Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Rosanna Beraldi"'
Autor:
Ryan D Geraets, Logan M Langin, Jacob T Cain, Camille M Parker, Rosanna Beraldi, Attila D Kovacs, Jill M Weimer, David A Pearce
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176526 (2017)
The Neuronal Ceroid Lipofuscinoses (NCLs), also known as Batten disease, result from mutations in over a dozen genes. Although, adults are susceptible, the NCLs are frequently classified as pediatric neurodegenerative diseases due to their greater pe
Externí odkaz:
https://doaj.org/article/f34a5113df834253a0b39fab17e9eda5
Autor:
Jessica Edwards, Timothy J. Nelson, Andre Terzic, Xing Li, Saji Oommen, Santiago Reyes, Saranya P. Wyles, Sybil C. L. Hrstka, Timothy M. Olson, Rosanna Beraldi
Publikováno v:
Human Molecular Genetics. 25:254-265
Dilated cardiomyopathy (DCM) is a leading cause of heart failure. In families with autosomal-dominant DCM, heterozygous missense mutations were identified in RNA-binding motif protein 20 (RBM20), a spliceosome protein induced during early cardiogenes
Autor:
David A. Pearce, Alexei Y. Savinov, Rosanna Beraldi, Attila D. Kovács, Ryan D. Geraets, Jill M. Weimer, Jordan A Dykstra, David K. Meyerholz
Ataxia telangiectasia (AT) is a progressive multisystem autosomal recessive disorder caused by mutations in the AT-mutated (ATM) gene. Early onset AT in children is characterized by cerebellar degeneration, leading to motor impairment. Lung disease a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7774fece0c72a0e2fb0d280648b77546
https://europepmc.org/articles/PMC5687068/
https://europepmc.org/articles/PMC5687068/
Autor:
Jacob T. Cain, Attila D. Kovács, Rosanna Beraldi, Jill M. Weimer, Logan Langin, David A. Pearce, Camille Parker, Ryan D. Geraets
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176526 (2017)
PLoS ONE
PLoS ONE
The Neuronal Ceroid Lipofuscinoses (NCLs), also known as Batten disease, result from mutations in over a dozen genes. Although, adults are susceptible, the NCLs are frequently classified as pediatric neurodegenerative diseases due to their greater pe
Publikováno v:
ISRN Stem Cells. 2014:1-10
Regenerative medicine offers a curative approach to treating heart disease through multiple emerging therapeutic concepts. Decellularized organ scaffolds are being optimized to guide and spatially organize stem cell differentiation in efforts to rebu
Autor:
Andre Terzic, Timothy J. Nelson, Timothy M. Olson, Frank J. Secreto, Rosanna Beraldi, Almudena Martinez Fernandez, Xing Li, Santiago Reyes
Publikováno v:
Human Molecular Genetics. 23:3779-3791
Dilated cardiomyopathy (DCM) due to mutations in RBM20, a gene encoding an RNA-binding protein, is associated with high familial penetrance, risk of progressive heart failure and sudden death. Although genetic investigations and physiological models
Autor:
Katherine A. White, David A. Pearce, Xiao-Jun Wang, Constantin Trantzas, Jason T. Struzynski, Christopher S. Rogers, Bryan T. Davis, Allyn M. Lambertz, Richard Van Rheeden, Brian A. Dacken, David K. Meyerholz, Krystal L. Weber, Benjamin W. Darbro, Frank Rohret, Judy A. Rohret, Chun-Hung Chan, Attila D. Kovács, Michael C. Kruer, Rosanna Beraldi, Jill M. Weimer
Publikováno v:
Human molecular genetics. 24(22)
Ataxia telangiectasia (AT) is a progressive multisystem disorder caused by mutations in the AT-mutated (ATM) gene. AT is a neurodegenerative disease primarily characterized by cerebellar degeneration in children leading to motor impairment. The disea
Publikováno v:
Molecular Reproduction and Development. 73:279-287
In higher eukaryotes, reverse transcriptase (RT) activities are encoded by a variety of endogenous retroviruses and retrotransposable elements. We previously found that mouse preimplantation embryos are endowed with an endogenous RT activity. Inhibit
Autor:
Michela Quirino, Rosanna Beraldi, Alessandra Cassano, Paola Sinibaldi-Vallebona, Enrico Garaci, Corrado Spadafora, Annalucia Serafino, Elisabetta Mattei, Ilaria Sciamanna, C. Pittoggi, Cristina Mearelli, Carlo Barone, Matteo Landriscina
Publikováno v:
Oncogene (Basingstoke) 24 (2005): 3923–3931. doi:10.1038/sj.onc.1208562
info:cnr-pdr/source/autori:Sciamanna I.1, Landriscina M.2, Pittoggi C.3, Quirino M.4, Mearelli C.5, Beraldi R.6, Mattei E.7, Serafino A.8, Cassano A.9, Sinibaldi-Vallebona P.10, Garaci E.11, Barone C.12, Spadafora C.13/titolo:Inhibition of endogenous reverse transcriptase antagonizes human tumor growth./doi:10.1038%2Fsj.onc.1208562/rivista:Oncogene (Basingstoke)/anno:2005/pagina_da:3923/pagina_a:3931/intervallo_pagine:3923–3931/volume:24
info:cnr-pdr/source/autori:Sciamanna I.1, Landriscina M.2, Pittoggi C.3, Quirino M.4, Mearelli C.5, Beraldi R.6, Mattei E.7, Serafino A.8, Cassano A.9, Sinibaldi-Vallebona P.10, Garaci E.11, Barone C.12, Spadafora C.13/titolo:Inhibition of endogenous reverse transcriptase antagonizes human tumor growth./doi:10.1038%2Fsj.onc.1208562/rivista:Oncogene (Basingstoke)/anno:2005/pagina_da:3923/pagina_a:3931/intervallo_pagine:3923–3931/volume:24
Undifferentiated cells and embryos express high levels of endogenous non-telomerase reverse transcriptase (RT) of retroposon/retroviral origin. We previously found that RT inhibitors modulate cell growth and differentiation in several cell lines. We
Autor:
Almudena Martinez-Fernandez, Andras Nagy, Andre Terzic, Santiago Reyes, Timothy J. Nelson, Carmen Perez-Terzic, Frank J. Secreto, Alexey E. Alekseev, Rosanna Beraldi, Hoon Ki Sung
Publikováno v:
Circulation. Cardiovascular genetics. 7(5)
Background— Nuclear reprogramming inculcates pluripotent capacity by which de novo tissue differentiation is enabled. Yet, introduction of ectopic reprogramming factors may desynchronize natural developmental schedules. This study aims to evaluate