Publications by authors named "Andreas W Kuss"

46Publications

miRNA Alterations Elicit Pathways Involved in Memory Decline and Synaptic Function in the Hippocampus of Aged Tg4-42 Mice.

Front Neurosci 2020 10;14:580524. Epub 2020 Sep 10.

Division of Molecular Psychiatry, Department of Psychiatry and Psychotherapy, University Medical Center Göttingen (UMG), Georg-August-University, Göttingen, Germany.

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http://dx.doi.org/10.3389/fnins.2020.580524DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511553PMC
September 2020

Genome-Wide DNA Alterations in X-Irradiated Human Gingiva Fibroblasts.

Int J Mol Sci 2020 Aug 12;21(16). Epub 2020 Aug 12.

Human Molecular Genetics Group, Department of Functional Genomics, Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, 17475 Greifswald, Germany.

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http://dx.doi.org/10.3390/ijms21165778DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460866PMC
August 2020

Ionizing Radiation Alters the Transition/Transversion Ratio in the Exome of Human Gingiva Fibroblasts.

Health Phys 2020 Jul;119(1):109-117

Department of Functional Genomics, Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.

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http://dx.doi.org/10.1097/HP.0000000000001251DOI Listing
July 2020

Exome Sequencing Discloses Ionizing-radiation-induced DNA Variants in the Genome of Human Gingiva Fibroblasts.

Health Phys 2018 07;115(1):151-160

Department of Functional Genomics, Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.

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http://dx.doi.org/10.1097/HP.0000000000000880DOI Listing
July 2018

FAM222B Is Not a Likely Novel Candidate Gene for Cerebral Cavernous Malformations.

Mol Syndromol 2016 Jul 18;7(3):144-52. Epub 2016 Jun 18.

Department of Human Genetics, University Medicine Greifswald and Interfaculty Institute of Genetics and Functional Genomics, University of Greifswald, Greifswald, Germany.

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http://dx.doi.org/10.1159/000446884DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988258PMC
July 2016

Transcriptome Alterations In X-Irradiated Human Gingiva Fibroblasts.

Health Phys 2016 08;111(2):75-84

*Department of Human Genetics, University Medicine Greifswald and Interfaculty Institute of Genetics and Functional Genomics, University of Greifswald, Greifswald, Germany; †Interfaculty Institute for Genetics and Functional Genomics, Department of Functional Genomics, University Medicine Greifswald, Germany; ‡Institut für Radiobiologie der Bundeswehr in Verbindung mit der Universität Ulm, München, Germany.

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http://dx.doi.org/10.1097/HP.0000000000000419DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936435PMC
August 2016

Morphological and behavioral characterization of adult mice deficient for SrGAP3.

Cell Tissue Res 2016 10 17;366(1):1-11. Epub 2016 May 17.

Institut für Anatomie und Zellbiologie, Universitätsmedizin Greifswald, Friedrich-Löffler-Straße-23c, 17487, Greifswald, Germany.

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http://dx.doi.org/10.1007/s00441-016-2413-yDOI Listing
October 2016

Gene Expression Profiling in the APP/PS1KI Mouse Model of Familial Alzheimer's Disease.

J Alzheimers Dis 2016 ;50(2):397-409

Division of Molecular Psychiatry, Department of Psychiatry and Psychotherapy, University Medical Center (UMG), Georg-August-University, Göttingen, Germany.

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http://dx.doi.org/10.3233/JAD-150745DOI Listing
November 2016

Subgroup-elimination transcriptomics identifies signaling proteins that define subclasses of TRPV1-positive neurons and a novel paracrine circuit.

PLoS One 2014 31;9(12):e115731. Epub 2014 Dec 31.

Department of Anesthesiology and Intensive Care Medicine, Experimental Anesthesiology and Pain Research, University Hospital of Cologne, Cologne, Germany; Department for Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0115731PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4281118PMC
October 2015

West syndrome caused by ST3Gal-III deficiency.

Epilepsia 2013 Feb 17;54(2):e24-7. Epub 2012 Dec 17.

Monique and Jacques Roboh Department of Genetic Research, the Department of Genetic and Metabolic Diseases, Hadassah, Hebrew University Medical Center, Jerusalem, Israel.

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http://dx.doi.org/10.1111/epi.12050DOI Listing
February 2013

A novel nonsense mutation in KDM5C/JARID1C gene causing intellectual disability, short stature and speech delay.

Neurosci Lett 2011 Jul 6;498(1):67-71. Epub 2011 May 6.

Department of Genetics, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro, Rio de Janeiro, Brazil.

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http://dx.doi.org/10.1016/j.neulet.2011.04.065DOI Listing
July 2011

OLA-DRB1 microsatellite variants are associated with ovine growth and reproduction traits.

Genet Sel Evol 2006 Jul-Aug;38(4):431-44. Epub 2006 Jun 23.

Department of Animal Breeding and Biotechnology, University of Hohenheim, D-70593 Stuttgart, Germany.

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http://dx.doi.org/10.1186/1297-9686-38-4-431DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2689294PMC
September 2006

Mitochondria-dependent caspase-9 activation is necessary for antigen receptor-mediated effector caspase activation and apoptosis in WEHI 231 lymphoma cells.

J Immunol 2002 Apr;168(8):3902-9

Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.

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http://dx.doi.org/10.4049/jimmunol.168.8.3902DOI Listing
April 2002