Thematische Bibliographien / Marmosets Anatomy / Zeitschriftenartikel
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Zeitschriftenartikel zum Thema „Marmosets Anatomy“

Autor: Grafiati
Veröffentlicht am 4. Juni 2021
Zuletzt aktualisiert am 31. Januar 2023

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1

Virley, David, Sarah J. Hadingham, Jenny C. Roberts, Belinda Farnfield, Heather Elliott, Greg Whelan, Jackie Golder, Chris David, Andrew A. Parsons, and A. Jackie Hunter. "A New Primate Model of Focal Stroke: Endothelin-1—Induced Middle Cerebral Artery Occlusion and Reperfusion in the Common Marmoset." Journal of Cerebral Blood Flow & Metabolism 24, no. 1 (January 2004): 24–41. http://dx.doi.org/10.1097/01.wcb.0000095801.98378.4a.

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The purpose of the present set of studies was to develop a new primate model of focal ischemia with reperfusion for long-term functional assessment in the common marmoset. Initially, the cerebral vascular anatomy of the marmoset was interrogated by Araldite-cast and ink-perfusion methods to determine the feasibility of an intravascular surgical approach. The methods showed that the internal carotid artery was highly tortuous in its passage, precluding the development of an extracranial method of inducing temporary middle cerebral artery occlusion in the marmoset. A pilot dose-response study in
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2

Harrison, Mary L., and Suzette D. Tardif. "Social implications of gummivory in marmosets." American Journal of Physical Anthropology 95, no. 4 (December 1994): 399–408. http://dx.doi.org/10.1002/ajpa.1330950404.

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3

Sussman, Robert W. "The Marmosets and Callimico: Phylogeny, Behavior, Anatomy and Conservation." Journal of Mammalian Evolution 18, no. 3 (April 12, 2011): 225–26. http://dx.doi.org/10.1007/s10914-011-9159-9.

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4

Marroig, Gabriel, Susan Cropp, and James M. Cheverud. "Systematics and evolution of the jacchus group of marmosets (Platyrrhini)." American Journal of Physical Anthropology 123, no. 1 (2003): 11–22. http://dx.doi.org/10.1002/ajpa.10146.

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5

Casteleyn, C., J. Bakker, S. Breugelmans, I. Kondova, J. Saunders, J. A. M. Langermans, P. Cornillie, et al. "Anatomical description and morphometry of the skeleton of the common marmoset (Callithrix jacchus)." Laboratory Animals 46, no. 2 (April 2012): 152–63. http://dx.doi.org/10.1258/la.2012.011167.

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Callithrix jacchus (common marmoset) is regularly used in biomedical research, including for studies involving the skeleton. To support these studies, skeletons of healthy animals that had been euthanized for reasons not interfering with skeletal anatomy were prepared. The marmoset dental formula 2I-1C-3P-2M of each oral quadrant is atypical for New World monkeys which commonly possess a third molar. Seven cervical, 12–13 thoracic, 7–6 lumbar, 2–3 sacral and 26–29 caudal vertebrae are present, the thoracolumbar region always comprising 19 vertebrae. A sigmoid clavicle connects the scapula with
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Harrison, Mary L., and Suzette D. Tardif. "Kin preference in marmosets and tamarins:Saguinus oedipus andCallithrix jacchus (callitrichidae, primates)." American Journal of Physical Anthropology 77, no. 3 (November 1988): 377–84. http://dx.doi.org/10.1002/ajpa.1330770310.

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7

Ford, Susan M. "Comment on the evolution of claw-like nails in callitrichids (marmosets/tamarins)." American Journal of Physical Anthropology 70, no. 1 (May 1986): 25–26. http://dx.doi.org/10.1002/ajpa.1330700106.

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8

Young, Jesse W. "Substrate determines asymmetrical gait dynamics in marmosets (Callithrix jacchus) and squirrel monkeys (Saimiri boliviensis)." American Journal of Physical Anthropology 138, no. 4 (April 2009): 403–20. http://dx.doi.org/10.1002/ajpa.20953.

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9

Francisco, Talitha Mayumi, Karina Lucas Barbosa Lopes-Mattos, Edgard Augusto de Toledo Picoli, Dayvid Rodrigues Couto, Juraci Alves Oliveira, José Cola Zanuncio, José Eduardo Serrão, Ita de Oliveira Silva, and Vanner Boere. "Feeding habits of marmosets: A case study of bark anatomy and chemical composition ofAnadenanthera peregrinagum." American Journal of Primatology 79, no. 3 (November 3, 2016): e22615. http://dx.doi.org/10.1002/ajp.22615.

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10

Smith, Timothy D., Thomas P. Eiting, Christopher J. Bonar, and Brent A. Craven. "Nasal Morphometry in Marmosets: Loss and Redistribution of Olfactory Surface Area." Anatomical Record 297, no. 11 (October 14, 2014): 2093–104. http://dx.doi.org/10.1002/ar.23029.

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11

Garde, Seema V., Anil R. Sheth, and Sujata A. Kulkarni. "FSH in testes of marmosets during development: Immunocytochemical localization and de novo biosynthesis." Anatomical Record 231, no. 1 (September 1991): 119–24. http://dx.doi.org/10.1002/ar.1092310113.

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12

Lowenstine, Linda J. "A Primer of Primate Pathology: Lesions and Nonlesions." Toxicologic Pathology 31, no. 1_suppl (January 2003): 92–102. http://dx.doi.org/10.1080/01926230390177668.

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Nonhuman primates are important laboratory animals for biomedical, pharmacology, and toxicology research. To effectively use primates as models, their gross and histologic anatomy, physiology and natural history, as well as common health problems and the source from which the primate is obtained, must be known and understood by pathologists involved in study design and/or interpretation. The first very important lesson in the “primer” is: there is no such thing as a generic monkey. Brand names (ie, species and subspecies) are important. Several taxonomic groups of primates are used in research
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13

Dumont, Elizabeth R., Julian L. Davis, Ian R. Grosse, and Anne M. Burrows. "Finite element analysis of performance in the skulls of marmosets and tamarins." Journal of Anatomy 218, no. 1 (December 15, 2010): 151–62. http://dx.doi.org/10.1111/j.1469-7580.2010.01247.x.

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14

Rosenberger, Alfred L. "Marmosets and tamarins: Systematics, behavior, and ecology. Edited by Anthony B. Rylands. New York: Oxford University Press. 1993. 396 pp. ISBN 0-19-85022-1. $75 (cloth)." American Journal of Physical Anthropology 97, no. 4 (August 1995): 457–58. http://dx.doi.org/10.1002/ajpa.1330970413.

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15

La Salles, Ana Yasha Ferreira de, Juliana Molina Martins, Brunna Muniz Rodrigues Falcão, José Rômulo Soares Dos Santos, Guildenor Xavier Medeiros, and Danilo José Ayres De Menezes. "Medullary Conus Topography in White-Tufted-Ear-Marmoset (Callithrix jacchus)." Acta Scientiae Veterinariae 45, no. 1 (June 20, 2017): 6. http://dx.doi.org/10.22456/1679-9216.80003.

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Background: The common marmoset (Callithrix jacchus) belongs to the family Cebidae and Subfamily Callitrichinae, a group formed by the smallest anthropoid primates. It is a very common species and adapts easily to captivity, an aspect that encourages the clandestine capture of these animals and makes them susceptible to wounds resulting from clandestine rearing and inadequate management, so that studies to understand the species are extremely important. With the objective of supplying anatomic bases for the practice of epidural anesthetic, data were studied regarding the topography of the comm
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Zimmerman, Shawn M., Mackenzie E. Long, Jeremy S. Dyke, Tomislav P. Jelesijevic, Frank Michel, Eric R. Lafontaine, and Robert J. Hogan. "Use of Immunohistochemistry to Demonstrate In Vivo Expression of the Burkholderia mallei Virulence Factor BpaB During Experimental Glanders." Veterinary Pathology 55, no. 2 (November 16, 2017): 258–67. http://dx.doi.org/10.1177/0300985817736113.

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Burkholderia mallei causes the highly contagious and debilitating zoonosis glanders, which infects via inhalation or percutaneous inoculation and often culminates in life-threatening pneumonia and sepsis. In humans, glanders is difficult to diagnose and requires prolonged antibiotic therapy with low success rates. No vaccine exists to protect against B. mallei, and there is concern regarding its use as a bioweapon. The authors previously identified the protein BpaB as a potential target for devising therapies due to its role in adherence to host cells and the formation of biofilms in vitro and
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17

Beattie, J. "The Anatomy of the Common Marmoset (Hapale jacchus Kuhl)." Proceedings of the Zoological Society of London 97, no. 3 (August 21, 2009): 593–718. http://dx.doi.org/10.1111/j.1469-7998.1927.tb07430.x.

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18

Mashiko, H., A. C. Yoshida, S. S. Kikuchi, K. Niimi, E. Takahashi, J. Aruga, H. Okano, and T. Shimogori. "Comparative Anatomy of Marmoset and Mouse Cortex from Genomic Expression." Journal of Neuroscience 32, no. 15 (April 11, 2012): 5039–53. http://dx.doi.org/10.1523/jneurosci.4788-11.2012.

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19

Moore, H. D. M., Sara Gems, and J. P. Hearn. "Early implantation stages in the marmoset monkey (Callithrix jacchus)." American Journal of Anatomy 172, no. 4 (April 1985): 265–78. http://dx.doi.org/10.1002/aja.1001720402.

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20

Dwyer, Barney E., Denson G. Fujikawa, and Claude G. Wasterlain. "Metabolic anatomy of generalized bicuculline seizures in the newborn marmoset monkey." Experimental Neurology 94, no. 1 (October 1986): 213–27. http://dx.doi.org/10.1016/0014-4886(86)90284-0.

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21

Falcão, Brunna Muniz Rodrigues, Joyce Galvão Souza, Ana Yasha Ferreira La Salles, Luan Nascimento Batista, Ediane Freitas Rocha, João Augusto Rodrigues Alves Diniz, Annielle Regina Fonseca Fernandes, José Rômulo Soares Santos, Danilo José Ayres Menezes, and Gildenor Xavier Medeiros. "Heart anatomy and topography of the common marmoset ( Callithrix jacchus Linnaeus, 1758)." Journal of Medical Primatology 49, no. 3 (February 5, 2020): 153–57. http://dx.doi.org/10.1111/jmp.12463.

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22

Haider, Syed G., Dieter Passia, Annemarie Treiber, and Susanne Milhorst. "Description of Eight Phases of Spermiogenesis in the Marmoset Testis." Cells Tissues Organs 135, no. 2 (1989): 180–84. http://dx.doi.org/10.1159/000146750.

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23

Wagner, Wencke M., and Robert M. Kirberger. "RADIOGRAPHIC ANATOMY OF THE THORAX AND ABDOMEN OF THE COMMON MARMOSET (CALLITHRIX JACCHUS)." Veterinary Radiology Ultrasound 46, no. 3 (May 2005): 217–24. http://dx.doi.org/10.1111/j.1740-8261.2005.00044.x.

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24

Graf, Renate, and R. Gossrau. "Cytochemistry of proteases in the mature rat and marmoset placenta." Histochemical Journal 17, no. 5 (May 1985): 567–71. http://dx.doi.org/10.1007/bf01003193.

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25

Kumar, R. Asok, and David M. Phillips. "Spermiation and sperm maturation in the marmoset." Anatomical Record 229, no. 3 (March 1991): 315–20. http://dx.doi.org/10.1002/ar.1092290305.

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26

Kaneko, Takaaki, Hiromasa Takemura, Franco Pestilli, Afonso C. Silva, Frank Q. Ye, and David A. Leopold. "Spatial organization of occipital white matter tracts in the common marmoset." Brain Structure and Function 225, no. 4 (April 6, 2020): 1313–26. http://dx.doi.org/10.1007/s00429-020-02060-3.

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27

Garde, Seema V., Anil R. Sheth, and Sujata A. Kulkarni. "Cellular distribution of inhibin in marmoset testes during development." Anatomical Record 229, no. 3 (March 1991): 334–38. http://dx.doi.org/10.1002/ar.1092290307.

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28

Ferreira Junior, Jair A., Daniel R. Rissi, Mônica A. Elias, André S. Leonardo, Karla A. Nascimento, Juliana T. S. A. Macêdo, and Pedro M. O. Pedroso. "Nephroblastoma in a black-tufted marmoset (Callithrix penicillata)." Pesquisa Veterinária Brasileira 38, no. 11 (November 2018): 2155–58. http://dx.doi.org/10.1590/1678-5150-pvb-5995.

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ABSTRACT: A renal nephroblastoma is described in a free-living black-tufted marmoset (Callithrix penicillata) in Central Brazil. The monkey was found dead and subjected to necropsy. Gross anatomic changes consisted of a ruptured left kidney, which was almost completely effaced by a white to yellow, partially encapsulated friable mass. The left ureter was distended due to obstruction by a red, spherical, 2mm in diameter friable mass. The urinary bladder was also distended. Histologically the renal and ureteral masses consisted of a triphasic embryonal neoplasm composed of embryonic epithelium f
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29

Clarke, Robert J., Maria-Luisa Aléssío, and Valdir F. Pessoa. "Distribution of Motoneurones Innervating Extraocular Muscles in the Brain of the Marmoset (Callithrixjacchus)." Cells Tissues Organs 130, no. 2 (1987): 191–96. http://dx.doi.org/10.1159/000146444.

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30

Bakken, Trygve E., Nikolas L. Jorstad, Qiwen Hu, Blue B. Lake, Wei Tian, Brian E. Kalmbach, Megan Crow, et al. "Comparative cellular analysis of motor cortex in human, marmoset and mouse." Nature 598, no. 7879 (October 6, 2021): 111–19. http://dx.doi.org/10.1038/s41586-021-03465-8.

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AbstractThe primary motor cortex (M1) is essential for voluntary fine-motor control and is functionally conserved across mammals1. Here, using high-throughput transcriptomic and epigenomic profiling of more than 450,000 single nuclei in humans, marmoset monkeys and mice, we demonstrate a broadly conserved cellular makeup of this region, with similarities that mirror evolutionary distance and are consistent between the transcriptome and epigenome. The core conserved molecular identities of neuronal and non-neuronal cell types allow us to generate a cross-species consensus classification of cell
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31

Bremer, Dietrich, Hans-Joachim Merker, and Reinhart Gossrau. "Ultrastructure and hydrolase cytochemistry of the developing marmoset yolk sac." Anatomy and Embryology 172, no. 1 (June 1985): 101–13. http://dx.doi.org/10.1007/bf00318949.

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32

Smith, Caroline A., H. D. M. Moore, and J. P. Hearn. "The ultrastructure of early implantation in the marmoset monkey (Callithrix jacchus)." Anatomy and Embryology 175, no. 3 (January 1987): 399–410. http://dx.doi.org/10.1007/bf00309853.

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33

Enders, Allen C., and Alexander Lopata. "Implantation in the marmoset monkey: Expansion of the early implantation site." Anatomical Record 256, no. 3 (November 1, 1999): 279–99. http://dx.doi.org/10.1002/(sici)1097-0185(19991101)256:3<279::aid-ar7>3.0.co;2-o.

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34

Woodward, Alexander, Rui Gong, Hiroshi Abe, Ken Nakae, Junichi Hata, Henrik Skibbe, Yoko Yamaguchi, et al. "The NanoZoomer artificial intelligence connectomics pipeline for tracer injection studies of the marmoset brain." Brain Structure and Function 225, no. 4 (May 2020): 1225–43. http://dx.doi.org/10.1007/s00429-020-02073-y.

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35

Clarke, R. J., C. J. P. Coimbra, and M. L. Aléssio. "Distribution of Parasympathetic Motoneurones in the Oculomotor Complex Innervating the Ciliary Ganglion in the Marmoset (Callithrix jacchus)." Cells Tissues Organs 121, no. 1 (1985): 53–58. http://dx.doi.org/10.1159/000145942.

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36

Aeckerle, Nelia, Ralf Dressel, and Rüdiger Behr. "Grafting of Neonatal Marmoset Monkey Testicular Single-Cell Suspensions into Immunodeficient Mice Leads to ex situ Testicular Cord Neomorphogenesis." Cells Tissues Organs 198, no. 3 (2013): 209–20. http://dx.doi.org/10.1159/000355339.

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37

Majka, Piotr, Marcello G. P. Rosa, Shi Bai, Jonathan M. Chan, Bing-Xing Huo, Natalia Jermakow, Meng K. Lin, et al. "Unidirectional monosynaptic connections from auditory areas to the primary visual cortex in the marmoset monkey." Brain Structure and Function 224, no. 1 (October 4, 2018): 111–31. http://dx.doi.org/10.1007/s00429-018-1764-4.

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38

Risser, Laurent, Amirouche Sadoun, Muriel Mescam, Kuzma Strelnikov, Sandra Lebreton, Samuel Boucher, Pascal Girard, Nathalie Vayssière, Marcello G. P. Rosa, and Caroline Fonta. "In vivo localization of cortical areas using a 3D computerized atlas of the marmoset brain." Brain Structure and Function 224, no. 5 (April 8, 2019): 1957–69. http://dx.doi.org/10.1007/s00429-019-01869-x.

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39

Rulle, Alexander, Nikoloz Tsikolia, Bernadette de Bakker, Charis Drummer, Rüdiger Behr, and Christoph Viebahn. "On the Enigma of the Human Neurenteric Canal." Cells Tissues Organs 205, no. 5-6 (2018): 256–78. http://dx.doi.org/10.1159/000493276.

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Existence and biomedical relevance of the neurenteric canal, a transient midline structure during early neurulation in the human embryo, have been controversially discussed for more than a century by embryologists and clinicians alike. In this study, the authors address the long-standing enigma by high-resolution histology and three-dimensional reconstruction using new and historic histological sections of 5 human 17- to 21-day-old embryos and of 2 marmoset monkey embryos of the species Callithrix jacchus at corresponding stages. The neurenteric canal presents itself as the classical vertical
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40

Ziegler, Toni E., Shelley L. Prudom, and Sofia R. Zahed. "Variations in male parenting behavior and physiology in the common marmoset." American Journal of Human Biology 21, no. 6 (November 2009): 739–44. http://dx.doi.org/10.1002/ajhb.20920.

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41

Roe, Anna Wang, Kerstin Fritsches, and John D. Pettigrew. "Optical imaging of functional organization of V1 and V2 in marmoset visual cortex." Anatomical Record Part A: Discoveries in Molecular, Cellular, and Evolutionary Biology 287A, no. 2 (2005): 1213–25. http://dx.doi.org/10.1002/ar.a.20248.

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42

Hendrickson, A., C. E. Warner, D. Possin, J. Huang, W. C. Kwan, and J. A. Bourne. "Retrograde transneuronal degeneration in the retina and lateral geniculate nucleus of the V1-lesioned marmoset monkey." Brain Structure and Function 220, no. 1 (October 31, 2013): 351–60. http://dx.doi.org/10.1007/s00429-013-0659-7.

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43

Lopata, Alex, D. J. Kohlman, L. G. Bowes, and W. B. Watkins. "Culture of marmoset blastocysts on matrigel: A model of differentiation during the implantation period." Anatomical Record 241, no. 4 (April 1995): 469–86. http://dx.doi.org/10.1002/ar.1092410405.

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44

Nishimura, Masataka, Makoto Takemoto, and Wen-Jie Song. "Organization of auditory areas in the superior temporal gyrus of marmoset monkeys revealed by real-time optical imaging." Brain Structure and Function 223, no. 4 (November 28, 2017): 1599–614. http://dx.doi.org/10.1007/s00429-017-1574-0.

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45

Jeong, Young-Gil, Nam-Seob Lee, Kyoung-Youl Lee, Seung-Hyuk Chung, In Koo Hwang, Jun-Gyo Suh, Tae-Cheon Kang, Byung-Hwa Hyun, Yang-Seok Oh, and Moo Ho Won. "Morphological characteristics of dopaminergic immunoreactive neurons in the olfactory bulb of the common marmoset monkey (Callithrix jacchus)." Annals of Anatomy - Anatomischer Anzeiger 185, no. 6 (December 2003): 543–47. http://dx.doi.org/10.1016/s0940-9602(03)80123-1.

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46

Niklaus, Andrea Louise, Christopher Raymond Murphy, and Alexander Lopata. "Characteristics of the uterine luminal surface epithelium at preovulatory and preimplantation stages in the marmoset monkey." Anatomical Record 264, no. 1 (2001): 82–92. http://dx.doi.org/10.1002/ar.1124.

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Senos, Rafael, Hildebrando Benedicto, Cristiane del Rio do Valle, Rodrigo del Rio do Valle, Penelope Nayudu, Mauro Roberto‐Rodrigues, and Pedro Primo Bombonato. "Collagen quantification in the ventricular walls of the heart of the common marmoset ( Callithrix jacchus )." Anatomical Record 304, no. 6 (April 19, 2021): 1275–79. http://dx.doi.org/10.1002/ar.24632.

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48

Atapour, Nafiseh, Katrina H. Worthy, Leo L. Lui, Hsin-Hao Yu, and Marcello G. P. Rosa. "Neuronal degeneration in the dorsal lateral geniculate nucleus following lesions of primary visual cortex: comparison of young adult and geriatric marmoset monkeys." Brain Structure and Function 222, no. 7 (March 22, 2017): 3283–93. http://dx.doi.org/10.1007/s00429-017-1404-4.

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49

Gossrau, R., and R. Graf. "Protease cytochemistry in the murine rodent, guinea-pig and marmoset placenta." Histochemistry 84, no. 4-6 (1986): 530–37. http://dx.doi.org/10.1007/bf00482987.

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50

Clarke, Robert J., Robert H. I. Blanks, and Roland A. Giolli. "Midbrain connections of the olivary pretectal nucleus in the marmoset ( Callithrix jacchus ): implications for the pupil light reflex pathway." Anatomy and Embryology 207, no. 2 (September 1, 2003): 149–55. http://dx.doi.org/10.1007/s00429-003-0339-0.

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