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1 ed to study the effect of Pitx2 depletion on extraocular muscle.
2 d receptor (PPAR)gamma were more abundant in extraocular muscle.
3 ase were only approximately 2-fold higher in extraocular muscle.
4 drug treatments to strengthen an underacting extraocular muscle.
5 as means of pharmacologically weakening the extraocular muscle.
6 gents that weaken and strengthen the treated extraocular muscle.
7 ated for patients with total paralysis of an extraocular muscle.
8 rhodamine-phalloidin, as does the zebrafish extraocular muscle.
9 system in association with the medial rectus extraocular muscle.
10 to all en plaque and en grappe endplates of extraocular muscle.
11 al extension of intramuscular haemangioma of extraocular muscle.
12 ismus, possibly by altering vergence tone in extraocular muscle.
13 ative image of the motor command sent to the extraocular muscles.
14 tly remodel the proximal segment of juvenile extraocular muscles.
15 f oculomotor axons to innervate their target extraocular muscles.
16 iation of the myogenic regulatory cascade in extraocular muscles.
17 phogenesis and gene expression in developing extraocular muscles.
18 by an outer mechanism driven by the oblique extraocular muscles.
19 imum [Ca2+]i and force significantly more in extraocular muscles.
20 sis that mitochondria serve as Ca2+ sinks in extraocular muscles.
21 educed muscle fiber diameters within treated extraocular muscles.
22 ic response of oculomotor nuclei to abnormal extraocular muscles.
23 issue biopsy for lesions not confined to the extraocular muscles.
24 motor nucleus, and contractility of isolated extraocular muscles.
25 related to the pattern of innervation of the extraocular muscles.
26 velopmental decision regions close to target extraocular muscles.
27 in patients with total paralysis of multiple extraocular muscles.
28 orbital inflammation primarily involving the extraocular muscles.
29 nd their corresponding alpha motoneurons and extraocular muscles.
30 lities result from myopathic fibrosis of the extraocular muscles.
31 omosome 12-linked congenital fibrosis of the extraocular muscles.
32 at they determine functional origins for the extraocular muscles.
33 luding dual or accessory muscle slips of the extraocular muscles.
34 ients (22/28 orbits) had enlargement of some extraocular muscles.
35 portion of slow fibers at birth, such as the extraocular muscles.
36 ar motor neurons and/or their innervation of extraocular muscles.
37 lmoplegia involving progressive paralysis of extraocular muscles.
38 plicating primary involvement of the oblique extraocular muscles.
39 ectivity between cranial motor axons and the extraocular muscles.
40 sessment of the pathophysiological status of extraocular muscles.
41 commonly affect the optic nerve, retina, and extraocular muscles.
42 GLUT1 and GLUT4 were detectable in extraocular muscles.
43 ated upstream activator of myogenesis in the extraocular muscles.
44 lability of substrate for energy pathways in extraocular muscles.
45 regulates [Ca2+]i and production of force in extraocular muscle; (2) mitochondrial content correlates
47 ated or syndromic congenital fibrosis of the extraocular muscles, a form of complex congenital strabi
48 uired at several steps in the development of extraocular muscles, acting first as an anti-apoptotic f
49 er candidates, including pulleys that affect extraocular-muscle action and the role of nasally biased
50 ults are consistent with the hypothesis that extraocular muscle afferent signals provide a feedback s
51 common singly-innervated muscle fiber (SIF), extraocular muscles also contain multiply-innervated mus
52 genetic locus for congenital fibrosis of the extraocular muscle, an autosomal dominant muscular dystr
53 All three Pitx2 isoforms were expressed by extraocular muscle and at higher levels than in other st
54 , slow-tonic MyHC and EOM-MyHC expression in extraocular muscle and its absence leads to increased ex
56 C are expressed in and around the developing extraocular muscles and cause growth cone collapse of oc
58 trophic factors strengthen juvenile maturing extraocular muscles and gain insight into mechanisms of
59 onance imaging revealed marked hypoplasia of extraocular muscles and intraorbital cranial nerves.
60 increases the dynamic response range of the extraocular muscles and matches metabolic demand to supp
62 uria, or fixed weakness, which often affects extraocular muscles and results in droopy eyelids (ptosi
63 amps, or fixed weakness, which often affects extraocular muscles and results in droopy eyelids (ptosi
64 ere detected in the posterior regions of the extraocular muscles and the connective tissues of the ex
65 cts of ocular motility are properties of the extraocular muscles and their associated connective tiss
66 The study of the oculomotor periphery, the extraocular muscles and their orbital attachments, is un
68 tion, and survival, leading to craniofacial, extraocular muscle, and ocular developmental abnormaliti
72 ted muscle fibers (MIFs) are peculiar to the extraocular muscles as they are non-twitch but produce a
74 fied five parameters of the superior oblique extraocular muscle at 2 weeks of age: contractile force,
77 eries with a minimum 50 patients; evaluating extraocular muscle BTXA injection for initial or repeat
79 sorder caused by aberrant innervation of the extraocular muscles by axons of brainstem motor neurons.
80 reported to cause congenital fibrosis of the extraocular muscles, c.1228G>A results in a TUBB3 E410K
81 (CN3) and applied to congenital fibrosis of extraocular muscles (CFEOM) and congenital oculomotor pa
82 ing of two CCDDs, congenital fibrosis of the extraocular muscles (CFEOM) and Duane retraction syndrom
83 egia, and include congenital fibrosis of the extraocular muscles (CFEOM) and Duane syndrome (DURS).
85 e classic form of congenital fibrosis of the extraocular muscles (CFEOM1) are born with bilateral pto
86 all three age groups in the Pitx2-deficient extraocular muscle compared with littermate controls.
93 Pitx2) is known to regulate the formation of extraocular muscle development and in this report we sho
94 comparable upstream factors required during extraocular muscle development have not been identified.
96 355 patients (81.1%, n = 355/438) had their extraocular muscles disinserted during surgery, with the
97 nd additional proteomic data, establish that extraocular muscle does not constitute a distinctive mus
100 e, especially in the presence of ipsilateral extraocular muscle enlargement, sinus disease, or focal
101 mably is the basis for the broad spectrum of extraocular muscle (EOM) contractile properties in drivi
104 graphy (AS-OCT) in measuring the distance of extraocular muscle (EOM) insertion to the limbus to impr
108 e quantitative measures of horizontal rectus extraocular muscle (EOM) morphology to determine the mag
112 ic resonance imaging (MRI) was used to study extraocular muscle (EOM) responses to head tilt in HTDHT
113 direct injection of ricin-mAb 35 into rabbit extraocular muscle (EOM) results in significant muscle l
114 re correlated with MRI studies demonstrating extraocular muscle (EOM) size, location, contractility,
115 mutation and MRI findings that demonstrated extraocular muscle (EOM) size, location, contractility,
116 ated that prolonged exposure of adult rabbit extraocular muscle (EOM) to insulin-like growth factor-1
117 es were analyzed quantitatively to determine extraocular muscle (EOM) volume, maximum diameter, and l
119 ative muscle classes, limb, masticatory, and extraocular muscle (EOM), in adult mice by high-density
126 erve as functional mechanical origins of the extraocular muscles (EOMs) and are normally stable relat
127 onance imaging (MRI) was used to demonstrate extraocular muscles (EOMs) and associated motor nerves i
128 ed magnetic resonance imaging (MRI) to study extraocular muscles (EOMs) and nerves in Duane-radial ra
130 n freshly dissected and cryosectioned rectus extraocular muscles (EOMs) and tibialis anterior (TA) mu
133 ness of almost all skeletal muscles, whereas extraocular muscles (EOMs) are comparatively spared.
137 ial DNA (mtDNA) defects were investigated in extraocular muscles (EOMs) collected from individuals co
143 e lateral rectus (LR) and medial rectus (MR) extraocular muscles (EOMs) have largely nonoverlapping s
144 mmon treatment for motility disorders of the extraocular muscles (EOMs) is a resection procedure in w
145 tramuscular innervation of horizontal rectus extraocular muscles (EOMs) is segregated into superior a
147 dings are nerve specializations found in the extraocular muscles (EOMs) of mammals, including primate
150 studies have shown that direct injection of extraocular muscles (EOMs) with insulin growth factor or
151 ry nerve terminal elimination at synapses in extraocular muscles (EOMs), a specialized set of muscles
152 sue structures constrain paths of the rectus extraocular muscles (EOMs), acting as pulleys and servin
153 Here, we investigated the morphogenesis of extraocular muscles (EOMs), an evolutionary conserved cr
154 l of compartmentalization in all four rectus extraocular muscles (EOMs), evidence was sought of possi
162 Populations of mature myofibers from all six extraocular muscles express N-CAM homogeneously on their
163 reported to have congenital fibrosis of the extraocular muscles, facial weakness, developmental dela
164 pothesis that there is greater complexity to extraocular muscle fiber types than the traditional desc
167 ous trophic factors regulate and/or maintain extraocular muscle force through a rapid mechanism that
168 fibers may either provide resistance against extraocular muscle forces or limit globe axial elongatio
171 h sensory-induced strabismus, innervation to extraocular muscles from motor nuclei produce the inappr
174 Modulation of Pitx2 expression can influence extraocular muscle function with long-term therapeutic i
175 nd in the multiply innervated slow fibers of extraocular muscle, gamma subunit expression persists in
177 ture; to date there are no reported cases of extraocular muscle haemangiomas extending into the brain
179 stablished several years ago that the rectus extraocular muscles have connective tissue pulleys, rece
180 al nerves grow toward, and connect with, six extraocular muscles in a stereotyped pattern, to control
181 (CT1) are known to increase the strength of extraocular muscles in adult and embryonic animals, but
182 Because of the exclusive involvement of the extraocular muscles in Graves' ophthalmopathy, the absen
184 lity of the rectus and superior oblique (SO) extraocular muscles in hypertropic and hypotropic eyes w
187 ng group in whom greater manipulation of the extraocular muscles inevitably occurs, are consistent wi
190 ubtypes, suggesting a potential link between extraocular muscle innervation, co-contraction, and corn
192 thorough clinical examination and imaging of extraocular muscle insertions on the Swept Source Anteri
193 eoperations based on preoperative imaging of extraocular muscle insertions, and whether the Anterior
197 7 patients with orbital metastasis, 5 showed extraocular muscle involvement with restricted ocular mo
200 in retinal pigment epithelium, optic nerve, extraocular muscle, iris, ciliary body, cornea, and seve
201 Ca2+ sinks; and (3) mitochondrial content in extraocular muscle is determined by the transcription fa
207 amount of residual function of the affected extraocular muscles is essential to determine which surg
208 tested the hypothesis that glucose uptake by extraocular muscles is not regulated by insulin or contr
210 y-induced strabismus, central innervation to extraocular muscles is responsible for setting the state
213 th the different loads and usage patterns of extraocular muscle layers, as proposed in the active pul
216 (AL) on globe rotational axis and horizontal extraocular muscle leverage during horizontal duction.
218 nversus syndrome, congenital fibrosis of the extraocular muscles, lymphedema-distichiasis syndrome, n
219 nition of the regulation of MyHC isoforms in extraocular muscle may allow their rational manipulation
221 risk factors for congenital fibrosis of the extraocular muscles, may play a role in SOP and conseque
222 Activity of complexes I and IV was lower in extraocular muscle mitochondria (approximately 50% the a
225 States 3, 4, and 5 respiration rates in extraocular muscle mitochondria were 40% to 60% lower th
227 of insulin-like growth factor II (IGF-II) on extraocular muscle morphometry and force generation were
231 t animals' (16 and 20 to 21 days) RPE and in extraocular muscle of a 16-day-old untreated mutant.
232 nalysis of triceps surae (a limb muscle) and extraocular muscles of adult male Sprague-Dawley rats.
234 Direct injection of ricin-mAb 35 into the extraocular muscles of rabbits results in a dose-related
235 M, was assessed immunohistochemically in the extraocular muscles of rabbits, monkeys, and humans to e
238 which the plant responds to neural drive to extraocular muscles on exclusively short, subsecond time
240 brachytherapy, type of strabismus developed, extraocular muscles operated, and modality of treatment
242 ll musculature, as well as the diaphragm and extraocular muscles, originate from MyoD+ progenitors.
246 bulbar anesthesia for cataract extraction is extraocular muscle paresis/restriction and is unique to
248 Pitx2 is important in maintaining the mature extraocular muscle phenotype and regulating the expressi
252 al eye position information (efference copy, extraocular muscle proprioception, or both) that is used
256 rst time that neuromuscular junctions of the extraocular muscles (responsible for the control of eye
258 nts evidence that congenital fibrosis of the extraocular muscles results from an abnormality in the d
260 disorder is genetically distinct from other extraocular muscle-specific disorders such as congenital
261 endogenous and exogenous trophic factors on extraocular muscle strength and mass were examined in th
264 identified in the Pitx2(Deltaflox/Deltaflox) extraocular muscle, suggesting that altered innervation
265 al mitochondrial clumping are found in other extraocular muscles, suggesting that the muscle patholog
269 Patients confirmed to have a history of extraocular muscle surgery targeting AHP and complete se
270 ates long-term motor and sensory outcomes of extraocular muscle surgery targeting AHP in patients wit
272 ouplings facilitate implementation by rectus extraocular muscle suspensions of a commutative ocular m
275 oscopic study of the enthesis site-where the extraocular muscle tendon inserts onto the sclera-in nor
277 xistence of a common tendinous origin of the extraocular muscles, that is continuous with the skull b
280 , from the genetics of disorders that affect extraocular muscles to the way in which the cerebral cor
281 fugal projection, the retinal image, and the extraocular muscles, to obtain an integrated picture of
284 es in humans with congenital fibrosis of the extraocular muscles type 1 (CFEOM1) due to missense muta
285 ve been linked to congenital fibrosis of the extraocular muscles type 1 (CFEOM1), a dominant disorder
287 otility disorder "Congenital fibrosis of the extraocular muscles type 1" (CFEOM1) results from hetero
288 abnormalities in congenital fibrosis of the extraocular muscles type 3 (CFEOM3), a disorder resultin
289 s consistent with congenital fibrosis of the extraocular muscles type 3 (CFEOM3); 1 patient harbored
293 We also analyzed the expression profile of extraocular muscle, which is divergent from other skelet
295 e ability of sustained treatment of a single extraocular muscle with glial cell line-derived neurotro