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Oogenesis in Xenopus laevis (Daudin). V. Relationships between developing oocytes and their investing follicular tissues

https://doi.org/10.1002/jmor.1051550106
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/aja.1001060207openalex-snapshot
The development of the zona pellucida of the mammalian ovum
inferredcites →https://doi.org/10.1002/aja.1001390406openalex-snapshot
Development of the zona pellucida in the rat oocyte
inferredcites →https://doi.org/10.1002/jcp.1040720407openalex-snapshot
The induced synthesis and transport of yolk proteins and their accumulation by the oocyte inXenopus laevis
inferredcites →https://doi.org/10.1002/jcp.1040760108openalex-snapshot
Extracellular concentrating of proteins in the cecropia moth follicle
inferredcites →https://doi.org/10.1002/jez.1400710109openalex-snapshot
Ovulation in the frog. II. Follicular rupture to fertilization
inferredcites →https://doi.org/10.1002/jez.1401790307openalex-snapshot
The passage of extracellular tracers through the follicular epithelium of lizard ovaries
inferredcites →https://doi.org/10.1002/jez.1401840305openalex-snapshot
Protein incorporation by isolated amphibian oocytes III. Optimum incubation conditions
inferredcites →https://doi.org/10.1002/jmor.1051290102openalex-snapshot
An autoradiographic analysis of yolk deposition in the cortex of the cecropia moth oocyte
inferredcites →https://doi.org/10.1002/jmor.1051290107openalex-snapshot
Oocyte‐follicle cell differentiation in two species of Amphineurans (Mollusca), Mopalia mucosa and Chaetopleura apiculata
inferredcites →https://doi.org/10.1002/jmor.1051360203openalex-snapshot
Oogenesis in Xenopus laevis (Daudin). I. Stages of oocyte development in laboratory maintained animals
inferredcites →https://doi.org/10.1002/jmor.1051360405openalex-snapshot
A cytological study of the ovary of Rhodnius prolixus. I. The ontogeny of the follicular epithelium
inferredcites →https://doi.org/10.1007/bf00209205openalex-snapshot
Oogenesis in Xenopus laevis (Daudin)
inferredcites →https://doi.org/10.1007/bf00214203openalex-snapshot
Further studies of the surface epithelium covering preovulatory rabbit follicles with special reference to lysosomal alterations
inferredcites →https://doi.org/10.1007/bf00324615openalex-snapshot
The cytology of the vitellogenic stages of oogenesis in Drosophila melanogaster
inferredcites →https://doi.org/10.1007/bf00335143openalex-snapshot
The origin and structure of the secondary coat of the egg of Drosophila melanogaster
inferredcites →https://doi.org/10.1007/bf00336618openalex-snapshot
The ultrastructure of the layers enveloping yolk-forming oocytes from Triturus viridescens
inferredcites →https://doi.org/10.1007/bf00339346openalex-snapshot
Experimentelle Untersuchungen �ber die Stoffaufnahme durch Pinocytose w�hrend der Vitellogenese des Amphibienoocyten
inferredcites →https://doi.org/10.1007/bf00342212openalex-snapshot
An electron microscope study of the formation of the zona pellucida in oocytes from Triturus viridescens
inferredcites →https://doi.org/10.1007/bf00342501openalex-snapshot
Elektronenmikroskopische und histochemische Studien �ber die Oogenese der Amphibieneizelle
inferredcites →https://doi.org/10.1007/bf00492287openalex-snapshot
An EM autoradiographic study on ovarian follicle cells of Drosophila melanogaster with special reference to the formation of egg coverings
inferredcites →https://doi.org/10.1007/bf02806021openalex-snapshot
Defined nutrient medium for the in vitro maintenance ofXenopus laevis oocytes
inferredcites →https://doi.org/10.1016/0012-1606(74)90189-4openalex-snapshot
Formation and structure of the fertilization envelope in Xenopus laevis
inferredcites →https://doi.org/10.1016/b978-0-12-455402-3.50008-5openalex-snapshot
REPRODUCTION
inferredcites →https://doi.org/10.1016/b978-0-12-455402-3.50009-7openalex-snapshot
THE PHYSIOLOGY OF VITELLOGENESIS
inferredcites →https://doi.org/10.1016/b978-1-4831-9952-8.50008-0openalex-snapshot
The Ultrastructure of the Cytoplasm of the Developing Amphibian Egg
inferredcites →https://doi.org/10.1016/s0022-5320(63)80009-xopenalex-snapshot
Ultrastructural studies on developing oocytes of the salamander Triturus viridescens
inferredcites →https://doi.org/10.1016/s0022-5320(76)80077-9openalex-snapshot
Oogenesis in Xenopus laevis (Daudin). III. Localization of negative charges on the surface of developing oocytes
inferredcites →https://doi.org/10.1016/s0040-8166(69)80037-6openalex-snapshot
A follicle cell contribution to the yolk spheres of moth oocytes
inferredcites →https://doi.org/10.1016/s0074-7696(08)60940-7openalex-snapshot
Structure and Function of Intercellular Junctions
inferredcites →https://doi.org/10.1016/s0074-7696(08)61653-8openalex-snapshot
Recent Advances in the Morphology, Histochemistry, and Biochemistry of Steroid-Synthesizing Cellular Sites in the Nonmammalian Vertebrate Ovary
inferredcites →https://doi.org/10.1021/ed049pa413openalex-snapshot
Scanning electron microscopy - Part I
inferredcites →https://doi.org/10.1083/jcb.26.1.49openalex-snapshot
PROTEIN UPTAKE IN THE OOCYTES OF THE CECROPIA MOTH
inferredcites →https://doi.org/10.1083/jcb.35.1.193openalex-snapshot
THE FORMATION OF THE PRIMARY ENVELOPE DURING OOCYTE DIFFERENTIATION IN TELEOSTS
inferredcites →https://doi.org/10.1083/jcb.39.1.1openalex-snapshot
ORGANIZATION AND ACTIVITY IN THE PRE- AND POSTOVULATORY FOLLICLE OF NECTURUS MACULOSUS
inferredcites →https://doi.org/10.1083/jcb.46.3.491openalex-snapshot
METABOLIC AND ULTRASTRUCTURAL CHANGES IN THE FROG OVARIAN FOLLICLE IN RESPONSE TO PITUITARY STIMULATION
inferredcites →https://doi.org/10.1083/jcb.50.1.201openalex-snapshot
PERMEABILITY OF THE OVARIAN FOLLICLE OF AEDES AEGYPTI MOSQUITOES
inferredcites →https://doi.org/10.1083/jcb.58.2.485openalex-snapshot
COMPLEX SURFACE INVAGINATIONS IN FROG OOCYTES
inferredcites →https://doi.org/10.1083/jcb.69.2.345openalex-snapshot
Protein incorporation by isolated amphibian oocytes. V. Specificity for vitellogenin incorporation.
inferredcites →https://doi.org/10.1093/icb/12.2.289openalex-snapshot
The Hormonal Control of the Amphibian Ovary
inferredcites →https://doi.org/10.1093/icb/14.4.1159openalex-snapshot
Amphibian Vitellogenin: Properties, Hormonal Regulation of Hepatic Synthesis and Ovarian Uptake, and Conversion to Yolk Proteins
inferredcites →https://doi.org/10.1111/j.2164-0947.1951.tb01007.xopenalex-snapshot
TECHNIQUES FOR THE PRESERVAATION OF THREE‐DIMENSIONAL STRUCTURE IN PREPARING SPECIMENS FOR THE ELECTRON MICROSCOPE*
inferredcites →https://doi.org/10.1242/jcs.s3-104.67.297openalex-snapshot
Studies on the ovarian follicle cells of Drosophila
inferredcites →https://doi.org/10.2307/1539007openalex-snapshot
THE SELECTIVE ACCUMULATION OF BLOOD PROTEINS BY THE OOCYTES OF SATURNIID MOTHS

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Mechanical Characterization of Xenopus Laevis Oocytes Using Atomic Force Microscopy
inferred← citeshttps://doi.org/10.1002/(sici)1097-010x(19960901)276:1<76::aid-jez9>3.0.co;2-2openalex-snapshot
Heterologous gap junctions between oocyte and follicle cells inBufo arenarum: Hormonal effects on their permeability and potential role in meiotic arrest
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(200002)55:2<229::aid-mrd13>3.0.co;2-6openalex-snapshot
?-spectrin has a stage-specific asymmetrical localization duringXenopus oogenesis
inferred← citeshttps://doi.org/10.1002/ar.1092290402openalex-snapshot
Localization of smooth‐muscle markers in the ovaries of some ectothermic vertebrates
inferred← citeshttps://doi.org/10.1002/jcp.1041210317openalex-snapshot
Maturation involves suppression of voltage‐gated currents in the frog oocyte
inferred← citeshttps://doi.org/10.1002/jcp.20184openalex-snapshot
Epithelium and/or theca are required for ATP‐elicited K+ current in follicle‐enclosed Xenopus oocytes
inferred← citeshttps://doi.org/10.1002/jemt.1060160302openalex-snapshot
Ultrastructural aspects of oogenesis and oocyte growth in fish and amphibians
inferred← citeshttps://doi.org/10.1002/jemt.1060160303openalex-snapshot
Transformation of the amphibian oocyte into the egg: Structural and biochemical events
inferred← citeshttps://doi.org/10.1002/jemt.1060170306openalex-snapshot
Structure and function of the extracellular matrix of anuran eggs
inferred← citeshttps://doi.org/10.1002/jez.1402040208openalex-snapshot
Oogenesis in Xenopus laevis (Daudin) VI. The route of injected tracer transport in the follicle and developing oocyte,
inferred← citeshttps://doi.org/10.1002/jez.1402300114openalex-snapshot
Intercellular junctions between the follicle cells and oocytes of Xenopus laevis
inferred← citeshttps://doi.org/10.1002/jez.1402310210openalex-snapshot
Electrophysiology of in vitro insulin‐ and progesterone‐induced reinitiation of oocyte meiosis in Rana pipiens
inferred← citeshttps://doi.org/10.1002/jmor.1051940310openalex-snapshot
Development of an avascular region (the stigma) in ovarian follicles of lizards (Anolis)
inferred← citeshttps://doi.org/10.1002/jmor.1051990306openalex-snapshot
Sex differentiation and early gonadal development in Bombina orientalis (anura: Discoglossidae)
inferred← citeshttps://doi.org/10.1002/jmor.1052090305openalex-snapshot
Ovary of the seahorse, Hippocampus erectus
inferred← citeshttps://doi.org/10.1002/mrd.1080390208openalex-snapshot
Formation of the vitelline envelope precedes the active uptake of vitellogenin during oocyte development in the rainbow trout,Oncorhynchus mykiss
inferred← citeshttps://doi.org/10.1002/mrd.1080420103openalex-snapshot
Molecular cloning, tissue distribution, and hormonal control in the ovary of Cx41 mRNA, a novel Xenopus connexin gene transcript
inferred← citeshttps://doi.org/10.1002/mrd.1120010307openalex-snapshot
Development of a culture medium for growing xenopus laevis oocytes
inferred← citeshttps://doi.org/10.1002/mrd.1120110209openalex-snapshot
Ovulation in the animal kingdom: A review with an emphasis on the role of contractile processes
inferred← citeshttps://doi.org/10.1006/dbio.2000.0120openalex-snapshot
Comparative Aspects of Animal Oogenesis
inferred← citeshttps://doi.org/10.1007/978-1-4613-1869-9_7openalex-snapshot
Endocrine Control of Oocyte Maturation
inferred← citeshttps://doi.org/10.1007/978-1-4613-1869-9_8openalex-snapshot
Ovulation: Insights About the Mechanisms Based on a Comparative Approach
inferred← citeshttps://doi.org/10.1007/978-1-4615-6814-8_3openalex-snapshot
Vitellogenesis and Oocyte Growth in Nonmammalian Vertebrates
inferred← citeshttps://doi.org/10.1007/978-1-4615-6814-8_5openalex-snapshot
Egg Envelopes in Vertebrates
inferred← citeshttps://doi.org/10.1007/978-1-4684-0682-5_3openalex-snapshot
Development of the Mature Egg Organization in Amphibians, Fish, and Starfish During the Concluding Stages of Oogenesis, in the Period of Maturation
inferred← citeshttps://doi.org/10.1007/978-1-4899-1775-1_6openalex-snapshot
ION Channels and Membrane Receptors in Follicle-Enclosed Xenopus Oocytes
inferred← citeshttps://doi.org/10.1007/978-1-59745-000-3_2openalex-snapshot
The Physiology of the Xenopus laevis Ovary
inferred← citeshttps://doi.org/10.1007/bf00210113openalex-snapshot
Microfilaments interacting with heavy meromyosin and deoxyribonuclease I in cells of the ovarian follicle of a lizard
inferred← citeshttps://doi.org/10.1007/bf00312049openalex-snapshot
Ultrastructure of developing ovarian follicles and ovulation in the lizard Anolis carolinensis (Reptilia)
inferred← citeshttps://doi.org/10.1007/bf00315955openalex-snapshot
The avian ovary is an open organ
inferred← citeshttps://doi.org/10.1007/bf00365833openalex-snapshot
Die Zona pellucida des S�ugetiereies
inferred← citeshttps://doi.org/10.1007/bf00384725openalex-snapshot
Smooth muscle cells in the walls of ovarian follicles in the Japanese quail
inferred← citeshttps://doi.org/10.1007/bf00581822openalex-snapshot
Expression of Ba currents in Xenopus oocyte injected with pregnant rat myometrium mRNA
inferred← citeshttps://doi.org/10.1007/bf00582635openalex-snapshot
Patch clamp measurements onXenopus laevis oocytes: currents through endogenous channels and implanted acetylcholine receptor and sodium channels
inferred← citeshttps://doi.org/10.1007/bf01868451openalex-snapshot
Use ofXenopus oocytes for the functional expression of plasma membrane proteins
inferred← citeshttps://doi.org/10.1007/bf01871240openalex-snapshot
Progesterone-induced down-regulation of an electrogenic Na+, K+-ATPase during the first meiotic division in amphibian oocytes
inferred← citeshttps://doi.org/10.1007/s00441-007-0523-2openalex-snapshot
Stages in follicle cell/oocyte interface during vitellogenesis in caecilians Ichthyophis tricolor and Gegeneophis ramaswamii: a transmission electron-microscopic study
inferred← citeshttps://doi.org/10.1016/0006-8993(94)91472-9openalex-snapshot
Potassium currents in epilepsy: effects of the epileptogenic agent pentylenetetrazol on a cloned potassium channel
inferred← citeshttps://doi.org/10.1016/0012-1606(81)90267-0openalex-snapshot
pH changes associated with meiotic maturation in oocytes of Xenopus laevis
inferred← citeshttps://doi.org/10.1016/0012-1606(81)90417-6openalex-snapshot
Electrical membrane properties of the Xenopus laevis oocyte during progesterone-induced meiotic maturation
inferred← citeshttps://doi.org/10.1016/0012-1606(83)90302-0openalex-snapshot
Developmental change of a depolarization-induced sodium permeability in the oocyte of Xenopus laevis
inferred← citeshttps://doi.org/10.1016/0012-1606(85)90343-4openalex-snapshot
Gonadotropins and the timing of progesterone-induced meiotic maturation of Xenopus laevis oocytes
inferred← citeshttps://doi.org/10.1016/0012-1606(90)90264-jopenalex-snapshot
Talin and vinculin in the oocytes, eggs, and early embryos of Xenopus laevis: A developmentally regulated change in distribution
inferred← citeshttps://doi.org/10.1016/0012-1606(91)90122-jopenalex-snapshot
A possible exchange in the follicle cells of Xenopus oocyte
inferred← citeshttps://doi.org/10.1016/0016-6480(80)90165-3openalex-snapshot
Oogenesis in Fundulus heteroclitus II. The transition from vitellogenesis into maturation
inferred← citeshttps://doi.org/10.1016/0016-6480(84)90038-8openalex-snapshot
Spontaneous, rhythmic contractions of the ovarian follicular wall of a lizard (Anolis carolinensis)
inferred← citeshttps://doi.org/10.1016/0092-8674(79)90260-5openalex-snapshot
Export of proteins from oocytes of Xenopus laevis
inferred← citeshttps://doi.org/10.1016/0092-8674(82)90329-4openalex-snapshot
Biosynthesis of the major zona pellucida glycoprotein secreted by oocytes during mammalian oogenesis
inferred← citeshttps://doi.org/10.1016/0165-0270(91)90090-mopenalex-snapshot
Recording of voltage and Ca2+-dependent currents in Xenopus oocytes using an intracellular perfusion method
inferred← citeshttps://doi.org/10.1016/0165-0270(95)00094-1openalex-snapshot
Improvement and testing of a concentration-clamp system for oocytes of Xenopus laevis
inferred← citeshttps://doi.org/10.1016/0166-2236(88)90102-6openalex-snapshot
The use of Xenopus oocytes to probe synaptic communication
inferred← citeshttps://doi.org/10.1016/0167-4889(82)90112-4openalex-snapshot
Specific binding of progesterone to the cell surface and its role in the meiotic divisions in Rana oocytes
inferred← citeshttps://doi.org/10.1016/0169-328x(86)90026-4openalex-snapshot
Involvement of a GTP-binding protein in mediation of serotonin and acetylcholine responses in Xenopus oocytes injected with rat brain messenger RNA
inferred← citeshttps://doi.org/10.1016/0304-3940(91)90927-lopenalex-snapshot
Interaction of Mg2+ and phencyclidine in use-dependent block of NMDA channels
inferred← citeshttps://doi.org/10.1016/0304-4157(88)90024-xopenalex-snapshot
Amino acid transport in developing animal oocytes and early conceptuses
inferred← citeshttps://doi.org/10.1016/0925-4773(93)90100-copenalex-snapshot
Maturation induced internalization of β1-integrin by Xenopus oocytes and formation of the maternal integrin pool
inferred← citeshttps://doi.org/10.1016/b978-0-12-185287-0.50020-xopenalex-snapshot
Methods for Expression of Excitability Proteins in Xenopus Oocytes
inferred← citeshttps://doi.org/10.1016/b978-0-12-377450-7.50024-1openalex-snapshot
Xenopus Oocyte as Model System to Study Receptor Coupling to Phospholipase C
inferred← citeshttps://doi.org/10.1016/b978-0-12-394815-1.00011-2openalex-snapshot
Comparative Aspects of Vertebrate Reproduction
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2024.10.011openalex-snapshot
Luteinizing hormone-induced changes in the structure of mammalian preovulatory follicles
inferred← citeshttps://doi.org/10.1016/j.autneu.2014.05.004openalex-snapshot
Innervation of amphibian reproductive system. Histological and ultrastructural studies
inferred← citeshttps://doi.org/10.1016/j.bbrc.2004.09.162openalex-snapshot
A technical consideration concerning the removal of oocyte vitelline membranes for patch clamp recording
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.104950openalex-snapshot
Follicular cells protect Xenopus oocyte from abnormal maturation via integrin signaling downregulation and O-GlcNAcylation control
inferred← citeshttps://doi.org/10.1016/j.jmbbm.2024.106648openalex-snapshot
Mechanical characterization of Xenopus laevis oocytes using atomic force microscopy
inferred← citeshttps://doi.org/10.1016/j.mce.2012.05.019openalex-snapshot
Naturally occurring steroids in Xenopus oocyte during meiotic maturation. Unexpected presence and role of steroid sulfates
inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.09.002openalex-snapshot
Gaps and barriers: Gap junctions as a channel of communication between the soma and the germline
inferred← citeshttps://doi.org/10.1016/j.ymeth.2010.01.015openalex-snapshot
Oocytes as an experimental system to analyze the ultrastructure of endogenous and ectopically expressed nuclear envelope components by field-emission scanning electron microscopy
inferred← citeshttps://doi.org/10.1016/s0005-2736(00)00148-6openalex-snapshot
Xenopus oocytes as an expression system for plant transporters
inferred← citeshttps://doi.org/10.1016/s0014-4835(05)80129-0openalex-snapshot
Ion, water and neutral solute transport in Xenopus oocytes expressing frog lens MIP
inferred← citeshttps://doi.org/10.1016/s0022-3565(24)37520-2openalex-snapshot
Antagonism of an Adenosine/ATP Receptor in Follicular Xenopus Oocytes
inferred← citeshttps://doi.org/10.1016/s0070-2153(08)60580-3openalex-snapshot
Chapter 4 The Fate of Genes, Messengers, and Proteins Introduced into Xenopus Oocytes
inferred← citeshttps://doi.org/10.1016/s0300-9629(96)00483-5openalex-snapshot
Measurement of elastic properties of Xenopus oocytes
inferred← citeshttps://doi.org/10.1016/s0925-4773(97)00048-8openalex-snapshot
A paired oocyte adhesion assay reveals the homophilic binding properties of the Xenopus maternal cadherins, XBU- and EP-cadherin
inferred← citeshttps://doi.org/10.1016/s1095-6433(98)00018-xopenalex-snapshot
Leucine transport in Xenopus laevis oocytes: Functional and morphological analysis of different defolliculation procedures
inferred← citeshttps://doi.org/10.1017/s0967199407004297openalex-snapshot
Ultrastructural changes in the follicular epithelium ofCeratophrys cranwelliprevitellogenic oocytes
inferred← citeshttps://doi.org/10.1017/s0967199407004327openalex-snapshot
Assembly of ovarian follicles in the caeciliansIchthyophis tricolorandGegeneophis ramaswamii:light and transmission electron microscopic study
inferred← citeshttps://doi.org/10.1023/a:1023352530873openalex-snapshot
Effects of Cycloheximide, Aminoglutethimide, Cytochalasin B, and Colchicine on Ovulation and the Ultrastructure of the Ovarian Follicle Wall in the Stellate Sturgeon Acipenser stellatus Pall
inferred← citeshttps://doi.org/10.1042/bj2680141openalex-snapshot
Metabolism of the biologically active inositol phosphates Ins(1,4,5)P3 and Ins(1,3,4,5)P4 by ovarian follicles of Xenopus laevis
inferred← citeshttps://doi.org/10.1046/j.1440-169x.1997.00009.xopenalex-snapshot
The developing Xenopus oocyte specifies the type of gonadotropin‐stimulated steroidogenesis performed by its associated follicle cells
inferred← citeshttps://doi.org/10.1073/pnas.75.11.5534openalex-snapshot
Long-term growth and differentiation of Xenopus oocytes in a defined medium.
inferred← citeshttps://doi.org/10.1073/pnas.78.5.3078openalex-snapshot
Full-grown oocytes from Xenopus laevis resume growth when placed in culture
inferred← citeshttps://doi.org/10.1073/pnas.84.12.4135openalex-snapshot
Hormonal activation of ionic currents in follicle-enclosed Xenopus oocytes.
inferred← citeshttps://doi.org/10.1073/pnas.87.4.1521openalex-snapshot
A serum factor that activates the phosphatidylinositol phosphate signaling system in Xenopus oocytes.
inferred← citeshttps://doi.org/10.1080/11250008409439457openalex-snapshot
A comparative analysis of the evolution of the egg envelopes and the origin of the yolk
inferred← citeshttps://doi.org/10.1080/12265071.2001.9647581openalex-snapshot
Ultrastructure of the follicular oocyte surface inRana dybowskii
inferred← citeshttps://doi.org/10.1083/jcb.90.2.362openalex-snapshot
Microfilament-mediated surface change in starfish oocytes in response to 1-methyladenine: implications for identifying the pathway and receptor sites for maturation-inducing hormones.
inferred← citeshttps://doi.org/10.1095/biolreprod18.5.762openalex-snapshot
Stimulation of Vitellogenin Uptake in Stage IV Xenopus Oocytes by Treatment with Chorionic Gonadotropin in vitro
inferred← citeshttps://doi.org/10.1095/biolreprod22.4.897openalex-snapshot
Structural Aspects of Ovulation in the Lamprey, Petromyzon marinus1
inferred← citeshttps://doi.org/10.1095/biolreprod61.3.692openalex-snapshot
Cadherin-Catenin Complexes During Zebrafish Oogenesis: Heterotypic Junctions Between Oocytes and Follicle Cells1
inferred← citeshttps://doi.org/10.1098/rspb.1987.0057openalex-snapshot
Membrane currents elicited by porcine vasoactive intestinal peptide (VIP) in follicle-enclosed Xenopus oocytes
inferred← citeshttps://doi.org/10.1098/rspb.1991.0044openalex-snapshot
Angiotensin II receptors in Xenopus oocytes
inferred← citeshttps://doi.org/10.1111/ahe.12569openalex-snapshot
Microvascular anatomy of ovary and oviduct in the adult African Clawed Toad (Xenopus laevis DAUDIN, 1802)–Histomorphology and scanning electron microscopy of vascular corrosion casts
inferred← citeshttps://doi.org/10.1111/j.1432-0436.1992.tb00695.xopenalex-snapshot
Identification of plakoglobin in oocytes and early embryos of Xenopus laevis: maternal expression of a gene encoding a junctional plaque protein
inferred← citeshttps://doi.org/10.1111/j.1432-1033.1980.tb06097.xopenalex-snapshot
The Xenopus Oocyte as a Surrogate Secretory System The Specificity of Protein Export
inferred← citeshttps://doi.org/10.1111/j.1432-1033.1983.tb07182.xopenalex-snapshot
The Fate of Xenopus and Locust Vitellogenins Made in Xenopus Oocytes
inferred← citeshttps://doi.org/10.1111/j.1432-1033.1983.tb07717.xopenalex-snapshot
Signal sequences, secondary modification and the turnover of miscompartmentalized secretory proteins in Xenopus oocytes
inferred← citeshttps://doi.org/10.1111/j.1440-169x.1983.00011.xopenalex-snapshot
Increased Potassium Conductance in Rana Follicles after Stimulation by Pituitary Extract
inferred← citeshttps://doi.org/10.1111/j.1440-169x.1986.00007.xopenalex-snapshot
Ultrastructure of Follicular Epithelia in the Ovary of Lepidochitona cinerea (L.) (Mollusca: Polyplacophora)
inferred← citeshttps://doi.org/10.1111/j.1440-169x.1987.00113.xopenalex-snapshot
The Differentiation of the Zona Pellucida (Vitelline Envelope) in the Lizard Tarentola mauritanica
inferred← citeshttps://doi.org/10.1111/j.1440-169x.1989.00085.xopenalex-snapshot
The Synthesis and Localization of Envelope Glycoproteins in Oocytes of Xenopus laevis using Immunocytochemical Methods
inferred← citeshttps://doi.org/10.1111/j.1440-169x.1992.00517.xopenalex-snapshot
In Vivo Study of Vitellogenin‐Gold Transport in the Ovarian Follicle and Oocyte of Xenopus laevis
inferred← citeshttps://doi.org/10.1111/j.1460-9568.1997.tb01636.xopenalex-snapshot
Follicular Tissues Reduce Drug Effects on Ion Channels in Oocytes of Xenopus laevis
inferred← citeshttps://doi.org/10.1113/jphysiol.1984.sp015310openalex-snapshot
Xenopus oocyte resting potential, muscarinic responses and the role of calcium and guanosine 3',5'‐cyclic monophosphate.
inferred← citeshttps://doi.org/10.1113/jphysiol.1984.sp015464openalex-snapshot
Induction and disappearance of excitability in the oocyte of Xenopus laevis: a voltage‐clamp study.
inferred← citeshttps://doi.org/10.1113/jphysiol.1985.sp015799openalex-snapshot
Role of calcium mobilization in mediation of acetylcholine‐evoked chloride currents in Xenopus laevis oocytes.
inferred← citeshttps://doi.org/10.1113/jphysiol.1987.sp016523openalex-snapshot
Properties of single sodium channels translated by Xenopus oocytes after injection with messenger ribonucleic acid.
inferred← citeshttps://doi.org/10.1113/jphysiol.1989.sp017718openalex-snapshot
Latencies of membrane currents evoked in Xenopus oocytes by receptor activation, inositol trisphosphate and calcium.
inferred← citeshttps://doi.org/10.1113/jphysiol.1989.sp017780openalex-snapshot
Effects of defolliculation on membrane current responses of Xenopus oocytes.
inferred← citeshttps://doi.org/10.1113/jphysiol.1989.sp017796openalex-snapshot
Membrane currents elicited by divalent cations in Xenopus oocytes.
inferred← citeshttps://doi.org/10.1126/science.569364openalex-snapshot
Oocyte-Follicle Cell Gap Junctions in Xenopus laevis and the Effects of Gonadotropin on Their Permeability
inferred← citeshttps://doi.org/10.1134/s1022795407100055openalex-snapshot
Basic aspects of ovarian development in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1134/s1062360413040024openalex-snapshot
Follicular cells of the amphibian ovary: Origin, structure, and functions
inferred← citeshttps://doi.org/10.1152/ajpcell.1990.259.5.c792openalex-snapshot
Xenopus oocyte K+ current. III. Phorbol esters and pH regulate current at gap junctions
inferred← citeshttps://doi.org/10.1152/ajpcell.1991.260.3.c652openalex-snapshot
Direct measurement of intracellular pressure
inferred← citeshttps://doi.org/10.1152/ajpcell.1994.266.6.c1586openalex-snapshot
Radiotracer studies of cystic fibrosis transmembrane conductance regulator expressed in Xenopus oocytes
inferred← citeshttps://doi.org/10.1186/s40851-023-00201-0openalex-snapshot
A review of the reproductive system in anuran amphibians
inferred← citeshttps://doi.org/10.1242/dev.114.2.533openalex-snapshot
U-cadherin in Xenopus oogenesis and oocyte maturation
inferred← citeshttps://doi.org/10.1242/dev.61.1.367openalex-snapshot
The secretion of proteinsin vitrofromXenopusoocytes and their accessory cells: a biochemical and morphological study
inferred← citeshttps://doi.org/10.1242/dev.83.1.169openalex-snapshot
Oocytes and early embryos of Xenopus laevis contain intermediate filaments which react with anti-mammalian vimentin antibodies
inferred← citeshttps://doi.org/10.1242/jcs.188367openalex-snapshot
The Ca2+-activated Cl− channel Ano1 controls microvilli length and membrane surface area in the oocyte
inferred← citeshttps://doi.org/10.1371/journal.pone.0039238openalex-snapshot
An Integrated Field-Effect Microdevice for Monitoring Membrane Transport in Xenopus laevis Oocytes via Lateral Proton Diffusion
inferred← citeshttps://doi.org/10.2108/zs170210openalex-snapshot
All Oocytes Attach to the Dorsal Ovarian Epithelium in the Ovary of Medaka, Oryzias latipes
inferred← citeshttps://doi.org/10.26807/remcb.v33i1-2.220openalex-snapshot
Crecimiento de oocitos biderianos en machos adultos de Rhinella marina (Linnaeus, 1758) mediante el uso de hormonas y disruptores endócrinos
inferred← citeshttps://doi.org/10.3109/10409238709086960openalex-snapshot
The Use ofXenopusOocytes for the Study of Ion Channel
inferred← citeshttps://doi.org/10.3389/fcell.2024.1365705openalex-snapshot
A maternal dorsoventral prepattern revealed by an asymmetric distribution of ventralizing molecules before fertilization in Xenopus laevis
inferred← citeshttps://doi.org/10.3791/55034openalex-snapshot
Xenopus Oocytes: Optimized Methods for Microinjection, Removal of Follicular Cell Layers, and Fast Solution Changes in Electrophysiological Experiments
inferred← citeshttps://doi.org/10.4322/jms.074214openalex-snapshot
Morphological characterization of the gonads of bullfrog tadpoles (Lithobates catesbeianus)
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