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DNA methylation changes during long-term in vitro cell culture are caused by epigenetic drift.
Published in:
Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02116-y
By:
- Franzen, Julia;
- Georgomanolis, Theodoros;
- Selich, Anton;
- Kuo, Chao-Chung;
- Stöger, Reinhard;
- Brant, Lilija;
- Mulabdić, Melita Sara;
- Fernandez-Rebollo, Eduardo;
- Grezella, Clara;
- Ostrowska, Alina;
- Begemann, Matthias;
- Nikolić, Miloš;
- Rath, Björn;
- Ho, Anthony D.;
- Rothe, Michael;
- Schambach, Axel;
- Papantonis, Argyris;
- Wagner, Wolfgang
Publication type:
Article
The lncRNA HOTAIR impacts on mesenchymal stem cells via triple helix formation.
Published in:
Nucleic Acids Research, 2016, v. 44, n. 22, p. 10631, doi. 10.1093/nar/gkw802
By:
- Kalwa, Marie;
- Hänzelmann, Sonja;
- Otto, Sabrina;
- Chao-Chung Kuo;
- Franzen, Julia;
- Joussen, Sylvia;
- Fernandez-Rebollo, Eduardo;
- Rath, Björn;
- Koch, Carmen;
- Hofmann, Andrea;
- Shih-Han Lee;
- Teschendorff, Andrew E.;
- Denecke, Bernd;
- Qiong Lin;
- Widschwendter, Martin;
- Weinhold, Elmar;
- Costa, Ivan G.;
- Wagner, Wolfgang
Publication type:
Article
Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locus.
Published in:
Journal of Bone & Mineral Research, 2011, v. 26, n. 8, p. 1864, doi. 10.1002/jbmr.369
By:
- Zazo, Celia;
- Thiele, Susanne;
- Martín, Cesar;
- Fernandez-Rebollo, Eduardo;
- Martinez-Indart, Lorea;
- Werner, Ralf;
- Garin, Intza;
- Group, Spanish PHP;
- Hiort, Olaf;
- Perez de Nanclares, Guiomar
Publication type:
Article
Exclusion of the GNAS locus in PHP-Ib patients with broad GNAS methylation changes: Evidence for an autosomal recessive form of PHP-Ib?
Published in:
Journal of Bone & Mineral Research, 2011, v. 26, n. 8, p. 1854, doi. 10.1002/jbmr.408
By:
- Fernández-Rebollo, Eduardo;
- Pérez de Nanclares, Guiomar;
- Lecumberri, Beatriz;
- Turan, Serap;
- Anda, Emma;
- Pérez-Nanclares, Gustavo;
- Feig, Denice;
- Nik-Zainal, Serena;
- Bastepe, Murat;
- Jüppner, Harald
Publication type:
Article
Jansen Metaphyseal Chondrodysplasia due to Heterozygous H223R-PTH1R Mutations With or Without Overt Hypercalcemia.
Published in:
2016
By:
- Nampoothiri, Sheela;
- Fernández-Rebollo, Eduardo;
- Yesodharan, Dhanya;
- Gardella, Thomas J.;
- Rush, Eric T.;
- Langman, Craig B.;
- Jüppner, Harald
Publication type:
journal article
Endocrine profile and phenotype-(epi)genotype correlation in Spanish patients with pseudohypoparathyroidism.
Published in:
2013
By:
- Fernández-Rebollo, Eduardo;
- Lecumberri, Beatriz;
- Gaztambide, Sonia;
- Martinez-Indart, Lorea;
- Perez de Nanclares, Guiomar;
- Castaño, Luis;
- Spanish PHP Group
Publication type:
journal article
Detection of hypomethylation syndrome among patients with epigenetic alterations at the GNAS locus.
Published in:
2012
By:
- Perez-Nanclares G;
- Romanelli V;
- Mayo S;
- Garin I;
- Zazo C;
- Fernandez-Rebollo E;
- Martínez F;
- Lapunzina P;
- de Nanclares GP;
- Spanish PHP Group;
- Perez-Nanclares, Gustavo;
- Romanelli, Valeria;
- Mayo, Sonia;
- Garin, Intza;
- Zazo, Celia;
- Fernandez-Rebollo, Eduardo;
- Martínez, Francisco;
- Lapunzina, Pablo;
- de Nanclares, Guiomar Pérez;
- Zazo Seco, Celia
Publication type:
journal article
New Splice Site Acceptor Mutation in <i>AIRE</i> Gene in Autoimmune Polyendocrine Syndrome Type 1.
Published in:
PLoS ONE, 2014, v. 9, n. 7, p. 1, doi. 10.1371/journal.pone.0101616
By:
- Mora, Mireia;
- Hanzu, Felicia A.;
- Pradas-Juni, Marta;
- Aranda, Gloria B.;
- Halperin, Irene;
- Puig-Domingo, Manuel;
- Aguiló, Sira;
- Fernández-Rebollo, Eduardo
Publication type:
Article
Differential Methylation of <i>TCF7L2</i> Promoter in Peripheral Blood DNA in Newly Diagnosed, Drug-Naïve Patients with Type 2 Diabetes.
Published in:
PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099310
By:
- Canivell, Silvia;
- Ruano, Elena G.;
- Sisó-Almirall, Antoni;
- Kostov, Belchin;
- González-de Paz, Luis;
- Fernandez-Rebollo, Eduardo;
- Hanzu, Felicia A.;
- Párrizas, Marcelina;
- Novials, Anna;
- Gomis, Ramon
Publication type:
Article
Gastric Inhibitory Polypeptide Receptor Methylation in Newly Diagnosed, Drug-Naïve Patients with Type 2 Diabetes: A Case-Control Study.
Published in:
PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0075474
By:
- Canivell, Silvia;
- Ruano, Elena G.;
- Sisó-Almirall, Antoni;
- Kostov, Belchin;
- González-de Paz, Luis;
- Fernandez-Rebollo, Eduardo;
- Hanzu, Felicia;
- Párrizas, Marcelina;
- Novials, Anna;
- Gomis, Ramon
Publication type:
Article
Intragenic GNAS deletion involving exon A/B in pseudohypoparathyroidism type 1A resulting in an apparent loss of exon A/B methylation: potential for misdiagnosis of pseudohypoparathyroidism type 1B.
Published in:
2010
By:
- Fernandez-Rebollo, Eduardo;
- García-Cuartero, Beatriz;
- Garin, Intza;
- Largo, Cristina;
- Martínez, Francisco;
- Garcia-Lacalle, Concepcion;
- Castaño, Luis;
- Bastepe, Murat;
- Pérez de Nanclares, Guiomar
Publication type:
journal article
Epigenetic Defects of GNAS in Patients with Pseudohypoparathyroidism and Mild Features of Albright’s Hereditary Osteodystrophy.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 6, p. 2370, doi. 10.1210/jc.2006-2287
By:
- de Nanclares, Guiomar Pérez;
- Fernández-Rebollo, Eduardo;
- Santin, Izortze;
- García-Cuartero, Beatriz;
- Gaztambide, Sonia;
- Menéndez, Edelmiro;
- Morales, Maria Jose;
- Pombo, Manuel;
- Bilbao, José Ramón;
- Barros, Francisco;
- Nuria Zazo;
- Ahrens, Wiebke;
- Jüppner, Harald;
- Hiort, Olaf;
- Castaño, Luis;
- Bastepe, Murat
Publication type:
Article
New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism.
Published in:
European Journal of Endocrinology, 2010, v. 163, n. 6, p. 953
By:
- Eduardo Fernández-Rebollo
Publication type:
Article
Two cases of deletion 2q37 associated with segregation of an unbalanced translocation 2;21: choanal atresia leading to misdiagnosis of CHARGE syndrome.
Published in:
European Journal of Endocrinology, 2009, v. 160, n. 4, p. 711
By:
- Eduardo Fernández-Rebollo
Publication type:
Article
Genetic barcoding reveals clonal dominance in iPSC-derived mesenchymal stromal cells.
Published in:
Stem Cell Research & Therapy, 2020, v. 11, n. 1, p. 1, doi. 10.1186/s13287-020-01619-5
By:
- Hollmann, Jonathan;
- Brecht, Johanna;
- Goetzke, Roman;
- Franzen, Julia;
- Selich, Anton;
- Schmidt, Marco;
- Eipel, Monika;
- Ostrowska, Alina;
- Hapala, Jan;
- Fernandez-Rebollo, Eduardo;
- Müller-Newen, Gerhard;
- Rothe, Michael;
- Eggermann, Thomas;
- Zenke, Martin;
- Wagner, Wolfgang
Publication type:
Article
LincRNA H19 protects from dietary obesity by constraining expression of monoallelic genes in brown fat.
Published in:
Nature Communications, 2018, p. 1, doi. 10.1038/s41467-018-05933-8
By:
- Schmidt, Elena;
- Dhaouadi, Ines;
- Gaziano, Isabella;
- Oliverio, Matteo;
- Klemm, Paul;
- Awazawa, Motoharu;
- Mitterer, Gerfried;
- Fernandez-Rebollo, Eduardo;
- Pradas-Juni, Marta;
- Wagner, Wolfgang;
- Hammerschmidt, Philipp;
- Loureiro, Rute;
- Kiefer, Christoph;
- Hansmeier, Nils R.;
- Khani, Sajjad;
- Bergami, Matteo;
- Heine, Markus;
- Ntini, Evgenia;
- Frommolt, Peter;
- Zentis, Peter
Publication type:
Article
Effects of senolytic drugs on human mesenchymal stromal cells.
Published in:
Stem Cell Research & Therapy, 2018, v. 9, n. 1, p. N.PAG, doi. 10.1186/s13287-018-0857-6
By:
- Grezella, Clara;
- Fernandez-Rebollo, Eduardo;
- Franzen, Julia;
- Ventura Ferreira, Mónica Sofia;
- Beier, Fabian;
- Wagner, Wolfgang
Publication type:
Article
Response to Letter to the Editor: Epigenetic Aging in Osteoporosis.
Published in:
2018
By:
- Jakob, Franz;
- Ebert, Regina;
- Fernandez‐Rebollo, Eduardo;
- Bischof, Oliver;
- Wagner, Wolfgang
Publication type:
Letter to the Editor
Primary Osteoporosis Is Not Reflected by Disease‐Specific DNA Methylation or Accelerated Epigenetic Age in Blood.
Published in:
Journal of Bone & Mineral Research, 2018, v. 33, n. 2, p. 356, doi. 10.1002/jbmr.3298
By:
- Fernandez‐Rebollo, Eduardo;
- Eipel, Monika;
- Wagner, Wolfgang;
- Seefried, Lothar;
- Jakob, Franz;
- Hoffmann, Per;
- Strathmann, Klaus
Publication type:
Article
Postnatal Establishment of Allelic Gαs Silencing as a Plausible Explanation for Delayed Onset of Parathyroid Hormone Resistance Owing to Heterozygous Gαs Disruption.
Published in:
Journal of Bone & Mineral Research, 2014, v. 29, n. 3, p. 749, doi. 10.1002/jbmr.2070
By:
- Turan, Serap;
- Fernandez-Rebollo, Eduardo;
- Aydin, Cumhur;
- Zoto, Teuta;
- Reyes, Monica;
- Bounoutas, George;
- Chen, Min;
- Weinstein, Lee S;
- Erben, Reinhold G;
- Marshansky, Vladimir;
- Bastepe, Murat
Publication type:
Article
New mutation type in pseudohypoparathyroidism type Ia.
Published in:
Clinical Endocrinology, 2008, v. 69, n. 5, p. 705, doi. 10.1111/j.1365-2265.2008.03255.x
By:
- Fernandez-Rebollo, Eduardo;
- Barrio, Raquel;
- Pérez-Nanclares, Gustavo;
- Carcavilla, Atilano;
- Garin, Intza;
- Castaño, Luis;
- de Nanclares, Guiomar Pérez
Publication type:
Article
Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients.
Published in:
Clinical Endocrinology, 2008, v. 68, n. 6, p. 873, doi. 10.1111/j.1365-2265.2008.03214.x
By:
- Garin, Intza;
- Rica, Itxaso;
- Estalella, Itziar;
- Oyarzabal, Mirentxu;
- Rodríguez-Rigual, Mercedes;
- San Pedro, Jose Ignacio;
- Pérez-Nanclares, Gustavo;
- Fernández-Rebollo, Eduardo;
- Busturia, Maria Angeles;
- Castaño, Luis;
- de Nanclares, Guiomar Pérez
Publication type:
Article

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