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1 vascularis, and in type 1 fibrocytes of the spiral ligament.
2 ; 2) basal loss of type IV fibrocytes in the spiral ligament; 3) apical loss of fibrocytes in spiral
3 rols, we localized AQP1 in fibrocytes in the spiral ligament and AQP4 in supporting epithelial cells
4 marrow-derived cells are concentrated in the spiral ligament and spiral limbus, areas that are known
6 an spiral limbus, osseous spiral lamina, and spiral ligament, and not in any other tissues in head an
7 in spiral ganglia neurons, fibrocytes of the spiral ligament, and supporting cells of the organ of Co
9 C activity was localized to pericytes in the spiral ligament as well as nerve fibers innervating oute
11 ase in Ngb in spiral ganglia neurons and rat spiral ligament, but not in supporting cells, following
15 orrelated with a substantial loss of type IV spiral ligament fibrocytes and a significant reduction o
16 -human specimens, GLAST was expressed in the spiral ligament fibrocytes but was not detected in the s
18 demonstrated that the inner ear fibrocytes (spiral ligament fibrocytes) are able to recognize nontyp
20 reactivity was detected in fibrocytes of the spiral ligament, from the basal to the apical portion of
21 e fibrocytes of the spiral limbus and of the spiral ligament in mouse and in human fetal and adult ti
22 e fibrocytes of the spiral limbus and of the spiral ligament in the cochlea, and in the fibrocytes of
23 decreased in spiral ganglia neurons and the spiral ligament in the prenatal and pre- and postnatal g
24 levels of TMC1 protein were observed in the spiral ligament of mutants when compared with wild-type
26 the differential expression of GLAST in the spiral ligament of the basal, middle, and apical turns o
27 oreover, KARS has strong localization to the spiral ligament region of the cochlea, as well as to Dei
28 ood vessels located in the stria vascularis, spiral ligament, sub-basilar region, stromal tissue, and
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