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17 Records found.
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1.
Ban, R. et al.: Biallelic COA7-variants leading to developmental regression with progressive spasticity and brain atrophy in a Chinese patient. Front. Genet. 12:685035 (2021)
2.
Molitor, L. ; Bacher, S. ; Burczyk, S.* & Niessing, D.: The molecular function of PURA andi Its implications in neurological diseases. Front. Genet. 12:638217 (2021)
3.
Ostner, J. ; Carcy, S. & Müller, C.: tascCODA: Bayesian tree-aggregated analysis of compositional amplicon and single-cell data Front. Genet. 12:766405 (2021)
4.
Pol-Fuster, J.* et al.: Familial psychosis associated with a missense mutation at MACF1 gene combined with the rare duplications DUP3p26.3 and DUP16q23.3, affecting the CNTN6 and CDH13 genes. Front. Genet. 12:622886 (2021)
5.
Xu, M. et al.: Identification of a novel variant in MT-CO3 causing MELAS. Front. Genet. 12:638749 (2021)
6.
Gusic, M. & Prokisch, H.: ncRNAs: New players in mitochondrial health and disease? Front. Genet. 11:95 (2020)
8.
Ummethum, H. & Hamperl, S.: Proximity labeling techniques to study chromatin. Front. Genet. 11:450 (2020)
9.
Contreras, R. ; Schriever, S.C. & Pfluger, P.T.: Physiological and epigenetic features of yoyo dieting and weight control. Front. Genet. 10:1015 (2019)
10.
Hawe, J. ; Theis, F.J. & Heinig, M.: Inferring interaction networks from multi-omics data. Front. Genet. 10:535 (2019)
11.
Shahryari, A. et al.: Development and clinical translation of approved gene therapy products for genetic disorders. Front. Genet. 10:868 (2019)
12.
Wang, Y.* et al.: Prognostic and predictive value of three DNA methylation signatures in lung adenocarcinoma. Front. Genet. 10:349 (2019)
13.
Westphal, D.S. ; Andres, S.* ; Makowski, C.* ; Meitinger, T. & Hoefele, J.*: MAP2 - A candidate gene for epilepsy, developmental delay and behavioral abnormalities in a patient with microdeletion 2q34. Front. Genet. 9:99 (2018)
14.
Ahting, U.* et al.: Clinical, biochemical, and genetic spectrum of seven new patients with NFU1 deficiency. Front. Genet. 6:123 (2015)
15.
Venco, P.* et al.: Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+. Front. Genet. 6:185 (2015)
16.
Sacco, F.* et al.: Combining affinity proteomics and network context to identify new phosphatase substrates and adapters in growth pathways. Front. Genet. 5:115 (2014)
17.
Jacobs, D.I.* et al.: Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: A novel candidate SNP approach. Front. Genet. 3:203 (2012)