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Lebenszykluskosten Von Straßen: Umsetzungsformen, Modulare Kalkulation, Optimierungspotentiale

Müller, Clemens

1, 2020

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Precipitation of Terephthalic Acid from Alkaline Solution: Influence of Temperature and Precipitation Acid

Industrial & engineering chemistry research, 2023-08, Vol.62 (30), p.12029-12040

2023

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Correlating Decoherence in Transmon Qubits: Low Frequency Noise by Single Fluctuators

Physical review letters, 2019-11, Vol.123 (19), p.190502-190502, Article 190502

2019

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A standardized framework for the validation and verification of clinical molecular genetic tests

European journal of human genetics : EJHG, 2010-12, Vol.18 (12), p.1276-1288

2010

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Dissipative Rabi model in the dispersive regime

Physical review research, 2020-07, Vol.2 (3), Article 033046

Müller, Clemens

2020

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Targeted Molecular Analysis in Adrenocortical Carcinomas: A Strategy Toward Improved Personalized Prognostication

The journal of clinical endocrinology and metabolism, 2018-12, Vol.103 (12), p.4511-4523

2018

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Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1

European journal of human genetics : EJHG, 2015-06, Vol.23 (6), p.808-816

2015

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Passive On-Chip Superconducting Circulator Using a Ring of Tunnel Junctions

Physical review letters, 2018-05, Vol.120 (21), p.213602-213602, Article 213602

2018

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The genetic basis of resistance to anticoagulants in rodents

Genetics (Austin), 2005-08, Vol.170 (4), p.1839-1847

2005

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Quantum Rifling: Protecting a Qubit from Measurement Back Action

Physical review letters, 2020-02, Vol.124 (7), p.070401-070401, Article 070401

2020

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Identification of deep intronic variants in 15 haemophilia A patients by next generation sequencing of the whole factor VIII gene

Thrombosis and haemostasis, 2015-10, Vol.114 (4), p.757-767

2015

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Human Vitamin K 2,3-Epoxide Reductase Complex Subunit 1-like 1 (VKORC1L1) Mediates Vitamin K-dependent Intracellular Antioxidant Function

The Journal of biological chemistry, 2011-04, Vol.286 (17), p.15085-15094

2011

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Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

Nature, 2004-02, Vol.427 (6974), p.537-541

2004

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Kalkulieren Im Ingenieurbau: Strategie - Kalkulation - Controlling

3., vollst. uberarb. und erw. Aufl. 2018 edition., 2018

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Human VKORC1 mutations cause variable degrees of 4-hydroxycoumarin resistance and affect putative warfarin binding interfaces

Blood, 2013-10, Vol.122 (15), p.2743-2750

2013

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Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6

European journal of human genetics : EJHG, 2014-02, Vol.22 (2), p.208-215

2014

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Mini-gene assays confirm the splicing effect of deep intronic variants in the factor VIII gene

Thrombosis and haemostasis, 2016-01, Vol.115 (1), p.222-224

2016

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Static Crystallization, an Alternative Methodology for Synthesis of High-Purity Aluminum

Metals (Basel ), 2023-01, Vol.13 (2), p.280

2023

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Particle Rearrangement and Pore Space Coarsening During Solid-State Sintering

Journal of the American Ceramic Society, 2009-07, Vol.92 (7), p.1384-1390

2009

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Early and lethal neurodegeneration with myasthenic and myopathic features: A new ALG14 -CDG

Neurology, 2017-08, Vol.89 (7), p.657-664

2017

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Identification of VKORC1 interaction partners by split-ubiquitin system and coimmunoprecipitation

Thrombosis and haemostasis, 2011-02, Vol.105 (2), p.285-294

2011

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Preinfection laboratory parameters may predict COVID‐19 severity in tumor patients

Cancer medicine (Malden, MA), 2021-07, Vol.10 (13), p.4424-4436

2021

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Identification of variants in MBNL1 in patients with a myotonic dystrophy-like phenotype

European journal of human genetics : EJHG, 2016-10, Vol.24 (10), p.1467-1472

2016

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Lebenszykluskosten Von Straßen: Umsetzungsformen, Modulare Kalkulation, Optimierungspotentiale

Precipitation of Terephthalic Acid from Alkaline Solution: Influence of Temperature and Precipitation Acid

Correlating Decoherence in Transmon Qubits: Low Frequency Noise by Single Fluctuators

A standardized framework for the validation and verification of clinical molecular genetic tests

Dissipative Rabi model in the dispersive regime

Targeted Molecular Analysis in Adrenocortical Carcinomas: A Strategy Toward Improved Personalized Prognostication

Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1

Passive On-Chip Superconducting Circulator Using a Ring of Tunnel Junctions

The genetic basis of resistance to anticoagulants in rodents

Quantum Rifling: Protecting a Qubit from Measurement Back Action

Identification of deep intronic variants in 15 haemophilia A patients by next generation sequencing of the whole factor VIII gene

Human Vitamin K 2,3-Epoxide Reductase Complex Subunit 1-like 1 (VKORC1L1) Mediates Vitamin K-dependent Intracellular Antioxidant Function

Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer

Kalkulieren Im Ingenieurbau: Strategie - Kalkulation - Controlling

Human VKORC1 mutations cause variable degrees of 4-hydroxycoumarin resistance and affect putative warfarin binding interfaces

Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6

Mini-gene assays confirm the splicing effect of deep intronic variants in the factor VIII gene

Static Crystallization, an Alternative Methodology for Synthesis of High-Purity Aluminum

Particle Rearrangement and Pore Space Coarsening During Solid-State Sintering

Early and lethal neurodegeneration with myasthenic and myopathic features: A new ALG14 -CDG

Identification of VKORC1 interaction partners by split-ubiquitin system and coimmunoprecipitation

Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer

Preinfection laboratory parameters may predict COVID‐19 severity in tumor patients

Identification of variants in MBNL1 in patients with a myotonic dystrophy-like phenotype

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