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 em 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 em 2009

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

Por Lührig, Sandra, Siamishi, Iliana, Tesmer-Wolf, Marieke, Zechner, Ulrich, Engel, Wolfgang, Nolte, Jessica
Publicado no Stem Cells Dev (2014)

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 no Endocr Connect (2017)

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 no Front Cell Neurosci (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 no Genes (Basel) (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 em 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 no Orphanet J Rare Dis (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 em 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 no EBioMedicine (2015)

Extreme Methylation Values of Imprinted Genes in Human Abortions and Stillbirths

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

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

Por Etzold, Anna, Galetzka, Danuta, Weis, Eva, Bartsch, Oliver, Haaf, Thomas, Spix, Claudia, Itzel, Timo, Schweiger, Susann, Strand, Dennis, Strand, Susanne, Zechner, Ulrich
Publicado no 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

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 no Diagn Pathol (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 em 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 no Nat Commun (2015)

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

Por 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.
Publicado em 2002

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 em 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 no PLoS One (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 em 2010

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

Por 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
Publicado em 2011