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...

Colistin resistance in Klebsiella pneumoniae

International journal of antimicrobial agents, 2014-07, Vol.44 (1), p.8-15

2014

Volltextzugriff (PDF)

The new HLA‐DQA103:50Q allele discovered by next‐generation sequencing in a Korean family

HLA, 2023-12, Vol.102 (6), p.770-772

2023

Volltextzugriff (PDF)

White blood cell differential count of maturation stages in bone marrow smear using dual-stage convolutional neural networks

PloS one, 2017-12, Vol.12 (12), p.e0189259-e0189259

2017

Volltextzugriff (PDF)

Idiopathic hypereosinophilia is clonal disorder? Clonality identified by targeted sequencing

PloS one, 2017-10, Vol.12 (10), p.e0185602-e0185602

2017

Volltextzugriff (PDF)

Overlooked KCNQ4 variants augment the risk of hearing loss

Experimental and Molecular Medicine, 2023, 55(0), , pp.844-859

2023

Volltextzugriff (PDF)

Metabolite Profiling and Characterization of LW6, a Novel HIF-1α Inhibitor, as an Antitumor Drug Candidate in Mice

Molecules (Basel, Switzerland), 2021-03, Vol.26 (7), p.1951

2021

Volltextzugriff (PDF)

Telomere length and its correlation with gene mutations in chronic lymphocytic leukemia in a Korean population

PloS one, 2019-07, Vol.14 (7), p.e0220177-e0220177

2019

Volltextzugriff (PDF)

A novel bi-alleleic DDX41 mutations in B-cell lymphoblastic leukemia: case report

BMC medical genomics, 2022-03, Vol.15 (1), p.46-46, Article 46

2022

Volltextzugriff (PDF)

Psychological Ownership and Ambivalent Employee Behaviors: A Moderated Mediation Model

SAGE open, 2023-01, Vol.13 (1)

2023

Volltextzugriff (PDF)

Telomere length and somatic mutations in correlation with response to immunosuppressive treatment in aplastic anaemia

British journal of haematology, 2017-08, Vol.178 (4), p.603-615

2017

Volltextzugriff (PDF)

Genomic Profile of Chronic Lymphocytic Leukemia in Korea Identified by Targeted Sequencing

PloS one, 2016-12, Vol.11 (12), p.e0167641-e0167641

2016

Volltextzugriff (PDF)

Effectiveness of pegfilgrastim prophylaxis in preventing febrile neutropenia during R-FC chemoimmunotherapy for chronic lymphocytic leukemia: A multicenter prospective phase II study

Frontiers in oncology, 2023-03, Vol.13, p.998014

2023

Volltextzugriff (PDF)

A rare case of primary plasma cell leukemia exhibiting the small-cell variant of plasma cells

Blood Research, 2022, 57(2), , pp.161-164

2022

Volltextzugriff (PDF)

ASXL1 is a molecular predictor in idiopathic cytopenia of undetermined significance

Leukemia & lymphoma, 2019-02, Vol.60 (3), p.756-763

2019

Volltextzugriff (PDF)

A Case of Acute Myeloid Leukemia With inv(16)(p13.1q22);CBFB-MYH11 Presenting With Faggot Cells

Annals of Laboratory Medicine, 2021, 41(3), , pp.333-335

2021

Volltextzugriff (PDF)

Underlying Microstructure of Parapapillary Deep-Layer Capillary Dropout Identified by Optical Coherence Tomography Angiography

Investigative ophthalmology & visual science, 2017-03, Vol.58 (3), p.1621-1627

2017

Volltextzugriff (PDF)

Asymmetric aneuploidy in mesenchymal stromal cells detected by in situ karyotyping and fluorescence in situ hybridization: suggestions for reference values for stem cells

Stem cells and development, 2015-01, Vol.24 (1), p.77-92

2015

Volltextzugriff (PDF)

CALR, JAK2, and MPL mutation profiles in patients with four different subtypes of myeloproliferative neoplasms: primary myelofibrosis, essential thrombocythemia, polycythemia vera, and myeloproliferative neoplasm, unclassifiable

American journal of clinical pathology, 2015-05, Vol.143 (5), p.635-644

2015

Volltextzugriff (PDF)

The novel HLA‐A allele, HLA‐A03:478, identified in a Korean individual

HLA, 2024-07, Vol.104 (1), p.e15595-n/a

2024

Volltextzugriff (PDF)

Human health and ecological assessment programs for Hebei Spirit oil spill accident of 2007: Status, lessons, and future challenges

Chemosphere (Oxford), 2017-04, Vol.173, p.180-189

2017

Volltextzugriff (PDF)

Leaching of Rare-Earth Elements and Their Adsorption by Using Blue-Green Algae

Materials transactions, 2011, Vol.52 (9), p.1799-1806

2011

Volltextzugriff (PDF)

Vestibular hair cells are more prone to damage by excessive acceleration insult in the mouse with KCNQ4 dysfunction

Scientific reports, 2024-07, Vol.14 (1), p.15260-17, Article 15260

2024

Volltextzugriff (PDF)

COCH-related autosomal dominant nonsyndromic hearing loss: a phenotype–genotype study

Human genetics, 2022-04, Vol.141 (3-4), p.889-901

2022

Volltextzugriff (PDF)

Associative Interactions among Zinc, Apolipoprotein E, and Amyloid-β in the Amyloid Pathology

International journal of molecular sciences, 2020-01, Vol.21 (3), p.802

2020

Volltextzugriff (PDF)

Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte

Orphanet journal of rare diseases, 2019-05, Vol.14 (1), p.114-114, Article 114

2019

Volltextzugriff (PDF)

1 – 25 von 6.437

Suche als RSS-Feed

Aktive Filter

ThemaOriginal

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(5.430)
Mit Volltextzugriff
(5.182)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

2 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(3.545)
Life Sciences & Biomedicine
(2.948)
Humans
(1.806)
Female
(1.128)
Male
(1.056)
Middle Aged
(760)
Adult
(733)
Animals
(610)
Aged
(564)
Oncology
(468)
Physical Sciences
(412)
Mice
(389)
Biological And Medical Sciences
(384)
Medicine
(356)
Science & Technology - Other Topics
(347)
Chemistry
(333)
Pharmacology & Pharmacy
(317)
Retrospective Studies
(311)
Technology
(311)
Biochemistry & Molecular Biology
(299)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Colistin resistance in Klebsiella pneumoniae

The new HLA‐DQA103:50Q allele discovered by next‐generation sequencing in a Korean family

White blood cell differential count of maturation stages in bone marrow smear using dual-stage convolutional neural networks

Idiopathic hypereosinophilia is clonal disorder? Clonality identified by targeted sequencing

Overlooked KCNQ4 variants augment the risk of hearing loss

Metabolite Profiling and Characterization of LW6, a Novel HIF-1α Inhibitor, as an Antitumor Drug Candidate in Mice

Telomere length and its correlation with gene mutations in chronic lymphocytic leukemia in a Korean population

A novel bi-alleleic DDX41 mutations in B-cell lymphoblastic leukemia: case report

Psychological Ownership and Ambivalent Employee Behaviors: A Moderated Mediation Model

Telomere length and somatic mutations in correlation with response to immunosuppressive treatment in aplastic anaemia

Genomic Profile of Chronic Lymphocytic Leukemia in Korea Identified by Targeted Sequencing

Effectiveness of pegfilgrastim prophylaxis in preventing febrile neutropenia during R-FC chemoimmunotherapy for chronic lymphocytic leukemia: A multicenter prospective phase II study

A rare case of primary plasma cell leukemia exhibiting the small-cell variant of plasma cells

ASXL1 is a molecular predictor in idiopathic cytopenia of undetermined significance

A Case of Acute Myeloid Leukemia With inv(16)(p13.1q22);CBFB-MYH11 Presenting With Faggot Cells

Underlying Microstructure of Parapapillary Deep-Layer Capillary Dropout Identified by Optical Coherence Tomography Angiography

Asymmetric aneuploidy in mesenchymal stromal cells detected by in situ karyotyping and fluorescence in situ hybridization: suggestions for reference values for stem cells

CALR, JAK2, and MPL mutation profiles in patients with four different subtypes of myeloproliferative neoplasms: primary myelofibrosis, essential thrombocythemia, polycythemia vera, and myeloproliferative neoplasm, unclassifiable

The novel HLA‐A allele, HLA‐A03:478, identified in a Korean individual

Human health and ecological assessment programs for Hebei Spirit oil spill accident of 2007: Status, lessons, and future challenges

Leaching of Rare-Earth Elements and Their Adsorption by Using Blue-Green Algae

Vestibular hair cells are more prone to damage by excessive acceleration insult in the mouse with KCNQ4 dysfunction

COCH-related autosomal dominant nonsyndromic hearing loss: a phenotype–genotype study

Associative Interactions among Zinc, Apolipoprotein E, and Amyloid-β in the Amyloid Pathology

Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte

Aktive Filter

Suchergebnisse filtern