Same as incurrent. Inoperculate. Without an operculum. Intercostate. Between the ribs or ridges. Invaginate. One part bending into another, as the tentacles of some land snails. Invertible.
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The tissue layers formed from the primitive streak invaginate together into the embryo and the induced mesenchymal stem cells will ingress and form the mesoderm. Mesodermal tissue will continue to differentiate and/or migrate throughout the embryo to ultimately form most connective tissue layers of the body.
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After the nuclei are positioned in a monolayer underneath the egg membrane, the membrane begins to slowly invaginate, thus separating the nuclei into cellular compartments; during this period, the egg is called a cellular blastoderm. The pole cells – the germline anlage – are the first cells to separate fully.
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After penetration, the pathogen produces infection vesicles which invaginate the cell membrane, and drain nutrients from the plant. Later in the pathogen's life cycle when the host's infected fruit or foliar flesh dies, the pathogen switches to the saprophytic life cycle to feed off of the dead tissue.
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Similarly to the red-billed buffalo weaver, the cassowary, a ratite, exhibits a pseudo-penis in both males and females. The male's pseudo- phallus is used to "invaginate", or to push the female’s pseudo-phallus inside-out, and then ejaculates from the cloaca to ensure a successful mating.
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At about 22 days into development, the ectoderm on each side of the rhombencephalon thickens to form otic placodes. These placodes invaginate to form otic pits, and then otic vesicles. The otic vesicles then form ventral and dorsal components. The ventral component forms the saccule and the cochlear duct.
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Mycorrhizas are commonly divided into ectomycorrhizas and endomycorrhizas. The two types are differentiated by the fact that the hyphae of ectomycorrhizal fungi do not penetrate individual cells within the root, while the hyphae of endomycorrhizal fungi penetrate the cell wall and invaginate the cell membrane.Harley, J.L. and S.E. Smith 1983. Mycorrhizal symbiosis (1st ed.).
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The occlusal surface is rough and mostly flat, adapted for crushing and grinding plant material. The body is covered with cementum both above and below the gingival line, below which is a layer of enamel covering the entire length of the body. The cementum and the enamel invaginate into the thick layer of dentin.
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Anillo means ring and shows that the name anillin references the observed enrichment of anillins at the contractile ring during cytokinesis. Anillins are also enriched at other actomyosin rings, most significantly, those at the leading edge of the Drosophila embryo during cellularization. These actomyosin rings invaginate to separate all nuclei for one another in the syncytial blastoderm.
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At the 4 mm stage, the lens placode is a single monolayer of columnar cells. As development progresses, the lens placode begins to deepen and invaginate. As the placode continues to deepen, the opening to the surface ectoderm constricts and the lens cells forms a structure known as the lens vesicle. By the 10 mm stage, the lens vesicle has completely separated from the surface ectoderm.
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After the 10th division, the pole cells form at the posterior end of the embryo, segregating the germ line from the syncytium. Finally, after the 13th division, cell membranes slowly invaginate, dividing the syncytium into individual somatic cells. Once this process is completed, gastrulation starts. Nuclear division in the early Drosophila embryo happens so quickly, no proper checkpoints exist, so mistakes may be made in division of the DNA.
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Embryologically, the defect is thought to occur around day 35 of gestation, when the vesicle fails to invaginate. Dysgenesis of the vesicle later in development may result in coloboma, a separate and less severe malformation of the ocular structures. CCE is almost always unilateral, but at least 2 cases of bilateral involvement have been described. Patients may also present with skin appendages attached to the skin surrounding the eyes.
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The sparganum larvae are white, wrinkled, and ribbon-shaped. They range from a few millimeters in length to several centimeters. The anterior end can invaginate and bears suggestions of the sucking grooves that are present in the scolex of the mature worm. The absence of a scolex or protoscolex in Spirometra is a key difference in differentiating between Taenia solium and Spirometra. The worm’s body is also characterized by a stromal network of smooth muscle.
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Ear development begins in about the third week of human embryonic development. Beginning with the formation of the Otic Placodes which are an extension of the early hind brain. By the fourth week of development the otic placodes invaginate, or sink inward forming pits which close themselves off for the outer surface ectoderm and begin forming the inner ear labyrinthe on the inside. Outer ear development begins in about the fifth week of human embryonic development.
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The earliest forms of laminar organization are shown in the diploblastic and triploblastic formation of the germ layers in the embryo. In the first week of human embryogenesis two layers of cells have formed, an external epiblast layer (the primitive ectoderm), and an internal hypoblast layer (primitive endoderm). This gives the early bilaminar disc. In the third week in the stage of gastrulation epiblast cells invaginate to form endoderm, and a third layer of cells known as mesoderm.
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Normally, the insular opercula begin to develop between the 20th and the 22nd weeks of pregnancy. At weeks 14 to 16 of fetal development, the insula begins to invaginate from the surface of the immature cerebrum of the brain, until at full term, the opercula completely cover the insula., as cited in note 3 of This process is called opercularization.Cheng-Yu Chen, Robert A. Zimmerman, Scott Faro, Beth Parrish, Zhiyue Wang, Larissa T. Bilaniuk, Ting-Ywan Chou.
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In Lobelioideae, pollen is, already in the bud stage, released into the tube formed by the anthers. During flowering, it is pushed up by the elongating style and "presented" to visiting pollinators at the apex of the tube, a mechanism described as a pollen pump. The style eventually protrudes through the anther tube, and becomes receptive to pollen. In Campanuloideae, the pollen is instead packed between hairs on the style, gradually being released as the hairs invaginate.
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The Frank and Ingram procedure is a common non-operative procedure used to increase function of the vaginal via dilators. The method uses graduated dilators to progressively invaginate the mucosa to dilate the opening, increasing depth and functionality of the vaginal over time. The Ingram modification involves using a bicycle seat positioned between the legs allowing direct contact with the perineum creating pressure on the vagina. Thus, by applying pressure to the mucosa, a neovagina forms.
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RickA, expressed on the rickettsial surface, activates Arp2/3 and causes actin polymerization. The rickettsiae use the actin to propel themselves throughout the cytosol to the surface of the host cell. This causes the host cell membrane to protrude outward and invaginate the membrane of an adjacent cell. The bacteria are then taken up by the neighboring cell in a double membrane vacuole that the bacteria can subsequently lyse, enabling spread from cell to cell without exposure to the extracellular environment.
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Two vascular fringes from the lower fold invaginate the roof and form the choroid plexus. The tela choroidea of the fourth ventricle (also known as the triangular lamella) is a double layer of pia mater and ependyma, between the cerebellum and the lower part of the roof of the fourth ventricle. The two layers are continuous with each other in front, and are mostly adherent throughout. The anterior layer of the fold, contains vascular fringes which make up the choroid plexus.
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Arbuscular mycorrhizas, or AM (formerly known as vesicular-arbuscular mycorrhizas, or VAM), are mycorrhizas whose hyphae penetrate plant cells, producing structures that are either balloon-like (vesicles) or dichotomously branching invaginations (arbuscules) as a means of nutrient exchange. The fungal hyphae do not in fact penetrate the protoplast (i.e. the interior of the cell), but invaginate the cell membrane. The structure of the arbuscules greatly increases the contact surface area between the hypha and the cell cytoplasm to facilitate the transfer of nutrients between them.
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Further induction by the chordamesoderm will form a protrusion: the optic vesicle. This vesicle will be subsequently invaginated by means of further inductions from the chordamesoderm. The optic vesicle will then induce the ectoderm that thickens (lens placode) and further invaginates to a point that detaches from the ectoderm and forms a neurogenic placode by itself. The lens placode is affected by the chordamesoderm making it to invaginate and forms the optic cup composed by an inner layer of neural retina and outer layer the pigmented retina that will unite and form the optic stalk.
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Similarly, E. tribuloides also possesses a larval skeleton that arises from a special lineage of cells. In contrast, however, the number and size of its micromeres can vary (from one to three), and they do not precociously invaginate; rather, they ingress during gastrulation and bud off from the tip of the growing archenteron. Although there are numerous molecular differences between the "spicule-forming cells" of E. tribuloides and the primary mesencyhme cells of euechinoids, these two cell lineages are thought to be homologous and have been contrasted in developmental evolution research.
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J. Urol. 159: 1951, 1998 With this technique, one, two or three “vest” sutures of 10-0 suture should be placed near the opening of the epididymal tubule to allow the epididymal tubule to “invaginate” into the vas deferens, theoretically creating a connection, that, based on studies in animal models, has an improved watertight seal and possibly a higher chance for success. Once the vas- deferens-epididymis connection is completed, the covering around the testis is replaced. Vasoepididymostomy is often considered one of the most technically challenging operations in the field of urology.
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Development 2007; 134(6): 1023-1034. The primitive knot is situated at the anterior end of the primitive streak and serves as the organizer for gastrulation, determining epiblast cell fate by inducing the differentiation of migrating epiblast cells during gastrulation. During gastrulation, migrating epiblast cells undergo epithelial-mesenchymal transition in order to lose cell-cell adhesion (E-cadherin), delaminate from the epiblast layer and migrate over the dorsal surface of the epiblast then down through the primitive streak. The first wave of epiblast cells to invaginate through the primitive streak invades and displaces the hypoblast to become the embryonic endoderm.
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Coats function to deform the donor membrane to produce a vesicle, and they also function in the selection of the vesicle cargo. Coat complexes that have been well characterized so far include coat protein-I (COP-I), COP-II, and clathrin. Clathrin coats are involved in two crucial transport steps: (i) receptor-mediated and fluid-phase endocytosis from the plasma membrane to early endosome and (ii) transport from the TGN to endosomes. In endocytosis, the clathrin coat is assembled on the cytoplasmic face of the plasma membrane, forming pits that invaginate to pinch off (scission) and become free CCVs.
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Endosis involves the invasion of one cell into another, where the intruder proliferates inside the host cell until it is digested by the host or forcibly pushes its way back out. Iwasa's questions and requirements for the model forced researchers to investigate the endosis mechanism in greater detail to accurately engineer an animation of this process. While working with Tomas Kirchausen, she created an animation on clathrin-mediated endocytosis, researching how clathrin triskelions operated and assembled on the inner surface of the plasma membrane to invaginate an extracellular particle. In 2010, Iwasa organized and taught a course on visualizing molecular and cellular processes with 3D animation in Porto, Portugal.
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Once the fungus has invaded the plant, it grows into plant mesophyll cells, producing specialized hyphae known as haustoria. The haustoria penetrate cell walls but not cell membrances: plant cell membranes invaginate around the main haustorial body forming a space known as the extra-haustorial matrix. An iron and phosphorus rich neck band bridges the plant and fungal membranes in the space between the cells for water flow, known as the apoplast, thus preventing the nutrients reaching the plant's cells. The haustorium contains amino acid and hexose sugar transporters and H+-ATPases which are used for active transport of nutrients from the plant, nourishing the fungus.
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In birds, the primitive streak formation is generated by a thickening of the epiblast called the Koller's sickle The Koller's sickle is created at the posterior edge of the area pellucida while the rest of the cells of the area pellucida remain at the surface, forming the epiblast. In chicks, the mesoderm cells don't invaginate like in amphibians, but they migrate medially and caudally from both sides and create a midline thickening called primitive streak. Which grows rapidly in length as more and more presumptive mesoderm cells continue to aggregate inward. Gastrulation begins in the area pellucida next to the posterior marginal zone, as the hypoblast and primitive streak both start there.
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For example, the ectoderm will give rise to the skin epidermis and the nervous system, the mesoderm will give rise to the vascular system, muscles, bone, and connective tissues, and the endoderm will give rise to organs of the digestive system and epithelium of the digestive system and respiratory system. Many visible changes in embryonic structure happen throughout gastrulation as the cells that make up the different germ layers migrate and cause the previously round embryo to fold or invaginate into a cup-like appearance. Past gastrulation, an embryo continues to develop into a mature multicellular organism by forming structures necessary for life outside of the womb or egg. As the name suggests, organogenesis is the stage of embryonic development when organs form.
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