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1 . Academic Journal
Thyroid hormones regulate cardiac repolarization and QT-interval related gene expression in hiPSC cardiomyocytes
저자
by
Alessandra Ulivieri
;
Luca Lavra
;
Fiorenza Magi
;
Alessandra Morgante
;
Leonardo Calò
, et al.
소스
Scientific Reports, Vol 12, Iss 1, Pp 1-13 (2022)
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7 . Academic Journal
Nonthyroidal illness syndrome (NTIS) in severe COVID-19 patients: role of T3 on the Na/K pump gene expression and on hydroelectrolytic equilibrium
저자
by
Salvatore Sciacchitano
;
Carlo Capalbo
;
Christian Napoli
;
Andrea Negro
;
Luciano De Biase
, et al.
소스
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-18 (2021)
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7 . Academic Journal
Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family
저자
by
Omid Daneshjoo
;
Pirooz Ebrahimi
;
Leila B. Salehi
;
Antonio Pizzuti
;
Masoud Garshasbi
.
소스
Clinical Case Reports, Vol 8, Iss 12, Pp 2333-2340 (2020)
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7 . Academic Journal
An enormous Italian pedigree of Marfan syndrome with a novel mutation in the FBN1 gene
저자
by
Omid Daneshjoo
;
Leila B. Salehi
;
Antonio Pizzuti
;
Giuseppe Novelli
;
Federica Sangiuolo
.
소스
Clinical Case Reports, Vol 8, Iss 8, Pp 1445-1451 (2020)
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7 . Academic Journal
Generation and characterization of the human induced pluripotent stem cell (hiPSC) line NCUFi001-A from a patient carrying KCNQ1 G314S mutation
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by
Luca Lavra
;
Fiorenza Magi
;
Alessandra Ulivieri
;
Alessandra Morgante
;
Marianna Paulis
, et al.
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Stem Cell Research, Vol 54, Iss , Pp 102418- (2021)
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7 . Academic Journal
Galectin-3: One Molecule for an Alphabet of Diseases, from A to Z
저자
by
Salvatore Sciacchitano
;
Luca Lavra
;
Alessandra Morgante
;
Alessandra Ulivieri
;
Fiorenza Magi
, et al.
소스
International Journal of Molecular Sciences, Vol 19, Iss 2, p 379 (2018)
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7 .
Copy number variation analysis implicates novel pathways in patients with oculo‐auriculo‐vertebral‐spectrum and congenital heart defects
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by
Maria Teresa Fadda
;
Sebastiano Bianca
;
Dario Cocciadiferro
;
Bruno Dallapiccola
;
Marina Goldoni
, et al.
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Clinical Genetics
. 100:268-279
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7 .
An enormous Italian pedigree of Marfan syndrome with a novel mutation in the FBN1 gene
저자
by
Federica Sangiuolo
;
Giuseppe Novelli
;
Antonio Pizzuti
;
Leila B. Salehi
;
Omid Daneshjoo
.
소스
Clinical Case Reports
Clinical Case Reports, Vol 8, Iss 8, Pp 1445-1451 (2020)
Open Access (Wiley)
Open Access (OpenAIRE)
Web of Science
Scopus
JCR 저널정보
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7 .
Generation and characterization of the human induced pluripotent stem cell (hiPSC) line NCUFi001-A from a patient carrying KCNQ1 G314S mutation
저자
by
Matteo Pedrazzini
;
Alessandra Morgante
;
Marianna Paulis
;
Salvatore Sciacchitano
;
Fiorenza Magi
, et al.
소스
Stem Cell Research, Vol 54, Iss, Pp 102418-(2021)
Open Access (OpenAIRE)
요약보기
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7 .
Nonthyroidal illness syndrome (NTIS) in severe COVID-19 patients: role of T3 on the Na/K pump gene expression and on hydroelectrolytic equilibrium
저자
by
Luca Lavra
;
Fiorenza Magi
;
Leila B. Salehi
;
Alessandra Ulivieri
;
Lea Petrella
, et al.
소스
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-18 (2021)
Journal of Translational Medicine
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