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1 d bipolar cells, and AII amacrine cells were immunonegative.
2 s in the substantia nigra pars compacta were immunonegative.
3 PV-negative basket cells, most of which were immunonegative.
4 growth lamina are taurine- and synaptotagmin-immunonegative.
5 tein trafficking mechanisms that render them immunonegative.
6 ls lining the extralobular ducts were TRAF-4 immunonegative.
7  which were glycine-immunonegative were GABA-immunonegative.
8 inals releasing inhibitory amino acids, were immunonegative.
9 lia and endothelial cells were GAD- and GABA-immunonegative.
10 ons and hippocampal pyramidal cells remained immunonegative.
11                                KC axons were immunonegative, but received direct input from, and cont
12 s than GABA-immunoreactive puncta on glycine-immunonegative cell bodies and (2) equal to or less nume
13 A, these results suggest that a subset of PV-immunonegative cells that express CB, most likely the so
14        All Type I neurons (n = 17) were ChAT immunonegative (ChAT-).
15 mmunopositive dendrites as well as with GABA-immunonegative dendrites of presumed granule cells.
16           However, the neuritic plaques were immunonegative for Abeta, whereas immunostaining for PrP
17 ble minority of GluR2/3-positive puncta were immunonegative for ABP.
18 sitive for cytokeratin and S-100 protein and immunonegative for adenohypophyseal hormones.
19 FR gene was amplified without truncation was immunonegative for both uPAR and phospho-Tyr-845.
20 osis (0 of 17) and Schwannoma (0 of 3), were immunonegative for DOG1.
21 euN) was used to visualize neurons that were immunonegative for FG or PV.
22        The MPNSTs, however, were essentially immunonegative for p16, with striking transitions in cas
23 immunopositive for pRb, and nine tumors were immunonegative for pRb.
24  for one antigen and only weakly positive or immunonegative for the other.
25                             Small cells were immunonegative for the receptor or weakly labelled.
26 d some brainstem nuclei became progressively immunonegative for trk, whereas neurons in the neocortic
27 uniculi at P0 compared with predominantly L1-immunonegative funicular axons in adults.
28                 Some chain elements are GABA immunonegative (GABA-) and are, thus, likely glycinergic
29                     Plasmacytomas were CPP32 immunonegative in 4 of 12 (33%) cases, in contrast to no
30 in taurine-positive laminae and occur in the immunonegative laminae between them.
31 ered that DNA loci of the immunopositive and immunonegative MHC-I neoantigens have distinct spatial d
32 in situ (DCIS) lesions were uniformly TRAF-4 immunonegative (n = 21).
33                                       PGP9.5-immunonegative nerves are strikingly similar to myelinat
34 ed; type 2, lightly stained; and type 3, DAT-immunonegative neuromelanin-containing perikarya.
35 ocalization of m2+/choline acetyltransferase-immunonegative neurons and the inhibitory neuropeptide g
36 llular reticular formation), many of the ASP-immunonegative neurons displayed colocalization with GAB
37 ominantly glycine-immunoreactive and glycine-immunonegative neurons, respectively.
38 glycine or for GABA; these were smaller than immunonegative neurons.
39  of numerous melanin-positive, but GTPCHI-ir immunonegative, neurons in the aged monkey and human nig
40 aurine-immunopositive laminae alternate with immunonegative ones.
41 , but most lymphocytes appeared to be TRAF-3 immunonegative or stained only weakly.
42 nant inhibitory drive of deep calbindin (CB)-immunonegative PCs that contrasts with a prominent depol
43 ergic terminals often encircled large, pale, immunonegative profiles that may be dendritic.
44 cted profiles in a single section; (2) large immunonegative profiles with dense-core vesicles were ab
45  terminals contacted both immunoreactive and immunonegative profiles.
46 alue of 33% of the G15242A mutation, whereas immunonegative, ragged-red fibers had a median value of
47 ncta formed pericellular baskets around GABA immunonegative somata in layers 2/3.
48 ority of LRNs were GABAergic and parvalbumin-immunonegative, some expressing calbindin; they innervat
49 munopositive stripes alternating with zebrin-immunonegative stripes.
50 rphology of GABA-immunoreactive (+) and GABA-immunonegative (-) synapses in the ICc.
51 ycine-immunoreactivity or which were glycine-immunonegative were GABA-immunonegative.
52 n the bone marrow were also typically TRAF-3 immunonegative, whereas myeloid progenitor cells and meg
53 migrating neurons in the cortical plate were immunonegative, whereas neurons deeper in the cortex tha
54 izontal cells, as well as Muller cells, were immunonegative, whereas retinal ganglion cells exhibited
55 ipheral blood lymphocytes were mostly TRAF-3 immunonegative, while granulocytes were TRAF-3 immunopos
56  are divided further into immunoreactive and immunonegative zones.