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1

Kim, Keun-Yong, Hong Keun Park, Seok-Gwan Choi, et al. "The full-length mitochondrial genome of the Fernholm’s hagfish, Myxine fernholmi (Myxini; Myxiniformes; Myxinidae)." Mitochondrial DNA Part B 4, no. 2 (2019): 3482–83. http://dx.doi.org/10.1080/23802359.2019.1674731.

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2

Cruz-Mena, O. "New records of hagfishes (Myxini: Myxiniformes: Myxinidae) from the Pacific coast of Costa Rica." Acta Ichthyologica et Piscatoria 45, no. 3 (2015): 323–29. http://dx.doi.org/10.3750/aip2015.45.3.13.

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3

Augustina, Treasa, Miriam Paul Sreeram, Sandhya Sukumaran, and Anjaly Jose. "A new species of six-gilled hagfish (Myxinidae: Eptatretus) from the Lakshadweep Sea." Zootaxa 5162, no. 2 (2022): 120–34. https://doi.org/10.11646/zootaxa.5162.2.2.

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Augustina, Treasa, Sreeram, Miriam Paul, Sukumaran, Sandhya, Jose, Anjaly (2022): A new species of six-gilled hagfish (Myxinidae: Eptatretus) from the Lakshadweep Sea. Zootaxa 5162 (2): 120-134, DOI: 10.11646/zootaxa.5162.2.2
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4

Claver, Cristina, Oriol Canals, and Naiara Rodriguez-Ezpeleta. "Assessing accuracy and completeness of GenBank for eDNA metabarcoding: towards a reliable marine fish reference database." ARPHA Conference Abstracts 4 (March 4, 2021): e64671. https://doi.org/10.3897/aca.4.e64671.

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Environmental DNA (eDNA) metabarcoding, the process of sequencing DNA collected from the environment for producing biodiversity inventories, is increasingly being applied to assess fish diversity and distribution in marine environments. Yet, the successful application of this technique deeply relies on accurate and complete reference databases used for taxonomic assignment. The most used markers for fish eDNA metabarcoding studies are the cytochrome C oxidase subunit 1 (COI), 16S ribosomal RNA (16S), the 12S ribosomal RNA (12S) and cytochrome b (cyt b) genes, whose sequences are usually retrie
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5

Song, Young Sun, and Jin-Koo Kim. "A new species of hagfish, Eptatretus wandoensis sp. nov. (Agnatha, Myxinidae), from the southwestern Sea of Korea." ZooKeys 926 (April 13, 2020): 81–94. https://doi.org/10.3897/zookeys.926.48745.

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Four specimens of the five-gilled white mid-dorsal line hagfish, Eptatretus wandoensis sp. nov. were recently collected from the southwestern Sea of Korea (Wando). This new species has five pairs of gill apertures, 14–18 prebranchial slime pores, 4 branchial slime pores, a dark brown back with a white mid-dorsal line and a white belly. These hagfish are similar to Eptatretus burgeri and Eptatretus minor in having a white mid-dorsal line, but can be readily distinguished by the numbers of gill apertures (5 vs. 6–7), gill pouches (5 vs. 6), and prebranchial slime pores (14–18 vs. > 18), as we
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Silva, Ana Serra, Groz Maria Pitta, Paula Leandro, Carlos A. Assis, and Rui Figueira. "Ichthyological collection of the Museu Oceanográfico D. Carlos I." ZooKeys 752 (April 23, 2018): 137–48. https://doi.org/10.3897/zookeys.752.20086.

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The collection of the Museu Oceanográfico D. Carlos I is a historical specimen, instrument, and document collection that has been housed at the Aquário Vasco da Gama since 1935. The collection is largely the result of several scientific campaigns conducted by Dom Carlos de Bragança between 1896 and 1907. Specifically, the ichthyological collection consists of 675 surviving catalogue records of specimens caught, acquired or offered to D. Carlos I between 1892 to 1907, and includes the type specimen for Odontaspis nasutus Bragança, 1904 (junior synonym of Mitsukurina owstoni Jordan, 1898), along
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7

Toop, T., J. A. Donald, and D. H. Evans. "Natriuretic peptide receptors in the kidney and the ventral and dorsal aortae of the Atlantic hagfish Myxine glutinosa (Agnatha)." Journal of Experimental Biology 198, no. 9 (1995): 1875–82. http://dx.doi.org/10.1242/jeb.198.9.1875.

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The character of natriuretic peptide receptors (NPRs) in the kidney and aortae of the Atlantic hagfish Myxine glutinosa was determined and compared with that of NPRs in hagfish gills. The relationship of hagfish kidney and aortic NPRs with NPRs from higher vertebrates was also examined. Iodinated atrial and C-type natriuretic peptides (NPs) (125I-ANP, 125I-CNP) were used in tissue section autoradiography, competition studies and guanylate cyclase (GC) assays. Rat atrial and porcine C-type NPs (rANP, pCNP) and rat des[Gln18, Ser19, Gly20, Leu21 Gly22]ANP-(4-23)-NH2 (C-ANF, which binds to the ma
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8

Viktorsson, Elvar Örn, Reidun Aesoy, Sindre Støa, et al. "New prodrugs and analogs of the phenazine 5,10-dioxide natural products iodinin and myxin promote selective cytotoxicity towards human acute myeloid leukemia cells." RSC Medicinal Chemistry 12, no. 5 (2021): 767–78. http://dx.doi.org/10.1039/d1md00020a.

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9

Mincarone, Michael. "Avaliação do risco de extinção do peixe-bruxa Myxine sotoi Mincarone, 2001 no Brasil." Biodiversidade Brasileira 2, no. 2 (2024): 162–65. https://doi.org/10.37002/biodiversidadebrasileira.v2i2.288.

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O risco de extinção do peixe-bruxa Myxine sotoi Mincarone, 2001 foi avaliado de acordo com os critérios da União Internacional para a Conservação da Natureza (IUCN 2001), com base nos dados disponíveis até 2009. A espécie foi categorizada como Vulnerável (VU).
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10

Pequeño, Germán, and Guillermo Figueroa-Muñoz. "Hallazgo de un tercer ejemplar de Myxine pequenoi (Ciclostomi, Myxinidae), con comentarios sobre los ciclóstomos marinos de Aysén, Chile." Revista de Biología Marina y Oceanografía 56, no. 2 (2021): 172–75. http://dx.doi.org/10.22370/rbmo.2021.56.2.3062.

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The capture of a specimen of Myxine pequenoi until 550 km south of the previously described distribution, specifically from Seno Magdalena, Puerto Cisnes, Aysén, is communicated. The extension of the geographic distribution of M. pequenoi was analyzed, in a wider spectrum about the marine cyclostomes, in the Chilean fjord’s region.
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11

Donadio, Stefano. "Myxing It Up to Study Chondramides." Chemistry & Biology 13, no. 6 (2006): 560–61. http://dx.doi.org/10.1016/j.chembiol.2006.06.004.

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12

ECHAVARRIA, MARCO A. ZUMBADO, EDWIN A. BARRANTES BARRANTES, CHARLES R. BARTLETT, ERICKA E. HELMICK, and BRIAN W. BAHDER. "A new species of planthopper in the genus Myxia (Hemiptera: Auchenorrhyncha: Cixiidae) from the Reserva Privada el Silencio de Los Angeles Cloud Forest in Costa Rica." Zootaxa 4915, no. 3 (2021): 351–63. http://dx.doi.org/10.11646/zootaxa.4915.3.4.

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A new species of Myxia Bahder & Bartlett (Cixiidae: Cixiinae: Oecleini) is established as Myxia baynardi sp. n. collected from native palms in cloud forest habitat in Costa Rica. Placement in the genus Myxia is supported by molecular analysis of the cytochrome c oxidase subunit I (COI) and 18S loci as well as morphological characters. Haplaxius delta (Kramer) was collected along the Caribbean coast as a new country record for Costa Rica. Based on morphological characters observed and molecular analysis of COI and 18S, H. delta is herein moved to the genus Myxia.
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13

ECHAVARRIA, MARCO A. ZUMBADO, EDWIN A. BARRANTES BARRANTES, CHARLES R. BARTLETT, ERICKA E. HELMICK, and BRIAN W. BAHDER. "A new species of Myxia (Hemiptera: Auchenorrhyncha: Cixiidae) collected on palms from the Reserva Privada el Silencio de Los Angeles Cloud Forest in Costa Rica." Zootaxa 5027, no. 3 (2021): 417–28. http://dx.doi.org/10.11646/zootaxa.5027.3.7.

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A new species of Myxia Bahder & Bartlett (Cixiidae: Cixiinae: Oecleini) is established as Myxia hernandezi sp. n. collected from native palms in cloud forest habitat in Costa Rica. Placement in the genus Myxia is supported by molecular analysis of the cytochrome c oxidase subunit I (COI) and 18S loci as well as morphological characters.
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14

Satchell, Geoffrey H. "Cardiac Function in the Hagfish,Myxine(Myxinoidea:Cyclostomata)." Acta Zoologica 67, no. 2 (1986): 115–22. http://dx.doi.org/10.1111/j.1463-6395.1986.tb00855.x.

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15

Morozov, A. I., V. A. Nevrovskii, V. I. Pistunovich, and A. N. Svechkopal. "Myxine design for an experimental Galathea reactor." Technical Physics 44, no. 4 (1999): 478–79. http://dx.doi.org/10.1134/1.1259329.

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16

Le Guyader, Hervé. "Le double effet du génome de la myxine." Pour la Science N° 559 – mai, no. 5 (2024): 92–94. http://dx.doi.org/10.3917/pls.559.0092.

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17

RETZIUS, GUSTAF. "Om epitelet i membrana olfactoria hos myxine glutinosa." Nordiskt Medicinskt Arkiv 11, no. 10 (2009): 1–8. http://dx.doi.org/10.1111/j.0954-6820.1879.tb01085.x.

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18

AXELSSON, MICHAEL, ANTHONY P. FARRELL, and STEFAN NILSSON. "Effects of Hypoxia and Drugs on the Cardiovascular Dynamics of the Atlantic Hagfish Myxine Glutinosa." Journal of Experimental Biology 151, no. 1 (1990): 297–316. http://dx.doi.org/10.1242/jeb.151.1.297.

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Cardiac output, ventral and dorsal aortic blood pressure and heart rate were recorded simultaneously in unanaesthetized hagfish, Myxine glutinosa L. Mean cardiac output was S.Tmlmin-1kg-1 and mean heart rate 22.3beatsmin-1. The absence of beat-to-beat oscillations in heart rate was consistent with the lack of an extrinsic cardiac innervation in hagfish. Mean blood pressures were 1.04 kPa (ventral aorta) and 0.77kPa (dorsal aorta). Injection of adrenaline into the caudal vein significantly increased cardiac output, stroke volume, heart rate and blood pressures of both aortas. Peak cardiac outpu
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19

McDONALD, D. G., V. CAVDEK, L. CALVERT, and C. L. MLLLIGAN. "Acid-Base Regulation in the Atlantic Hagfish Myxine Glutinosa." Journal of Experimental Biology 161, no. 1 (1991): 201–15. http://dx.doi.org/10.1242/jeb.161.1.201.

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Blood acid-base status and net transfers of acidic equivalents to the external environment were studied in hagfish, Myxine glutinosa, infused with ammonium sulphate (4mequivkg−1 NH4+) or with sulphuric acid (3mequiv kg−1 H+). Hagfish extracellular fluids (ECF) play a greater role in acid-base regulation than in teleosts. This is because hagfish have a much larger blood volume relative to teleosts, despite a relatively low blood buffering capacity. Consequently, infusion of ammonium sulphate produced only half of the acidosis produced in marine teleosts in comparable studies, and hagfish readil
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20

Schützinger, S., H. S. Choi, R. A. Patzner, and H. Adam. "Estrogens in Plasma of the Hagfish,Myxine glutinosa(Cyclostomata)." Acta Zoologica 68, no. 4 (1987): 263–66. http://dx.doi.org/10.1111/j.1463-6395.1987.tb00893.x.

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21

Muller, G. "Water regulates oxygen binding in hagfish (Myxine glutinosa) hemoglobin." Journal of Experimental Biology 206, no. 8 (2003): 1389–95. http://dx.doi.org/10.1242/jeb.00278.

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22

Jacobi, Kevin, Nelson Bovcon, Ximena Navoa, David Galván, and Pablo Cochia. "First records of Myxine affinis Günther, 1870 and Myxine knappi Wisner & McMillan, 1995 in San Jorge Gulf, central Patagonia, Southwestern Atlantic." Revista del Museo Argentino de Ciencias Naturales 25 (2023): 199–206. http://dx.doi.org/10.22179/revmacn.25.814.

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23

BARRANTES, EDWIN A. BARRANTES, MARCO A. ZUMBADO ECHAVARRIA, CHARLES R. BARTLETT, ERICKA E. HELMICK, and BRIAN W. BAHDER. "A new species of planthopper in the genus Myxia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacoidea: Cixiidae) from the cloud forest in Costa Rica." Zootaxa 5481, no. 4 (2024): 440–52. http://dx.doi.org/10.11646/zootaxa.5481.4.2.

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A new species of Myxia is described from light collecting in Villa Blanca, Costa Rica. The new species possesses an unusual large areolet on the anterior portion of the vertex. Maximum Likelihood analyses based on the 18S rRNA gene, D9–D10 expansion region of the 28S gene, H3 gene and 5’ region of the COI gene support the monophyly of Myxia, with the new species nested deeply within the genus.
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24

Andres, K. H., and M. von Düring. "Lamellated receptors in the skin of the hagfish, Myxine glutinosa." Neuroscience Letters 151, no. 1 (1993): 74–76. http://dx.doi.org/10.1016/0304-3940(93)90049-q.

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25

Alesci, Alessio, Gioele Capillo, Angelo Fumia, et al. "Confocal Characterization of Intestinal Dendritic Cells from Myxines to Teleosts." Biology 11, no. 7 (2022): 1045. http://dx.doi.org/10.3390/biology11071045.

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Dendritic cells (DCs) are antigen-presenting cells (APCs) that regulate the beginning of adaptive immune responses. The mechanisms of tolerance to antigens moving through the digestive tract are known to be regulated by intestinal DCs. Agnatha and Gnathostoma are descendants of a common ancestor. The Ostracoderms gave rise to Cyclostomes, whereas the Placoderms gave rise to Chondrichthyes. Sarcopterygii and Actinopterygii are two evolutionary lines of bony fishes. Brachiopterygii and Neopterygii descend from the Actinopterygii. From Neopterygii, Holostei and Teleostei evolved. Using immunohist
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Cantisani, Marco, Marilisa Leone, Eleonora Mignogna, et al. "Structure-Activity Relations of Myxinidin, an Antibacterial Peptide Derived from the Epidermal Mucus of Hagfish." Antimicrobial Agents and Chemotherapy 57, no. 11 (2013): 5665–73. http://dx.doi.org/10.1128/aac.01341-13.

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ABSTRACTThe structure-activity relations of myxinidin, a peptide derived from epidermal mucus of hagfish,Myxine glutinosaL., were investigated. Analysis of key residues allowed us to design new peptides with increased efficiency. Antimicrobial activity of native and modified peptides demonstrated the key role of uncharged residues in the sequence; the loss of these residues reduces almost entirely myxinidin antimicrobial activity, while insertion of arginine at charged and uncharged position increases antimicrobial activity compared with that of native myxinidin. Particularly, we designed a pe
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Jensen, F. B. "Haemoglobin H+ equilibria in lamprey (Lampetra fluviatilis) and hagfish (Myxine glutinosa)." Journal of Experimental Biology 202, no. 14 (1999): 1963–68. http://dx.doi.org/10.1242/jeb.202.14.1963.

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Agnathans, comprising lamprey and hagfish species, have been reported to be practically devoid of HCO3-/Cl- exchange across the red blood cell membrane. This suggests that the capacity of their haemoglobin (Hb) to remove H+ is essential for obtaining a high CO2-carrying capacity in the blood. Hydrogen ion titrations were performed on oxygenated and deoxygenated composite Hbs from river lamprey and from Atlantic hagfish at 15 degrees C and an ionic strength of 0.1 (0.1 mol l-1 KCl). Lamprey Hb was characterised by very low buffer values when the degree of oxygenation was constant, whereas the f
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BURNE, R. H. "2. On the Presence of a Branchial Basket in Myxine glutinosa." Proceedings of the Zoological Society of London 60, no. 4 (2009): 706–8. http://dx.doi.org/10.1111/j.1096-3642.1892.tb01790.x.

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29

McLeese, Jennifer M., Glenda M. Wright, John H. Youson, and J. Geoffrey Eales. "Deiodination activity in extrathyroidal tissues of the Atlantic hagfish,Myxine glutinosa." Journal of Experimental Zoology 287, no. 6 (2000): 445–52. http://dx.doi.org/10.1002/1097-010x(20001101)287:6<445::aid-jez6>3.0.co;2-a.

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Sanders, Michael, Bonnie Mathews, David Sutherland, Weily Soong, Harry Giles, and Leo Pezzementi. "Biochemical and molecular characterization of acetylcholinesterase from the hagfish Myxine glutinosa." Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology 115, no. 1 (1996): 97–109. http://dx.doi.org/10.1016/0305-0491(96)00088-0.

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31

Johnsson, M., and M. Axelsson. "Control of the systemic heart and the portal heart of Myxine glutinosa." Journal of Experimental Biology 199, no. 6 (1996): 1429–34. http://dx.doi.org/10.1242/jeb.199.6.1429.

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The effects of preload and afterload on the performance of the systemic heart of the hagfish Myxine glutinosa were investigated before and during sotalol treatment using an in situ perfusion technique. Elevation of input pressure (preload) increased flow by means of increased stroke volume and heart rate in accordance with Starling's law of the heart, while increased output pressure (afterload) decreased flow mainly because of decreased stroke volume. Treatment with the beta-adrenoceptor antagonist sotalol did not change the quality of the responses to increased preload or afterload, although
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32

McVvean, Alistair. "Velocity and displacement receptors in the skin of the hagfish Myxine glutinosa." Journal of Zoology 219, no. 2 (1989): 251–67. http://dx.doi.org/10.1111/j.1469-7998.1989.tb02581.x.

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33

Kavanaugh, Scott I., Mickie L. Powell, and Stacia A. Sower. "Seasonal changes of gonadotropin-releasing hormone in the Atlantic hagfish Myxine glutinosa." General and Comparative Endocrinology 140, no. 2 (2005): 136–43. http://dx.doi.org/10.1016/j.ygcen.2004.10.015.

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Powell, Mickie L., Scott Kavanaugh, and Stacia A. Sower. "Identification of a functional corpus luteum in the Atlantic hagfish, Myxine glutinosa." General and Comparative Endocrinology 148, no. 1 (2006): 95–101. http://dx.doi.org/10.1016/j.ygcen.2006.01.003.

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35

Rasmussen, Ann-Sofie, Axel Janke, and Ulfur Arnason. "The mitochondrial DNA molecule of the hagfish (myxine glutinosa) and vertebrate phylogeny." Journal of Molecular Evolution 46, no. 4 (1998): 382–88. http://dx.doi.org/10.1007/pl00006317.

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Feng, Jun, Kiichiro Yano, Rita Monahan-Earley, et al. "Vascular bed-specific endothelium-dependent vasomomotor relaxation in the hagfish, Myxine glutinosa." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 293, no. 2 (2007): R894—R900. http://dx.doi.org/10.1152/ajpregu.00080.2007.

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The last common ancestor of hagfish and gnathostomes was also the last common ancestor of all extant vertebrates that lived some time more than 500 million years ago. Features that are shared between hagfish and gnathostomes can be inferred to have already been present in this ancestral vertebrate. We recently reported that hagfish endothelium displays phenotypic heterogeneity in ultrastructure, lectin binding, and mechanisms of leukocyte adhesion. Thus, phenotypic cell heterogeneity evolved as an early feature of the endothelium. In the present study, we wanted to extend these observations by
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Grant, Marianne A., David L. Beeler, Katherine C. Spokes, et al. "Identification of extant vertebrate Myxine glutinosa VWF: evolutionary conservation of primary hemostasis." Blood 130, no. 23 (2017): 2548–58. http://dx.doi.org/10.1182/blood-2017-02-770792.

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Key Points The extant vertebrate hagfish, M glutinosa, has a single, functional vwf gene, structurally simpler than in higher vertebrates. VWF appeared in an ancestral vertebrate as a hemostatic protein lacking functional domains required for primary hemostasis under high flow.
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Peters, T., R. E. Forster, and G. Gros. "Hagfish (Myxine glutinosa) red cell membrane exhibits no bicarbonate permeability as detected by (18)O exchange." Journal of Experimental Biology 203, no. 10 (2000): 1551–60. http://dx.doi.org/10.1242/jeb.203.10.1551.

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The bicarbonate permeability of the plasma membrane of intact hagfish (Myxine glutinosa) red blood cells and the intracellular carbonic anhydrase activity of these cells were determined by applying the (18)O exchange reaction using a special mass spectrometric technique. When the macromolecular carbonic anhydrase inhibitor Prontosil-Dextran was used to suppress any extracellular carbonic anhydrase activity, the mean intracellular acceleration of the CO(2) hydration/HCO(3)(−) dehydration reaction over the uncatalyzed reaction (referred to as intracellular carbonic anhydrase activity A(i)) was 2
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Leigh, Katharine L., Jed P. Sparks, and William E. Bemis. "Food Preferences of Atlantic Hagfish,Myxine glutinosa, Assessed by Experimental Baiting of Traps." Copeia 104, no. 3 (2016): 623–27. http://dx.doi.org/10.1643/ce-15-353.

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40

Jansson, L., and S. Falkmer. "Blood Flow to the Pancreatic Islet Parenchyma of the Atlantic Hagfish(Myxine glutinosa)." Hormone and Metabolic Research 30, no. 04 (1998): 182–87. http://dx.doi.org/10.1055/s-2007-978863.

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Fels, Lüder M., Pedro M. Sanz-Altamira, Brigitte Deeker, Bernd Elger, and Hilmar Stolte. "Filtration Characteristics of the Single Isolated Perfused Glomerulus of Myxine glutinosa." Kidney and Blood Pressure Research 16, no. 5 (1993): 276–84. http://dx.doi.org/10.1159/000173773.

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Gürsoy, Halil-Cem, Dorota Koper, and Bernd-Joachim Benecke. "The Vertebrate 7S K RNA Separates Hagfish (Myxine glutinosa) and Lamprey (Lampetra fluviatilis)." Journal of Molecular Evolution 50, no. 5 (2000): 456–64. http://dx.doi.org/10.1007/s002390010048.

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43

Fago, Angela, and Roy E. Weber. "The hemoglobin system of the hagfish Myxine glutinosa: aggregation state and functional properties." Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology 1249, no. 1 (1995): 109–15. http://dx.doi.org/10.1016/0167-4838(95)00031-o.

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Reinecke, Manfred. "Substance P is a vasoactive hormone in the atlantic hagfish Myxine glutinosa (Cyclostomata)." General and Comparative Endocrinology 66, no. 2 (1987): 291–96. http://dx.doi.org/10.1016/0016-6480(87)90279-6.

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45

Donald, John A., Tes Toop, and David H. Evans. "Natriuretic peptide binding sites in the brain of the Atlantic hagfish,Myxine glutinosa." Journal of Experimental Zoology 284, no. 4 (1999): 407–13. http://dx.doi.org/10.1002/(sici)1097-010x(19990901)284:4<407::aid-jez7>3.0.co;2-9.

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46

Foster, Glen D., and T. W. Moon. "Enzyme activities in the Atlantic hagfish, Myxine glutinosa: changes with captivity and food deprivation." Canadian Journal of Zoology 64, no. 5 (1986): 1080–85. http://dx.doi.org/10.1139/z86-162.

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Selected Krebs cycle enzymes and carbohydrate, amino acid, and lipid metabolizing enzymes were assayed in the muscle and liver of newly captured (April, 4 °C; August, 15 °C), fed (for 7 months), and food-deprived (for 7 and 11 months) hagfish, Myxine glutinosa. Seasonal differences were found in the glycogen content of the muscle and liver of newly captured hagfish (lower in the cold temperature), while consistently high levels were maintained in the fed group. Food deprivation decreased the content. All enzymes measured were found in both tissues, except glucose-6-phosphate dehydrogenase (liv
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47

Lim, J. L., and T. M. Winegard. "Diverse anguilliform swimming kinematics in Pacific hagfish (Eptatretus stoutii) and Atlantic hagfish (Myxine glutinosa)." Canadian Journal of Zoology 93, no. 3 (2015): 213–23. http://dx.doi.org/10.1139/cjz-2014-0260.

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Abstract:
Anguilliform mode swimmers pass waves of lateral bending down their elongate bodies to propel forward. Hagfishes (Myxinidae) are classified as anguilliform swimmers, but their unique habits and reduced morphology—including a flexible body lacking a vertebral column—have the potential to translate into unique swimming behaviour within this broad classification. Their roles as active scavengers and hunters can require considerable bouts of swimming, yet quantitative data on hagfish locomotion are limited. Here, we aim to provide a more complete mechanistic understanding of hagfish swimming by qu
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48

Edwards, Susan L., Justin Arnold, Salvatore D. Blair, et al. "Ammonia excretion in the Atlantic hagfish (Myxine glutinosa) and responses of an Rhc glycoprotein." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 308, no. 9 (2015): R769—R778. http://dx.doi.org/10.1152/ajpregu.00355.2014.

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Hagfishes, the most ancient of the extant craniates, demonstrate a high tolerance for a number of unfavorable environmental conditions, including elevated ammonia. Proposed mechanisms of ammonia excretion in aquatic organisms include vesicular NH4+ transport and release by exocytosis in marine crabs, and passive NH3 diffusion, active NH4+ transport, and paracellular leakage of NH3 or NH4+ across the gills of fishes. Recently, an emerging paradigm suggests that Rhesus glycoproteins play a vital role in ammonia transport in both aquatic invertebrates and vertebrates. This study has identified an
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49

Robson, P., G. M. Wright, and F. W. Keeley. "Distinct non-collagen based cartilages comprising the endoskeleton of the Atlantic hagfish, Myxine glutinosa." Anatomy and Embryology 202, no. 4 (2000): 281–90. http://dx.doi.org/10.1007/s004290000113.

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50

Elger, M. "The branchial circulation and the gill epithelia in the Atlantic hagfish, Myxine glutinosa L." Anatomy and Embryology 175, no. 4 (1987): 489–504. http://dx.doi.org/10.1007/bf00309684.

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