1 rocytes with abnormal enzyme expression were
immunolocalized.
2 expressed in Chinese hamster ovary cells and
immunolocalized.
3 We
immunolocalized a broad range of these regulators in tis
4 s are infiltrated by IgA PCs, the cells were
immunolocalized and quantitated in tissue sections taken
5 In wild type mice, claudin 14 was
immunolocalized at hair cell and supporting cell TJs.
6 PRG4 was
immunolocalized at the articular cartilage surface, but
7 Similarly, the GS holoprotein is
immunolocalized exclusively to the uninfected nodule tis
8 In aspen stem primary tissues, PtCAD was
immunolocalized exclusively to xylem elements in which o
9 We
immunolocalized FGF receptors and analyzed changes in FG
10 We
immunolocalized Fkn to RA ST macrophages, fibroblasts, e
11 We have
immunolocalized HA-tagged Kar3p to the spindle pole body
12 ice against the isolated recombinant protein
immunolocalized HSP60 in the cytoplasm and wall of paras
13 ocytes expressed Fras1 transcripts and Fras1
immunolocalized in a glomerular BM-like pattern.
14 Immunoglobulin G (IgG) was
immunolocalized in adjacent sections to demonstrate area
15 Both isoforms were
immunolocalized in ameloblasts, principally at maturatio
16 human RA synovial tissue confirmed that PBEF
immunolocalized in apical synovial membrane cells, endot
17 Last, the Trichoplax channel was
immunolocalized in cells that express an endomorphin-lik
18 Aedae-KR was
immunolocalized in contact chemosensory neurons in proth
19 lpha SMA, desmin, and PDGFR beta prominently
immunolocalized in cortical peritubular locations.
20 HO-1 was
immunolocalized in fixed sections of brain 24 h to 7 day
21 HO-1 was
immunolocalized in fixed sections of brain 3 h to 5 days
22 We show that MENT is
immunolocalized in granulocyte heterochromatin, where it
23 NTs were
immunolocalized in HTM tissues and cultured HTM cells ar
24 The Menkes and Wilson proteins were
immunolocalized in human and mouse retinas and in the AR
25 ADAMTS-5 was
immunolocalized in human arthritic synovium, where stain
26 lin receptor substrate 1 (IRS-1) was readily
immunolocalized in islet beta-cells.
27 HO-2 was
immunolocalized in neurons both before and after TBI, wh
28 sequenced, chromosome-mapped, expressed and
immunolocalized in parasitic cells.
29 CTGF protein was
immunolocalized in rat corneas after photorefractive ker
30 etween 7 and 14 d after injury, where it was
immunolocalized in reactive astrocytes bordering the les
31 PP1 was
immunolocalized in slime plugs and P-protein bodies in s
32 F in human corneal fibroblasts, and CTGF was
immunolocalized in the cells.
33 70), a marker of neuronal stress/injury, was
immunolocalized in the cortex.
34 beta-catenin, and focal adhesion kinase were
immunolocalized in the cultured epithelial cells, and hi
35 CTGF was
immunolocalized in the cultured fibroblasts by using a s
36 Although native galectin was
immunolocalized in the cytoplasm of Bge cells and the pl
37 Zic1 was
immunolocalized in the cytosol and nucleus of the murine
38 th factor (TGF) beta1, a fibrogenic cytokine
immunolocalized in the endomysial connective tissue of p
39 in 1 hour after wounding, EGFR was no longer
immunolocalized in the membranes of cells migrating into
40 HO-1 was
immunolocalized in the normal cord and along the axis of
41 MYH9 was
immunolocalized in the organ of Corti, the subcentral re
42 Type IX collagen was
immunolocalized in the preliminary matrix organized in g
43 of hippocampal neurons by microinjection and
immunolocalized it to the dendrites.
44 d P2Y12-R mRNA expression in rat kidney, and
immunolocalized its protein and aquaporin-2 (AQP2) in CD
45 luorescent staining with specific antibodies
immunolocalized MMP proteins in situ.
46 istochemical studies of normal human tissues
immunolocalized NEU1 and NEU3 proteins to both pulmonary
47 Notch receptors and ligands were
immunolocalized on conjunctival biopsies by confocal mic
48 In acute MS lesions both AIIt and LRP were
immunolocalized on macrophages and astrocytes while LRP
49 BAMT was
immunolocalized predominantly in the conical cells of th
50 ne are affected, phosphorylated Smad1/5/8 is
immunolocalized predominantly to granule cell precursors
51 TBC1D24 in the mouse inner ear was
immunolocalized predominantly to spiral ganglion neurons
52 d in cystathionine beta-synthase expression,
immunolocalized principally to the trophoblast, in patho
53 To test this hypothesis, we have
immunolocalized the CFTR and Na,K-ATPase proteins in int
54 We have
immunolocalized the InsP3 receptor to the inner nuclear
55 Now we have
immunolocalized the Shh protein and the Patched receptor
56 Notch1, Notch3, and Jagged1 were
immunolocalized throughout the conjunctival epithelium,
57 Both Fas and FasL were
immunolocalized to a greater extent in the patients who
58 In wild-type mice, Cx43 was
immunolocalized to apical and lateral regions of lens ep
59 Although NOX4 protein
immunolocalized to both nuclear membranes and intranucle
60 ocal microscopy and flow cytometry, NEU1 was
immunolocalized to both the plasma membrane and the peri
61 r and outer hair cells, and HCN1 protein was
immunolocalized to cochlear hair cell stereocilia.
62 HCN1 was
immunolocalized to discrete sites on saccular hair cell
63 nin biosynthetic enzymes but TKPR2 have been
immunolocalized to endoplasmic reticulum of anther tapet
64 FFA3 was
immunolocalized to enteroendocrine cells and to the ente
65 CN1 transcript, and HCN1 and HCN2 protein is
immunolocalized to hair-cell stereocilia by both z-stack
66 EphA2 was
immunolocalized to human corneal epithelial cells in viv
67 All cathepsins, except for cat K, were
immunolocalized to macrophages in BPD.
68 All of these proteins have been
immunolocalized to microfibrils.
69 All three proteins were
immunolocalized to mononuclear cells in perivascular cuf
70 triene C4 synthase, and cyclooxygenase, were
immunolocalized to native as well as newly induced lipid
71 cted protoplasts, the CP66:6G:g5 protein was
immunolocalized to nuclei.
72 pared with NOF cartilage, and matriptase was
immunolocalized to OA chondrocytes.
73 VEGF-A was
immunolocalized to peritoneal mesothelium and TGF-beta1
74 Zyme is
immunolocalized to perivascular cells in monkey cortex a
75 MMP-2 and MMP-9
immunolocalized to punctate structures within the neurop
76 VLA-4
immunolocalized to RA ST, SF, or PB, monocytes, macropha
77 e development, SUTs, other than SbSUT4, were
immunolocalized to sieve elements, while for elongating
78 The mouse DACH1 protein was
immunolocalized to specific cell types within the develo
79 Both HGF and its receptor
immunolocalized to subsynovial macrophages as well.
80 d PRG4 secretion, and the source of PRG4 was
immunolocalized to superficial cells.
81 e developing tooth organ, TIP39 and tuftelin
immunolocalized to the apical pole of secretory amelobla
82 ue inhibitor of metalloproteinase-1 was also
immunolocalized to the basement membrane zone and superf
83 Gelatinase B was
immunolocalized to the basement membrane zone and superf
84 TNF-alpha was
immunolocalized to the cardiac myocyte, suggesting that
85 epitope-tagged receptor (C-Tag-hPTH1-Rc) was
immunolocalized to the cell membrane and, to a lesser ex
86 Pir proteins have been
immunolocalized to the cell wall.
87 At the subcellular level, LeAGP-1
immunolocalized to the cell walls of these particular ce
88 in COS-7 cells as a FLAG fusion protein and
immunolocalized to the cytoplasm.
89 The EGFR
immunolocalized to the DCT and EGFR tyrosine kinase inhi
90 Gelatinase A was
immunolocalized to the epithelium and stroma of normal c
91 Tissue inhibitor of metalloproteinase-2 was
immunolocalized to the epithelium in normal and wounded
92 Collagen XVIII was
immunolocalized to the human corneal epithelium, epithel
93 Vps10p has been
immunolocalized to the late-Golgi compartment where CPY
94 odulin-dependent protein kinase type IV-were
immunolocalized to the lateral wall of the OHC.
95 s, where, surprisingly, it was predominantly
immunolocalized to the lumenal surface of dysplastic gla
96 In normal human embryos, OFD1a
immunolocalized to the metanephric mesenchyme, oral muco
97 Type XVIII collagen was
immunolocalized to the mouse corneal epithelium, epithel
98 To address these hypotheses, STELLA was
immunolocalized to the mouse gastrula between Early Stre
99 In addition, the protein was
immunolocalized to the Muller cells in the retina as wel
100 rum to the recombinant protein, Ac-GST-1 was
immunolocalized to the parasite hypodermis and muscle ti
101 Anti-E-cadherin antibodies injected i.v.
immunolocalized to the pulmonary lymphovascular emboli o
102 parasitic cycle, and the mature protein was
immunolocalized to the surface of endospores.
103 A transport protein was
immunolocalized to the symbiosomal membrane separating t
104 vation of caspase-3 on Western blotting, and
immunolocalized to the syncytiotrophoblast; necrosis was
105 tite geminivirus squash leaf curl virus, was
immunolocalized to unique approximately 40-nm tubules th
106 In situ, pVHL
immunolocalized to villous cytotrophoblast stem cells, a
107 We
immunolocalized two of the minicell-enriched proteins, O
108 Connexins were
immunolocalized using specific antibodies.
109 anted human hearts with advanced CAV, RANTES
immunolocalized with graft-infiltrating mononuclear cell
110 alpha1-antitrypsin, transgene expression was
immunolocalized within keratinocytes of the stratum gran