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Maria Rossing

Showing results (101-110 of 127) with videos related to

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Endocrine Connections|May 16, 2018
Incidence and prevalence of sporadic and hereditary MTC in Denmark 1960-2014: a nationwide studyJes Sloth Mathiesen, Jens Peter Kroustrup, Peter Vestergaard, et al.
Cancers|February 13, 2025
<i>RET</i> C611Y Germline Variant in Multiple Endocrine Neoplasia Type 2A in Denmark 1930-2021: A Nationwide StudyAnders Würgler Hansen, Peter Vestergaard, Morten Møller Poulsen, et al.
Cancer Research Communications|November 26, 2024
Beyond HRD Status: Unraveling Genetic Variants Impacting PARP Inhibitor Sensitivity in Advanced Ovarian CancerMaj K Kjeldsen, Morten Jørgensen, Dina Sofie B Grønseth, et al.
British Journal of Cancer|September 17, 2020
Breast cancer survival in Nordic BRCA2 mutation carriers-unconventional association with oestrogen receptor statusElinborg J Olafsdottir, Ake Borg, Maj-Britt Jensen, et al.
Breast Cancer Research : BCR|January 9, 2024
Male with an apparently normal phenotype carrying a BRCA1 exon 20 duplication in trans to a BRCA1 frameshift variantInes Block, Àngels Mateu-Regué, Thi Tuyet Nhu Do, et al.
Plos Genetics|December 17, 2020
Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromesAnna Byrjalsen, Thomas V O Hansen, Ulrik K Stoltze, et al.
Orphanet Journal of Rare Diseases|July 31, 2024
DAHEAN: A Danish nationwide study ensuring quality assurance through real-world data for suspected hereditary anemia patientsAndreas Glenthøj, Andreas Ørslev Rasmussen, Selma Kofoed Bendtsen, et al.
Acta Oncologica (Stockholm, Sweden)|October 18, 2022
Dihydropyrimidine dehydrogenase (DPD) genotype and phenotype among Danish cancer patients: prevalence and correlation between <i>DPYD</i>-genotype variants and P-uracil concentrationsNiels Herluf Paulsen, Camilla Qvortrup, Fie Juhl Vojdeman, et al.
BMC Genomics|January 30, 2020
Assessment of branch point prediction tools to predict physiological branch points and their alteration by variantsRaphaël Leman, Hélène Tubeuf, Sabine Raad, et al.
Nucleic Acids Research|October 16, 2018
Corrigendum: Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effortRaphaël Leman, Pascaline Gaildrat, Gérald L Gac, et al.
Pageof 13

Showing results (101-110 of 127) with videos related to

Sort By:
Pageof 13
Endocrine Connections|May 16, 2018
Incidence and prevalence of sporadic and hereditary MTC in Denmark 1960-2014: a nationwide studyJes Sloth Mathiesen, Jens Peter Kroustrup, Peter Vestergaard, et al.
Cancers|February 13, 2025
<i>RET</i> C611Y Germline Variant in Multiple Endocrine Neoplasia Type 2A in Denmark 1930-2021: A Nationwide StudyAnders Würgler Hansen, Peter Vestergaard, Morten Møller Poulsen, et al.
Cancer Research Communications|November 26, 2024
Beyond HRD Status: Unraveling Genetic Variants Impacting PARP Inhibitor Sensitivity in Advanced Ovarian CancerMaj K Kjeldsen, Morten Jørgensen, Dina Sofie B Grønseth, et al.
British Journal of Cancer|September 17, 2020
Breast cancer survival in Nordic BRCA2 mutation carriers-unconventional association with oestrogen receptor statusElinborg J Olafsdottir, Ake Borg, Maj-Britt Jensen, et al.
Breast Cancer Research : BCR|January 9, 2024
Male with an apparently normal phenotype carrying a BRCA1 exon 20 duplication in trans to a BRCA1 frameshift variantInes Block, Àngels Mateu-Regué, Thi Tuyet Nhu Do, et al.
Plos Genetics|December 17, 2020
Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromesAnna Byrjalsen, Thomas V O Hansen, Ulrik K Stoltze, et al.
Orphanet Journal of Rare Diseases|July 31, 2024
DAHEAN: A Danish nationwide study ensuring quality assurance through real-world data for suspected hereditary anemia patientsAndreas Glenthøj, Andreas Ørslev Rasmussen, Selma Kofoed Bendtsen, et al.
Acta Oncologica (Stockholm, Sweden)|October 18, 2022
Dihydropyrimidine dehydrogenase (DPD) genotype and phenotype among Danish cancer patients: prevalence and correlation between <i>DPYD</i>-genotype variants and P-uracil concentrationsNiels Herluf Paulsen, Camilla Qvortrup, Fie Juhl Vojdeman, et al.
BMC Genomics|January 30, 2020
Assessment of branch point prediction tools to predict physiological branch points and their alteration by variantsRaphaël Leman, Hélène Tubeuf, Sabine Raad, et al.
Nucleic Acids Research|October 16, 2018
Corrigendum: Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effortRaphaël Leman, Pascaline Gaildrat, Gérald L Gac, et al.
Pageof 13