Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Adeeb Naser Eddin"'
Autor:
Maria Gabelli, Polina Stepensky, Giorgio Ottaviano, Khushnuma Mullanfiroze, Arina Lazareva, Irina Zaidman, Ehud Even-Or, Giovanna Lucchini, Robert Chiesa, Juliana Silva, Stuart Adams, Susanne Kricke, Maria Finch, Annette Hill, Rachel Mead, Delphine Veys, Yael Dinur Schejter, Adeeb Naser Eddin, Austen Worth, Persis J. Amrolia, Kanchan Rao
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d916ecab56ed5f2f35473daf471e50e
https://hdl.handle.net/11577/3473038
https://hdl.handle.net/11577/3473038
Autor:
Ehud Even-Or, Bella Shadur, Mohammad Najajreh, Adeeb Naser Eddin, Irina Zaidman, Orly Zelig, Polina Stepensky, Yael Dinur Schejter
Publikováno v:
Pediatric bloodcancerREFERENCES. 67(1)
Autoimmune cytopenias (AIC) following allogeneic hematopoietic stem cell transplantation (HSCT) may cause significant morbidity and mortality and are often challenging to treat. We present a case of a pediatric patient with primary myelofibrosis of i
Autor:
Natalia Simanovsky, Abril Gijsbers, Katherine H. Kim, Davide Altamura, Talia Dor, Joel Charrow, Arnulfo Bautista-Santos, Alfonso Méndez-Godoy, Orly Elpeleg, Montserrat Chacón-Flores, Nuria Sánchez-Puig, Omar Abuzaitoun, Dritan Siliqi, Polina Stepensky, Adeeb Naser Eddin
Publikováno v:
Journal of medical genetics
54 (2017): 558–566. doi:10.1136/jmedgenet-2016-104366
info:cnr-pdr/source/autori:Stepensky P.; Chacon-Flores M.; Kim K.H.; Abuzaitoun O.; Bautista-Santos A.; Simanovsky N.; Siliqi D.; Altamura D.; Mendez-Godoy A.; Gijsbers A.; Eddin A.N.; Dor T.; Charrow J.; Sanchez-Puig N.; Elpeleg O./titolo:Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in a Shwachman-Diamond like syndrome/doi:10.1136%2Fjmedgenet-2016-104366/rivista:Journal of medical genetics (Print)/anno:2017/pagina_da:558/pagina_a:566/intervallo_pagine:558–566/volume:54
54 (2017): 558–566. doi:10.1136/jmedgenet-2016-104366
info:cnr-pdr/source/autori:Stepensky P.; Chacon-Flores M.; Kim K.H.; Abuzaitoun O.; Bautista-Santos A.; Simanovsky N.; Siliqi D.; Altamura D.; Mendez-Godoy A.; Gijsbers A.; Eddin A.N.; Dor T.; Charrow J.; Sanchez-Puig N.; Elpeleg O./titolo:Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in a Shwachman-Diamond like syndrome/doi:10.1136%2Fjmedgenet-2016-104366/rivista:Journal of medical genetics (Print)/anno:2017/pagina_da:558/pagina_a:566/intervallo_pagine:558–566/volume:54
Background For the final step of the maturation of the ribosome, the nascent 40S and 60S subunits are exported from the nucleus to the cell cytoplasm. To prevent premature association of these ribosomal subunits, eukaryotic initiation factor 6 (eIF6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30b7642090c05571e86401fc8a58f2a9
http://www.cnr.it/prodotto/i/376032
http://www.cnr.it/prodotto/i/376032