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  • 1
    Publication Date: 2010-05-15
    Description: Clinical malaria is associated with the proliferation of Plasmodium parasites in human erythrocytes. The coordinated processes of parasite egress from and invasion into erythrocytes are rapid and tightly regulated. We have found that the plant-like calcium-dependent protein kinase PfCDPK5, which is expressed in invasive merozoite forms of Plasmodium falciparum, was critical for egress. Parasites deficient in PfCDPK5 arrested as mature schizonts with intact membranes, despite normal maturation of egress proteases and invasion ligands. Merozoites physically released from stalled schizonts were capable of invading new erythrocytes, separating the pathways of egress and invasion. The arrest was downstream of cyclic guanosine monophosphate-dependent protein kinase (PfPKG) function and independent of protease processing. Thus, PfCDPK5 plays an essential role during the blood stage of malaria replication.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3109083/" 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/PMC3109083/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dvorin, Jeffrey D -- Martyn, Derek C -- Patel, Saurabh D -- Grimley, Joshua S -- Collins, Christine R -- Hopp, Christine S -- Bright, A Taylor -- Westenberger, Scott -- Winzeler, Elizabeth -- Blackman, Michael J -- Baker, David A -- Wandless, Thomas J -- Duraisingh, Manoj T -- 086550/Wellcome Trust/United Kingdom -- G1000779/Medical Research Council/United Kingdom -- GM073046/GM/NIGMS NIH HHS/ -- K08 AI087874/AI/NIAID NIH HHS/ -- K12-HD000850/HD/NICHD NIH HHS/ -- MC_U117532063/Medical Research Council/United Kingdom -- R01 AI057919/AI/NIAID NIH HHS/ -- R01 AI057919-05/AI/NIAID NIH HHS/ -- R01 GM073046/GM/NIGMS NIH HHS/ -- R01AI057919/AI/NIAID NIH HHS/ -- U117532063/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2010 May 14;328(5980):910-2. doi: 10.1126/science.1188191.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/20466936" target="_blank"〉PubMed〈/a〉
    Keywords: Calcium-Binding Proteins/chemistry/genetics/*metabolism ; Cyclic GMP-Dependent Protein Kinases/antagonists & inhibitors/metabolism ; Enzyme Inhibitors/pharmacology ; Erythrocytes/*parasitology ; Host-Parasite Interactions ; Humans ; Ligands ; Merozoites/enzymology/physiology ; Models, Biological ; Morpholines/metabolism ; Plasmodium falciparum/cytology/enzymology/growth & development/*physiology ; Protein Kinases/chemistry/genetics/*metabolism ; Protozoan Proteins/chemistry/genetics/*metabolism ; Pyridines/pharmacology ; Pyrroles/pharmacology ; Recombinant Fusion Proteins/chemistry/metabolism ; Schizonts/cytology/enzymology/physiology
    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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  • 2
    Publication Date: 2014-02-28
    Description: The life cycles of many parasites involve transitions between disparate host species, requiring these parasites to go through multiple developmental stages adapted to each of these specialized niches. Transmission of malaria parasites (Plasmodium spp.) from humans to the mosquito vector requires differentiation from asexual stages replicating within red blood cells into non-dividing male and female gametocytes. Although gametocytes were first described in 1880, our understanding of the molecular mechanisms involved in commitment to gametocyte formation is extremely limited, and disrupting this critical developmental transition remains a long-standing goal. Here we show that expression levels of the DNA-binding protein PfAP2-G correlate strongly with levels of gametocyte formation. Using independent forward and reverse genetics approaches, we demonstrate that PfAP2-G function is essential for parasite sexual differentiation. By combining genome-wide PfAP2-G cognate motif occurrence with global transcriptional changes resulting from PfAP2-G ablation, we identify early gametocyte genes as probable targets of PfAP2-G and show that their regulation by PfAP2-G is critical for their wild-type level expression. In the asexual blood-stage parasites pfap2-g appears to be among a set of epigenetically silenced loci prone to spontaneous activation. Stochastic activation presents a simple mechanism for a low baseline of gametocyte production. Overall, these findings identify PfAP2-G as a master regulator of sexual-stage development in malaria parasites and mark the first discovery of a transcriptional switch controlling a differentiation decision in protozoan parasites.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4040541/" 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/PMC4040541/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kafsack, Bjorn F C -- Rovira-Graells, Nuria -- Clark, Taane G -- Bancells, Cristina -- Crowley, Valerie M -- Campino, Susana G -- Williams, April E -- Drought, Laura G -- Kwiatkowski, Dominic P -- Baker, David A -- Cortes, Alfred -- Llinas, Manuel -- 090532/Wellcome Trust/United Kingdom -- 090532/Z/09/Z/Wellcome Trust/United Kingdom -- 090770/Wellcome Trust/United Kingdom -- 094752/Wellcome Trust/United Kingdom -- 098051/Wellcome Trust/United Kingdom -- G0600230/Medical Research Council/United Kingdom -- G0600718/Medical Research Council/United Kingdom -- J005398/Medical Research Council/United Kingdom -- P50GM071508/GM/NIGMS NIH HHS/ -- R01 AI076276/AI/NIAID NIH HHS/ -- T32 GM007388/GM/NIGMS NIH HHS/ -- Biotechnology and Biological Sciences Research Council/United Kingdom -- Howard Hughes Medical Institute/ -- England -- Nature. 2014 Mar 13;507(7491):248-52. doi: 10.1038/nature12920. Epub 2014 Feb 23.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey 08544, USA [2] Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA (B.F.C.K.); Department of Molecular Biology and Center for Infectious Disease Dynamics, The Pennsylvania State University, State College, Pennsylvania 16802, USA (V.M.C., M.L.). ; 1] Barcelona Centre for International Health Research (CRESIB, Hospital Clinic-Universitat de Barcelona), Barcelona, 08036 Catalonia, Spain [2] Institute for Research in Biomedicine (IRB), Barcelona, 08028 Catalonia, Spain. ; 1] Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London WC1E 7HT, UK [2] Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London WC1E 7HT, UK. ; Barcelona Centre for International Health Research (CRESIB, Hospital Clinic-Universitat de Barcelona), Barcelona, 08036 Catalonia, Spain. ; 1] Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey 08544, USA [2] Institute for Research in Biomedicine (IRB), Barcelona, 08028 Catalonia, Spain [3] Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA (B.F.C.K.); Department of Molecular Biology and Center for Infectious Disease Dynamics, The Pennsylvania State University, State College, Pennsylvania 16802, USA (V.M.C., M.L.). ; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton CB10 1SA, UK. ; Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA. ; Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London WC1E 7HT, UK. ; 1] Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton CB10 1SA, UK [2] Wellcome Trust Sanger Centre for Human Genetics, Oxford OX3 7BN, UK. ; 1] Barcelona Centre for International Health Research (CRESIB, Hospital Clinic-Universitat de Barcelona), Barcelona, 08036 Catalonia, Spain [2] Institute for Research in Biomedicine (IRB), Barcelona, 08028 Catalonia, Spain [3] Catalan Institution for Research and Advanced Studies (ICREA), Barcelona, 08010 Catalonia, Spain. ; 1] Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey 08544, USA [2] Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA [3] Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA (B.F.C.K.); Department of Molecular Biology and Center for Infectious Disease Dynamics, The Pennsylvania State University, State College, Pennsylvania 16802, USA (V.M.C., M.L.).〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24572369" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; DNA-Binding Proteins/deficiency/genetics/metabolism ; Female ; Gene Expression Regulation/*genetics ; Gene Silencing ; Genes, Protozoan/genetics ; Genome, Protozoan/genetics ; Germ Cells/cytology/*growth & development/metabolism ; Malaria/*parasitology ; Male ; Parasites/cytology/genetics/*physiology ; Plasmodium falciparum/cytology/*genetics/physiology ; Protozoan Proteins/genetics/metabolism ; Reproduction, Asexual ; Sex Differentiation/genetics ; Sexual Development/*genetics ; Transcription, Genetic/*genetics
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 97 (1975), S. 4076-4083 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 60 (1989), S. 3475-3477 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: Measurement of distribution of velocities of phases in pipe flow of a dense gas-solid suspension was facilitated by the use of an ion source in the form of a localized corona discharge and a downstream traversing electrostatic probe. The system utilizes the transient behavior of a corona discharge which provides a distinction of times of arrival of ions and solid particles of modified charges at a downstream probe. This probe system does not suffer the handicap of other available probe systems in a dense solid phase.
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Physics of Fluids 31 (1988), S. 3152-3155 
    ISSN: 1089-7666
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Empirical modeling of the dependence of loop voltage on edge plasma conditions in the reversed field pinch is discussed. Specific concerns are raised regarding magnetohydrodynamic-based models that assume a large local dissipation of magnetic helicity at the plasma edge. A kinetic model is presented in which loop voltage can be affected by fast electrons carrying momentum directly to the walls or limiters, without a large edge helicity dissipation.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1089-7666
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Steady-state current sustainment by oscillating field current drive (OFCD) utilizes a technique in which the toroidal and poloidal magnetic fields at the plasma surface are modulated at audio frequencies in quadrature. Experiments on the ZT-40M reversed field pinch [Fusion Technol. 8, 1571 (1985)] have examined OFCD over a range of modulation amplitude, frequency, and phase. For all cases examined, the magnitude of the plasma current is dependent on the phase of the modulations as predicted by theory. However, evidence of current drive has only been observed at relatively low levels of injected power. For larger modulation amplitudes, the data suggest that substantial current drive is offset by increased plasma resistance as a result of modulation enhanced plasma–wall interactions. The initial experimental results and supporting theoretical interpretations of OFCD are discussed.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 68 (1986), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Moderate water stresses in the range 0 to −0.6 MPa applied with PEG 6000 to excised roots of Zea mays L. var. LG 11 induced increases of up to four-fold in the amount of abscisic acid (ABA) determined in the tissue after a 12 h period of xylem exudation. The ABA concentration of xylem exudate collected after a 2 h water stress also increased by up to four-fold. Salt stresses, induced with NaCl solutions, resulted in similar increases in the ABA concentrations. ABA concentrations in both root tissue and xylem exudate were highest 4 h after removal of the stress and then declined over a subsequent 8 h period. These results are interpreted in support of the concept that root-produced ABA may have a role in the fine control of the plant's water balance.
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 56 (1982), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 205 (1965), S. 306-307 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Coleus is particularly suitable for an investigation of this kind because the main vascular bundles are situated at the angles of the square stem. We used CaldwelFs split root technique on Coleus frederici. Cuttings were taken and a fortnight later the rooted stumps were carefully split from the ...
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Planta 112 (1973), S. 293-299 
    ISSN: 1432-2048
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The accumulation of 86Rb labelled potassium by isolated stelar and cortical tissues from 7-day-old roots of Zea mays has been compared with the levels accumulated by these tissues in the intact root. Cortical tissues have similar uptake eapacities in these two conditions whereas stelar tissues only exhibit an uptake capacity in the intact root system. The uncoupler carbonylcyanide m-chlorophenylhydrazone caused a considerable decrease in the uptake of potassium by these tissues. In the intact root system it prevented ions from the bathing medium reaching the stelar tissues. The efflux pattern from preloaded isolated stelar and cortical tissues was considerably altered by the inhibitor, a promotion of the efflux occurring in both of these tissues. It is concluded that stelar tissues only accumulated ions when these are supplied through the root symplasm and that the stelar plasmalemma has only a limited uptake capacity per se. Stelar uptake is thus a reflection of vacuolar accumulation across the tonoplast. There is no evidence in the present study of a carrier-mediated active secretion of ions across the stelar plasmalemma. The fact that the efflux was promoted rather than depressed by the uncoupler supports the postulate that a passive leakage is the final stage in the transport of ions across the plant root.
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