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LuTHy: a double‐readout bioluminescence‐based two‐hybrid technology for quantitative mapping of protein–protein interactions in mammalian cells

Molecular systems biology, 2018-07, Vol.14 (7), p.e8071-n/a

2018

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Current Approaches Toward Quantitative Mapping of the Interactome

Frontiers in genetics, 2016-05, Vol.7, p.74-74

2016

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SNPs in the coding region of the metastasis-inducing gene MACC1 and clinical outcome in colorectal cancer

Molecular cancer, 2012-07, Vol.11 (1), p.49-49, Article 49

2012

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An integer programming framework for inferring disease complexes from network data

Bioinformatics, 2016-06, Vol.32 (12), p.i271-i277

2016

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Schizophrenia risk candidate protein ZNF804A interacts with STAT2 and influences interferon-mediated gene transcription in mammalian cells

Journal of molecular biology, 2021-09, Vol.433 (19), p.167184-167184, Article 167184

2021

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An integer programming framework for inferring disease complexes from network data

Bioinformatics (Oxford, England), 2016-12, Vol.32 (24), p.3855-3855

2016

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mHTT Seeding Activity: A Marker of Disease Progression and Neurotoxicity in Models of Huntington’s Disease

Molecular cell, 2018-09, Vol.71 (5), p.675-688.e6

2018

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Self-assembly of Mutant Huntingtin Exon-1 Fragments into Large Complex Fibrillar Structures Involves Nucleated Branching

Journal of molecular biology, 2018-06, Vol.430 (12), p.1725-1744

2018

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Interaction Networks and Perturbed Cellular Functions in Schizophrenia

Klockmeier, Konrad

2019

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DULIP: A Dual Luminescence-Based Co-Immunoprecipitation Assay for Interactome Mapping in Mammalian Cells

Journal of molecular biology, 2015-10, Vol.427 (21), p.3375-3388

2015

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F129EXOME SEQUENCING WITH SUBSEQUENT MULTI-TIER ANALYSES IN A LARGE COHORT OF MULTIPLY AFFECTED FAMILIES PROVIDES NEW INSIGHT INTO SCHIZOPHRENIA

European neuropsychopharmacology, 2019, Vol.29, p.S1180-S1181

2019

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M92 - EXOME-SEQUENCING IN DENSLY AFFECTED PEDIGREES IDENTIFIES NEW CANDIDATE GENES FOR SCHIZOPHRENIA

European neuropsychopharmacology, 2019, Vol.29, p.S1005-S1005

2019

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EXOME-SEQUENCING IN DENSLY AFFECTED PEDIGREES IDENTIFIES NEW CANDIDATE GENES FOR SCHIZOPHRENIA

European neuropsychopharmacology, 2019, Vol.29, p.S1005

2019

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Lu TH y: a double‐readout bioluminescence‐based two‐hybrid technology for quantitative mapping of protein–protein interactions in mammalian cells

Molecular systems biology, 2018-07, Vol.14 (7)

2018

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Novel potential of NADPH-oxidase and RHO-kinase pathways inhibition in a genetic in-vitro Parkinson's disease model

Proceedings for Annual Meeting of The Japanese Pharmacological Society, 2018, Vol.WCP2018, p.PO4-1-139

2018

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LuTHy: a double‐readout bioluminescence‐based two‐hybrid technology for quantitative mapping of protein–protein interactions in mammalian cells

Current Approaches Toward Quantitative Mapping of the Interactome

SNPs in the coding region of the metastasis-inducing gene MACC1 and clinical outcome in colorectal cancer

Systematic interaction network filtering identifies CRMP1 as a novel suppressor of huntingtin misfolding and neurotoxicity

An integer programming framework for inferring disease complexes from network data

Schizophrenia risk candidate protein ZNF804A interacts with STAT2 and influences interferon-mediated gene transcription in mammalian cells

An integer programming framework for inferring disease complexes from network data

mHTT Seeding Activity: A Marker of Disease Progression and Neurotoxicity in Models of Huntington’s Disease

Self-assembly of Mutant Huntingtin Exon-1 Fragments into Large Complex Fibrillar Structures Involves Nucleated Branching

Interaction Networks and Perturbed Cellular Functions in Schizophrenia

DULIP: A Dual Luminescence-Based Co-Immunoprecipitation Assay for Interactome Mapping in Mammalian Cells

F129EXOME SEQUENCING WITH SUBSEQUENT MULTI-TIER ANALYSES IN A LARGE COHORT OF MULTIPLY AFFECTED FAMILIES PROVIDES NEW INSIGHT INTO SCHIZOPHRENIA

M92 - EXOME-SEQUENCING IN DENSLY AFFECTED PEDIGREES IDENTIFIES NEW CANDIDATE GENES FOR SCHIZOPHRENIA

EXOME-SEQUENCING IN DENSLY AFFECTED PEDIGREES IDENTIFIES NEW CANDIDATE GENES FOR SCHIZOPHRENIA

Lu TH y: a double‐readout bioluminescence‐based two‐hybrid technology for quantitative mapping of protein–protein interactions in mammalian cells

Novel potential of NADPH-oxidase and RHO-kinase pathways inhibition in a genetic in-vitro Parkinson's disease model

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