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Institution

Forest Research Institute

FacilityDehra Dūn, India
About: Forest Research Institute is a facility organization based out in Dehra Dūn, India. It is known for research contribution in the topics: Population & Forest management. The organization has 5320 authors who have published 7625 publications receiving 185876 citations.


Papers
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Journal ArticleDOI
TL;DR: In this paper, the authors measured CO2 exchange and vegetation dynamics over two growing seasons along a mire chronosequence on the land uplift coast of the Bay of Bothnia in western Finland.
Abstract: Vegetation succession in mires is rather well identified using the paleoecological approach. Recently, the ecological succession concept has been extended to ecosystem functions, e.g., carbon dioxide (CO2) dynamics. Although a strong link between mire vegetation and carbon dynamics is well acknowledged, the successional changes in mire ecosystem functions have remained practically unstudied, especially under the same climatic control. To study the patterns and dynamics of CO2 exchange during mire succession, we measured CO2 exchange and vegetation dynamics over 2 growing seasons along a mire chronosequence on the land uplift coast of the Bay of Bothnia in western Finland. The study showed a decrease in photosynthesis during mire succession that was linked to compositional change in vegetation, i.e., replacement of sedge and herb dominance with the dominance of dwarf shrubs and Sphagna. Similarly, the study revealed decreased variation in gross photosynthesis (PG) and ecosystem respiration (RE) ov...

56 citations

Journal ArticleDOI
TL;DR: The increase in phospholipids and decrease in fibrosis are opposite to features of choline-deficient models of liver disease and suggest HSD17B13 as an attractive therapeutic target.
Abstract: Carriers of the hydroxysteroid 17-β dehydrogenase 13 (HSD17B13) gene variant (rs72613567:TA) have a reduced risk of NASH and cirrhosis but not steatosis. We determined its effect on liver histology, lipidome, and transcriptome using ultra performance liquid chromatography-mass spectrometry and RNA-seq. In carriers and noncarriers of the gene variant, we also measured pathways of hepatic fatty acids (de novo lipogenesis [DNL] and adipose tissue lipolysis [ATL] using 2H2O and 2H-glycerol) and insulin sensitivity using 3H-glucose and euglycemic-hyperinsulinemic clamp) and plasma cytokines. Carriers and noncarriers had similar age, sex and BMI. Fibrosis was significantly less frequent while phospholipids, but not other lipids, were enriched in the liver in carriers compared with noncarriers. Expression of 274 genes was altered in carriers compared with noncarriers, consisting predominantly of downregulated inflammation-related gene sets. Plasma IL-6 concentrations were lower, but DNL, ATL and hepatic insulin sensitivity were similar between the groups. In conclusion, carriers of the HSD17B13 variant have decreased fibrosis and expression of inflammation-related genes but increased phospholipids in the liver. These changes are not secondary to steatosis, DNL, ATL, or hepatic insulin sensitivity. The increase in phospholipids and decrease in fibrosis are opposite to features of choline-deficient models of liver disease and suggest HSD17B13 as an attractive therapeutic target.

56 citations

Journal ArticleDOI
TL;DR: The results demonstrate that PtrMYB119 and PtrmyB120 function as transcriptional activators of anthocyanin accumulation in both Arabidopsis and poplar.
Abstract: Anthocyanins are a group of colorful and bioactive natural pigments with important physiological and ecological functions in plants. We found an MYB transcription factor (PtrMYB119) from Populus trichocarpa that positively regulates anthocyanin production when expressed under the control of the CaMV 35S promoter in transgenic Arabidopsis Amino acid sequence analysis revealed that PtrMYB119 is highly homologous to Arabidopsis PAP1 (PRODUCTION OF ANTHOCYANIN PIGMENT1), a well-known transcriptional activator of anthocyanin biosynthesis. Independently produced transgenic poplars overexpressing PtrMYB119 or PtrMYB120 (a paralogous gene to PtrMYB119) (i.e., 35S::PtrMYB119 and 35S::PtrMYB120, respectively) showed elevated accumulation of anthocyanins in the whole plants, including leaf, stem and even root tissues. Using a reverse-phase high-performance liquid chromatography, we confirmed that the majority of the accumulated anthocyanin in our transgenic poplar is cyanidin-3-O-glucoside. Gene expression analyses revealed that most of the genes involved in the anthocyanin biosynthetic pathway were highly upregulated in 35S::PtrMYB119 poplars compared with the nontransformed control poplar. Among these genes, expression of PtrCHS1 (Chalcone Synthase1) and PtrANS2 (Anthocyanin Synthase2), which catalyze the initial and last steps of anthocyanin biosynthesis, respectively, was upregulated by up to 350-fold. Subsequent transient activation assays confirmed that PtrMYB119 activated the transcription of both PtrCHS1 and PtrANS2 Interestingly, expression of MYB182, a repressor of both anthocyanin and proanthocyanidin (PA) biosynthesis, was largely suppressed in 35S::PtrMYB119 poplars, while expression of MYB134, an activator of PA biosynthesis, was not changed significantly. More interestingly, high-level accumulation of anthocyanins in 35S::PtrMYB119 poplars did not have an adverse effect on plant growth. Taken together, our results demonstrate that PtrMYB119 and PtrMYB120 function as transcriptional activators of anthocyanin accumulation in both Arabidopsis and poplar.

56 citations

Journal ArticleDOI
TL;DR: Effective management of COPD and prevention of exacerbations may lead to improved patient outcomes and reduction in total healthcare costs for long-term management of CopD.
Abstract: Background:Exacerbations are a major contributor to the large burden of treating chronic obstructive pulmonary disease (COPD). Estimates of exacerbation costs in the United States are limited.Objective:To estimate incremental costs associated with COPD exacerbation, particularly severe exacerbation, in the United States.Methods:COPD patients with at least one exacerbation were identified in the Thomson Reuters MarketScan administrative claims database. A COPD exacerbation was defined as patient use of oral or parenteral corticosteroids on the same day or within 7 days following a claim with a COPD diagnosis. Severe exacerbation was further defined if the exacerbation was associated with hospitalization or death. Healthcare costs and exacerbations were evaluated at quarterly intervals starting from patients’ first observed claim with COPD diagnostic code in the database. Incremental costs associated with exacerbation were estimated as cost differences between quarters with exacerbation and quarters...

56 citations

Book ChapterDOI
TL;DR: In this paper, the authors demonstrate that the compaction of soils during forestry operations reduces the rate of establishment of natural regeneration, reduces tree growth for periods spanning at least a decade and can have deleterious effects on tree form.
Abstract: Summary Experiments conducted under controlled conditions in greenhouses and observations of tree growth in the field demonstrate that the compaction of soils during forestry operations reduces the rate of establishment of natural regeneration, reduces tree growth for periods spanning at least a decade and can have deleterious effects on tree form. The intensity of compaction is greatest during harvesting, but by judicious choice of harvesting systems, machines and running gear, based on considerations of slope and soil water conditions, the impact on the soil can be reduced. Other options available to reduce the intensity of compaction are the laying of slash beds on the main extraction trails, the grading of terrain into areas suitable for logging during the wet and dry periods of the year, based on soil type and drainage conditions, and, if necessary, the rehabilitation of soils by cultivation or deep ripping and the application of fertilizer.

56 citations


Authors

Showing all 5332 results

NameH-indexPapersCitations
Kari Alitalo174817114231
Jaakko Kaprio1631532126320
Glenn D. Prestwich8869042758
John K. Volkman7821221931
Petri T. Kovanen7743227171
Hailong Wang6964719652
Mika Ala-Korpela6531918048
Heikki Henttonen6427114536
Zhihong Xu5743811832
Kari Pulkki5421511166
Louis A. Schipper531929224
Sang Young Lee532719917
Young-Joon Ahn522889121
Venkatesh Narayanamurti492589399
Francis M. Kelliher491248599
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20236
202226
2021504
2020503
2019440
2018381