Academic literature on the topic 'Lamellar body'

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Lamellar body.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Lamellar body"

1

Neerhof, Mark G., James C. Dohnal, Edward R. Ashwood, In-Sik Lee, and Maurizio M. Anceschi. "LAMELLAR BODY COUNTS." Obstetrics & Gynecology 97, no. 2 (February 2001): 318–20. http://dx.doi.org/10.1097/00006250-200102000-00029.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Delivopoulos, S. G., and P. Kugrens. "Thylakoid formation from coiled lamellar bodies during carposporogenesis in Faucheocolax attenuata Setch. (Rhodophyta, Rhodymeniales)." Journal of Cell Science 75, no. 1 (April 1, 1985): 215–24. http://dx.doi.org/10.1242/jcs.75.1.215.

Full text
Abstract:
Chloroplast development during carposporogenesis in the parasitic red alga Faucheocolax attenuata Setch. was studied by electron microscopy. Proplastids are usually found in the peripheral cytoplasm of young carpospores and are characterized by the presence of portions of a peripheral thylakoid and coiled lamellar bodies that range in size up to 0.5 micron. One type of coiled lamellar body occurs in the peripheral region of the proplastid and is continuous with the peripheral thylakoid, while the other type is found in the central portion of the stroma. These coiled lamellae separate and expand, adding membranes to both thylakoid systems, thereby functioning as thylakoid-forming bodies. As each coiled lamella unravels, it forms an undulated double-membraned structure having the same width as a thylakoid. After substantial expansion, the developing thylakoids begin to straighten and assume a parallel orientation to each other, thus becoming mature thylakoids. Small coiled lamellae often persist in mature carpospore chloroplasts, and are utilized in additional thylakoid formation during carpospore germination.
APA, Harvard, Vancouver, ISO, and other styles
3

LEWIS, PAMELA S., MICHELE R. LAURIA, JEFFERY DZIECZKOWSKI, GREGORY O. UTTER, and MITCHELL P. DOMBROWSKI. "Amniotic Fluid Lamellar Body Count." Obstetrics & Gynecology 93, no. 3 (March 1999): 387–91. http://dx.doi.org/10.1097/00006250-199903000-00015.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Mol, Ben W. J., Anjoke Huisjes, and Arie Franx. "AMNIOTIC FLUID LAMELLAR BODY COUNT." Obstetrics & Gynecology 94, no. 3 (September 1999): 481–82. http://dx.doi.org/10.1097/00006250-199909000-00035.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Lewis, Pamela Sue. "AMNIOTIC FLUID LAMELLAR BODY COUNT." Obstetrics & Gynecology 94, no. 3 (September 1999): 482. http://dx.doi.org/10.1097/00006250-199909000-00036.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Schaller-Bals, S., S. R. Bates, K. Notarfrancesco, J. Q. Tao, A. B. Fisher, and H. Shuman. "Surface-expressed lamellar body membrane is recycled to lamellar bodies." American Journal of Physiology-Lung Cellular and Molecular Physiology 279, no. 4 (October 1, 2000): L631—L640. http://dx.doi.org/10.1152/ajplung.2000.279.4.l631.

Full text
Abstract:
Monoclonal antibody (MAb) 3C9, an antibody generated to the lamellar body of rat lung type II pneumocytes, specifically labels the luminal face of the lamellar body membrane. To follow the retrieval of lamellar body membrane from the cell surface in these cells, MAb 3C9 was instilled into rat lungs. In vivo, it was endocytosed by type II cells but not by other lung cells. In type II cells that were isolated from rat lungs by elastase digestion and cultured on plastic for 24 h, MAb 3C9 first bound to the cell surface, then was found in endosomes, vesicular structures, and multivesicular bodies and, finally, clustered on the luminal face of lamellar body membranes. The amount internalized reached a plateau after 1.5 h of incubation and was stimulated with the secretagogue ATP. In double-labeling experiments, internalized MAb 3C9 did not completely colocalize with NBD-PC liposomes or the nonspecific endocytic marker TMA-DPH, suggesting that lamellar body membrane is retrieved back to existing lamellar bodies by a pathway different from that of bulk membrane and may be one pathway for surfactant endocytosis. The lamellar body membrane components are retrieved as subunits that are redistributed among the preexisting lamellar bodies in the cell.
APA, Harvard, Vancouver, ISO, and other styles
7

Neerhof, Mark, Elaine Haney, James Dohnal, and Nicholas Hobart. "Maturity cutoffs for lamellar body counts." American Journal of Obstetrics and Gynecology 191, no. 6 (December 2004): S83. http://dx.doi.org/10.1016/j.ajog.2004.10.177.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Colvard, MD, SH Ashrafi, OK Alonge, and GA Cordell. "Smokeless tobacco-induced lamellar body abnormalities." Oral Diseases 12, no. 3 (May 2006): 343–48. http://dx.doi.org/10.1111/j.1601-0825.2005.01211.x.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Bates, Sandra R., Jian-Qin Tao, Susanne Schaller, Aron B. Fisher, and Henry Shuman. "Lamellar body membrane turnover is stimulated by secretagogues." American Journal of Physiology-Lung Cellular and Molecular Physiology 278, no. 3 (March 1, 2000): L443—L452. http://dx.doi.org/10.1152/ajplung.2000.278.3.l443.

Full text
Abstract:
Lamellar bodies are specialized cellular organelles used for storage of surfactant by alveolar type II cells of the lung. We utilized monoclonal antibody (MAb) 3C9, which recognizes an integral lamellar body-limiting membrane protein of 180 kDa, to follow lamellar body trafficking. 125I-labeled MAb 3C9 bound to the surface of type II cells and was internalized by the cells in a time- and concentration-dependent manner that was inhibitable by excess unlabeled antibody. The internalized antibody remained undegraded over a 4-h time period. The L2 rat lung cell line that does not have lamellar bodies did not bind iodinated 3C9. Exposure of type II cells to the secretagogues ATP, phorbol 12-myristate 13-acetate, and cAMP resulted in a 1.5- to 2-fold enhancement of binding and uptake of MAb 3C9. Calphostin C inhibited phorbol 12-myristate 13-acetate-stimulated phospholipid secretion and also reduced binding and uptake of MAb 3C9 by type II cells. Treatment of type II cells with phenylarsine oxide to obstruct clathrin-mediated endocytosis had no effect on the internalization of MAb 3C9 while markedly blocking the uptake of surfactant protein A and transferrin. An actin-mediated process was important for lamellar body membrane uptake because incubation with cytochalasin D partially inhibited MAb 3C9 incorporation by type II cells. These studies are compatible with enhanced lamellar body membrane turnover associated with surfactant secretion and indicate that this process can be monitored by the trafficking of the antigen reporter MAb 3C9.
APA, Harvard, Vancouver, ISO, and other styles
10

HUGHES, GEORGE M., STEVEN F. PERRY, and JOHANNES PIIPER. "Morphometry of the Gills of the Elasmobranch Scyliorhinus Stellaris in Relation to Body Size." Journal of Experimental Biology 121, no. 1 (March 1, 1986): 27–42. http://dx.doi.org/10.1242/jeb.121.1.27.

Full text
Abstract:
In order to study the dependence of the dimensions of the respiratory apparatus on body size and to provide a morphometric basis for the analysis of branchial gas exchange function, the gills of 12 specimens of Scyliorhinus stellaris L., weighing 0.58-2.62 kg, were examined morphometrically. The average values and the local variations of the structural parameters determining diffusive gas transfer properties of the gills were determined. Particular attention was paid to corrections for shrinkage effects in surface area measurements and to corrections for the Holmes and slant effects in measurements of paraffin sections. The shape and size of secondary lamellae varied according to the sampling site on the filament, and filament length varied with its location on the gill arch. Also the water-blood distance varied, mainly because of frequent occurrence of thickenings at mid-height of the secondary lamellae. The total gill surface area increased proportionally to (body mass)0.78, mainly because of an increase in surface area of individual lamellae rather than an increase in their number. Since the thickness of the secondary lamellae varied little with body mass, the observed increase in total filament length in proportion to body mass is attributed to an increase in interlamellar distance. The water-blood distance varied little with body mass. The extent of shrinkage was found to be about 10% of filament length, but because of the compensating increase in secondary lamellar frequency this had no effect on gill area estimates, although it did affect the interlamellar dimensions. Shrinkage of individual secondary lamellae was extremely difficult to estimate, partly because of non-isometric shrinkage within the gill system. Underestimation of secondary lamellar area using paraffin sections could approach 30% mainly because of a reduction in the proportion of the pillar cell system exposed above the level of the gill filaments.
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Lamellar body"

1

Korogi, Yohei. "In Vitro Disease Modeling of Hermansky-Pudlak Syndrome Type 2 Using Human Induced Pluripotent Stem Cell-Derived Alveolar Organoids." Kyoto University, 2019. http://hdl.handle.net/2433/243303.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

渡部, 百合子, and Yuriko Watanabe. "Amniotic lamellar body count and congenital diaphragmatic hernia in humans and in a rat model." Thesis, 2014. http://hdl.handle.net/2237/20384.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Syue, Yu-Ren, and 薛喻仁. "Are Biomimetic Lipid Lamellae of Healthy and Atopic Eczema Stratum Corneum Phase Change Materials for Body Heat Conductivity and Thermal Protection?" Thesis, 2012. http://ndltd.ncl.edu.tw/handle/19163204780944457641.

Full text
Abstract:
博士
國立中央大學
化學工程與材料工程研究所
100
Skin is the outermost and the largest organ of the mammals, and stratum corneum (SC) is the outermost tissue of the skin. There is not much research in the thermal properties of the SC. We use palmitic acid, cholesterol, and ceramide type IV (mass ratio of PA/CHOL/CER4(EOH)=1/1/2) to mimic the healthy SC lipid lamellae. The molten method is used to prepare the lipid mixtures. Use low-temperature differential scanning calorimetry (LTDSC) is used to analyze the equilibrium state of the lipid mixtures. Small angle X-ray scattering (SAXS), powder X-ray diffraction (PXRD) diffraction and hot stage optical microscopy (HSOM) are employed to study the phase transformation and nanostructures of the SC lipid blends. In this study, the morphology and thermal property differences between the lipid mixtures of the healthy SC and atopic dermatitis (AD, mass ratio of PA/CHOL/CER4(EOH)=1/1/1.13) are compared. Not only the lamellar structures are 9.5 nm and 9.3 nm, respectively, but also some structures change are observed in SAXS diffraction patterns. The packing of the healthy SC and AD lipid mixtures are hexagonal and orthorhombic phases, respectively. Thermal properties such as specific heat, conductivity and heat of fusion of the health SC and AD lipid mixtures are determined by temperature-history method. Apparently, the role of SC is not for thermal regulation, because of the relatively values of specific heat (3.23±0.14 kJ kg-1K-1), heat conductivity (0.226±0.087 Wm-1K-1), and latent heat (kJ kg-1). The large area of the SC and hairless skin surface mainly are for the sense of touch. The melting point of 66oC prevents SC of early human from melting in Africa of 50oC. The specific heat of AD lipid mixtures is larger than the healthy SC lipid mixtures, and it is one of the reasons of the sensitivity and exacerbation of the AD patients in cold weather.
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Lamellar body"

1

Aharony, Amnon. "Magnetism and Superconductivity in Doped Lamellar Copper Oxide Systems." In Recent Progress in Many-Body Theories, 33–34. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3798-4_4.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Krstić, Radivoj V. "Bony Tissue. Osteons or Haversian Systems of Lamellae." In General Histology of the Mammal, 218–19. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70420-8_107.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

"The Epidermal Lamellar Body as a Multifunctional Secretory Organelle." In Skin Barrier, 281–92. CRC Press, 2005. http://dx.doi.org/10.1201/b14173-19.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Lucarelli, Mark J. "Management of Blepharoptosis." In Surgery of the Eyelid, Lacrimal System, and Orbit. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780195340211.003.0014.

Full text
Abstract:
A thorough understanding of upper eyelid anatomy is essential for the ptosis surgeon. The upper eyelid consists of skin, orbicularis, septum, tarsus, levator, Muller’s muscle, and conjunctiva. The skin and orbicularis form the anterior lamella. Conceptually, the orbicularis may be subdivided according to its topography into pretarsal, preseptal, and orbital components (over the orbital rim and extending to the frontalis muscle superiorly). The orbital septum is a fibrous lamellar structure arising from the periosteum over the superior and inferior orbital rims. In the upper eyelid, the orbital septum fuses with the levator aponeurosis approximately 2 to 5 mm above the superior tarsal border in Caucasians. In Asian patients, the septum extends further inferiorly into the eyelid. Preaponeurotic orbital fat is normally located behind the orbital septum in the preaponeurotic space. The preaponeurotic fat is an important landmark for surgeons as it lies immediately anterior to the levator aponeurosis. The tarsus of the upper eyelid is a firm, dense connective-tissue plate that provides rigidity to the eyelid. The upper tarsal plate measures approximately 10 mm vertically in the center of the eyelid. The tarsal plate is usually 1 mm thick. The levator complex originates from the periorbita of the lesser wing of the sphenoid at the annulus of Zinn. The muscular portion of the levator in adults is approximately 36 mm long, while the aponeurosis is 14 to 20 mm long. The bony attachments of the aponeurosis are via its horizontal expansions, the medial and lateral horns. The lateral horn, which is much stronger than the medial horn, passes through the lacrimal gland and divides it into the palpebral and orbital lobes. The lateral horn attaches to the periorbita of the orbital tubercle and to the lateral canthal tendon. The medial horn is a thin, delicate structure. It attaches loosely with the posterior portion of the medial canthal tendon and curves medially and posteriorly to insert at the posterior lacrimal crest and the adjacent periorbita of the medial orbital wall. Whitnall’s superior transverse ligament (Whitnall’s ligament) is a condensation of the fascial sheaths of the levator muscle located superior to the area of transition of the levator muscle to the levator aponeurosis (musculoaponeurotic junction).
APA, Harvard, Vancouver, ISO, and other styles
5

Robinson, Max, Keith Hunter, Michael Pemberton, and Philip Sloan. "Disorders of bone." In Soames' & Southam's Oral Pathology. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780199697786.003.0012.

Full text
Abstract:
Most invasive dental procedures involving removal of teeth or bone are followed by uneventful healing. However, dentists should be aware that generalized abnormalities of bone, such as osteoporosis and Paget’s dis­ease of bone, may complicate these procedures and, rarely, can lead to ongoing clinical problems. The effects of radiotherapy to the jaws and bisphosphonate treatment are well-described causes of osteonecrosis and delayed healing. Diagnosis of bone disorders often depends on integrating the results of clinical, imaging, pathological, genetic, and biochemical investigations. Although the bony skeleton is often thought of as forming just a rigid framework, it should be remembered that bone is a living, responsive tissue that plays an important role in metabolism. During development, some bones develop from a cartilaginous template and others, such as most of the craniofacial bones, form in fibrous membranes. Bone matrix is laid down by osteoblasts that are derived from the extensive meshwork of bone-lining cells that cover the bone surfaces. The bone matrix contains osteocytes that are responsive to mechanical stresses. Bone matrix is removed by osteoclasts that move over the bone sur­face, resulting in scalloped pits termed Howship’s lacunae. Bone mat­rix can be woven or lamellar in pattern. Pathologists often examine sections of bony lesions in polarized light to determine whether the pattern of the collagenous matrix is woven or lamellar, because it can be pivotal for diagnosis. It is also important for clinicians to be aware that, in order to produce a histological section of bone, the tissue must first be fixed and then demineralized to soften the matrix. When a bone biopsy is performed, the patient should be made aware that additional time will be needed to process the biopsy. Following extraction of a tooth, the socket rapidly fills with blood, which then clots. Granulation tissue, which consists of proliferating endothelial cells and fibroblasts derived from remnants of the periodontal ligament and surrounding alveolar bone, grows into the clot and organization commences. Osteoclasts begin to remodel the crestal bone and remove any small spicules of bone detached during the extraction.
APA, Harvard, Vancouver, ISO, and other styles
6

Edmonds III, Radcliffe G. "Curses for All Occasions: Malefic and Binding Magic." In Drawing Down the Moon, 53–90. Princeton University Press, 2019. http://dx.doi.org/10.23943/princeton/9780691156934.003.0003.

Full text
Abstract:
This chapter examines the place of curse tablets within the ancient Greco-Roman world. The curse tablet, the thin sheet of metal (lamella) with mysterious writings on it, appears as part of the standard equipment of the malevolent magician. One of the first types of magical evidence to be systematically collected and cataloged, the curse tablets have been the object of scholarly study for over a hundred years, and a number of recent studies have analyzed particular features of the curse tablet, elucidating the rules of the genre and illuminating the characteristic poetics of the magical curse. Indeed, more than 1,700 curse tablets from the ancient Greco-Roman world have been published, and many more remain unpublished, awaiting the analysis of scholars. These tablets of metal inscribed with malevolent wishes present a good body of evidence for scholars of ancient magic, since most of these curses seem to fall within everyone's intuitive definition of magic. They clearly intend harm to the target, they are mostly made and deposited in secret, and they use strange words to compel suprahuman powers to take concrete action against another for the personal benefit of the curser.
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Lamellar body"

1

Frick, Manfred, Pika Miklavc, Oliver Wittekindt, Thomas Haller, and Paul Dietl. "Fusion-Activated Ca2+ Entry (FACE): Vesicular Calcium Channels Regulating The Postfusion Stage Of Lamellar Body Exocytosis?" In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a5098.

Full text
APA, Harvard, Vancouver, ISO, and other styles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography