Oliver Plottner
Overview
Explore the profile of Oliver Plottner including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
213
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Recent Articles
1.
Popp O, Moser S, Zielonka J, Ruger P, Hansen S, Plottner O
MAbs
. 2017 Nov;
10(2):290-303.
PMID: 29173063
Novel biotherapeutic glycoproteins, like recombinant monoclonal antibodies (mAbs) are widely used for the treatment of numerous diseases. The N-glycans attached to the constant region of an antibody have been demonstrated...
2.
Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders
Stoll G, Pietilainen O, Linder B, Suvisaari J, Brosi C, Hennah W, et al.
Nat Neurosci
. 2013 Aug;
16(9):1228-1237.
PMID: 23912948
Implicating particular genes in the generation of complex brain and behavior phenotypes requires multiple lines of evidence. The rarity of most high-impact genetic variants typically precludes the possibility of accruing...
3.
Guenther U, Handoko L, Laggerbauer B, Jablonka S, Chari A, Alzheimer M, et al.
Hum Mol Genet
. 2009 Jan;
18(7):1288-300.
PMID: 19158098
Distal spinal muscular atrophy type 1 (DSMA1) is an autosomal recessive disease that is clinically characterized by distal limb weakness and respiratory distress. In this disease, the degeneration of alpha-motoneurons...
4.
Linder B, Plottner O, Kroiss M, Hartmann E, Laggerbauer B, Meister G, et al.
Hum Mol Genet
. 2008 Jul;
17(20):3236-46.
PMID: 18664458
Tudor domains are widespread among proteins involved in RNA metabolism, but only in a few cases their cellular function has been analyzed in detail. Here, we report on the characterization...
5.
Malatesta M, Scassellati C, Meister G, Plottner O, Buhler D, Sowa G, et al.
Exp Cell Res
. 2003 Dec;
292(2):312-21.
PMID: 14697339
Mutations in the survival of motor neuron (SMN) gene are the major cause of spinal muscular atrophy (SMA). The SMN gene encodes a 38-kDa protein that localises in the cytoplasm...