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2009 Universities Across the Country
LIFE IN HALE : A Few Words from the Chair... Volume VIII As many of you may know, the recent national economic downturn has severely affected many state Summer 2009 universities across the country. Ironically, CU has been spared the worst effects because it receives only 9% of its annual budget from the State of Colorado. This reminds us how important student tui- tion, external research grants, and private contributions are for the future of Anthropology at CU Boulder. Fortunately, the department continues to enjoy high enrollments, active research agendas, and generous support from its alumni. The major philanthropic gifts we have received from Gregg Goldstein and Tom Lennon have made an especially important impact this year by providing our graduate students with fellowship and fieldwork support. If you are interested in exploring the op- tions for making an endowed donation or a legacy bequest to sustain the future of Colorado anthro- pology, I would be happy to discuss this with you. rooms and corridors of Hale. Meanwhile, it is high summer in the Rockies, and Hope you will find this edition at least 50% of our faculty and grad students are of CU Anthropology Press presently “in the field” in various parts of the intriguing and informative as world collecting data for their research projects, we make the transition from while our three-person departmental staff make paper & print to on-line web- preparations for the Fall 2009 semester. We will based publication. Please be joined by two new faculty colleagues (see send us your latest news so story below) and a fresh cohort of graduate and that we can share your sto- Dennis McGilvray undergraduate students to enliven the class- ries and stay in touch. -
The Evolutionary History of the Human Face
This is a repository copy of The evolutionary history of the human face. White Rose Research Online URL for this paper: https://eprints.whiterose.ac.uk/145560/ Version: Accepted Version Article: Lacruz, Rodrigo S, Stringer, Chris B, Kimbel, William H et al. (5 more authors) (2019) The evolutionary history of the human face. Nature Ecology and Evolution. pp. 726-736. ISSN 2397-334X https://doi.org/10.1038/s41559-019-0865-7 Reuse Items deposited in White Rose Research Online are protected by copyright, with all rights reserved unless indicated otherwise. They may be downloaded and/or printed for private study, or other acts as permitted by national copyright laws. The publisher or other rights holders may allow further reproduction and re-use of the full text version. This is indicated by the licence information on the White Rose Research Online record for the item. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ THE EVOLUTIONARY HISTORY OF THE HUMAN FACE Rodrigo S. Lacruz1*, Chris B. Stringer2, William H. Kimbel3, Bernard Wood4, Katerina Harvati5, Paul O’Higgins6, Timothy G. Bromage7, Juan-Luis Arsuaga8 1* Department of Basic Science and Craniofacial Biology, New York University College of Dentistry; and NYCEP, New York, USA. 2 Department of Earth Sciences, Natural History Museum, London, UK 3 Institute of Human Origins and School of Human Evolution and Social Change, Arizona State University, Tempe, AZ. -
Upper Pleistocene Human Remains from Vindija Cave, Croatia, Yugoslavia
AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY 54~499-545(1981) Upper Pleistocene Human Remains From Vindija Cave, Croatia, Yugoslavia MILFORD H. WOLPOFF, FRED H. SMITH, MIRKO MALEZ, JAKOV RADOVCIC, AND DARKO RUKAVINA Department of Anthropology, University of Michigan, Ann Arbor, Michigan 48109 (MH.W.1,Department of Anthropology, University of Tennessee, Kmxuille, Tennessee 37916 (FHS.),and Institute for Paleontology and Quaternary Geology, Yugoslav Academy of Sciences and Arts, 41000 Zagreb, Yugoslavia (M.M., J.R., D.R.) KEY WORDS Vindija, Neandertal, South Central Europe, Modern Homo sapiens origin, Evolution ABSTRACT Human remains excavated from Vindija cave include a large although fragmentary sample of late Mousterian-associated specimens and a few additional individuals from the overlying early Upper Paleolithic levels. The Mousterian-associated sample is similar to European Neandertals from other regions. Compared with earlier Neandertals from south central Europe, this sam- ple evinces evolutionary trends in the direction of Upper Paleolithic Europeans. Compared with the western European Neandertals, the same trends can be demon- strated, although the magnitude of difference is less, and there is a potential for confusing temporal with regional sources of variation. The early Upper Paleo- lithic-associated sample cannot be distinguished from the Mousterian-associated hominids. We believe that this site provides support for Hrdlicka’s “Neandertal phase” of human evolution, as it was originally applied in Europe. The Pannonian Basin and surrounding val- the earliest chronometrically dated Upper leys of south central Europe have yielded a Paleolithic-associated hominid in Europe large and significant series of Upper Pleisto- (Smith, 1976a). cene fossil hominids (e.g. Jelinek, 1969) as well This report presents a detailed comparative as extensive evidence of their cultural behavior description of a sample of fossil hominids re- (e.g. -
SEC23IP (NM 007190) Human Recombinant Protein – TP309056
OriGene Technologies, Inc. 9620 Medical Center Drive, Ste 200 Rockville, MD 20850, US Phone: +1-888-267-4436 [email protected] EU: [email protected] CN: [email protected] Product datasheet for TP309056 SEC23IP (NM_007190) Human Recombinant Protein Product data: Product Type: Recombinant Proteins Description: Recombinant protein of human SEC23 interacting protein (SEC23IP) Species: Human Expression Host: HEK293T Tag: C-Myc/DDK Predicted MW: 110.9 kDa Concentration: >50 ug/mL as determined by microplate BCA method Purity: > 80% as determined by SDS-PAGE and Coomassie blue staining Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol Preparation: Recombinant protein was captured through anti-DDK affinity column followed by conventional chromatography steps. Storage: Store at -80°C. Stability: Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. RefSeq: NP_009121 Locus ID: 11196 UniProt ID: Q9Y6Y8 RefSeq Size: 7306 Cytogenetics: 10q26.11-q26.12 RefSeq ORF: 3000 Synonyms: iPLA1beta; MSTP053; P125; P125A Summary: This gene encodes a member of the phosphatidic acid preferring-phospholipase A1 family. The encoded protein is localized to endoplasmic reticulum exit sites and plays a critical role in ER-Golgi transport as part of the multimeric coat protein II complex. An orthologous gene in frogs is required for normal neural crest cell development, suggesting that this gene may play a role in Waardenburg syndrome neural crest defects. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Feb 2011] This product is to be used for laboratory only. -
Genes in Eyecare Geneseyedoc 3 W.M
Genes in Eyecare geneseyedoc 3 W.M. Lyle and T.D. Williams 15 Mar 04 This information has been gathered from several sources; however, the principal source is V. A. McKusick’s Mendelian Inheritance in Man on CD-ROM. Baltimore, Johns Hopkins University Press, 1998. Other sources include McKusick’s, Mendelian Inheritance in Man. Catalogs of Human Genes and Genetic Disorders. Baltimore. Johns Hopkins University Press 1998 (12th edition). http://www.ncbi.nlm.nih.gov/Omim See also S.P.Daiger, L.S. Sullivan, and B.J.F. Rossiter Ret Net http://www.sph.uth.tmc.edu/Retnet disease.htm/. Also E.I. Traboulsi’s, Genetic Diseases of the Eye, New York, Oxford University Press, 1998. And Genetics in Primary Eyecare and Clinical Medicine by M.R. Seashore and R.S.Wappner, Appleton and Lange 1996. M. Ridley’s book Genome published in 2000 by Perennial provides additional information. Ridley estimates that we have 60,000 to 80,000 genes. See also R.M. Henig’s book The Monk in the Garden: The Lost and Found Genius of Gregor Mendel, published by Houghton Mifflin in 2001 which tells about the Father of Genetics. The 3rd edition of F. H. Roy’s book Ocular Syndromes and Systemic Diseases published by Lippincott Williams & Wilkins in 2002 facilitates differential diagnosis. Additional information is provided in D. Pavan-Langston’s Manual of Ocular Diagnosis and Therapy (5th edition) published by Lippincott Williams & Wilkins in 2002. M.A. Foote wrote Basic Human Genetics for Medical Writers in the AMWA Journal 2002;17:7-17. A compilation such as this might suggest that one gene = one disease. -
September 2017 N°17
ISSN 2499-1341 EXPRESSION quarterly e-journal of atelier in cooperation with uispp-cisenp. international scientific commission on the intellectual and spiritual expressions of non-literate peoples N°17 September 2017 CULT SITES AND ART Anthropomorphic face on the entrance slab of a circular ceremonial structure from Har Karkom, Negev desert, Israel (Pre-pottery Neolithic site BK 608). EDITORIAL NOTES accompany them. What echoes accompanied CULT SITES the paintings in the prehistoric caves? What performances, if any, were taking place in front AND ART of the decorated rock surfaces? The visual art stresses myths, mythical beings Walking along a narrow trail, on the edge of and/or historical facts, which are related to the a steep valley in the middle of a deep forest, cult and to the sanctity of the site. It is the visual we suddenly heard noises of human presen- memory that justifes the function of the site. ce, voices that were neither speeches nor son- Was it the same in prehistoric times? In front of gs, something in between. We reached a cave where a number of people were assembled in rock art sites, in the Camonica Valley, Italy, or a corner and an old bearded man was standing in Kakadu in Arnhem Land, Australia, or in the on an upper step of the rock talking ... perhaps Drakensberg caves, South Africa, or in the Al- talking, perhaps declaiming, perhaps singing, tamira cave, Spain, the presence of prehistoric but not to the people below. He was talking or art awakens a sense of sacredness, we feel that performing or praying in front of a white rock these were and are special places but .. -
Genetic Variant in 3' Untranslated Region of the Mouse Pycard Gene
bioRxiv preprint doi: https://doi.org/10.1101/2021.03.26.437184; this version posted March 26, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 1 2 3 Title: 4 Genetic Variant in 3’ Untranslated Region of the Mouse Pycard Gene Regulates Inflammasome 5 Activity 6 Running Title: 7 3’UTR SNP in Pycard regulates inflammasome activity 8 Authors: 9 Brian Ritchey1*, Qimin Hai1*, Juying Han1, John Barnard2, Jonathan D. Smith1,3 10 1Department of Cardiovascular & Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, 11 Cleveland, OH 44195 12 2Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 13 44195 14 3Department of Molecular Medicine, Cleveland Clinic Lerner College of Medicine of Case Western 15 Reserve University, Cleveland, OH 44195 16 *, These authors contributed equally to this study. 17 Address correspondence to Jonathan D. Smith: email [email protected]; ORCID ID 0000-0002-0415-386X; 18 mailing address: Cleveland Clinic, Box NC-10, 9500 Euclid Avenue, Cleveland, OH 44195, USA. 19 1 bioRxiv preprint doi: https://doi.org/10.1101/2021.03.26.437184; this version posted March 26, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 20 Abstract 21 Quantitative trait locus mapping for interleukin-1 release after inflammasome priming and activation 22 was performed on bone marrow-derived macrophages (BMDM) from an AKRxDBA/2 strain intercross. -
Mechanical Ventilation in the Critically Ill Obese Patient
Mechanical Ventilation in the Critically Ill Obese Patient Antonio M. Esquinas Malcolm Lemyze Editors 123 Mechanical Ventilation in the Critically Ill Obese Patient Antonio M. Esquinas • Malcolm Lemyze Editors Mechanical Ventilation in the Critically Ill Obese Patient Editors Antonio M. Esquinas Malcolm Lemyze Intensive Care and Non Invasive Department Respiratory and CC Medicine Ventilatory Unit Schaffner Hospital Hospital Morales Meseguer Lens Murcia France Spain ISBN 978-3-319-49252-0 ISBN 978-3-319-49253-7 (eBook) https://doi.org/10.1007/978-3-319-49253-7 Library of Congress Control Number: 2017955688 © Springer International Publishing AG 2018 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. The use of general descriptive names, registered names, trademarks, service marks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. The publisher, the authors and the editors are safe to assume that the advice and information in this book are believed to be true and accurate at the date of publication. Neither the publisher nor the authors or the editors give a warranty, express or implied, with respect to the material contained herein or for any errors or omissions that may have been made. -
Differential Stromal Reprogramming in Benign and Malignant Naturally Occurring Canine Mammary Tumours Identifies Disease-Promoting Stromal Components
bioRxiv preprint doi: https://doi.org/10.1101/783621; this version posted September 26, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Differential stromal reprogramming in benign and malignant naturally occurring canine mammary tumours identifies disease-promoting stromal components Parisa Amini 1,a, Sina Nassiri 2,a, Alexandra Malbon 3,4 and Enni Markkanen 1,* 1 Institute of Veterinary Pharmacology and Toxicology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland 2 Bioinformatics Core Facility, SIB Swiss Institute of Bioinformatics, Lausanne, Switzerland 3 Institute of Veterinary Pathology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland 4 current address: The Royal (Dick) School of Veterinary Studies and The Roslin Institute Easter Bush Campus, Midlothian, EH25 9RG a these authors contributed equally to the manuscript * Correspondence: [email protected]; ORCID: 0000-0001-7780-8233 Keywords Laser-capture microdissection, canine mammary carcinoma, canine mammary adenoma, breast cancer, tumour stroma, tumour microenvironment Summary statement: RNasequencing-based analysis of stromal reprogramming between benign and malignant naturally occurring canine mammary tumours identifies potential molecular drivers in cancer-associated stroma that support tumour growth and malignancy. Abstract The importance of cancer-associated stroma (CaS) for initiation and progression of cancer is well accepted. However, as stromal changes in benign forms of naturally occurring tumours are poorly understood, it remains unclear how CaS from benign and malignant tumours compare. Spontaneous canine mammary tumours are viewed as excellent models of human mammary carcinomas (mCa). -
Ancient Hominins and the Species Question Erin Hurley Coastal Carolina University, [email protected]
Coastal Carolina University CCU Digital Commons Honors College and Center for Interdisciplinary Honors Theses Studies Winter 12-14-2018 Drawing the Line: Ancient Hominins and the Species Question Erin Hurley Coastal Carolina University, [email protected] Carolyn Dillian [email protected] Follow this and additional works at: https://digitalcommons.coastal.edu/honors-theses Part of the Biological and Physical Anthropology Commons Recommended Citation Hurley, Erin and Dillian, Carolyn, "Drawing the Line: Ancient Hominins and the Species Question" (2018). Honors Theses. 322. https://digitalcommons.coastal.edu/honors-theses/322 This Thesis is brought to you for free and open access by the Honors College and Center for Interdisciplinary Studies at CCU Digital Commons. It has been accepted for inclusion in Honors Theses by an authorized administrator of CCU Digital Commons. For more information, please contact [email protected]. Running head: DRAWAING THE LINE 1 Drawing the Line Ancient Hominins and the Species Question Erin Hurley Coastal Carolina University DRAWING THE LINE 2 Abstract The present paper asserts that groups such as Neandertals and Denisovans should be considered subspecies of H. sapiens. This contention is based upon the biological species concept and the fact that these groups interbred to create viable offspring. It is also stated that introgression from these groups made several positive contributions to the evolution of H. sapiens and their genome that may have served to promote the persistence of H. sapiens in Eurasia. DRAWING THE LINE 3 Drawing the Line: Ancient Hominins and the Species Question Since the first discoveries of fossil hominins, these “other” human-like creatures of the past have captivated the imagination. -
CEMIP Sirna (H): Sc-90061
SANTA CRUZ BIOTECHNOLOGY, INC. CEMIP siRNA (h): sc-90061 BACKGROUND STORAGE AND RESUSPENSION Encoding more than 700 genes, chromosome 15 is made up of approximately Store lyophilized siRNA duplex at -20° C with desiccant. Stable for at least 106 million base pairs and is about 3% of the human genome. Angelman and one year from the date of shipment. Once resuspended, store at -20° C, Prader-Willi syndromes are associated with loss of function or deletion of avoid contact with RNAses and repeated freeze thaw cycles. genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss Resuspend lyophilized siRNA duplex in 330 µl of the RNAse-free water is due to inactivity of the maternal 15q11-q13-encoded UBE3A gene in the provided. Resuspension of the siRNA duplex in 330 µl of RNAse-free water brain by either chromosomal deletion or mutation. In cases of Prader-Willi makes a 10 µM solution in a 10 µM Tris-HCl, pH 8.0, 20 mM NaCl, 1 mM syndrome, there is a partial or complete deletion of this region from the pater- EDTA buffered solution. nal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. APPLICATIONS Marfan syndrome is associated with chromosome 15 through the FBN1 gene. CEMIP siRNA (h) is recommended for the inhibition of CEMIP expression in REFERENCES human cells. 1. Hurowitz, G.I., et al. 1993. Neuropsychiatric aspects of adult-onset SUPPORT REAGENTS Tay-Sachs disease: two case reports with several new findings. -
A Unique and Specific Interaction Between Αt-Catenin and Plakophilin
2126 Research Article A unique and specific interaction between ␣T-catenin and plakophilin-2 in the area composita, the mixed-type junctional structure of cardiac intercalated discs Steven Goossens1,2,*, Barbara Janssens1,2,*,‡, Stefan Bonné1,2,§, Riet De Rycke1,2, Filip Braet1,2,¶, Jolanda van Hengel1,2 and Frans van Roy1,2,** 1Department for Molecular Biomedical Research, VIB and 2Department of Molecular Biology, Ghent University, B-9052 Ghent, Belgium *These authors contributed equally to this work ‡Present address: Wiley-VCH, Boschstrasse 12, D-69469 Weinheim, Germany §Present address: Diabetes Research Center, Brussels Free University (VUB), Laarbeeklaan 103, B-1090 Brussels, Belgium ¶Present address: Australian Key Centre for Microscopy and Microanalysis, The University of Sydney, NSW 2006, Australia **Author for correspondence (e-mail: [email protected]) Accepted 24 April 2007 Journal of Cell Science 120, 2126-2136 Published by The Company of Biologists 2007 doi:10.1242/jcs.004713 Summary Alpha-catenins play key functional roles in cadherin- desmosomal proteins in the heart localize not only to the catenin cell-cell adhesion complexes. We previously desmosomes in the intercalated discs but also at adhering reported on ␣T-catenin, a novel member of the ␣-catenin junctions with hybrid composition. We found that in the protein family. ␣T-catenin is expressed predominantly in latter junctions, endogenous plakophilin-2 colocalizes with cardiomyocytes, where it colocalizes with ␣E-catenin at the ␣T-catenin. By providing an extra link between the intercalated discs. Whether ␣T- and ␣E-catenin have cadherin-catenin complex and intermediate filaments, the specific or synergistic functions remains unknown. In this binding of ␣T-catenin to plakophilin-2 is proposed to be a study we used the yeast two-hybrid approach to identify means of modulating and strengthening cell-cell adhesion specific functions of ␣T-catenin.