Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Andrea Oneglia"'
Autor:
Guan Wang, Cunling Zhang, Hiroto Kambara, Cheryl Dambrot, Xuemei Xie, Li Zhao, Rong Xu, Andrea Oneglia, Fei Liu, Hongbo R. Luo
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
The MRP8-Cre-ires/EGFP transgenic mouse (Mrp8creTg, on C57BL/6J genetic background) is popular in immunological and hematological research for specifically expressing Cre recombinase and an EGFP reporter in neutrophils. It is often crossed with other
Externí odkaz:
https://doaj.org/article/c826001d08e2462ab085ded2c74ed7f4
Autor:
Jessica Piché, Natacha Gosset, Lisa-Marie Legault, Alain Pacis, Andrea Oneglia, Maxime Caron, Philippe Chetaille, Luis Barreiro, Donghai Liu, Xioyan Qi, Stanley Nattel, Séverine Leclerc, Mélanie Breton-Larrivée, Serge McGraw, Gregor Andelfinger, Jeroen Bakkers, Bart Loeys, Michel Pucéat
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 7, Iss 2, Pp 411-431 (2019)
Background & Aims: A generalized human pacemaking syndrome, chronic atrial and intestinal dysrhythmia (CAID) (OMIM 616201), is caused by a homozygous SGO1 mutation (K23E), leading to chronic intestinal pseudo-obstruction and arrhythmias. Because CAID
Externí odkaz:
https://doaj.org/article/8a8bdcb4983c41069d137c85a56a870e
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice.
Autor:
Andrea Freschi, Stella K Hur, Federica Maria Valente, Folami Y Ideraabdullah, Angela Sparago, Maria Teresa Gentile, Andrea Oneglia, Diego Di Nucci, Luca Colucci-D'Amato, Joanne L Thorvaldsen, Marisa S Bartolomei, Andrea Riccio, Flavia Cerrato
Publikováno v:
PLoS Genetics, Vol 14, Iss 2, p e1007243 (2018)
Differential DNA methylation defects of H19/IGF2 are associated with congenital growth disorders characterized by opposite clinical pictures. Due to structural differences between human and mouse, the mechanisms by which mutations of the H19/IGF2 Imp
Externí odkaz:
https://doaj.org/article/42197b0275b04922acbf4d0c0614bb84
Autor:
Angela Sparago, Andrea Oneglia, Marisa S. Bartolomei, Flavia Cerrato, Stella K. Hur, Luca Colucci-D'Amato, Andrea Freschi, Diego Di Nucci, Maria Teresa Gentile, Folami Y. Ideraabdullah, Federica Maria Valente, Andrea Riccio, Joanne L. Thorvaldsen
Publikováno v:
PLoS Genetics
PLOS genetics (Online) 14 (2018). doi:10.1371/journal.pgen.1007243
info:cnr-pdr/source/autori:Freschi A.; Hur S.K.; Valente F.M.; Ideraabdullah F.Y.; Sparago A.; Gentile M.T.; Oneglia A.; Di Nucci D.; Colucci-D'Amato L.; Thorvaldsen J.L.; Bartolomei M.S.; Riccio A.; Cerrato F./titolo:Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice/doi:10.1371%2Fjournal.pgen.1007243/rivista:PLOS genetics (Online)/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:14
PLoS Genetics, Vol 14, Iss 2, p e1007243 (2018)
PLOS genetics (Online) 14 (2018). doi:10.1371/journal.pgen.1007243
info:cnr-pdr/source/autori:Freschi A.; Hur S.K.; Valente F.M.; Ideraabdullah F.Y.; Sparago A.; Gentile M.T.; Oneglia A.; Di Nucci D.; Colucci-D'Amato L.; Thorvaldsen J.L.; Bartolomei M.S.; Riccio A.; Cerrato F./titolo:Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice/doi:10.1371%2Fjournal.pgen.1007243/rivista:PLOS genetics (Online)/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:14
PLoS Genetics, Vol 14, Iss 2, p e1007243 (2018)
Differential DNA methylation defects of H19/IGF2 are associated with congenital growth disorders characterized by opposite clinical pictures. Due to structural differences between human and mouse, the mechanisms by which mutations of the H19/IGF2 Imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d62f896bbd49c20a0b780a5140d58d8
http://hdl.handle.net/11591/387083
http://hdl.handle.net/11591/387083
