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 ""Zeevi DA"" wg kryterium: Autor

  Lista filtrów
Wyrównaj
    Wyświetlanie 1-6 z 6
    Tytuł:
    SHaploseek is a sequencing-only, high-resolution method for comprehensive preimplantation genetic testing.
    Autorzy:
    Backenroth D; Braun School of Public Health and Community Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
    Altarescu G; PGT Unit, Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.; Faculty of Medicine, Hebrew University, Jerusalem, Israel.
    Zahdeh F; Translational Genomics Lab, Medical Genetics Institute, Shaare Zedek Medical Center, Bayit Str. 12, P.O.Box 3235, 91031, Jerusalem, Israel.
    Mann T; Translational Genomics Lab, Medical Genetics Institute, Shaare Zedek Medical Center, Bayit Str. 12, P.O.Box 3235, 91031, Jerusalem, Israel.
    Murik O; Translational Genomics Lab, Medical Genetics Institute, Shaare Zedek Medical Center, Bayit Str. 12, P.O.Box 3235, 91031, Jerusalem, Israel.
    Renbaum P; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Segel R; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Zeligson S; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Hakam-Spector E; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Carmi S; Braun School of Public Health and Community Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
    Zeevi DA; Translational Genomics Lab, Medical Genetics Institute, Shaare Zedek Medical Center, Bayit Str. 12, P.O.Box 3235, 91031, Jerusalem, Israel. .
    Pokaż więcej
    Źródło:
    Scientific reports [Sci Rep] 2023 Oct 21; Vol. 13 (1), pp. 18036. Date of Electronic Publication: 2023 Oct 21.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Preimplantation Diagnosis*/methods
    Pregnancy ; Female ; Child ; Humans ; Genetic Testing/methods ; Haplotypes ; Embryo, Mammalian ; High-Throughput Nucleotide Sequencing/methods ; DNA ; Aneuploidy ; Blastocyst
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Detection of single nucleotide and copy number variants in the Fabry disease-associated GLA gene using nanopore sequencing.
    Autorzy:
    Nowak A; Department of Endocrinology and Clinical Nutrition, University Hospital Zurich and University of Zurich, Zurich, Switzerland. .; Department of Internal Medicine, Psychiatry University Hospital Zurich, Zurich, Switzerland. .
    Murik O; Medical Genetics Institute and Translational Genomics Lab, Shaare Zedek Medical Center, Jerusalem, Israel.
    Mann T; Medical Genetics Institute and Translational Genomics Lab, Shaare Zedek Medical Center, Jerusalem, Israel.
    Zeevi DA; Medical Genetics Institute and Translational Genomics Lab, Shaare Zedek Medical Center, Jerusalem, Israel.
    Altarescu G; Medical Genetics Institute and Translational Genomics Lab, Shaare Zedek Medical Center, Jerusalem, Israel. .
    Pokaż więcej
    Źródło:
    Scientific reports [Sci Rep] 2021 Nov 16; Vol. 11 (1), pp. 22372. Date of Electronic Publication: 2021 Nov 16.
    Typ publikacji:
    Clinical Trial; Journal Article
    MeSH Terms:
    Base Sequence*
    Mutation, Missense*
    Polymorphism, Single Nucleotide*
    Sequence Deletion*
    Fabry Disease/*genetics
    alpha-Galactosidase/*genetics
    Adult ; High-Throughput Nucleotide Sequencing ; Humans ; Male ; Middle Aged
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Recommendation of premarital genetic screening in the Syrian Jewish community based on mutation carrier frequencies within Syrian Jewish cohorts.
    Autorzy:
    Zeevi DA; Dor Yeshorim, The Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel.
    Chung WK; Columbia University, New York, NY, USA.
    Levi C; Dor Yeshorim, The Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel.
    Scher SY; Dor Yeshorim, The Committee for Prevention of Jewish Genetic Diseases, Brooklyn, NY, USA.
    Bringer R; Dor Yeshorim, The Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel.
    Kahan Y; Dor Yeshorim, The Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel.
    Muallem H; Dor Yeshorim, The Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel.
    Benel R; Dor Yeshorim, The Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel.
    Hirsch Y; Dor Yeshorim, The Committee for Prevention of Jewish Genetic Diseases, Brooklyn, NY, USA.
    Weiden T; Dor Yeshorim, The Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel.
    Ekstein A; Dor Yeshorim, The Committee for Prevention of Jewish Genetic Diseases, Jerusalem, Israel.
    Ekstein J; Dor Yeshorim, The Committee for Prevention of Jewish Genetic Diseases, Brooklyn, NY, USA.
    Pokaż więcej
    Źródło:
    Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2021 Aug; Vol. 9 (8), pp. e1756. Date of Electronic Publication: 2021 Jul 20.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Gene Frequency*
    Practice Guidelines as Topic*
    Genetic Carrier Screening/*standards
    Genetic Diseases, Inborn/*genetics
    Jews/*genetics
    Genetic Carrier Screening/methods ; Genetic Carrier Screening/statistics & numerical data ; Genetic Counseling/standards ; Genetic Diseases, Inborn/diagnosis ; Genetic Diseases, Inborn/ethnology ; Humans ; Premarital Examinations/standards ; Syria
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    The utility of MALDI-TOF MS for outbreak investigation in the neonatal intensive care unit.
    Autorzy:
    Bar-Meir M; Infectious Diseases, Shaare-Zedek Medical Center, Jerusalem, Israel. .; Faculty of Medicine, Hebrew University, Jerusalem, Israel. .
    Berliner E; Pediatrics, Shaare-Zedek Medical Center, Jerusalem, Israel.
    Kashat L; The Microbiology Laboratory, Shaare-Zedek Medical Center, Jerusalem, Israel.
    Zeevi DA; Medical Genetics Institute - Shaare-Zedek Medical Center, Jerusalem, Israel.
    Assous MV; Faculty of Medicine, Hebrew University, Jerusalem, Israel.; The Microbiology Laboratory, Shaare-Zedek Medical Center, Jerusalem, Israel.
    Pokaż więcej
    Źródło:
    European journal of pediatrics [Eur J Pediatr] 2020 Dec; Vol. 179 (12), pp. 1843-1849. Date of Electronic Publication: 2020 Jun 10.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Intensive Care Units, Neonatal*
    Klebsiella Infections*/diagnosis
    Klebsiella pneumoniae*/genetics
    Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization*
    Disease Outbreaks ; Humans ; Infant, Newborn ; Multilocus Sequence Typing
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Noninvasive paternal exclusion testing for cystic fibrosis in the first five to eight weeks of gestation.
    Autorzy:
    Zeevi DA; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel. .
    Zahdeh F; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Kling Y; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Rosen T; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Renbaum P; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Ron-El R; Infertility and IVF Unit, Assaf Harofeh Medical Center, Zerifin, Israel.
    Eldar-Geva T; IVF Unit, Division of Obstetrics and Gynecology, Shaare Zedek Medical Center, Jerusalem, Israel.; Hebrew University Faculty of Medicine, Jerusalem, Israel.
    Holzer HEG; IVF Unit, Division of Obstetrics and Gynecology, Shaare Zedek Medical Center, Jerusalem, Israel.
    Levy-Lahad E; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.; Hebrew University Faculty of Medicine, Jerusalem, Israel.
    Altarescu G; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.; Hebrew University Faculty of Medicine, Jerusalem, Israel.
    Pokaż więcej
    Źródło:
    Scientific reports [Sci Rep] 2018 Oct 29; Vol. 8 (1), pp. 15941. Date of Electronic Publication: 2018 Oct 29.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Cystic Fibrosis/*diagnosis
    Cystic Fibrosis Transmembrane Conductance Regulator/*genetics
    Genetic Testing/*methods
    Prenatal Diagnosis/*methods
    Alleles ; Cystic Fibrosis/genetics ; DNA/chemistry ; DNA/isolation & purification ; DNA/metabolism ; Female ; Genotype ; Gestational Age ; Haplotypes ; High-Throughput Nucleotide Sequencing ; Humans ; Male ; Polymorphism, Single Nucleotide ; Pregnancy ; Sequence Analysis, DNA
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) Repair.
    Autorzy:
    Gazy I; Human Genetics, Hebrew University Medical School, Jerusalem, Israel; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Zeevi DA; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Renbaum P; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Zeligson S; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Eini L; Department of Genetics, Alexander Silberman Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel.
    Bashari D; The Mina and Everard Goodman Faculty of Life Science, Bar Ilan University, Ramat Gan, Israel.
    Smith Y; Genomic Data Analysis Unit, Hebrew University Medical School, Jerusalem, Israel.
    Lahad A; Department of Family Medicine, Hebrew University Medical School, Jerusalem, Israel; Clalit Health Services, Jerusalem, Israel.
    Goldberg M; Department of Genetics, Alexander Silberman Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel.
    Ginsberg D; The Mina and Everard Goodman Faculty of Life Science, Bar Ilan University, Ramat Gan, Israel.
    Levy-Lahad E; Human Genetics, Hebrew University Medical School, Jerusalem, Israel; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.
    Pokaż więcej
    Źródło:
    PloS one [PLoS One] 2015 Jul 31; Vol. 10 (7), pp. e0134120. Date of Electronic Publication: 2015 Jul 31 (Print Publication: 2015).
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    DNA Repair*
    RNA, Long Noncoding/*genetics
    Rad51 Recombinase/*genetics
    DNA Damage ; Humans ; Rad51 Recombinase/physiology
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
      Wyświetlanie 1-6 z 6

      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