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1 lassified as nuclear, cortical, or posterior subcapsular.
2 eneously, 109 had a smooth surface, 101 were subcapsular, 89 had ill-defined margins, and 62 had a ce
5 nset of heart failure and the development of subcapsular and cortical cataracts is observed in Mbnl3(
6 vital dyes, to determine whether age-related subcapsular and cortical cataracts were linked to the fa
7 oped that initially appeared to be posterior subcapsular and gradually matured to involve the entire
8 lipopolysaccharide, were very visible in the subcapsular and medullary sinuses but were largely exclu
9 a recta in the renal medulla, the lymph node subcapsular and medullary sinuses, and some capillaries
10 ly associated with the severity of posterior subcapsular and nuclear cataracts, which was the only fe
14 sults in the accumulation of NK cells in the subcapsular area of the draining lymph node and their ac
15 gions in the medullary, interfollicular, and subcapsular areas where viral infection was initially co
16 itating reticulum cells of T zones, cells in subcapsular areas, and cells of the reticular network we
18 ciated with a higher prevalence of posterior subcapsular cataract (PSC) (OR, 1.29; 95% CI, 1.07-1.55)
19 te a possible relationship between posterior subcapsular cataract (PSC) formation and expression of t
20 cities formed during recovery from posterior subcapsular cataract (PSC) in Royal College of Surgeons
21 presence of cortical, nuclear, or posterior subcapsular cataract (PSC) opacification in at least one
23 ty, except for variable mild local posterior subcapsular cataract and local retinal toxicity with hig
25 95% CI, 1.27-2.87; P = 0.002); and posterior subcapsular cataract increase of 5% or more versus less
27 ers (OR, 1.28; 95% CI, 0.79-2.08); posterior subcapsular cataract occurred in 3.0% of statin users an
29 act, 1.95 (95% CI: 0.48, 7.95) for posterior subcapsular cataract, 1.82 (95% CI: 0.91, 3.66) for soft
30 95% CI, 0.78-1.65; P = 0.519); and posterior subcapsular cataract, 3.05 (95% CI, 1.79-5.19; P < 0.001
31 The associations of lens features (posterior subcapsular cataract, nuclear color, nuclear white scatt
32 .82, 95% CI: 0.68, 0.97; primarily posterior subcapsular cataract, RR = 0.90, 95% CI: 0.71, 1.13).
33 ear white scatter, cortical spokes, anterior subcapsular cataract, vacuoles, waterclefts, coronary fl
36 es regarding the pathophysiology of anterior subcapsular cataracts secondary to posterior chamber pIO
38 ar incident nuclear, cortical, and posterior subcapsular cataracts, but was related to incident catar
44 al dominant "progressive childhood posterior subcapsular" cataracts segregating in a white family to
46 is triggered by the interaction of bacterial subcapsular components and bone marrow-derived DC (likel
48 th hydrocortisone induced both medullary and subcapsular cortical TE cells to express CK6, a differen
49 gitidis and that in each case, the bacterial subcapsular domain markedly influences the Ig response t
51 mains unresolved whether different bacterial subcapsular domains can exert differential effects on PS
52 sues, high endothelial venules and basal and subcapsular epithelia are CD164 class II-positive, while
53 le negative thymoctyes and laminin 5 made by subcapsular epithelial cells is required for the surviva
55 differentiating fibers of the bow region and subcapsular fibers of the central zone, whereas the lens
56 oneal implants, intratumoral hemorrhage, and subcapsular fluid, showed a significant association with
58 icities of these two important streptococcal subcapsular group polysaccharides to fully understand th
60 s, ureteropelvic junction obstruction, renal subcapsular hematoma, cholelithiasis, medullary calcinos
64 l vascular abnormalities, including aberrant subcapsular hepatic veins, enlarged glomeruli, intestina
65 murine model of chronic kidney disease, with subcapsular hydrogel injections acting as a delivery dep
66 aft model of kidney cancer, characterized by subcapsular implantation of Caki-1 clear cell human kidn
68 ix pancreatic cancer cell lines and a spleen subcapsular inoculation nude mouse model were also used.
71 ll to glucose challenge, comparable to renal subcapsular islet grafts, despite a marginal islet dose,
72 4 to prevent recurrence of diabetes in renal subcapsular islet isografts in DR-BB (RT1uu) rats with e
76 onsive (>120 days) Lewis recipients of renal subcapsular islets underwent nephrectomy of the islet be
80 receptor CCR7 for their transition from the subcapsular lymph node sinus into the parenchyma, a migr
83 d.HGF-transduced NHP islets in vivo, a renal subcapsular marginal mass islet transplant model was dev
87 anticipated from earlier studies, posterior subcapsular, nuclear, and cortical cataracts were associ
88 d to UVB exhibited accelerated anterior lens subcapsular opacification, which was more pronounced in
91 d cortical opacities as grade > or = 0.5 and subcapsular opacities as grade > or =0.3 of the Lens Opa
93 tations, 2 eyes had progression of posterior subcapsular opacities, although neither required surgery
94 graded for nuclear, cortical, and posterior subcapsular opacities, and the amount of liquid vitreous
95 iring nearwork, nuclear opacities, posterior subcapsular opacities, glaucoma, and ocular hypertension
96 tical opacity as grade >/=1.0, and posterior subcapsular opacity as grade >/=0.5 according to the Len
97 OL showed either stage 5 (complete posterior subcapsular opacity) or stage 6 (mature) cataracts, wher
99 (OR, 1.57; 95% CI, 1.13-2.20) and posterior subcapsular (OR, 1.73; 95% CI, 1.10-2.72) cataract, but
100 stant cell renewal, involving recruitment of subcapsular progenitors to ZG fate and subsequent lineag
101 graded for nuclear, cortical, and posterior subcapsular (PSC) cataract, following the Wisconsin Cata
102 presence of nuclear, cortical, or posterior subcapsular (PSC) cataract, from standardized grading of
106 entage involvement of cortical and posterior subcapsular (PSC) lens opacities within the central 5 mm
107 viduals with nuclear, cortical, or posterior subcapsular (PSC) opacities and individuals with no cata
108 ens for presence of nuclear (NSC), posterior subcapsular (PSC), and cortical cataract (CC), using the
109 tes assemble in clusters in the cords of the subcapsular red pulp and are distinct from macrophages a
111 nsplanted, but most biopsies sample only the subcapsular region and may not accurately represent the
116 onized by newly produced antibodies from the subcapsular region to the germinal center, and affinity
118 a predominance of sclerosis in the kidney's subcapsular region, the area predominantly sampled by th
122 elop cataracts in the anterior and posterior subcapsular regions as well as punctate opacities in the
123 n DCs from the early stage in the lymph node subcapsular regions, and COX-2 inhibition markedly suppr
124 lant survival and blood glucose control in a subcapsular renal graft model in immuno-incompetent diab
126 tain innate-like lymphocytes that survey the subcapsular sinus (SCS) and associated macrophages for p
127 CD169+MHCII+ macrophages on the floor of the subcapsular sinus (SCS) and in the medulla of lymph node
129 inate via lymphatics and preferentially bind subcapsular sinus (SCS) CD169(+) macrophages in tumor-dr
130 ) alpha1beta2, which maintained a protective subcapsular sinus (SCS) macrophage phenotype within viru
131 were found associated with CD169(+)-positive subcapsular sinus (SCS) macrophages and collagen fibers.
133 y than naive T cells, relocalized toward the subcapsular sinus (SCS) near invaded macrophages, and en
134 b(+)CD169(+) macrophages, which populate the subcapsular sinus (SCS) of LNs, are critical for the cle
135 in-water emulsion adjuvant MF59 localizes in subcapsular sinus and medullary macrophage compartments
136 Our findings identify macrophages lining the subcapsular sinus as an important site of B cell encount
137 , small numbers of beads were present in the subcapsular sinus as early as 6 h after inhalation.
140 ng by lymphatic endothelial cells lining the subcapsular sinus ceiling stabilizes interfollicular CCL
141 borne antigens and chemoattractants from the subcapsular sinus directly to the B cell follicles.
142 ure that macrophages of the mouse lymph node subcapsular sinus facilitate B cell activation in vivo b
143 broblastic reticular cells that connects the subcapsular sinus floor and the HEVs by intertwining wit
145 t contain the unprocessed Ag are captured by subcapsular sinus macrophages and are transferred onto f
146 resulting from S. flexneri interactions with subcapsular sinus macrophages and dendritic cells, and r
147 By contrast, large antigens were bound by subcapsular sinus macrophages and subsequently transferr
149 cate that NK-cell recruitment is mediated by subcapsular sinus macrophages, IFN-gamma, and CXCR3 duri
150 acquisition did not require dendritic cells, subcapsular sinus macrophages, or B cell movement to the
154 s (Mo) and B cell areas in the spleen and to subcapsular sinus Mo in lymph nodes of naive mice (CR-Fc
155 ymph node, exosomes were not retained in the subcapsular sinus of CD169(-/-) mice but penetrated deep
156 cells were identified in the paracortex and subcapsular sinus of the draining internal iliac lymph n
159 in the DLN, most of the LPS was found in the subcapsular sinus or medulla, near or within lymphatic e
160 antigens diffuse directly from lymph in the subcapsular sinus to be acquired by antigen-specific B c
163 luding chemokines, traveled rapidly from the subcapsular sinus to the HEVs using the reticular networ
164 njection, first in the region closest to the subcapsular sinus where lymph enters the lymph node.
165 endothelial cells lining the ceiling of the subcapsular sinus, but not those lining the floor, expre
166 luorophore-labeled molecules highlighted the subcapsular sinus, the reticular fibers, and the ablumin
176 In addition, the spatially limited renal subcapsular site restricts the mass of islet tissue that
178 st, porcine islets transplanted to the liver subcapsular space do not survive, although autologous is
179 2500, were transplanted into the left renal subcapsular space of a syngeneic adult mouse made diabet
180 -2d) islets were transplanted into the renal subcapsular space of diabetic c-Rel-/- C57BL/6 (H-2b) mi
181 ncreatic islets of Langerhans into the renal subcapsular space of immunodeficient BALB/c.rag2(-/-).cg
182 regeneration of prostatic structures in the subcapsular space of the kidney was observed within 4-8
183 ically, its expression was restricted to the subcapsular space of the LN during early inflammation, w
184 mokidney by thymic autografting to the renal subcapsular space results in normal thymic growth and fu
186 n as few as 10 islets implanted in the renal subcapsular space, intrahepatic, intraabdominal, and sub
189 sorganized TEBs characterized by exaggerated subcapsular spaces, breaks in basal lamina, dissociated
190 These results suggest the presence of common subcapsular surface antigens, such as outer membrane pro
195 fat planes obscured, retroperitoneal fluid (subcapsular vs extracapsular), ascites beyond the cul-de
196 tes downregulate CCR9 and migrate toward the subcapsular zone where they recombine their TCR beta-cha
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