Resultats de la cerca - David Gurwitz

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  1. 1
    Angiotensin receptor blockers as tentative SARS‐CoV‐2 therapeutics

    Angiotensin receptor blockers as tentative SARS‐CoV‐2 therapeutics per David Gurwitz

    Publicat 2020
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  2. 2
    Estradiol reduces <scp><i>ACE2</i></scp> and <scp><i>TMPRSS2</i> mRNA</scp> levels in <scp>A549</scp> human lung epithelial cells

    Estradiol reduces <scp><i>ACE2</i></scp> and <scp><i>TMPRSS2</i> mRNA</scp> levels in <scp>A549</scp> human lung epithelial cells per Gabriele Baristaite, David Gurwitz

    Publicat 2022
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  3. 3
    Personal genomics services: whose genomes?

    Personal genomics services: whose genomes? per David Gurwitz, Yael Bregman-Eschet

    Publicat 2009
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  4. 4
    Thrombin modulates and reverses neuroblastoma neurite outgrowth.

    Thrombin modulates and reverses neuroblastoma neurite outgrowth. per David Gurwitz, Dennis D. Cunningham

    Publicat 1988
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  5. 5
    Effects of age and sex on recovery from COVID-19: Analysis of 5769 Israeli patients

    Effects of age and sex on recovery from COVID-19: Analysis of 5769 Israeli patients per Irena Voinsky, Gabriele Baristaite, David Gurwitz

    Publicat 2020
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  6. 6
    Ethnic differences in alpha‐1 antitrypsin deficiency allele frequencies may partially explain national differences in COVID‐19 fatality rates

    Ethnic differences in alpha‐1 antitrypsin deficiency allele frequencies may partially explain national differences in COVID‐19 fatality rates per Guy Shapira, Noam Shomron, David Gurwitz

    Publicat 2020
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  7. 7
    Pharmacogenetics in Europe: Barriers and Opportunities

    Pharmacogenetics in Europe: Barriers and Opportunities per David Gurwitz, Eleni Zika, Michael M. Hopkins, Sibylle Gaisser, Dolores Ibarreta

    Publicat 2009
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  8. 8
    Machine Learning-Based Blood RNA Signature for Diagnosis of Autism Spectrum Disorder

    Machine Learning-Based Blood RNA Signature for Diagnosis of Autism Spectrum Disorder per Irena Voinsky, Oleg Y. Fridland, Adi Aran, Richard E. Frye, David Gurwitz

    Publicat 2023
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  9. 9
    Genome-wide expression profiling of human lymphoblastoid cell lines implicates integrin beta-3 in the mode of action of antidepressants

    Genome-wide expression profiling of human lymphoblastoid cell lines implicates integrin beta-3 in the mode of action of antidepressants per Keren Oved, Ayelet Morag, Metsada Pasmanik‐Chor, Moshe Rehavi, Noam Shomron, David Gurwitz

    Publicat 2013
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  10. 10
    Assessment of pharmacogenetic tests: presenting measures of clinical validity and potential population impact in association studies

    Assessment of pharmacogenetic tests: presenting measures of clinical validity and potential population impact in association studies per Elisa C.M. Tonk, David Gurwitz, Anke H. Maitland‐van der Zee, A. Cecile J.W. Janssens

    Publicat 2016
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  11. 11
    Protease nexin-1, an antithrombin with neurite outgrowth activity, is reduced in Alzheimer disease.

    Protease nexin-1, an antithrombin with neurite outgrowth activity, is reduced in Alzheimer disease. per Steven L. Wagner, James W. Geddes, CW Cotman, Alice Lau, David Gurwitz, Paul J. Isackson, Dennis D. Cunningham

    Publicat 1989
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  12. 12
    Identification of thioredoxin-interacting protein (TXNIP) as a downstream target for IGF1 action

    Identification of thioredoxin-interacting protein (TXNIP) as a downstream target for IGF1 action per Karthik Nagaraj, Lena Lapkina-Gendler, Rive Sarfstein, David Gurwitz, Metsada Pasmanik‐Chor, Zvi Laron, Shoshana Yakar, Haim Werner

    Publicat 2018
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  13. 13
    The EU-ADR corpus: Annotated drugs, diseases, targets, and their relationships

    The EU-ADR corpus: Annotated drugs, diseases, targets, and their relationships per Erik M. van Mulligen, Annie Fourrier‐Réglat, David Gurwitz, Mariam Molokhia, Ainhoa Nieto, Gianluca Trifirõ, Jan A. Kors, Laura I. Furlong

    Publicat 2012
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  14. 14
    SIRT1, miR-132 and miR-212 link human longevity to Alzheimer’s Disease

    SIRT1, miR-132 and miR-212 link human longevity to Alzheimer’s Disease per Adva Hadar, Elena Milanesi, Marta Walczak, Monika Puzianowska‐Kuźnicka, Jacek Kuźnicki, Alessio Squassina, Paola Niola, Caterina Chillotti, Johannes Attems, Illana Gozes, David Gurwitz

    Publicat 2018
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  15. 15
    Discovery of autism/intellectual disability somatic mutations in Alzheimer's brains: mutated ADNP cytoskeletal impairments and repair as a case study

    Discovery of autism/intellectual disability somatic mutations in Alzheimer's brains: mutated ADNP cytoskeletal impairments and repair as a case study per Yanina Ivashko‐Pachima, Adva Hadar, Iris Grigg, Vlasta Korenková, Oxana Kapitansky, Gidon Karmon, Michael Gershovits, Carmen Laura Sayas, R. Frank Kooy, Johannes Attems, David Gurwitz, Illana Gozes

    Publicat 2019
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  16. 16
    Ethnicity-Related Polymorphisms and Haplotypes in the Human <i>ABCB1</i> Gene

    Ethnicity-Related Polymorphisms and Haplotypes in the Human <i>ABCB1</i> Gene per Chava Kimchi‐Sarfaty, Andrew Marple, Shiri Shinar, Avraham M Kimchi, David Scavo, M Isabella Roma, In‐Wha Kim, Adam P. Jones, Mili Arora, John J. Gribar, David Gurwitz, Michael M. Gottesman

    Publicat 2006
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  17. 17
    MtDNA evidence for a genetic bottleneck in the early history of the Ashkenazi Jewish population

    MtDNA evidence for a genetic bottleneck in the early history of the Ashkenazi Jewish population per Doron M. Behar, Michael F. Hammer, Daniel Garrigan, Richard Villems, Batsheva Bonné‐Tamir, Martin Richards, David Gurwitz, Dror Rosengarten, Matthew E. Kaplan, Sergio Della Pergola, Lluís Quintana‐Murci, Karl Skorecki

    Publicat 2004
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  18. 18
    Counting the Founders: The Matrilineal Genetic Ancestry of the Jewish Diaspora

    Counting the Founders: The Matrilineal Genetic Ancestry of the Jewish Diaspora per Doron M. Behar, Ene Metspalu, Toomas Kivisild, Saharon Rosset, Shay Tzur, Yarin Hadid, Guennady Yudkovsky, Dror Rosengarten, Luı́sa Pereira, António Amorim, Ildus Kutuev, David Gurwitz, Batsheva Bonné‐Tamir, Richard Villems, Karl Skorecki

    Publicat 2008
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  19. 19
    Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families

    Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families per Hashem Shahin, Tom Walsh, Amal Abu Rayyan, Ming K. Lee, Jake Higgins, Diane E. Dickel, Kristen Lewis, James Thompson, Carl Baker, Alex S. Nord, Sunday M. Stray, David Gurwitz, Karen B. Avraham, Mary‐Claire King, Moien Kanaan

    Publicat 2009
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  20. 20
    Ancestry inference of 96 population samples using microhaplotypes

    Ancestry inference of 96 population samples using microhaplotypes per Özlem Bülbül, A.J. Pakstis, Usha Soundararajan, Cemal Gürkan, Jane E. Brissenden, Janet Roscoe, Baigalmaa Evsanaa, Ariunaa Togtokh, Peristera Paschou, Elena L. Grigorenko, David Gurwitz, Sharon Wootton, Robert Lagacé, Joseph Chang, William C. Speed, Kenneth K. Kídd

    Publicat 2017
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