戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ice leads to increased lipid droplet size in fat tissue.
2 ry effect of insulin on glucose transport in fat tissue.
3  addition Hmgic-/- mice have a deficiency in fat tissue.
4 pendent of the quantity of the LA periatrial fat tissue.
5 kine production systemically and in visceral fat tissue.
6 ing assay and indirect immunofluorescence on fat tissue.
7 extract could be used to induce lipolysis on fat tissue.
8 atic vessels within acutely inflamed orbital fat tissue.
9 e echogenicity of the surrounding mesenteric fat tissue.
10 es, which were filled with only subcutaneous fat tissue.
11 the exercise-induced browning effect on this fat tissue.
12 d diverse changes in alternative splicing in fat tissue.
13 ells and tumor invasion into the surrounding fat tissue.
14 de concentration in aqueous solutions and in fat tissue.
15 ation of lean mice with almost no detectable fat tissue.
16  features of growth regulation by the insect fat tissue.
17 fatty acids, enabling homeostasis of healthy fat tissue.
18  insulin insensitivity in muscle, liver, and fat tissues.
19 g the induction of brown adipocytes in white fat tissues.
20 he insulin receptor signalling in muscle and fat tissues.
21  Dm-dNK expression was low in both liver and fat tissues.
22 n the atypical growth of certain cancers and fat tissues.
23 ssed in the avian spleen, lung, kidneys, and fat tissues.
24 ssion of UCP1 and other thermogenic genes in fat tissues.
25  to suppress the actions of BMP4 on dorsally fated tissues.
26 for studying development of multiple cardiac-fated tissues.
27 ng acute infection, loss of body weight from fat tissue; a compensation period during which macaques
28 r adulthood but also showed markedly reduced fat tissue accumulation compared to their ob/ob litterma
29 ipocyte [Ad]-knockout [KO]) have a defect in fat tissue accumulation despite having larger lipid drop
30                                        Mouse fat tissue activin A increased with aging.
31 e endogenous brown fat, this synthetic brown fat tissue acts as a sink for glucose uptake, as determi
32 ns can directly influence the laying down of fat tissue (adiposity).
33 ally important to determine how hypertrophic fat tissue alters T cell balance to drive inflammation.
34 ess approximately twofold more TNFR2 mRNA in fat tissue and approximately sixfold more soluble TNFR2
35 increased adiponectin expression in visceral fat tissue and in serum.
36 es, lymphocytes, and macrophages in both the fat tissue and myocardium separately.
37 on in the kidneys, brain, heart, intestines, fat tissue and pancreas.
38 differentiation, increases with aging in rat fat tissue and preadipocytes.
39 activity increased twofold in the epididymal fat tissue and remained unchanged in muscle and liver of
40 strate that PTHrP mediates energy wasting in fat tissues and contributes to the broader aspects of ca
41 urces, including bone marrow, spleen, liver, fat tissues and the adventitia of the arterial wall.
42 t promotes inflammation in the kidney, lung, fat tissue, and elsewhere.
43 ater loss in body-mass index, abdominal fat, fat tissue, and lean tissue, compared with that in SIV-i
44 reased density of the surrounding mesenteric fat tissue, and mesenteric lymph nodes.
45 ll layer, distributed in the lung, heart and fat tissues, and was finally eliminated through the dial
46                             In the heart and fat tissue, ANP was reported to affect lipid peroxidatio
47 rinated biphenyls (PCB) measured in blood or fat tissue are associated with increased risk of NHL.
48 hysiological consequences of having no white fat tissue are profound.
49  aromatic characteristics of cell-cultivated fat tissue as a flavor enhancer for meat alternatives.
50 to thermogenic stimuli, peroxisomes in brown fat tissue (BAT) undergo selective remodeling and expand
51 egulate adipocytes and thereby contribute to fat tissue biology.
52  cell-autonomous function for Foxa3 in white fat tissue browning.
53  macaques lost a greater percentage of total fat tissue but had more subcutaneous-fat deposition than
54 Importantly, reduced expression of Thrap3 in fat tissue by antisense oligonucleotides (ASOs) regulate
55  cachexia and wasting of skeletal muscle and fat tissue by as yet poorly understood mechanisms.
56 e measured the quantity of the LA periatrial fat tissue by the area (millimeter square) and the quali
57 as a mediator of the side effects induced in fat tissues by chronic treatment with synthetic steroids
58 ug usage including measurements of abdominal fat tissue, cardiovascular health, and lipid metabolism
59  into background air, lung, soft-tissue, and fat tissue classes, followed by the assignment of predef
60 ed and mainly expressed in intestine, liver, fat tissues, colon, muscle, and heart, in the order of h
61 lls purified from Ebf2(GFP) embryos or brown fat tissue did not express myoblast or dermal cell marke
62 f leptin activity, is increased in CD36-null fat tissue disproportionately to leptin levels.
63  reveal variability in women's glandular and fat tissue distribution, suggesting that milk production
64 at cells as the stromal-vascular fraction of fat tissue does not contain adipoQ mRNA.
65 Grb10 determines the proportions of lean and fat tissue during development, thereby influencing energ
66 ges that shift activity away from regions of fat tissue during PET image reconstruction.
67 stance and metabolic syndrome accompanied by fat tissue dysregulation.
68 sgenic mice develop a selective abundance of fat tissue early in life, show marked adipose tissue inf
69 ent a method of producing bulk cell-cultured fat tissue for food applications.
70 e and versatile strategy to produce cultured fat tissue for food-related applications, thereby addres
71 the possibilities to harness immune cells in fat tissue for the treatment of chronic metabolic condit
72 minant-negative construct not only abrogated fat tissue formation but also reduced angiogenesis.
73 perimeter coverage was found with increasing fat tissue fraction at marrow cellularities between 50%
74                           Back and abdominal fat tissues from 11 adult emus were biopsied at four tim
75 evels were significantly lower in epididymal fat tissues from db/db and high fat diet-induced obese m
76 ory form of IRS-1 was observed in muscle and fat tissues from obese rats.
77  adipose-derived stem cells (ASCs) and whole-fat tissues from the abdominal subcutaneous fat of obese
78 , and highlight the use of explants to study fat tissue function in wildlife.
79 cesses contributing to regional variation in fat tissue function.
80 l as glucose and fat oxidation in muscle and fat tissue, gluconeogenesis in liver, and even glucose-r
81 and protein, adipocytes from mouse and human fat tissue had almost undetectable Thy1 levels.
82  The 3D fat tissues were visually similar to fat tissue harvested from animals, with matching texture
83 F1 in the regulation of energy metabolism in fat tissues; however, whether HSF1 is differentially exp
84 erestingly, Ebf2-expressing cells from white fat tissue in adult animals differentiated into brown-li
85  inhibitors in its complete elimination from fat tissue in hCETP transgenic mice as evident within 21
86 ligand Delta-like 4 (Dll4) in atheromata and fat tissue in LDL-receptor-deficient mice.
87 ect on WISP1 gene expression in subcutaneous fat tissue in overweight subjects who had undergone hype
88 x vivo activity of PDH in muscle, liver, and fat tissues in normal Sprague-Dawley rats.
89 re relative to their expression in the adult fat tissues in vivo, i.e. inguinal fat for white adipocy
90 that the juxtaposition of dorsal and ventral fated tissue in the eye leads to an enrichment of emc ex
91 , inflammation was associated with increased fat tissue index (P=0.01) and male gender (P=0.04).
92 e (r = 0.203), triceps skinfold (r = 0.197), fat tissue index (r = 0.150), serum insulin (r = 0.280),
93                                       Higher fat tissue index (whole-body multifrequency bioimpedance
94 ific-Tlr9-deficient mice exhibited increased fat tissue inflammation, weight gain, and impaired gluco
95                       In skeletal muscle and fat tissue, inositol phospholipid 3-kinase plays an inte
96  from BAT, inguinal fat, and retroperitoneal fat tissue interact with the CRE2 motif (CGTCA) in a spe
97  preparation and transformation of ASCs from fat tissue into mouse iPSCs in feeder-free conditions an
98    We also show that upon transplantation of fat tissue into these mice, triglyceride content in musc
99                             The expansion of fat tissue involves a complex interaction of endocrine f
100 Conclusions The quality of the LA periatrial fat tissue is an independent predictor of recurrence aft
101                         In humans, the brown fat tissue is composed of discrete depots found througho
102 r porcine adipocytes in 2D, after which bulk fat tissue is produced by mechanically harvesting and ag
103 mes (Kliposome/water), (iii) human abdominal fat tissues (KAFT/water) from seven individuals, and (iv
104 In each phantom, 0-3 additional 1.5-cm-thick fat tissue layers were added to derive 4 phantoms repres
105                 Adipogenesis and increase in fat tissue mass are mechanosensitive processes and hence
106               Adipoq(-/+) offspring had more fat tissue mass at both birth and adulthood.
107 showed that maternal obesity increased fetal fat tissue mass, with a significant elevation in fetal b
108 tenuated maternal obesity-induced high fetal fat tissue mass.
109  in mice and speculate that the reduction in fat tissue may negatively affect insulin sensitivity, as
110 esized that the quality of the LA periatrial fat tissue, measured by the mean computed tomography att
111 ng-term dietary interventions on pericardial fat tissue mobilization are sparse.We sought to evaluate
112 58/12%), wound infections (n = 45/9, 3%) and fat tissue necrosis (n = 41/8%).
113 ons; and patients' age, resection weight for fat tissue necrosis.
114 -3 activity did not change in the epididymal fat tissue of A/J mice, regardless of the type of diet t
115 of insulin resistance and type 2 diabetes in fat tissue of C57BL/6J mice, and implicate GSK-3 as a po
116      We have examined gene expression in the fat tissue of normal mice at the onset of diet-induced o
117 pididymal, retroperitoneal, and subcutaneous fat tissue of normal, but not of leptin-receptor-defecti
118 cant IR down-regulation was also observed in fat tissue of obese human subjects and in 3T3-L1 adipocy
119 dipogenic and lipogenic genes was altered in fat tissue of rats at 2 weeks and 2 months of age.
120 e mitochondrial uncoupling protein (UCP1) in fat tissues of A/J and C57BL/6J inbred strains of mice v
121 sion in the gonads, gizzard and subcutaneous fat tissues of chickens.
122  cultured mouse hepatocytes and in liver and fat tissues of diet-induced obese (DIO) mice and ob/ob m
123 E3B mRNA levels in heart and white and brown fat tissues of JCR:LA-cp rats revealed that PDE3B mRNA a
124  isolated MSCs from cardiac and subcutaneous fat tissues of mice with LVD 28 days after myocardial in
125  wk of thermal burn injury in the muscle and fat tissues of patients from the large-scale collaborati
126          Further, GPR30 expression levels in fat tissues of WT obese female mice were greatly increas
127 Thus, manipulations of NPY2R activity within fat tissue offer new ways to remodel fat and treat obesi
128 ngth; orbital, optic nerve (ON), and orbital fat tissue (OFT) volume; and implant position.
129 e has a much higher metabolic rate than does fat tissue, older individuals generally develop lower me
130                                              Fat tissue, overgrowing in obesity, promotes the progres
131 own fat, large differences occurred in white fat tissues, particularly in retroperitoneal fat.
132  quantity of the left atrial (LA) periatrial fat tissue predicts recurrence after catheter ablation o
133                                     Visceral fat tissue primarily consists of adipocytes that secrete
134 ell as level of TNF-alpha mRNA expression in fat tissue (r = 0.56, P < 0.001).
135                               White adipose (fat) tissues regulate metabolism, reproduction, and life
136         Adiponectin, a novel hormone made by fat tissue, regulates energy metabolism and endothelial
137                                              Fat tissue-related systemic inflammation acts as the lin
138 e depots and how its levels are regulated in fat tissues remain unclear.
139                                 Lipolysis in fat tissue represents a major source of circulating fatt
140           Transgenic expression of Prdm16 in fat tissue robustly induced the development of brown-lik
141 d 2,4-di-tert-butyl-phenol (DBP), in humans (fat tissues, serum, urine, breast milk, and fingernails)
142              Brown adipose tissue (BAT) is a fat tissue specialized in heat production (non-shivering
143                                 We generated fat tissue-specific adenosine A2AR KO mice to assess the
144  not 1866, treated cells isolated from white fat tissue (stromal vesicular fraction) produced the ant
145 levels of the pP65 protein in the epididymal fat tissue, suggesting less activation of the nuclear fa
146 activation of the sympathetic innervation of fat tissue, suppression of leptin, and a reduction in ca
147  levels are higher in brown and subcutaneous fat tissues than in those in the visceral depot and that
148 in metabolically more favorable hyperplastic fat tissue that contains an increased number of smaller
149  Brown adipose tissue (BAT) is a specialized fat tissue that is dedicated to thermoregulation.
150 ompared to controls, and were highest in the fat tissue; there was no significant difference in fibro
151 e generated a transgenic mouse with no white fat tissue throughout life.
152                                        Since fat tissue turns over throughout life, preadipocyte char
153 uticle imaging is due to the air sacs and/or fat tissue underneath the head cuticle.
154 uctures, closely resembling in vivo tissues (fat tissue, vasculature, etc.).
155 ISP1 expression in visceral and subcutaneous fat tissue was associated with markers of insulin resist
156 eptinemic and pair-fed animals, identifiable fat tissue was completely ablated only in the former gro
157 it TAF7, is enriched in adipocytes and white fat tissue (WAT) in mouse.
158 stin gene (Retn) expression is restricted to fat tissue, we identified an adipocyte-specific enhancer
159 nd expression profiling of developing murine fat tissues-we identified Atf4 as expressed in invertebr
160 significantly reduced the body weight, total fat tissue weight, and plasma lipid concentrations in th
161 effect on their food intake, body weight, or fat tissue weight.
162        The mechanical properties of cultured fat tissues were based on binder choice and concentratio
163                                       The 3D fat tissues were visually similar to fat tissue harveste
164 robed the APOA4 interactome in mouse gonadal fat tissue, where ApoA4 gene is not transcribed but APOA
165 order characterized by a paucity of adipose (fat) tissue which is evident at birth and is accompanied
166 n be used as an indicator of muscle mass and fat tissue, which are distributed differently in men and
167 actor-alpha, levels of which are elevated in fat tissue with aging, increased CUGBP1 protein, CUGBP1
168 issue attenuation (minimum range: 8.4 HU for fat tissue with the Sensation 16; maximum range: 63.4 HU

 
Page Top