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Wyszukujesz frazę ""Amann, G"" wg kryterium: Autor


Wyświetlanie 1-14 z 14
Tytuł :
The genetic tumor background is an important determinant for heterogeneous MYCN-amplified neuroblastoma.
Autorzy :
Bogen D; Department of Tumor Biology, CCRI, Children's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
Brunner C; Department of Tumor Biology, CCRI, Children's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
Walder D; Department of Tumor Biology, CCRI, Children's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
Ziegler A; Department of Tumor Biology, CCRI, Children's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
Abbasi R; Department of Tumor Biology, CCRI, Children's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
Ladenstein RL; S2IRP, CCRI, Children's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.; Department of Pediatrics, Medical University of Vienna, Vienna, Austria.
Noguera R; Pathology Department, Medical School, University of Valencia, INCLIVA, Valencia, Spain.
Martinsson T; Department of Clinical Genetics, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Amann G; Department of Clinical Pathology, Medical University of Vienna, Vienna, Austria.
Schilling FH; Pediatric Oncology, Olgahospital, Klinikum Stuttgart, Stuttgart, Germany.
Ussowicz M; Department of Pediatric Oncology, Hematology and BMT, Wroclaw Medical University, Wroclaw, Poland.
Benesch M; Division of Pediatric Hematology/Oncology, Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
Ambros PF; Department of Tumor Biology, CCRI, Children's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.; Department of Pediatrics, Medical University of Vienna, Vienna, Austria.
Ambros IM; Department of Tumor Biology, CCRI, Children's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
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Źródło :
International journal of cancer [Int J Cancer] 2016 Jul 01; Vol. 139 (1), pp. 153-63. Date of Electronic Publication: 2016 Mar 22.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Amplification*
Genetic Heterogeneity*
Neuroblastoma/*genetics
Nuclear Proteins/*genetics
Oncogene Proteins/*genetics
Adolescent ; Aneuploidy ; Child ; Child, Preschool ; Chromosome Aberrations ; Chromosome Deletion ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Infant ; Male ; N-Myc Proto-Oncogene Protein ; Neuroblastoma/pathology ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Tytuł :
Intratumoural heterogeneity of 1p deletions and MYCN amplification in neuroblastomas.
Autorzy :
Ambros PF; CCRI, Children's Cancer Research Institute, St Anna Kinderspital, Vienna, Austria. />Ambros IM
Kerbl R
Luegmayr A
Rumpler S
Ladenstein R
Amann G
Kovar H
Horcher E
De Bernardi B
Michon J
Gadner H
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Źródło :
Medical and pediatric oncology [Med Pediatr Oncol] 2001 Jan; Vol. 36 (1), pp. 1-4.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Amplification*
Genes, myc*
Chromosomes, Human, Pair 1/*genetics
Neuroblastoma/*genetics
Chromosomes, Human, Pair 1/ultrastructure ; Clone Cells/ultrastructure ; Disease Progression ; Humans ; In Situ Hybridization, Fluorescence ; Loss of Heterozygosity ; Neoplasm Invasiveness ; Neoplasm Metastasis ; Neoplasm Recurrence, Local ; Neoplastic Stem Cells/ultrastructure ; Neuroblastoma/pathology ; Prognosis
Czasopismo naukowe
Tytuł :
Familial cryptic translocation with del 4q34-->qter and dup 12pter-->p13 in sibs with tracheal stenosis: clinical, classical and molecular cytogenetic studies and CGH analyses from archival placental tissues evidencing tertiary trisomy 4 in one abortion specimen.
Autorzy :
Fritz B; Institut für Klinische Genetik, Philipps-Universität, Marburg, Germany.
Greber-Platzer S
Frischer T
Streubel B
Gröblacher J
Amann G
Ventruba P
Rehder H
Fonatsch C
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Źródło :
American journal of medical genetics [Am J Med Genet] 2000 Oct 02; Vol. 94 (4), pp. 271-80.
Typ publikacji :
Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Deletion*
Chromosomes, Human, Pair 12/*genetics
Chromosomes, Human, Pair 4/*genetics
Tracheal Stenosis/*genetics
Translocation, Genetic/*genetics
Trisomy/*genetics
Adult ; Child ; Fatal Outcome ; Female ; Humans ; Infant ; Karyotyping ; Male ; Nuclear Family ; Nucleic Acid Hybridization ; Pregnancy ; Tracheal Stenosis/diagnosis ; Tracheal Stenosis/pathology ; Trisomy/diagnosis ; Trisomy/pathology
Czasopismo naukowe
Tytuł :
Neuroblastoma screening in infants postponed after the sixth month of age: a trial to reduce "overdiagnosis" and to detect cases with "unfavorable" biologic features.
Autorzy :
Kerbl R; University Children's Hospital (Division of Hematology/Oncology), Graz, Austria.
Urban CE
Ladenstein R
Ambros IM
Spuller E
Mutz I
Amann G
Kovar H
Gadner H
Ambros PF
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Źródło :
Medical and pediatric oncology [Med Pediatr Oncol] 1997 Jul; Vol. 29 (1), pp. 1-10.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Mass Screening*
Neuroblastoma/*diagnosis
Age Factors ; Austria/epidemiology ; Humans ; Incidence ; Infant ; Neoplasm Staging ; Neuroblastoma/epidemiology ; Neuroblastoma/pathology ; Neuroblastoma/prevention & control
Czasopismo naukowe
Tytuł :
Proof of the reactive nature of the Schwann cell in neuroblastoma and its clinical implications.
Autorzy :
Ambros IM; Children's Cancer Research Institute (CCRI), St. Anna Kinderspital, Vienna, Austria.
Zellner A
Stock C
Amann G
Gadner H
Ambros PF
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Źródło :
Progress in clinical and biological research [Prog Clin Biol Res] 1994; Vol. 385, pp. 331-7.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Neuroblastoma/*pathology
Schwann Cells/*pathology
Chromosome Aberrations ; Chromosome Deletion ; Chromosome Disorders ; Chromosomes, Human, Pair 1 ; DNA Probes ; DNA, Neoplasm/analysis ; Humans ; In Situ Hybridization ; Neuroblastoma/genetics
Czasopismo naukowe
Tytuł :
Cyclopia as a result of an unbalanced familial translocation, rcp(7;18)(q34;q21)
Autorzy :
Smart RD
Ross J
Amann G
Nelson MM
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Źródło :
American journal of medical genetics [Am J Med Genet] 1986 Jun; Vol. 24 (2), pp. 269-72.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Chromosomes, Human, 16-18*
Chromosomes, Human, 6-12 and X*
Eye Abnormalities*
Translocation, Genetic*
Chromosome Aberrations/*genetics
Chromosome Disorders ; Female ; Humans
Czasopismo naukowe
    Wyświetlanie 1-14 z 14

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