UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 209

Sortiert nach

Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

American journal of human genetics, 2012-05, Vol.90 (5), p.856-863

2012

Link zum Volltext

Verfügbarkeit prüfen

Direct Measurement of the Elastohydrodynamic Lift Force at the Nanoscale

Physical review letters, 2020-02, Vol.124 (5), p.054502-054502, Article 054502

2020

Link zum Volltext

Verfügbarkeit prüfen

Forecasted E/P Ratio and ROE: Shanghai Stock Exchange (SSE), China

SAGE open, 2021-04, Vol.11 (2), p.215824402110231

Arshad, Muhammad Usman

2021

Link zum Volltext

Verfügbarkeit prüfen

Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability

American journal of human genetics, 2014-12, Vol.95 (6), p.721-728

2014

Link zum Volltext

Verfügbarkeit prüfen

A simplistic approach to evaluate the power conversion efficiencies for hybrid charge transport layers in open-air fabricated perovskite solar cells

Journal of materials research, 2022-04, Vol.37 (7), p.1323-1340

2022

Link zum Volltext

Verfügbarkeit prüfen

Deficiency in Aim2 affects viability and calcification of vascular smooth muscle cells from murine aortas and angiotensin-II induced aortic aneurysms

Molecular medicine (Cambridge, Mass.), 2020-09, Vol.26 (1), p.87-87, Article 87

2020

Link zum Volltext

Verfügbarkeit prüfen

Faculty Members’ Perception of Learning Organization: A Case of Higher Education Institutions

SAGE Open, 2023-01, Vol.13 (1), p.215824402311544

2023

Link zum Volltext

Verfügbarkeit prüfen

Scalable fabrication of hemispherical solid immersion lenses in silicon carbide through grayscale hard-mask lithography

Applied physics letters, 2023-04, Vol.122 (17)

2023

Link zum Volltext

Verfügbarkeit prüfen

Does Financial Sector Promote Economic Growth in Pakistan? Empirical Evidences From Markov Switching Model

SAGE open, 2020-10, Vol.10 (4), p.215824402096306

2020

Link zum Volltext

Verfügbarkeit prüfen

Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

American journal of human genetics, 2011-07, Vol.89 (1), p.176-182

2011

Link zum Volltext

Verfügbarkeit prüfen

Alterations in the Immune Cell Composition in Premalignant Breast Tissue that Precede Breast Cancer Development

Clinical cancer research, 2017-07, Vol.23 (14), p.3945-3952

2017

Link zum Volltext

Verfügbarkeit prüfen

Oligodontia Is Caused by Mutation in LTBP3, the Gene Encoding Latent TGF-β Binding Protein 3

American journal of human genetics, 2009-04, Vol.84 (4), p.519-523

2009

Link zum Volltext

Verfügbarkeit prüfen

Meta-Analysis on the Efficacy of Novel Glucose-Lowering Agents in Older Patients With Type 2 Diabetes Mellitus

The American journal of cardiology, 2023-01, Vol.187, p.127-130

2023

Link zum Volltext

Verfügbarkeit prüfen

A comprehensive author ranking evaluation of network and bibliographic indices

Malaysian journal of library & information science, 2020-01, Vol.25 (1), p.31-45

2020

Link zum Volltext

Verfügbarkeit prüfen

An Individual Patient-Level Meta-Analysis of Ischemic Versus Nonischemic Cardiomyopathy and Trajectory of Decongestion in Patients With Acute Decompensated Heart Failure

The American journal of cardiology, 2023-08, Vol.200, p.32-39

2023

Link zum Volltext

Verfügbarkeit prüfen

Entropy variation of rotating BTZ black hole under Hawking radiation

Physica scripta, 2022-04, Vol.97 (4), p.45005

2022

Link zum Volltext

Verfügbarkeit prüfen

Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopment

Human molecular genetics, 2015-06, Vol.24 (11), p.3172-3180

2015

Link zum Volltext

Verfügbarkeit prüfen

Readmissions in Patients With Heart Failure and Mental Health Disorders (from a National Database)

The American journal of cardiology, 2021-11, Vol.159, p.142-143

2021

Link zum Volltext

Verfügbarkeit prüfen

Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation

American journal of human genetics, 2009-12, Vol.85 (6), p.909-915

2009

Link zum Volltext

Verfügbarkeit prüfen

Optical in situ monitoring of plasma-enhanced atomic layer deposition process

Japanese Journal of Applied Physics, 2018-06, Vol.57 (6S2), p.6

2018

Link zum Volltext

Verfügbarkeit prüfen

Trade Openness and Public Innovation: A Causality Analysis

SAGE open, 2023-07, Vol.13 (3)

2023

Link zum Volltext

Verfügbarkeit prüfen

Crucial and diverse role of the interleukin-33/ST2 axis in infectious diseases

Infection and immunity, 2015-05, Vol.83 (5), p.1738-1748

2015

Link zum Volltext

Verfügbarkeit prüfen

Disparities in adult critical care resources across Pakistan: findings from a national survey and assessment using a novel scoring system

Critical care (London, England), 2022-07, Vol.26 (1), p.1-209, Article 209

2022

Link zum Volltext

Verfügbarkeit prüfen

Wheat Gluten: High Molecular Weight Glutenin Subunits-Structure, Genetics, and Relation to Dough Elasticity

Journal of food science, 2007-04, Vol.72 (3), p.R56-R63

2007

Link zum Volltext

Verfügbarkeit prüfen

Utilization of Implantable Cardioverter-Defibrillators in Patients With Heart Transplant (from National Inpatient Sample Database)

The American journal of cardiology, 2022-07, Vol.175, p.65-71

2022

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 209

Suche als RSS-Feed

Aktive Filter

ThemaEnvironmental Sciences & Ecology

KollektionSingle Journals

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(202)
Mit Volltextzugriff
(166)

Publikationsform

Artikel
(207)
magazinearticle
(2)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

Direct Measurement of the Elastohydrodynamic Lift Force at the Nanoscale

Forecasted E/P Ratio and ROE: Shanghai Stock Exchange (SSE), China

Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability

A simplistic approach to evaluate the power conversion efficiencies for hybrid charge transport layers in open-air fabricated perovskite solar cells

Deficiency in Aim2 affects viability and calcification of vascular smooth muscle cells from murine aortas and angiotensin-II induced aortic aneurysms

Faculty Members’ Perception of Learning Organization: A Case of Higher Education Institutions

Scalable fabrication of hemispherical solid immersion lenses in silicon carbide through grayscale hard-mask lithography

Does Financial Sector Promote Economic Growth in Pakistan? Empirical Evidences From Markov Switching Model

Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

Alterations in the Immune Cell Composition in Premalignant Breast Tissue that Precede Breast Cancer Development

Oligodontia Is Caused by Mutation in LTBP3, the Gene Encoding Latent TGF-β Binding Protein 3

Meta-Analysis on the Efficacy of Novel Glucose-Lowering Agents in Older Patients With Type 2 Diabetes Mellitus

A comprehensive author ranking evaluation of network and bibliographic indices

An Individual Patient-Level Meta-Analysis of Ischemic Versus Nonischemic Cardiomyopathy and Trajectory of Decongestion in Patients With Acute Decompensated Heart Failure

Entropy variation of rotating BTZ black hole under Hawking radiation

Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopment

Readmissions in Patients With Heart Failure and Mental Health Disorders (from a National Database)

Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation

Optical in situ monitoring of plasma-enhanced atomic layer deposition process

Trade Openness and Public Innovation: A Causality Analysis

Crucial and diverse role of the interleukin-33/ST2 axis in infectious diseases

Disparities in adult critical care resources across Pakistan: findings from a national survey and assessment using a novel scoring system

Wheat Gluten: High Molecular Weight Glutenin Subunits-Structure, Genetics, and Relation to Dough Elasticity

Utilization of Implantable Cardioverter-Defibrillators in Patients With Heart Transplant (from National Inpatient Sample Database)

Aktive Filter

Suchergebnisse filtern