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List of works by Eduardo Fernandez-Rebollo

A MAFG-lncRNA axis links systemic nutrient abundance to hepatic glucose metabolism

scientific article published on 31 January 2020

DNA-methylation changes in replicative senescence and aging: two sides of the same coin?

scientific article published on 23 December 2015

Detection of hypomethylation syndrome among patients with epigenetic alterations at the GNAS locus.

scientific article published on 4 April 2012

Differential methylation of TCF7L2 promoter in peripheral blood DNA in newly diagnosed, drug-naïve patients with type 2 diabetes

scientific article (publication date: 2014)

Differential transcriptional and posttranslational transcription factor 7-like regulation among nondiabetic individuals and type 2 diabetic patients.

scientific article

Effects of senolytic drugs on human mesenchymal stromal cells.

scientific article

Effects of sex steroids on the pattern of methylation and expression of the promoter region of estrogen and androgen receptors in people with gender dysphoria under cross-sex hormone treatment.

scientific article

Endocrine profile and phenotype-(epi)genotype correlation in Spanish patients with pseudohypoparathyroidism.

scientific article published on 26 March 2013

Exclusion of the GNAS locus in PHP-Ib patients with broad GNAS methylation changes: evidence for an autosomal recessive form of PHP-Ib?

scientific article published on August 2011

Gastric inhibitory polypeptide receptor methylation in newly diagnosed, drug-naïve patients with type 2 diabetes: a case-control study

scientific article (publication date: 2013)

Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locus

article

Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients.

scientific article

Human Platelet Lysate versus Fetal Calf Serum: These Supplements Do Not Select for Different Mesenchymal Stromal Cells.

scientific article published on 11 July 2017

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

scientific article

Jansen Metaphyseal Chondrodysplasia due to Heterozygous H223R-PTH1R Mutations With or Without Overt Hypercalcemia

scientific article published on 13 July 2016

LincRNA H19 protects from dietary obesity by constraining expression of monoallelic genes in brown fat

scientific article published in Nature Communications

Loss of XLαs (extra-large αs) imprinting results in early postnatal hypoglycemia and lethality in a mouse model of pseudohypoparathyroidism Ib.

scientific article published on 10 April 2012

New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism

scientific article published on 13 September 2010

New mutation type in pseudohypoparathyroidism type Ia.

scientific article published on 3 April 2008

New splice site acceptor mutation in AIRE gene in autoimmune polyendocrine syndrome type 1.

scientific article

Postnatal establishment of allelic Gαs silencing as a plausible explanation for delayed onset of parathyroid hormone resistance owing to heterozygous Gαs disruption

scientific article published on March 2014

Primary Osteoporosis Is Not Reflected by Disease-Specific DNA Methylation or Accelerated Epigenetic Age in Blood

scientific article

Response to Letter to the Editor: Epigenetic Aging in Osteoporosis

scientific article published on 14 September 2018

The lncRNA HOTAIR impacts on mesenchymal stem cells via triple helix formation

scientific article published on 14 September 2016

The majority of cases of neonatal diabetes in Spain can be explained by known genetic abnormalities

article

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