关注
Eduardo Fernandez-Rebollo
Eduardo Fernandez-Rebollo
DanStem
在 sund.ku.dk 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis
I Garin, EL Edghill, I Akerman, O Rubio-Cabezas, I Rica, JM Locke, ...
Proceedings of the National Academy of Sciences 107 (7), 3105-3110, 2010
2192010
Epigenetic Defects of GNAS in Patients with Pseudohypoparathyroidism and Mild Features of Albright’s Hereditary Osteodystrophy
GP De Nanclares, E Fernández-Rebollo, I Santin, B García-Cuartero, ...
The Journal of Clinical Endocrinology & Metabolism 92 (6), 2370-2373, 2007
1672007
The lncRNA HOTAIR impacts on mesenchymal stem cells via triple helix formation
M Kalwa, S Hänzelmann, S Otto, CC Kuo, J Franzen, S Joussen, ...
Nucleic acids research 44 (22), 10631-10643, 2016
1602016
LincRNA H19 protects from dietary obesity by constraining expression of monoallelic genes in brown fat
E Schmidt, I Dhaouadi, I Gaziano, M Oliverio, P Klemm, M Awazawa, ...
Nature communications 9 (1), 3622, 2018
1212018
Human Platelet Lysate versus Fetal Calf Serum: These Supplements Do Not Select for Different Mesenchymal Stromal Cells
E Fernandez-Rebollo, B Mentrup, R Ebert, J Franzen, G Abagnale, ...
Scientific reports 7 (1), 5132, 2017
842017
New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism
E Fernández-Rebollo, B Lecumberri, I Garin, J Arroyo, A Bernal-Chico
Eur J Endocrinol 163, 953-962, 2010
822010
Senescence-associated metabolomic phenotype in primary and iPSC-derived mesenchymal stromal cells
E Fernandez-Rebollo, J Franzen, R Goetzke, J Hollmann, A Ostrowska, ...
Stem cell reports 14 (2), 201-209, 2020
702020
Effects of senolytic drugs on human mesenchymal stromal cells
C Grezella, E Fernandez-Rebollo, J Franzen, MS Ventura Ferreira, ...
Stem cell research & therapy 9, 1-6, 2018
702018
Postnatal establishment of allelic Gαs silencing as a plausible explanation for delayed onset of parathyroid hormone resistance owing to heterozygous Gαs disruption
S Turan, E Fernandez‐Rebollo, C Aydin, T Zoto, M Reyes, G Bounoutas, ...
Journal of Bone and Mineral Research 29 (3), 749-760, 2014
692014
Endocrine profile and phenotype-(epi) genotype correlation in Spanish patients with pseudohypoparathyroidism
E Fernández-Rebollo, B Lecumberri, S Gaztambide, L Martinez-Indart, ...
The Journal of Clinical Endocrinology & Metabolism 98 (5), E996-E1006, 2013
582013
Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locus
C Zazo, S Thiele, C Martín, E Fernandez‐Rebollo, L Martinez‐Indart, ...
Journal of Bone and Mineral Research 26 (8), 1864-1870, 2011
562011
Detection of Hypomethylation Syndrome among Patients with Epigenetic Alterations at the GNAS Locus
G Perez-Nanclares, V Romanelli, S Mayo, I Garin, C Zazo, ...
The Journal of Clinical Endocrinology & Metabolism 97 (6), E1060-E1067, 2012
462012
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 …
G Aranda, E Fernández-Rebollo, M Pradas-Juni, FA Hanzu, SG Kalko, ...
The Journal of steroid biochemistry and molecular biology 172, 20-28, 2017
432017
Exclusion of the GNAS locus in PHP‐Ib patients with broad GNAS methylation changes: Evidence for an autosomal recessive form of PHP‐Ib?
E Fernández‐Rebollo, G Pérez de Nanclares, B Lecumberri, S Turan, ...
Journal of Bone and Mineral Research 26 (8), 1854-1863, 2011
432011
Coexistence of two different pseudohypoparathyroidism subtypes (Ia and Ib) in the same kindred with independent Gsα coding mutations and GNAS imprinting defects
B Lecumberri, E Fernandez-Rebollo, L Sentchordi, P Saavedra, ...
Journal of medical genetics 47 (4), 276-280, 2010
432010
Intragenic GNAS Deletion Involving Exon A/B in Pseudohypoparathyroidism Type 1A Resulting in an Apparent Loss of Exon A/B Methylation: Potential for …
E Fernandez-Rebollo, B García-Cuartero, I Garin, C Largo, F Martínez, ...
The Journal of Clinical Endocrinology & Metabolism 95 (2), 765-771, 2010
422010
DNA methylation changes during long-term in vitro cell culture are caused by epigenetic drift
J Franzen, T Georgomanolis, A Selich, CC Kuo, R Stöger, L Brant, ...
Communications biology 4 (1), 598, 2021
402021
Primary osteoporosis is not reflected by disease‐specific DNA methylation or accelerated epigenetic age in blood
E Fernandez‐Rebollo, M Eipel, L Seefried, P Hoffmann, K Strathmann, ...
Journal of Bone and Mineral Research 33 (2), 356-361, 2018
392018
Differential Methylation of TCF7L2 Promoter in Peripheral Blood DNA in Newly Diagnosed, Drug-Naïve Patients with Type 2 Diabetes
S Canivell, EG Ruano, A Siso-Almirall, B Kostov, L Gonzalez-de Paz, ...
PLoS One 9 (6), e99310, 2014
392014
Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients
I Garin, I Rica, I Estalella, M Oyarzabal, M Rodríguez‐Rigual, JIS Pedro, ...
Clinical Endocrinology 68 (6), 873-878, 2008
382008
系统目前无法执行此操作,请稍后再试。
文章 1–20