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  • 1
    Online Resource
    Online Resource
    Milton :Taylor & Francis Group,
    Keywords: Notochord-Evolution. ; Electronic books.
    Description / Table of Contents: Although it is the defining organ of Chordates, the notochord is perhaps the least understood of vertebrate organs because it is usually considered a transient structure only present in early embryonic development.
    Type of Medium: Online Resource
    Pages: 1 online resource (267 pages)
    Edition: 1st ed.
    ISBN: 9781498787925
    Series Statement: Evolutionary Cell Biology Series
    DDC: 591.3
    Language: English
    Note: Cover -- Half Title -- Title Page -- Copyright Page -- Table of Contents -- Series Preface -- Preface -- Acknowledgments -- Authors -- Section I: Development and Evolutionary Origin of the Notochord -- Chapter 1 Introduction to the Notochord and to Notochord Cells -- 1.1 Introduction -- 1.2 Structure of the Notochord -- A. Notochord Cells (Chordocytes) -- B. The Notochord Sheath -- 1.3 Function of the Notochord and Notochord Cells -- A. The Primary Chordate Axial Skeleton -- B. Signals for Neural and Ectodermal Induction -- C. Signals for Somitic Mesodermal Induction -- D. Integration of Axial Structures at the Phylotypic Stage -- E. Fate in Later Ontogeny -- 1.4 Differentiation of Notochord Cells -- A. Stack of Coins -- B. Notochord Epithelium -- C. Development of the Notochord Sheath -- 1.5 Notochord as Cartilage -- 1.6 Summary -- Chapter 2 Discovery and Evolutionary Origin of the Notochord -- 2.1 Introduction -- 2.2 Chordates -- A. Cephalochordates -- B. Tunicates -- 2.3 Hemichordates: A Phylum Outside the Chordates -- 2.4 Discovery that Amphioxus and Ascidians Possess a Notochord -- A. Amphioxus -- B. Ascidians (Tunicates) -- 2.5 Annelids as Chordate Ancestors -- A. The 1870s: Midline Structures, Segmentation and an Annelid Origin for Chordates -- B. The 20th C: Dorso-Ventral Inversion -- C. The 1990s: The Stomochord, Axochord and Gene-Based Homology Hypotheses -- 2.6 Vertebrates -- A. Albert Kölliker's 1859 Paper -- B. Notochord Structure and Function in Vertebrates -- 2.7 Searching for Chordates and Early Vertebrates in the Fossil Record -- A. Cambrian Fossils: Candidate Chordates -- B. Candidate Vertebrate: Jamoytius kerwoodi, Conodonts and the "Tully Monster" -- a. Jamoytius kerwoodi -- b. Conodonts -- c. The "Tully Monster" -- 2.8 Developmental Biology and Palaeontology -- 2.9 Summary. , Chapter 3 Germ-Layer Origin of the Notochord: Endoderm or Mesoderm -- 3.1 Introduction -- 3.2 The Notochord, Vertebral Column and Neural Tube -- 3.3 Developmental Origin of the Notochord -- A. Notochord as Endodermal -- B. Notochord as Mesodermal -- C. Notochord as Ectodermal -- D. Chordamesoderm and the Organizer -- E. The Dorsal Organizer -- F. The Anterior Notochord -- 3.4 The Notochord in Human Embryos -- 3.5 The Tail Bud, Secondary Neurulation and Secondary Notochord Extension -- 3.6 External Tails in Humans -- 3.7 Summary -- Section II: Function of the Notochord and Notochord Sheath -- Chapter 4 Function of the Notochord in Early Embryonic Development -- 4.1 Introduction -- 4.2 Midline Dorso-Ventral Organization: The Floor Plate -- 4.3 Notochord-Mesoderm Signaling Segregates Myotome from Sclerotome -- 4.4 The Notochord and Chondrogenesis of Sclerotomal Mesoderm in Tetrapods -- A. Removal or Transplantation of the Notochord and/or Neural Tube -- B. Molecular Signaling Cascades and Vertebral Chondrogenesis -- a. Shh, Noggin and Gremlin1 -- b. Pax1, Pax9 and Sox9 -- 4.5 Notochord Signaling and Vertebral Morphogenesis in Tetrapods -- A. Notochord, Neural Tube and Pax1 -- B. Notochord and Spinal Ganglia -- 4.6 Segmental Hox Gene Expression in the Teleost Notochord -- 4.7 Summary -- Chapter 5 Notochord Cells and Notochord Sheath Formation -- 5.1 Introduction -- 5.2 A Stack of Coins and the First Layer of the Notochord Sheath -- 5.3 The Notochord Sheath -- A. Notochord Sheath Formation -- B. Invasion of Cells into the Notochord Sheath -- 5.4 Notochord Cells -- A. The Notochord Epithelium -- B. Vacuolated Cells and the Expansion of the Notochord -- 5.5 The Amniote Notochord is Special -- A. The Notochord and what we Consider as Cartilage Matrix Components -- B. The Notochord Makes Cartilage Collagens, or the Other Way Round? -- 5.6 Summary. , Section III: Nature and Fate of the Notochord and Vertebrae across the Vertebrates -- Chapter 6 The Role of the Notochord in Vertebral Body Development -- 6.1 Do Somites Rule Over the Notochord? -- A. Resegmentation and Leaky-Resegmentation -- B. The Notochord and Vertebral Body Development -- 6.2 The Chordacentrum -- 6.3 In Half of All Vertebrate Species, Notochord Sheath Mineralization and Not Chondrogenesis Creates the Anlage of the Vertebral Centrum -- A. Are Notochord Signals Involved? -- B. How the Notochord Generates Vertebral Body Anlagen -- C. Variations of Vertebral Body Centra Anlagen Formation -- 6.4 How Common Is Notochord Sheath Mineralization? -- 6.5 Development of Cartilaginous Vertebral Bodies from the Notochord -- 6.6 A New Start of Vertebral Column Development -- 6.7 Summary -- Chapter 7 The Notochord in Adult Vertebrates -- 7.1 Introduction -- 7.2 Non-Constricted Notochords in Adult Vertebrates -- A. The Naked Notochord of Jawless Vertebrates -- B. Notochords of Extant Sarcopterygians -- C. Non-Constricted Notochords and Vertebral Centrum Regression -- 7.3 Constricted Notochords in Adult Vertebrates -- A. Notochord Constriction in Non-Mammalian Tetrapods -- B. Notochord Expansion Forms the Actinopterygian Intervertebral Disk -- C. A Neopterygian Notochord that Follows the Tetrapod Scheme -- D. Constricted and Non-Constricted Chondrichthyan Notochords -- 7.4 The Discontinuous Mammalian Notochord -- 7.5 Discontinuous Notochords in Non-Mammalian Vertebrates -- 7.6 Summary -- Section IV: Relationships: Notochord-Cartilage, Notochord-Vertebrae, Notochord-Vertebral Column -- Chapter 8 Relationships between Notochord and Chondrogenic Cells and Tissues: Transformational Series -- 8.1 Introduction -- 8.2 Shared Morphological Features of Notochord and Chondrogenic Cells. , 8.3 Similar Glycosaminoglycans in the Notochord Sheath and Cartilage Extracellular Matrix -- A. Notochord Secretes the Glycosaminoglycans of the Notochord Sheath -- B. Aggrecan -- C. Chondromodulin-1 -- 8.4 Similar Collagens in the Notochord Sheath and Cartilage Extracellular Matrix -- A. Collagen Type II -- B. Other Fibrillar Collagens -- C. Secretion of Type X Collagen -- 8.5 Shared Genes and Transcription Factors -- A. Brachyury -- B. Sox5 and Sox6 -- C. Sox9 -- 8.6 Transformations between Notochord and Chondrogenic Cells -- A. Chordoid and Chondroid -- B. Chordomas and Chondromas -- C. The Origins of Intervertebral and Intravertebral Cartilages -- a. Intervertebral Cartilage -- b. Intravertebral Cartilage -- D. Terminal Cartilaginous Notochord Extension -- 8.7 Notochord as a Type of Cartilage -- 8.8 Summary -- Chapter 9 The Notochord and Hypotheses about the Evolution of the Vertebral Column -- 9.1 The Notochord as Viewed in Life Science Disciplines -- 9.2 The Notochord's Struggle with the Arcualia Hypothesis -- 9.3 The Notochord and Autocentra -- 9.4 Centra from Notochord, Arches from Somites -- 9.5 The Fusion of Chordacentra and Autocentra -- 9.6 Joint Formation, a Key for Vertebral Column Homology -- 9.7 Summary -- References -- Index -- Series Page.
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  • 2
    In: Journal of virology, Washington, DC : ASM, 1967, 79(2005), 3, Seite 1842-1852, 0022-538X
    In: volume:79
    In: year:2005
    In: number:3
    In: pages:1842-1852
    Description / Table of Contents: The zebrafish, Danio rerio, has become recognized as a valuable model for the study of development, genetics, and toxicology. Recently, the zebrafish has been recognized as a useful model for infectious disease and immunity. In this study, the pathogenesis and antiviral immune response of zebrafish to experimental snakehead rhabdovirus (SHRV) infection was characterized. Zebrafish 24 h postfertilization to 30 days postfertilization were susceptible to infection by immersion in 10 6 50% tissue culture infective doses (TCID50) of SHRV/ml, and adult zebrafish were susceptible to infection by intraperitoneal (i.p.) injection of 10 5 TCID50 of SHRV/ml. Mortalities exceeded 40% in infected fish, and clinical presentation of infection included petechial hemorrhaging, redness of the abdomen, and erratic swim behavior. Virus reisolation and reverse transcription-PCR analysis of the viral nucleocapsid gene confirmed the presence of SHRV. Histological sections of moribund embryonic and juvenile fish revealed necrosis of the pharyngeal epithelium and liver, in addition to congestion of the swim bladder by cell debris. Histopathology in adult fish injected i.p. was confined to the site of injection. The antiviral response in zebrafish was monitored by quantitative real-time PCR analysis of zebrafish interferon (IFN) and Mx expression. IFN and Mx levels were elevated in zebrafish exposed to SHRV, although expression and intensity differed with age and route of infection. This study is the first to examine the pathogenesis of SHRV infection in zebrafish. Furthermore, this study is the first to describe experimental infection of zebrafish embryos with a viral pathogen, which will be important for future experiments involving targeted gene disruption and forward genetic screens.
    Type of Medium: Online Resource
    Pages: Ill., graph. Darst
    ISSN: 0022-538X
    Language: English
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  • 3
    ISSN: 1432-0878
    Keywords: Key words: Fish bone ; Acellular bone ; Bone resorption ; Tartrate-resistant acid phosphatase ; Mononucleated osteoclasts ; Osteoblasts ; Oreochromis niloticus (Teleostei)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. Bone resorption by mononucleated cells was studied in the acellular bone of a teleost fish (Oreochromis niloticus) by histological and enzyme histochemical observations and by transmission electron microscopy. Bone resorbing cells (osteoclasts) were identified by their location at the sites of bone resorption, their frequent association with a band of concentrated activity of tartrate-resistant acid phosphatase at the bone surface and by the presence or lack of certain enzymes. Tartrate-resistant acid phosphatase was used as a marker for osteoclasts, and alkaline phosphatase as a marker for osteoblasts. Osteoclasts in O. niloticus are not multinucleated; however, during intense bone resorption, they form cell aggregations that resemble multinucleated giant cells in mammals. Conversely, during less intense bone degradation, osteoclasts are flat, have long narrow cytoplasmic processes and resemble the bone-lining cells of mammals. All bone-resorbing cells in O. niloticus are mononucleated and lack a ruffled border. Similarities to and differences from bone resorption by mononucleated cells in mammals are discussed.
    Type of Medium: Electronic Resource
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  • 4
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    Wiley
    In:  Journal of Morphology, 260 . p. 301.
    Publication Date: 2018-04-03
    Description: Nonmammalian tooth-bearing vertebrates usually replace their teeth throughout life. Much about how a replacement pattern is generated has been learned from zebrafish. However, to understand general mechanisms of tooth replacement, advantage can be taken from studying other, “nonmodel” species. We have mapped the patterns of tooth replacement in widely divergent aquatic osteichthyans using 2D charts, in which one axis is time, the other linear spacing along the tooth row. New teeth that are generated simultaneously are considered part of the same odontogenic wave. Using this approach, it appears that a similar, general pattern underlies very distinctive dentitions in distantly related species. A simple shift in spacing of odontogenic waves, or in distance between subsequent tooth positions along a row (or both), can produce dramatically different dentitions between life stages within a species, or between closely related species. Examples will be presented from salmonids, cyprinids, and cichlids. Our observations suggest that lines linking subsequent positions may have more biological significance than replacement waves (usually linking alternate positions), often used to explain the generation of patterns. The presence of a general pattern raises questions about common control mechanisms. There is now increasing evidence, at least for the zebrafish, to support a role for stem cells in continuous tooth renewal and control of replacement patterns.
    Type: Article , NonPeerReviewed
    Format: text
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  • 5
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    Wiley
    In:  Journal of Experimental Zoology Part B: Molecular and Developmental Evolution, 306B (3). pp. 204-215.
    Publication Date: 2017-07-11
    Description: The dentition of osteichthyans presents an astonishing diversity with regard to the distribution of teeth in the oral cavity, tooth numbers, arrangements, shapes, and sizes. Taking examples from three unrelated teleosts—the most speciose group of osteichthyans—and from the literature, this study explores how the initial tooth pattern is set up, and how this relates to the establishment and maintenance (or modification) of the tooth replacement pattern. In teleosts, first-generation teeth (the very first teeth in ontogeny to develop at a particular locus) are commonly initiated in adjacent or in alternate (odd and even) positions. The mechanisms responsible for these divergent developmental patterns remain to be elucidated, in particular, whether they reflect a field or local type of control. However, patterns of adjacent or alternate tooth initiation, set up by the first-generation teeth, can easily turn into replacement patterns where new teeth are initiated simultaneously every second, or even every third position, by synchronizing the formation of new first-generation teeth to the formation of replacement teeth at older loci. Our observations suggest that, once established, the replacement pattern appears to be maintained, as a kind of “default” state. Variations and modifications in this pattern are nevertheless common and suggest that tooth replacement is under local control, exerted at the level of the initiation of replacement teeth. Further studies are needed to test the hypothesis that regular replacement patterns are more frequent in association with the plesiomorphic condition of extramedullary replacement (replacement on the surface of the dentigerous bone) and more rare in the derived condition of intramedullary replacement (replacement within the medullary cavity of the dentigerous bone)
    Type: Article , NonPeerReviewed
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  • 6
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    In:  Palaeontological Association Newsletter, 58 . pp. 26-31.
    Publication Date: 2017-01-05
    Type: Article , NonPeerReviewed
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  • 7
    Publication Date: 2017-01-06
    Description: The short tail phenotype represents one of the main causes for downgrading of farmed Atlantic salmon (Salmo salar) at slaughterhouses. Prevalence of short tail is variable and the aetiology is suspected to be multi-factorial. Risk factors have been identified but descriptions of the aetiology and the pathology of the condition are still rare. In the current study, a radiological and histological analysis of short tails has been performed, examining six normal and six downgraded individuals from a slaughterhouse in southern Norway. In the short tail phenotype, vertebral bodies were shifted and bent at the contact zone of adjacent vertebral bodies. Changes either affected the entire spine or were located at the medial caudal-spine. While the internal bone structure of the vertebrae was similar in deformed and non-deformed animals, a lack of intervertebral space apparently caused a shortening of the vertebral column and corresponded to an elevated condition factor in deformed individuals. Histological analysis revealed different degrees of proliferation of cartilaginous tissues, which replaced the intervertebral notochord tissue. The displacement of adjacent vertebral bodies and the development of cartilage in between vertebral bodies suggest mechanical forces as a possible cause for the observed deformations, since mechanically-induced overload and a subsequent direct contact of bones are factors that can stimulate heterotopic cartilage development and pseudoarthrosis
    Type: Article , NonPeerReviewed
    Format: text
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  • 8
    Publication Date: 2017-01-05
    Type: Article , NonPeerReviewed
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  • 9
    Publication Date: 2018-04-03
    Type: Article , NonPeerReviewed
    Format: text
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  • 10
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    Wiley
    In:  Journal of Morphology, 260 . pp. 340-341.
    Publication Date: 2018-04-03
    Type: Article , NonPeerReviewed
    Format: text
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