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1 cathelicidin-related antimicrobial peptide (CRAMP).
2 mice genetically defective in production of CRAMP.
3 epsis by LzMPC treatment required endogenous CRAMP.
4 ent the penetration of the inner membrane by CRAMP.
5 of FPRL1/mouse formyl peptide receptor-2 by CRAMP.
6 ystonias, including torticollis and writer's cramp.
7 tor tasks that elicited dystonia or writer's cramp.
8 e in the patients with dystonia and writer's cramp.
9 cally inhibit S. aureus killing by synthetic CRAMP.
10 by enhanced expression of beta-defensins and CRAMP.
11 not been previously investigated in writer's cramp.
12 oth the CCR2 ligand CCL2 and an Fpr2 agonist CRAMP.
13 ficient sleep time or nocturnal leg jerks or cramps.
14 include bloody diarrhea and severe abdominal cramps.
15 tools with fever, prostration, and abdominal cramps.
16 women, is characterized by painful menstrual cramps.
17 villous blunting that leads to diarrhea and cramping.
18 somotor symptoms (0.96 vs 0.85, P<.001), leg cramps (1.10 vs 0.91, P<.001), and bladder control sympt
19 had nausea (20 [30%] vs 4 [6%]) and stomach cramps (15 [23%] vs 2 [3%]) more often than those receiv
23 ted nausea (95%), dizziness (72%), abdominal cramps (58%), headache (52%), vomiting (51%), chills (48
26 Patients reported diarrhea (100%), abdominal cramps (93%), fever (93%), bloody stools (72%), and vomi
28 h staphylocidal activities demonstrated that CRAMP, a cationic antimicrobial peptide, is primarily re
29 luate further the expression and function of CRAMP, a peptide corresponding to the predicted COOH-ter
30 but at the expense of symptoms that include cramping abdominal pain, fecal urgency, and diarrhea.
32 lectron microscopy that the primary locus of CRAMP activity appears to be intracytoplasmic, rather th
35 to cathelin-related anti-microbial peptide (CRAMP), an anti-microbial peptide expressed at high leve
36 t in cathelin-related antimicrobial peptide (CRAMP; an ortholog of the sole human cathelicidin, LL-37
38 bduction movements in patients with writer's cramp and compared them with those of normal aged-matche
39 e further identified increased expression of Cramp and formation of neutrophil extracellular traps in
40 amellar body-derived antimicrobial peptides, CRAMP and mBD3, declined after Ox challenges, parallelin
42 mplicated in the pathophysiology of writer's cramp and other primary dystonias, endogenous dopamine r
49 of inhibitors that extend from the polar and cramped (and so not easily druggable) substrate-binding
50 the antimicrobial peptides beta-defensin 3, CRAMP, and chemokine CXCL10 and its receptor CXCR3 in co
52 oms of frequency, nocturnal bowel movements, cramping, and bleeding returned close to baseline values
57 ecological problems, vasomotor symptoms, leg cramps, and bladder control problems, whereas women in t
60 , one characterized by exercise intolerance, cramps, and myoglobinuria, and the other dominated by fi
61 elevated CK levels, muscle weakness, muscle cramps, and persistent myalgia and CK elevations after s
64 cathelicidin-related antimicrobial peptide (CRAMP), are important effectors of the innate immune sys
66 ed in middle life with incapacitating muscle cramps associated with calf hypertrophy and only mild cl
70 ion in patients with arthritis and menstrual cramps, but they have not provided any benefit to patien
71 concentrations of human (LL-37) and murine (CRAMP) cathelicidins, human alpha-defensin (HBD-1, HBD-2
72 e of antimicrobial human (LL-37) and murine (CRAMP [cathelin-related antimicrobial peptide]) cathelic
74 DBS treatment of tardive dystonia, writer's cramp, cranial dystonia, myoclonus dystonia, and off-sta
75 oprotein E-deficient mice, pDC depletion and Cramp-deficiency in bone marrow reduced atherosclerosis
79 yed early neutrophil influx were observed in CRAMP-deficient mice infected with Pseudomonas aeruginos
80 evident as early as 1 hour after infection, CRAMP-deficient mice showed no baseline alterations in i
81 n was delayed early but increased by 48 h in CRAMP-deficient mice, which was associated with enhanced
84 ne marrow chimera experiments indicated that CRAMP derived from bone marrow cells rather than structu
85 dmitted to the hospital because of abdominal cramping, diarrhea, hematochezia, fever to a peak temper
88 be stimulated to produce interferon-alpha by Cramp/DNA complexes, and we further identified increased
89 that the murine mature cathelicidin peptide (CRAMP), encoded by the mouse gene (Camp), is functionall
92 tase-polymerase chain reaction also detected CRAMP expression in adult testis, spleen, stomach, and i
93 l ligation and puncture caused a decrease in CRAMP expression in the liver, whereas enteral administr
95 yokymia, neuromyotonia, Isaacs' syndrome and Cramp-Fasciculation Syndrome to describe the motor manif
96 1 had significantly (P < .05) more abdominal cramps, fatigue, transient hearing loss, febrile neutrop
101 , mBD4 (short interfering RNA knockdown), or CRAMP (genetic knockout) exhibited enhanced disease seve
106 rine cathelin-related antimicrobial peptide (CRAMP) has been reported to inhibit S. Typhimurium growt
107 tients with task-specific dystonia (writer's cramp) have impaired cortical inhibition likely arising
108 n of cathelin-related antimicrobial peptide (CRAMP; human LL-37 orthologue), and mouse beta defensin
112 lapse of symptoms such as abdominal pain and cramping in patients with irritable bowel syndrome.
113 erved except for mild diarrhea and abdominal cramping in the infusion group on the infusion day.
114 city was grade 3/4 diarrhea and/or abdominal cramps in six of 12 patients treated at 24 mg/m(2), desp
115 idin cathelin-related antimicrobial peptide (CRAMP) in a murine model of Fusarium solani keratitis.
116 cathelicidin-related antimicrobial peptide (CRAMP) in macrophages and enhanced bactericidal activity
117 l-derived cathelicidins (human: LL37, mouse: CRAMP) induce adhesion of classical monocytes but not of
122 aken together, our findings demonstrate that CRAMP is an important contributor to effective host muco
124 by permeability barrier requirements and (2) CRAMP is required for permeability barrier homeostasis.
126 um toxin is clinically effective in writer's cramp, it does not reverse the associated dysfunction of
127 ccinia pox formation occurred in four of six CRAMP knockout animals and in only one of 15 control mic
131 ased expression of the antimicrobial peptide Cramp/LL37 in atherosclerotic lesions may thus stimulate
134 xel-based results also suggest that writer's cramp may be associated with reduced striatal dopamine r
135 findings suggest that patients with writer's cramp may have divergent responses in striatal dopamine
136 BD-3 production ex vivo and was required for CRAMP, mBD-3, and mBD-14 expression in response to S. au
137 to Fpr2(-/-) mice, in the inflamed airway of CRAMP(-/-) mice, DC trafficking into the peribronchiolar
138 espite an apparent increase in mBD3 protein, CRAMP-/- mice delayed permeability barrier recovery, att
142 and cathelin-related antimicrobial peptide (CRAMP) (murine homologues of hBD2 and LL-37, respectivel
144 erse events attributed to X-82 including leg cramps (n = 2), elevated alanine aminotransferase (n = 2
146 ed rotation and multiple pulse spectroscopy (CRAMPS) NMR spin exchange measurements in combination wi
148 zol--elevated liver-enzyme levels and muscle cramps--of grade 2 or less occurred in 41% and 33% of th
150 scle, causing exercise intolerance, myalgia, cramps, or fixed weakness, which often affects extraocul
152 patients with fever and abdominal symptoms (cramping, pain, distention, diarrhea, GI bleeding), shou
154 reased serum creatinine level, insomnia, leg cramps, paresthesias, and tremor, were managed with dose
157 ians; repetitive tasks, prolonged or awkward/cramped positions, and bending/twisting were contributor
158 the same task repeatedly, working in awkward/cramped positions, working in the same position for long
162 ccommodated in the shallow and comparatively cramped recognition pocket; it has fewer hydrogen bondin
163 eletal muscle, causing exercise intolerance, cramps, recurrent myoglobinuria, or fixed weakness, whic
165 The human and mouse cathelicidins (LL-37 and CRAMP, respectively) are expressed at select epithelial
168 nd unaffected hand in patients with writer's cramp showed significantly less reduction in 20- to 30-H
169 e side chains and that confined movements of cramped side chains within and through the tunnel fine-t
170 In atherosclerotic aortas, we could detect CRAMP specifically in neutrophils, but not in monocytes
171 n (CPE) is responsible for the diarrheal and cramping symptoms of human C. perfringens type A food po
173 of increasingly severe neuropathic pain and cramps that have been poorly responsive to a variety of
174 Cathelin-related antimicrobial peptide (CRAMP), the orthologue of human cathelicidin/LL-37, is t
175 ic GI symptoms (eg, gas, diarrhea, abdominal cramping), there were no significant differences between
176 enty-five patients (89%) experienced pain or cramps/tired muscles, whereas 3 (11%) remained symptom-f
178 lly, simultaneous administration of OVA with CRAMP to mice promoted both humoral and cellular Ag-spec
179 both Mig-14 and VirK inhibit the binding of CRAMP to Salmonella, and demonstrate that Mig-14 is an i
180 cathelicidin-related antimicrobial peptide (CRAMP), to innate mucosal immunity in a mouse model of G
181 atients with torticollis, nine with writer's cramp, two with blepharospasm and 16 healthy control sub
182 ns, the anti-microbial activity of LL-37 and CRAMP was determined against the common wound pathogen g
185 ed rotation and multiple pulse spectroscopy (CRAMPS), water adsorption, and nitrogen measurements rev
187 ors reported more musculoskeletal stiffness, cramps, weakness and joint swelling (P < .001), cataract
188 oss-correlograms from patients with writer's cramp were either flat or modulated by a 11-12-Hz tremor
189 these antimicrobial peptides, and LL-37 and CRAMP were rapidly cleaved by released amebic cysteine p
192 ases, except the mouse antimicrobial peptide CRAMP, which we speculate works in part by inhibiting cy
193 control subjects and patients with writer's cramp while they write a stereotyped word repetitively a
194 or a mouse macrophage antimicrobial peptide (CRAMP), while SodCI remained tethered within the peripla
195 r acute effects included diarrhea and muscle cramping, while with repeated dosing, anorexia and fatig
197 logy of two idiopathic focal dystonias: hand cramp with excessive cocontractions of agonist and antag
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