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1 he region of the human genome containing the OB gene.
2 transduced into increased expression of the ob gene.
3 al-like tranposon in the first intron of the ob gene.
4 om 78 families at markers flanking the human OB gene.
5 capable of directing expression of the mouse ob gene.
6 of leptin, the protein product of the obese (ob) gene.
7 treme obesity have an allelic variant of the OB gene, although other nearby genes could contribute to
10 isolation and partial sequence of the human OB gene and the screening of 105 obese patients for muta
11 f calories from fat) without mutation of the ob gene, and in four genetic models of obesity in mice:
16 al adipose tissue-specific expression of the ob gene as well as enhanced expression by C/EBPalpha.
17 tially thought to be adipocyte-specific, the OB gene, as well as the leptin receptor, have been found
18 cal-by-descent for the region containing the OB gene at greater than chance levels (corrected P = 0.0
23 While the 5' flanking region of the mouse ob gene contains several consensus C/EBP binding sites,
25 oreover, we found that the expression of the ob gene could be manipulated by pharmacologically blocki
26 that mutations in the coding sequence of the OB gene do not constitute a common cause of increased bo
29 These data suggest that insulin regulates OB gene expression and leptin production indirectly, pro
30 nsulin and dexamethasone to acutely modulate ob gene expression and leptin secretion in rat adipocyte
31 In this report, we present evidence that ob gene expression in cultured cells suppresses acetyl-C
32 we provide evidence for rapid activation of ob gene expression in skeletal muscle by glucosamine.
36 ocorticoids, which supports the concept that ob gene expression is under hormonal control, which is e
37 of sequence elements and factors regulating ob gene expression should be of major importance in the
38 etes mellitus to examine the relationship of ob gene expression to obesity and non-insulin-dependent
41 taken to investigate the changes in obesity (OB) gene expression and production of leptin in response
42 by increased fat accretion, elevated obese (ob) gene expression, and high plasma leptin levels, simi
45 Leptin, a fat-derived protein encoded by the ob gene, has been postulated to be a sensor of energy st
47 this study we examined the expression of the ob gene in a dietary model in which moderate obesity dev
48 db/db mice, decreased the expression of the ob gene in these animal models of obesity and non-insuli
49 sults demonstrate that the expression of the ob gene is up-regulated in these two rodent models of di
50 ferentiation, expression of the mouse obese (ob) gene is immediately preceded by the expression of C/
56 ch is a 16 kilodalton protein-encoded by the OB gene, is involved in the regulation of food intake, b
59 Leptin, the protein product of the obese (ob) gene, is a type-I cytokine hormone secreted by fat t
60 EP), the human homolog of the mouse obesity (ob) gene, is positioned near the linkage peak and is the
64 Leptin, the protein encoded by the obese (ob) gene, is secreted from adipose tissue and is thought
65 Leptin, the protein encoded by the obese (ob) gene, is synthesized and released in response to inc
72 A mild decline in subcutaneous adipocyte ob gene mRNA and a marked fall in serum leptin were obse
75 f the K(ATP) channel opener diazoxide or the ob gene product leptin mimicked the effect of glucose re
76 murine hematopoietic stem cells and that the ob gene product leptin stimulated hemato- and lymphopoie
85 recently published receptor for the obesity (ob) gene product (leptin) is an isoform of B219 with a n
87 alpha as a transcriptional activator of the ob gene promoter and identify the functional C/EBP bindi
88 o 3T3-L1 cells with a series of 5' truncated ob gene promoter constructs activated reporter gene expr
89 ge inhibition patterns (footprinting) of the ob gene promoter revealed that recombinant C/EBP alpha,
91 evidence for linkage between markers in the OB gene region and various traits, as follows: D7S514 an
92 es to the literature on linkage in the human OB gene region, we are able to show that the evidence fo
96 tely upstream of the first exon of the mouse ob gene revealed DNA sequences corresponding to presumpt
98 hese results indicate that expression of the ob gene serves as a sensor of fat cell hypertrophy, inde
99 Furthermore, one haplotype containing the OB gene was transmitted by heterozygous parents to extre
101 is a lack of leptin due to a mutation in the ob gene, we tested the hypothesis that leptin targets a
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