Institute of Human Genetics


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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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Abstract

Journal

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