Search research articles
Contact Us
Filters
Showing results (231-240 of 336) with videos related to
Page
of 34
Sort By:
Frontiers in Oncology
|
July 25, 2022
Clonal Evolution at First Sight: A Combined Visualization of Diverse Diagnostic Methods Improves Understanding of Leukemic Progression
Sarah Sandmann, Yvonne Lisa Behrens, Claudia Davenport, et al.
Studies in Health Technology and Informatics
|
May 17, 2025
Quality of Life Trajectories with EHR Integration
Martin Dugas, Robin Fleige, Stephan Christoph Feder, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
April 23, 2004
Global gene expression in human myocardium-oligonucleotide microarray analysis of regional diversity and transcriptional regulation in heart failure
Stefan Kääb, Andreas S Barth, Daniel Margerie, et al.
Blood Advances
|
September 24, 2021
Calcitonin receptor-like (CALCRL) is a marker of stemness and an independent predictor of outcome in pediatric AML
Linus Angenendt, Marius Wöste, Jan-Henrik Mikesch, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 19, 2022
A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels
Maria Schubert, Lina Pérez Lanuza, Marius Wöste, et al.
Journal of Medical Internet Research
|
January 11, 2022
Understanding the Nature of Metadata: Systematic Review
Hannes Ulrich, Ann-Kristin Kock-Schoppenhauer, Noemi Deppenwiese, et al.
Clinical Epigenetics
|
August 22, 2021
Whole-genome methylation analysis of testicular germ cells from cryptozoospermic men points to recurrent and functionally relevant DNA methylation changes
Sara Di Persio, Elsa Leitão, Marius Wöste, et al.
Oncology Reports
|
June 2, 2010
Low SMC1A protein expression predicts poor survival in acute myeloid leukemia
Claudia Hömme, Utz Krug, Nicola Tidow, et al.
Haematologica
|
January 16, 2009
Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype
Tadayuki Akagi, Seishi Ogawa, Martin Dugas, et al.
Human Mutation
|
July 29, 2014
A new workflow for whole-genome sequencing of single human cells
Vera Binder, Christoph Bartenhagen, Vera Okpanyi, et al.
Page
of 34
Search research articles
Search
Showing results (231-240 of 336) with videos related to
Sort By:
Page
of 34
Frontiers in Oncology
|
July 25, 2022
Clonal Evolution at First Sight: A Combined Visualization of Diverse Diagnostic Methods Improves Understanding of Leukemic Progression
Sarah Sandmann, Yvonne Lisa Behrens, Claudia Davenport, et al.
Studies in Health Technology and Informatics
|
May 17, 2025
Quality of Life Trajectories with EHR Integration
Martin Dugas, Robin Fleige, Stephan Christoph Feder, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
April 23, 2004
Global gene expression in human myocardium-oligonucleotide microarray analysis of regional diversity and transcriptional regulation in heart failure
Stefan Kääb, Andreas S Barth, Daniel Margerie, et al.
Blood Advances
|
September 24, 2021
Calcitonin receptor-like (CALCRL) is a marker of stemness and an independent predictor of outcome in pediatric AML
Linus Angenendt, Marius Wöste, Jan-Henrik Mikesch, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 19, 2022
A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels
Maria Schubert, Lina Pérez Lanuza, Marius Wöste, et al.
Journal of Medical Internet Research
|
January 11, 2022
Understanding the Nature of Metadata: Systematic Review
Hannes Ulrich, Ann-Kristin Kock-Schoppenhauer, Noemi Deppenwiese, et al.
Clinical Epigenetics
|
August 22, 2021
Whole-genome methylation analysis of testicular germ cells from cryptozoospermic men points to recurrent and functionally relevant DNA methylation changes
Sara Di Persio, Elsa Leitão, Marius Wöste, et al.
Oncology Reports
|
June 2, 2010
Low SMC1A protein expression predicts poor survival in acute myeloid leukemia
Claudia Hömme, Utz Krug, Nicola Tidow, et al.
Haematologica
|
January 16, 2009
Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype
Tadayuki Akagi, Seishi Ogawa, Martin Dugas, et al.
Human Mutation
|
July 29, 2014
A new workflow for whole-genome sequencing of single human cells
Vera Binder, Christoph Bartenhagen, Vera Okpanyi, et al.
Page
of 34