Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

English (EN)·Polski (PL)·Ukraiński (UK)
Przejdź do strony domowej biblioteki Uniwersytet Ekonomiczny we Wrocławiu Link otwiera się w nowym oknie Logo biblioteki Prolib Integro - strona głównaUniwersytet Ekonomiczny we Wrocławiu

Wyszukujesz frazę ""Richardson CE"" wg kryterium: Autor

  Lista filtrów
Wyrównaj
    Wyświetlanie 1-19 z 19
    Tytuł:
    Obesity in post menopausal women with a family history of breast cancer: prevalence and risk awareness.
    Autorzy:
    Begum P
    Richardson CE
    Carmichael AR
    Pokaż więcej
    Źródło:
    International Seminars in Surgical Oncology; 2009, Vol. 6, p5p-5p, 1p
    Czasopismo naukowe
    Szczegóły
    Tytuł:
    Genetically targeted chemical assembly of functional materials in living cells, tissues, and animals.
    Autorzy:
    Liu J; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
    Kim YS; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.
    Richardson CE; Department of Biology, Stanford University, Stanford, CA 94305, USA.
    Tom A; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.
    Ramakrishnan C; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.
    Birey F; Department of Psychiatry, Stanford University, Stanford, CA 94305, USA.
    Katsumata T; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
    Chen S; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
    Wang C; Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley CA 94720, USA.
    Wang X; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.
    Joubert LM; Cell Sciences Imaging Facility, Stanford University, Stanford, CA 94305, USA.
    Jiang Y; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
    Wang H; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.
    Fenno LE; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.; Department of Psychiatry, Stanford University, Stanford, CA 94305, USA.
    Tok JB; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
    Pașca SP; Department of Psychiatry, Stanford University, Stanford, CA 94305, USA.
    Shen K; Department of Biology, Stanford University, Stanford, CA 94305, USA.; Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA.
    Bao Z; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA. .
    Deisseroth K; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA. .; Department of Psychiatry, Stanford University, Stanford, CA 94305, USA.; Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA.
    Pokaż więcej
    Źródło:
    Science (New York, N.Y.) [Science] 2020 Mar 20; Vol. 367 (6484), pp. 1372-1376.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
    MeSH Terms:
    Genetic Engineering*
    Aniline Compounds/*chemistry
    Ascorbate Peroxidases/*genetics
    Neurons/*physiology
    Nitro Compounds/*chemistry
    Phenylenediamines/*chemistry
    Polymers/*chemistry
    Action Potentials ; Animals ; Ascorbate Peroxidases/metabolism ; Caenorhabditis elegans ; Cell Membrane/metabolism ; Cell Survival ; Cells, Cultured ; Electric Conductivity ; HEK293 Cells ; Hippocampus ; Humans ; Membrane Potentials ; Mice ; Motor Neurons/physiology ; Muscle Cells/physiology ; Neurons/enzymology ; Patch-Clamp Techniques ; Polymers/metabolism ; Rats ; Transduction, Genetic
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    A hormone receptor pathway cell-autonomously delays neuron morphological aging by suppressing endocytosis.
    Autorzy:
    Richardson CE; Department of Biology, Stanford University, Stanford, California, United States of America.
    Yee C; Department of Biology, Stanford University, Stanford, California, United States of America.
    Shen K; Department of Biology, Stanford University, Stanford, California, United States of America.; Howard Hughes Medical Institute, Department of Biology, Stanford University, Stanford, California, United States of America.
    Pokaż więcej
    Źródło:
    PLoS biology [PLoS Biol] 2019 Oct 07; Vol. 17 (10), pp. e3000452. Date of Electronic Publication: 2019 Oct 07 (Print Publication: 2019).
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Caenorhabditis elegans/*genetics
    Caenorhabditis elegans Proteins/*genetics
    Diapause/*genetics
    Longevity/*genetics
    Neurons/*metabolism
    Receptors, Cytoplasmic and Nuclear/*genetics
    T-Lymphoma Invasion and Metastasis-inducing Protein 1/*genetics
    Animals ; Caenorhabditis elegans/growth & development ; Caenorhabditis elegans/metabolism ; Caenorhabditis elegans Proteins/metabolism ; Cellular Senescence/genetics ; Endocytosis/genetics ; Endosomes/metabolism ; Gene Expression Regulation, Developmental ; Genotype ; Neurons/cytology ; Receptors, Cytoplasmic and Nuclear/metabolism ; Signal Transduction ; T-Lymphoma Invasion and Metastasis-inducing Protein 1/metabolism
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Mutations in Nonessential eIF3k and eIF3l Genes Confer Lifespan Extension and Enhanced Resistance to ER Stress in Caenorhabditis elegans.
    Autorzy:
    Cattie DJ; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
    Richardson CE; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
    Reddy KC; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
    Ness-Cohn EM; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
    Droste R; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.; Howard Hughes Medical Institute, McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
    Thompson MK; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
    Gilbert WV; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
    Kim DH; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
    Pokaż więcej
    Źródło:
    PLoS genetics [PLoS Genet] 2016 Sep 30; Vol. 12 (9), pp. e1006326. Date of Electronic Publication: 2016 Sep 30 (Print Publication: 2016).
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
    MeSH Terms:
    Caenorhabditis elegans*/genetics
    Caenorhabditis elegans*/metabolism
    Caenorhabditis elegans Proteins/*genetics
    Endoplasmic Reticulum Stress/*genetics
    Eukaryotic Initiation Factor-3/*genetics
    Longevity/*genetics
    Microtubule-Associated Proteins/*genetics
    Adaptation, Physiological/genetics ; Aging/genetics ; Animals ; Animals, Genetically Modified ; Mutation ; Stress, Physiological/genetics
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Physiological IRE-1-XBP-1 and PEK-1 signaling in Caenorhabditis elegans larval development and immunity.
    Autorzy:
    Richardson CE; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
    Kinkel S
    Kim DH
    Pokaż więcej
    Źródło:
    PLoS genetics [PLoS Genet] 2011 Nov; Vol. 7 (11), pp. e1002391. Date of Electronic Publication: 2011 Nov 17.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural
    MeSH Terms:
    Caenorhabditis elegans/*growth & development
    Caenorhabditis elegans/*immunology
    Caenorhabditis elegans Proteins/*genetics
    Carrier Proteins/*genetics
    Cell Cycle Proteins/*genetics
    Immunity/*genetics
    MAP Kinase Kinase 1/*genetics
    Protein Serine-Threonine Kinases/*genetics
    Animals ; Caenorhabditis elegans/genetics ; Caenorhabditis elegans Proteins/metabolism ; Carrier Proteins/metabolism ; Cell Cycle Proteins/metabolism ; Endoplasmic Reticulum Stress/drug effects ; Endoplasmic Reticulum Stress/genetics ; Feedback, Physiological ; Gene Expression Regulation, Developmental ; Homeostasis/genetics ; Homeostasis/physiology ; Larva/genetics ; Larva/growth & development ; MAP Kinase Kinase 1/metabolism ; Mutant Proteins/genetics ; Mutant Proteins/metabolism ; Protein Serine-Threonine Kinases/metabolism ; Signal Transduction ; Temperature ; Tunicamycin/pharmacology ; Unfolded Protein Response/genetics ; Unfolded Protein Response/physiology
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Phosphorylation of the conserved transcription factor ATF-7 by PMK-1 p38 MAPK regulates innate immunity in Caenorhabditis elegans.
    Autorzy:
    Shivers RP; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
    Pagano DJ
    Kooistra T
    Richardson CE
    Reddy KC
    Whitney JK
    Kamanzi O
    Matsumoto K
    Hisamoto N
    Kim DH
    Pokaż więcej
    Źródło:
    PLoS genetics [PLoS Genet] 2010 Apr 01; Vol. 6 (4), pp. e1000892. Date of Electronic Publication: 2010 Apr 01.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Immunity, Innate*/genetics
    Activating Transcription Factors/*metabolism
    Caenorhabditis elegans/*enzymology
    Caenorhabditis elegans/*immunology
    Caenorhabditis elegans Proteins/*genetics
    Caenorhabditis elegans Proteins/*metabolism
    Mitogen-Activated Protein Kinases/*metabolism
    Transcription Factors/*genetics
    Transcription Factors/*metabolism
    Activating Transcription Factors/genetics ; Amino Acid Sequence ; Animals ; Caenorhabditis elegans/genetics ; Genes, Helminth ; Mitogen-Activated Protein Kinases/genetics ; Molecular Sequence Data ; Phosphorylation ; Phylogeny ; Sequence Alignment
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    An essential role for XBP-1 in host protection against immune activation in C. elegans.
    Autorzy:
    Richardson CE; Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
    Kooistra T
    Kim DH
    Pokaż więcej
    Źródło:
    Nature [Nature] 2010 Feb 25; Vol. 463 (7284), pp. 1092-5.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Genes, Essential*
    Caenorhabditis elegans/*immunology
    Caenorhabditis elegans Proteins/*metabolism
    Carrier Proteins/*metabolism
    Endoplasmic Reticulum/*pathology
    Immunity, Innate/*immunology
    Unfolded Protein Response/*physiology
    Animals ; Caenorhabditis elegans/growth & development ; Caenorhabditis elegans/microbiology ; Caenorhabditis elegans Proteins/genetics ; Caenorhabditis elegans Proteins/immunology ; Carrier Proteins/genetics ; Carrier Proteins/immunology ; Endoplasmic Reticulum/immunology ; Endoplasmic Reticulum/metabolism ; Enzyme Activation ; Humans ; Larva/growth & development ; Larva/immunology ; Larva/microbiology ; Mitogen-Activated Protein Kinases/immunology ; Mitogen-Activated Protein Kinases/metabolism ; Mutation/genetics ; Phenotype ; Protein Serine-Threonine Kinases/metabolism ; Pseudomonas aeruginosa/immunology ; Pseudomonas aeruginosa/pathogenicity ; Pseudomonas aeruginosa/physiology ; Survival Analysis ; Unfolded Protein Response/immunology
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Effect of semen on vaginal fluid cytokines and secretory leukocyte protease inhibitor.
    Autorzy:
    Agnew KJ; Department of Obstetrics and Gynecology, University of Washington, 1959 NE Pacific Street, Box 356460, Seattle, WA 98195, USA. />Aura J
    Nunez N
    Lee Z
    Lawler R
    Richardson CE
    Culhane J
    Hitti J
    Pokaż więcej
    Źródło:
    Infectious diseases in obstetrics and gynecology [Infect Dis Obstet Gynecol] 2008; Vol. 2008, pp. 820845.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Interleukins/*metabolism
    Secretory Leukocyte Peptidase Inhibitor/*metabolism
    Semen/*physiology
    Vaginal Discharge/*immunology
    Acid Phosphatase ; Adult ; Cohort Studies ; Coitus ; Enzyme-Linked Immunosorbent Assay/methods ; Female ; Humans ; Interleukin-1beta/analysis ; Interleukin-1beta/metabolism ; Interleukin-6/analysis ; Interleukin-6/metabolism ; Interleukin-8/analysis ; Interleukin-8/metabolism ; Interleukins/analysis ; Male ; Pregnancy ; Prospective Studies ; Secretory Leukocyte Peptidase Inhibitor/analysis ; Vagina/physiology
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
      Wyświetlanie 1-19 z 19

      Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies