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Lista de obras de Eduardo Fernandez-Rebollo

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

artículo científico publicado en 2020

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

artículo científico publicado en 2015

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

artículo científico publicado en 2012

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

Effects of senolytic drugs on human mesenchymal stromal cells.

artículo científico publicado en 2018

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.

artículo científico publicado en 2017

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

artículo científico

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

artículo científico publicado en 2011

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

artículo científico publicado en 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.

artículo científico publicado en 2008

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

artículo científico publicado en 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

artículo científico publicado en 2009

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

artículo científico publicado en 2016

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

artículo científico publicado en 2018

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

artículo científico publicado en 2012

New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism

artículo científico publicado en 2010

New mutation type in pseudohypoparathyroidism type Ia.

artículo científico publicado en 2008

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

artículo científico publicado en 2014

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

artículo científico publicado en 2017

Response to Letter to the Editor: Epigenetic Aging in Osteoporosis

artículo científico publicado en 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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