UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Cytogenetic testing by fluorescence in situ hybridization is improved by plasma cell sorting in multiple myeloma

Scientific reports, 2022-05, Vol.12 (1), p.8287-8287, Article 8287

2022

Volltextzugriff (PDF)

Exosome-based detection of EGFR T790M in plasma and pleural fluid of prospectively enrolled non-small cell lung cancer patients after first-line tyrosine kinase inhibitor therapy

Cancer cell international, 2021-01, Vol.21 (1), p.50-50, Article 50

2021

Volltextzugriff (PDF)

Clonal Spread of Extended-Spectrum Cephalosporin-Resistant Enterobacteriaceae Between Companion Animals and Humans in South Korea

Frontiers in microbiology, 2019-06, Vol.10, p.1371-1371

2019

Volltextzugriff (PDF)

A Comparative Study for Detection of EGFR Mutations in Plasma Cell-Free DNA in Korean Clinical Diagnostic Laboratories

BioMed research international, 2018-01, Vol.2018 (2018), p.1-11

2018

Volltextzugriff (PDF)

Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy

Brain & development (Tokyo. 1979), 2020-06, Vol.42 (6), p.438-448

2020

Volltextzugriff (PDF)

Development and validation of sensitive BCR::ABL1 fusion gene quantitation using next-generation sequencing

Cancer cell international, 2023-05, Vol.23 (1), p.106-106, Article 106

2023

Volltextzugriff (PDF)

A Case of STIL-TAL1 -positive T-lymphoblastic Leukemia With a Minor Philadelphia-positive Clone

Annals of Laboratory Medicine, 2023, 43(1), , pp.100-103

2023

Volltextzugriff (PDF)

Enhancing mutation detection in multiple myeloma with an error-corrected ultra-sensitive NGS assay without plasma cell enrichment

Cancer cell international, 2024-08, Vol.24 (1), p.1-10, Article 282

2024

Volltextzugriff (PDF)

Real-World Clinical Utility of Targeted RNA Sequencing in Leukemia Diagnosis and Management

Cancers, 2024-07, Vol.16 (13), p.2467

2024

Volltextzugriff (PDF)

Selecting short length nucleic acids localized in exosomes improves plasma EGFR mutation detection in NSCLC patients

Cancer cell international, 2019-10, Vol.19 (1), p.251-251, Article 251

2019

Volltextzugriff (PDF)

Clinical Practice Guidelines for Pre-Analytical Procedures of Plasma Epidermal Growth Factor Receptor Variant Testing

Annals of Laboratory Medicine, 2022, 42(2), , pp.141-149

2022

Volltextzugriff (PDF)

NUP214 Rearrangements in Leukemia Patients: A Case Series From a Single Institution

Annals of Laboratory Medicine, 2024, 44(4), , pp.335-342

2024

Volltextzugriff (PDF)

Genetic diagnosis of inborn errors of immunity using clinical exome sequencing

Frontiers in immunology, 2023-05, Vol.14, p.1178582-1178582

2023

Volltextzugriff (PDF)

Application of CRISPR/Cas9-based mutant enrichment technique to improve the clinical sensitivity of plasma EGFR testing in patients with non-small cell lung cancer

Cancer cell international, 2022-02, Vol.22 (1), p.82-82, Article 82

2022

Volltextzugriff (PDF)

Emergence of multidrug-resistant Providencia rettgeri isolates co-producing NDM-1 carbapenemase and PER-1 extended-spectrum β-lactamase causing a first outbreak in Korea

Annals of clinical microbiology and antimicrobials, 2018-05, Vol.17 (1), p.20-20, Article 20

2018

Volltextzugriff (PDF)

Comprehensive insights into AML relapse: genetic mutations, clonal evolution, and clinical outcomes

Cancer cell international, 2024-05, Vol.24 (1), p.174-174, Article 174

2024

Volltextzugriff (PDF)

Evaluation of Combined Cancer Markers With Lactate Dehydrogenase and Application of Machine Learning Algorithms for Differentiating Benign Disease From Malignant Ovarian Cancer

Cancer control, 2021-01, Vol.28, p.10732748211033401-10732748211033401

2021

Volltextzugriff (PDF)

Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort

Genes, 2021-12, Vol.13 (1), p.27

2021

Volltextzugriff (PDF)

A comparative study of next-generation sequencing and fragment analysis for the detection and allelic ratio determination of FLT3 internal tandem duplication

Diagnostic pathology, 2022-01, Vol.17 (1), p.14-8, Article 14

2022

Volltextzugriff (PDF)

Monitoring measurable residual disease in paediatric acute lymphoblastic leukaemia using immunoglobulin gene clonality based on next-generation sequencing

Cancer cell international, 2024-06, Vol.24 (1), p.1-10, Article 218

2024

Volltextzugriff (PDF)

Corrigendum: Genetic diagnosis of inborn errors of immunity using clinical exome sequencing

Frontiers in immunology, 2023-06, Vol.14, p.1235318-1235318

2023

Volltextzugriff (PDF)

Unraveling trajectories from aplastic anemia to hematologic malignancies: genetic and molecular insights

Frontiers in oncology, 2024-03, Vol.14, p.1365614-1365614

2024

Volltextzugriff (PDF)

The Genotype-Phenotype Correlation in Human 5α-Reductase Type 2 Deficiency: Classified and Analyzed from a SRD5A2 Structural Perspective

International journal of molecular sciences, 2023-02, Vol.24 (4), p.3297

2023

Volltextzugriff (PDF)

Diagnostic yield of targeted next-generation sequencing for pediatric hereditary hemolytic anemia

BMC medical genomics, 2023-09, Vol.16 (1), p.1-7, Article 215

2023

Volltextzugriff (PDF)

Optical genome mapping identifies clinically relevant genomic rearrangements in prostate cancer biopsy sample

Cancer cell international, 2022-10, Vol.22 (1), p.1-306, Article 306

2022

Volltextzugriff (PDF)

1 – 25 von 158

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(139)
Mit Volltextzugriff
(119)

Publikationsform

Artikel
(146)
Berichte
(12)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(96)
Life Sciences & Biomedicine
(93)
Humans
(56)
Medical Laboratory Technology
(34)
Female
(28)
Mutation
(26)
Oncology
(25)
Next-Generation Sequencing
(24)
병리학
(23)
Male
(21)
Patients
(21)
Genetic Aspects
(14)
High-Throughput Nucleotide Sequencing
(13)
Letter To The Editor
(13)
Republic Of Korea
(13)
Middle Aged
(12)
Original
(12)
Hematology
(11)
Adult
(10)
Bone Marrow
(10)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Cytogenetic testing by fluorescence in situ hybridization is improved by plasma cell sorting in multiple myeloma

Exosome-based detection of EGFR T790M in plasma and pleural fluid of prospectively enrolled non-small cell lung cancer patients after first-line tyrosine kinase inhibitor therapy

Clonal Spread of Extended-Spectrum Cephalosporin-Resistant Enterobacteriaceae Between Companion Animals and Humans in South Korea

A Comparative Study for Detection of EGFR Mutations in Plasma Cell-Free DNA in Korean Clinical Diagnostic Laboratories

Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy

Development and validation of sensitive BCR::ABL1 fusion gene quantitation using next-generation sequencing

A Case of STIL-TAL1 -positive T-lymphoblastic Leukemia With a Minor Philadelphia-positive Clone

Enhancing mutation detection in multiple myeloma with an error-corrected ultra-sensitive NGS assay without plasma cell enrichment

Real-World Clinical Utility of Targeted RNA Sequencing in Leukemia Diagnosis and Management

Selecting short length nucleic acids localized in exosomes improves plasma EGFR mutation detection in NSCLC patients

Clinical Practice Guidelines for Pre-Analytical Procedures of Plasma Epidermal Growth Factor Receptor Variant Testing

NUP214 Rearrangements in Leukemia Patients: A Case Series From a Single Institution

Genetic diagnosis of inborn errors of immunity using clinical exome sequencing

Application of CRISPR/Cas9-based mutant enrichment technique to improve the clinical sensitivity of plasma EGFR testing in patients with non-small cell lung cancer

Emergence of multidrug-resistant Providencia rettgeri isolates co-producing NDM-1 carbapenemase and PER-1 extended-spectrum β-lactamase causing a first outbreak in Korea

Comprehensive insights into AML relapse: genetic mutations, clonal evolution, and clinical outcomes

Evaluation of Combined Cancer Markers With Lactate Dehydrogenase and Application of Machine Learning Algorithms for Differentiating Benign Disease From Malignant Ovarian Cancer

Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort

A comparative study of next-generation sequencing and fragment analysis for the detection and allelic ratio determination of FLT3 internal tandem duplication

Monitoring measurable residual disease in paediatric acute lymphoblastic leukaemia using immunoglobulin gene clonality based on next-generation sequencing

Corrigendum: Genetic diagnosis of inborn errors of immunity using clinical exome sequencing

Unraveling trajectories from aplastic anemia to hematologic malignancies: genetic and molecular insights

The Genotype-Phenotype Correlation in Human 5α-Reductase Type 2 Deficiency: Classified and Analyzed from a SRD5A2 Structural Perspective

Diagnostic yield of targeted next-generation sequencing for pediatric hereditary hemolytic anemia

Optical genome mapping identifies clinically relevant genomic rearrangements in prostate cancer biopsy sample

Suchergebnisse filtern