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Bernd Auber

Showing results (41-50 of 75) with videos related to

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Journal of Neurology|May 25, 2020
SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegiaAlma Osmanovic, Maylin Widjaja, Alisa Förster, et al.
Leukemia|February 27, 2024
Germline variants in patients developing second malignant neoplasms after therapy for pediatric acute lymphoblastic leukemia-a case-control studyStefanie V Junk, Alisa Förster, Gunnar Schmidt, et al.
Haematologica|November 4, 2017
<i>MDS1</i> and <i>EVI1</i> complex locus (MECOM): a novel candidate gene for hereditary hematological malignanciesTim Ripperger, Winfried Hofmann, Jan C Koch, et al.
NPJ Breast Cancer|June 30, 2026
Multi-omics analysis in suspected hereditary breast and ovarian cancer cases reveals novel candidate susceptibility factorsB Aldrige Allister, Winfried Hofmann, Jonathan L Lühmann, et al.
Breast Cancer Research and Treatment|September 8, 2018
A tandem duplication of BRCA1 exons 1-19 through DHX8 exon 2 in four families with hereditary breast and ovarian cancer syndromeChen Du, Dorothea Mark, Barbara Wappenschmidt, et al.
Breast Cancer Research : BCR|August 9, 2018
Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredityJudith Penkert, Gunnar Schmidt, Winfried Hofmann, et al.
Journal of Clinical Immunology|October 30, 2021
Biomarkers of DNA Damage Response Enable Flow Cytometry-Based Diagnostic to Identify Inborn DNA Repair Defects in Primary ImmunodeficienciesKerstin Felgentreff, Ulrich Baumann, Christian Klemann, et al.
JACC. Cardiooncology|August 16, 2021
Increased Cancer Prevalence in Peripartum CardiomyopathyTobias J Pfeffer, Stella Schlothauer, Stefan Pietzsch, et al.
Frontiers in Oncology|April 26, 2021
Plasma Metabolome Signature Indicative of <i>BRCA1</i> Germline Status Independent of Cancer IncidenceJudith Penkert, Andre Märtens, Martin Seifert, et al.
Clinical Genetics|July 7, 2020
De novo missense variants in the RAP1B gene identified in two patients with syndromic thrombocytopeniaJan Hendrik Niemann, Chen Du, Susanne Morlot, et al.
Pageof 8

Showing results (41-50 of 75) with videos related to

Sort By:
Pageof 8
Journal of Neurology|May 25, 2020
SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegiaAlma Osmanovic, Maylin Widjaja, Alisa Förster, et al.
Leukemia|February 27, 2024
Germline variants in patients developing second malignant neoplasms after therapy for pediatric acute lymphoblastic leukemia-a case-control studyStefanie V Junk, Alisa Förster, Gunnar Schmidt, et al.
Haematologica|November 4, 2017
<i>MDS1</i> and <i>EVI1</i> complex locus (MECOM): a novel candidate gene for hereditary hematological malignanciesTim Ripperger, Winfried Hofmann, Jan C Koch, et al.
NPJ Breast Cancer|June 30, 2026
Multi-omics analysis in suspected hereditary breast and ovarian cancer cases reveals novel candidate susceptibility factorsB Aldrige Allister, Winfried Hofmann, Jonathan L Lühmann, et al.
Breast Cancer Research and Treatment|September 8, 2018
A tandem duplication of BRCA1 exons 1-19 through DHX8 exon 2 in four families with hereditary breast and ovarian cancer syndromeChen Du, Dorothea Mark, Barbara Wappenschmidt, et al.
Breast Cancer Research : BCR|August 9, 2018
Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredityJudith Penkert, Gunnar Schmidt, Winfried Hofmann, et al.
Journal of Clinical Immunology|October 30, 2021
Biomarkers of DNA Damage Response Enable Flow Cytometry-Based Diagnostic to Identify Inborn DNA Repair Defects in Primary ImmunodeficienciesKerstin Felgentreff, Ulrich Baumann, Christian Klemann, et al.
JACC. Cardiooncology|August 16, 2021
Increased Cancer Prevalence in Peripartum CardiomyopathyTobias J Pfeffer, Stella Schlothauer, Stefan Pietzsch, et al.
Frontiers in Oncology|April 26, 2021
Plasma Metabolome Signature Indicative of <i>BRCA1</i> Germline Status Independent of Cancer IncidenceJudith Penkert, Andre Märtens, Martin Seifert, et al.
Clinical Genetics|July 7, 2020
De novo missense variants in the RAP1B gene identified in two patients with syndromic thrombocytopeniaJan Hendrik Niemann, Chen Du, Susanne Morlot, et al.
Pageof 8