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1 nctate lines of density that run through the rootlet.
2 the acetylated microtubules and along the D4 rootlet.
3 f the gene for rootletin, a component of the rootlet.
4 g-sought structural component of the ciliary rootlet.
5 m their normal localization near microvillar rootlets.
6     It was originally cloned from human hair rootlets.
7 mal basal bodies and cytoplasmic microtubule rootlets.
8 lation of neurons among the trigeminal motor rootlets.
9 exist between the sciatic notch to the nerve rootlets.
10 er ear hair cell cytoskeleton, forming dense rootlets.
11 tous actin density and abnormal stereociliar rootlets.
12  at the junction between the lower and upper rootlets.
13 iate preferential binding to centrioles over rootlets.
14 tly, via microtubules, to some stereociliary rootlets.
15 rrelated with shorter acetylated microtubule rootlets.
16  hereditary deafness DFNB28, is localized to rootlets.
17 number of single spindle afferents in dorsal rootlets.
18 t the ciliary base in photoreceptors lacking rootlets.
19  In the mutant, ciliated cells are devoid of rootlets.
20 P holds a preference for binding directly to rootlet actin remains an open question.
21 s indicate that pericentriolar fibres termed rootlets, also known as the centrosome linker, entangle
22 he evolution of terminal rooting axes called rootlets among the rhizomorphic lycopsids.
23 at support microvilli have their pointed-end rootlets anchored in a filamentous meshwork referred to
24  propose a model of eyespot assembly wherein rootlet and photoreceptor direct EYE2 to an area of the
25 aex8) mice develop normally but fail to form rootlets and are easier to deflect and damage.
26 ate with the basal bodies and their striated rootlets and form complexes named ciliary adhesions (CAs
27                     Root mutant neurons lack rootlets and have dramatically impaired sensory function
28 Gene expression signatures of I. echinospora rootlets and leaves were different.
29  functional paradigm for Nesprin1 at ciliary rootlets and suggest that the wide spectrum of human pat
30  of Nesprin1alpha with photoreceptor ciliary rootlets and the functional interaction between rootleti
31                              The function of rootlets and the molecules responsible for their formati
32 ceptor patches were not restricted to the D4 rootlet, and more anterior eyespots correlated with shor
33  it localizes with basal bodies, basal feet, rootlets, and actin filaments.
34  localizes to cilia-forming basal bodies and rootlets, and is required for ciliary adhesion complexes
35  function of the rotational stiffness of the rootlets; and 4) how the standing tension of the tip lin
36              In retinal photoreceptors where rootlets appear particularly robust, rootlets extend fro
37                                  Stereocilia rootlets are angled toward the center of the bundle, ten
38                       Our data indicate that rootlets are composed of homopolymeric rootletin protofi
39                                              Rootlets are critical for the sensory and motile functio
40 l tissue sections, we found that microvillar rootlets are decorated with the severing protein, cofili
41                        The other states that rootlets are modified leaves.
42                                      Ciliary rootlets are striated bundles of filaments that connect
43  consistent with the hypothesis that Isoetes rootlets are true roots and not modified leaves.
44                   One hypothesis states that rootlets are true roots, like roots in other lycopsids.
45                We show, however, that normal rootlet assembly requires centrioles.
46                                              Rootlet axon RFs in adult cats were used to approximate
47 n brewer's spent grain (BSG) and barley malt rootlets (BMR), common waste products of beer processing
48 e input from these same digits within dorsal rootlets bordering the lesion site.
49 ristae associated with photoreceptor ciliary rootlet bundles.
50 s into uniquely dense bundles reminiscent of rootlets but distinct from bundles formed by espin, an a
51 ls of pejvakin-deficient mice develop normal rootlets, but hair bundle morphology and mechanotransduc
52 on of the intercentriolar linker and ciliary rootlet component rootletin, and rootletin knockdown in
53   Pejvakin binds to and colocalizes with the rootlet component TRIOBP at the base of stereocilia in i
54  the daughter four-membered (D4) microtubule rootlet, comprises an elliptical patch of rhodopsin phot
55                                         Some rootlets contact the tight junctions that underlie the e
56                                              Rootlets contain spectrin, tropomyosin, and beta- and ga
57                                       Barley rootlets contained the highest hydroxycinnamoylagmatine
58                                       Dorsal rootlets containing electrophysiologically identified ax
59 in reveal, respectively, the way stereocilia rootlets contribute to the hair bundle's mechanical prop
60                       The number of cervical rootlet contributions for each trapezius branch varied f
61 muscle insertion, and the number of cervical rootlet contributions.
62 ioned adjacent to the daughter four-membered rootlet (D4), a unique bundle of acetylated microtubules
63 hoot axes, and largely unbranched stigmarian rootlets developed from rhizomorphs axes.
64 e base of microvilli, including to the actin rootlet devoid of ezrin or plasma membrane.
65 s and in a mix of afferents in lumbar dorsal rootlets (dorsal root potential [DRP]) with bipolar elec
66 s where rootlets appear particularly robust, rootlets extend from the basal bodies to the synaptic te
67 e packed more densely at the base, forming a rootlet extending into the cell body.
68 spectroscopy after their purification from a rootlet extract.
69 nds and binds TRIOBP-5, which itself bundles rootlet F-actin.
70                                  The ciliary rootlet, first recognized over a century ago, is a promi
71 cilium, they are especially dependent on the rootlet for structural integrity and long-term survival.
72 strategically located to augment stereocilia rootlet formation and their pivot point flexibility for
73 radiating from the centrioles and resembling rootlets found in vivo.
74 ructions of membrane-associated and purified rootlets from mouse retina using cryo-electron tomograph
75 r plate, and a severing of the hair-bundle's rootlets from the actin cores of the stereocilia.
76                                          The rootlets have a thick central core that widens at the an
77  developed largely unbranched, root-hairless rootlets, here we report that stigmarian rootlets were h
78 is positioned along, and adjacent to, the D4 rootlet in the absence of pigment granules.
79 oreover, pejvakin localizes to stereociliary rootlets in hair cells and is required for stereocilia m
80  cells, and ANKRD24 no longer localizes with rootlets in mice lacking TRIOBP-5; exogenous DsRed-TRIOB
81 sRed-TRIOBP-5 restores endogenous ANKRD24 to rootlets in these mice.
82  cord explants and formation of "miniventral rootlets." In neonatal mice, PTN protected the facial mo
83 eurography, which separates intradural nerve rootlets into normal, partial mild, severe, and complete
84                              The stereocilia rootlet is a key structure in vertebrate hair cells, anc
85                         The striated ciliary rootlet is a prominent cytoskeleton originating from bas
86             In vitro assays suggest that the rootlet is among the least dynamic of all cytoskeletons
87                They suggest that the ciliary rootlet is involved in cellular transport and stabilizes
88              Thus, a primary function of the rootlet is to provide structural support for the cilium.
89          A robust ridged pedicle with distal rootlets is preserved, together with a lophophore and ot
90  a major structural component of the ciliary rootlet, is located at the basal bodies and centrosomes
91        Within a particular frequency region, rootlet length correlates with stereociliary height but
92 of basal stereocilia in equivalent rows, but rootlet lengths increase much less.
93  a cytoskeletal structure called the ciliary rootlet links the cilium to the cell body.
94 es the apical plasma membrane with the lower rootlet, maintaining a normal distribution of TRIOBP-5.
95 etain defects in basal body structure and in rootlet microtubule positioning.
96 striated fiber is incomplete in this mutant, rootlet microtubules can be misplaced, and multiflagella
97 d activity was recorded from the hypoglossal rootlet of 700- to 800-microm medullary sections.
98 , and Dvl2 has been shown to localize to the rootlet of motile cilia.
99 ure that in the algal ancestor served as the rootlet of the flagellar basal bodies is required for pa
100  protein, designated rootletin, found in the rootlets of ciliated cells.
101 astructure, with membranes lifting away from rootlets of core bundles.
102 aralogs Rootletin and C-Nap1, assembles into rootlets of diverse lengths among sensory neuron subtype
103 estigating gene expression in the leaves and rootlets of Isoetes echinospora.
104 ss the subapical domain, which transects the rootlets of microvillar actin bundles.
105  Nesprin1 are integral components of ciliary rootlets of multiciliated ependymal and tracheal cells.
106 tletin recruits Nesprin1alpha at the ciliary rootlets of photoreceptors and identify asymmetric NE ag
107 Nerve impulses were recorded from the dorsal rootlets of the L7-S1 segments of the spinal cord, and a
108 ith respect to flagellar number, microtubule rootlet organization, cleavage furrow positioning, and b
109 t due to a lack of structural information of rootlet organization.
110 t a density of approximately 25,600 terminal rootlets per meter of rhizomorph, and were covered in ro
111 flections of up to +/-35 degrees, ruling out rootlet prestressing as the basis for sliding adhesion.
112 n mAb widely used as a marker for vertebrate rootlets recognizes an epitope in rootletin.
113 investigated the structure and dimensions of rootlets relative to the stereocilia in apical (low-freq
114                          In contrast, dorsal rootlet rhizotomy led to a significant increase in corti
115 on; or (2) diminishing their input by dorsal rootlet rhizotomy.
116                                          The rootlet's filamentous architecture, with frequent membra
117 eferentially expressed in the I. echinospora rootlets, S. moellendorffii roots and A. thaliana roots
118 and content were observed in fourteen barley rootlet samples.
119                               Vagal afferent rootlet section eliminated pancreatic secretions evoked
120 physiologically 15-25 weeks after the dorsal rootlet section to define this reactivation.
121 eate nucleus at 15-25 weeks after the dorsal rootlet section, than those mapped only 7 days postlesio
122         In four others (Group 2), additional rootlets shown to innervate the middle finger and thenar
123 n of four brewing by-products, namely barley rootlets, spent grain, hot trub, and cold trub.
124                      These data suggest that rootlets strengthen the ankle region to provide durabili
125 nk membranes may serve as part of the stable rootlet structure for anchoring the tip links of stereoc
126 ar plates and association with stereociliary rootlets suggest that this isozyme participates in rigid
127 s-positive vesicles adjacent to the striated rootlet suggests a transport role for this cytoskeletal
128              Previous studies indicated that rootlets support the long-term stability of some cilia.
129 -bands, associated with accumulations on the rootlet surface, and discrete (D)-bands corresponding to
130     We show that flexible protrusions on the rootlet surface, which emanate from the cross-striations
131 extinct rhizomorphic lycopsids have the same rootlet system architecture.
132                  After section of the dorsal rootlets that enervate the macaque's thumb and index fin
133                       Stereocilia have dense rootlets that extend through the ankle region to anchor
134 root entry zone and the lateral funiculi via rootlets that had become adherent to the lateral spinal
135 neous rhythmic activity in hypoglossal (XII) rootlets that occur in synchrony with periodic bursts of
136 ortical fibers in oral apparatus and ciliary rootlets, the apical filament ring and to inner arm (14S
137                                  In purified rootlets, the striations were classified into amorphous
138    Together with TRIOBP-5, ANKRD24 organizes rootlets to enable hearing with long-term resilience.
139            The most abundant compound in all rootlets was the glycosylated 4-O-7'/3-8'-linked heterod
140 f C-NAP1, although components of the ciliary rootlet were aberrantly localized away from the base of
141 fting with preceding normal intradural nerve rootlets were diagnosed by an experienced neuroradiologi
142 ess rootlets, here we report that stigmarian rootlets were highly branched, developed at a density of
143 gene expression signatures of I. echinospora rootlets were similar to gene expression signatures of t
144     Annular ANKRD24 continues into the lower rootlet, where it surrounds and binds TRIOBP-5, which it
145 ler that localizes specifically to the basal rootlets, where the pointed ends of core bundle filament
146 ubule-based trafficking selective for the D4 rootlet, which is perturbed in mlt1 mutant cells.
147    Stereocilia that lack TPRN develop warped rootlets with gradual loss of TRIOBP-5 and ANKRD24 from
148  or the XIIMN while recording from XII nerve rootlets (XIIn) as an index of respiratory motor output.

 
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