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Arndt Borkhardt

Heinrich Heine University Dusseldorf

Universitätsklinikum Düsseldorf

SCHOLARLY PAPERS

3

DOWNLOADS

91

TOTAL CITATIONS

1

Scholarly Papers (3)

1.

Osteosarcoma and Causes of Death. A Report of 1.520 Deceased Patients from the Cooperative Osteosarcoma Study Group (COSS)

Number of pages: 19 Posted: 30 May 2022
Stuttgart Cancer Center, Stuttgart Cancer Center, Heinrich Heine University Dusseldorf, Semmelweis University, University of Hamburg - University Medical Center Hamburg-Eppendorf, Motol University Hospital, St. Anna Children's Cancer Research Institute (CCRI), University of Münster, Hannover Medical School, University Children's Hospital beider Basel, Stuttgart Cancer Center, Goethe University Frankfurt, University Hospital Ulm, Stuttgart Cancer Center, Friedrich-Alexander-Universität Erlangen-Nürnberg - Department of Pediatrics and Adolescent Medicine, Helios Klinikum Berlin-Buch, Universitätsklinikum Münster, Stuttgart Cancer Center, Technische Universität München (TUM), Medizinische Universität Wien and Stuttgart Cancer Center
Downloads 42 (1,170,409)
Citation 1

Abstract:

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Osteosarcoma, survival, Child, Adolescent, adult

2.

Progressive Short Stature in Pearson Syndrome and the Impact of Organ Failure

Number of pages: 17 Posted: 03 Mar 2026
University of Freiburg, affiliation not provided to SSRN, affiliation not provided to SSRN, RWTH Aachen University, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, Heinrich Heine University Dusseldorf, affiliation not provided to SSRN, affiliation not provided to SSRN, Friedrich-Alexander-Universität Erlangen-Nürnberg - Department of Pediatrics and Adolescent Medicine, Medical University of Innsbruck, University of Freiburg, University of Freiburg and University of Freiburg
Downloads 25 (1,399,036)

Abstract:

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Pearson syndrome, height, weight, body mass index, growth, failure to thrive

3.

UBQLN1-Mediated Repression of Homologous Recombination is an Actionable Target for Cancer Therapy

Number of pages: 86 Posted: 01 Apr 2026
Max Planck Institute for Biology of Ageing, Max Planck Institute for Biology of Ageing, Max Planck Institute for Biology of Ageing, Max Planck Institute for Biology of Ageing, University of Cologne, University of Seville, University of Seville, Max Planck Institute for Biology of Ageing, Max Planck Institute for Biology of Ageing, Max Planck Institute for Biology of Ageing, Max Planck Institute for Biology of Ageing, Max Planck Institute for Biology of Ageing, Max Planck Institute for Biology of Ageing, Max Planck Institute for Biology of Ageing, Max Planck Institute for Biology of Ageing, University of Cologne, Max Planck Institute for Biology of Ageing, Max Planck Institute for Biology of Ageing, University of Cologne, University of Cologne, Max Planck Institute for Biology of Ageing, Providence Saint John's Health Center (SJHC), University of Duisburg-Essen - University Hospital Essen, Max Planck Institute for Biochemistry, University of Cologne, Max Planck Institute for Biology of Ageing, Max Planck Institute for Metabolism Research, Max Planck Institute for Biology of Ageing, University of Cologne - University Hospital of Cologne, Tel Aviv University, Providence Saint John's Health Center (SJHC), University of Cologne, University of Cologne, University of Cologne, Zeynep Kamil Maternity and Children's Training and Research Hospital, Baylor College of Medicine, Baylor College of Medicine, University of Cologne, Max Planck Institute for Biology of Ageing, University of Seville, Heinrich Heine University Dusseldorf, Heinrich Heine University Dusseldorf, University of Cologne, University of Cologne, Saint John’s Cancer Institute at Providence Saint John’s Health Center, University of Cologne, Heinrich Heine University Dusseldorf, Department of Hematology and Stem Cell Transplantation, University of Duisburg-Essen and Max Planck Institute for Biology of Ageing
Downloads 24 (1,436,435)

Abstract:

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DNA damage, DNA double-strand break repair, Homologous recombination, cancer, targeted cancer therapy, UBQLN1 deficiency syndrome, UBQLN1, RAD51, MRE11, genome instability, syndrome, Ubiquitin, proteasomal degradation, Lung Cancer, PARP, ICB