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  • 1
    UID:
    edoccha_BV036069134
    Format: 1 Online-Ressource (XII, 229 Seiten) : , Illustrationen, Diagramme.
    ISBN: 978-3-318-01461-7
    Series Statement: Monographs in human genetics Vol. 15
    Content: Fanconi anemia (FA) is a rare genetic disease discovered 80 years ago by Guido Fanconi, an eminent Swiss pediatrician. It is characterized by short stature, skeletal anomalies, increased incidence of solid tumors and leukemias, bone marrow failure and cellular sensitivity to DNA damaging agents.Following a historical account, exemplary case reports and the current status of FA genes and their mutations, this volume discusses neoplasia in FA as well as current approaches to pre- and postnatal diagnosis. Further topics include revertant mosaicism as a kind of ‘natural gene therapy’ and hematopoietic stem cell transplantation as the only curative approach in FA. The final chapters investigate evolutionary aspects of the FA genes with special emphasis on the avian genome and the involvement of FA genes in recombinational types of DNA repair.Physicians and researchers in the fields of pediatrics, hematology, cancer, genetics, DNA repair and aging will benefit from understanding this disease, which illustrates the complex network of genomic maintenance systems that protect us from cancer and premature aging
    Note: Literaturangaben. - elucidates the connection between genetic instability, cancer and premature aging
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-8277-3
    Language: English
    Subjects: Biology , Medicine
    RVK:
    RVK:
    Keywords: Fanconi-Anämie ; Aufsatzsammlung
    Author information: Schindler, Detlev 1950-
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    UID:
    almahu_BV036069134
    Format: 1 Online-Ressource (XII, 229 Seiten) : , Illustrationen, Diagramme.
    ISBN: 978-3-318-01461-7
    Series Statement: Monographs in human genetics Vol. 15
    Content: Fanconi anemia (FA) is a rare genetic disease discovered 80 years ago by Guido Fanconi, an eminent Swiss pediatrician. It is characterized by short stature, skeletal anomalies, increased incidence of solid tumors and leukemias, bone marrow failure and cellular sensitivity to DNA damaging agents.Following a historical account, exemplary case reports and the current status of FA genes and their mutations, this volume discusses neoplasia in FA as well as current approaches to pre- and postnatal diagnosis. Further topics include revertant mosaicism as a kind of ‘natural gene therapy’ and hematopoietic stem cell transplantation as the only curative approach in FA. The final chapters investigate evolutionary aspects of the FA genes with special emphasis on the avian genome and the involvement of FA genes in recombinational types of DNA repair.Physicians and researchers in the fields of pediatrics, hematology, cancer, genetics, DNA repair and aging will benefit from understanding this disease, which illustrates the complex network of genomic maintenance systems that protect us from cancer and premature aging
    Note: Literaturangaben. - elucidates the connection between genetic instability, cancer and premature aging
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-8277-3
    Language: English
    Subjects: Biology , Medicine
    RVK:
    RVK:
    Keywords: Fanconi-Anämie ; Aufsatzsammlung
    Author information: Schindler, Detlev 1950-
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    UID:
    b3kat_BV036069134
    Format: 1 Online-Ressource (XII, 229 Seiten) , Illustrationen, Diagramme
    ISBN: 9783318014617
    Series Statement: Monographs in human genetics Vol. 15
    Content: Fanconi anemia (FA) is a rare genetic disease discovered 80 years ago by Guido Fanconi, an eminent Swiss pediatrician. It is characterized by short stature, skeletal anomalies, increased incidence of solid tumors and leukemias, bone marrow failure and cellular sensitivity to DNA damaging agents.Following a historical account, exemplary case reports and the current status of FA genes and their mutations, this volume discusses neoplasia in FA as well as current approaches to pre- and postnatal diagnosis. Further topics include revertant mosaicism as a kind of ‘natural gene therapy’ and hematopoietic stem cell transplantation as the only curative approach in FA. The final chapters investigate evolutionary aspects of the FA genes with special emphasis on the avian genome and the involvement of FA genes in recombinational types of DNA repair.Physicians and researchers in the fields of pediatrics, hematology, cancer, genetics, DNA repair and aging will benefit from understanding this disease, which illustrates the complex network of genomic maintenance systems that protect us from cancer and premature aging
    Note: Literaturangaben , elucidates the connection between genetic instability, cancer and premature aging
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-8277-3
    Language: English
    Subjects: Biology , Medicine
    RVK:
    RVK:
    Keywords: Fanconi-Anämie ; Aufsatzsammlung
    Author information: Schindler, Detlev 1950-
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    UID:
    almafu_BV036069134
    Format: 1 Online-Ressource (XII, 229 Seiten) : , Illustrationen, Diagramme.
    ISBN: 978-3-318-01461-7
    Series Statement: Monographs in human genetics Vol. 15
    Content: Fanconi anemia (FA) is a rare genetic disease discovered 80 years ago by Guido Fanconi, an eminent Swiss pediatrician. It is characterized by short stature, skeletal anomalies, increased incidence of solid tumors and leukemias, bone marrow failure and cellular sensitivity to DNA damaging agents.Following a historical account, exemplary case reports and the current status of FA genes and their mutations, this volume discusses neoplasia in FA as well as current approaches to pre- and postnatal diagnosis. Further topics include revertant mosaicism as a kind of ‘natural gene therapy’ and hematopoietic stem cell transplantation as the only curative approach in FA. The final chapters investigate evolutionary aspects of the FA genes with special emphasis on the avian genome and the involvement of FA genes in recombinational types of DNA repair.Physicians and researchers in the fields of pediatrics, hematology, cancer, genetics, DNA repair and aging will benefit from understanding this disease, which illustrates the complex network of genomic maintenance systems that protect us from cancer and premature aging
    Note: Literaturangaben. - elucidates the connection between genetic instability, cancer and premature aging
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-8055-8277-3
    Language: English
    Subjects: Biology , Medicine
    RVK:
    RVK:
    Keywords: Fanconi-Anämie ; Aufsatzsammlung
    Author information: Schindler, Detlev 1950-
    Library Location Call Number Volume/Issue/Year Availability
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  • 5
    UID:
    almafu_9958095822402883
    Format: 1 online resource (243 p.)
    ISBN: 1-280-84352-7 , 9786610843527 , 3-318-01461-3
    Series Statement: Monographs in human genetics, v. 15
    Content: Fanconi anemia (FA) is a rare genetic disease discovered 80 years ago by Guido Fanconi, an eminent Swiss pediatrician. It is characterized by short stature, skeletal anomalies, increased incidence of solid tumors and leukemias, bone marrow failure and cellular sensitivity to DNA damaging agents. Following a historical account, exemplary case reports and the current status of FA genes and their mutations, this volume discusses neoplasia in FA as well as current approaches to pre- and postnatal diagnosis. Further topics include revertant mosaicism as a kind of 'natural gene therapy' and hematopo
    Note: Description based upon print version of record. , Why, what, and how can we learn from a rare disease like Fanconi anemia? / Schroeder-Kurth, T. -- Fanconi anemia: a disease with many faces / Dietrich, R., Velleuer, E. -- Milestones in Fanconi anemia research / Digweed, M., Hoehn, H., Sperling K. -- Fanconi anemia genes: structure, mutations, and genotype-phenotype correlations / Kalb, R. ... [et al.] -- Cancer in Fanconi anemia and Fanconi anemia genes in cancer / Neveling, K., Kalb, R., Schindler, D. -- Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: results and implications / Neitzel H. ... [et al.] -- Interphase FISH-assay for the detection of MDS- and AML-associated chromosomal imbalances in native bone marrow and peripheral blood cells / Tonnies, H. ... [et al.] -- Applications of cell cycle testing in Fanconi anemia / Schindler, D. ... [et al.] -- Prenatal diagnosis of Fanconi anemia: functional and molecular testing / Bechtold, A. ... [et al.] -- Revertant mosaicism in Fanconi anemia: natural gene therapy at work / Hoehn, H. ... [et al.] -- Stem cell transplantation in Fanconi anemia, recent advances with alternative donors / Eyrich, M., Winkler, B., Schlegel, P.G. -- Fanconi anemia genes in vertebrates: evolutionary conservation, sex-linkage, and embryonic expression of FANCC and FANCG in avian cells / Nanda, I. ... [et al.] -- Studying homologous recombination in Fanconi anemia / Demuth, I., Digweed, M. -- Functional knock-down of human RAD51 for testing the Fanconi anemia-BRCA connection / Rio, P., Hanenberg, H. , English
    Additional Edition: ISBN 3-8055-8277-3
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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  • 6
    Book
    Book
    München : Verl. Med. Genetik
    UID:
    kobvindex_ZLB13718703
    Format: 117 Seiten , Ill., graph. Darst. , 30 cm
    Series Statement: Medizinische Genetik
    Note: Literaturangaben
    Language: German
    Keywords: Fanconi-Anämie ; Humangenetik ; Aufsatzsammlung ; Aufsatzsammlung ; Aufsatzsammlung
    Author information: Schindler, Detlev
    Library Location Call Number Volume/Issue/Year Availability
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  • 7
    UID:
    b3kat_BV026014135
    Format: Getr. Zähl.
    Language: Undetermined
    Author information: Schindler, Detlev 1950-
    Library Location Call Number Volume/Issue/Year Availability
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  • 8
    UID:
    almafu_BV026320275
    Format: 56 S. : , Ill., graph. Darst.
    Note: Würzburg, Univ., Diss., 1984
    Language: German
    Keywords: Hochschulschrift
    Author information: Schindler, Detlev 1950-
    Library Location Call Number Volume/Issue/Year Availability
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  • 9
    UID:
    almahu_BV024920152
    Format: 56 S. : , Ill.
    Note: Würzburg, Univ., Diss., 1984
    Language: German
    Keywords: Hochschulschrift
    Author information: Schindler, Detlev, 1950-
    Library Location Call Number Volume/Issue/Year Availability
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