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Model-Based System Testing Using Visual Contracts

2009 35th Euromicro Conference on Software Engineering and Advanced Applications, 2009, p.121-124

2009

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Holistic Model-Based Testing for Business Information Systems

2010 Third International Conference on Software Testing, Verification and Validation, 2010, p.327-330

Mlynarski, Michael

2010

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Model-Based Testing: Achievements and Future Challenges

Advances In Computers, 2012, Vol.86, p.1-39

2012

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KnowledgeBus – An Architecture to Support Intelligent and Flexible Knowledge Management

Creating New Learning Experiences on a Global Scale, p.487-492

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From design models to test models by means of test ideas

Proceedings of the 6th International Workshop on Model-Driven Engineering, Verification and Validation, 2009, p.1-10

2009

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Effort Comparison for Model-Based Testing Scenarios

2010 Third International Conference on Software Testing, Verification, and Validation Workshops, 2010, p.28-36

2010

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Mobile Testing und Usability Testing?

Softwaretechnik-Trends, 2013-05, Vol.33 (2), p.77-78

2013

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TSC1 loss increases risk for tauopathy by inducing tau acetylation and preventing tau clearance via chaperone-mediated autophagy

Science advances, 2021-11, Vol.7 (45), p.eabg3897-eabg3897

2021

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Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood

Diabetes (New York, N.Y.), 2008-04, Vol.57 (4), p.1034

2008

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Abstract 4523: Inhibition of arginase in combination with anti-PDL1 leads to increased infiltration and activation of CD8+ T cells, NK cells, and CD103+ dendritic cells in mouse syngeneic tumor models

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.4523-4523

2020

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Hematopoietic Stem Cell Transplantation Positively Affects the Natural History of Cancer in Nijmegen Breakage Syndrome

Clinical cancer research, 2021-01, Vol.27 (2), p.575-584

2021

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A common haplotype at the CD36 locus is associated with high free fatty acid levels and increased cardiovascular risk in Caucasians

Human molecular genetics, 2004-10, Vol.13 (19), p.2197-2205

2004

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Electrochromic Bragg Mirror: ECBM

Advanced materials (Weinheim), 2012-09, Vol.24 (35), p.OP265-OP269

2012

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Diabolische Vigilanz: Studien zur Inszenierung von Wachsamkeit in Teufelserzählungen des Spätmittelalters und der Frühen Neuzeit

2022

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se enwysten nicht, dat he was eyn deeff“. Zur scheiternden Vigilanz im Broder Rusche

Diabolische Vigilanz, 2022, Vol.2, p.45-64

2022

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Common Haplotypes at the Adiponectin Receptor 1 (ADIPOR1) Locus Are Associated With Increased Risk of Coronary Artery Disease in Type 2 Diabetes

Diabetes (New York, N.Y.), 2006-10, Vol.55 (10), p.2763-2770

2006

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Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

Circulation. Cardiovascular genetics, 2017-10, Vol.10 (5)

2017

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Whole genome sequencing of Caribbean Hispanic families with late‐onset Alzheimer's disease

Annals of clinical and translational neurology, 2018-04, Vol.5 (4), p.406-417

2018

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From Bare Metal Powders to Colloidally Stable TCO Dispersions and Transparent Nanoporous Conducting Metal Oxide Thin Films

Small (Weinheim an der Bergstrasse, Germany), 2012-12, Vol.8 (24), p.3806-3809

2012

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unique late-replicating XY to autosome translocation in Peromyscus melanophrys

Chromosome research, 2010-02, Vol.18 (2), p.179-189

2010

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Genetic variability at the leptin receptor ( LEPR ) locus is a determinant of plasma fibrinogen and C-reactive protein levels

Atherosclerosis, 2007-03, Vol.191 (1), p.121-127

2007

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A common haplotype at the CD36 locus is associated with high free fatty acid levels and increased cardiovascular risk in Caucasians

Human molecular genetics, 2005-12, Vol.14 (24), p.3973-3973

2005

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Model-Based System Testing Using Visual Contracts

Holistic Model-Based Testing for Business Information Systems

Model-Based Testing: Achievements and Future Challenges

KnowledgeBus – An Architecture to Support Intelligent and Flexible Knowledge Management

From design models to test models by means of test ideas

Effort Comparison for Model-Based Testing Scenarios

Mobile Testing und Usability Testing?

Copy Number Variation of the glucose transporter gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome

TSC1 loss increases risk for tauopathy by inducing tau acetylation and preventing tau clearance via chaperone-mediated autophagy

Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood

Abstract 4523: Inhibition of arginase in combination with anti-PDL1 leads to increased infiltration and activation of CD8+ T cells, NK cells, and CD103+ dendritic cells in mouse syngeneic tumor models

Hematopoietic Stem Cell Transplantation Positively Affects the Natural History of Cancer in Nijmegen Breakage Syndrome

A common haplotype at the CD36 locus is associated with high free fatty acid levels and increased cardiovascular risk in Caucasians

Electrochromic Bragg Mirror: ECBM

Diabolische Vigilanz: Studien zur Inszenierung von Wachsamkeit in Teufelserzählungen des Spätmittelalters und der Frühen Neuzeit

se enwysten nicht, dat he was eyn deeff“. Zur scheiternden Vigilanz im Broder Rusche

Common Haplotypes at the Adiponectin Receptor 1 (ADIPOR1) Locus Are Associated With Increased Risk of Coronary Artery Disease in Type 2 Diabetes

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

Whole genome sequencing of Caribbean Hispanic families with late‐onset Alzheimer's disease

From Bare Metal Powders to Colloidally Stable TCO Dispersions and Transparent Nanoporous Conducting Metal Oxide Thin Films

unique late-replicating XY to autosome translocation in Peromyscus melanophrys

Genetic variability at the leptin receptor ( LEPR ) locus is a determinant of plasma fibrinogen and C-reactive protein levels

A common haplotype at the CD36 locus is associated with high free fatty acid levels and increased cardiovascular risk in Caucasians

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