PuSH - Publication Server of Helmholtz Zentrum München

29 Records found.
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1.
Philippe, H.* et al.: Mitigating anticipated effects of systematic errors supports sister-group relationship between Xenacoelomorpha and Ambulacraria. Curr. Biol. 29, 1818-1826.e6 (2019)
2.
Schneider, T.* et al.: Combinatorial recognition of clustered RNA elements by the multidomain RNA-binding protein IMP3. Nat. Commun. 10:2266 (2019)
3.
Braun, F.* et al.: Structure-based design and profiling of novel 17 beta-HSD14 inhibitors. Eur. J. Med. Chem. 155, 61-76 (2018)
4.
Jensen, L.R.* et al.: A mouse model for intellectual disability caused by mutations in the X-linked 2′‑O‑methyltransferase Ftsj1 gene. Biochim. Biophys. Acta-Mol. Basis Dis., accepted (2018)
5.
Cossarizza, A.* et al.: Guidelines for the use of flow cytometry and cell sorting in immunological studies. Eur. J. Immunol. 47, 1584-1797 (2017)
6.
Müller, S.* ; Stumpp, C. ; Sørensen, J.H.* & Jessen, S.*: Spatiotemporal variation of stable isotopic composition in precipitation: Post-condensational effects in a humid area. Hydrol. Process. 31, 3146-3159 (2017)
7.
Wiessner, M.* et al.: Mutations in INPP5K, encoding a phosphoinositide 5-phosphatase, cause congenital muscular dystrophy with cataracts and mild cognitive impairment. Am. J. Hum. Genet. 100, 523-536 (2017)
8.
Kirsch, J.* et al.: Endothelial dysfunction, and a prothrombotic, proinflammatory phenotype is caused by loss of mitochondrial thioredoxin reductase in endothelium. Arterioscler. Thromb. Vasc. Biol. 36, 1891-1899 (2016)
9.
Maresch, R.* et al.: Multiplexed pancreatic genome engineering and cancer induction by transfection-based CRISPR/Cas9 delivery in mice. Nat. Commun. 7:10770 (2016)
10.
Hrabě de Angelis, M. et al.: Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics. Nat. Genet. 47, 969-978 (2015)
11.
Müller, S.* et al.: Next-generation sequencing reveals novel differentially regulated mRNAs, lncRNAs, miRNAs, sdRNAs and a piRNA in pancreatic cancer. Mol. Cancer 14:94 (2015)
12.
Müller, S.* et al.: Erratum to: Next-generation sequencing reveals novel differentially regulated mRNAs, lncRNAs, miRNAs, sdRNAs and a piRNA in pancreatic cancer. Mol. Cancer 14:144 (2015)
13.
Andor, N. ; Harness, J.V.* ; Müller, S.* ; Mewes, H.-W. & Petritsch, C.*: EXPANDS: Expanding ploidy and allele frequency on nested subpopulations. Bioinformatics 30, 50-60 (2014)
14.
Endes, C.* et al.: Risk assessment of released cellulose nanocrystals-mimicking inhalatory exposure. J. Phys. Conf. Ser. 429, IOP:012008 (2013)
15.
Hartwig, S.* et al.: Secretome profiling of primary human skeletal muscle cells. Biochim. Biophys. Acta-Proteins Proteom. 1844, 1011-1017 (2013)
16.
Müller, S.* ; Eickholz, P.* ; Reitmeir, P. & Eger, T.*: Long-term tooth loss in periodontally compromised but treated patients according to the type of prosthodontic treatment. A retrospective study. J. Oral Rehabil. 40, 358-367 (2013)
17.
Oelkrug, R.* et al.: Brown fat in a protoendothermic mammal fuels eutherian evolution. Nat. Commun. 4:2140 (2013)
18.
Ishikawa, K.* et al.: Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians. Neurology 77, 1853-1855 (2011)
19.
Haindl, M.* ; Harasim, T. ; Eick, D. & Müller, S.*: The nucleolar SUMO-specific protease SENP3 reverses SUMO modification of nucleophosmin and is required for rRNA processing. EMBO Rep. 9, 273-279 (2008)
20.
Bolzer, A.* et al.: Three-dimensional maps of all chromosomes in human male fibroblast nuclei and prometaphase rosetts. PLoS Biol. 3, 826-842:e157 (2005)