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Institute of Human Genetics
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Overview
Publications
(768)
Research Grants
(8)
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Journal article
Journal article
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Transcriptome sequencing reveals maelstrom as a novel target gene of the terminal system in the red flour beetle Tribolium castaneum (2017)
Pridöhl F, Weißkopf M, Koniszewski N, Sulzmaier A, Uebe S, Ekici AB, Schoppmeier M
Journal article
Cardiac injury of the newborn mammalian heart accelerates cardiomyocyte terminal differentiation (2017)
Zebrowski D, Jensen CH, Becker R, Ferrazzi F, Baun C, Hvidsten S, Sheikh SP, et al.
Journal article
Rhinovirus species/genotypes and interferon-λ: subtypes, receptor and polymorphisms - missing pieces of the puzzle of childhood asthma? (2017)
Bergauer A, Sopel N, Kro B, Vuorinen T, Xepapadaki P, Weiss ST, Blau A, et al.
Journal article
FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum (2017)
Reuter M, Riess A, Moog U, Briggs TA, Chandler KE, Rauch A, Stampfer M, et al.
Journal article
A spinal epidural abscess due to Streptobacillus moniliformis infection following a rat bite: case report (2017)
Hammer A, Wolff D, Geißdörfer W, Schrey M, Ziegler R, Steiner HH, Bogdan C
Journal article
FAM13A is associated with non-small cell lung cancer (NSCLC) progression and controls tumor cell proliferation and survival (2017)
Eisenhut F, Heim L, Trump S, Mittler S, Sopel N, Andreev K, Ferrazzi F, et al.
Journal article
Posttranscriptional Regulation of LOXL1 Expression Via Alternative Splicing and Nonsense-Mediated mRNA Decay as an Adaptive Stress Response (2017)
Berner D, Zenkel M, Pasutto F, Hoja U, Liravi P, Gusek-Schneider GC, Kruse F, et al.
Journal article
Novel STRA6 null mutations in the original family described with Matthew-Wood syndrome (2017)
Pasutto F, Flinter F, Rauch A, Reis A
Journal article
Histopathological proof of the pathogenicity of a rare GFAP mutation in a patient with flaccid paraparesis (2017)
Brackmann F, Coras R, Rössler K, Kraus C, Rompel O, Trollmann R
Journal article
STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability (2017)
Lehalle D, Mosca-Boidron AL, Begtrup A, Boute-Benejean O, Charles P, Cho MT, Clarkson A, et al.
Journal article
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