Bones and Bone Structure
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ICRS Heritage Summit 1
ICRS Heritage Summit 1 20th Anniversary www.cartilage.org of the ICRS ICRS Heritage Summit June 29 – July 01, 2017 Gothia Towers, Gothenburg, Sweden Final Programme & Abstract Book #ICRSSUMMIT www.cartilage.org Picture Copyright: Zürich Tourismus 2 The one-step procedure for the treatment of chondral and osteochondral lesions Aesculap Biologics Facing a New Frontier in Cartilage Repair Visit Anika at Booth #16 Easy and fast to be applied via arthroscopy. Fixation is not required in most cases. The only entirely hyaluronic acid-based scaffold supporting hyaline-like cartilage regeneration Biologic approaches to tissue repair and regeneration represent the future in healthcare worldwide. Available Sizes Aesculap Biologics is leading the way. 2x2 cm Learn more at www.aesculapbiologics.com 5x5 cm NEW SIZE Aesculap Biologics, LLC | 866-229-3002 | www.aesculapusa.com Aesculap Biologics, LLC - a B. Braun company Website: http://hyalofast.anikatherapeutics.com E-mail: [email protected] Telephone: +39 (0)49 295 8324 ICRS Heritage Summit 3 The one-step procedure for the treatment of chondral and osteochondral lesions Visit Anika at Booth #16 Easy and fast to be applied via arthroscopy. Fixation is not required in most cases. The only entirely hyaluronic acid-based scaffold supporting hyaline-like cartilage regeneration Available Sizes 2x2 cm 5x5 cm NEW SIZE Website: http://hyalofast.anikatherapeutics.com E-mail: [email protected] Telephone: +39 (0)49 295 8324 4 Level 1 Study Proves Efficacy of ACP in -
Applications of Chondrocyte-Based Cartilage Engineering: an Overview
Hindawi Publishing Corporation BioMed Research International Volume 2016, Article ID 1879837, 17 pages http://dx.doi.org/10.1155/2016/1879837 Review Article Applications of Chondrocyte-Based Cartilage Engineering: An Overview Abdul-Rehman Phull,1 Seong-Hui Eo,1 Qamar Abbas,1 Madiha Ahmed,2 and Song Ja Kim1 1 Department of Biological Sciences, College of Natural Sciences, Kongju National University, Gongjudaehakro 56, Gongju 32588, Republic of Korea 2Department of Pharmacy, Quaid-i-Azam University, Islamabad 45320, Pakistan Correspondence should be addressed to Song Ja Kim; [email protected] Received 14 May 2016; Revised 24 June 2016; Accepted 26 June 2016 Academic Editor: Magali Cucchiarini Copyright © 2016 Abdul-Rehman Phull et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Chondrocytes are the exclusive cells residing in cartilage and maintain the functionality of cartilage tissue. Series of biocomponents such as different growth factors, cytokines, and transcriptional factors regulate the mesenchymal stem cells (MSCs) differentiation to chondrocytes. The number of chondrocytes and dedifferentiation are the key limitations in subsequent clinical application of the chondrocytes. Different culture methods are being developed to overcome such issues. Using tissue engineering and cell based approaches, chondrocytes offer prominent therapeutic option specifically in orthopedics for cartilage repair and to treat ailments such as tracheal defects, facial reconstruction, and urinary incontinence. Matrix-assisted autologous chondrocyte transplantation/implantation is an improved version of traditional autologous chondrocyte transplantation (ACT) method. An increasing number of studies show the clinical significance of this technique for the chondral lesions treatment. -
Development of the Endochondral Skeleton
Downloaded from http://cshperspectives.cshlp.org/ on September 24, 2021 - Published by Cold Spring Harbor Laboratory Press Development of the Endochondral Skeleton Fanxin Long1,2 and David M. Ornitz2 1Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110 2Department of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri 63110 Correspondence: fl[email protected] SUMMARY Much of the mammalian skeleton is composed of bones that originate from cartilage templates through endochondral ossification. Elucidating the mechanisms that control endochondral bone development is critical for understanding human skeletal diseases, injury response, and aging. Mouse genetic studies in the past 15 years have provided unprecedented insights about molecules regulating chondrocyte formation, chondrocyte maturation, and osteoblast differ- entiation, all key processes of endochondral bone development. These include the roles of the secreted proteins IHH, PTHrP, BMPs, WNTs, and FGFs, their receptors, and transcription factors such as SOX9, RUNX2, and OSX, in regulating chondrocyte and osteoblast biology. This review aims to integrate the known functions of extracellular signals and transcription factors that regulate development of the endochondral skeleton. Outline 1 Introduction 5 Osteoblastogenesis 2 Mesenchymal condensation 6 Closing remarks 3 Chondrocyte differentiation References 4 Growth plate development Editors: Patrick P.L. Tam, W. James Nelson, and Janet Rossant Additional Perspectives on Mammalian Development available at www.cshperspectives.org Copyright # 2013 Cold Spring Harbor Laboratory Press; all rights reserved; doi: 10.1101/cshperspect.a008334 Cite this article as Cold Spring Harb Perspect Biol 2013;5:a008334 1 Downloaded from http://cshperspectives.cshlp.org/ on September 24, 2021 - Published by Cold Spring Harbor Laboratory Press F. -
Comparative Anatomy of the Lower Respiratory Tract of the Gray Short-Tailed Opossum (Monodelphis Domestica) and North American Opossum (Didelphis Virginiana)
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Doctoral Dissertations Graduate School 12-2001 Comparative Anatomy of the Lower Respiratory Tract of the Gray Short-tailed Opossum (Monodelphis domestica) and North American Opossum (Didelphis virginiana) Lee Anne Cope University of Tennessee - Knoxville Follow this and additional works at: https://trace.tennessee.edu/utk_graddiss Part of the Animal Sciences Commons Recommended Citation Cope, Lee Anne, "Comparative Anatomy of the Lower Respiratory Tract of the Gray Short-tailed Opossum (Monodelphis domestica) and North American Opossum (Didelphis virginiana). " PhD diss., University of Tennessee, 2001. https://trace.tennessee.edu/utk_graddiss/2046 This Dissertation is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a dissertation written by Lee Anne Cope entitled "Comparative Anatomy of the Lower Respiratory Tract of the Gray Short-tailed Opossum (Monodelphis domestica) and North American Opossum (Didelphis virginiana)." I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Doctor of Philosophy, with a major in Animal Science. Robert W. Henry, Major Professor We have read this dissertation and recommend its acceptance: Dr. R.B. Reed, Dr. C. Mendis-Handagama, Dr. J. Schumacher, Dr. S.E. Orosz Accepted for the Council: Carolyn R. -
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. -
PE2812 Breaking Arm Bones a Second Time
Breaking Arm Bones a Second Time Children who have broken arm bones are at higher risk for breaking the same arm bones again if they do not go through the right treatment, for the right amount of time. How likely is it that There is up to a 5% chance (1 out of every 20 cases) of breaking forearm my child’s arm bones a second time, in the same place. There is a higher risk to break these bones again if the first fracture is in the middle of the forearm bones (as bones will break seen in the pictures below). There is a lower risk if the fracture is closer to again? the hand. Most repeat fractures tend to happen within six months after the first injury heals. First fracture Same fracture after healing for about 6 weeks 1 of 2 To Learn More Free Interpreter Services • Orthopedics and Sports Medicine • In the hospital, ask your nurse. 206-987-2109 • From outside the hospital, call the • Ask your child’s healthcare provider toll-free Family Interpreting Line, 1-866-583-1527. Tell the interpreter • seattlechildrens.org the name or extension you need. Breaking Arm Bones a Second Time How can I help my Wearing a cast for at least six weeks lowers the risk of breaking the same child lower the risk arm bones again. After wearing a cast, we recommend your child wear a brace for 4 weeks in order to protect the injured area and start improving of having a wrist movement. While your child wears a brace, we recommend they do repeated bone not participate in contact sports (e.g., soccer, football or dodge ball). -
Study Guide Medical Terminology by Thea Liza Batan About the Author
Study Guide Medical Terminology By Thea Liza Batan About the Author Thea Liza Batan earned a Master of Science in Nursing Administration in 2007 from Xavier University in Cincinnati, Ohio. She has worked as a staff nurse, nurse instructor, and level department head. She currently works as a simulation coordinator and a free- lance writer specializing in nursing and healthcare. All terms mentioned in this text that are known to be trademarks or service marks have been appropriately capitalized. Use of a term in this text shouldn’t be regarded as affecting the validity of any trademark or service mark. Copyright © 2017 by Penn Foster, Inc. All rights reserved. No part of the material protected by this copyright may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system, without permission in writing from the copyright owner. Requests for permission to make copies of any part of the work should be mailed to Copyright Permissions, Penn Foster, 925 Oak Street, Scranton, Pennsylvania 18515. Printed in the United States of America CONTENTS INSTRUCTIONS 1 READING ASSIGNMENTS 3 LESSON 1: THE FUNDAMENTALS OF MEDICAL TERMINOLOGY 5 LESSON 2: DIAGNOSIS, INTERVENTION, AND HUMAN BODY TERMS 28 LESSON 3: MUSCULOSKELETAL, CIRCULATORY, AND RESPIRATORY SYSTEM TERMS 44 LESSON 4: DIGESTIVE, URINARY, AND REPRODUCTIVE SYSTEM TERMS 69 LESSON 5: INTEGUMENTARY, NERVOUS, AND ENDOCRINE S YSTEM TERMS 96 SELF-CHECK ANSWERS 134 © PENN FOSTER, INC. 2017 MEDICAL TERMINOLOGY PAGE III Contents INSTRUCTIONS INTRODUCTION Welcome to your course on medical terminology. You’re taking this course because you’re most likely interested in pursuing a health and science career, which entails proficiencyincommunicatingwithhealthcareprofessionalssuchasphysicians,nurses, or dentists. -
REVIEW ARTICLE Interactions Between GH, IGF-I, Glucocorticoids
0031-3998/02/5202-0137 PEDIATRIC RESEARCH Vol. 52, No. 2, 2002 Copyright © 2002 International Pediatric Research Foundation, Inc. Printed in U.S.A. REVIEW ARTICLE Interactions between GH, IGF-I, Glucocorticoids, and Thyroid Hormones during Skeletal Growth HELEN ROBSON, THOMAS SIEBLER, STEPHEN M. SHALET, AND GRAHAM R. WILLIAMS Department of Clinical Research [H.R.], Department of Endocrinology [S.M.S.], Christie Hospital National Health Service Trust, Manchester, U.K.; University Children’s Hospital, University of Leipzig, Leipzig, Germany [T.S.]; IC Molecular Endocrinology Group, Division of Medicine and MRC Clinical Sciences Centre, Faculty of Medicine, Imperial College School of Science Technology and Medicine, Hammersmith Hospital, London, U.K. [G.R.W.] ABSTRACT Linear growth occurs during development and the childhood Abbreviations years until epiphyseal fusion occurs. This process results from 5'-DI, 5'-iodothyronine deiodinase endochondral ossification in the growth plates of long bones and FGF, fibroblast growth factor is regulated by systemic hormones and paracrine or autocrine FGFR, fibroblast growth factor receptor factors. The major regulators of developmental and childhood GC, glucocorticoid growth are GH, IGF-I, glucocorticoids, and thyroid hormone. GHR, GH receptor Sex steroids are responsible for the pubertal growth spurt and GR, glucocorticoid receptor epiphyseal fusion. This review will consider interactions between HSPG, heparan sulfate proteoglycan GH, IGF-I, glucocorticoids, and thyroid hormone during linear 11HSD, 11-hydroxysteroid dehydrogenase growth. It is well known from physiologic and clinical studies IGF-IR, IGF-I receptor that these hormones interact at the level of the hypothalamus and IGFBP, IGF binding protein pituitary. Interacting effects on peripheral tissues such as liver are Ihh, Indian hedgehog also well understood, but we concentrate here on the epiphyseal JAK-2, Janus-activated kinase-2 growth plate as an important and newly appreciated target organ PTHrP, PTH-related peptide for convergent hormone action. -
Upper Limb Development
Upper Limb Development Alphonsus Chong Department of Hand and Reconstructive Microsurgery National University Hospital Why bother? Most congenital limb anomalies are due to: Disorders of embryogenesis or Problems during fetal development Some terminology Embryogenesis 0-8 weeks – new organ systems appear Fetal period Appearance of primary ossification center in humerus Differentiation, maturation and enlargement of existing organs Limb Development Limb Patterning Tissue Differentiation Why is it an arm and not Skeletal a leg? Joint Vascular Nerve Muscle and Tendon Positional Information and Axes of the upper limb Limb Bud in E3 Chick Embryo Limb bud (lateral plate) Loose mesenchymal cells from lateral plate mesoderm Ectodermal epithelial cells Migrating cells Somites --> Muscle Nerves Vasculature Limb Bud Development Limb bud Ectoderm and mesenchyme Not fully differentiated yet but all ingredients there If transplanted ectopic limb Limb Bud Regions AER Progress zone Zone of polarizing activity AER – Proximal to Distal formation Zone of Polarizing Actvity – AP development Morphogen Gradient Model Dorsal / ventral patterning less well understood Separation of Digits Apoptosis (Programmed cell death) of interdigital mesenchyme BMPs important Starts post-axial to pre-axial Mesoderm specifies amount of apoptosis How does this relate to pathogensis? Picture from Greene Learning Points UE development occurs early in embryogenesis – most risk of development congenital anomalies Pattern of limb development follows a body plan Digit formation is by apoptosis Thank You Further Reading Principles of Development 3rd Ed by Lewis Wolpert. Oxford University Press Growing Hand. Amit Gupta and Louisville Group. -
Pg 131 Chondroblast -> Chondrocyte (Lacunae) Firm Ground Substance
Figure 4.8g Connective tissues. Chondroblast ‐> Chondrocyte (Lacunae) Firm ground substance (chondroitin sulfate and water) Collagenous and elastic fibers (g) Cartilage: hyaline No BV or nerves Description: Amorphous but firm Perichondrium (dense irregular) matrix; collagen fibers form an imperceptible network; chondroblasts produce the matrix and when mature (chondrocytes) lie in lacunae. Function: Supports and reinforces; has resilient cushioning properties; resists compressive stress. Location: Forms most of the embryonic skeleton; covers the ends Chondrocyte of long bones in joint cavities; forms in lacuna costal cartilages of the ribs; cartilages of the nose, trachea, and larynx. Matrix Costal Photomicrograph: Hyaline cartilage from the cartilages trachea (750x). Thickness? Metabolism? Copyright © 2010 Pearson Education, Inc. Pg 131 Figure 6.1 The bones and cartilages of the human skeleton. Epiglottis Support Thyroid Larynx Smooth Cartilage in Cartilages in cartilage external ear nose surface Cricoid Trachea Articular Lung Cushions cartilage Cartilage of a joint Cartilage in Costal Intervertebral cartilage disc Respiratory tube cartilages in neck and thorax Pubic Bones of skeleton symphysis Meniscus (padlike Axial skeleton cartilage in Appendicular skeleton knee joint) Cartilages Articular cartilage of a joint Hyaline cartilages Elastic cartilages Fibrocartilages Pg 174 Copyright © 2010 Pearson Education, Inc. Figure 4.8g Connective tissues. (g) Cartilage: hyaline Description: Amorphous but firm matrix; collagen fibers form an imperceptible network; chondroblasts produce the matrix and when mature (chondrocytes) lie in lacunae. Function: Supports and reinforces; has resilient cushioning properties; resists compressive stress. Location: Forms most of the embryonic skeleton; covers the ends Chondrocyte of long bones in joint cavities; forms in lacuna costal cartilages of the ribs; cartilages of the nose, trachea, and larynx. -
GLOSSARY of MEDICAL and ANATOMICAL TERMS
GLOSSARY of MEDICAL and ANATOMICAL TERMS Abbreviations: • A. Arabic • abb. = abbreviation • c. circa = about • F. French • adj. adjective • G. Greek • Ge. German • cf. compare • L. Latin • dim. = diminutive • OF. Old French • ( ) plural form in brackets A-band abb. of anisotropic band G. anisos = unequal + tropos = turning; meaning having not equal properties in every direction; transverse bands in living skeletal muscle which rotate the plane of polarised light, cf. I-band. Abbé, Ernst. 1840-1905. German physicist; mathematical analysis of optics as a basis for constructing better microscopes; devised oil immersion lens; Abbé condenser. absorption L. absorbere = to suck up. acervulus L. = sand, gritty; brain sand (cf. psammoma body). acetylcholine an ester of choline found in many tissue, synapses & neuromuscular junctions, where it is a neural transmitter. acetylcholinesterase enzyme at motor end-plate responsible for rapid destruction of acetylcholine, a neurotransmitter. acidophilic adj. L. acidus = sour + G. philein = to love; affinity for an acidic dye, such as eosin staining cytoplasmic proteins. acinus (-i) L. = a juicy berry, a grape; applied to small, rounded terminal secretory units of compound exocrine glands that have a small lumen (adj. acinar). acrosome G. akron = extremity + soma = body; head of spermatozoon. actin polymer protein filament found in the intracellular cytoskeleton, particularly in the thin (I-) bands of striated muscle. adenohypophysis G. ade = an acorn + hypophyses = an undergrowth; anterior lobe of hypophysis (cf. pituitary). adenoid G. " + -oeides = in form of; in the form of a gland, glandular; the pharyngeal tonsil. adipocyte L. adeps = fat (of an animal) + G. kytos = a container; cells responsible for storage and metabolism of lipids, found in white fat and brown fat. -
Bone Markings / Features on Bones
08/05/2016 Bone Markings : Skeletal System Search Custom Search Like Tweet Home Health News Human Body Biology Chemistry Glossary Textbooks Bone Disorders Ads by Google ► Bone Tissue ► Bone Marrow ► Human Skull Bone ► Bone on Bone Knee Sun 8 May 2016 Bone Markings / Features on Bones Human Body Study Section Bone markings and the features of bones (including the correct words used to describe them) are often required by firstlevel courses in human anatomy and associated health science subjects. It is important to be familiar with the terminology used to Human Body Index refer to bone markings in order to communicate effectively with professionals involved in healthcare, research, forensics, and Health Glossary related disciplines. More about Bones and the Skeletal System: The following terms used to describe bone markings or features on bones are in alphabetical order with short definitions: Human Skeleton Axial and Appendicular Word / Term Meaning / Description Type of Example(s) Skeleton (Bone Marking or bone The Structure and Feature) marking Functions of Bones Types of Bones 1. Angle A corner Feature of Inferior angle (lower) and superior angle (upper) are Bone Markings & Features shape of bone the rounded angles or "corners" of the scapula. on Bones Disorders of the Skeletal 2. Body The main portion of a bone The diaphysis of long bones such as the humerus. System Curvature of the Spine 3. Condyle Rounded bump or large rounded Process The medial condyle of the femur (bone), upperleg. prominence. Such rounded surfaces forms joints Types of Joints usually fit into a fossa on another bone to Specific bones: form a joint.