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3 Embryology and Development
BIOL 6505 − INTRODUCTION TO FETAL MEDICINE 3. EMBRYOLOGY AND DEVELOPMENT Arlet G. Kurkchubasche, M.D. INTRODUCTION Embryology – the field of study that pertains to the developing organism/human Basic embryology –usually taught in the chronologic sequence of events. These events are the basis for understanding the congenital anomalies that we encounter in the fetus, and help explain the relationships to other organ system concerns. Below is a synopsis of some of the critical steps in embryogenesis from the anatomic rather than molecular basis. These concepts will be more intuitive and evident in conjunction with diagrams and animated sequences. This text is a synopsis of material provided in Langman’s Medical Embryology, 9th ed. First week – ovulation to fertilization to implantation Fertilization restores 1) the diploid number of chromosomes, 2) determines the chromosomal sex and 3) initiates cleavage. Cleavage of the fertilized ovum results in mitotic divisions generating blastomeres that form a 16-cell morula. The dense morula develops a central cavity and now forms the blastocyst, which restructures into 2 components. The inner cell mass forms the embryoblast and outer cell mass the trophoblast. Consequences for fetal management: Variances in cleavage, i.e. splitting of the zygote at various stages/locations - leads to monozygotic twinning with various relationships of the fetal membranes. Cleavage at later weeks will lead to conjoined twinning. Second week: the week of twos – marked by bilaminar germ disc formation. Commences with blastocyst partially embedded in endometrial stroma Trophoblast forms – 1) cytotrophoblast – mitotic cells that coalesce to form 2) syncytiotrophoblast – erodes into maternal tissues, forms lacunae which are critical to development of the uteroplacental circulation. -
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 -
1 Male Checklist Male Reproductive System Components of the Male
Male Checklist Male Reproductive System Components of the male Testes; accessory glands and ducts; the penis; and reproductive system the scrotum. Functions of the male The male reproductive system produces sperm cells that reproductive system can be transferred to the female, resulting in fertilization and the formation of a new individual. It also produces sex hormones responsible for the normal development of the adult male body and sexual behavior. Penis The penis functions as the common outlet for semen (sperm cells and glandular secretions) and urine. The penis is also the male copulatory organ, containing tissue that can fill with blood resulting in erection of the penis. Prepuce A fold of skin over the distal end of the penis. Circumcision is the surgical removal of the prepuce. Corpus spongiosum A spongy body consisting of erectile tissue. It surrounds the urethra. Sexual excitement can cause erectile tissue to fill with blood. As a result, the penis becomes erect. Glans penis The expanded, distal end of the corpus spongiosum. It is also called the head of the penis. Bulb of the penis The proximal end of the corpus spongiosum. Bulbospongiosus muscle One of two skeletal muscles surrounding the bulb of the penis. At the end of urination, contraction of the bulbospongiosus muscles forces any remaining urine out of the urethra. During ejaculation, contractions of the bulbospongiosus muscles ejects semen from the penis. Contraction of the bulbospongiosus muscles compresses the corpus spongiosum, helping to maintain an erection. Corpus cavernosum One of two spongy bodies consisting of erectile tissue that (pl., corpora cavernosa) form the sides and front of the penis. -
Pancreatic B-Cell Replacement: Advances in Protocols Used for Differentiation of Pancreatic Progenitors to B-Like Cells
FOLIA HISTOCHEMICA REVIEW ET CYTOBIOLOGICA Vol. 57, No. 3, 2019 pp. 101–115 Pancreatic b-cell replacement: advances in protocols used for differentiation of pancreatic progenitors to b-like cells Muhammad Waseem Ghani1, Li Ye1, Zhao Yi1, Hammad Ghani2, Muhammad Waseem Birmani1, Aamir Nawab1, Lang Guan Cun1, Liu Bin1, Xiao Mei1 1Department of Livestock Production and Management, Agricultural College, Guangdong Ocean University, Zhanjiang, Guangdong, China 2Nawaz Sharif Medical College University of Gujrat, Punjab, Pakistan Abstract Insulin-producing cells derived from in vitro differentiation of stem cells and non-stem cells by using different factors can spare the need for genetic manipulation and provide a cure for diabetes. In this context, pancreatic progenitors differentiating to b-like cells garner increasing attention as b-cell replacement source. This kind of cell therapy has the potential to cure diabetes, but is still on its way of being clinically useful. The primary restriction for in vitro production of mature and functional b-cells is developing a physiologically relevant in vitro culture system which can mimic in vivo pathways of islet development. In order to achieve this target, different approaches have been attempted for the differentiation of pancreatic stem/progenitor cells to b-like cells. Here, we will review some of the state-of-the-art protocols for the differentiation of pancreatic progenitors and differentiated pancreatic cells into b-like cells with a focus on pancreatic duct cells. (Folia Histochemica et Cytobiologica -
Cell-Cell Interactions
7 Cell-Cell Interactions Concept Outline 7.1 Cells signal one another with chemicals. Receptor Proteins and Signaling between Cells. Receptor proteins embedded in the plasma membrane change shape when they bind specific signal molecules, triggering a chain of events within the cell. Types of Cell Signaling. Cell signaling can occur between adjacent cells, although chemical signals called hormones act over long distances. 7.2 Proteins in the cell and on its surface receive signals from other cells. Intracellular Receptors. Some receptors are located within the cell cytoplasm. These receptors respond to lipid- soluble signals, such as steroid hormones. Cell Surface Receptors. Many cell-to-cell signals are water-soluble and cannot penetrate membranes. Instead, the signals are received by transmembrane proteins protruding out from the cell surface. 7.3 Follow the journey of information into the cell. FIGURE 7.1 Persimmon cells in close contact with one another. These Initiating the Intracellular Signal. Cell surface receptors plant cells and all cells, no matter what their function, interact often use “second messengers” to transmit a signal to the with their environment, including the cells around them. cytoplasm. Amplifying the Signal: Protein Kinase Cascades. Surface receptors and second messengers amplify signals as id you know that each of the 100 trillion cells of your they travel into the cell, often toward the cell nucleus. Dbody shares one key feature with the cells of tigers, bumblebees, and persimmons (figure 7.1)—a feature that 7.4 Cell surface proteins mediate cell-cell interactions. most bacteria and protists lack? Your cells touch and com- The Expression of Cell Identity. -
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. -
© Copyright 2016 Wendy Yang
© Copyright 2016 Wendy Yang Role for cell-to-cell communication in stem cell specification toward pancreatic progenitors: relevance to the design of novel therapies for diabetes. Wendy Yang A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy University of Washington 2016 Reading Committee: Vincenzo Cirulli, Chair Laura Crisa Paul D. Lampe Program Authorized to Offer Degree: Pharmacology University of Washington Abstract Role for cell-to-cell communication in stem cell specification toward pancreatic progenitors: relevance to the design of novel therapies for diabetes. Wendy Yang Chair of the Supervisory Committee: Vincenzo Cirulli Metabolism, Endocrinology & Nutrition Pancreatic islets of Langerhans, responsible for the production of hormones such as insulin and glucagon, develop from pluripotent pancreatic progenitors following their specification toward an endocrine phenotype. Based on the established role of cell-to-cell communication as an important mechanism regulating developmental decisions during embryonic life, I investigated the expression pattern of Connexins (Cxs), the building blocks of Gap Junction channels, in the developing human pancreas, and in an in vitro model of pancreatic progenitor differentiation from human embryonic stem cells (hESC). I also investigated the role of β1 integrins and an associated downstream effector, integrin-linked kinase (ILK), on islet development in mice. In a first series of experiments, I investigated the expression pattern of Cxs in the developing human pancreas. Results from these studies revealed that while Cx32 is predominantly expressed in the acinar tissue, Cx36 is primarily expressed in developing islet β- cells. Cx43 exhibited the most interesting expression pattern, being primarily detected in putative islet cell progenitors that delaminate from the pancreatic ductal epithelium and aggregate with developing islet cell clusters. -
Cooperative Coupling of Cell-Matrix and Cell–Cell Adhesions in Cardiac Muscle
Cooperative coupling of cell-matrix and cell–cell adhesions in cardiac muscle Megan L. McCaina, Hyungsuk Leea,1, Yvonne Aratyn-Schausa, André G. Kléberb, and Kevin Kit Parkera,2 aDisease Biophysics Group, Wyss Institute for Biologically Inspired Engineering, School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138; and bDepartment of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215 Edited by Robert Langer, Massachusetts Institute of Technology, Cambridge, MA, and approved May 1, 2012 (received for review February 21, 2012) Adhesion between cardiac myocytes is essential for the heart to serve as cues for remodeling adhesions and assembling tissues. In function as an electromechanical syncytium. Although cell-matrix vitro studies have demonstrated that cytoskeletal tension (27) and and cell–cell adhesions reorganize during development and dis- exogenous cyclic strain (28, 29) promote cell–cell adhesion and ease, the hierarchical cooperation between these subcellular struc- tissue assembly in many cell types. Culturing noncardiac cells tures is poorly understood. We reasoned that, during cardiac on stiff substrates tips the balance of adhesion in favor of focal development, focal adhesions mechanically stabilize cells and tis- adhesions and away from cell–cell adhesions (30–32), suggesting sues during myofibrillogenesis and intercalated disc assembly. As that mechanical forces can modulate the assembly or disassembly the intercalated disc matures, we postulated that focal -
ATG9 Regulates Autophagosome Progression from the Endoplasmic Reticulum in Arabidopsis
ATG9 regulates autophagosome progression from the endoplasmic reticulum in Arabidopsis Xiaohong Zhuanga,b,1, Kin Pan Chunga,b,1, Yong Cuia,b,1, Weili Lina,b, Caiji Gaoa,b,2, Byung-Ho Kanga,b, and Liwen Jianga,b,c,3 aCentre for Cell & Developmental Biology, School of Life Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China; bState Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China; and cThe Chinese University of Hong Kong Shenzhen Research Institute, Shenzhen 518057, China Edited by Diane C. Bassham, Iowa State University, Ames, IA, and accepted by Editorial Board Member Maarten J. Chrispeels December 8, 2016 (received for review October 6, 2016) Autophagy is a conserved pathway for bulk degradationofcytoplasmic autophagy pathway because ATG9 was required for the biogenesis material by a double-membrane structure named the autophagosome. of ER-derived compartments during the unfolded protein response The initiation of autophagosome formation requires the recruitment of (9). However, whether ATG9 plays a direct role in the early stages autophagy-related protein 9 (ATG9) vesicles to the preautophagosomal of autophagosome formation or in a specific autophagy process structure. However, the functional relationship between ATG9 vesicles remainstobeinvestigatedinplants.Onemajorchallengeisthelack and the phagophore is controversial in different systems, and the mo- of morphologically informative visualization that might correlate the lecular function of ATG9 remains unknown in plants. Here, we demon- early autophagosomal structures and ATG9 vesicles in real-time and strate that ATG9 is essential for endoplasmic reticulum (ER)-derived in three dimensions. autophagosome formation in plants. -
Clinical Pelvic Anatomy
SECTION ONE • Fundamentals 1 Clinical pelvic anatomy Introduction 1 Anatomical points for obstetric analgesia 3 Obstetric anatomy 1 Gynaecological anatomy 5 The pelvic organs during pregnancy 1 Anatomy of the lower urinary tract 13 the necks of the femora tends to compress the pelvis Introduction from the sides, reducing the transverse diameters of this part of the pelvis (Fig. 1.1). At an intermediate level, opposite A thorough understanding of pelvic anatomy is essential for the third segment of the sacrum, the canal retains a circular clinical practice. Not only does it facilitate an understanding cross-section. With this picture in mind, the ‘average’ of the process of labour, it also allows an appreciation of diameters of the pelvis at brim, cavity, and outlet levels can the mechanisms of sexual function and reproduction, and be readily understood (Table 1.1). establishes a background to the understanding of gynae- The distortions from a circular cross-section, however, cological pathology. Congenital abnormalities are discussed are very modest. If, in circumstances of malnutrition or in Chapter 3. metabolic bone disease, the consolidation of bone is impaired, more gross distortion of the pelvic shape is liable to occur, and labour is likely to involve mechanical difficulty. Obstetric anatomy This is termed cephalopelvic disproportion. The changing cross-sectional shape of the true pelvis at different levels The bony pelvis – transverse oval at the brim and anteroposterior oval at the outlet – usually determines a fundamental feature of The girdle of bones formed by the sacrum and the two labour, i.e. that the ovoid fetal head enters the brim with its innominate bones has several important functions (Fig. -
Roles of Sigma-1 Receptors on Mitochondrial Functions Relevant to Neurodegenerative Diseases Tzu-Yu Weng1,2, Shang-Yi Anne Tsai1 and Tsung-Ping Su1*
Weng et al. Journal of Biomedical Science (2017) 24:74 DOI 10.1186/s12929-017-0380-6 REVIEW Open Access Roles of sigma-1 receptors on mitochondrial functions relevant to neurodegenerative diseases Tzu-Yu Weng1,2, Shang-Yi Anne Tsai1 and Tsung-Ping Su1* Abstract The sigma-1 receptor (Sig-1R) is a chaperone that resides mainly at the mitochondrion-associated endoplasmic reticulum (ER) membrane (called the MAMs) and acts as a dynamic pluripotent modulator in living systems. At the MAM, the Sig-1R is known to play a role in regulating the Ca2+ signaling between ER and mitochondria and in maintaining the structural integrity of the MAM. The MAM serves as bridges between ER and mitochondria regulating multiple functions such as Ca2+ transfer, energy exchange, lipid synthesis and transports, and protein folding that are pivotal to cell survival and defense. Recently, emerging evidences indicate that the MAM is critical in maintaining neuronal homeostasis. Thus, given the specific localization of the Sig-1R at the MAM, we highlight and propose that the direct or indirect regulations of the Sig-1R on mitochondrial functions may relate to neurodegenerative diseases including Alzheimer’s disease (AD), Parkinson’s disease (PD), Huntington’s disease (HD) and amyotrophic lateral sclerosis (ALS). In addition, the promising use of Sig-1R ligands to rescue mitochondrial dysfunction-induced neurodegeneration is addressed. Keywords: Sigma-1 receptor, Mitochondria, Mitochondrion-associated ER membrane (MAM), Neurodegenerative disorders Background also regulates Ca2+ influx by attenuating the coupling of The sigma-1 receptor (Sig-1R) is an endoplasmic the ER Ca2+ sensor STIM1 to Orai1 [3]. -
Histology Histology
HISTOLOGY HISTOLOGY ОДЕСЬКИЙ НАЦІОНАЛЬНИЙ МЕДИЧНИЙ УНІВЕРСИТЕТ THE ODESSA NATIONAL MEDICAL UNIVERSITY Áiáëiîòåêà ñòóäåíòà-ìåäèêà Medical Student’s Library Серія заснована в 1999 р. на честь 100-річчя Одеського державного медичного університету (1900–2000 рр.) The series is initiated in 1999 to mark the Centenary of the Odessa State Medical University (1900–2000) 1 L. V. Arnautova O. A. Ulyantseva HISTÎLÎGY A course of lectures A manual Odessa The Odessa National Medical University 2011 UDC 616-018: 378.16 BBC 28.8я73 Series “Medical Student’s Library” Initiated in 1999 Authors: L. V. Arnautova, O. A. Ulyantseva Reviewers: Professor V. I. Shepitko, MD, the head of the Department of Histology, Cytology and Embryology of the Ukrainian Medical Stomatologic Academy Professor O. Yu. Shapovalova, MD, the head of the Department of Histology, Cytology and Embryology of the Crimean State Medical University named after S. I. Georgiyevsky It is published according to the decision of the Central Coordinational Methodical Committee of the Odessa National Medical University Proceedings N1 from 22.09.2010 Навчальний посібник містить лекції з гістології, цитології та ембріології у відповідності до програми. Викладено матеріали теоретичного курсу по всіх темах загальної та спеціальної гістології та ембріології. Посібник призначений для підготовки студентів до практичних занять та ліцензійного екзамену “Крок-1”. Arnautova L. V. Histology. A course of lectures : a manual / L. V. Arnautova, O. A. Ulyantseva. — Оdessa : The Оdessa National Medical University, 2010. — 336 p. — (Series “Medical Student’s Library”). ISBN 978-966-443-034-7 The manual contains the lecture course on histology, cytology and embryol- ogy in correspondence with the program.