plasma membrane.
259 green fluorescent fusion protein (DRP1C-GFP) was localized at the division plane in dividing cells an
260 en fluorescent protein--CalS1 fusion protein was localized at the growing cell plate, that expression
261      Reaction product in photoreceptor cells was localized at the inner/outer segment junction and in
262                                       apfp-1 was localized at the interface between stiff byssus and
263                                   C4d in PTC was localized at the interface of endothelium and baseme
264 se C were at the apical membrane, E-cadherin was localized at the lateral membrane, and beta-catenin
265 lized EGF exhibited higher pPLCgamma1, which was localized at the leading edge.
266 hoxyphenol and p-hydroquinone, respectively) was localized at the main heme access channel.
267                                       Necl-5 was localized at the membrane of midlobular and centrilo
268                                       PvGAMA was localized at the microneme in the mature schizont-st
269                                When the UASG was localized at the nucleosomal pseudodyad, relative oc
270                          Interestingly, NOX5 was localized at the outer membrane of the mitochondria
271 ulture demonstrated that phosphorylated sst2 was localized at the plasma membrane after 10 seconds of
272 o wild type occludin, its Y398A/Y402A mutant was localized at the plasma membrane and cell-cell conta
273 ectron microscopy revealed that polycystin-1 was localized at the plasma membrane and sarcoplasmic re
274 ana leaves, SYMRK-yellow fluorescent protein was localized at the plasma membrane, and interaction wi
275 rescence studies showed that alpha1D protein was localized at the plasma membrane, in cytosol and cel
276 fluorescence analysis demonstrated that FFHA was localized at the plasma membrane, whereas GFP was pr
277  whereas FGF-2 in normal corneal endothelium was localized at the plasma membrane.
278 ivIVA, which is required for an ovoid shape, was localized at the poles and septum of pneumococcal ch
279 scence in situ hybridization, the mBD-1 gene was localized at the proximal portion of chromosome 8, t
280 ulation site, and the central common pathway was localized at the region between the intersections of
281 pproximately 700 s(-1) mM(-1), respectively) was localized at the same exposed Trp-164 responsible fo
282 ed fibers expressing NFATc-GFP, fluorescence was localized at the sarcomeric z-lines and absent from
283 laudin-1 expressing Can 10 clones, Claudin-1 was localized at the TJ and paracellular permeability wa
284 tions suggest that the DA storage impairment was localized at the VMAT2 protein itself.
285                                         MYPN was localized at the Z-line in control skeletal muscles
286 evealed that most Mkc7p and Yap3p activities were localized at the cell surface.
287                      The exogenous connexins were localized at the cell surfaces in junctional macula
288 rs after antigen challenge, immune complexes were localized at the ciliary body and iris of receptor-
289                  In all nuclei, m2 receptors were localized at the membrane of motoneuronal perikarya
290                       Initially, osteoclasts were localized at the periosteum next to the synovial me
291 n of the infected immune cell population and were localized at the periphery of parasite plaques.
292                 Both HA-TRHR and HA-K338STOP were localized at the plasma membrane of untreated cells
293            None of the RGS proteins examined were localized at the plasma membrane.
294 reover, the majority of infected tumor cells were localized at the tumor margin.
295 ally insertions or deletions (1-142 bp) that were localized at the ZFN cleavage site and likely deriv
296                            Major differences are localized at two regions: residues 29-31 and residue
297  these results suggest that the core of PHF6 is localized at VYK, and the interaction between small a
298 ORFs, is seen exclusively in the nucleus and is localized at Xic.
299 edly, the gene encoding this protein, FANCB, is localized at Xp22.31 and subject to X-chromosome inac
300 at glycerol-3-phosphate dehydrogenase (GPDH) is localized at Z-discs and M-lines.

 
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