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

av Lehnen, Harald, Zechner, Ulrich, Haaf, Thomas
Publicerad 2013

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

av Herlyn, Holger, Zechner, Ulrich, Oswald, Franz, Pfeufer, Arne, Zischler, Hans, Haaf, Thomas
Publicerad 2009

Lrrc34, a Novel Nucleolar Protein, Interacts with Npm1 and Ncl and Has an Impact on Pluripotent Stem Cells

av Lührig, Sandra, Siamishi, Iliana, Tesmer-Wolf, Marieke, Zechner, Ulrich, Engel, Wolfgang, Nolte, Jessica
I publikationen Stem Cells Dev (2014)

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

av Gerber, Tiemo S, Schad, Arno, Hartmann, Nils, Springer, Erik, Zechner, Ulrich, Musholt, Thomas J
I publikationen Endocr Connect (2017)

The FOXP2-Driven Network in Developmental Disorders and Neurodegeneration

av Oswald, Franz, Klöble, Patricia, Ruland, André, Rosenkranz, David, Hinz, Bastian, Butter, Falk, Ramljak, Sanja, Zechner, Ulrich, Herlyn, Holger
I publikationen Front Cell Neurosci (2017)

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

av Birtel, Johannes, Gliem, Martin, Hess, Kristina, Birtel, Theresa H., Holz, Frank G., Zechner, Ulrich, Bolz, Hanno J., Herrmann, Philipp
I publikationen Genes (Basel) (2020)

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

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

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

av Komlosi, Katalin, Diederich, Stefan, Fend-Guella, Desiree Lucia, Bartsch, Oliver, Winter, Jennifer, Zechner, Ulrich, Beck, Michael, Meyer, Peter, Schweiger, Susann
I publikationen Orphanet J Rare Dis (2018)

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

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

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

av Wilmanns, Christoph, Cooper, Alexis, Wockner, Leesa, Katsandris, Sotirios, Glaser, Nadine, Meyer, Alexander, Bartsch, Oliver, Binder, Harald, Walter, Paul Karl, Zechner, Ulrich
I publikationen EBioMedicine (2015)

Extreme Methylation Values of Imprinted Genes in Human Abortions and Stillbirths

av Pliushch, Galyna, Schneider, Eberhard, Weise, Daniela, El Hajj, Nady, Tresch, Achim, Seidmann, Larissa, Coerdt, Wiltrud, Müller, Annette M., Zechner, Ulrich, Haaf, Thomas
Publicerad 2010

CAF-like state in primary skin fibroblasts with constitutional BRCA1 epimutation sheds new light on tumor suppressor deficiency-related changes in healthy tissue

av Etzold, Anna, Galetzka, Danuta, Weis, Eva, Bartsch, Oliver, Haaf, Thomas, Spix, Claudia, Itzel, Timo, Schweiger, Susann, Strand, Dennis, Strand, Susanne, Zechner, Ulrich
I publikationen Epigenetics (2016)

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

av Šutić, Maja, Baranašić, Jurica, Bilić, Lana Kovač, Bilić, Mario, Jakovčević, Antonija, Brčić, Luka, Seiwerth, Sven, Jakopović, Marko, Samaržija, Miroslav, Zechner, Ulrich, Knežević, Jelena
I publikationen Diagn Pathol (2021)

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

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

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

av Xu, Xingbo, Smorag, Lukasz, Nakamura, Toshinobu, Kimura, Tohru, Dressel, Ralf, Fitzner, Antje, Tan, Xiaoying, Linke, Matthias, Zechner, Ulrich, Engel, Wolfgang, Krishna Pantakani, D. V.
I publikationen Nat Commun (2015)

SHARP is a novel component of the Notch/RBP-Jκ signalling pathway

av Oswald, Franz, Kostezka, Ulrike, Astrahantseff, Kathy, Bourteele, Soizic, Dillinger, Karin, Zechner, Ulrich, Ludwig, Leopold, Wilda, Monika, Hameister, Horst, Knöchel, Walter, Liptay, Susanne, Schmid, Roland M.
Publicerad 2002

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

av 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
Publicerad 2013

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

av 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
I publikationen PLoS One (2016)

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

av 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
Publicerad 2010

Limiting dilution bisulfite (pyro)sequencing reveals parent-specific methylation patterns in single early mouse embryos and bovine oocytes

av El Hajj, Nady, Trapphoff, Tom, Linke, Matthias, May, Andreas, Hansmann, Tamara, Kuhtz, Juliane, Reifenberg, Kurt, Heinzmann, Julia, Niemann, Heiner, Daser, Angelika, Eichenlaub-Ritter, Ursula, Zechner, Ulrich, Haaf, Thomas
Publicerad 2011