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1 Twelve patients were cachectic.
2 population, 16% of patients were found to be cachectic.
3 within 2 weeks) developed ascites and became cachectic.
5 eart failure (CHF), classified clinically as cachectic (8% to 35% weight loss over > or = 6 months be
11 s (mean age, 61.9+/-10.9 years; 95% male; 25 cachectics) and 24 age-matched normal subjects (mean age
16 l compared EPA diethyl ester with placebo in cachectic cancer patients for effects on weight and lean
17 he 24K material was also present in urine of cachectic cancer patients, but was absent from normal su
18 2 on the alpha-subunit in skeletal muscle of cachectic cancer patients, which would lead to muscle at
24 Plasma leptin levels are elevated in non-cachectic CHF, suggesting the possibility that leptin mi
28 rogeroid features, including short lifespan, cachectic dwarfism, lordokyphosis, cataracts, loss of su
34 The 24-kDa peak may be identified as the cachectic factor, a glycoprotein, whereas the peak at 67
35 o and in vivo models of muscle wasting, that cachectic factors are remarkably selective in targeting
38 stent and increased kidney production of pro-cachectic factors, combined with a lack of kidney cleara
39 ion and elevated blood levels of soluble pro-cachectic factors, including activin A, directly linking
41 an and cellular-level functional deficits in cachectic hearts outside of the catabolic in vivo enviro
44 more, Pax7 was induced by serum factors from cachectic mice and patients, in an NF-kappaB-dependent m
45 so declined in Tibialis Anterior muscle from cachectic mice bearing murine colon adenocarcinoma or hu
46 induced chronic cachexia model revealed that cachectic mice develop perivascular fibrosis in major me
47 ock myostatin pathway signaling in normal or cachectic mice leads to hypertrophy or prevention of mus
53 e results suggest that UBR2 up-regulation in cachectic muscle is mediated by the p38beta-C/EBPbeta si
57 of this pathway (that is, SDF1 or CXCR4) in cachectic muscles increased the fiber area by 20%, prote
58 whose expression is specifically altered in cachectic muscles of Yoshida hepatoma-bearing rodents bu
59 ed SIRT1 loss induced NF-kappaB signaling in cachectic muscles that enhanced the expression of FOXO t
62 was found to have a stronger correlation to cachectic organ volume loss than tumor volume, giving su
63 he ergoreflex was particularly overactive in cachectics (P<0.05), accompanied by marked muscle mass d
66 ion are increased in both morbidly obese and cachectic patients compared with normal-weight recipient
67 not increased in morbidly obese patients but cachectic patients had a significantly lower incidence o
69 control subjects and noncachectic patients, cachectic patients had reduced plasma sodium and increas
74 th factor-I (IGF-I) axis were compared in 21 cachectic patients with CHF, 51 noncachectic patients an
75 Shortened survival applies particularly to cachectic patients with localized disease, thereby reinf
76 3B gradually increased from precachectic to cachectic patients, without differences in E3 ubiquitin
86 y was seen at 30 days for morbidly obese and cachectic recipients (12.7% and 17.7%, respectively) ver
89 s underlying mitochondrial remodeling in the cachectic skeletal muscle, through an integrative explor
96 L-1alpha, IL-1beta, and TNFalpha can mediate cachectic states, how these molecules affect energy expe
98 e N-end rule pathway that is up-regulated by cachectic stimuli including proinflammatory cytokines an
99 -1alpha is elevated in the sera and liver of cachectic, suggesting a mechanism by which chronic IL-1R
102 S) confirmed the high tCho level observed in cachectic tumors that occurred because of an increase of
103 to identify metabolic signatures typical of cachectic tumors, using this information to analyze the