PuSH - Publikationsserver des Helmholtz Zentrums München

Fneish, Z.* ; Becker, J.* ; Mulenge, F.* ; Fneish, F.* ; Costa, B.* ; Traidl-Hoffmann, C. ; Gilles, S. ; Kalinke, U.*

Birch pollen-induced signatures in dendritic cells are maintained upon additional cytomegalovirus exposure.

Gene 927:148649 (2024)

Westphal, D.S.* ; Mastantuono, E.* ; Seidel, H.* ; Riedhammer, K.M.* ; Hahn, A.* ; Vill, K.* ; Wagner, M.

There is more to it than just congenital heart defects – The phenotypic spectrum of TAB2-related syndrome.

Gene 814:146167 (2022)

Brugger, M.* ; Brunet, T.* ; Wagner, M. ; Orec, L.E.* ; Schwaibold, E.M.C.* ; Boy, N.*

Locus heterogeneity in two siblings presenting with developmental delay, intellectual disability and autism spectrum disorder.

Gene 768:145260 (2021)

Boonsimma, P.* ; Gasser, M.M.* ; Netbaramee, W.* ; Wechapinan, T.* ; Srichomthong, C.* ; Ittiwut, C.* ; Wagner, M. ; Krenn, M.* ; Zimprich, F.* ; Abicht, A.* ; Biskup, S.* ; Roser, T.* ; Borggraefe, I.* ; Suphapeetiporn, K.* ; Shotelersuk, V.*

Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases.

Gene 749:144709 (2020)

Brunet, T.* ; Westphal, D.S.* ; Weber, S. ; Juenger, H.* ; Vlaho, S.* ; Hoefele, J.* ; Meitinger, T.* ; Rieger-Fackeldey, E.* ; Wagner, M.

A novel pathogenic variant in MYO18B associating early-onset muscular hypotonia, and characteristic dysmorphic features, delineation of the phenotypic spectrum of MYO18B-related conditions.

Gene 742:144542 (2020)

Klinner, J.* ; Krüger, M.* ; Brunet, T.* ; Makowski, C.* ; Riedhammer, K.M.* ; Mollweide, A.* ; Wagner, M. ; Hoefele, J.*

Congenital lymphedema as a rare and first symptom of tuberous sclerosis complex.

Gene 753:144815 (2020)

Günthner, R.* ; Wagner, M. ; Thurm, T.* ; Ponsel, S.* ; Höfele, J.* ; Lange-Sperandio, B.*

Identification of co-occurrence in a patient with Dent's disease and ADA2-deficiency by exome sequencing.

Gene 649, 23-26 (2018)

Leszinski, G.S.* ; Warncke, K.* ; Hoefele, J.* ; Wagner, M.

A case report and review of the literature indicate that HMGA2 should be added as a disease gene for Silver-Russell syndrome.

Gene 663, 110-114 (2018)

Westphal, D.S. ; Andres, S.* ; Beitzel, K.I.* ; Makowski, C.* ; Meitinger, T. ; Hoefele, J.*

Identification of a de novo microdeletion 1q44 in a patient with hypogenesis of the corpus callosum, seizures and microcephaly - A case report.

Gene 616, 41-44 (2017)

Vauti, F.* ; Goller, T.* ; Beine, R.* ; Becker, L.* ; Klopstock, T.* ; Hölter, S.M. ; Wurst, W. ; Fuchs, H. ; Gailus-Durner, V. ; Hrabě de Angelis, M. ; Arnold, H.-H.*

The mouse Trm1-like gene is expressed in neural tissues and plays a role in motor coordination and exploratory behaviour.

Gene 389, 174-185 (2007)

Zeilfelder, U.* ; Frank, O.* ; Sparacio, S.* ; Schön, U. ; Bosch, V.* ; Seifarth, W.* ; Leib-Mösch, C.

The potential of retroviral vectors to cotransfer human endogenous retroviruses (HERVs) from human packaging cell lines.

Gene 390, 175-179 (2007)

Guimera, J. ; Vogt Weisenhorn, D.M. ; Echevarria, D.* ; Martinez, S.* ; Wurst, W.

Molecular characterization, structure and developmental expression of Megane bHLH factor.

Gene 377, 65-76 (2006)

Kramer-Hämmerle, S. ; Hahn, A.* ; Brack-Werner, R. ; Werner, T.*

Elucidating effects of long-term expression of HIV-1 Nef on astrocytes by microarray, promoter, and literature analyses.

Gene 358, 31-38 (2005)

Feederle, R.* ; Delecluse, H.J.* ; Rouault, J.P.* ; Schepers, A. ; Hammerschmidt, W.