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...

Nanoarray Digital Polymerase Chain Reaction with High-Resolution Melt for Enabling Broad Bacteria Identification and Pheno–Molecular Antimicrobial Susceptibility Test

Analytical chemistry (Washington), 2019-10, Vol.91 (20), p.12784-12792

2019

Volltextzugriff (PDF)

Highly Efficient Real-Time Droplet Analysis Platform for High-Throughput Interrogation of DNA Sequences by Melt

Analytical chemistry (Washington), 2019-09, Vol.91 (17), p.11275-11282

2019

Volltextzugriff (PDF)

Confidentiality and Differential Privacy in the Dissemination of Frequency Tables

Statistical science, 2018-08, Vol.33 (3), p.358-385

2018

Volltextzugriff (PDF)

Facile Coupling of Droplet Magnetofluidic-Enabled Automated Sample Preparation for Digital Nucleic Acid Amplification Testing and Analysis

Analytical chemistry (Washington), 2020-10, Vol.92 (19), p.13254-13261

2020

Volltextzugriff (PDF)

Biomedical data privacy: problems, perspectives, and recent advances

Journal of the American Medical Informatics Association : JAMIA, 2013-01, Vol.20 (1), p.2-6

2013

Volltextzugriff (PDF)

Individual privacy versus public good: protecting confidentiality in health research

Statistics in medicine, 2015-10, Vol.34 (23), p.3081-3103

2015

Volltextzugriff (PDF)

Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML

Blood, 2008-02, Vol.111 (3), p.1534-1542

2008

Volltextzugriff (PDF)

Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

Blood, 2010-04, Vol.115 (14), p.2731-2739

2010

Volltextzugriff (PDF)

Multilayer microfluidic array for highly efficient sample loading and digital melt analysis of DNA methylation

Lab on a chip, 2019-01, Vol.19 (3), p.444-451

2019

Volltextzugriff (PDF)

Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms

Blood, 2009-06, Vol.113 (25), p.6403-6410

2009

Volltextzugriff (PDF)

Fabrication of Multilayer Microfluidic Arrays for Passive, Efficient DNA Trapping and Profiling

Methods in molecular biology (Clifton, N.J.), 2023, Vol.2679, p.315

2023

Volltextzugriff (PDF)

250K Single Nucleotide Polymorphism Array Karyotyping Identifies Acquired Uniparental Disomy and Homozygous Mutations, Including Novel Missense Substitutions of c-Cbl, in Myeloid Malignancies

Cancer research (Chicago, Ill.), 2008-12, Vol.68 (24), p.10349-10357

2008

Volltextzugriff (PDF)

Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies

Blood, 2011-04, Vol.117 (17), p.4552-4560

2011

Volltextzugriff (PDF)

SNP array–based karyotyping: differences and similarities between aplastic anemia and hypocellular myelodysplastic syndromes

Blood, 2011-06, Vol.117 (25), p.6876-6884

2011

Volltextzugriff (PDF)

Aberrant DNA methylation is a dominant mechanism in MDS progression to AML

Blood, 2009-02, Vol.113 (6), p.1315-1325

2009

Volltextzugriff (PDF)

Application of array‐based whole genome scanning technologies as a cytogenetic tool in haematological malignancies

British journal of haematology, 2009-09, Vol.146 (5), p.479-488

2009

Volltextzugriff (PDF)

Multiplex Digital Methylation‐Specific PCR for Noninvasive Screening of Lung Cancer

Advanced science, 2023-06, Vol.10 (16), p.e2206518-n/a

2023

Volltextzugriff (PDF)

Anonymization for outputs of population health and health services research conducted via an online data center

Journal of the American Medical Informatics Association : JAMIA, 2017-05, Vol.24 (3), p.544-549

2017

Volltextzugriff (PDF)

Advancing the ethical use of digital data in human research: challenges and strategies to promote ethical practice

Ethics and information technology, 2019-03, Vol.21 (1), p.59-73

2019

Volltextzugriff (PDF)

Topography, Clinical, and Genomic Correlates of 5q Myeloid Malignancies Revisited

Journal of clinical oncology, 2012-04, Vol.30 (12), p.1343-1349

2012

Volltextzugriff (PDF)

Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis

Blood, 2012-06, Vol.119 (25), p.6109-6117

2012

Volltextzugriff (PDF)

SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromes

Blood, 2012-10, Vol.120 (16), p.3173-3186

2012

Volltextzugriff (PDF)

Assessing privacy risks in population health publications using a checklist-based approach

Journal of the American Medical Informatics Association : JAMIA, 2018-03, Vol.25 (3), p.315-320

2018

Volltextzugriff (PDF)

Comparison of Two Remote Access Systems Recently Developed and Implemented in Australia

Privacy in Statistical Databases, 2014, p.299-311

2014

Volltextzugriff (PDF)

CBL, CBLB, TET2, ASXL1, and IDH1/2 mutations and additional chromosomal aberrations constitute molecular events in chronic myelogenous leukemia

Blood, 2011-05, Vol.117 (21), p.e198-e206

2011

Volltextzugriff (PDF)

1 – 25 von 331

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(296)
Mit Volltextzugriff
(303)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(329)

Erscheinungsjahr

n.n

Thema

Science & Technology
(157)
Life Sciences & Biomedicine
(106)
Humans
(88)
Male
(51)
Female
(45)
Middle Aged
(40)
Physical Sciences
(35)
Aged
(34)
Adult
(33)
Biological And Medical Sciences
(29)
Hematology
(28)
Mathematics
(26)
Technology
(26)
Medical Sciences
(25)
Computer Science
(21)
Immunology
(21)
Confidentiality
(19)
Hematologic And Hematopoietic Diseases
(19)
Polymorphism, Single Nucleotide
(17)
Adolescent
(16)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Nanoarray Digital Polymerase Chain Reaction with High-Resolution Melt for Enabling Broad Bacteria Identification and Pheno–Molecular Antimicrobial Susceptibility Test

Highly Efficient Real-Time Droplet Analysis Platform for High-Throughput Interrogation of DNA Sequences by Melt

Confidentiality and Differential Privacy in the Dissemination of Frequency Tables

Facile Coupling of Droplet Magnetofluidic-Enabled Automated Sample Preparation for Digital Nucleic Acid Amplification Testing and Analysis

Biomedical data privacy: problems, perspectives, and recent advances

Individual privacy versus public good: protecting confidentiality in health research

Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML

Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

Multilayer microfluidic array for highly efficient sample loading and digital melt analysis of DNA methylation

Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms

Fabrication of Multilayer Microfluidic Arrays for Passive, Efficient DNA Trapping and Profiling

250K Single Nucleotide Polymorphism Array Karyotyping Identifies Acquired Uniparental Disomy and Homozygous Mutations, Including Novel Missense Substitutions of c-Cbl, in Myeloid Malignancies

Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies

SNP array–based karyotyping: differences and similarities between aplastic anemia and hypocellular myelodysplastic syndromes

Aberrant DNA methylation is a dominant mechanism in MDS progression to AML

Application of array‐based whole genome scanning technologies as a cytogenetic tool in haematological malignancies

Multiplex Digital Methylation‐Specific PCR for Noninvasive Screening of Lung Cancer

Anonymization for outputs of population health and health services research conducted via an online data center

Advancing the ethical use of digital data in human research: challenges and strategies to promote ethical practice

Topography, Clinical, and Genomic Correlates of 5q Myeloid Malignancies Revisited

Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis

SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromes

Assessing privacy risks in population health publications using a checklist-based approach

Comparison of Two Remote Access Systems Recently Developed and Implemented in Australia

CBL, CBLB, TET2, ASXL1, and IDH1/2 mutations and additional chromosomal aberrations constitute molecular events in chronic myelogenous leukemia

Suchergebnisse filtern