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

由 Lehnen, Harald, Zechner, Ulrich, Haaf, Thomas
出版 2013

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

由 Herlyn, Holger, Zechner, Ulrich, Oswald, Franz, Pfeufer, Arne, Zischler, Hans, Haaf, Thomas
出版 2009

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

由 Lührig, Sandra, Siamishi, Iliana, Tesmer-Wolf, Marieke, Zechner, Ulrich, Engel, Wolfgang, Nolte, Jessica
發表在 Stem Cells Dev (2014)

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

由 Gerber, Tiemo S, Schad, Arno, Hartmann, Nils, Springer, Erik, Zechner, Ulrich, Musholt, Thomas J
發表在 Endocr Connect (2017)

The FOXP2-Driven Network in Developmental Disorders and Neurodegeneration

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

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

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

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

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

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

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

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

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

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

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

Extreme Methylation Values of Imprinted Genes in Human Abortions and Stillbirths

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

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

由 Etzold, Anna, Galetzka, Danuta, Weis, Eva, Bartsch, Oliver, Haaf, Thomas, Spix, Claudia, Itzel, Timo, Schweiger, Susann, Strand, Dennis, Strand, Susanne, Zechner, Ulrich
發表在 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

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

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

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

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

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

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

由 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.
出版 2002

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

由 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
出版 2013

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

由 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
發表在 PLoS One (2016)

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

由 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
出版 2010

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

由 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
出版 2011