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 ""Liehr, T."" wg kryterium: Autor

  Lista filtrów
Wyrównaj
Wyświetlanie 1-20 z 179
Tytuł:
Thoughts on the Etiology of Cherubism.
Autorzy:
Hyckel P; Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, 07747 Jena, Germany.
Liehr T; Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, 07747 Jena, Germany.
Pokaż więcej
Źródło:
Journal of clinical medicine [J Clin Med] 2024 Apr 03; Vol. 13 (7). Date of Electronic Publication: 2024 Apr 03.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Chromosomes of Asian cyprinid fishes: Novel insight into the chromosomal evolution of Labeoninae (Teleostei, Cyprinidae).
Autorzy:
Khensuwan S; Department of Biology, Faculty of Science, Khon Kaen University, Muang, Khon Kaen, Thailand.
de Menezes Cavalcante Sassi F; Departamento de Genética e Evolução, Laboratório de Citogenética de Peixes, Universidade Federal de São Carlos, São Carlos, São Paulo, Brazil.
Rosa de Moraes RL; Departamento de Genética e Evolução, Laboratório de Citogenética de Peixes, Universidade Federal de São Carlos, São Carlos, São Paulo, Brazil.
Rab P; Institute of Animal Physiology and Genetics, Laboratory of Fish Genetics, Czech Academy of Sciences, Rumburská, Liběchov, Czech Republic.
Liehr T; Institute of Human Genetics, University Hospital Jena, Jena, Germany.
Supiwong W; Faculty of Interdisciplinary Studies, Khon Kaen University, Nong Khai Campus, Muang, Nong Khai, Thailand.
Seetapan K; School of Agriculture and Natural Resources, University of Phayao, Tumbol Maeka, Muang, Phayao, Thailand.
Tanomtong A; Department of Biology, Faculty of Science, Khon Kaen University, Muang, Khon Kaen, Thailand.
Tantisuwichwong N; Department of Biology, Faculty of Science, Khon Kaen University, Muang, Khon Kaen, Thailand.
Arunsang S; Program in Animal Science, Faculty of Agricultural Technology and Agro-Industry, Rajamangala University of Technology Suvarnabhumi, Phra Nakhon Si Ayutthaya, Ayutthaya, Thailand.
Buasriyot P; Faculty of Science and Technology, Rajamangala University of Technology Suvarnabhumi, Mueang Nonthaburi, Nonthaburi, Thailand.
Tongnunui S; Department of Conservation Biology, Mahidol University, Kanchanburi Campus, Sai Yok, Kanchanaburi Province, Thailand.
Cioffi MB; Departamento de Genética e Evolução, Laboratório de Citogenética de Peixes, Universidade Federal de São Carlos, São Carlos, São Paulo, Brazil.
Pokaż więcej
Źródło:
PloS one [PLoS One] 2024 Feb 07; Vol. 19 (2), pp. e0292689. Date of Electronic Publication: 2024 Feb 07 (Print Publication: 2024).
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes*/genetics
Cyprinidae*/genetics
Animals ; Phylogeny ; Karyotype ; Chromosome Aberrations ; DNA, Ribosomal/genetics ; Thailand ; Evolution, Molecular
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Homeology of sex chromosomes in Amazonian Harttia armored catfishes supports the X-fission hypothesis for the X 1 X 2 Y sex chromosome system origin.
Autorzy:
de Menezes Cavalcante Sassi F; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, SP, 13565-905, Brazil.
Sember A; Laboratory of Fish Genetics, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, Rumburská, 89, Liběchov, Czech Republic.
Deon GA; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, SP, 13565-905, Brazil.
Liehr T; Institut für Humangenetik, Universitätsklinikum Jena, 07747, Jena, Germany. thomas.liehr@med-uni.jena.de.
Padutsch N; Institut für Humangenetik, Universitätsklinikum Jena, 07747, Jena, Germany.
Oyakawa OT; Museu de Zoologia, Universidade de São Paulo, São Paulo, SP, 04263-000, Brazil.
Vicari MR; Departamento de Biologia Estrutural, Molecular e Genética, Universidade Estadual de Ponta Grossa, Ponta Grossa, PR, Brazil.
Bertollo LAC; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, SP, 13565-905, Brazil.
Moreira-Filho O; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, SP, 13565-905, Brazil.
de Bello Cioffi M; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, SP, 13565-905, Brazil.
Pokaż więcej
Źródło:
Scientific reports [Sci Rep] 2023 Sep 21; Vol. 13 (1), pp. 15756. Date of Electronic Publication: 2023 Sep 21.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Catfishes*/genetics
Animals ; In Situ Hybridization, Fluorescence ; Phylogeny ; Sex Chromosomes/genetics ; Y Chromosome
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The Diagnostic, Prognostic, and Therapeutic Potential of Cell-Free DNA with a Special Focus on COVID-19 and Other Viral Infections.
Autorzy:
Hovhannisyan G; Department of Genetics and Cytology, Yerevan State University, Alex Manoogian 1, Yerevan 0025, Armenia.
Harutyunyan T; Department of Genetics and Cytology, Yerevan State University, Alex Manoogian 1, Yerevan 0025, Armenia.
Aroutiounian R; Department of Genetics and Cytology, Yerevan State University, Alex Manoogian 1, Yerevan 0025, Armenia.
Liehr T; Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Am Klinikum 1, 07747 Jena, Germany.
Pokaż więcej
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Sep 15; Vol. 24 (18). Date of Electronic Publication: 2023 Sep 15.
Typ publikacji:
Journal Article; Review
MeSH Terms:
COVID-19*/diagnosis
Cell-Free Nucleic Acids*
Virus Diseases*
Body Fluids*
Humans ; Prognosis ; COVID-19 Testing
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Chromosomal Rearrangements and Satellite DNAs: Extensive Chromosome Reshuffling and the Evolution of Neo-Sex Chromosomes in the Genus Pyrrhulina (Teleostei; Characiformes).
Autorzy:
de Moraes RLR; Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos 13565-905, SP, Brazil.; Institute of Human Genetics, University Hospital Jena, 07747 Jena, Germany.
de Menezes Cavalcante Sassi F; Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos 13565-905, SP, Brazil.; Institute of Human Genetics, University Hospital Jena, 07747 Jena, Germany.
Vidal JAD; Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos 13565-905, SP, Brazil.
Goes CAG; Faculdade de Ciências, UNESP, Bauru 17033-36, SP, Brazil.
Dos Santos RZ; Faculdade de Ciências, UNESP, Bauru 17033-36, SP, Brazil.
Stornioli JHF; Institute of Biological Sciences and Health, Universidade Federal Rural do Rio de Janeiro, Seropédica 23890-000, RJ, Brazil.
Porto-Foresti F; Faculdade de Ciências, UNESP, Bauru 17033-36, SP, Brazil.
Liehr T; Institute of Human Genetics, University Hospital Jena, 07747 Jena, Germany.
Utsunomia R; Faculdade de Ciências, UNESP, Bauru 17033-36, SP, Brazil.
de Bello Cioffi M; Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos 13565-905, SP, Brazil.; Institute of Human Genetics, University Hospital Jena, 07747 Jena, Germany.
Pokaż więcej
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Sep 04; Vol. 24 (17). Date of Electronic Publication: 2023 Sep 04.
Typ publikacji:
Journal Article
MeSH Terms:
Characiformes*
Animals ; DNA, Satellite/genetics ; Sex Chromosomes/genetics ; Chromosome Aberrations ; Karyotyping
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Cytogenetics Meets Genomics: Cytotaxonomy and Genomic Relationships among Color Variants of the Asian Arowana Scleropages formosus .
Autorzy:
Toma GA; Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos 13565-905, SP, Brazil.
Dos Santos N; Faculdade de Ciências, UNESP, Bauru 17033-36, SP, Brazil.
Dos Santos R; Faculdade de Ciências, UNESP, Bauru 17033-36, SP, Brazil.
Rab P; Laboratory of Fish Genetics, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, Rumburská 89, 27721 Liběchov, Czech Republic.
Kretschmer R; Departamento de Ecologia, Zoologia e Genética, Universidade Federal de Pelotas, Pelotas 96010-900, RS, Brazil.
Ezaz T; Institute for Aplied Ecology, University of Canberra, Canberra 2617, Australia.
Bertollo LAC; Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos 13565-905, SP, Brazil.
Liehr T; Institute of Human Genetics, University Hospital Jena, 07747 Jena, Germany.
Porto-Foresti F; Faculdade de Ciências, UNESP, Bauru 17033-36, SP, Brazil.
Hatanaka T; Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos 13565-905, SP, Brazil.
Tanomtong A; Department of Biology, Faculty of Science, Khon Kaen University, Muang, Khon Kaen 40002, Thailand.
Utsunomia R; Faculdade de Ciências, UNESP, Bauru 17033-36, SP, Brazil.
Cioffi MB; Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos 13565-905, SP, Brazil.
Pokaż więcej
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 May 19; Vol. 24 (10). Date of Electronic Publication: 2023 May 19.
Typ publikacji:
Journal Article
MeSH Terms:
Genome*
Genomics*
Animals ; Fishes/genetics ; Karyotype ; Cytogenetic Analysis
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Giant Sex Chromosomes in Omophoita Species (Coleoptera, Chrysomelidae): Structural and Evolutionary Relationships Revealed by Zoo-FISH and Comparative Genomic Hybridization (CGH).
Autorzy:
Vidal JAD; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos (UFSCar), Rodovia Washington Luiz Km. 235, C.P. 676, São Carlos 13565-905, Brazil.; Laboratório de Genética e Evolução, Departamento de Biologia Estrutural Molecular e Genética, Universidade Estadual de Ponta Grossa (UEPG), Av. Carlos Cavalcanti, 4748, Ponta Grossa 84030-900, Brazil.
Sassi FMC; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos (UFSCar), Rodovia Washington Luiz Km. 235, C.P. 676, São Carlos 13565-905, Brazil.
de Moraes RLR; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos (UFSCar), Rodovia Washington Luiz Km. 235, C.P. 676, São Carlos 13565-905, Brazil.
Artoni RF; Laboratório de Genética e Evolução, Departamento de Biologia Estrutural Molecular e Genética, Universidade Estadual de Ponta Grossa (UEPG), Av. Carlos Cavalcanti, 4748, Ponta Grossa 84030-900, Brazil.
Liehr T; Institute of Human Genetics, University Hospital Jena, 07747 Jena, Germany.
Cioffi MB; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos (UFSCar), Rodovia Washington Luiz Km. 235, C.P. 676, São Carlos 13565-905, Brazil.; Institute of Human Genetics, University Hospital Jena, 07747 Jena, Germany.
de Almeida MC; Laboratório de Genética e Evolução, Departamento de Biologia Estrutural Molecular e Genética, Universidade Estadual de Ponta Grossa (UEPG), Av. Carlos Cavalcanti, 4748, Ponta Grossa 84030-900, Brazil.
Pokaż więcej
Źródło:
Insects [Insects] 2023 May 04; Vol. 14 (5). Date of Electronic Publication: 2023 May 04.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Chromosomes of Asian Cyprinid Fishes: Genomic Differences in Conserved Karyotypes of 'Poropuntiinae' (Teleostei, Cyprinidae).
Autorzy:
Khensuwan S; Department of Biology, Faculty of Science, Khon Kaen University, Muang, Khon Kaen 40002, Thailand.
Sassi FMC; Departamento de Genética e Evolução, Universidade Federal de São Carlos (UFSCar), Rodovia Washington Luiz Km. 235, C.P. 676, São Carlos 13565-905, Brazil.
Moraes RLR; Departamento de Genética e Evolução, Universidade Federal de São Carlos (UFSCar), Rodovia Washington Luiz Km. 235, C.P. 676, São Carlos 13565-905, Brazil.
Jantarat S; Department of Science, Faculty of Science and Technology, Prince of Songkla University, Pattani 94000, Thailand.
Seetapan K; School of Agriculture and Natural Resources, University of Phayao, Tumbol Maeka, Muang, Phayao 56000, Thailand.
Phintong K; Department of Fundamental Science, Faculty of Science and Technology, Surindra Rajabhat University, Muang, Surin 32000, Thailand.
Thongnetr W; Division of Biology, Department of Science, Faculty of Science and Technology, Rajamangala University of Technology Krungthep, Bangkok 10120, Thailand.
Kaewsri S; Program in Biology, Faculty of Science, Buriram Rajabhat University, Muang, Buriram 31000, Thailand.
Jumrusthanasan S; Program in Biology, Faculty of Science, Buriram Rajabhat University, Muang, Buriram 31000, Thailand.
Supiwong W; Faculty of Applied Science and Engineering, Khon Kaen University, Nong Khai Campus, Muang, Nong Khai 43000, Thailand.
Rab P; Laboratory of Fish Genetics, Institute of Animal Physiology and Genetics, Czech Academy of Sciences, Rumburská 89, 277 21 Liběchov, Czech Republic.
Tanomtong A; Department of Biology, Faculty of Science, Khon Kaen University, Muang, Khon Kaen 40002, Thailand.
Liehr T; Institute of Human Genetics, University Hospital Jena, 07747 Jena, Germany.
Cioffi MB; Departamento de Genética e Evolução, Universidade Federal de São Carlos (UFSCar), Rodovia Washington Luiz Km. 235, C.P. 676, São Carlos 13565-905, Brazil.
Pokaż więcej
Źródło:
Animals : an open access journal from MDPI [Animals (Basel)] 2023 Apr 20; Vol. 13 (8). Date of Electronic Publication: 2023 Apr 20.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Functional Characterization of Transgenic Mice Overexpressing Human 15-Lipoxygenase-1 (ALOX15) under the Control of the aP2 Promoter.
Autorzy:
Heydeck D; Department of Biochemistry, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, Charitéplatz 1, D-10117 Berlin, Germany.
Ufer C; Department of Biochemistry, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, Charitéplatz 1, D-10117 Berlin, Germany.
Kakularam KR; Department of Biochemistry, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, Charitéplatz 1, D-10117 Berlin, Germany.
Rothe M; Lipidomix GmbH, Robert-Roessle-Str. 10, D-13125 Berlin, Germany.
Liehr T; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Am Klinikum 1, D-07747 Jena, Germany.
Poulain P; Genfit, Parc Eurasanté 885, Avenue Eugène Avinée, 59120 Loos, France.
Kuhn H; Department of Biochemistry, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, Charitéplatz 1, D-10117 Berlin, Germany.
Pokaż więcej
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Mar 02; Vol. 24 (5). Date of Electronic Publication: 2023 Mar 02.
Typ publikacji:
Journal Article
MeSH Terms:
Arachidonate 15-Lipoxygenase*/genetics
Arachidonate 15-Lipoxygenase*/metabolism
Tandem Mass Spectrometry*
Gene Expression*
Adult ; Animals ; Humans ; Mice ; Arachidonate 12-Lipoxygenase/metabolism ; Chromatography, Liquid ; In Situ Hybridization, Fluorescence ; Mice, Transgenic
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Molecular cytogenetic and phenotypic characterization of Phelan McDermid and 22q13 duplication syndrome: a case report.
Autorzy:
Khalifa Y; Department of Pediatrics, Bahrain Defence Force Hospital, Riffa, Kingdom of Bahrain.
Hassan HY; Banoon ART and Cytogenetics Centre, Bahrain Defence Force Hospital, P.O. Box: 28743, Riffa, Kingdom of Bahrain. .
Weise A; University Hospital Jena, Friedrich, Jena, Germany.
Liehr T; University Hospital Jena, Friedrich, Jena, Germany.
Alkhayyat H; Department of Pediatrics, Bahrain Defence Force Hospital, Riffa, Kingdom of Bahrain.
Pokaż więcej
Źródło:
Molecular cytogenetics [Mol Cytogenet] 2022 Dec 17; Vol. 15 (1), pp. 52. Date of Electronic Publication: 2022 Dec 17.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Intrachromosomal amplification of BCR expressed as homogenously staining region (hsr) in a case of acute myeloid leukemia with myelodysplasia-related changes.
Autorzy:
Mohanty P; Department of Cancer Cytogenetics, Advanced Centre for Treatment, Research and Education in Cancer (ACTREC), Tata Memorial Center, Navi Mumbai, India.
Shetty D; Department of Cancer Cytogenetics, Advanced Centre for Treatment, Research and Education in Cancer (ACTREC), Tata Memorial Center, Navi Mumbai, India.; Homi Bhabha National Institute (HBNI), Training School Complex, Mumbai, India.
Liehr T; Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Jena, Germany.
Mrasek K; Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Jena, Germany.
Khattry N; Homi Bhabha National Institute (HBNI), Training School Complex, Mumbai, India.; Department of Medical Oncology, Advanced Centre for Treatment, Research and Education in Cancer (ACTREC), Tata Memorial Centre, Navi Mumbai, India.
Pokaż więcej
Źródło:
International journal of laboratory hematology [Int J Lab Hematol] 2022 Dec; Vol. 44 (6), pp. 993-994. Date of Electronic Publication: 2022 May 09.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Myelodysplastic Syndromes*/genetics
Leukemia, Myeloid, Acute*/genetics
Humans ; Chromosome Aberrations ; Staining and Labeling
Raport
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Molecular combing and its application in clinical settings.
Autorzy:
Wang Y; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Am Klinikum 1, 07747, Jena, Germany.; Jinze Group Beijing Jinze Medical Laboratory, Building A, National Engineering Center for Protein Drugs, Building 1, 33 Science Park Road, Huilongguan Town, Changping District, Beijing, 1F, China.
Kumar KR; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Am Klinikum 1, 07747, Jena, Germany.
Liehr T; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Am Klinikum 1, 07747, Jena, Germany. Thomas.Liehr@med.uni-jena.de.
Pokaż więcej
Źródło:
Molecular cytogenetics [Mol Cytogenet] 2022 Nov 16; Vol. 15 (1), pp. 50. Date of Electronic Publication: 2022 Nov 16.
Typ publikacji:
Journal Article; Review
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The role of Calmodulin Binding Transcription Activator 1 (CAMTA1) gene and its putative genetic partners in the human nervous system.
Autorzy:
Alves G; Circulating Biomarkers Laboratory, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Ornellas MH; Circulating Biomarkers Laboratory, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Liehr T; Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Jena, Germany.
Pokaż więcej
Źródło:
Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society [Psychogeriatrics] 2022 Nov; Vol. 22 (6), pp. 869-878. Date of Electronic Publication: 2022 Aug 10.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Trans-Activators*/genetics
Trans-Activators*/metabolism
Neuroblastoma*/genetics
Neuroblastoma*/metabolism
Neuroblastoma*/pathology
Humans ; Calcium-Binding Proteins/genetics ; Calcium-Binding Proteins/metabolism ; Calmodulin/metabolism ; Nervous System/metabolism ; Nervous System/pathology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Partial Reduction in BRCA1 Gene Dose Modulates DNA Replication Stress Level and Thereby Contributes to Sensitivity or Resistance.
Autorzy:
Classen S; Laboratory of Radiobiology and Experimental Radiooncology, Center of Oncology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Rahlf E; Laboratory of Radiobiology and Experimental Radiooncology, Center of Oncology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Jungwirth J; Project Group Biochemistry, Leibniz Institute on Aging-Fritz Lipmann Institute, 07745 Jena, Germany.
Albers N; Laboratory of Radiobiology and Experimental Radiooncology, Center of Oncology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Hebestreit LP; Laboratory of Radiobiology and Experimental Radiooncology, Center of Oncology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Zielinski A; Laboratory of Radiobiology and Experimental Radiooncology, Center of Oncology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Poole L; Laboratory of Radiobiology and Experimental Radiooncology, Center of Oncology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Groth M; CF Next-Generation Sequencing, Leibniz Institute on Aging-Fritz Lipmann Institute, Beutenbergstrasse 11, 07745 Jena, Germany.
Koch P; CF Life Science Computing, Leibniz Institute on Aging-Fritz Lipmann Institute, Beutenbergstrasse 11, 07745 Jena, Germany.
Liehr T; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Am Klinikum 1, 07747 Jena, Germany.
Kankel S; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Am Klinikum 1, 07747 Jena, Germany.
Cordes N; OncoRay-National Center for Radiation Research in Oncology, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, Fetscherstr. 74, PF 41, 01307 Dresden, Germany.; National Center for Tumor Diseases, Partner Site Dresden: German Cancer Research Center, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.; Department of Radiotherapy and Radiation Oncology, University Hospital Carl Gustav Carus, Technische Universität Dresden, Fetscherstr. 74, PF 50, 01307 Dresden, Germany.; Helmholtz-Zentrum Dresden-Rossendorf, Institute of Radiooncology-OncoRay, Bautzner Landstr. 400, 01328 Dresden, Germany.; German Cancer Consortium (DKTK), Partner Site Dresden, and German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69192 Heidelberg, Germany.
Petersen C; Department of Radiotherapy and Radiooncology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Rothkamm K; Laboratory of Radiobiology and Experimental Radiooncology, Center of Oncology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Pospiech H; Project Group Biochemistry, Leibniz Institute on Aging-Fritz Lipmann Institute, 07745 Jena, Germany.; Faculty of Biochemistry and Molecular Medicine, University of Oulu, 90014 Oulu, Finland.
Borgmann K; Laboratory of Radiobiology and Experimental Radiooncology, Center of Oncology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Pokaż więcej
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Nov 01; Vol. 23 (21). Date of Electronic Publication: 2022 Nov 01.
Typ publikacji:
Journal Article
MeSH Terms:
Genes, BRCA1*
Breast Neoplasms*/genetics
Breast Neoplasms*/drug therapy
Humans ; Female ; Cell Line, Tumor ; BRCA1 Protein/genetics ; BRCA1 Protein/metabolism ; Homologous Recombination ; DNA Repair/genetics ; DNA Replication ; DNA Damage
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Chromosomal Heteromorphisms and Cancer Susceptibility Revisited.
Autorzy:
Liehr T; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, 07747 Jena, Germany.
Pokaż więcej
Źródło:
Cells [Cells] 2022 Oct 15; Vol. 11 (20). Date of Electronic Publication: 2022 Oct 15.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Repetitive Sequences, Nucleic Acid*
Neoplasms*/genetics
Humans ; DNA ; DNA Copy Number Variations/genetics ; RNA
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability.
Autorzy:
El Amrani Z; RABAT Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
Elalaoui SC; RABAT Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
Jdioui W; médicale, Centre des consultations et des explorations externes, Hopital d'enfants, CHU Ibn SinaConsultation de génétique, Rabat, Marocco.
Sbiti A; RABAT Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
Ratbi I; RABAT Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
Liehr T; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Jena, Germany.
Sefiani A; RABAT Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
Natiq A; RABAT Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.; Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.
Pokaż więcej
Źródło:
Ophthalmic genetics [Ophthalmic Genet] 2022 Oct; Vol. 43 (5), pp. 689-692. Date of Electronic Publication: 2022 Jun 06.
Typ publikacji:
Journal Article
MeSH Terms:
Intellectual Disability*/genetics
Retinal Neoplasms*/genetics
Retinoblastoma*/genetics
Retinoblastoma*/pathology
Chromosome Aberrations ; Chromosome Deletion ; Genes, Retinoblastoma ; Humans ; Karyotyping ; Translocation, Genetic
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
False-positives and false-negatives in non-invasive prenatal testing (NIPT): what can we learn from a meta-analyses on > 750,000 tests?
Autorzy:
Liehr T; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Am Klinikum 1, 07747, Jena, Germany. Thomas.Liehr@med.uni-jena.de.
Pokaż więcej
Źródło:
Molecular cytogenetics [Mol Cytogenet] 2022 Aug 19; Vol. 15 (1), pp. 36. Date of Electronic Publication: 2022 Aug 19.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Genomic Organization of Microsatellites and LINE-1- like Retrotransposons: Evolutionary Implications for Ctenomys minutus (Rodentia: Ctenomyidae) Cytotypes.
Autorzy:
de Oliveira TD; Programa de Pós-Graduação em Biologia Animal, Universidade Federal do Rio Grande do Sul, Porto Alegre 91501-970, Brazil.
Bertocchi NA; Programa de Pós-Graduação em Genética e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre 91501-970, Brazil.
Kretschmer R; Departamento de Ecologia, Zoologia e Genética, Instituto de Biologia, Universidade Federal de Pelotas, Pelotas 96010-900, Brazil.
de Oliveira EHC; Instituto de Ciências Exatas e Naturais, Universidade Federal do Pará, Belém 66075-110, Brazil.; Laboratório de Cultura de Tecidos e Citogenética, SAMAM, Instituto Evandro Chagas, Ananindeua 67030-000, Brazil.
Cioffi MB; Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos 13565-905, Brazil.
Liehr T; Institute of Human Genetics, University Hospital Jena, Friedrich Schiller University, 07747 Jena, Germany.
de Freitas TRO; Programa de Pós-Graduação em Biologia Animal, Universidade Federal do Rio Grande do Sul, Porto Alegre 91501-970, Brazil.; Programa de Pós-Graduação em Genética e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre 91501-970, Brazil.
Pokaż więcej
Źródło:
Animals : an open access journal from MDPI [Animals (Basel)] 2022 Aug 16; Vol. 12 (16). Date of Electronic Publication: 2022 Aug 16.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes.
Autorzy:
Baba N; Institute of Human Genetics, University of Jena, Jena, Germany.; Praxis Für Humangenetik, Zentrum Für Ambulante Medizin, Jena, Germany.
Lengyel A; 2Nd Department of Pediatrics, Semmelweis University Budapest, Budapest, Hungary.
Pinti E; 2Nd Department of Pediatrics, Semmelweis University Budapest, Budapest, Hungary.
Yapici E; Institute of Human Genetics, Medical Faculty, RWTH Aachen University, Pauwelsstr. 30, 52074, Aachen, Germany.
Schreyer I; Institute of Human Genetics, University of Jena, Jena, Germany.; Praxis Für Humangenetik, Zentrum Für Ambulante Medizin, Jena, Germany.
Liehr T; Institute of Human Genetics, University of Jena, Jena, Germany.
Fekete G; 2Nd Department of Pediatrics, Semmelweis University Budapest, Budapest, Hungary.
Eggermann T; Institute of Human Genetics, Medical Faculty, RWTH Aachen University, Pauwelsstr. 30, 52074, Aachen, Germany. .
Pokaż więcej
Źródło:
Molecular cytogenetics [Mol Cytogenet] 2022 May 13; Vol. 15 (1), pp. 19. Date of Electronic Publication: 2022 May 13.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Uniparental disomy is a chromosomic disorder in the first place.
Autorzy:
Liehr T; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Am Klinikum 1, 07747, Jena, Germany. Thomas.Liehr@med.uni-jena.de.
Pokaż więcej
Źródło:
Molecular cytogenetics [Mol Cytogenet] 2022 Feb 17; Vol. 15 (1), pp. 5. Date of Electronic Publication: 2022 Feb 17.
Typ publikacji:
Journal Article
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 1-20 z 179

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