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Cytochemical techniques for basic proteins reveal that as spermatid nuclei begin to elongate they have the somatic histone complement, and as they complete elongation they contain a very arginine‐rich, TCA‐extractable complement, or the salmon sperm histone type. After the nuclei have developed their ultimate corkscrew shape the final transition takes place to a very arginine‐rich, TCA‐stable complement, or the mammalian sperm histone type. These nuclei were not rich in sulfhydryl groups, but they were extractable with sodium thioglycolate. 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Biol., 67, 202a",{},{"id":19,"text":465,"url":19,"identifiers":466},"Kossel A., 1928, The Protamines and Histones",{},{"id":19,"text":468,"url":19,"identifiers":469},"10.1007\u002FBF00306423",{"doi":468},{"id":19,"text":471,"url":19,"identifiers":472},"10.1002\u002Fjmor.1051120202",{"doi":471},{"id":19,"text":320,"url":19,"identifiers":474},{"doi":320},{"id":476,"createTime":477,"updateTime":477,"relativeEntities":478,"slug":479,"properties":480,"entityType":107,"verifyStatus":108,"verifyTime":477,"verifyNote":109,"syncStatus":18,"languages":492,"translateLanguages":19,"viewCount":20,"primaryUrl":493,"fullTextUrl":19,"authors":494,"publicationType":187,"publisherRelationship":534,"citationCount":561,"citationInfo":562,"publishDate":565,"publishYear":566,"citationAnalyzeStatus":18,"lastCitationAnalyze":19,"indexDatabases":19,"openAccess":19,"references":567,"isForceReanalyzing":341},"3f15c5bd-e02f-46ae-b4cb-294503d0b169","2024-09-28T23:04:19.141+00:00",[],"The-time-course-of-seawater-acclimation-in-i-Fundulus-heteroclitus-i-L-",{"mag":481,"keywords":483,"openalex":484,"abstract":486,"title":488,"doi":490},{"VOID":482},"1966924009",{},{"VOID":485},"W1966924009",{"EN":487},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Serum Na\u003Cjats:sup>+\u003C\u002Fjats:sup> and osmolality increased significantly within 12–24 hours after transfer of \u003Cjats:italic>Fundulus heteroclitus\u003C\u002Fjats:italic> to seawater (SW) but returned to freshwater (FW) levels after 4 days in SW. Na\u003Cjats:sup>+\u003C\u002Fjats:sup>K\u003Cjats:sup>+\u003C\u002Fjats:sup>‐adenosine triphosphatase (ATPase) remained low during the first 2 days in SW but increased to a level characteristic of fully acclimated fish within 4 days. Serum cortisol did not display a marked elevation during the rise in Na\u003Cjats:sup>+\u003C\u002Fjats:sup>K\u003Cjats:sup>+\u003C\u002Fjats:sup>‐ATPase. Thus, the pattern of SW‐acclimation in \u003Cjats:italic>F. heteroclitus\u003C\u002Fjats:italic> is similar to that of the eel (\u003Cjats:italic>Anguilla rostrata\u003C\u002Fjats:italic>), but acclimation is accomplished somewhat more rapidly in \u003Cjats:italic>F. heteroclitus\u003C\u002Fjats:italic> and the prolonged period of elevated serum cortisol observed in the eel does not occur.\u003C\u002Fjats:p>\u003Cjats:p>A distinct peak in cortisol was observed during acclimation to FW when gill Na\u003Cjats:sup>+\u003C\u002Fjats:sup>K\u003Cjats:sup>+\u003C\u002Fjats:sup>‐ATPase and serum osmolality were declining. This indicates that elevated serum cortisol does not always lead to an increase in Na\u003Cjats:sup>+\u003C\u002Fjats:sup>K\u003Cjats:sup>+\u003C\u002Fjats:sup>‐ATPase activity.\u003C\u002Fjats:p>",{"EN":489},"The time course of seawater acclimation in \u003Ci>Fundulus heteroclitus\u003C\u002Fi> L.",{"VOID":491},"10.1002\u002Fjez.1402280105",[111],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.1402280105",[495,514],{"id":496,"sortIndex":20,"researcher":19,"roles":497,"affiliations":498,"properties":509},"6df4a970-ed38-4b52-ba54-9ec162c8e6c2",[],[499],{"id":500,"sortIndex":20,"affiliation":501,"properties":19},"6072a22d-d88f-4f3c-8ced-c01c82782637",{"id":502,"createTime":503,"updateTime":503,"relativeEntities":504,"slug":505,"properties":506,"entityType":129,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"270282e0-ba9e-4329-bc10-c2672fdd7ea9","2024-09-28T23:04:19.154+00:00",[],"College-of-Marine-Studies-and-School-of-Life-and-Health-Sciences-University-of-Delaware-Newark-Delaware-19711",{"title":507},{"EN":508},"College of Marine Studies and School of Life and Health Sciences, University of Delaware, Newark, Delaware 19711",{"openalex":510,"title":512},{"VOID":511},"A5058025223",{"EN":513},"William F. 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H., 1969, Sodium and potassium activated adenosine triphosphatase in kidneys of Fundulus heteroclitus adapted to fresh and salt water, Yale J. Biol. Med., 41, 388",{},{"id":19,"text":593,"url":19,"identifiers":594},"Evans D. H., 1980, Kinetic studies of ion transport by fish gill epithelium, Am. J. Physiol., 228, R224",{},{"id":19,"text":596,"url":19,"identifiers":597},"10.1007\u002FBF00706591",{"doi":596},{"id":19,"text":599,"url":19,"identifiers":600},"10.1016\u002FS0021-9258(18)84756-1",{"doi":599},{"id":19,"text":602,"url":19,"identifiers":603},"10.1007\u002FBF00455957",{"doi":602},{"id":19,"text":605,"url":19,"identifiers":606},"Forrest J. N., 1973, Na transport and Na\u002FK‐ATPase in gills during adaptation to seawater: Effects of cortisol, Am. J. Physiol., 224, 709, 10.1152\u002Fajplegacy.1973.224.3.709",{"doi":607},"10.1152\u002Fajplegacy.1973.224.3.709",{"id":19,"text":609,"url":19,"identifiers":610},"Forrest J. N., 1973, Plasma cortisol response to saltwater adaptation in the American eel Anguilla rostrata, Am. J. Physiol., 224, 714, 10.1152\u002Fajplegacy.1973.224.3.714",{"doi":611},"10.1152\u002Fajplegacy.1973.224.3.714",{"id":19,"text":613,"url":19,"identifiers":614},"10.1016\u002F0016-6480(79)90081-9",{"doi":613},{"id":19,"text":616,"url":19,"identifiers":617},"Hendler E. D., 1972, Effects of adrenalectomy and hormone replacement on Na‐K‐ATPase in renal tissue, Am. J. Physiol., 222, 754, 10.1152\u002Fajplegacy.1972.222.3.754",{"doi":618},"10.1152\u002Fajplegacy.1972.222.3.754",{"id":19,"text":620,"url":19,"identifiers":621},"10.1016\u002F0005-2744(68)90176-9",{"doi":620},{"id":19,"text":623,"url":19,"identifiers":624},"10.1083\u002Fjcb.70.1.157",{"doi":623},{"id":19,"text":626,"url":19,"identifiers":627},"10.1016\u002F0300-9629(77)90188-8",{"doi":626},{"id":19,"text":629,"url":19,"identifiers":630},"10.1016\u002F0016-6480(80)90191-4",{"doi":629},{"id":19,"text":632,"url":19,"identifiers":633},"10.1016\u002FS0021-9258(19)52451-6",{"doi":632},{"id":19,"text":635,"url":19,"identifiers":636},"10.1016\u002F0016-6480(74)90090-2",{"doi":635},{"id":19,"text":638,"url":19,"identifiers":639},"10.1016\u002F0016-6480(69)90040-9",{"doi":638},{"id":19,"text":641,"url":19,"identifiers":642},"Maetz J., 1967, Evolution de la balance minérale du sodium chez Fundulus heteroclitus au cours du transfert d'eau de mer en eau douce: Effets de l'hypophysectomie et de la prolactine, Gen. Comp. Endocrinol., 8, 63",{},{"id":19,"text":644,"url":19,"identifiers":645},"10.1038\u002F2141118a0",{"doi":644},{"id":19,"text":647,"url":19,"identifiers":648},"10.1085\u002Fjgp.50.2.391",{"doi":647},{"id":19,"text":650,"url":19,"identifiers":651},"Pickford G. E., 1969, Studies on the blood serum of the Cyprinodont fish Fundulus heteroclitus, adapted to fresh or salt water, Trans. Connecticut Acad. 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The agnathan hagfishes have primitive gill pouches, while the lampreys have arch‐like gills similar to the higher fishes. In the lampreys and elasmobranchs, the gill filaments are supported by a complete interbranchial septum and water exits via external branchial slits or pores. In contrast, the teleost interbranchial septum is much reduced, leaving the ends of the filaments unattached, and the multiple gill openings are replaced by the single caudal opening of the operculum. The basic functional unit of the gill is the filament, which supports rows of plate‐like lamellae. The lamellae are designed for gas exchange with a large surface area and a thin epithelium surrounding a well‐vascularized core of pillar cell capillaries. The lamellae are positioned for the blood flow to be counter‐current to the water flow over the gills. Despite marked differences in the gross anatomy of the gill among the various groups, the cellular constituents of the epithelium are remarkably similar. The lamellar gas‐exchange surface is covered by squamous pavement cells, while large, mitochondria‐rich, ionocytes and mucocytes are found in greatest frequency in the filament epithelium. Demands for ionoregulation can often upset this balance. There has been much study of the structure and function of the branchial mitochondria‐rich cells. These cells are generally characterized by a high mitochondrial density and an amplification of the basolateral membrane through folding or the presence of an intracellular tubular system. Morphological subtypes of MRCs as well as some methods of MRC detection are discussed. © 2002 Wiley‐Liss, Inc.\u003C\u002Fjats:p>",{"EN":690},"Fish gill morphology: inside out",{"VOID":692},"12115897",{"VOID":694},"10.1002\u002Fjez.10124",[111],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.10124",[698,730],{"id":699,"sortIndex":45,"researcher":19,"roles":700,"affiliations":701,"properties":723},"b9bb2995-4fec-47b5-801f-be869b0e77e8",[],[702,713],{"id":703,"sortIndex":45,"affiliation":704,"properties":19},"4b60ead5-2f2a-40a8-858a-be00442663df",{"id":705,"createTime":706,"updateTime":707,"relativeEntities":708,"slug":709,"properties":710,"entityType":129,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"1882e57d-fa9c-4a3e-a4a9-c89e1d109b27","2023-12-26T12:51:25.077+00:00","2024-10-06T15:22:53.340+00:00",[],"Department-of-Biology-McMaster-University-Hamilton-Ontario-Canada-L8S-4K1",{"title":711},{"VI":712},"Department of Biology, McMaster University, Hamilton, Ontario, Canada, L8S 4K1",{"id":714,"sortIndex":20,"affiliation":715,"properties":19},"652220cb-4099-4cb1-acf5-c5006f28fa20",{"id":716,"createTime":717,"updateTime":717,"relativeEntities":718,"slug":719,"properties":720,"entityType":129,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"db64a755-81e0-4429-8377-05f8fd3af05d","2024-09-28T23:04:12.442+00:00",[],"Centre-d-Ecologie-et-de-Physiologie-Energ%C3%A9tiques-CNRS-Strasbourg-67037-France",{"title":721},{"EN":722},"Centre d'Ecologie et de Physiologie Energétiques, CNRS, Strasbourg, 67037 France",{"openalex":724,"orcid":726,"title":728},{"VOID":725},"A5042763634",{"VOID":727},"https:\u002F\u002Forcid.org\u002F0000-0002-1435-9298",{"EN":729},"Pierre Laurent",{"id":731,"sortIndex":20,"researcher":19,"roles":732,"affiliations":733,"properties":745},"b7617326-a573-4c9d-81e3-1779767c03e6",[],[734],{"id":735,"sortIndex":20,"affiliation":736,"properties":19},"531f9a91-3cdd-4c71-a959-4e4e54c8c276",{"id":737,"createTime":738,"updateTime":739,"relativeEntities":740,"slug":741,"properties":742,"entityType":129,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"060921ed-42fe-48ab-8f0a-0f96630d79a9","2024-09-28T23:04:12.429+00:00","2025-06-11T19:09:12.014+00:00",[],"Centro-Interdisciplinar-de-Investiga%C3%A7%C3%A3o-Marinha-e-Ambiental-CIIMAR-4150-180-Porto-Portugal",{"title":743},{"EN":744},"Centro Interdisciplinar de Investigação Marinha e Ambiental (CIIMAR), 4150‐180 Porto, Portugal",{"openalex":746,"orcid":748,"title":750},{"VOID":747},"A5087372555",{"VOID":749},"https:\u002F\u002Forcid.org\u002F0000-0003-3681-1166",{"EN":751},"Jonathan M. 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In freshwater (FW) teleost gill, the mechanism of NaCl uptake is more controversial and involves apical V‐type H\u003Cjats:sup>+\u003C\u002Fjats:sup>‐ATPase linked to an apical Na\u003Cjats:sup>+\u003C\u002Fjats:sup> channel, apical Cl\u003Cjats:sup>−\u003C\u002Fjats:sup>–HCO\u003Cjats:inline-graphic xmlns:xlink=\"http:\u002F\u002Fwww.w3.org\u002F1999\u002Fxlink\" xlink:href=\"graphic\u002Ftex2gif-stack-1.gif\" xlink:title=\"urn:x-wiley:0022104X:media:JEZ10127:tex2gif-stack-1\" \u002F> exchange and basolateral Na\u003Cjats:sup>+\u003C\u002Fjats:sup>,K\u003Cjats:sup>+\u003C\u002Fjats:sup>‐ATPase. Ca\u003Cjats:sup>2+\u003C\u002Fjats:sup> uptake (in FW and SW) is via Ca\u003Cjats:sup>2+\u003C\u002Fjats:sup> channels in the apical membrane and Ca\u003Cjats:sup>2+\u003C\u002Fjats:sup>‐ATPase in the basolateral membrane. Mainly this transport occurs in mitochondria rich (MR) chloride cells, but there is a role for the pavement cells also. Future research will likely expand in two major directions, molded by methodology: first in physiological genomics of all the transporters, including their expression, trafficking, operation, and regulation at the molecular level, and second in biotelemetry to examine multivariable components in behavioral physiological ecology, thus widening the integration of physiology from the molecular to the environmental levels while deepening understanding at all levels. © 2002 Wiley‐Liss, Inc.\u003C\u002Fjats:p>",{"EN":1131},"Na\u003Csup>+\u003C\u002Fsup>, Cl\u003Csup>−\u003C\u002Fsup>, Ca\u003Csup>2+\u003C\u002Fsup> and Zn\u003Csup>2+\u003C\u002Fsup> transport by fish gills: retrospective review and prospective synthesis",{"VOID":1133},"12115901",{"VOID":1135},"10.1002\u002Fjez.10127","2024-09-28T23:04:11.440+00:00",[111],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.10127",[1140],{"id":1141,"sortIndex":20,"researcher":19,"roles":1142,"affiliations":1143,"properties":1155},"bdcfaa25-d0d5-4d81-b8f1-9fd91eba2037",[],[1144],{"id":1145,"sortIndex":20,"affiliation":1146,"properties":19},"bc3fc9f5-7690-4e8f-9651-7fd9a687ec21",{"id":1147,"createTime":1148,"updateTime":1149,"relativeEntities":1150,"slug":1151,"properties":1152,"entityType":129,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"870360fd-fe9f-4561-8e5a-314abd150b86","2023-12-19T12:13:25.741+00:00","2024-09-28T23:04:11.459+00:00",[],"Department-of-Biology-St-Francis-Xavier-University-Antigonish-Nova-Scotia-Canada-B2G-2W5-",{"title":1153},{"VI":1154},"Department of Biology, St. Francis Xavier University, Antigonish, Nova Scotia, Canada B2G 2W5, ",{"openalex":1156,"orcid":1158,"title":1160},{"VOID":1157},"A5033145743",{"VOID":1159},"https:\u002F\u002Forcid.org\u002F0000-0002-5792-8710",{"EN":1161},"William S. 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10.1242\u002Fjeb.204.4.701",{"doi":1630},"10.1242\u002Fjeb.204.4.701",{"id":19,"text":1632,"url":19,"identifiers":1633},"10.1111\u002Fj.1095-8649.2000.tb00259.x",{"doi":1632},{"id":19,"text":671,"url":19,"identifiers":1635},{"doi":671},{"id":19,"text":1637,"url":19,"identifiers":1638},"10.1023\u002FA:1007755008204",{"doi":1637},{"id":19,"text":1640,"url":19,"identifiers":1641},"10.2108\u002Fzsj.13.655",{"doi":1640},{"id":19,"text":1643,"url":19,"identifiers":1644},"10.1007\u002Fs003600050066",{"doi":1643},{"id":19,"text":1646,"url":19,"identifiers":1647},"10.1007\u002Fs004240050674",{"doi":1646},{"id":19,"text":1649,"url":19,"identifiers":1650},"Wilson JM, 2000, NaCl uptake by the branchial epithelium in freshwater teleost fish: an immunological approach to ion transport protein localization, J Exp Biol, 203, 2279, 10.1242\u002Fjeb.203.15.2279",{"doi":1096},{"id":19,"text":1652,"url":19,"identifiers":1653},"Wilson JM, 2000, Immunolocalization of ion transport proteins to branchial epithelium mitochondria rich cells in the mudskipper (Periophthalmodon schlosseri), J Exp Biol, 203, 2297, 10.1242\u002Fjeb.203.15.2297",{"doi":1101},{"id":19,"text":1655,"url":19,"identifiers":1656},"10.1152\u002Fajpregu.1999.277.2.R517",{"doi":1655},{"id":19,"text":1658,"url":19,"identifiers":1659},"10.2307\u002F1352333",{"doi":1658},{"id":19,"text":1661,"url":19,"identifiers":1662},"Wood CM, 1997, Cultured branchial epithelia from freshwater fish gills, J Exp Biol, 200, 1047, 10.1242\u002Fjeb.200.6.1047",{"doi":1663},"10.1242\u002Fjeb.200.6.1047",{"id":19,"text":1665,"url":19,"identifiers":1666},"10.1016\u002FS1095-6433(97)00403-0",{"doi":1665},{"id":19,"text":1668,"url":19,"identifiers":1669},"10.1016\u002FS0734-9750(99)00035-X",{"doi":1668},{"id":19,"text":1671,"url":19,"identifiers":1672},"10.1074\u002Fjbc.M008209200",{"doi":1671},{"id":19,"text":1674,"url":19,"identifiers":1675},"10.1007\u002FBF00233449",{"doi":1674},{"id":1677,"createTime":1678,"updateTime":1678,"relativeEntities":1679,"slug":1680,"properties":1681,"entityType":107,"verifyStatus":108,"verifyTime":1695,"verifyNote":109,"syncStatus":18,"languages":1696,"translateLanguages":19,"viewCount":20,"primaryUrl":1697,"fullTextUrl":19,"authors":1698,"publicationType":187,"publisherRelationship":1808,"citationCount":1835,"citationInfo":1836,"publishDate":1839,"publishYear":788,"citationAnalyzeStatus":18,"lastCitationAnalyze":19,"indexDatabases":19,"openAccess":19,"references":1840,"isForceReanalyzing":341},"e82d980d-f3c3-460c-bcb3-1df7fe34c3f0","2024-09-28T23:04:00.243+00:00",[],"Dynamics-of-Na-sup-sup-K-sup-sup-2Cl-sup-sup-cotransporter-and-Na-sup-sup-K-sup-sup-ATPase-expression-in-the-branchial-epithelium-of-brown-trout-i-Salmo-trutta-i-and-atlantic-salmon-i-Salmo-salar-i-",{"mag":1682,"keywords":1684,"openalex":1685,"abstract":1687,"title":1689,"pm":1691,"doi":1693},{"VOID":1683},"2085908073",{},{"VOID":1686},"W2085908073",{"EN":1688},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>The dynamics of branchial Na\u003Cjats:sup>+\u003C\u002Fjats:sup>,K\u003Cjats:sup>+\u003C\u002Fjats:sup>,2Cl\u003Cjats:sup>−\u003C\u002Fjats:sup> cotransporter (NKCC) and Na\u003Cjats:sup>+\u003C\u002Fjats:sup>,K\u003Cjats:sup>+\u003C\u002Fjats:sup>‐ATPase (NKA) expression were investigated in brown trout and Atlantic salmon during salinity shifts and the parr‐smolt transformation, respectively. In the brown trout, Western blotting revealed that NKCC and NKA abundance increased gradually and in parallel (30‐ and ten‐fold, respectively) after transfer to seawater (SW). The NKA hydrolytic activity increased ten‐fold after SW‐transfer. Following back‐transfer to fresh water (FW), the levels of both proteins and NKA activity decreased. The NKCC immunostaining in the gill of SW‐acclimated trout was strong, and mainly localized in large cells in the filament and around the bases of the lamellae. In FW‐acclimated trout, immunostaining was less intense and more diffuse. Partial cDNAs of the secretory NKCC1 isoform were cloned and sequenced from both brown trout and Atlantic salmon gills. Two differently sized transcripts were detected by Northern blotting in the gill but not in other osmoregulatory tissues (kidney, pyloric caeca, intestine). The abundance in the gill of these transcripts and of the associated NKCC protein increased four‐ and 30‐fold, respectively, during parr‐smolt transformation. The abundance of NKA α‐subunit protein also increased in the gill during parr‐smolt transformation though to a lesser extent than enzymatic activity (2.5‐ and eight‐fold, respectively). In separate series of in vitro experiments, cortisol directly stimulated the expression of NKCC mRNA in gill tissue of both salmonids. The study demonstrates the coordinated regulation of NKCC and NKA proteins in the gill during salinity shifts and parr‐smolt transformation of salmonids. © 2002 Wiley‐Liss, Inc.\u003C\u002Fjats:p>",{"EN":1690},"Dynamics of Na\u003Csup>+\u003C\u002Fsup>,K\u003Csup>+\u003C\u002Fsup>,2Cl\u003Csup>−\u003C\u002Fsup> cotransporter and Na\u003Csup>+\u003C\u002Fsup>,K\u003Csup>+\u003C\u002Fsup>‐ATPase expression in the branchial epithelium of brown trout (\u003Ci>Salmo trutta\u003C\u002Fi>) and atlantic salmon (\u003Ci>Salmo salar\u003C\u002Fi>)",{"VOID":1692},"12115907",{"VOID":1694},"10.1002\u002Fjez.10118","2024-09-28T23:04:00.242+00:00",[111],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.10118",[1699,1720,1740,1759,1776,1793],{"id":1700,"sortIndex":45,"researcher":19,"roles":1701,"affiliations":1702,"properties":1713},"590ef8be-b22e-4b87-a917-072ada9cd55c",[],[1703],{"id":1704,"sortIndex":20,"affiliation":1705,"properties":19},"7202bf83-8f95-4b08-a228-6f6d502f1069",{"id":1706,"createTime":1707,"updateTime":1707,"relativeEntities":1708,"slug":1709,"properties":1710,"entityType":129,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"83528a7f-490f-4f85-a2ec-6883d9badad9","2024-09-28T23:04:00.262+00:00",[],"Institute-of-Biology-University-of-Southern-Denmark-Main-Campus-Odense-University-DK-5230-Odense-M-Denmark",{"title":1711},{"EN":1712},"Institute of Biology, University of Southern Denmark-Main Campus: Odense University, DK-5230 Odense M, Denmark",{"openalex":1714,"orcid":1716,"title":1718},{"VOID":1715},"A5057824760",{"VOID":1717},"https:\u002F\u002Forcid.org\u002F0000-0002-5785-7094",{"EN":1719},"Steffen S. 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Anz., 97, 169",{},{"id":19,"text":2162,"url":19,"identifiers":2163},"Krüger P., 1952, Tetanus und Tonus der Quergestreiften Skelettmuskeln der Wirbeltiere und des Menschen",{},{"id":19,"text":2165,"url":19,"identifiers":2166},"10.1113\u002Fjphysiol.1953.sp004949",{"doi":2165},{"id":19,"text":2168,"url":19,"identifiers":2169},"10.1111\u002Fj.1748-1716.1966.tb03427.x",{"doi":2168},{"id":19,"text":2171,"url":19,"identifiers":2172},"10.1016\u002FB978-0-12-395555-5.50009-8",{"doi":2171},{"id":19,"text":2174,"url":19,"identifiers":2175},"Milonig G., 1962, Electron Microscopy",{},{"id":19,"text":2177,"url":19,"identifiers":2178},"10.1083\u002Fjcb.26.2.477",{"doi":2177},{"id":19,"text":2180,"url":19,"identifiers":2181},"Peachey L. 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Biophys., 10, 237",{},{"id":19,"text":2204,"url":19,"identifiers":2205},"10.1007\u002FBF01723355",{"doi":2204},{"id":19,"text":2207,"url":19,"identifiers":2208},"10.1007\u002FBF01752143",{"doi":2207},{"id":2210,"createTime":2211,"updateTime":2211,"relativeEntities":2212,"slug":2213,"properties":2214,"entityType":107,"verifyStatus":108,"verifyTime":2211,"verifyNote":109,"syncStatus":18,"languages":2228,"translateLanguages":19,"viewCount":20,"primaryUrl":2229,"fullTextUrl":19,"authors":2230,"publicationType":187,"publisherRelationship":2271,"citationCount":83,"citationInfo":2298,"publishDate":2300,"publishYear":2301,"citationAnalyzeStatus":18,"lastCitationAnalyze":19,"indexDatabases":19,"openAccess":19,"references":2302,"isForceReanalyzing":341},"742f31da-a71b-405f-9067-78b39aff85d5","2024-09-29T22:01:23.108+00:00",[],"Effect-of-sensory-input-from-the-tongue-on-jaw-movement-in-normal-feeding-in-the-opossum",{"mag":2215,"keywords":2217,"openalex":2218,"abstract":2220,"title":2222,"pm":2224,"doi":2226},{"VOID":2216},"2114243589",{},{"VOID":2219},"W2114243589",{"EN":2221},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Opossums were presented with solid and liquid foods. The movements of the jaw and tongue were recorded cineradiographically together with recordings of the EMG activity in muscles opening the jaw and moving the base of the tongue (hyoid). The jaw opening in each cycle was in two stages–01 and 02; 01 had a constant amplitude irrespective of the food ingested. Ingestion of liquid (which involved continuous accumulation of a liquid bolus in the valleculae prior to swallowing) was associated with cycles of oral movement in which 02 was small; tongue retraction was associated with this opening. In contrast, solid and semisolid food ingestion was associated with large angles of jaw opening in 02 that also coincided with the tongue retraction. In this latter case a characteristic pattern of EMG activity, in which all the muscles moving the hyoid were simultaneously active, was added to the pattern seen in lapping; this additional activity had an EMG pattern that was consistent with a jaw opening reflex. The findings contrast with other reports that the jaw opening reflex is suppressed in mastication. Experimentally induced tongue contact with a variety of solid surfaces during lapping (an activity involving accumulation of a liquid bolus in the valleculae) induced neither increased jaw opening nor the additional EMG pattern. However, in situations when there was no bolus in the valleculae, additional jaw opening activity was elicited when the tongue contracted solids intra‐ or extra‐orally. It is suggested that the ability of sensory input, from the anterior tongue, to elicit a jaw opening reflex and to change the type of jaw\u002Ftongue cycle was dependent upon the extent of bolus accumulation in the valleculae and therefore indirectly upon the consistency of the food.\u003C\u002Fjats:p>",{"EN":2223},"Effect of sensory input from the tongue on jaw movement in normal feeding in the opossum",{"VOID":2225},"2760570",{"VOID":2227},"10.1002\u002Fjez.1402500302",[111],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.1402500302",[2231,2252],{"id":2232,"sortIndex":45,"researcher":19,"roles":2233,"affiliations":2234,"properties":2245},"10495207-964b-4b6e-ab06-df01c18d2d3b",[],[2235],{"id":2236,"sortIndex":20,"affiliation":2237,"properties":19},"5bee77e6-4010-4fda-8f69-f0e8d04305a2",{"id":2238,"createTime":2239,"updateTime":2239,"relativeEntities":2240,"slug":2241,"properties":2242,"entityType":129,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"f8c8b43f-2b4d-4213-ba3b-daad934f8c04","2024-09-29T22:01:23.148+00:00",[],"M-C-Z-Harvard-University-Cambridge-MA-02138",{"title":2243},{"EN":2244},"M.C.Z. 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P., 1984, Oro‐Facial Pain and Neuromuscular Dysfunction: Mechanisms and clinical correlates, 51",{},{"id":19,"text":2382,"url":19,"identifiers":2383},"10.1159\u002F000118860",{"doi":2382},{"id":19,"text":2385,"url":19,"identifiers":2386},"10.1139\u002Fy83-168",{"doi":2385},{"id":19,"text":2388,"url":19,"identifiers":2389},"10.1016\u002F0166-2236(83)90219-9",{"doi":2388},{"id":19,"text":2391,"url":19,"identifiers":2392},"10.1016\u002F0306-4522(81)90247-5",{"doi":2391},{"id":19,"text":2394,"url":19,"identifiers":2395},"10.1139\u002Fy81-104",{"doi":2394},{"id":19,"text":2397,"url":19,"identifiers":2398},"10.1016\u002F0003-9969(81)90137-0",{"doi":2397},{"id":19,"text":2400,"url":19,"identifiers":2401},"10.1152\u002Fphysrev.1982.62.1.129",{"doi":2400},{"id":19,"text":2403,"url":19,"identifiers":2404},"10.1113\u002Fexpphysiol.1915.sp000201",{"doi":2403},{"id":19,"text":2406,"url":19,"identifiers":2407},"10.1002\u002Fjmor.1051850203",{"doi":2406},{"id":19,"text":2409,"url":19,"identifiers":2410},"10.1113\u002Fjphysiol.1917.sp001809",{"doi":2409},{"id":19,"text":2412,"url":19,"identifiers":2413},"10.1111\u002Fj.1469-7998.1984.tb04290.x",{"doi":2412},{"id":19,"text":2415,"url":19,"identifiers":2416},"10.1007\u002FBF00592290",{"doi":2415},{"id":19,"text":2418,"url":19,"identifiers":2419},"10.1016\u002F0003-9969(73)90178-7",{"doi":2418},{"id":19,"text":2421,"url":19,"identifiers":2422},"10.1016\u002F0006-8993(74)90058-4",{"doi":2421},{"id":19,"text":2424,"url":19,"identifiers":2425},"10.1177\u002F014107688407701205",{"doi":2424},{"id":19,"text":2427,"url":19,"identifiers":2428},"10.1016\u002F0006-8993(79)90510-9",{"doi":2427},{"id":19,"text":2430,"url":19,"identifiers":2431},"10.1152\u002Fjn.1980.44.3.456",{"doi":2430},{"id":19,"text":2433,"url":19,"identifiers":2434},"10.1159\u002F000118859",{"doi":2433},{"id":19,"text":2436,"url":19,"identifiers":2437},"10.1016\u002F0014-4886(87)90172-5",{"doi":2436},{"id":19,"text":2439,"url":19,"identifiers":2440},"10.1016\u002F0003-9969(82)90032-2",{"doi":2439},{"id":19,"text":2442,"url":19,"identifiers":2443},"10.1016\u002F0003-9969(78)90015-8",{"doi":2442},{"id":19,"text":2445,"url":19,"identifiers":2446},"10.2170\u002Fjjphysiol.24.73",{"doi":2445},{"id":2448,"createTime":2449,"updateTime":2449,"relativeEntities":2450,"slug":2451,"properties":2452,"entityType":107,"verifyStatus":108,"verifyTime":2449,"verifyNote":109,"syncStatus":18,"languages":2466,"translateLanguages":19,"viewCount":20,"primaryUrl":2467,"fullTextUrl":19,"authors":2468,"publicationType":187,"publisherRelationship":2503,"citationCount":2530,"citationInfo":2531,"publishDate":2533,"publishYear":2534,"citationAnalyzeStatus":18,"lastCitationAnalyze":19,"indexDatabases":19,"openAccess":19,"references":2535,"isForceReanalyzing":341},"9f9c9f2b-d6e0-49f5-b9d7-e2cacee92c5b","2024-09-26T21:41:37.285+00:00",[],"RNA-in-Cecropia-moth-ovaries-Sites-of-synthesis-transport-and-storage",{"mag":2453,"keywords":2455,"openalex":2456,"abstract":2458,"title":2460,"pm":2462,"doi":2464},{"VOID":2454},"2143893072",{},{"VOID":2457},"W2143893072",{"EN":2459},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Azure B staining of Cecropia moth ovarian follicles indicated that the pattern of RNA concentrations characteristic of vitellogenic oocytes is disrupted by a gross redistribution and dispersion, beginning with the final discharge of the cytoplasm of the nurse cells into the oocyte. The cytoplasmic redistribution is largely complete two days later when chorion formation begins, the germinal vesicle breaks down, and the first meiotic spindle forms.\u003C\u002Fjats:p>\u003Cjats:p>At this stage the follicle contains 30 μg of RNA, of which 27 μg are in the follicle cells and only 3 μg in the oocyte itself. The proportionately large amount of follicle cell RNA apparently reflects the synthetic functions of these cells in the formation of yolk and the secretion of chorion. Of the 3 μg in the oocyte, only 1 μg is incorporated into the early embryo while the remainder is found in the yolk cells and serosa.\u003C\u002Fjats:p>\u003Cjats:p>Autoradiography of follicles labeled with H\u003Cjats:sup>3\u003C\u002Fjats:sup>‐uridine either \u003Cjats:italic>in vivo\u003C\u002Fjats:italic> or by a “pulsechase” procedure \u003Cjats:italic>in vitro\u003C\u002Fjats:italic> indicated that, as in other polytrophic insect ovaries, the nurse cell nuclei are the most conspicuous source of oocyte RNA. The germinal vesicle incorporated labeled uridine in previtellogenic follicles. In vitellogenic and later stages neither a germinal vesicle nor a follicle cell contribution to oocyte RNA was detected by the procedures used.\u003C\u002Fjats:p>",{"EN":2461},"RNA in Cecropia moth ovaries: Sites of synthesis, transport, and storage",{"VOID":2463},"5813697",{"VOID":2465},"10.1002\u002Fjez.1401700102",[111],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.1401700102",[2469,2488],{"id":2470,"sortIndex":20,"researcher":19,"roles":2471,"affiliations":2472,"properties":2483},"39df56d1-6872-4711-a637-b10968f9da0d",[],[2473],{"id":2474,"sortIndex":20,"affiliation":2475,"properties":19},"e035d4d5-9c5f-4d1b-a81a-d69441273921",{"id":2476,"createTime":2477,"updateTime":2477,"relativeEntities":2478,"slug":2479,"properties":2480,"entityType":129,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"51444bb9-470c-48e1-ae2d-f40559dc8e2c","2024-09-26T21:41:37.305+00:00",[],"Biology-Department-University-of-Pennsylvania-and-Anatomy-Department-Women-s-Medical-College-of-Pennsylvania",{"title":2481},{"EN":2482},"Biology Department, University of Pennsylvania, and Anatomy Department, Women's Medical College of Pennsylvania",{"openalex":2484,"title":2486},{"VOID":2485},"A5103706023",{"EN":2487},"Sylvia B. 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Jb. Physiol., 71, 371",{},{"id":19,"text":2549,"url":19,"identifiers":2550},"10.1007\u002FBF00594513",{"doi":2549},{"id":19,"text":2552,"url":19,"identifiers":2553},"10.1007\u002FBF00331114",{"doi":2552},{"id":19,"text":2555,"url":19,"identifiers":2556},"10.1073\u002Fpnas.51.1.139",{"doi":2555},{"id":19,"text":2558,"url":19,"identifiers":2559},"10.1016\u002FS0022-2836(64)80116-9",{"doi":2558},{"id":19,"text":2561,"url":19,"identifiers":2562},"Brown D. D., 1966, The nucleolus and synthesis of ribosomal RNA during oogenesis and embryogenesis of Xenopus laevis, Natl. Cancer Inst. 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C., 1960, Oogenesis in adult Drosophila melanogaster. IX. Studies on the cytochemistry and ultrastructure of developing oocytes, Growth, 24, 265",{},{"id":19,"text":2591,"url":19,"identifiers":2592},"King R. C., 1965, Oogenesis in Hyalophora cecropia, Growth, 29, 17",{},{"id":19,"text":2594,"url":19,"identifiers":2595},"10.1126\u002Fscience.129.3364.1674",{"doi":2594},{"id":19,"text":2597,"url":19,"identifiers":2598},"10.1002\u002Fjez.1401270205",{"doi":2597},{"id":19,"text":2600,"url":19,"identifiers":2601},"10.1083\u002Fjcb.30.1.177",{"doi":2600},{"id":19,"text":2603,"url":19,"identifiers":2604},"10.1126\u002Fscience.154.3750.775",{"doi":2603},{"id":19,"text":2606,"url":19,"identifiers":2607},"Melius M. E.1966An autoradiographic analysis of blood protein uptake and protein yolk sphere formation by Cecropia moth oocytes. Ph. D. Thesis University of Pennsylvania.",{},{"id":19,"text":2609,"url":19,"identifiers":2610},"10.1016\u002FS0014-4827(64)81008-9",{"doi":2609},{"id":19,"text":2612,"url":19,"identifiers":2613},"Ogur M., 1950, The nucleic acids of plant tissues. I. The extraction and estimation of desoxypentose nucleic acid and pentose nucleic acid, Arch. Biochem., 25, 262",{},{"id":19,"text":2615,"url":19,"identifiers":2616},"10.1016\u002F0003-9861(52)90381-0",{"doi":2615},{"id":19,"text":2618,"url":19,"identifiers":2619},"Pollack S. B.1967Synthesis and distribution of RNA in Cecropia oocyte differentiation. Ph. D. Thesis University of Pennsylvania.",{},{"id":19,"text":2621,"url":19,"identifiers":2622},"10.1007\u002FBF00600761",{"doi":2621},{"id":19,"text":2624,"url":19,"identifiers":2625},"10.1083\u002Fjcb.20.2.313",{"doi":2624},{"id":19,"text":2627,"url":19,"identifiers":2628},"Schmidt G., 1945, A method for the determination of desoxyribonucleic acid, ribonucleic acid, and phosphoprotein in animal tissues, J. Biol. Chem., 161, 83, 10.1016\u002FS0021-9258(17)41524-9",{"doi":2629},"10.1016\u002FS0021-9258(17)41524-9",{"id":19,"text":2631,"url":19,"identifiers":2632},"Schneider K., 1917, Die Entwicklung des Eierstockes und Eies von Deilephila euphorbiae, Arch. Zellforsch., 14, 79",{},{"id":19,"text":2634,"url":19,"identifiers":2635},"10.1016\u002F0014-4827(60)90158-0",{"doi":2634},{"id":19,"text":2637,"url":19,"identifiers":2638},"10.1126\u002Fscience.150.3697.777",{"doi":2637},{"id":19,"text":2640,"url":19,"identifiers":2641},"10.1083\u002Fjcb.26.1.49",{"doi":2640},{"id":19,"text":2643,"url":19,"identifiers":2644},"10.1085\u002Fjgp.37.4.539",{"doi":2643},{"id":19,"text":2646,"url":19,"identifiers":2647},"10.2307\u002F1539007",{"doi":2646},{"id":19,"text":2649,"url":19,"identifiers":2650},"10.1083\u002Fjcb.9.4.747",{"doi":2649},{"id":19,"text":2652,"url":19,"identifiers":2653},"10.1016\u002F0012-1606(68)90002-X",{"doi":2652},{"id":19,"text":2655,"url":19,"identifiers":2656},"10.2307\u002F1539008",{"doi":2655},{"id":19,"text":2658,"url":19,"identifiers":2659},"Urbani E., 1964, Osserva zioni citochimiche e autoradiografiche sulmetabolisimo degli acidi nucleici nella oogenesis di Dytiscus marginalis L, Rend. Inst. Sci. Univ. di Camerino, 5, 19",{},{"id":19,"text":2661,"url":19,"identifiers":2662},"10.2307\u002F1539367",{"doi":2661},{"id":19,"text":2664,"url":19,"identifiers":2665},"Verhien A., 1921, Die Eibildung der Muscider Zool Jahrb, Abt. f. Anat. u. Ont., 42, 150",{},{"id":19,"text":2667,"url":19,"identifiers":2668},"Wallace R. A. andJ. N.Dumont1969The induced synthesis and transport of yolk proteins and their accumulation by the oocyte inXenopus. J. Cell. Physiol. In press.",{},{"id":19,"text":2670,"url":19,"identifiers":2671},"10.1016\u002F0014-4827(60)90049-5",{"doi":2670},{"id":19,"text":2673,"url":19,"identifiers":2674},"Zalokar M.1961Ribonucleic acid and the control of cellular processes. In: Control Mechanisn in Cellular Processes D. M. Bonner ed. p.87–140.",{},{"id":2676,"createTime":2677,"updateTime":2677,"relativeEntities":2678,"slug":2679,"properties":2680,"entityType":107,"verifyStatus":108,"verifyTime":2694,"verifyNote":109,"syncStatus":18,"languages":2695,"translateLanguages":19,"viewCount":20,"primaryUrl":2696,"fullTextUrl":19,"authors":2697,"publicationType":187,"publisherRelationship":2717,"citationCount":66,"citationInfo":2745,"publishDate":2747,"publishYear":2072,"citationAnalyzeStatus":18,"lastCitationAnalyze":19,"indexDatabases":19,"openAccess":19,"references":2748,"isForceReanalyzing":341},"8247089d-5095-49fd-b3c1-f0ad4c344e62","2024-09-26T21:41:22.397+00:00",[],"The-regulation-of-ovulation-in-the-tsetse-fly-i-Glossina-pallidipes-i-Austen",{"mag":2681,"keywords":2683,"openalex":2684,"abstract":2686,"title":2688,"pm":2690,"doi":2692},{"VOID":2682},"2053122581",{},{"VOID":2685},"W2053122581",{"EN":2687},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>The tsetse‐fly female matures a single oocyte at a time. It ovulates this into the uterus, where it hatches, develops into a fully‐grown larva, and is later larviposited by the mother. It is only then that the next mature oocyte is ovulated, and the whole sequence is repeated. Thus, in this insect, it is possible to differentiate clearly four processes of egg production: (1) oogenesis, (2) oocyte growth and vitellogenesis, (3) ovulation, and (4) oviposition (in this case, larviposition). Mating is necessary to initiate the process of ovulation, but it is not necessary for the earlier processes. In virgin females, oogenesis, oocyte growth and vitellogenesis takes place normally; but the sequentially matured oocytes are lysed within the egg chambers without being ovulated.\u003C\u002Fjats:p>",{"EN":2689},"The regulation of ovulation in the tsetse‐fly, \u003Ci>Glossina pallidipes\u003C\u002Fi> Austen",{"VOID":2691},"5130027",{"VOID":2693},"10.1002\u002Fjez.1401770406","2024-09-26T21:41:22.396+00:00",[111],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.1401770406",[2698],{"id":2699,"sortIndex":20,"researcher":19,"roles":2700,"affiliations":2701,"properties":2712},"fb20065f-8bec-44b2-9838-3ece5f0a0abe",[],[2702],{"id":2703,"sortIndex":20,"affiliation":2704,"properties":19},"b3984c99-8bb7-4a4d-a850-d638f368a600",{"id":2705,"createTime":2706,"updateTime":2706,"relativeEntities":2707,"slug":2708,"properties":2709,"entityType":129,"verifyStatus":18,"verifyTime":19,"verifyNote":19,"syncStatus":18,"languages":19,"translateLanguages":19,"viewCount":20},"0cf459a2-e624-4f7d-b056-3e5388bfa1e5","2024-09-26T21:41:22.415+00:00",[],"Department-of-Entomology-University-of-Nairobi-P-O-Box-30197-Nairobi-and-The-International-Centre-of-Insect-Physiology-and-Ecology-P-O-Box-30772-Nairobi-Kenya",{"title":2710},{"EN":2711},"Department of Entomology, University of Nairobi, P.O. 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