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...

Mutant U2AF1 Expression Alters Hematopoiesis and Pre-mRNA Splicing In Vivo

Cancer cell, 2015-05, Vol.27 (5), p.631-643

2015

Volltextzugriff (PDF)

Cellular stressors contribute to the expansion of hematopoietic clones of varying leukemic potential

Nature communications, 2018-01, Vol.9 (1), p.455-10, Article 455

2018

Volltextzugriff (PDF)

Mutation Clearance after Transplantation for Myelodysplastic Syndrome

The New England journal of medicine, 2018-09, Vol.379 (11), p.1028-1041

2018

Volltextzugriff (PDF)

Comparison of Clinical Targeted Next-Generation Sequence Data from Formalin-Fixed and Fresh-Frozen Tissue Specimens

The Journal of molecular diagnostics : JMD, 2013-09, Vol.15 (5), p.623-633

2013

Volltextzugriff (PDF)

Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches

Cancer genetics, 2013-12, Vol.206 (12), p.432-440

2013

Volltextzugriff (PDF)

TGF-β signaling in myeloproliferative neoplasms contributes to myelofibrosis without disrupting the hematopoietic niche

The Journal of clinical investigation, 2022-06, Vol.132 (11)

2022

Volltextzugriff (PDF)

TP53 immunohistochemistry correlates with TP53 mutation status and clearance in decitabine-treated patients with myeloid malignancies

Haematologica (Roma), 2019-08, Vol.104 (8), p.e345-e348

2019

Volltextzugriff (PDF)

MED12 exon 2 mutations in uterine and extrauterine smooth muscle tumors

Human pathology, 2014, Vol.45 (1), p.65-70

2014

Volltextzugriff (PDF)

Targeted next‐generation sequencing using fine‐needle aspirates from adenocarcinomas of the lung

Cancer cytopathology, 2014-02, Vol.122 (2), p.104-113

2014

Volltextzugriff (PDF)

T-cell clonality assessment by next-generation sequencing improves detection sensitivity in mycosis fungoides

Journal of the American Academy of Dermatology, 2015-08, Vol.73 (2), p.228-236.e2

2015

Volltextzugriff (PDF)

Performance of Common Analysis Methods for Detecting Low-Frequency Single Nucleotide Variants in Targeted Next-Generation Sequence Data

The Journal of molecular diagnostics : JMD, 2014, Vol.16 (1), p.75-88

2014

Volltextzugriff (PDF)

Retinoblastoma gene mutations detected by whole exome sequencing of Merkel cell carcinoma

Modern pathology, 2014-08, Vol.27 (8), p.1073-1087

2014

Volltextzugriff (PDF)

Targeted next generation sequencing of clinically significant gene mutations and translocations in leukemia

Modern pathology, 2012-06, Vol.25 (6), p.795-804

2012

Volltextzugriff (PDF)

Sequencing-Based Measurable Residual Disease Testing in Acute Myeloid Leukemia

Frontiers in cell and developmental biology, 2020-05, Vol.8, p.249-249

2020

Volltextzugriff (PDF)

Detection of FLT3 Internal Tandem Duplication in Targeted, Short-Read-Length, Next-Generation Sequencing Data

The Journal of molecular diagnostics : JMD, 2013, Vol.15 (1), p.81-93

2013

Volltextzugriff (PDF)

The evaluation of the delayed swollen breast in patients with a history of breast implants

Frontiers in oncology, 2023-07, Vol.13, p.1174173-1174173

2023

Volltextzugriff (PDF)

Tumor suppressor function of WT1 in acute promyelocytic leukemia

Haematologica (Roma), 2022-01, Vol.107 (1), p.342-346

2022

Volltextzugriff (PDF)

Discriminating a common somatic ASXL1 mutation (c.1934dup; p.G646Wfs12) from artifact in myeloid malignancies using NGS

Leukemia, 2018-08, Vol.32 (8), p.1874-1878

2018

Volltextzugriff (PDF)

A Model Study of In Silico Proficiency Testing for Clinical Next-Generation Sequencing

Archives of pathology & laboratory medicine (1976), 2016-10, Vol.140 (10), p.1085-1091

2016

Volltextzugriff (PDF)

Spectrum of mutations in leiomyosarcomas identified by clinical targeted next-generation sequencing

Experimental and molecular pathology, 2017-02, Vol.102 (1), p.156-161

2017

Volltextzugriff (PDF)

Occult Specimen Contamination in Routine Clinical Next-Generation Sequencing Testing

American journal of clinical pathology, 2015-10, Vol.144 (4), p.667-674

2015

Volltextzugriff (PDF)

CD163 immunohistochemistry is superior to CD68 in predicting outcome in classical Hodgkin lymphoma

American journal of clinical pathology, 2014-03, Vol.141 (3), p.381-387

2014

Volltextzugriff (PDF)

Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists

The Journal of molecular diagnostics : JMD, 2017-01, Vol.19 (1), p.4-23

2017

Volltextzugriff (PDF)

Exome analysis of treatment‐related AML after APL suggests secondary evolution

British journal of haematology, 2019-06, Vol.185 (5), p.984-987

2019

Volltextzugriff (PDF)

Detection of Gene Rearrangements in Targeted Clinical Next-Generation Sequencing

The Journal of molecular diagnostics : JMD, 2014-07, Vol.16 (4), p.405-417

2014

Volltextzugriff (PDF)

1 – 25 von 144

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(139)
Mit Volltextzugriff
(132)

Publikationsform

Artikel
(143)
Berichte
(1)

Sprache

Englisch
(144)

Erscheinungsjahr

n.n

Thema

Science & Technology
(98)
Life Sciences & Biomedicine
(97)
Humans
(75)
Pathology
(47)
Mutation
(37)
Female
(28)
Male
(25)
Middle Aged
(25)
Hematology
(24)
Adult
(22)
Oncology
(22)
Aged
(21)
Leukemia, Myeloid, Acute - Genetics
(16)
High-Throughput Nucleotide Sequencing - Methods
(15)
Leukemia
(14)
Myelodysplastic Syndromes - Genetics
(13)
Medicine
(12)
Acute Myeloid Leukemia
(11)
Aged, 80 And Over
(11)
High-Throughput Nucleotide Sequencing
(11)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Mutant U2AF1 Expression Alters Hematopoiesis and Pre-mRNA Splicing In Vivo

Cellular stressors contribute to the expansion of hematopoietic clones of varying leukemic potential

Mutation Clearance after Transplantation for Myelodysplastic Syndrome

Comparison of Clinical Targeted Next-Generation Sequence Data from Formalin-Fixed and Fresh-Frozen Tissue Specimens

Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches

TGF-β signaling in myeloproliferative neoplasms contributes to myelofibrosis without disrupting the hematopoietic niche

TP53 immunohistochemistry correlates with TP53 mutation status and clearance in decitabine-treated patients with myeloid malignancies

MED12 exon 2 mutations in uterine and extrauterine smooth muscle tumors

Targeted next‐generation sequencing using fine‐needle aspirates from adenocarcinomas of the lung

T-cell clonality assessment by next-generation sequencing improves detection sensitivity in mycosis fungoides

Performance of Common Analysis Methods for Detecting Low-Frequency Single Nucleotide Variants in Targeted Next-Generation Sequence Data

Retinoblastoma gene mutations detected by whole exome sequencing of Merkel cell carcinoma

Targeted next generation sequencing of clinically significant gene mutations and translocations in leukemia

Sequencing-Based Measurable Residual Disease Testing in Acute Myeloid Leukemia

Detection of FLT3 Internal Tandem Duplication in Targeted, Short-Read-Length, Next-Generation Sequencing Data

The evaluation of the delayed swollen breast in patients with a history of breast implants

Tumor suppressor function of WT1 in acute promyelocytic leukemia

Discriminating a common somatic ASXL1 mutation (c.1934dup; p.G646Wfs12) from artifact in myeloid malignancies using NGS

A Model Study of In Silico Proficiency Testing for Clinical Next-Generation Sequencing

Spectrum of mutations in leiomyosarcomas identified by clinical targeted next-generation sequencing

Occult Specimen Contamination in Routine Clinical Next-Generation Sequencing Testing

CD163 immunohistochemistry is superior to CD68 in predicting outcome in classical Hodgkin lymphoma

Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists

Exome analysis of treatment‐related AML after APL suggests secondary evolution

Detection of Gene Rearrangements in Targeted Clinical Next-Generation Sequencing

Suchergebnisse filtern