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21 . Academic Journal
RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 Pathway
저자
by
De Rosa, Gianluca
;
Andolfo, Immacolata
;
Marra, Roberta
;
Manna, Francesco
;
Rosato, Barbara Eleni
, et al.
소스
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
; AUG 2020, 21 15, p5577 11p.
Scopus
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27 .
Unraveling the molecular basis of iron overload in rare hereditary anemias: Dehydrated hereditary stomatocytosis and Congenital dyserythropoietic anemia type II
저자
by
Rosato, Barbara Eleni
.
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Open Access (OpenAIRE)
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23 . Academic Journal
SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic Cells.
저자
by
Rosato, Barbara Eleni
;
Marra, Roberta
;
D'Onofrio, Vanessa
;
Del Giudice, Federica
;
Della Monica, Simone
, et al.
소스
International Journal of Molecular Sciences
. Feb2022, Vol. 23 Issue 3, p1304-N.PAG. 1p.
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27 .
PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosis
저자
by
Antonella Gambale
;
Barbara Eleni Rosato
;
Roberta Marra
;
Gianluca De Rosa
;
Lucia De Franceschi
, et al.
소스
Haematologica
. 103:e94-e97
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27 .
Common variants at 21q22.3 locus influence MX1 and TMPRSS2 gene expression and susceptibility to severe COVID-19
저자
by
Ivan Gentile
;
Roberta Russo
;
Romolo Villani
;
Pellegrino Cerino
;
Vito Alessandro Lasorsa
, et al.
소스
iScience
iScience, Vol 24, Iss 4, Pp 102322-(2021)
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27 . Academic Journal
Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients.
저자
by
Andolfo, Immacolata
;
Martone, Stefania
;
Rosato, Barbara Eleni
;
Marra, Roberta
;
Gambale, Antonella
, et al.
소스
Genes
. Jul2021, Vol. 12 Issue 7, p958. 1p.
Web of Science
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27 .
PIEZO1 Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood Cells
저자
by
Immacolata Andolfo
;
Gianluca De Rosa
;
Edoardo Errichiello
;
Francesco Manna
;
Barbara Eleni Rosato
, et al.
소스
Frontiers in Physiology
Frontiers in Physiology, Vol 10 (2019)
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27 .
The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variant
저자
by
Francesco Manna
;
Roberta Marra
;
Gianluca De Rosa
;
Achille Iolascon
;
Immacolata Andolfo
, et al.
소스
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27 . Academic Journal
Regulatory Noncoding and Predicted Pathogenic Coding Variants of CCR5 Predispose to Severe COVID-19.
저자
by
Cantalupo, Sueva
;
Lasorsa, Vito Alessandro
;
Russo, Roberta
;
Andolfo, Immacolata
;
D'Alterio, Giuseppe
, et al.
소스
International Journal of Molecular Sciences
. May2021, Vol. 22 Issue 10, p5372-5372. 1p.
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27 . Academic Journal
PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosis
저자
by
Andolfo, Immacolata
;
Manna, Francesco
;
De Rosa, Gianluca
;
Rosato, Barbara Eleni
;
Gambale, Antonella
, et al.
소스
HAEMATOLOGICA
; FEB 28 2018, 103 3, pE94-pE97, 4p.
Scopus
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