Search Results - "FREGIN, ANDREAS" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

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

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

by Oldenburg, Johannes, Rost, Simone, Fregin, Andreas, Ivaskevicius, Vytautas, Conzelmann, Ernst, Hörtnagel, Konstanze, Pelz, Hans-Joachim, Lappegard, Knut, Seifried, Erhard, Scharrer, Inge, Tuddenham, Edward G. D, Müller, Clemens R, Strom, Tim M
Published in Nature (05.02.2004)

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Journal Article

The genetic basis of resistance to anticoagulants in rodents

The genetic basis of resistance to anticoagulants in rodents

by Pelz, Hans-Joachim, Rost, Simone, Hünerberg, Mirja, Fregin, Andreas, Heiberg, Ann-Charlotte, Baert, Kristof, MacNicoll, Alan D, Prescott, Colin V, Walker, Anne-Sophie, Oldenburg, Johannes, Müller, Clemens R
Published in Genetics (Austin) (01.08.2005)

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Journal Article

Current pharmacogenetic developments in oral anticoagulation therapy: the influence of variant VKORC1 and CYP2C9 alleles

Current pharmacogenetic developments in oral anticoagulation therapy: the influence of variant VKORC1 and CYP2C9 alleles

by Oldenburg, Johannes, Bevans, Carville G, Fregin, Andreas, Geisen, Christof, Müller-Reible, Clemens, Watzka, Matthias
Published in Thrombosis and haemostasis (01.09.2007)

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Journal Article

Site-directed mutagenesis of coumarin-type anticoagulant-sensitive VKORC1: evidence that highly conserved amino acids define structural requirements for enzymatic activity and inhibition by warfarin

Site-directed mutagenesis of coumarin-type anticoagulant-sensitive VKORC1: evidence that highly conserved amino acids define structural requirements for enzymatic activity and inhibition by warfarin

by Rost, Simone, Fregin, Andreas, Hünerberg, Mirja, Bevans, Carville G, Müller, Clemens R, Oldenburg, Johannes
Published in Thrombosis and haemostasis (01.10.2005)

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Journal Article

Feature detectors for traffic light recognition

Feature detectors for traffic light recognition

by Fregin, Andreas, Muller, Julian, Dietmayer, Klaus
Published in 2017 IEEE 20th International Conference on Intelligent Transportation Systems (ITSC) (01.10.2017)

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Conference Proceeding

Missense mutations at ALA‐10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapy

Missense mutations at ALA‐10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapy

by Oldenburg, Johannes, Quenzel, Ernst‐Markus, Harbrecht, Uschi, Fregin, Andreas, Kress, Wolfram, Müller, Clemens Rainer, Hertfelder, Hans‐Jörg, Schwaab, Rainer, Brackmann, Hans‐Hermann, Hanfland, Peter
Published in British journal of haematology (01.07.1997)

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Journal Article

Disparity Sliding Window: Object Proposals from Disparity Images

Disparity Sliding Window: Object Proposals from Disparity Images

by Muller, Julian, Fregin, Andreas, Dietmayer, Klaus
Published in 2018 IEEE/RSJ International Conference on Intelligent Robots and Systems (IROS) (01.10.2018)

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Conference Proceeding

Compound heterozygous mutations in the γ‐glutamyl carboxylase gene cause combined deficiency of all vitamin K‐dependent blood coagulation factors

Compound heterozygous mutations in the γ‐glutamyl carboxylase gene cause combined deficiency of all vitamin K‐dependent blood coagulation factors

by Rost, Simone, Fregin, Andreas, Koch, Dieter, Compes, Markus, Müller, Clemens R., Oldenburg, Johannes
Published in British journal of haematology (01.08.2004)

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Journal Article

Learning Traffic Light Colors

Learning Traffic Light Colors

by Fregin, Andreas, Dietmayer, Klaus
Published in 2018 21st International Conference on Intelligent Transportation Systems (ITSC) (01.11.2018)

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Conference Proceeding

Somatic Mosaicism in Hemophilia A: A Fairly Common Event

Somatic Mosaicism in Hemophilia A: A Fairly Common Event

by Leuer, Marco, Oldenburg, Johannes, Lavergne, Jean-Maurice, Ludwig, Michael, Fregin, Andreas, Eigel, Anton, Ljung, Rolf, Goodeve, Anne, Peake, Ian, Olek, Klaus
Published in American journal of human genetics (01.07.2001)

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Journal Article

A closer look on traffic light detection evaluation metrics

A closer look on traffic light detection evaluation metrics

by Fregin, Andreas, Dietmayer, Klaus
Published in 2016 IEEE 19th International Conference on Intelligent Transportation Systems (ITSC) (01.11.2016)

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Conference Proceeding

The DriveU Traffic Light Dataset: Introduction and Comparison with Existing Datasets

The DriveU Traffic Light Dataset: Introduction and Comparison with Existing Datasets

by Fregin, Andreas, Muller, Julian, Krebel, Ulrich, Dietmayer, Klaus
Published in 2018 IEEE International Conference on Robotics and Automation (ICRA) (01.05.2018)

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Conference Proceeding

Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K–dependent clotting factors to the centromeric region of chromosome 16

Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K–dependent clotting factors to the centromeric region of chromosome 16

by Fregin, Andreas, Rost, Simone, Wolz, Werner, Krebsova, Alice, Muller, Clemens R., Oldenburg, Johannes
Published in Blood (01.11.2002)

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Journal Article

Three ways of using stereo vision for traffic light recognition

Three ways of using stereo vision for traffic light recognition

by Fregin, Andreas, Muller, Julian, Dietmayer, Klaus
Published in 2017 IEEE Intelligent Vehicles Symposium (IV) (01.06.2017)

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Conference Proceeding

Founder mutation Arg485Pro led to recurrent compound heterozygous GGCX genotypes in two German patients with VKCFD type 1

Founder mutation Arg485Pro led to recurrent compound heterozygous GGCX genotypes in two German patients with VKCFD type 1

by Rost, Simone, Geisen, Christof, Fregin, Andreas, Seifried, Erhard, Müller, Clemens R, Oldenburg, Johannes
Published in Blood coagulation & fibrinolysis (01.09.2006)

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Journal Article

Compound heterozygous mutations in the [gamma]-glutamyl carboxylase gene cause combined deficiency of all vitamin K-dependent blood coagulation factors

Compound heterozygous mutations in the [gamma]-glutamyl carboxylase gene cause combined deficiency of all vitamin K-dependent blood coagulation factors

by Rost, Simone, Fregin, Andreas, Koch, Dieter, Compes, Markus
Published in British journal of haematology (02.08.2004)

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Journal Article

Disparity Sliding Window: Object Proposals From Disparity Images

Disparity Sliding Window: Object Proposals From Disparity Images

by Müller, Julian, Fregin, Andreas, Dietmayer, Klaus
Year of Publication 17.05.2018

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Journal Article

Multi-camera system for traffic light detection: About camera setup and mapping of detections

Multi-camera system for traffic light detection: About camera setup and mapping of detections

by Muller, Julian, Fregin, Andreas, Dietmayer, Klaus
Published in 2017 IEEE 20th International Conference on Intelligent Transportation Systems (ITSC) (01.10.2017)

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Conference Proceeding

Mutations in the VKORC1 Gene Cause Warfarin Resistance, Warfarin Sensitivity and Combined Deficiency of Vitamin K Dependent Coagulation Factors

Mutations in the VKORC1 Gene Cause Warfarin Resistance, Warfarin Sensitivity and Combined Deficiency of Vitamin K Dependent Coagulation Factors

by Oldenburg, Johannes, Rost, Simone, Fregin, Andreas, Geisen, Christof, Ivaskevicius, Vytautas, Seifried, Erhard, Scharrer, Inge, Heistinger, Maximilian, Tuddenham, Edward, Muller-Reible, Clemens, Zieger, Barbara
Published in Blood (16.11.2004)

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Journal Article

Alkaptonuria in Slovakia: thirty-two years of research on phenotype and genotype

Alkaptonuria in Slovakia: thirty-two years of research on phenotype and genotype

by Srsen, Stefan, Müller, Clemens R., Fregin, Andreas, Srsnova, Klara
Published in Molecular genetics and metabolism (01.04.2002)

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Journal Article