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Molecular Therapy. Methods & Clinical Development
|
December 24, 2025
Targeted inhibition of <i>ELANE</i> expression using adenine base editing to treat severe congenital neutropenia
Betül Findik, Benjamin Dannenmann, Franka Bernhard, et al.
Cancers
|
June 28, 2023
CAR-NK Cells Targeting HER1 (EGFR) Show Efficient Anti-Tumor Activity against Head and Neck Squamous Cell Carcinoma (HNSCC)
Juliette Nowak, Marco Bentele, Ivana Kutle, et al.
The Journal of Allergy and Clinical Immunology
|
January 25, 2017
Myb-like, SWIRM, and MPN domains 1 (MYSM1) deficiency: Genotoxic stress-associated bone marrow failure and developmental aberrations
Ehsan Bahrami, Maximilian Witzel, Tomas Racek, et al.
Hemasphere
|
September 24, 2024
Comprehensive sequential genetic analysis delineating frequency, patterns, and prognostic impact of genomic dynamics in a real-world cohort of patients with lower-risk MDS
Paolo Mazzeo, Christina Ganster, John Wiedenhöft, et al.
European Journal of Human Genetics : EJHG
|
August 10, 2018
A patient-specific induced pluripotent stem cell model for West syndrome caused by ST3GAL3 deficiency
Laura van Diepen, Falk F R Buettner, Dirk Hoffmann, et al.
Scientific Reports
|
December 3, 2016
Improved bi-allelic modification of a transcriptionally silent locus in patient-derived iPSC by Cas9 nickase
Reto Eggenschwiler, Mohsen Moslem, Mariane Serra Fráguas, et al.
International Journal of Cancer
|
November 15, 2018
The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants
Stephanie Schubert, Jana L van Luttikhuizen, Bernd Auber, et al.
Annals of Hematology
|
February 21, 2020
Implementation of RNA sequencing and array CGH in the diagnostic workflow of the AIEOP-BFM ALL 2017 trial on acute lymphoblastic leukemia
Maximilian Schieck, Jana Lentes, Kathrin Thomay, et al.
Journal of Hepatology
|
June 10, 2026
In vivo base editing alleviates hepatic iron accumulation and fibrosis in models of HFE-related hereditary hemochromatosis
Vanessa Hamann, Sebastian Hook, Pimpan Sujariyakul, et al.
Molecular & Cellular Proteomics : MCP
|
January 21, 2016
Glycomic Characterization of Induced Pluripotent Stem Cells Derived from a Patient Suffering from Phosphomannomutase 2 Congenital Disorder of Glycosylation (PMM2-CDG)
Christina T Thiesler, Samanta Cajic, Dirk Hoffmann, et al.
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of 14
Search research articles
Search
Showing results (91-100 of 138) with videos related to
Sort By:
Page
of 14
Molecular Therapy. Methods & Clinical Development
|
December 24, 2025
Targeted inhibition of <i>ELANE</i> expression using adenine base editing to treat severe congenital neutropenia
Betül Findik, Benjamin Dannenmann, Franka Bernhard, et al.
Cancers
|
June 28, 2023
CAR-NK Cells Targeting HER1 (EGFR) Show Efficient Anti-Tumor Activity against Head and Neck Squamous Cell Carcinoma (HNSCC)
Juliette Nowak, Marco Bentele, Ivana Kutle, et al.
The Journal of Allergy and Clinical Immunology
|
January 25, 2017
Myb-like, SWIRM, and MPN domains 1 (MYSM1) deficiency: Genotoxic stress-associated bone marrow failure and developmental aberrations
Ehsan Bahrami, Maximilian Witzel, Tomas Racek, et al.
Hemasphere
|
September 24, 2024
Comprehensive sequential genetic analysis delineating frequency, patterns, and prognostic impact of genomic dynamics in a real-world cohort of patients with lower-risk MDS
Paolo Mazzeo, Christina Ganster, John Wiedenhöft, et al.
European Journal of Human Genetics : EJHG
|
August 10, 2018
A patient-specific induced pluripotent stem cell model for West syndrome caused by ST3GAL3 deficiency
Laura van Diepen, Falk F R Buettner, Dirk Hoffmann, et al.
Scientific Reports
|
December 3, 2016
Improved bi-allelic modification of a transcriptionally silent locus in patient-derived iPSC by Cas9 nickase
Reto Eggenschwiler, Mohsen Moslem, Mariane Serra Fráguas, et al.
International Journal of Cancer
|
November 15, 2018
The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants
Stephanie Schubert, Jana L van Luttikhuizen, Bernd Auber, et al.
Annals of Hematology
|
February 21, 2020
Implementation of RNA sequencing and array CGH in the diagnostic workflow of the AIEOP-BFM ALL 2017 trial on acute lymphoblastic leukemia
Maximilian Schieck, Jana Lentes, Kathrin Thomay, et al.
Journal of Hepatology
|
June 10, 2026
In vivo base editing alleviates hepatic iron accumulation and fibrosis in models of HFE-related hereditary hemochromatosis
Vanessa Hamann, Sebastian Hook, Pimpan Sujariyakul, et al.
Molecular & Cellular Proteomics : MCP
|
January 21, 2016
Glycomic Characterization of Induced Pluripotent Stem Cells Derived from a Patient Suffering from Phosphomannomutase 2 Congenital Disorder of Glycosylation (PMM2-CDG)
Christina T Thiesler, Samanta Cajic, Dirk Hoffmann, et al.
Page
of 14