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  • 1
    Publication Date: 2016-05-28
    Description: The Journal of Physical Chemistry B DOI: 10.1021/acs.jpcb.6b01459
    Electronic ISSN: 1520-5207
    Topics: Chemistry and Pharmacology , Physics
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  • 2
    Publication Date: 2016-04-04
    Description: Three bright molecular line sources in G333 have recently been shown to exhibit signatures of infall. We describe a molecular line radiative transfer (RT) modelling process which is required to extract the infall signature from Mopra and Nanten2 data. The observed line profiles differ greatly between individual sources but are reproduced well by variations upon a common unified model where the outflow viewing angle is the most significant difference between the sources. The models and data together suggest that the observed properties of the high-mass star-forming regions such as infall, turbulence and mass are consistent with scaled-up versions of the low-mass case with turbulent velocities that are supersonic and an order of magnitude larger than those found in low-mass star-forming regions. Using detailed RT modelling, we show that the G333 cores are essentially undergoing a scaled-up version of low-mass star formation. This is an extension of earlier work in that the degree of infall and the chemical abundances are constrained by the RT modelling in a way that is not practical with a standard analysis of observational data. We also find high velocity infall and high infall mass rates, possibly suggesting accelerated collapse due to external pressure. Molecular depletion due to freeze-out on to dust grains in central regions of the cores is suggested by low molecular abundances of several species. Strong evidence for a local enhancement of 13 C-bearing species towards the outflow cloud cores is discussed, consistent with the presence of shocks caused by the supersonic motions within them.
    Print ISSN: 0035-8711
    Electronic ISSN: 1365-2966
    Topics: Physics
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  • 3
    Publication Date: 2008-04-25
    Description: Papaya, a fruit crop cultivated in tropical and subtropical regions, is known for its nutritional benefits and medicinal applications. Here we report a 3x draft genome sequence of 'SunUp' papaya, the first commercial virus-resistant transgenic fruit tree to be sequenced. The papaya genome is three times the size of the Arabidopsis genome, but contains fewer genes, including significantly fewer disease-resistance gene analogues. Comparison of the five sequenced genomes suggests a minimal angiosperm gene set of 13,311. A lack of recent genome duplication, atypical of other angiosperm genomes sequenced so far, may account for the smaller papaya gene number in most functional groups. Nonetheless, striking amplifications in gene number within particular functional groups suggest roles in the evolution of tree-like habit, deposition and remobilization of starch reserves, attraction of seed dispersal agents, and adaptation to tropical daylengths. Transgenesis at three locations is closely associated with chloroplast insertions into the nuclear genome, and with topoisomerase I recognition sites. Papaya offers numerous advantages as a system for fruit-tree functional genomics, and this draft genome sequence provides the foundation for revealing the basis of Carica's distinguishing morpho-physiological, medicinal and nutritional properties.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2836516/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2836516/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ming, Ray -- Hou, Shaobin -- Feng, Yun -- Yu, Qingyi -- Dionne-Laporte, Alexandre -- Saw, Jimmy H -- Senin, Pavel -- Wang, Wei -- Ly, Benjamin V -- Lewis, Kanako L T -- Salzberg, Steven L -- Feng, Lu -- Jones, Meghan R -- Skelton, Rachel L -- Murray, Jan E -- Chen, Cuixia -- Qian, Wubin -- Shen, Junguo -- Du, Peng -- Eustice, Moriah -- Tong, Eric -- Tang, Haibao -- Lyons, Eric -- Paull, Robert E -- Michael, Todd P -- Wall, Kerr -- Rice, Danny W -- Albert, Henrik -- Wang, Ming-Li -- Zhu, Yun J -- Schatz, Michael -- Nagarajan, Niranjan -- Acob, Ricelle A -- Guan, Peizhu -- Blas, Andrea -- Wai, Ching Man -- Ackerman, Christine M -- Ren, Yan -- Liu, Chao -- Wang, Jianmei -- Wang, Jianping -- Na, Jong-Kuk -- Shakirov, Eugene V -- Haas, Brian -- Thimmapuram, Jyothi -- Nelson, David -- Wang, Xiyin -- Bowers, John E -- Gschwend, Andrea R -- Delcher, Arthur L -- Singh, Ratnesh -- Suzuki, Jon Y -- Tripathi, Savarni -- Neupane, Kabi -- Wei, Hairong -- Irikura, Beth -- Paidi, Maya -- Jiang, Ning -- Zhang, Wenli -- Presting, Gernot -- Windsor, Aaron -- Navajas-Perez, Rafael -- Torres, Manuel J -- Feltus, F Alex -- Porter, Brad -- Li, Yingjun -- Burroughs, A Max -- Luo, Ming-Cheng -- Liu, Lei -- Christopher, David A -- Mount, Stephen M -- Moore, Paul H -- Sugimura, Tak -- Jiang, Jiming -- Schuler, Mary A -- Friedman, Vikki -- Mitchell-Olds, Thomas -- Shippen, Dorothy E -- dePamphilis, Claude W -- Palmer, Jeffrey D -- Freeling, Michael -- Paterson, Andrew H -- Gonsalves, Dennis -- Wang, Lei -- Alam, Maqsudul -- R01 GM083873/GM/NIGMS NIH HHS/ -- R01 GM083873-05/GM/NIGMS NIH HHS/ -- R01 LM006845/LM/NLM NIH HHS/ -- R01 LM006845-08/LM/NLM NIH HHS/ -- England -- Nature. 2008 Apr 24;452(7190):991-6. doi: 10.1038/nature06856.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Hawaii Agriculture Research Center, Aiea, Hawaii 96701, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18432245" target="_blank"〉PubMed〈/a〉
    Keywords: Arabidopsis/genetics ; Carica/*genetics ; Contig Mapping ; Databases, Genetic ; Genes, Plant/genetics ; Genome, Plant/*genetics ; Molecular Sequence Data ; Plants, Genetically Modified/genetics ; Sequence Alignment ; Sequence Analysis, DNA ; Transcription Factors/genetics ; Tropical Climate
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2010-12-18
    Description: The adipose-derived hormone leptin maintains energy balance in part through central nervous system-mediated increases in sympathetic outflow that enhance fat burning. Triggering of beta-adrenergic receptors in adipocytes stimulates energy expenditure by cyclic AMP (cAMP)-dependent increases in lipolysis and fatty-acid oxidation. Although the mechanism is unclear, catecholamine signalling is thought to be disrupted in obesity, leading to the development of insulin resistance. Here we show that the cAMP response element binding (CREB) coactivator Crtc3 promotes obesity by attenuating beta-adrenergic receptor signalling in adipose tissue. Crtc3 was activated in response to catecholamine signals, when it reduced adenyl cyclase activity by upregulating the expression of Rgs2, a GTPase-activating protein that also inhibits adenyl cyclase activity. As a common human CRTC3 variant with increased transcriptional activity is associated with adiposity in two distinct Mexican-American cohorts, these results suggest that adipocyte CRTC3 may play a role in the development of obesity in humans.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025711/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025711/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Song, Youngsup -- Altarejos, Judith -- Goodarzi, Mark O -- Inoue, Hiroshi -- Guo, Xiuqing -- Berdeaux, Rebecca -- Kim, Jeong-Ho -- Goode, Jason -- Igata, Motoyuki -- Paz, Jose C -- Hogan, Meghan F -- Singh, Pankaj K -- Goebel, Naomi -- Vera, Lili -- Miller, Nina -- Cui, Jinrui -- Jones, Michelle R -- CHARGE Consortium -- GIANT Consortium -- Chen, Yii-Der I -- Taylor, Kent D -- Hsueh, Willa A -- Rotter, Jerome I -- Montminy, Marc -- M01 RR000425-36/RR/NCRR NIH HHS/ -- M01-RR00425/RR/NCRR NIH HHS/ -- N01 HC095159/HC/NHLBI NIH HHS/ -- N01-HC95159/HC/NHLBI NIH HHS/ -- N02 HL64278/HL/NHLBI NIH HHS/ -- N02-HL64278/HL/NHLBI NIH HHS/ -- P30 DK063491/DK/NIDDK NIH HHS/ -- P30 DK063491-09/DK/NIDDK NIH HHS/ -- P30-DK063491/DK/NIDDK NIH HHS/ -- R01 DK033651/DK/NIDDK NIH HHS/ -- R01 DK049777/DK/NIDDK NIH HHS/ -- R01 DK049777-18/DK/NIDDK NIH HHS/ -- R01 DK079888/DK/NIDDK NIH HHS/ -- R01 DK079888-05/DK/NIDDK NIH HHS/ -- R01 HL071205/HL/NHLBI NIH HHS/ -- R01 HL071205-05/HL/NHLBI NIH HHS/ -- R01 HL088457/HL/NHLBI NIH HHS/ -- R01 HL088457-04/HL/NHLBI NIH HHS/ -- R01-DK049777/DK/NIDDK NIH HHS/ -- R01-DK083834/DK/NIDDK NIH HHS/ -- R01-DK79888/DK/NIDDK NIH HHS/ -- R01-HL088457/HL/NHLBI NIH HHS/ -- R01-L071205/PHS HHS/ -- R37 DK083834/DK/NIDDK NIH HHS/ -- R37 DK083834-26/DK/NIDDK NIH HHS/ -- R37 DK083834-27/DK/NIDDK NIH HHS/ -- England -- Nature. 2010 Dec 16;468(7326):933-9. doi: 10.1038/nature09564.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, California 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21164481" target="_blank"〉PubMed〈/a〉
    Keywords: Adipocytes/drug effects/metabolism ; Adipose Tissue/drug effects/metabolism ; Animals ; Body Temperature ; Catecholamines/*metabolism ; Cells, Cultured ; Cyclic AMP/metabolism ; Cyclic AMP Response Element-Binding Protein/antagonists & inhibitors/metabolism ; Dietary Fats/pharmacology ; *Energy Metabolism/genetics ; Female ; Genome-Wide Association Study ; Humans ; Insulin Resistance ; Mexican Americans/genetics ; Mice ; Obesity/chemically induced/genetics/metabolism ; Phosphorylation ; RGS Proteins/biosynthesis/genetics ; Receptors, Adrenergic, beta/metabolism ; Signal Transduction/drug effects/*physiology ; Transcription Factors/chemistry/deficiency/genetics/*metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2011-10-15
    Description: A current limitation in nanoparticle superlattice engineering is that the identities of the particles being assembled often determine the structures that can be synthesized. Therefore, specific crystallographic symmetries or lattice parameters can only be achieved using specific nanoparticles as building blocks (and vice versa). We present six design rules that can be used to deliberately prepare nine distinct colloidal crystal structures, with control over lattice parameters on the 25- to 150-nanometer length scale. These design rules outline a strategy to independently adjust each of the relevant crystallographic parameters, including particle size (5 to 60 nanometers), periodicity, and interparticle distance. As such, this work represents an advance in synthesizing tailorable macroscale architectures comprising nanoscale materials in a predictable fashion.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Macfarlane, Robert J -- Lee, Byeongdu -- Jones, Matthew R -- Harris, Nadine -- Schatz, George C -- Mirkin, Chad A -- New York, N.Y. -- Science. 2011 Oct 14;334(6053):204-8. doi: 10.1126/science.1210493.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry, Northwestern University, Evanston, IL 60208, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21998382" target="_blank"〉PubMed〈/a〉
    Keywords: Base Sequence ; Crystallization ; Crystallography ; DNA/*chemistry ; Engineering ; Metal Nanoparticles/*chemistry ; Microscopy, Electron, Transmission ; Nucleic Acid Hybridization ; Oligonucleotides/chemistry ; Particle Size ; Scattering, Small Angle ; Thermodynamics
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2013-08-24
    Description: The directed assembly of nanoparticle building blocks is a promising method for generating sophisticated three-dimensional materials by design. In this work, we have used DNA linkers to synthesize nanoparticle superlattices that have greater complexity than simple binary systems using the process of topotactic intercalation-the insertion of a third nanoparticle component at predetermined sites within a preformed binary lattice. Five distinct crystals were synthesized with this methodology, three of which have no equivalent in atomic or molecular crystals, demonstrating a general approach for assembling highly ordered ternary nanoparticle superlattices whose structures can be predicted before their synthesis. Additionally, the intercalation process was demonstrated to be completely reversible; the inserted nanoparticles could be expelled into solution by raising the temperature, and the ternary superlattice could be recovered by cooling.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Macfarlane, Robert J -- Jones, Matthew R -- Lee, Byeongdu -- Auyeung, Evelyn -- Mirkin, Chad A -- New York, N.Y. -- Science. 2013 Sep 13;341(6151):1222-5. doi: 10.1126/science.1241402. Epub 2013 Aug 22.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry, 2145 Sheridan Road, Evanston, IL 60208, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23970559" target="_blank"〉PubMed〈/a〉
    Keywords: DNA/*chemistry ; Microscopy, Electron, Transmission ; Nanoparticles/*chemistry ; Scattering, Small Angle ; X-Ray Diffraction
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 7
    Publication Date: 2012-11-07
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jones, Matthew R -- Mirkin, Chad A -- England -- Nature. 2012 Nov 1;491(7422):42-3. doi: 10.1038/491042a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23128220" target="_blank"〉PubMed〈/a〉
    Keywords: Colloids/*chemistry
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 8
    Publication Date: 2015-02-24
    Description: For over half a century, the biological roles of nucleic acids as catalytic enzymes, intracellular regulatory molecules, and the carriers of genetic information have been studied extensively. More recently, the sequence-specific binding properties of DNA have been exploited to direct the assembly of materials at the nanoscale. Integral to any methodology focused on assembling matter from smaller pieces is the idea that final structures have well-defined spacings, orientations, and stereo-relationships. This requirement can be met by using DNA-based constructs that present oriented nanoscale bonding elements from rigid core units. Here, we draw analogy between such building blocks and the familiar chemical concepts of "bonds" and "valency" and review two distinct but related strategies that have used this design principle in constructing new configurations of matter.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jones, Matthew R -- Seeman, Nadrian C -- Mirkin, Chad A -- New York, N.Y. -- Science. 2015 Feb 20;347(6224):1260901. doi: 10.1126/science.1260901.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA. ; Department of Chemistry, New York University, New York, NY 10003, USA. chadnano@northwestern.edu ned.seeman@nyu.edu. ; Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA. Department of Chemistry and International Institute for Nanotechnology, Northwestern University, Evanston, IL 60208, USA. chadnano@northwestern.edu ned.seeman@nyu.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25700524" target="_blank"〉PubMed〈/a〉
    Keywords: DNA/*chemistry ; Nanostructures/*chemistry ; Nucleic Acid Conformation ; Nucleic Acid Hybridization
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 9
    Publication Date: 2016-02-26
    Description: Unlike conventional inorganic materials, biological systems are exquisitely adapted to respond to their surroundings. Proteins and other biological molecules can process a complex set of chemical binding events as informational inputs and respond accordingly via a change in structure and function. We applied this principle to the design and synthesis of inorganic materials by preparing nanoparticles with reconfigurable surface ligands, where interparticle bonding can be programmed in response to specific chemical cues in a dynamic manner. As a result, a nascent set of "transmutable nanoparticles" can be driven to crystallize along multiple thermodynamic trajectories, resulting in rational control over the phase and time evolution of nanoparticle-based matter.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kim, Youngeun -- Macfarlane, Robert J -- Jones, Matthew R -- Mirkin, Chad A -- New York, N.Y. -- Science. 2016 Feb 5;351(6273):579-82. doi: 10.1126/science.aad2212.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA. International Institute of Nanotechnology, Northwestern University, Evanston, IL 60208, USA. ; International Institute of Nanotechnology, Northwestern University, Evanston, IL 60208, USA. Department of Chemistry, Northwestern University, Evanston, IL 60208, USA. ; Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA. International Institute of Nanotechnology, Northwestern University, Evanston, IL 60208, USA. Department of Chemistry, Northwestern University, Evanston, IL 60208, USA. chadnano@northwestern.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26912697" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 10
    Publication Date: 2016-09-18
    Description: We have analysed the chemical and kinematic properties of the 20 and 50 km s –1 molecular clouds in the Central Molecular Zone of the Milky Way Galaxy, as well as those of the molecular ridge bridging these two clouds. Our work has utilized 37 molecular transitions in the 0.65, 3 and 7-mm wavebands, from the Mopra and NANTEN2 telescopes. The 0.65-mm NANTEN2 data highlights a dense condensation of emission within the western part of the 20 km s –1 cloud, visible in only four other transitions, which are 3-mm H 13 CN (1–0), H 13 CO + (1–0), HNC (1–0) and N 2 H + (1–0), suggesting that the condensation is moderately optically thick and cold. We find that while the relative chemical abundances between both clouds are alike in many transitions, suggesting little variation in the chemistry between both clouds; the 20 km s –1 , cold cloud is brighter than the 50 km s –1 cloud in shock and high density tracers. The spatial distribution of enhanced emission is widespread in the 20 km s –1 cloud, as shown via line ratio maps. The position velocity diagrams across both clouds indicate that the gas is well mixed. We show that the molecular ridge is most likely part of the 20 km s –1 cloud and that both of them may possibly extend to include the 50 km s –1 cloud, as part of one larger cloud. Furthermore, we expect that the 20 km s –1 cloud is being tidally sheared as a result of the gravitational potential from Sgr A*
    Print ISSN: 0035-8711
    Electronic ISSN: 1365-2966
    Topics: Physics
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