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  • 1
    Online Resource
    Online Resource
    Milton :Taylor & Francis Group,
    Keywords: Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (169 pages)
    Edition: 1st ed.
    ISBN: 9781351093019
    Language: English
    Note: Cover -- Title -- Copyright -- THE AUTHOR -- Contents -- Chapter 11 Predator-Prey Coccidia: The Sarcocystidae -- Family Sarcocystidae -- Subfamily Sarcocystinae -- Genus Sarcocystis -- Genus Frenkelia -- Genus Arthrocystis -- Subfamily Toxoplasmatinae -- Genus Toxoplasma -- Genus Besnoitia -- Chapter 12 Blood Parasites: The Malaria and Related Parasites -- Class Aconoidasida -- Order Haemospororida -- Family Plasmodiidae -- Genus Plasmodium -- Genus Nycteria -- Genus Polychromophilus -- Genus Dionisia -- Genus Mesnilium -- Genus Hepatocystis -- Genus Rayella -- Genus Haemoproteus -- Genus Leucocytozoon -- Genus Saurocytozoon -- Chapter 13 Blood Parasites: The Piroplasms -- Order Piroplasmorida -- Family Anthemosomatidae -- Genus Anthemosoma -- Family Babesiidae -- Genus Babesia -- Genus Echinozoon -- Family Theileriidae -- Genus Theileria -- Family Haemohormidiidae -- Genus Haemohormidium -- Genus Sauroplasma -- Chapter 14 Parasites of Uncertain Affinities (Incertae Sedis) -- Genus Cristalloidophora -- Genus Echinococcidium -- Genus Elleipsisoma -- Genus Globidiellum -- Genus Joyeuxella -- Genus Rhabdospora -- Genus Serpentoplasma -- Genus Spermatobium -- Genus Spiriopsis -- Genus Spirogregarina -- Genus Toxocystis -- Genus Trophosphaera -- References -- Appendix 1 Nomina Dubia, Nomina Nuda, Non-Apicomplexa, Etc -- Appendix 2 Superseded Generic Names -- Index.
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  • 2
    Online Resource
    Online Resource
    Milton :Taylor & Francis Group,
    Keywords: Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (218 pages)
    Edition: 1st ed.
    ISBN: 9781351084550
    Language: English
    Note: Cover -- Title -- Copyright -- THE AUTHOR -- Contents -- Chapter 1 Introduction -- Chapter 2 Class Perkinsasida -- Family Perkinsidae -- Genus Perkinsus -- Chapter 3 The Gregarines: Archigregarines -- Class Conoidasida -- Subclass Gregarinasina -- Order Archigregarinorida -- Family Selenidioididae -- Genus Selenidioides -- Genus Meroselenidium -- Genus Merogregarina -- Family Exoschizonidae -- Genus Exoschizon -- Chapter 4 The Gregarines: Blastogregarines -- Order Eugregarinorida -- Suborder Blastogregarinorina -- Family Siedleckiidae -- Genus Siedleckia -- Chapter 5 The Gregarines: Aseptate Eugregarines -- Suborder Aseptatorina -- Family Selenidiidae -- Genus Selenidium -- Genus Selenocystis -- Genus Ditrypanocystis -- Genus Heterospora -- Family Lecudinidae -- Genus Lecudina -- Genus Polyrhabdina -- Genus Ulivina -- Genus Sycia -- Genus Pontesia -- Genus Bhatiella -- Genus Viviera -- Genus Cochleomeritus -- Genus Ancora -- Genus Hentschelia -- Genus Lecythion -- Genus Hyperidion -- Genus Zygosoma -- Genus Filipodium -- Genus Diplauxis -- Genus Chlamydocystis -- Genus Contortiocorpa -- Genus Lankesteria -- Genus Monocystella -- Genus Ascogregarina -- Genus Kofoidina -- Genus Ophioidina -- Genus Paraophioidina -- Genus Lateroprotomeritus -- Genus Extremocystis -- Family Urosporidae -- Genus Urospora -- Genus Gonospora -- Genus Lithocystis -- Genus Ceratospora -- Genus Pterospora -- Genus Paragonospora -- Family Aikinetocystidae -- Genus Aikinetocystis -- Genus Nellocystis -- Family Monocystidae -- Subfamily Monocystinae -- Genus Monocystis -- Genus Nematocystis -- Genus Rhabdocystis -- Genus Apolocystis -- Genus Cephalocystis -- Genus Trigonepimerus -- Genus Mastocystis -- Subfamily Zygocystinae -- Genus Zygocystis -- Genus Adelphocystis -- Genus Pleurocystis -- Subfamily Rhynchocystinae -- Genus Rhynchocystis -- Genus Dirhynchocystis. , Genus Grayallia -- Subfamily Stomatophorinae -- Genus Stomatophora -- Genus Craterocystis -- Genus Astrocystella -- Genus Albertisella -- Genus Beccaricystis -- Genus Parachoanocystoides -- Genus Choanocystoides -- Genus Zeylanocystis -- Genus Arborocystis -- Genus Chakravartiella -- Subfamily Oligochaetocystinae -- Genus Oligochaetocystis -- Genus Echiurocystis -- Genus Neomonocystis -- Genus Acarogregarina -- Family Diplocystidae -- Genus Diplocystis -- Family Allantocystidae -- Genus Allantocystis -- Family Schaudinnellidae -- Genus Schaudinnella -- Family Enterocystidae -- Genus Enterocystis -- Family Ganymedidae -- Genus Ganymedes -- Chapter 6 The Gregarines: Septate Eugregarines -- Suborder Septatorina -- Superfamily Porosporicae -- Family Porosporidae -- Genus Porospora -- Genus Nematopsis -- Genus Pachyporospora -- Superfamily Gregarinicae -- Family Cephaloidophoridae -- Genus Cephaloidophora -- Genus Caridohabitans -- Genus Rotundula -- Family Cephalolobidae -- Genus Cephalolobus -- Genus Callynthrochlamys -- Family Uradiophoridae -- Genus Uradiophora -- Genus Heliospora -- Genus Pyxinioides -- Genus Nematoides -- Genus Bifilida -- Family Gregarinidae -- Genus Gregarina -- Genus Erhardovina -- Genus Gymnospora -- Genus Triseptata -- Genus Gamocystis -- Genus Anisolobus -- Genus Garnhamia -- Genus Torogregarina -- Genus Faucispora -- Genus Spinispora -- Genus Bolivia -- Genus Degiustia -- Genus Cirrigregarina -- Genus Molluskocystis -- Family Metameridae -- Genus Metamera -- Genus Gopaliella -- Genus Deuteromera -- Genus Cognettiella -- Family Didymophyidae -- Genus Didymophyes -- Genus Liposcelisus -- Genus Quadruhyalodiscus -- Family Hirmocystidae -- Genus Hirmocystis -- Genus Hyalospora -- Genus Tettigonospora -- Genus Euspora -- Genus Tintinospora -- Genus Arachnocystis -- Genus Protomagalhaensia -- Genus Pintospora -- Genus Endomycola. , Genus Retractocephalus -- Superfamily Stenophoricae -- Family Stenophoridae -- Genus Stenophora -- Genus Fonsecaia -- Genus Hyalosporina -- Family Leidyanidae -- Genus Leidyana -- Family Cnemidosporidae -- Genus Cnemidospora -- Family Monoductidae -- Genus Monoductus -- Genus Stenoductus -- Genus Phleobum -- Family Sphaerocystidae -- Genus Sphaerocystis -- Genus Schneideria -- Genus Paraschneideria -- Genus Neoschneideria -- Family Trichorhynchidae -- Genus Trichorhynchus -- Family Dactylophoridae -- Genus Dactylophorus -- Genus Echinomera -- Genus Grebnickiella -- Genus Rhopalonia -- Genus Acutispora -- Genus Seticephalus -- Genus Dendrorhynchus -- Genus Mecistophora -- Family Stylocephalidae -- Genus Stylocephalus -- Genus Stylocephaloides -- Genus Cystocephalus -- Genus Bulbocephalus -- Genus Xiphocephalus -- Genus Lophocephalus -- Genus Lophocephaloides -- Genus Sphaerorhynchus -- Genus Oocephalus -- Genus Campanacephalus -- Genus Clavicephalus -- Genus Cystocephaloides -- Genus Orbocephalus -- Genus Lepismatophila -- Genus Colepismatophila -- Family Actinocephalidae -- Subfamily Actinocephalinae -- Genus Actinocephalus -- Genus Caulocephalus -- Genus Cornimeritus -- Genus Umbracephalus -- Genus Urnaepimeritus -- Genus Asterophora -- Genus Pileocephalus -- Genus Gemmicephalus -- Genus Pilidiophora -- Genus Geneiorhynchus -- Genus Acanthoepimeritus -- Genus Phialoides -- Genus Legeria -- Genus Pyxinia -- Genus Discorhynchus -- Genus Steinina -- Genus Bothriopsides -- Genus Pomania -- Genus Stictospora -- Genus Coleorhynchus -- Genus Stylocystis -- Genus Amphoroides -- Genus Taeniocystis -- Genus Sciadiophora -- Genus Anthorhynchus -- Genus Agrippina -- Genus Globulocephalus -- Genus Alaspora -- Genus Ascocephalus -- Genus Amphorocephalus -- Genus Tricystis -- Genus Thalicola -- Genus Epicavus -- Genus Gryllotalpia -- Genus Chilogregarina. , Genus Crucocephalus -- Genus Harendraia -- Genus Levinea -- Subfamily Acanthosporinae -- Genus Acanthospora -- Genus Grenoblia -- Genus Corycella -- Genus Ancyrophora -- Genus Rhizionella -- Genus Cometoides -- Genus Prismatospora -- Genus Tetraedrospora -- Genus Ramicephalus -- Genus Coronoepimeritus -- Genus Dinematospora -- Genus Doliospora -- Genus Acanthosporidium -- Genus Quadruspinospora -- Genus Contospora -- Genus Tetractinospora -- Genus Echinoocysta -- Genus Mukundaella -- Genus Tetrameridionospinispora -- Subfamily Menosporinae -- Genus Menospora -- Genus Hoplorhynchus -- Genus Odonaticola -- Family Brustiosporidae -- Genus Brustiospora -- Family Acutidae -- Genus Acuta -- Genus Apigregarina -- Family Monoicidae -- Genus Monoica -- Superfamily Fusionicae -- Family Fusionidae -- Genus Fusiona -- Chapter 7 The Gregarines: Neogregarines -- Order Neogregarinorida -- Family Gigaductidae -- Genus Gigaductus -- Family Ophryoystidae -- Genus Ophryocystis -- Family Schizocystidae -- Genus Schizocystis -- Genus Machadoella -- Genus Lymphotropha -- Family Caulleryellidae -- Genus Caulleryella -- Genus Tipulocystis -- Family Syncystidae -- Genus Syncystis -- Family Lipotrophidae -- Genus Lipotropha -- Genus Menzbieria -- Genus Mattesia -- Genus Lipocystis -- Genus Farinocystis -- Incertae Sedis -- Genus Sawayella -- Chapter 8 The Coccidia: Agamococcidiorida, Protococcidiorida, and Ixorheorida -- Subclass Coccidiasina -- Order Agamococcidiorida -- Family Rhytidocystidae -- Genus Rhytidocystis -- Order Ixorheorida -- Family Ixorheidae -- Genus Ixorheis -- Order Protococcidiorida -- Family Grellidae -- Genus Grellia -- Genus Coelotropha -- Family Myriosporidae -- Genus Myriospora -- Genus Myriosporides -- Genus Mackinnonia -- Family Angeiocystidae -- Genus Angeiocystis -- Family Eleutheroschizonidae -- Genus Eleutheroschizon. , Chapter 9 The Coccidia: Adeleinorina -- Order Eucoccidiorida -- Suborder Adeleorina -- Family Adeleidae -- Genus Adelea -- Genus Adelina -- Genus Klossia -- Genus Orcheobius -- Genus Chagasella -- Genus Ithania -- Genus Rasajeyna -- Genus Ganapatiella -- Genus Gibbsia -- Family Legerellidae -- Genus Legerella -- Family Haemogregarinidae -- Genus Haemogregarina -- Genus Karyolysus -- Genus Hepatozoon -- Genus Cyrilia -- Family Klossiellidae -- Genus Klossiella -- Chapter 10 The Coccidia: Eimeriorina -- Suborder Eimeriorina -- Family Spirocystidae -- Genus Spirocystis -- Family Selenococcidiidae -- Genus Selenococcidium -- Family Dobellidae -- Genus Dobellia -- Family Aggregatidae -- Genus Aggregata -- Genus Merocystis -- Genus Pseudoklossia -- Genus Grasseella -- Genus Ovivora -- Genus Selysina -- Family Caryotrophidae -- Genus Caryotropha -- Genus Dorisiella -- Family Cryptosporidiidae -- Genus Cryptosporidium -- Family Pfeifferinellidae -- Genus Pfeifferinella -- Family Eimeriidae -- Genus Tyzzeria -- Genus Alveocystis -- Genus Eimeria -- Genus Epieimeria -- Genus Mantonella -- Genus Cyclospora -- Genus Caryospora -- Genus Isospora -- Genus Dorisa -- Genus Wenyonella -- Genus Octosporella -- Genus Hoarella -- Genus Sivatoshella -- Genus Pythonella -- Genus Gousseffia -- Genus Skrjabinella -- Genus Diaspora -- Family Barrouxiidae -- Genus Barrouxia -- Genus Goussia -- Genus Defretinella -- Genus Crystallospora -- Family Atoxoplasmatidae -- Genus Atoxoplasma -- Family Lankesterellidae -- Genus Lankesterella -- Family Dactylosomatidae -- Genus Dactylosoma -- Genus Schellackia -- Family Calyptosporidae -- Genus Calyptospora -- Index.
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 35 (1988), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: A total of 169 cross-transmission attempts has been made with 44 (11.8%) of the 372 named species of Eimeria of rodents. Of these, 161 were rodent-to-rodent, 6 rodent-to-lagomorph, and 1 each rodent-to-carnivore and rodent-to-bird. None of the last three categories was successful. In the rodent-to-rodent combinations, 39 (80%) of the 49 attempts to transmit a coccidian species from one rodent species to another of the same genus were successful, and only 14 (12.5%) of the 112 attempts to transmit a coccidium to a rodent of a different genus were successful. Eight of the successful attempts were with E. chinchillae, which was the only truly euryxenous species of Eimeria in the group. Two successful attempts were between the closely related rodent genera Spermophilus and Cynomys, and two were both of E. separata from Rattus norvegicus to some genetic strains but not to others of Mus musculus. One attempt with E. vermiformis from Mus musculus to Rattus norvegicus required treatment of the rat with the immunosuppressant dexamethasone to succeed. More cross-transmission studies are needed to determine the host-spectra of the species of Eimeria and other coccidian genera, and to determine the roles of genetics and immunosuppression in their transmission.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    British journal of psychotherapy 4 (1988), S. 0 
    ISSN: 1752-0118
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine , Psychology
    Notes: SUMMARY: Personal therapy for therapists is generally seen as an invaluable component of training. A review of the empirical literature on personal therapy in training found that approximately two-thirds of trainees find their personal therapy satisfactory. 15-40% however, report unsatisfactory outcomes or negative effects. Personal therapy in the early stages of training may have a deleterious effect on the therapist's work with patients. No evidence was found to support the view that personal therapy significantly enhances therapeutic effectiveness. Some reasons for this negative conclusion are mentioned and suggestions are offered for further research in this area.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1476-5535
    Keywords: Aflatoxin miniassay ; Fluorescence analysis ; Aspergillus flavus ; Aspergillus parasiticus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A convenient miniassay for aflatoxin has been developed for cultures ofAspergillus flavus andA. parasiticus grown for 3–10 days in 10 ml of a coconut extract medium. The sensitivity of the assay, as measured by photofluorometry (365 nm maximum excitation; 445 nm maximum emission), is of the order of 0.01 μM (3.12 ng/ml) for aflatoxin B1 dissolved in aqueous iodine (0.26 mM). High performance liquid chromatography, monitored by fluorometric analysis of both an aflatoxin B1 standard and selected culture filtrates, confirmed the sensitivity of the assay and indicated specificity for iodine-enhanced fluorescence of aflatoxin in the coconut extract medium. Thin layer chromatography further confirmed the aflatoxin titers and the specificity for enhancement of aflatoxins B1 and G1 in culture filtrates.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Diabetologia 31 (1988), S. 703-707 
    ISSN: 1432-0428
    Keywords: Diabetes ; zinc ; immune system ; lymphocyte mitogenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary To evaluate the role of zinc status in immune system dysfunction in diabetic animals, the interleukin-2 production and the lymphocyte mitogenic response to phytohaemagglutinin, concanavalin A and lipopolysaccharide were measured in streptozotocin-induced diabetic rats, diabetic rats treated with insulin and their non-diabetic controls maintained on low zinc, normal zinc and high zinc diets for 3 weeks. Unstimulated lymphocyte proliferation was significantly lower in diabetic rats compared to nondiabetic control rats maintained on normal zinc diet (1505±318 vs 3447±497 cpm) (p〈0.005) or low zinc diet (546±191 vs 4011±628cpm) (p〈0.005). High zinc diet attenuated the difference between the diabetic rats (2404±833 cpm) and control rats (3929±713 cpm). Insulinised diabetic rats were similar to control rats. Phytohaemagglutinin-stimulated lymphocyte proliferation was not significantly altered with dietary zinc changes, but diabetic rats on low zinc diet had significantly lower (p〈0.025) values compared to control rats on the same diet (41470±7874 vs 72308±8895 cpm). Insulinisation did not normalise phytohemaegglutinin-stimulated lymphocyte proliferation (40711±3666 cpm). Similarly, cells from diabetic rats on low zinc diet, unlike their controls, failed to respond to concanavalin A stimulation. Compared to control rats the diabetic rats on either low or normal zinc diets had lower lipopolysaccharide-stimulated lymphocyte proliferation. High zinc diet or insulinisation normalised mitogenic response of lymphocytes to lipopolysaccharide. Unlike the diabetic rats alterations in dietary zinc intake did not significantly affect the lymphocyte proliferation in control rats. Neither the diabetic state nor zinc status had any significant effect on interleukin-2 production. Thus, zinc status of the animal is an important determinant of cell-mediated immunity, but additional factors peculiar to the diabetic state may be involved in the modulation of the immune system in diabetes.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Behavior genetics 18 (1988), S. 571-581 
    ISSN: 1573-3297
    Keywords: Mus domesticus ; house mice ; vocalization ; diallel analysis ; genetic dominance ; threshold model
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Psychology
    Notes: Abstract Rates of vocalization in response to experimenter handling were assessed in eight inbred parent strains and their F1 crosses. Use of a stimulation level greater than that previously used by Whitney and a normalizing transformation of response rates provided evidence for a threshold-of-response model for vocalization. The diallel analysis indicated that a simple additive-dominance model fit the normalized data well. Substantial additive genetic variance and incomplete dominance favoring vocalization to handling were observed. Vocalization rates of recently domesticated wild-trapped mice did not differ from the diallel average, nor was there a strong relationship between vocalization rates of the strains tested and other assessments of wildness or temperament reported for these strains. Taken together, Whitney's work and the present data provide an extended testing environment for the vocalization response, producing a more comprehensive picture of the genetic architecture of the response than is possible from either study alone.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-7381
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The occurrence of neuropeptides in rat brown adipose tissue has been investigated. Immunohistochemical studies on interscapular and perirenal brown fat have demonstrated unequivocally the presence of substance-P (SP)-like, neuropeptide-Y (NPY)-like and calcitonin gene related-peptide (CGRP)-like immunoreactive elements (putative nerves) in adventitial distribution on inter- and intralobular supply arteries and in accompanying nerve bundles. At a more peripheral level, some NPY-like immunoreactive elements and a greater number of CGRP-like immunoreactive elements were observed in the parenchymal field. Somatostatin, bombesin, neurotensin, enkephalin, and vasoactive-intestinal-polypeptide immunoreactivities were not detected. No differences in neuropeptide distribution were noted between interscapular and perirenal brown fat. There is a degree of coincident distribution of SP, NPY and CGRP with that of noradrenergic nervous elements as visualized by condensation histochemistry. Since after 6-hydroxydopamine treatment not all the nerve terminals in rat brown adipose tissue are stigmatized (earlier report), the present results have been discussed in the light of a possible pluralism in innervation of brown adipose tissue.
    Type of Medium: Electronic Resource
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