Epigenetics of gestational diabetes mellitus and offspring health: the time for action is in early stages of life

por Lehnen, Harald, Zechner, Ulrich, Haaf, Thomas
Publicado 2013

Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes

por Herlyn, Holger, Zechner, Ulrich, Oswald, Franz, Pfeufer, Arne, Zischler, Hans, Haaf, Thomas
Publicado 2009

Targeted next-generation sequencing of cancer genes in poorly differentiated thyroid cancer

por Gerber, Tiemo S, Schad, Arno, Hartmann, Nils, Springer, Erik, Zechner, Ulrich, Musholt, Thomas J
Publicado 2017

A novel large in-frame FBN1 deletion causes neonatal Marfan syndrome

por Elgaz, Sümeyye, Wittekindt, Boris, Esmaeili, Anoosh, Fischer, Sebastian, Bolz, Hanno J., Zechner, Ulrich, Buxmann, Horst
Publicado 2022

The FOXP2-Driven Network in Developmental Disorders and Neurodegeneration

por Oswald, Franz, Klöble, Patricia, Ruland, André, Rosenkranz, David, Hinz, Bastian, Butter, Falk, Ramljak, Sanja, Zechner, Ulrich, Herlyn, Holger
Publicado 2017

Comprehensive Geno- and Phenotyping in a Complex Pedigree Including Four Different Inherited Retinal Dystrophies

por Birtel, Johannes, Gliem, Martin, Hess, Kristina, Birtel, Theresa H., Holz, Frank G., Zechner, Ulrich, Bolz, Hanno J., Herrmann, Philipp
Publicado 2020

Stage-Specific Germ-Cell Marker Genes Are Expressed in All Mouse Pluripotent Cell Types and Emerge Early during Induced Pluripotency

por Xu, Xingbo, Pantakani, D. V. Krishna, Lührig, Sandra, Tan, Xiaoying, Khromov, Tatjana, Nolte, Jessica, Dressel, Ralf, Zechner, Ulrich, Engel, Wolfgang
Publicado 2011

Targeted next-generation sequencing analysis in couples at increased risk for autosomal recessive disorders

por Komlosi, Katalin, Diederich, Stefan, Fend-Guella, Desiree Lucia, Bartsch, Oliver, Winter, Jennifer, Zechner, Ulrich, Beck, Michael, Meyer, Peter, Schweiger, Susann
Publicado 2018

Metabolic Programming of MEST DNA Methylation by Intrauterine Exposure to Gestational Diabetes Mellitus

por El Hajj, Nady, Pliushch, Galyna, Schneider, Eberhard, Dittrich, Marcus, Müller, Tobias, Korenkov, Michael, Aretz, Melanie, Zechner, Ulrich, Lehnen, Harald, Haaf, Thomas
Publicado 2013

Morphology and Progression in Primary Varicose Vein Disorder Due to 677C>T and 1298A>C Variants of MTHFR

por Wilmanns, Christoph, Cooper, Alexis, Wockner, Leesa, Katsandris, Sotirios, Glaser, Nadine, Meyer, Alexander, Bartsch, Oliver, Binder, Harald, Walter, Paul Karl, Zechner, Ulrich
Publicado 2015

CpG islands in MyD88 and ASC/PYCARD/TMS1 promoter regions are differentially methylated in head and neck squamous cell carcinoma and primary lung squamous cell carcinoma

por Šutić, Maja, Baranašić, Jurica, Bilić, Lana Kovač, Bilić, Mario, Jakovčević, Antonija, Brčić, Luka, Seiwerth, Sven, Jakopović, Marko, Samaržija, Miroslav, Zechner, Ulrich, Knežević, Jelena
Publicado 2021

A boy with homozygous microdeletion of NEUROG1 presents with a congenital cranial dysinnervation disorder [Moebius syndrome variant]

por Schröder, Julia C, Läßig, Anne K, Galetzka, Danuta, Peters, Angelika, Castle, John C, Diederich, Stefan, Zechner, Ulrich, Müller-Forell, Wibke, Keilmann, Annerose, Bartsch, Oliver
Publicado 2013

Dppa3 expression is critical for generation of fully reprogrammed iPS cells and maintenance of Dlk1-Dio3 imprinting

por Xu, Xingbo, Smorag, Lukasz, Nakamura, Toshinobu, Kimura, Tohru, Dressel, Ralf, Fitzner, Antje, Tan, Xiaoying, Linke, Matthias, Zechner, Ulrich, Engel, Wolfgang, Krishna Pantakani, D. V.
Publicado 2015

The Disease-Specific Phenotype in Cardiomyocytes Derived from Induced Pluripotent Stem Cells of Two Long QT Syndrome Type 3 Patients

por Fatima, Azra, Kaifeng, Shao, Dittmann, Sven, Xu, Guoxing, Gupta, Manoj K., Linke, Matthias, Zechner, Ulrich, Nguemo, Filomain, Milting, Hendrik, Farr, Martin, Hescheler, Jürgen, Šarić, Tomo
Publicado 2013

Abnormal Hypermethylation at Imprinting Control Regions in Patients with S-Adenosylhomocysteine Hydrolase (AHCY) Deficiency

por Motzek, Antje, Knežević, Jelena, Switzeny, Olivier J., Cooper, Alexis, Barić, Ivo, Beluzić, Robert, Strauss, Kevin A., Puffenberger, Erik G., Mudd, S. Harvey, Vugrek, Oliver, Zechner, Ulrich
Publicado 2016

Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns

por Schneider, Eberhard, Pliushch, Galyna, El Hajj, Nady, Galetzka, Danuta, Puhl, Alexander, Schorsch, Martin, Frauenknecht, Katrin, Riepert, Thomas, Tresch, Achim, Müller, Annette M., Coerdt, Wiltrud, Zechner, Ulrich, Haaf, Thomas
Publicado 2010

Monozygotic twins discordant for constitutive BRCA1 promoter methylation, childhood cancer and secondary cancer

por Galetzka, Danuta, Hansmann, Tamara, El Hajj, Nady, Weis, Eva, Irmscher, Benjamin, Ludwig, Marco, Schneider-Rätzke, Brigitte, Kohlschmidt, Nicolai, Beyer, Vera, Bartsch, Oliver, Zechner, Ulrich, Spix, Claudia, Haaf, Thomas
Publicado 2012

Inhibition of histone deacetylation rescues phenotype in a mouse model of Birk-Barel intellectual disability syndrome

por Cooper, Alexis, Butto, Tamer, Hammer, Niklas, Jagannath, Somanath, Fend-Guella, Desiree Lucia, Akhtar, Junaid, Radyushkin, Konstantin, Lesage, Florian, Winter, Jennifer, Strand, Susanne, Roeper, Jochen, Zechner, Ulrich, Schweiger, Susann
Publicado 2020

Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation

por Bohne, Florian, Langer, David, Martiné, Ursula, Eider, Claudia S., Cencic, Regina, Begemann, Matthias, Elbracht, Miriam, Bülow, Luzie, Eggermann, Thomas, Zechner, Ulrich, Pelletier, Jerry, Zabel, Bernhard Ulrich, Enklaar, Thorsten, Prawitt, Dirk
Publicado 2016

Early-life adversity selectively impairs α2-GABA(A) receptor expression in the mouse nucleus accumbens and influences the behavioral effects of cocaine

por Mitchell, Scott J., Maguire, Edward P., Cunningham, Linda, Gunn, Benjamin G., Linke, Matthias, Zechner, Ulrich, Dixon, Claire I., King, Sarah L., Stephens, David N., Swinny, Jerome D., Belelli, Delia, Lambert, Jeremy J.
Publicado 2018