Peter Nürnberg

Peter Nürnberg

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Peter Nürnberg

Peter Nürnberg

Publications by authors named "Peter Nürnberg"

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17Publications

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Novel mutations in SLC6A5 with benign course in hyperekplexia.

Cold Spring Harb Mol Case Stud 2019 Oct 11. Epub 2019 Oct 11.

University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Pediatrics and Center for Molecular Medicine (CMMC);

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http://dx.doi.org/10.1101/mcs.a004465DOI Listing
October 2019

A novel C8orf37 splice mutation and genotype-phenotype correlation for cone-rod dystrophy.

Ophthalmic Genet 2016 09 11;37(3):294-300. Epub 2016 Feb 11.

a Medical Faculty, Institute of Human Genetics and Anthropology, Heinrich-Heine University , Düsseldorf , Germany.

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http://dx.doi.org/10.3109/13816810.2015.1071408DOI Listing
September 2016

Label-Free Protein-RNA Interactome Analysis Identifies Khsrp Signaling Downstream of the p38/Mk2 Kinase Complex as a Critical Modulator of Cell Cycle Progression.

PLoS One 2015 20;10(5):e0125745. Epub 2015 May 20.

Department I of Internal Medicine, University Hospital of Cologne, Weyertal 115B, 50931, Cologne, Germany; Cologne Excellence Cluster on Cellular Stress Response in Aging-Associated Diseases, University of Cologne, Weyertal 115B, 50931, Cologne, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0125745PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439058PMC
February 2016

Beijing clades of Mycobacterium tuberculosis are associated with differential survival in HIV-negative Russian patients.

Infect Genet Evol 2015 Dec 28;36:517-523. Epub 2015 Aug 28.

Clinical TB and HIV Group, Blizard Institute, Queen Mary, University of London, 2 Newark Street, London E12AT, UK; Department of Infectious Diseases, Imperial College London, DuCane Road, London W12 ONN, UK.

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http://dx.doi.org/10.1016/j.meegid.2015.08.028DOI Listing
December 2015

A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family.

Mol Vis 2006 May 22;12:518-22. Epub 2006 May 22.

Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, Punjab, India.

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May 2006