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Expression and Localization of Myosin VI in Developing Mouse Spermatids
Histochem Cell Biol DOI 10.1007/s00418-017-1579-z ORIGINAL PAPER Expression and localization of myosin VI in developing mouse spermatids Przemysław Zakrzewski1 · Robert Lenartowski2 · Maria Jolanta Re˛dowicz3 · Kathryn G. Miller4 · Marta Lenartowska1 Accepted: 4 May 2017 © The Author(s) 2017. This article is an open access publication Abstract Myosin VI (MVI) is a versatile actin-based and Sertoli cell actin hoops. Since this is the frst report of motor protein that has been implicated in a variety of dif- MVI expression and localization during mouse spermio- ferent cellular processes, including endo- and exocytic genesis and MVI partners in developing sperm have not yet vesicle traffcking, Golgi morphology, and actin structure been identifed, we discuss some probable roles for MVI stabilization. A role for MVI in crucial actin-based pro- in this process. During early stages, MVI is hypothesized cesses involved in sperm maturation was demonstrated in to play a role in Golgi morphology and function as well Drosophila. Because of the prominence and importance of as in actin dynamics regulation important for attachment actin structures in mammalian spermiogenesis, we inves- of developing acrosome to the nuclear envelope. Next, tigated whether MVI was associated with actin-mediated the protein might also play anchoring roles to help gener- maturation events in mammals. Both immunofuorescence ate forces needed for spermatid head elongation. Moreo- and ultrastructural analyses using immunogold labeling ver, association of MVI with actin that accumulates in showed that MVI was strongly linked with key structures the Sertoli cell ectoplasmic specialization and other actin involved in sperm development and maturation. -
Te2, Part Iii
TERMINOLOGIA EMBRYOLOGICA Second Edition International Embryological Terminology FIPAT The Federative International Programme for Anatomical Terminology A programme of the International Federation of Associations of Anatomists (IFAA) TE2, PART III Contents Caput V: Organogenesis Chapter 5: Organogenesis (continued) Systema respiratorium Respiratory system Systema urinarium Urinary system Systemata genitalia Genital systems Coeloma Coelom Glandulae endocrinae Endocrine glands Systema cardiovasculare Cardiovascular system Systema lymphoideum Lymphoid system Bibliographic Reference Citation: FIPAT. Terminologia Embryologica. 2nd ed. FIPAT.library.dal.ca. Federative International Programme for Anatomical Terminology, February 2017 Published pending approval by the General Assembly at the next Congress of IFAA (2019) Creative Commons License: The publication of Terminologia Embryologica is under a Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0) license The individual terms in this terminology are within the public domain. Statements about terms being part of this international standard terminology should use the above bibliographic reference to cite this terminology. The unaltered PDF files of this terminology may be freely copied and distributed by users. IFAA member societies are authorized to publish translations of this terminology. Authors of other works that might be considered derivative should write to the Chair of FIPAT for permission to publish a derivative work. Caput V: ORGANOGENESIS Chapter 5: ORGANOGENESIS -
Pfeiffer Syndrome Type II Discovered Perinatally
Diagnostic and Interventional Imaging (2012) 93, 785—789 CORE Metadata, citation and similar papers at core.ac.uk Provided by Elsevier - Publisher Connector LETTER / Musculoskeletal imaging Pfeiffer syndrome type II discovered perinatally: Report of an observation and review of the literature a,∗ a a a H. Ben Hamouda , Y. Tlili , S. Ghanmi , H. Soua , b c b a S. Jerbi , M.M. Souissi , H. Hamza , M.T. Sfar a Unité de néonatologie, service de pédiatrie, CHU Tahar Sfar, 5111 Mahdia, Tunisia b Service de radiologie, CHU Tahar Sfar, 5111 Mahdia, Tunisia c Service de gynéco-obstétrique, CHU Tahar Sfar, 5111 Mahdia, Tunisia Pfeiffer syndrome, described for the first time by Pfeiffer in 1964, is a rare hereditary KEYWORDS condition combining osteochondrodysplasia with craniosynostosis [1]. This syndrome is Pfeiffer syndrome; also called acrocephalosyndactyly type 5, which is divided into three sub-types. Type I Cloverleaf skull; is the classic Pfeiffer syndrome, with autosomal dominant transmission, often associated Craniosynostosis; with normal intelligence. Types II and III occur as sporadic cases in individuals who have Syndactyly; craniosynostosis with broad thumbs, broad big toes, ankylosis of the elbows and visceral Prenatal diagnosis abnormalities [2]. We report a case of Pfeiffer syndrome type II, discovered perinatally, which is distinguished from type III by the skull appearing like a cloverleaf, and we shall discuss the clinical, radiological and evolutive features and the advantage of prenatal diagnosis of this syndrome with a review of the literature. Observation The case involved a male premature baby born at 36 weeks of amenorrhoea with multiple deformities at birth. The parents were not blood-related and in good health who had two other boys and a girl with normal morphology. -
EQUINE CONCEPTUS DEVELOPMENT – a MINI REVIEW Maria Gaivão 1, Tom Stout
Gaivão & Stout Equine conceptus development – a mini review EQUINE CONCEPTUS DEVELOPMENT – A MINI REVIEW DESENVOLVIMENTO DO CONCEPTO DE EQUINO – MINI REVISÃO Maria Gaivão 1, Tom Stout 2 1 - CICV – Faculdade de Medicina Veterinária; ULHT – Universidade Lusófona de Humanidades e Tecnologias; [email protected] 2 - Utrecht University, Department of Equine Sciences, Section of Reproduction, The Netherlands. Abstract: Many aspects of early embryonic development in the horse are unusual or unique; this is of scientific interest and, in some cases, considerable practical significance. During early development the number of different cell types increases rapidly and the organization of these increasingly differentiated cells becomes increasingly intricate as a result of various inter-related processes that occur step-wise or simultaneously in different parts of the conceptus (i.e., the embryo proper and its associated membranes and fluid). Equine conceptus development is of practical interest for many reasons. Most significantly, following a high rate of successful fertilization (71-96%) (Ball, 1988), as many as 30-40% of developing embryos fail to survive beyond the first two weeks of gestation (Ball, 1988), the time at which gastrulation begins. Indeed, despite considerable progress in the development of treatments for common causes of sub-fertility and of assisted reproductive techniques to enhance reproductive efficiency, the need to monitor and rebreed mares that lose a pregnancy or the failure to produce a foal, remain sources of considerable economic loss to the equine breeding industry. Of course, the potential causes of early embryonic death are numerous and varied (e.g. persistent mating induced endometritis, endometrial gland insufficiency, cervical incompetence, corpus luteum (CL) failure, chromosomal, genetic and other unknown factors (LeBlanc, 2004). -
2020 WSES Guidelines for the Detection and Management of Bile
Edinburgh Research Explorer 2020 WSES guidelines for the detection and management of bile duct injury during cholecystectomy Citation for published version: De’angelis, N, Catena, F, Memeo, R, Coccolini, F, Martínez-pérez, A, Romeo, OM, De Simone, B, Di Saverio, S, Brustia, R, Rhaiem, R, Piardi, T, Conticchio, M, Marchegiani, F, Beghdadi, N, Abu-zidan, FM, Alikhanov, R, Allard, M, Allievi, N, Amaddeo, G, Ansaloni, L, Andersson, R, Andolfi, E, Azfar, M, Bala, M, Benkabbou, A, Ben-ishay, O, Bianchi, G, Biffl, WL, Brunetti, F, Carra, MC, Casanova, D, Celentano, V, Ceresoli, M, Chiara, O, Cimbanassi, S, Bini, R, Coimbra, R, Luigi De’angelis, G, Decembrino, F, De Palma, A, De Reuver, PR, Domingo, C, Cotsoglou, C, Ferrero, A, Fraga, GP, Gaiani, F, Gheza, F, Gurrado, A, Harrison, E, Henriquez, A, Hofmeyr, S, Iadarola, R, Kashuk, JL, Kianmanesh, R, Kirkpatrick, AW, Kluger, Y, Landi, F, Langella, S, Lapointe, R, Le Roy, B, Luciani, A, Machado, F, Maggi, U, Maier, RV, Mefire, AC, Hiramatsu, K, Ordoñez, C, Patrizi, F, Planells, M, Peitzman, AB, Pekolj, J, Perdigao, F, Pereira, BM, Pessaux, P, Pisano, M, Puyana, JC, Rizoli, S, Portigliotti, L, Romito, R, Sakakushev, B, Sanei, B, Scatton, O, Serradilla-martin, M, Schneck, A, Sissoko, ML, Sobhani, I, Ten Broek, RP, Testini, M, Valinas, R, Veloudis, G, Vitali, GC, Weber, D, Zorcolo, L, Giuliante, F, Gavriilidis, P, Fuks, D & Sommacale, D 2021, '2020 WSES guidelines for the detection and management of bile duct injury during cholecystectomy', World Journal of Emergency Surgery, vol. 16, no. 1, 30. https://doi.org/10.1186/s13017-021-00369-w -
Vocabulario De Morfoloxía, Anatomía E Citoloxía Veterinaria
Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) Servizo de Normalización Lingüística Universidade de Santiago de Compostela COLECCIÓN VOCABULARIOS TEMÁTICOS N.º 4 SERVIZO DE NORMALIZACIÓN LINGÜÍSTICA Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) 2008 UNIVERSIDADE DE SANTIAGO DE COMPOSTELA VOCABULARIO de morfoloxía, anatomía e citoloxía veterinaria : (galego-español- inglés) / coordinador Xusto A. Rodríguez Río, Servizo de Normalización Lingüística ; autores Matilde Lombardero Fernández ... [et al.]. – Santiago de Compostela : Universidade de Santiago de Compostela, Servizo de Publicacións e Intercambio Científico, 2008. – 369 p. ; 21 cm. – (Vocabularios temáticos ; 4). - D.L. C 2458-2008. – ISBN 978-84-9887-018-3 1.Medicina �������������������������������������������������������������������������veterinaria-Diccionarios�������������������������������������������������. 2.Galego (Lingua)-Glosarios, vocabularios, etc. políglotas. I.Lombardero Fernández, Matilde. II.Rodríguez Rio, Xusto A. coord. III. Universidade de Santiago de Compostela. Servizo de Normalización Lingüística, coord. IV.Universidade de Santiago de Compostela. Servizo de Publicacións e Intercambio Científico, ed. V.Serie. 591.4(038)=699=60=20 Coordinador Xusto A. Rodríguez Río (Área de Terminoloxía. Servizo de Normalización Lingüística. Universidade de Santiago de Compostela) Autoras/res Matilde Lombardero Fernández (doutora en Veterinaria e profesora do Departamento de Anatomía e Produción Animal. -
Human Pluripotent Stem Cells As a Model of Trophoblast Differentiation in Both Normal Development and Disease
Human pluripotent stem cells as a model of trophoblast differentiation in both normal development and disease Mariko Horiia,b,1, Yingchun Lia,b,1, Anna K. Wakelanda,b,1, Donald P. Pizzoa, Katharine K. Nelsona,b, Karen Sabatinib,c, Louise Chang Laurentb,c, Ying Liud,e,f, and Mana M. Parasta,b,2 aDepartment of Pathology, University of California, San Diego, La Jolla, CA 92093; bSanford Consortium for Regenerative Medicine, University of California, San Diego, La Jolla, CA 92093; cDepartment of Reproductive Medicine, University of California, San Diego, La Jolla, CA 92093; dDepartment of Neurosurgery, Center for Stem Cell and Regenerative Medicine, University of Texas Health Sciences Center, Houston, TX 77030; eThe Senator Lloyd and B. A. Bentsen Center for Stroke Research, University of Texas Health Sciences Center, Houston, TX 77030; and fThe Brown Foundation Institute of Molecular Medicine for the Prevention of Human Diseases, University of Texas Health Sciences Center, Houston, TX 77030 Edited by R. Michael Roberts, University of Missouri–Columbia, Columbia, MO, and approved May 25, 2016 (received for review March 24, 2016) Trophoblast is the primary epithelial cell type in the placenta, a Elf5 (Ets domain transcription factor) and Eomes (Eomeso- transient organ required for proper fetal growth and develop- dermin), also have been shown to be required for maintenance of ment. Different trophoblast subtypes are responsible for gas/nutrient the TSC fate in the mouse (8, 9). exchange (syncytiotrophoblasts, STBs) and invasion and maternal Significantly less is known about TE specification and the TSC vascular remodeling (extravillous trophoblasts, EVTs). Studies of niche in the human embryo (10, 11). -
Download PDF File
Folia Morphol. Vol. 77, No. 2, pp. 386–392 DOI: 10.5603/FM.a2017.0080 O R I G I N A L A R T I C L E Copyright © 2018 Via Medica ISSN 0015–5659 www.fm.viamedica.pl Incidental imaging findings of congenital rib abnormalities: a case series and review of developmental concepts A.M. Aignătoaei1, C.E. Moldoveanu2, I.-D. Căruntu3, S.E. Giuşcă3, S. Partene Vicoleanu3, A.H. Nedelcu3 1Department of Pathology, “Sf. Spiridon” Clinic Hospital, 1, Independenţei Square, Iaşi, Romania 2Department of Radiology, Pneumology Clinic Hospital, 30, dr. Iosif Cihac Street, Iaşi, Romania 3Department of Morphofunctional Sciences, “Grigore T. Popa” University, 16, University Street, Iaşi, Romania [Received: 12 June 2017; Accepted: 24 July 2017] Background: Congenital rib abnormalities are found in approximately 2% of the general population. Usually, they occur in isolation and are rarely symptomatic, but they can also be associated with other malformations. Materials and methods: We reviewed imaging examinations performed over a period of 2 years (2014–2015), enabling us to identify isolated rib abnormalities in 6 adult patients. Results: The case series consisted in 3 cases with bilateral cervical ribs and 1 case each with bifid rib, costal fusion and rib pseudarthrosis. In all patients, the costal anomalies were discovered incidentally. All rib malformations were detected at thoracic radiography, except for the rib pseudarthrosis, which was identified at computed tomography (CT) scan. Differential diagnosis was made between cer- vical ribs and abnormalities of the C7 transverse process and of the first rib, while the other costal malformations were distinguished from tumoural, traumatic or inflammatory lesions of the chest wall, lung and pleura. -
Epithelium 2 : Glandular Epithelium Histology Laboratory -‐ Year 1, Fall Term Dr
Epithelium 2 : Glandular Epithelium Histology Laboratory -‐ Year 1, Fall Term Dr. Heather Yule ([email protected]) October 21, 2014 Slides for study: 75 (Salivary Gland), 355 (Pancreas Tail), 48 (Atrophic Mammary Gland), 49 (Active Mammary Gland) and 50 (Resting Mammary Gland) Electron micrographs for : study EM: Serous acinus in parotid gland EM: Mucous acinus in mixed salivary gland EM: Pancreatic acinar cell Main Objective: Understand key histological features of glandular epithelium and relate structure to function. Specific Objectives: 1. Describe key histological differences between endocrine and exocrine glands including their development. 2. Compare three modes of secretion in glands; holocrine, apocrine and merocrine. 3. Explain the functional significance of polarization of glandular epithelial cells. 4. Define the terms parenchyma, stroma, mucous acinus, serous acinus and serous a demilune and be able to them identify in glandular tissue. 5. Distinguish exocrine and endocrine pancreas. 6. Compare the histology of resting, lactating and postmenopausal mammary glands. Keywords: endocrine gland, exocrine gland, holocrine, apocrine, merocrine, polarity, parenchyma, stroma, acinus, myoepithelial cell, mucous gland, serous gland, mixed or seromucous gland, serous demilune, exocrine pancreas, endocrine pancreas (pancreatic islets), resting mammary gland, lactating mammary gland, postmenopausal mammary gland “This copy is made solely for your personal use for research, private study, education, parody, satire, criticism, or review -
Liver • Gallbladder
NORMAL BODY Microscopic Anatomy! Accessory Glands of the GI Tract,! lecture 2! ! • Liver • Gallbladder John Klingensmith [email protected] Objectives! By the end of this lecture, students will be able to: ! • trace the flow of blood and bile within the liver • describe the structure of the liver in regard to its functions • indicate the major cell types of the liver and their functions • distinguish the microanatomy of exocrine and endocrine function by the hepatocytes • explain the functional organization of the gallbladder at the cellular level (Lecture plan: overview of structure and function, then increasing resolution of microanatomy and cellular function) Liver and Gallbladder Liver October is “Liver Awareness Month” -- http://www.liverfoundation.org Liver • Encapsulated by CT sheath and mesothelium • Lobes largely composed of hepatocytes in parenchyma • Receives blood from small intestine and general circulation Major functions of the liver • Production and secretion of digestive fluids to small intestine (exocrine) • Production of plasma proteins and lipoproteins (endocrine) • Storage and control of blood glucose • Detoxification of absorbed compounds • Source of embyronic hematopoiesis The liver lobule • Functional unit of the parenchyma • Delimited by CT septa, invisible in humans (pig is shown) • Surrounds the central vein • Bordered by portal tracts Central vein, muralia and sinusoids Parenchyma: Muralia and sinusoids • Hepatocyte basolateral membrane faces sinusoidal lumen • Bile canaliculi occur between adjacent hepatocytes • Cords anastomose Vascularization of the liver • Receives veinous blood from small intestine via portal vein • Receives freshly oxygenated blood from hepatic artery • Discharges blood into vena cava via hepatic vein Blood flow in the liver lobes • flows in via the portal vein and hepatic artery • oozes through the liver lobules to central veins • flows out via the hepatic vein Portal Tract! (aka portal triad) • Portal venule • Hepatic arteriole • Bile duct • Lymph vessel • Nerves • Connective tissue Central vein! (a.k.a. -
Modeling Congenital Disease and Inborn Errors of Development in Drosophila Melanogaster Matthew J
© 2016. Published by The Company of Biologists Ltd | Disease Models & Mechanisms (2016) 9, 253-269 doi:10.1242/dmm.023564 REVIEW SUBJECT COLLECTION: TRANSLATIONAL IMPACT OF DROSOPHILA Modeling congenital disease and inborn errors of development in Drosophila melanogaster Matthew J. Moulton and Anthea Letsou* ABSTRACT particularly difficult to manage clinically {e.g. CHARGE syndrome Fly models that faithfully recapitulate various aspects of human manifesting coloboma [emboldened words and phrases are defined disease and human health-related biology are being used for in the glossary (see Box 1)], heart defects, choanal atresia, growth research into disease diagnosis and prevention. Established and retardation, genitourinary malformation and ear abnormalities new genetic strategies in Drosophila have yielded numerous (Hsu et al., 2014), and velocardiofacial or Shprinstzens syndrome substantial successes in modeling congenital disorders or inborn manifesting cardiac anomaly, velopharyngeal insufficiency, errors of human development, as well as neurodegenerative disease aberrant calcium metabolism and immune dysfunction (Chinnadurai and cancer. Moreover, although our ability to generate sequence and Goudy, 2012)}. Estimates suggest that the cause of at least 50% of datasets continues to outpace our ability to analyze these datasets, congenital abnormalities remains unknown (Lobo and Zhaurova, the development of high-throughput analysis platforms in Drosophila 2008). It is vital that we understand the etiology of congenital has provided access through the bottleneck in the identification of anomalies because this knowledge provides a foundation for improved disease gene candidates. In this Review, we describe both the diagnostics as well as the design of preventatives and therapeutics that traditional and newer methods that are facilitating the incorporation of can effectively alleviate or abolish the effects of disease. -
Ultrastrucure of Germ Cells During Spermatogenesis
Korean J. Malacol. 26(1): 33-43, 2010 Ultrastrucure of Germ Cells during Spermatogenesis and Some Characteristics of Sperm Morphology in Male Mytilus coruscus (Bivalvia: Mytilidae) on the West Coast of Korea Jin Hee Kim1, Ee-Yung Chung2, Ki-Ho Choi3, Kwan Ha Park4, and Sung-Woo Park4 1Korea Inter-University Unstitute of Ocean Science, Pukyong National University, Busan 608-737, Korea 2Korea Marine Environment & Ecosystem Institute, Dive Korea, Bucheon 420-857, Korea 3West Sea Fisheries Research Institute, National Fisheries Research and Development Institute, Incheon 400-420, Korea 4Department of Aquatic Life Medicine, Kunsan National University, Kunsan 573-701, Korea ABSTRACT The ultrastructure of germ cells during spermatogenesis and some characteristics of sperm morphology in male Mytilus coruscus, which was collected on the coastal waters of Gyeokpo in western Korea, were investigated by transmission electron microscope observations. The morphology of the spermatozoon has a primitive type and is similar to those of other bivalves in that it contains a short midpiece with five mitochondria surrounding the centrioles. The morphologies of the sperm nucleus type and the acrosome shape of this species have an oval and modified cone shape, respectively. In particular, the axial rod is observed between the nucleus and acrosome of the sperm. The spermatozoon is approximately 45-50 μm in length including a sperm nucleus (about 1.46 μm in length), an acrosome (about 3.94 μm in length) and tail flagellum (approximately 40-45 μm). The axoneme of the sperm tail flagellum consists of nine pairs of microtubules at the periphery and a pair at the center.