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1 nal and in the afferent fiber outside of the corpuscle.
2  in terminal Schwann cells within Meissner's corpuscles.
3 e the medullary niches surrounding Hassall's corpuscles.
4 endritic cells as well as enlarged Hassall's corpuscles.
5 ifferentiated epithelium including Hassall's corpuscles.
6 ongitudinal lanceolate endings, and Pacinian corpuscles.
7  size and density of innervation to Meissner corpuscles.
8 endritic cells and TSLP-expressing Hassall's corpuscles.
9 ecialized sensory receptors such as Meissner corpuscles.
10  receptors: Meissner corpuscles and Pacinian corpuscles.
11 redominantly in type C nevus cells and nevic corpuscles.
12 alized mainly in the medulla and in Hassle's corpuscles.
13 d subsequent loss of innervation in Meissner corpuscles, a mechanoreceptor expressing the BDNF recept
14 architecture of the avian Meissner (Grandry) corpuscle acquired using enhanced focused ion beam scann
15 , selective optogenetic activation of Krause corpuscle afferent terminals evoked penile erection in m
16  imaging experiments showed that both Krause corpuscle afferent types are A-fibre rapid-adapting low-
17 le afferents, along with a putative Pacinian corpuscle afferent, were recovered from 2-7-day-old neon
18 ls found in Golgi tendon organs and Pacinian corpuscles after nerve resection in the early neonatal p
19 more, encapsulated nerve endings in Pacinian corpuscles also contain reaction product following immun
20                                     Pacinian corpuscles also deteriorated.
21 receptor nerve-endings within the Meissner's corpuscle and in hair follicle lanceolate endings that b
22 ree-dimensional architecture of the Pacinian corpuscle and reveal the role of its cellular components
23 te complex, Meissner corpuscle, and Pacinian corpuscle and the subcellular distribution of Piezo2 wit
24 was measurable using the density of Meissner corpuscles and associated with an accumulation of intra-
25                       The extent of Meissner corpuscles and dermal nerve bundles were comparable betw
26  signaling components are devoid of Pacinian corpuscles and exhibit a dramatic disruption of RA mecha
27 erated mice that selectively lacked Meissner corpuscles and found them to be deficient in both percei
28  distinct subtypes associated with Hassall's corpuscles and identify divergence in the timing of medu
29 t hybrid morphologies, forming both Meissner corpuscles and lanceolate endings.
30 associated with fingerprint ridges (Meissner corpuscles and Merkel cell neurite complexes, respective
31 acinian corpuscles deep in the dermis, small corpuscles and Merkel endings around the base of dermal
32     Hypertrophy also occurred among Meissner corpuscles and Merkel endings supplied by Abeta fibers.
33 ry end-organs, such as Meissner and Pacinian corpuscles and others.
34 re mediated by two major receptors: Meissner corpuscles and Pacinian corpuscles.
35                                    The white corpuscles and the other cells capable of doing this hav
36 hymus (epithelial cells inside the Hassall's corpuscles), and brain (neurons, ependymal cells, and ma
37 e hair follicle lanceolate complex, Meissner corpuscle, and Pacinian corpuscle and the subcellular di
38 rs, which form Meissner corpuscles, Pacinian corpuscles, and longitudinal lanceolate endings.
39 Merkel cell-neurite complexes, Meissner-like corpuscles, and small lamellated corpuscles, specialized
40                                              Corpuscles are composed of a mechanoreceptor afferent su
41 nvironmental vibrations captured by Pacinian corpuscles are encoded in the auditory midbrain to media
42                       We found that Meissner corpuscles are innervated by two mechanoreceptor subtype
43                                     Meissner corpuscles are mechanosensory end organs that densely oc
44                                     Meissner corpuscles are most sensitive to frequencies around 10-5
45 es around 10-50 Hz (flutter), while Pacinian corpuscles are most sensitive to high frequency (100-300
46             Golgi tendon organs and Pacinian corpuscles are peripheral mechanoreceptors that disappea
47           "Nature has provided, in the white corpuscles as you call them-in the phagocytes as we call
48 mast cells, Langerhans cells, and Meissner's corpuscles, as well as in hair follicles, sweat glands,
49 pendent responses, the responses of Pacinian corpuscle-associated (PC) fibers are most strongly modul
50 f the cell column, and a single encapsulated corpuscle beneath the cell column, in the connective tis
51 he cortical response to stimulation of these corpuscles can be tested by taking advantage of the diff
52                                          The corpuscle comprises a stack of LCs interdigitated with t
53 erely truncated nephrons consisting of renal corpuscles connected to collecting ducts by an abnormall
54                                          The corpuscle contains a mechanoreceptor afferent surrounded
55  ventral glabrous skin terminate as Pacinian corpuscles deep in the dermis, small corpuscles and Merk
56                               Mechanosensory corpuscles detect transient touch and vibration in the s
57                                     Pacinian corpuscles detect transient touch and vibration in verte
58          Here we report that human Hassall's corpuscles express thymic stromal lymphopoietin (TSLP).
59         The neural component of the Meissner corpuscle filled the capsule of the mechanoreceptors tha
60                                    Hassall's corpuscles-first described in the human thymus over 150
61               However, the diabetic Meissner corpuscles had an abnormal structure and immunochemistry
62                                     Meissner corpuscles had normal density but were located deeper in
63 within the thymus, the function of Hassall's corpuscles has remained an enigma.
64        These findings suggest that Hassall's corpuscles have a critical role in dendritic-cell-mediat
65                           Although Hassall's corpuscles have been proposed to act in both the removal
66 ng type II (SAII) primary afferents, Ruffini corpuscles have rarely been reported in the skin, despit
67 iological properties and functions of Krause corpuscles have remained unclear since their discovery.
68  medullar epithelial cells forming Hassall's corpuscles (HC).
69    After longer-term hyperglycemia, Meissner corpuscle hypertrophy declined but the number of corpusc
70 emale mice, while genetic ablation of Krause corpuscles impaired intromission and ejaculation of male
71  mouse pinna, and sweat ducts and Meissner's corpuscle in the human fingertip skin-features that are
72 afferents are likely to terminate as Ruffini corpuscles in human glabrous skin.
73                                     Pacinian corpuscles in mammals and touch receptor neurons (TRNs)
74 rent terminal innervating Grandry (Meissner) corpuscles in the bill skin of a tactile specialist duck
75         We observed a high density of Krause corpuscles in the clitoris compared with the penis.
76 the distribution of Ruffini and Ruffini-like corpuscles in the distal phalanx of the index finger.
77 ells were seen in early capillary loop renal corpuscles in the mutant, but fewer than in the controls
78 nsing neurons are associated with Meissner's corpuscles in the skin.
79 ced by the epithelial cells of the Hassall's corpuscles, induced differentiation of CD4(+)CD25(-) thy
80 ow contains a high density of mechanosensory corpuscles innervated by functional rapidly adapting tri
81 e to retrograde degeneration of the Meissner-corpuscle innervating Abeta axons and aberrant formation
82      Thus, functional tuning of the Pacinian corpuscle is enabled by an interplay between mechanosens
83  not reform, and the reformation of Pacinian corpuscles is greatly impaired.
84 nerve terminals are associated with Meissner corpuscles, longitudinal lanceolate endings, and Pacinia
85                                   Meissner's corpuscle (MC) density in the fingertips was assessed us
86                                   Meissner's corpuscles (MCs) are cutaneous mechanoreceptors found in
87 elinated mechanoreceptors that form Meissner corpuscles, Merkel cell-neurite complexes, and circumfer
88 eceptors in neurons is critical for Meissner corpuscle morphology.
89                                     Pacinian corpuscle neurons are specialized low-threshold mechanor
90 l vibrations detected by the body's Pacinian corpuscle neurons, which are distinguished by their abil
91 nsory thresholds via an endocrine organ, the corpuscle of Stannius (CS), which is essential in zebraf
92                                    The renal corpuscle of the kidney comprises a glomerular vasculatu
93 ensory neuron subtypes that innervate Krause corpuscles of both the clitoris and penis and project to
94 afish pronephros is also associated with the corpuscles of Stannius (CS), endocrine glands that regul
95 d the heart, liver, somite muscle, fins, and corpuscles of Stannius.
96 y the accumulation of mobile cells, of white corpuscles of the blood in particular which absorb the m
97                                 Thus, Krause corpuscles of the clitoris and penis are highly sensitiv
98 mical and physiological properties of Krause corpuscles of the mouse clitoris and penis and their rol
99 e soon encircled by a compact mass of moving corpuscles; others, farther away, only found themselves
100 are RA mechanoreceptors, which form Meissner corpuscles, Pacinian corpuscles, and longitudinal lanceo
101                                 The Pacinian corpuscle (PC), a cutaneous mechanoreceptor located deep
102                                     Pacinian corpuscles (PCs) are tactile receptors composed of a ner
103 ced by a thymic cell type known as Hassall's corpuscles) positively select regulatory T cells within
104 ting mechanoreceptors innervating Meissner's corpuscles, recorded from Ush2a(-/-) mice, showed large
105 expression of SIRT1 in skin induced Meissner corpuscle reinnervation and regeneration, resulting in s
106 uscle hypertrophy declined but the number of corpuscles remained higher than in age-matched nondiabet
107 inct receptor types (Meissner's and Pacinian corpuscle, respectively), which may engage different neu
108   Using optogenetics we show that Meissner's corpuscle Schwann cells are necessary for the perception
109           In nonhairy plantar skin, Meissner corpuscle sensory endings were larger, and the number of
110 ncreased hair follicle innervation, Meissner corpuscle size, and Merkel cell number in glabrous skin,
111 issner-like corpuscles, and small lamellated corpuscles, specialized mechanosensory structures of the
112 ysis revealed no significant change in renal corpuscle structure.
113 sis of the two Meissner afferents within the corpuscle supports a model in which the extent of lamell
114                      Like mammalian Pacinian corpuscles, these neurons depolarized with both positive
115 tion includes the direct response of tactile corpuscles to environmental stimuli and psychological pa
116                            Within Meissner's corpuscles, two molecularly and functionally distinct se
117 ce of viable thymic epithelium and Hassall's corpuscles under the renal capsule and in the omental im
118  previous report, the formation of the renal corpuscle was defective in the absence of beta-catenin.
119                 Only one presumptive Ruffini corpuscle was found in the skin processed for double imm
120                         No cutaneous Ruffini corpuscles were found anywhere on the digit.
121 eta axons and aberrant formation of Meissner corpuscles which may have increased the mechanosensitivi
122  Glomerular volume, volume of the glomerular corpuscle, which is tuft, and the fractional volumes of
123 ture and bicellular sensory mechanism in the corpuscles, which comprises the afferents and LCs, creat
124                                       Krause corpuscles, which were discovered in the 1850s, are spec
125 ting glabrous (non-hairy) skin form Meissner corpuscles, while in hairy skin, they associate with hai

 
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