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  • 1
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 112, No. 10 ( 2015-03-10)
    Abstract: Two decades after the discovery of the first animal microRNA (miRNA), the number of miRNAs in animal genomes remains a vexing question. Here, we report findings from analyzing 1,323 short RNA sequencing samples (RNA-seq) from 13 different human tissue types. Using stringent thresholding criteria, we identified 3,707 statistically significant novel mature miRNAs at a false discovery rate of ≤0.05 arising from 3,494 novel precursors; 91.5% of these novel miRNAs were identified independently in 10 or more of the processed samples. Analysis of these novel miRNAs revealed tissue-specific dependencies and a commensurate low Jaccard similarity index in intertissue comparisons. Of these novel miRNAs, 1,657 (45%) were identified in 43 datasets that were generated by cross-linking followed by Argonaute immunoprecipitation and sequencing (Ago CLIP-seq) and represented 3 of the 13 tissues, indicating that these miRNAs are active in the RNA interference pathway. Moreover, experimental investigation through stem-loop PCR of a random collection of newly discovered miRNAs in 12 cell lines representing 5 tissues confirmed their presence and tissue dependence. Among the newly identified miRNAs are many novel miRNA clusters, new members of known miRNA clusters, previously unreported products from uncharacterized arms of miRNA precursors, and previously unrecognized paralogues of functionally important miRNA families (e.g., miR-15/107). Examination of the sequence conservation across vertebrate and invertebrate organisms showed 56.7% of the newly discovered miRNAs to be human-specific whereas the majority (94.4%) are primate lineage-specific. Our findings suggest that the repertoire of human miRNAs is far more extensive than currently represented by public repositories and that there is a significant number of lineage- and/or tissue-specific miRNAs that are uncharacterized.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
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    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2015
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  • 2
    Online Resource
    Online Resource
    Wiley ; 1998
    In:  Annals of the New York Academy of Sciences Vol. 855, No. 1 ( 1998-11), p. 165-168
    In: Annals of the New York Academy of Sciences, Wiley, Vol. 855, No. 1 ( 1998-11), p. 165-168
    Abstract: ABSTRACT: We previously demonstrated that taste receptor cells (TRCs) respond to cis ‐polyunsaturated fatty acids (PUFAs) through an inhibition of delayed rectifying K channels (K DR ), 1 which may represent the transduction mechanism for dietary fat. To determine if there is a link between the sensitivity of fungiform TRCs to PUFAs and dietary fat preferences, we compared the PUFA‐sensitivity of TRCs using patch clamp techniques from Osborne‐Mendel (O‐M) and S5B/Pl rats, which display dietary preferences for fat over carbohydrate and carbohydrate over fat, respectively. 3 In isolated TRCs, the PUFAs, linoleic (C18:2), linolenic (C18:3) and arachidonic acid (C20:4) inhibit K DR in a concentration‐dependent manner in both strains, while the unsaturated lauric acid (C12:0) was ineffective. K DR from TRCs of S5B/Pl rats were significantly more sensitive to inhibition by all three PUFAs (10 μM) than were TRCs from O‐M rats. We are currently investigating whether this differential responsiveness is due to (i) the relative affinity of the interaction between cis‐PUFAs and the delayed rectifying K channels or (ii) the relative density of delayed rectifying K channels in the two rat strains. Whatever the mechanism, these data suggest an inverse correlation between peripheral gustatory sensitivity to PUFAs and the dietary preference for fat. This finding may provide insight into the mechanism for sensing dietary fat that allows the S5B rats to reduce fat intake on a high‐fat diet and avoid the obesity which results when O‐M rats eat a high‐fat diet.
    Type of Medium: Online Resource
    ISSN: 0077-8923 , 1749-6632
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 1998
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  • 3
    Online Resource
    Online Resource
    Wiley ; 1961
    In:  Annals of the New York Academy of Sciences Vol. 92, No. 1 ( 1961-04), p. 115-127
    In: Annals of the New York Academy of Sciences, Wiley, Vol. 92, No. 1 ( 1961-04), p. 115-127
    Type of Medium: Online Resource
    ISSN: 0077-8923 , 1749-6632
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 1961
    detail.hit.zdb_id: 2834079-6
    detail.hit.zdb_id: 211003-9
    detail.hit.zdb_id: 2071584-5
    SSG: 11
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  • 4
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2000
    In:  Nature Vol. 404, No. 6778 ( 2000-4), p. 672-677
    In: Nature, Springer Science and Business Media LLC, Vol. 404, No. 6778 ( 2000-4), p. 672-677
    Type of Medium: Online Resource
    ISSN: 0028-0836 , 1476-4687
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    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2000
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    detail.hit.zdb_id: 1413423-8
    SSG: 11
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  • 5
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 1978
    In:  Proceedings of the National Academy of Sciences Vol. 75, No. 1 ( 1978-01), p. 477-481
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 75, No. 1 ( 1978-01), p. 477-481
    Abstract: Genetically obese ( ob/ob ) mice, mice that became obese after treatment with gold thioglucose, and lean animals were studied in the euthyroid state, after induction of hypothyroidism, and after treatment with triiodothyronine. The activity of glycerol 3-phosphate dehydrogenase ( sn -glycerol-3-phosphate:(acceptor) oxidoreductase; EC 1.1.99.5] was reduced in the livers from hypothyroid animals and was increased by treatment with triiodothyronine in all groups. The activity of the ouabain-suppressible sodium- and potassium-dependent ATPase (ATP phosphohydrolase; EC 3.6.1.3) was increased by triiodothyronine and reduced by hypothyroidism in the lean and gold thioglucose-treated obese animals. In the obese ( ob/ob ) mice, on the other hand, treatment with triiodothyronine did not increase the activity of this enzyme, which remained at the level found in hypothyroid animals. This enzymatic activity was reduced in both liver and kidney. Adenylate cyclase [ATP pyrophosphate-lyase (cyclizing); EC 4.6.1.1] activity in liver membranes, however, was similar in all three groups of mice. This enzyme complex was activated by glucagon and was unaffected by treatment with thyroid hormones. The lack of a thyroid-dependent ouabain-suppressible (Na + + K + )-ATPase in the tissues of the obese ( ob/ob ) mouse could explain most, if not all, of the abnormalities that have been described in this animal.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 1978
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    SSG: 11
    SSG: 12
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  • 6
    Online Resource
    Online Resource
    American Association for the Advancement of Science (AAAS) ; 1981
    In:  Science Vol. 213, No. 4512 ( 1981-09-04), p. 1125-1127
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 213, No. 4512 ( 1981-09-04), p. 1125-1127
    Abstract: The weight of interscapular brown fat in the rat and its rate of respiration increased in response to a single meal. These data suggest that brown adipose tissue plays a role in the thermic effect of meals and that diet-induced thermogenesis may reflect the summation of the thermic effects of single meals during prolonged overeating.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 1981
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  • 7
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 1978
    In:  Nature Vol. 274, No. 5674 ( 1978-8), p. 900-902
    In: Nature, Springer Science and Business Media LLC, Vol. 274, No. 5674 ( 1978-8), p. 900-902
    Type of Medium: Online Resource
    ISSN: 0028-0836 , 1476-4687
    RVK:
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    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1978
    detail.hit.zdb_id: 120714-3
    detail.hit.zdb_id: 1413423-8
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  • 8
    Online Resource
    Online Resource
    Wiley ; 1993
    In:  Annals of the New York Academy of Sciences Vol. 676, No. 1 ( 1993-03), p. 223-241
    In: Annals of the New York Academy of Sciences, Wiley, Vol. 676, No. 1 ( 1993-03), p. 223-241
    Type of Medium: Online Resource
    ISSN: 0077-8923 , 1749-6632
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 1993
    detail.hit.zdb_id: 2834079-6
    detail.hit.zdb_id: 211003-9
    detail.hit.zdb_id: 2071584-5
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  • 9
    Online Resource
    Online Resource
    Wiley ; 2014
    In:  Annals of the New York Academy of Sciences Vol. 1311, No. 1 ( 2014-04), p. 1-13
    In: Annals of the New York Academy of Sciences, Wiley, Vol. 1311, No. 1 ( 2014-04), p. 1-13
    Abstract: There are two groups of approved drugs that can be used to manage weight in patients with obesity: medications approved for obesity per se and medications that affect body weight for obese patients who have complications from their obesity and are receiving these medications for chronic disease management. For obesity per se, treatment is with one of the three drugs currently approved for long‐term treatment of obesity or one of a few others that can be used for short‐term treatment. Among these, orlistat partially blocks intestinal digestion of fat and produces weight loss of 5–8 kg but major limitations are associated gastrointestinal symptoms; lorcaserin, a serotonin‐2C agonist with few side effects, produces a mean weight loss of 4–7 kg; and the combination of phentermine and topiramate (extended release) produces a mean weight loss of 8–10 kg, but should only be used after verifying a woman is not pregnant. Failure to lose more than 3% of body weight within 3 months with any of these agents should lead to reevaluation of therapy. The short‐term drugs for treating obesity per se are sympathomimetics, with phentermine being most widely used. The second group of drugs is for weight‐centric prescribing for patients with a chronic disease such as diabetes, depression, or psychiatric disorders. For each disorder, some drugs produce weight gain, others are weight neutral, but the best choice for these patients is the combination of drugs that treat the underlying condition and also produce weight loss.
    Type of Medium: Online Resource
    ISSN: 0077-8923 , 1749-6632
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2014
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  • 10
    Online Resource
    Online Resource
    Wiley ; 1987
    In:  Annals of the New York Academy of Sciences Vol. 499, No. 1 ( 1987-06), p. 14-28
    In: Annals of the New York Academy of Sciences, Wiley, Vol. 499, No. 1 ( 1987-06), p. 14-28
    Type of Medium: Online Resource
    ISSN: 0077-8923 , 1749-6632
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 1987
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    SSG: 11
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