Zobrazeno 1 - 10
of 10
pro vyhledávání: '"M G, Sanna"'
Autor:
A. Meloni, L. Pistoia, N. Martini, D. Visceglie, P. M. G. Sanna, M. Murgia, A. Barone, P. Giovangrossi, G. Alberini, V. Positano, F. Cademartiri
Publikováno v:
HemaSphere, Vol 6, Pp 1393-1394 (2022)
Externí odkaz:
https://doaj.org/article/b662533544f34eabb133470ed47d6826
Autor:
Laura Pistoia, S Renne, Massimiliano Missere, P M G Sanna, Emanuele Grassedonio, S Pulini, N Giunta, Antonella Meloni, M. Pasin, Vincenzo Positano, G Peritore, A Pepe
Publikováno v:
European Heart Journal. 40
Background In non transfusion dependent thalassemia (NTDT) the lack of a clear genotype-phenotype relationship complicates the already complex and extensive scenario in clinical practice. Purpose Our aim was to detect if the presence of a β°/β° h
Autor:
P Giuliano, Positano, P M G Sanna, A Carollo, Paolo Preziosi, Alessia Pepe, M. G. Roberti, Antonella Meloni, Vinci, M. Mangione, Laura Pistoia, M. Murgia
Publikováno v:
European Heart Journal. 39
Autor:
Laura Pistoia, P M G Sanna, L. Cuccia, Domenico Giuseppe D'Ascola, P. Ricchi, G Peritore, Antonella Meloni, L. Pitrolo, Vincenzo Positano, A. Barone, Riccardo Righi, A. Pepe
Publikováno v:
HemaSphere. 3:1064
Autor:
Antonella Quarta, P M G Sanna, Massimo Lombardi, Gianluca Valeri, Alessia Pepe, Paolo Preziosi, Antonella Meloni, L. Gulino, Daniele De Marchi, Giovan Battista Ruffo
Publikováno v:
European Heart Journal. 34:P2919-P2919
Purpose: Sickle-thalassemia is an inherited hemoglobin disorder resulting from the combined heterozygosity for sickle-cell and β-thalassemia genes. Myocardial iron overload in patients with sickle-thalassemia has been poorly studied; however, a repo
Autor:
M G Sanna, Melvin I. Simon
Publikováno v:
Journal of bacteriology. 178(21)
Bacterial chemotaxis results from the ability of flagellated bacteria to control the frequency of switching between smooth-swimming and tumbling episodes in response to changes in concentration of extracellular substances. High levels of phosphorylat
Autor:
G, Fogu, B, Spano, R, Sanna, A G, Angius, P M, Campus, M G, Olzai, M G, Sanna, A, Balata, A, Chiarolini
Publikováno v:
La Pediatria medica e chirurgica : Medical and surgical pediatrics. 13(4)
We report a case of Edward's syndrome showing some symptoms infrequently described in trisomy 18. The authors suggest that the phenotypic expression of symptoms rarely observed in the syndrome may be better interpreted as non specific consequence of
Publikováno v:
La Pediatria medica e chirurgica : Medical and surgical pediatrics. 12(4)
The study of gene/dosage effect may be essential in tracing the pathogenetic steps which lead from an unbalanced chromosome anomaly to a pathological phenotype. We present a newborn with a clinical and pathological picture compatible with a diagnosis
Publikováno v:
Scopus-Elsevier
Osmoregulation of the Shigella flexneri ompC gene and the role of OmpC in Shigella virulence have been investigated. OmpC was highly expressed when bacteria were grown in medium of either low or high osmolarity. This constitutive expression is in con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbbfdf6db0e817801c121b319c3691a2
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027261249&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027261249&partnerID=MN8TOARS
Publikováno v:
Scopus-Elsevier
An expressed sequence tag homologous to cheA was previously isolated by random sequencing of Thermotoga maritima cDNA clones (C. W. Kim, P. Markiewicz, J. J. Lee, C. F. Schierle, and J. H. Miller, J. Mol. Biol. 231: 960-981, 1993). Oligonucleotides c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5ed98e30a8a14bfdf8c294dce55e147
http://www.scopus.com/inward/record.url?eid=2-s2.0-0030031939&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0030031939&partnerID=MN8TOARS