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Relevant bibliographies by topics / Mammalian / Journal articles

Journal articles on the topic 'Mammalian'

To see the other types of publications on this topic, follow the link: Mammalian.

Author: Grafiati

Published: 4 June 2021

Last updated: 21 February 2023

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1

Kostopoulos, Dimitris S., Kalliopi K. Koliadimou, and George D. Koufos. "The giraffids (Mammalia, Artiodactyla) from the Late Miocene Mammalian localities of Nikiti (Macedonia, Greece)." Palaeontographica Abteilung A 239, no. 1-3 (April 23, 1996): 61–88. http://dx.doi.org/10.1127/pala/239/1996/61.

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2

Senter, Phil, and John G. Moch. "A critical survey of vestigial structures in the postcranial skeletons of extant mammals." PeerJ 3 (November 24, 2015): e1439. http://dx.doi.org/10.7717/peerj.1439.

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In the Mammalia, vestigial skeletal structures abound but have not previously been the focus of study, with a few exceptions (e.g., whale pelves). Here we use a phylogenetic bracketing approach to identify vestigial structures in mammalian postcranial skeletons and present a descriptive survey of such structures in the Mammalia. We also correct previous misidentifications, including the previous misidentification of vestigial caviid metatarsals as sesamoids. We also examine the phylogenetic distribution of vestigiality and loss. This distribution indicates multiple vestigialization and loss events in mammalian skeletal structures, especially in the hand and foot, and reveals no correlation in such events between mammalian fore and hind limbs.

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3

Braun, Thomas, and Thilo Borchardt. "Cardiovascular regeneration in non-mammalian model systems: What are the differences between newts and man?" Thrombosis and Haemostasis 98, no. 08 (2007): 311–18. http://dx.doi.org/10.1160/th07-02-0153.

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SummaryThe mammalian heart cannot regenerate substantial cardiac injuries, while certain non-mammalian vertebrates such as certain fish (Danio rerio) and amphibiae (Notophthalmus viridescens) are able to repair the heart without functional impairment. In mammalians, the prevailing repair process is accompanied by fibrosis and scarring, while zebrafish and newts can replace lost contractile tissue by newly formed cardiac muscle with only little or no scar formation.A better understanding of cardiac regeneration in non-mammalian vertebrates might provide new insights for the manipulation of regenerative pathways in the human heart. Here, we summarize the current knowledge in cardiac regeneration of newts and the principal differences to repair processes in mammalian hearts.

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4

Rogers, Nedra. "Mammalian." Fourth Genre: Explorations in Nonfiction 9, no. 1 (2007): 1–6. http://dx.doi.org/10.1353/fge.2007.0017.

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5

Armitage, Kenneth B. "Mammalian Function Mammalian Physiology J. Homer Ferguson." BioScience 37, no. 10 (November 1987): 748. http://dx.doi.org/10.2307/1310495.

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6

Behringer, Richard R., Guy S. Eakin, and Marilyn B. Renfree. "Mammalian diversity: gametes, embryos and reproduction." Reproduction, Fertility and Development 18, no. 2 (2006): 99. http://dx.doi.org/10.1071/rd05137.

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The class Mammalia is composed of approximately 4800 extant species. These mammalian species are divided into three subclasses that include the monotremes, marsupials and eutherians. Monotremes are remarkable because these mammals are born from eggs laid outside of the mother’s body. Marsupial mammals have relatively short gestation periods and give birth to highly altricial young that continue a significant amount of ‘fetal’ development after birth, supported by a highly sophisticated lactation. Less than 10% of mammalian species are monotremes or marsupials, so the great majority of mammals are grouped into the subclass Eutheria, including mouse and human. Mammals exhibit great variety in morphology, physiology and reproduction. In the present article, we highlight some of this remarkable diversity relative to the mouse, one of the most widely used mammalian model organisms, and human. This diversity creates challenges and opportunities for gamete and embryo collection, culture and transfer technologies.

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7

Ročková, Š., V. Rada, J. Havlík, R. Švejstil, E. Vlková, V. Bunešová, K. Janda, and I. Profousová. "Growth of bifidobacteria in mammalian milk." Czech Journal of Animal Science 58, No. 3 (March 4, 2013): 99–105. http://dx.doi.org/10.17221/6666-cjas.

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Microbial colonization of the mammalian intestine begins at birth, when from a sterile state a newborn infant is exposed to an external environment rich in various bacterial species. An important group of intestinal bacteria comprises bifidobacteria. Bifidobacteria represent major intestinal microbiota during the breast-feeding period. Animal milk contains all crucial nutrients for babies’ intestinal microflora. The aim of our work was to test the influence of different mammalian milk on the growth of bifidobacteria. The growth of seven strains of bifidobacteria in human milk, the colostrum of swine, cow’s milk, sheep’s milk, and rabbit’s milk was tested. Good growth accompanied by the production of lactic acid was observed not only in human milk, but also in the other kinds of milk in all three strains of Bifidobacterium bifidum of different origin. Human milk selectively supported the production of lactic acid of human bifidobacterial isolates, especially the Bifidobacterium bifidum species. The promotion of bifidobacteria by milk is species-specific. Human milk contains a key factor for the growth of specific species or strains of human-origin bifidobacteria compared to other kinds of milk. In contrast, some components (maybe lysozyme) of human milk inhibited the growth of Bifidobacterium animalis. Animal-origin strains of bifidobacteria were not able to significantly grow even in milk of animal origin, with the exception of B. animalis subsp. lactis 1,2, which slightly grew in sheep’s milk.

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8

Folin, Marcella, and Eva Contiero. "Electrophoretic analysis of mammalian hair keratins." Anthropologischer Anzeiger 54, no. 4 (December 12, 1996): 331–39. http://dx.doi.org/10.1127/anthranz/54/1996/331.

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9

Conley, A. "Mammalian aromatases." Reproduction 121, no. 5 (May 1, 2001): 685–95. http://dx.doi.org/10.1530/reprod/121.5.685.

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10

Salamat, Muhammad Khalid, Carola Munoz-Montesino, Mohammed Moudjou, Human Rezaei, Hubert Laude, Vincent Béringue, and Michel Dron. "Mammalian prions." Prion 7, no. 2 (March 2013): 131–35. http://dx.doi.org/10.4161/pri.23110.

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11

Savistchenko, Jimmy, Zaira E. Arellano-Anaya, Olivier Andréoletti, and Didier Vilette. "Mammalian prions." Prion 5, no. 2 (April 2011): 84–87. http://dx.doi.org/10.4161/pri.5.2.16096.

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12

Liberles, Stephen D. "Mammalian Pheromones." Annual Review of Physiology 76, no. 1 (February 10, 2014): 151–75. http://dx.doi.org/10.1146/annurev-physiol-021113-170334.

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13

Fu, Qi, and P. Jeremy Wang. "Mammalian piRNAs." Spermatogenesis 4, no. 1 (January 2014): e27889. http://dx.doi.org/10.4161/spmg.27889.

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14

Printz, R. L., M. A. Magnuson, and D. K. Granner. "Mammalian Glucokinase." Annual Review of Nutrition 13, no. 1 (July 1993): 463–96. http://dx.doi.org/10.1146/annurev.nu.13.070193.002335.

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15

Wasson, K., and R. L. Peper. "Mammalian Microsporidiosis." Veterinary Pathology 37, no. 2 (March 2000): 113–28. http://dx.doi.org/10.1354/vp.37-2-113.

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The phylum Microspora contains a diverse group of single-celled, obligate intracellular protozoa sharing a unique organelle, the polar filament, and parasitizing a wide variety of invertebrate and vertebrate animals, including insects, fish, birds, and mammals. Encephalitozoon cuniculi is the classic microsporidial parasite of mammals, and encephalitozoonosis in rabbits and rodents has been and continues to be recognized as a confounding variable in animal-based biomedical research. Although contemporary research colonies are screened for infection with this parasite, E. cuniculi remains a cause of morbidity and mortality in pet and conventionally raised rabbits. In addition, E. cuniculi is a potential pathogen of immature domestic dogs and farm-raised foxes. The recent discovery and identification of Encephalitozoon intestinalis, Encephalitozoon hellem, and Enterocytozoon bieneusi, in addition to E. cuniculi, as opportunistic pathogens of humans have renewed interest in the Microspora. Veterinary pathologists, trained in the comparative anatomy of multiple animal species and infectious disease processes, are in a unique position to contribute to the diagnosis and knowledge of the pathogenesis of these parasitic diseases. This review article covers the life cycle, ultrastructure, and biology of mammalian microsporaidia and the clinical disease and lesions seen in laboratory and domestic animals, particularly as they relate to Encephalitozoon species. Human microsporidial disease and animal models of human infection are also addressed. Often thought of as rabbit pathogens of historical importance, E. cuniculi and the related mammalian microsporidia are emerging as significant opportunistic pathogens of immunocompromised individuals.

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16

Richardson, Miles. "Mammalian Man." Anthropology Humanism Quarterly 15, no. 1 (February 1990): 30. http://dx.doi.org/10.1525/ahu.1990.15.1.30.2.

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17

Kannikeswaran, Nirupama, and Deepak Kamat. "Mammalian Bites." Clinical Pediatrics 48, no. 2 (October 2, 2008): 145–48. http://dx.doi.org/10.1177/0009922808324494.

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18

BOCK, JASON B., and RICHARD H. SCHELLER. "Mammalian SNAREs." Nature 387, no. 6629 (May 1997): 134. http://dx.doi.org/10.1038/387134a0.

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19

Weitzman, Jonathan B. "Mammalian RNAi." Genome Biology 2 (2001): spotlight—20010525–01. http://dx.doi.org/10.1186/gb-spotlight-20010525-01.

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20

Wiley, James F. "Mammalian Bites." Clinical Pediatrics 29, no. 5 (May 1990): 283–87. http://dx.doi.org/10.1177/000992289002900506.

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21

Esposito, Carla, and Ivana Caputo. "Mammalian transglutaminases." FEBS Journal 272, no. 3 (January 10, 2005): 615–31. http://dx.doi.org/10.1111/j.1742-4658.2004.04476.x.

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22

Wayne, R. K., and E. A. Ostrander. "Mammalian genomics:." Heredity 92, no. 4 (March 24, 2004): 273–74. http://dx.doi.org/10.1038/sj.hdy.6800428.

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23

Deininger, P. L. "Mammalian Retroelements." Genome Research 12, no. 10 (October 1, 2002): 1455–65. http://dx.doi.org/10.1101/gr.282402.

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24

Blackall, Linda L. "Mammalian microbiomes." Microbiology Australia 36, no. 1 (2015): 3. http://dx.doi.org/10.1071/ma15002.

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25

Chew, Amy. "MAMMALIAN EVOLUTION." Quarterly Review of Biology 82, no. 3 (September 2007): 251–55. http://dx.doi.org/10.1086/519967.

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26

Lundelius, E. L. "Mammalian Evolution." Science 264, no. 5167 (June 24, 1994): 1953–54. http://dx.doi.org/10.1126/science.264.5167.1953.

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27

Wang, Aijun, and Edward A. Dennis. "Mammalian lysophospholipases." Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids 1439, no. 1 (July 1999): 1–16. http://dx.doi.org/10.1016/s1388-1981(99)00063-3.

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28

Wassarman, Paul M. "Mammalian Fertilization." Cell 96, no. 2 (January 1999): 175–83. http://dx.doi.org/10.1016/s0092-8674(00)80558-9.

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29

Prothero, Donald R. "Mammalian Evolution." Short Courses in Paleontology 7 (1994): 238–70. http://dx.doi.org/10.1017/s2475263000001343.

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The evolution of certain mammalian lineages has become the favorite examples of nearly every introductory textbook in historical geology, paleontology, and evolutionary biology. The evolution of the horse is the most frequently used, since it emerged in 1851 and has been reproduced many times in nearly 150 years (see Gould, 1987, and MacFadden, 1992). Occasionally, one sees a revival of one of Osborn's (1929) evolutionary sequences of brontotheres, and some books may show a sequence of mammoths and mastodonts. In most historical geology books, the discussion of fossil mammals usually consists of just these selected examples, since the authors seem to think that a fuller account of Cenozoic mammal evolution is beyond the level of their readers. Children's books, trade books, and museum displays typically show little more than the evolution of the horse and few selected pictures of spectacular beasts such as saber-toothed cats, ground sloths, mammoths, and the gigantic hornless rhinocerosParaceratherium(called by the obsolete namesBaluchitheriumorIndricotheriumin virtually every caption). Given these conditions, one cannot fault students or the general public for thinking that only horses have a good fossil record, or that there are no other well-studied groups of fossil mammals.

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30

Camerino, Giovanna, and Peter N. Goodfellow. "Mammalian genetics." Current Opinion in Genetics & Development 2, no. 3 (January 1992): 385–86. http://dx.doi.org/10.1016/s0959-437x(05)80146-7.

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31

Abbot, Patrick, and Antonis Rokas. "Mammalian pregnancy." Current Biology 27, no. 4 (February 2017): R127—R128. http://dx.doi.org/10.1016/j.cub.2016.10.046.

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32

Bond, Judith S., and Robert J. Beynon. "Mammalian metalloendopeptidases." International Journal of Biochemistry 17, no. 5 (January 1985): 565–74. http://dx.doi.org/10.1016/0020-711x(85)90287-3.

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33

Shur, Barry D., Carey Rodeheffer, and Michael A. Ensslin. "Mammalian fertilization." Current Biology 14, no. 17 (September 2004): R691—R692. http://dx.doi.org/10.1016/j.cub.2004.08.037.

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34

Meserve, Lee A. "Mammalian Neuroendocrinology." Trends in Endocrinology & Metabolism 5, no. 10 (December 1994): 430. http://dx.doi.org/10.1016/1043-2760(94)90025-6.

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35

Beintema, Jaap J. "Mammalian ribonucleases." FEBS Letters 185, no. 1 (June 3, 1985): 115–20. http://dx.doi.org/10.1016/0014-5793(85)80752-3.

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36

Stanley, Keith K. "Mammalian ectoenzymes." Trends in Biochemical Sciences 13, no. 11 (November 1988): 456–57. http://dx.doi.org/10.1016/0968-0004(88)90224-1.

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37

Hansson, Lennart. "Mammalian landscapes." Trends in Ecology & Evolution 15, no. 5 (May 2000): 212. http://dx.doi.org/10.1016/s0169-5347(00)01841-3.

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38

Kägi, Jeremias H. R., and Peter Hunziker. "Mammalian metallothionein." Biological Trace Element Research 21, no. 1 (July 1989): 111–18. http://dx.doi.org/10.1007/bf02917243.

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39

Silver, Lee M., Joe Nadeau, and Jan Klein. "Mammalian Genome." Mammalian Genome 1, no. 1 (1991): 1. http://dx.doi.org/10.1007/bf00350840.

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40

Moayedi, Yalda, Masashi Nakatani, and Ellen Lumpkin. "Mammalian mechanoreception." Scholarpedia 10, no. 3 (2015): 7265. http://dx.doi.org/10.4249/scholarpedia.7265.

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41

Wakayama, Teruhiko. "Mammalian Clone." Journal of Mammalian Ova Research 22, no. 2 (June 2005): 49–58. http://dx.doi.org/10.1274/jmor.22.49.

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42

Hurchinson, J. S. M. "Mammalian neuroendocrinology." Animal Reproduction Science 36, no. 1-2 (July 1994): 172–73. http://dx.doi.org/10.1016/0378-4320(94)90065-5.

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43

Xiuhui, Wang, Chen Yan, and Gao Zhongxin. "Mammalian sociality." Journal of Forestry Research 8, no. 3 (September 1997): 182–85. http://dx.doi.org/10.1007/bf02855415.

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44

Strasser, Peter, Mario Gimona, Herbert Moessler, Monika Herzog, and J. Victor Small. "Mammalian calponin." FEBS Letters 330, no. 1 (September 6, 1993): 13–18. http://dx.doi.org/10.1016/0014-5793(93)80909-e.

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45

Galloway, Russell E. "Mammalian bites." Journal of Emergency Medicine 6, no. 4 (July 1988): 325–31. http://dx.doi.org/10.1016/0736-4679(88)90370-8.

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46

Staunton, Hugh. "Mammalian sleep." Naturwissenschaften 92, no. 5 (April 21, 2005): 203–20. http://dx.doi.org/10.1007/s00114-005-0618-0.

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47

Francke, Uta. "Mammalian Cells Mammalian Cell Genetics Martin L. Hooper." BioScience 37, no. 10 (November 1987): 741–42. http://dx.doi.org/10.2307/1310484.

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48

Brown, Steve D. M., Joseph H. Nadeau, Sara Wells, Ann-Marie Mallon, Lydia Teboul, Christopher K. Tuggle, and Lawrence B. Schook. "Introduction to Mammalian Genome Special Issue: Mammalian Genetic Resources." Mammalian Genome 33, no. 1 (January 19, 2022): 1–3. http://dx.doi.org/10.1007/s00335-022-09942-3.

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49

Wang, Li-Ting, Shih-Jong Wang, and Shih-Hsien Hsu. "Functional characterization of mammalian Wntless homolog in mammalian system." Kaohsiung Journal of Medical Sciences 28, no. 7 (July 2012): 355–61. http://dx.doi.org/10.1016/j.kjms.2012.02.001.

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50

Vázquez, José. "Mammalian Brain Biology." American Biology Teacher 67, no. 9 (November 1, 2005): 568–69. http://dx.doi.org/10.2307/4451910.

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