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Blood
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April 22, 2016
Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndrome
Simon Völkl, Anne Rensing-Ehl, Andrea Allgäuer, et al.
Nature Communications
|
December 4, 2015
Exome sequencing of osteosarcoma reveals mutation signatures reminiscent of BRCA deficiency
Michal Kovac, Claudia Blattmann, Sebastian Ribi, et al.
NPJ Precision Oncology
|
May 5, 2026
An international framework for clinical translation of molecular classifiers in osteosarcoma
Amanda E Marinoff, Michaela Nathrath, David S Shulman, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
October 9, 2025
Investigation of DNA Damage Response Genes Validates the Role of DNA Repair in Pediatric Cancer Risk and Identifies <i>SMARCAL1</i> as a Novel Osteosarcoma Predisposition Gene
Ninad Oak, Wenan Chen, Alise Blake, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 4, 2025
Comprehensive investigation of DNA damage repair genes in children with cancer identifies <i>SMARCAL1</i> as novel osteosarcoma predisposition gene
Ninad Oak, Wenan Chen, Alise Blake, et al.
Blood
|
November 22, 2023
Survival in primary hemophagocytic lymphohistiocytosis, 2016 to 2021: etoposide is better than its reputation
Svea Böhm, Katharina Wustrau, Jana Pachlopnik Schmid, et al.
Journal of Medical Genetics
|
September 9, 2019
High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers
Maribel González-Acosta, Fátima Marín, Benjamin Puliafito, et al.
Human Mutation
|
February 12, 2019
A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes
Richard Gallon, Barbara Mühlegger, Sören-Sebastian Wenzel, et al.
The Journal of Clinical Investigation
|
May 9, 2023
Patient-tailored adoptive immunotherapy with EBV-specific T cells from related and unrelated donors
Agnes Bonifacius, Britta Lamottke, Sabine Tischer-Zimmermann, et al.
Journal of Human Immunity
|
June 18, 2026
ADA2 genotype and enzyme activity may predict vasculitic or hematologic DADA2 phenotype
Philipp Peters, Johanna Schepp, Michael H Albert, et al.
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of 9
Search research articles
Search
Showing results (61-70 of 86) with videos related to
Sort By:
Page
of 9
Blood
|
April 22, 2016
Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndrome
Simon Völkl, Anne Rensing-Ehl, Andrea Allgäuer, et al.
Nature Communications
|
December 4, 2015
Exome sequencing of osteosarcoma reveals mutation signatures reminiscent of BRCA deficiency
Michal Kovac, Claudia Blattmann, Sebastian Ribi, et al.
NPJ Precision Oncology
|
May 5, 2026
An international framework for clinical translation of molecular classifiers in osteosarcoma
Amanda E Marinoff, Michaela Nathrath, David S Shulman, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
October 9, 2025
Investigation of DNA Damage Response Genes Validates the Role of DNA Repair in Pediatric Cancer Risk and Identifies <i>SMARCAL1</i> as a Novel Osteosarcoma Predisposition Gene
Ninad Oak, Wenan Chen, Alise Blake, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 4, 2025
Comprehensive investigation of DNA damage repair genes in children with cancer identifies <i>SMARCAL1</i> as novel osteosarcoma predisposition gene
Ninad Oak, Wenan Chen, Alise Blake, et al.
Blood
|
November 22, 2023
Survival in primary hemophagocytic lymphohistiocytosis, 2016 to 2021: etoposide is better than its reputation
Svea Böhm, Katharina Wustrau, Jana Pachlopnik Schmid, et al.
Journal of Medical Genetics
|
September 9, 2019
High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers
Maribel González-Acosta, Fátima Marín, Benjamin Puliafito, et al.
Human Mutation
|
February 12, 2019
A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes
Richard Gallon, Barbara Mühlegger, Sören-Sebastian Wenzel, et al.
The Journal of Clinical Investigation
|
May 9, 2023
Patient-tailored adoptive immunotherapy with EBV-specific T cells from related and unrelated donors
Agnes Bonifacius, Britta Lamottke, Sabine Tischer-Zimmermann, et al.
Journal of Human Immunity
|
June 18, 2026
ADA2 genotype and enzyme activity may predict vasculitic or hematologic DADA2 phenotype
Philipp Peters, Johanna Schepp, Michael H Albert, et al.
Page
of 9