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For: Dzyuba V, Cosson J. Motility of fish spermatozoa: from external signaling to flagella response. Reprod Biol 2014;14:165-75. [PMID: 25152513 DOI: 10.1016/j.repbio.2013.12.005] [Cited by in Crossref: 60] [Cited by in F6Publishing: 52] [Article Influence: 7.5] [Reference Citation Analysis]
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6 Contreras P, Ulloa P, Merino O, Valdebenito I, Figueroa E, Farías J, Risopatrón J. Effect of short-term storage on sperm function in Patagonian blenny (Eleginops maclovinus) sperm. Aquaculture 2017;481:58-63. [DOI: 10.1016/j.aquaculture.2017.08.022] [Cited by in Crossref: 14] [Cited by in F6Publishing: 7] [Article Influence: 2.8] [Reference Citation Analysis]
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10 Liu Y, Torres L, Tiersch TR. Cryopreservation of sperm bundles (spermatozeugmata) from endangered livebearing goodeids. Cryobiology 2018;82:49-56. [PMID: 29665384 DOI: 10.1016/j.cryobiol.2018.04.009] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
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12 Dadras H, Dzyuba B, Cosson J, Golpour A, Siddique MAM, Linhart O. Effect of water temperature on the physiology of fish spermatozoon function: a brief review. Aquac Res 2017;48:729-40. [DOI: 10.1111/are.13049] [Cited by in Crossref: 41] [Cited by in F6Publishing: 23] [Article Influence: 6.8] [Reference Citation Analysis]
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14 de Jesus Paula DA, Murgas LDS, Castro TFD, de Lima Assis I, Neto RVR, Marcussi S. Effects of cooling rates on the quality of Prochilodus lineatus (Valenciennes, 1836) sperm. Reprod Domest Anim 2019;54:1034-43. [PMID: 31077452 DOI: 10.1111/rda.13459] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]
15 Lee-Estevez M, Herrera L, Díaz R, Beltrán J, Figueroa E, Dumorné K, Ulloa-Rodríguez P, Short S, Risopatrón J, Valdebenito I, Farías J. Effects of cryopreservation on cAMP-dependent protein kinase and AMP-activated protein kinase in Atlantic salmon (Salmo salar) spermatozoa: Relation with post-thaw motility. Anim Reprod Sci 2019;209:106133. [PMID: 31514940 DOI: 10.1016/j.anireprosci.2019.106133] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
16 Judycka S, Szczepkowski M, Ciereszko A, Dietrich GJ. New extender for cryopreservation of Siberian sturgeon (Acipenser baerii) semen. Cryobiology 2015;70:184-9. [PMID: 25725469 DOI: 10.1016/j.cryobiol.2015.02.005] [Cited by in Crossref: 20] [Cited by in F6Publishing: 14] [Article Influence: 2.9] [Reference Citation Analysis]
17 Dzyuba V, Sampels S, Ninhaus-Silveira A, Kahanec M, Veríssimo-Silveira R, Rodina M, Cosson J, Boryshpolets S, Selinger M, Sterba J, Dzyuba B. Sperm motility and lipid composition in internally fertilizing ocellate river stingray Potamotrygon motoro. Theriogenology 2019;130:26-35. [PMID: 30856412 DOI: 10.1016/j.theriogenology.2019.02.029] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
18 Nynca J, Słowińska M, Judycka S, Dobosz S, Ciereszko A. Acquiring the potential for motility is accompanied by profound changes in the testicular sperm proteome of sex-reversed female and normal male rainbow trout. Aquaculture 2020;521:735033. [DOI: 10.1016/j.aquaculture.2020.735033] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
19 Liu Y, Yang H, Torres L, Tiersch TR. Activation of free sperm and dissociation of sperm bundles (spermatozeugmata) of an endangered viviparous fish, Xenotoca eiseni. Comp Biochem Physiol A Mol Integr Physiol 2018;218:35-45. [PMID: 29371117 DOI: 10.1016/j.cbpa.2018.01.006] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
20 Rudolfsen G, Serrano JV, Folstad I. Own, but not foreign seminal fluid inhibits sperm activation in a vertebrate with external fertilization. Front Ecol Evol 2015;3. [DOI: 10.3389/fevo.2015.00092] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 0.9] [Reference Citation Analysis]
21 Siddique M, Linhart O, Kujawa R, Krejszeff S, Butts I. Composition of seminal plasma and ovarian fluid in Ide Leuciscus idus and Northern pike Esox lucius. Reprod Dom Anim 2016;51:960-9. [DOI: 10.1111/rda.12773] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
22 Silveira CR, Varela Junior AS, Corcini CD, Soares SL, Anciuti AN, Kütter MT, Martínez PE. Effects of Bisphenol A on redox balance in red blood and sperm cells and spermatic quality in zebrafish Danio rerio. Ecotoxicology 2019;28:913-22. [PMID: 31396792 DOI: 10.1007/s10646-019-02091-5] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
23 Kekäläinen J, Jokiniemi A, Janhunen M, Huuskonen H. Offspring phenotype is shaped by the nonsperm fraction of semen. J Evol Biol 2020;33:584-94. [PMID: 31984576 DOI: 10.1111/jeb.13592] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
24 Dzyuba B, Legendre M, Baroiller JF, Cosson J. Sperm motility of the Nile tilapia (Oreochromis niloticus): Effects of temperature on the swimming characteristics. Anim Reprod Sci 2019;202:65-72. [PMID: 30717995 DOI: 10.1016/j.anireprosci.2019.01.010] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
25 França TS, Motta NC, Egger RC, Oliveira AV, Murgas LDS. Impact of activation solutions on fresh and frozen-thawed sperm motility and fertilization success for two species of migratory freshwater fishes. Theriogenology 2020;149:6-15. [PMID: 32224378 DOI: 10.1016/j.theriogenology.2020.03.016] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
26 Bondarenko V, Cosson J. Structure and beating behavior of the sperm motility apparatus in aquatic animals. Theriogenology 2019;135:152-63. [DOI: 10.1016/j.theriogenology.2019.06.005] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 2.7] [Reference Citation Analysis]
27 Nichols ZG, Rikard S, Alavi SMH, Walton WC, Butts IAE. Regulation of sperm motility in Eastern oyster (Crassostrea virginica) spawning naturally in seawater with low salinity. PLoS One 2021;16:e0243569. [PMID: 33735238 DOI: 10.1371/journal.pone.0243569] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Yang S, Huang W, Chen H, Huang M, Liufu Y, Meng Z. Effect of chilled storage on sperm quality of basa catfish (Pangasius bocourti). Fish Physiol Biochem 2020;46:2133-41. [PMID: 32829474 DOI: 10.1007/s10695-020-00860-2] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
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30 Cosson J. A 40 years journey with fish spermatozoa as companions as I personally experienced it. Fish Physiol Biochem 2021;47:757-65. [PMID: 33083947 DOI: 10.1007/s10695-020-00882-w] [Reference Citation Analysis]
31 Liu Y, Blackburn H, Taylor SS, Tiersch TR. Development of germplasm repositories to assist conservation of endangered fishes: Examples from small-bodied livebearing fishes. Theriogenology 2019;135:138-51. [PMID: 31220687 DOI: 10.1016/j.theriogenology.2019.05.020] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]
32 Butts IAE, Hilmarsdóttir GS, Zadmajid V, Gallego V, Støttrup JG, Jacobsen C, Krüger-johnsen M, Politis SN, Asturiano JF, Holst LK, Tomkiewicz J. Dietary amino acids impact sperm performance traits for a catadromous fish, Anguilla anguilla reared in captivity. Aquaculture 2020;518:734602. [DOI: 10.1016/j.aquaculture.2019.734602] [Cited by in Crossref: 9] [Cited by in F6Publishing: 2] [Article Influence: 4.5] [Reference Citation Analysis]
33 Dadras H, Sampels S, Golpour A, Dzyuba V, Cosson J, Dzyuba B. Analysis of common carp Cyprinus carpio sperm motility and lipid composition using different in vitro temperatures. Anim Reprod Sci 2017;180:37-43. [PMID: 28302333 DOI: 10.1016/j.anireprosci.2017.02.011] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 2.6] [Reference Citation Analysis]
34 Figueroa E, Valdebenito I, Zepeda AB, Figueroa CA, Dumorné K, Castillo RL, Farias JG. Effects of cryopreservation on mitochondria of fish spermatozoa. Rev Aquacult 2017;9:76-87. [DOI: 10.1111/raq.12105] [Cited by in Crossref: 33] [Cited by in F6Publishing: 14] [Article Influence: 4.7] [Reference Citation Analysis]
35 Magnotti C, Cerqueira V, Villasante A, Romero J, Watanabe I, Oliveira R, Farias J, Merino O, Valdebenito, Figueroa E. Spermatological characteristics and effects of cryopreservation in Lebranche mullet spermatozoa (Mugil liza Valenciennes, 1836): first report of ultra-rapid freezing. Animal Reproduction Science 2022. [DOI: 10.1016/j.anireprosci.2022.106986] [Reference Citation Analysis]
36 Lissabet JFB, Belén LH, Lee-Estevez M, Farias JG. Role of voltage-gated L-type calcium channel in the spermatozoa motility of Atlantic salmon (Salmo salar). Comp Biochem Physiol A Mol Integr Physiol 2020;241:110633. [PMID: 31839589 DOI: 10.1016/j.cbpa.2019.110633] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
37 İnanan BE, Öğretmen F. Determination of differences in the biochemical properties of sperm activating and non-activating ovarian fluids and their influences on sperm motility in rainbow trout (Oncorhynchus mykiss). Aquaculture 2015;448:539-44. [DOI: 10.1016/j.aquaculture.2015.06.018] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 1.4] [Reference Citation Analysis]
38 Prokopchuk G, Dzyuba B, Bondarenko O, Rodina M, Cosson J. Motility initiation of sterlet sturgeon (Acipenser ruthenus) spermatozoa: Describing the propagation of the first flagellar waves. Theriogenology 2015;84:51-61. [PMID: 25794841 DOI: 10.1016/j.theriogenology.2015.02.011] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
39 Dumorné K, Figueroa E, Cosson J, Lee-estevez M, Ulloa-rodríguez P, Valdebenito I, Farías JG. Protein phosphorylation and ions effects on salmonid sperm motility activation. Rev Aquacult 2018;10:727-37. [DOI: 10.1111/raq.12198] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 1.4] [Reference Citation Analysis]
40 Bernardes Júnior JJ, Jimenez JE, Bombardelli RA, Nuñer APDO. Changes in external osmolality and ionic composition affect Megaleporinus obtusidens sperm motility. Animal Reproduction Science 2018;190:63-74. [DOI: 10.1016/j.anireprosci.2018.01.008] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
41 Nynca J, Słowińska M, Judycka S, Ciereszko A. Maladaptation of trout spermatozoa to fresh water is related to oxidative stress and proteome changes. Reproduction 2019;157:485-99. [PMID: 30921765 DOI: 10.1530/REP-19-0012] [Cited by in Crossref: 2] [Article Influence: 0.7] [Reference Citation Analysis]
42 Balamurugan R, Prapaporn W, Munuswamy N. Sperm activation and effects of cryopreservation on motility, ultrastructure and DNA integrity in Grey mullet Mugil cephalus. Aquaculture Reports 2019;14:100204. [DOI: 10.1016/j.aqrep.2019.100204] [Cited by in Crossref: 6] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
43 Kholodnyy V, Gadêlha H, Cosson J, Boryshpolets S. How do freshwater fish sperm find the egg? The physicochemical factors guiding the gamete encounters of externally fertilizing freshwater fish. Rev Aquacult 2020;12:1165-92. [DOI: 10.1111/raq.12378] [Cited by in Crossref: 13] [Cited by in F6Publishing: 5] [Article Influence: 4.3] [Reference Citation Analysis]
44 Dietrich MA, Dietrich GJ, Mostek A, Ciereszko A. Motility of carp spermatozoa is associated with profound changes in the sperm proteome. J Proteomics 2016;138:124-35. [PMID: 26926441 DOI: 10.1016/j.jprot.2016.02.029] [Cited by in Crossref: 21] [Cited by in F6Publishing: 20] [Article Influence: 3.5] [Reference Citation Analysis]
45 Fabbrocini A, Silvestri F, Vitiello V, Pelosi S, Sansone G, D'adamo R. A step towards using the semen of the common pandora Pagellus erythrinus for practical applications of cryo-research: The computer-assessed sperm motility pattern in long-term cryostored samples. Aquaculture 2020;528:735604. [DOI: 10.1016/j.aquaculture.2020.735604] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
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48 Alcántar‐vázquez JP, Fernández‐santos J, Meza‐villalvazo VM. Sperm kinetics and motility subpopulation in XY and YY Nile tilapia ( Oreochromis niloticus ) males. Aquaculture Research 2022;53:932-9. [DOI: 10.1111/are.15634] [Reference Citation Analysis]
49 Zhang J, Ma W, Xie B, Gui J, Mei J. Beneficial effect and potential molecular mechanism of chloroquine on sperm motility and fertilizing ability in yellow catfish. Aquaculture 2017;468:307-13. [DOI: 10.1016/j.aquaculture.2016.10.028] [Cited by in Crossref: 9] [Cited by in F6Publishing: 3] [Article Influence: 1.8] [Reference Citation Analysis]
50 Yamaner G, Tunçelli G, Tosun DD, Çanak Ö, Memiş D. Sperm activation in Black Sea Trout ( Salmo trutta labrax ): Effect of ions and osmolality on spermatozoa motility. Aquaculture Research. [DOI: 10.1111/are.15773] [Reference Citation Analysis]
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52 Caldas JS, Godoy L. Sperm characterization of the endangered Amazonian fish Hypancistrus zebra: Basic knowledge for reproduction and conservation strategies. Animal Reproduction Science 2019;204:117-24. [DOI: 10.1016/j.anireprosci.2019.03.012] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
53 Niedźwiecka N, Gronczewska J, Skorkowski EF. NAD-preferring malic enzyme: localization, regulation and its potential role in herring (Clupea harengus) sperm cells. Fish Physiol Biochem 2017;43:351-60. [PMID: 27630022 DOI: 10.1007/s10695-016-0291-6] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.2] [Reference Citation Analysis]
54 Ulloa-Rodríguez P, Contreras P, Dumorné K, Figueroa E, Risopatrón J, Valdebenito I, Farías JG. Sperm morphology and ultrastructure of Patagonian blenny (Eleginops maclovinus). Tissue Cell 2019;57:66-9. [PMID: 30947965 DOI: 10.1016/j.tice.2019.02.006] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
55 Motta NC, Machado GJ, Ferreira IS, García JL, Martínez Chávez CC, Martı Nez-Palacios CA, Solis Murgas LD. Sperm characterization and cryopreservation of the endangered freshwater fish Chirostoma estor (Atheriniformes). Cryobiology 2021:S0011-2240(21)00150-4. [PMID: 34537224 DOI: 10.1016/j.cryobiol.2021.09.004] [Reference Citation Analysis]
56 Yang J, Dong D, Peng G, Sun Q, Yang C, Gao Y, Ji H, Dong W. Melatonin regulates ATP content and fertilising capacity of Onychostoma macrolepis spermatozoa by inhibiting ROS accumulation during semen storage in vitro. Reprod Fertil Dev 2020;32:1212-22. [PMID: 33019961 DOI: 10.1071/RD20153] [Reference Citation Analysis]
57 Taugbøl A, Mazzarella AB, Cramer ERA, Laskemoen T. Salinity-induced phenotypic plasticity in threespine stickleback sperm activation. Biol Lett 2017;13:20170516. [PMID: 29021318 DOI: 10.1098/rsbl.2017.0516] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
58 Özgür ME, Maraş Z, Erdoğan S. The relationship between semen seminal plasma ions and sperm cell velocities of wild-caught longspine scraper, Capoeta trutta. Arch Anim Breed 2019;62:557-64. [PMID: 31807667 DOI: 10.5194/aab-62-557-2019] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]