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...

MiR-151a: a robust endogenous control for normalizing small extracellular vesicle cargo in human cancer

Biomarker research, 2023-10, Vol.11 (1), p.1-94, Article 94

2023

Volltextzugriff (PDF)

Functional Analysis of 3′UTR Variants at the LDLR and PCSK9 Genes in Patients with Familial Hypercholesterolemia

Human mutation, 2024-02, Vol.2024, p.1-15

2024

Volltextzugriff (PDF)

Analytical validation of a laboratory-development multigene pharmacogenetic assay

Pharmacogenetics and genomics, 2021-10, Vol.31 (8), p.177-184

2021

Volltextzugriff (PDF)

The impact of next-generation sequencing on the DNA methylation–based translational cancer research

Translational research : the journal of laboratory and clinical medicine, 2016-03, Vol.169, p.1-18.e1

2016

Volltextzugriff (PDF)

Evaluation of the clinical use of MGMT methylation in extracellular vesicle-based liquid biopsy as a tool for glioblastoma patient management

Scientific reports, 2024-05, Vol.14 (1), p.11398-11398, Article 11398

2024

Volltextzugriff (PDF)

Molecular diagnosis of cystic fibrosis by RNA obtained from nasal epithelial cells

Journal of cystic fibrosis, 2024-07, Vol.23 (4), p.788-795

2024

Volltextzugriff (PDF)

Prognostic Impact of Dihydropyrimidine Dehydrogenase Germline Variants in Unresectable Non-Small Cell Lung Cancer Patients Treated with Platin-Based Chemotherapy

International journal of molecular sciences, 2023-06, Vol.24 (12), p.9843

2023

Volltextzugriff (PDF)

DNA Methylation of miR-7 is a Mechanism Involved in Platinum Response through MAFG Overexpression in Cancer Cells

Theranostics, 2017-01, Vol.7 (17), p.4118-4134

2017

Volltextzugriff (PDF)

Transcriptional epigenetic regulation of Fkbp1/Pax9 genes is associated with impaired sensitivity to platinum treatment in ovarian cancer

Clinical epigenetics, 2021-12, Vol.13 (1), p.167-167, Article 167

2021

Volltextzugriff (PDF)

An epigenomic approach to identifying differential overlapping and cis-acting lncRNAs in cisplatin-resistant cancer cells

Epigenetics, 2018-03, Vol.13 (3), p.251-263

2018

Volltextzugriff (PDF)

Evaluation of two automated low-cost RNA extraction protocols for SARS-CoV-2 detection

PloS one, 2021-02, Vol.16 (2), p.e0246302-e0246302

2021

Volltextzugriff (PDF)

Symptomatic heterozygous X-Linked myotubular myopathy female patient with a large deletion at Xq28 and decrease expression of normal allele

European journal of medical genetics, 2021-04, Vol.64 (4), p.104170-104170, Article 104170

2021

Volltextzugriff (PDF)

miR-124 as a Liquid Biopsy Prognostic Biomarker in Small Extracellular Vesicles from NSCLC Patients

International journal of molecular sciences, 2023-07, Vol.24 (14), p.11464

2023

Volltextzugriff (PDF)

Role of Dusp6 Phosphatase as a Tumor Suppressor in Non-Small Cell Lung Cancer

International journal of molecular sciences, 2019-04, Vol.20 (8), p.2036

2019

Volltextzugriff (PDF)

Clinical validation of a novel quantitative assay for the detection of MGMT methylation in glioblastoma patients

Clinical epigenetics, 2021-03, Vol.13 (1), p.52-52, Article 52

2021

Volltextzugriff (PDF)

A Novel Role for the Tumor Suppressor Gene ITF2 in Tumorigenesis and Chemotherapy Response

Cancers, 2020-03, Vol.12 (4), p.786

2020

Volltextzugriff (PDF)

Artificial Intelligence Will Not Replace Health Professionals, but the Proper Use of Artificial Intelligence Will Make Health Professionals Better

Cancer research (Chicago, Ill.), 2020-05, Vol.80 (10), p.1912-1913

Rodriguez-Antolin, Carlos

2020

Volltextzugriff (PDF)

Functional analysis of new variants at the low‐density lipoprotein receptor associated with familial hypercholesterolemia

Human mutation, 2019-08, Vol.40 (8), p.1181-1190, Article humu.23801

2019

Volltextzugriff (PDF)

A SCN4A mutation causing paramyotonia congenita

Neuromuscular disorders : NMD, 2017-12, Vol.27 (12), p.1123-1125

2017

Volltextzugriff (PDF)

Optimizing the Procedure to Manufacture Clinical-Grade NK Cells for Adoptive Immunotherapy

Cancers, 2021-02, Vol.13 (3), p.577

2021

Volltextzugriff (PDF)

Hereditary spastic paraplegia associated with a novel homozygous intronic noncanonical splice site variant in the AP4B1 gene

Annals of human genetics, 2022-05, Vol.86 (3), p.109-118

2022

Volltextzugriff (PDF)

Abstract 2381: miRNome exosomal characterization reveals a distinct signature able to predict cisplatin-response in NSCLC patients

Cancer research (Chicago, Ill.), 2021-07, Vol.81 (13_Supplement), p.2381-2381

2021

Volltextzugriff (PDF)

Novel SLC12A2‐ROS1 Fusion in Non‐Small Cell Lung Cancer with a Significant Response to Crizotinib: The Importance of Choosing the Appropriate Next‐Generation Sequencing Assay

The oncologist (Dayton, Ohio), 2021-06, Vol.26 (6), p.e908-e912

2021

Volltextzugriff (PDF)

Advancing pharmacogenetic testing in a tertiary hospital: a retrospective analysis after 10 years of activity

Frontiers in pharmacology, 2023-10, Vol.14, p.1292416-1292416

2023

Volltextzugriff (PDF)

NKG2D-CAR memory T cells target pediatric T-cell acute lymphoblastic leukemia in vitro and in vivo but fail to eliminate leukemia initiating cells

Frontiers in immunology, 2023-10, Vol.14, p.1187665-1187665

2023

Volltextzugriff (PDF)

1 – 25 von 51

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(47)
Mit Volltextzugriff
(46)

Publikationsform

Artikel
(50)
magazinearticle
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

MiR-151a: a robust endogenous control for normalizing small extracellular vesicle cargo in human cancer

Functional Analysis of 3′UTR Variants at the LDLR and PCSK9 Genes in Patients with Familial Hypercholesterolemia

Analytical validation of a laboratory-development multigene pharmacogenetic assay

The impact of next-generation sequencing on the DNA methylation–based translational cancer research

Evaluation of the clinical use of MGMT methylation in extracellular vesicle-based liquid biopsy as a tool for glioblastoma patient management

Molecular diagnosis of cystic fibrosis by RNA obtained from nasal epithelial cells

Prognostic Impact of Dihydropyrimidine Dehydrogenase Germline Variants in Unresectable Non-Small Cell Lung Cancer Patients Treated with Platin-Based Chemotherapy

DNA Methylation of miR-7 is a Mechanism Involved in Platinum Response through MAFG Overexpression in Cancer Cells

Transcriptional epigenetic regulation of Fkbp1/Pax9 genes is associated with impaired sensitivity to platinum treatment in ovarian cancer

An epigenomic approach to identifying differential overlapping and cis-acting lncRNAs in cisplatin-resistant cancer cells

Evaluation of two automated low-cost RNA extraction protocols for SARS-CoV-2 detection

Symptomatic heterozygous X-Linked myotubular myopathy female patient with a large deletion at Xq28 and decrease expression of normal allele

miR-124 as a Liquid Biopsy Prognostic Biomarker in Small Extracellular Vesicles from NSCLC Patients

Role of Dusp6 Phosphatase as a Tumor Suppressor in Non-Small Cell Lung Cancer

Clinical validation of a novel quantitative assay for the detection of MGMT methylation in glioblastoma patients

A Novel Role for the Tumor Suppressor Gene ITF2 in Tumorigenesis and Chemotherapy Response

Artificial Intelligence Will Not Replace Health Professionals, but the Proper Use of Artificial Intelligence Will Make Health Professionals Better

Functional analysis of new variants at the low‐density lipoprotein receptor associated with familial hypercholesterolemia

A SCN4A mutation causing paramyotonia congenita

Optimizing the Procedure to Manufacture Clinical-Grade NK Cells for Adoptive Immunotherapy

Hereditary spastic paraplegia associated with a novel homozygous intronic noncanonical splice site variant in the AP4B1 gene

Abstract 2381: miRNome exosomal characterization reveals a distinct signature able to predict cisplatin-response in NSCLC patients

Novel SLC12A2‐ROS1 Fusion in Non‐Small Cell Lung Cancer with a Significant Response to Crizotinib: The Importance of Choosing the Appropriate Next‐Generation Sequencing Assay

Advancing pharmacogenetic testing in a tertiary hospital: a retrospective analysis after 10 years of activity

NKG2D-CAR memory T cells target pediatric T-cell acute lymphoblastic leukemia in vitro and in vivo but fail to eliminate leukemia initiating cells

Suchergebnisse filtern