Zobrazeno 1 - 10 of 12 pro vyhledávání: '"Leticia Villalba-Benito"'
1
Akademický článek
RMRP, RMST, FTX and IPW: novel potential long non-coding RNAs in medullary thyroid cancer
Autor: Berta Luzón-Toro, Leticia Villalba-Benito, Raquel María Fernández, Ana Torroglosa, Guillermo Antiñolo, Salud Borrego
Publikováno v: Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-7 (2021)
Abstract The relevant role of long non-coding RNAs (lncRNAs) in cancer is currently a matter of increasing interest. Medullary thyroid cancer (MTC) is a rare neuroendocrine tumor (2–5% of all thyroid cancer) derived from the parafollicular C-cells
Externí odkaz: https://doaj.org/article/1ac9788288b64ae5b60c58be3fede86e
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2
Akademický článek
Overexpression of DNMT3b target genes during Enteric Nervous System development contribute to the onset of Hirschsprung disease
Autor: Leticia Villalba-Benito, Ana Torroglosa, Raquel María Fernández, Macarena Ruíz-Ferrer, María José Moya-Jiménez, Guillermo Antiñolo, Salud Borrego
Publikováno v: Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
Abstract Hirschsprung disease (HSCR) is attributed to a failure of neural crest cells (NCCs) to migrate, proliferate, differentiate and/or survive in the bowel wall during embryonic Enteric Nervous System (ENS) development. ENS formation is the resul
Externí odkaz: https://doaj.org/article/793aabe852e5456db9fa289db4eacdb4
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4
What is new about the genetic background of Hirschsprung disease?
Autor: Salud Borrego, Berta Luzón-Toro, Leticia Villalba-Benito, Raquel M. Fernández, Guillermo Antiñolo, Ana Torroglosa
Publikováno v: Clinical Genetics. 97:114-124
Hirschsprung disease (HSCR) is a rare congenital disorder caused by an incorrect enteric nervous system development due to a failure in migration, proliferation, differentiation and/or survival of enteric neural crest cells. HSCR is a complex genetic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37fb43135b9ae43931f95db9013d2936
https://doi.org/10.1111/cge.13615
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5
Genome-wide analysis of DNA methylation in Hirschsprung enteric precursor cells: unraveling the epigenetic landscape of enteric nervous system development
Autor: Joaquín Dopazo, Leticia Villalba-Benito, Berta Luzón-Toro, Raquel M. Fernández, Salud Borrego, Daniel Lopez-Lopez, María José Moya-Jiménez, Carlos S. Casimiro-Soriguer, Guillermo Antiñolo, Ana Torroglosa
Publikováno v: Clinical Epigenetics
Digital.CSIC. Repositorio Institucional del CSIC
instname
[Background] Hirschsprung disease (HSCR, OMIM 142623) is a rare congenital disorder that results from a failure to fully colonize the gut by enteric precursor cells (EPCs) derived from the neural crest. Such incomplete gut colonization is due to alte
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5943a3b8d560ced4eae11d8d636e9cfd
http://hdl.handle.net/10261/265803
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6
RMRP, RMST, FTX and IPW: novel potential long non-coding RNAs in medullary thyroid cancer
Autor: Salud Borrego, Guillermo Antiñolo, Raquel M. Fernández, Leticia Villalba-Benito, Berta Luzón-Toro, Ana Torroglosa
Publikováno v: Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-7 (2021)
The relevant role of long non-coding RNAs (lncRNAs) in cancer is currently a matter of increasing interest. Medullary thyroid cancer (MTC) is a rare neuroendocrine tumor (2–5% of all thyroid cancer) derived from the parafollicular C-cells which sec
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3acdcf68368796ce06c6cf1751cf01b8
https://hdl.handle.net/10668/16931
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7
Identification of New Potential LncRNA Biomarkers in Hirschsprung Disease
Autor: Leticia Villalba-Benito, María José Moya-Jiménez, Raquel M. Fernández, Ana Torroglosa, Salud Borrego, Guillermo Antiñolo, Berta Luzón-Toro
Publikováno v: International Journal of Molecular Sciences
Digital.CSIC. Repositorio Institucional del CSIC
instname
International Journal of Molecular Sciences, Vol 21, Iss 5534, p 5534 (2020)
This article belongs to the Special Issue Biomarkers in Rare Diseases.
Hirschsprung disease (HSCR) is a neurocristopathy defined by intestinal aganglionosis due to alterations during the development of the Enteric Nervous System (ENS). A wide sp
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dfa35eb15dfa685225096edc191809c
https://pubmed.ncbi.nlm.nih.gov/32748823
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8
Influencers on Thyroid Cancer Onset: Molecular Genetic Basis
Autor: Guillermo Antiñolo, Berta Luzón-Toro, Raquel M. Fernández, Salud Borrego, Ana Torroglosa, Leticia Villalba-Benito
Publikováno v: Digital.CSIC. Repositorio Institucional del CSIC
instname
idUS: Depósito de Investigación de la Universidad de Sevilla
Universidad de Sevilla (US)
idUS. Depósito de Investigación de la Universidad de Sevilla
Genes, Vol 10, Iss 11, p 913 (2019)
Genes
© 2019 by the authors.
Thyroid cancer, a cancerous tumor or growth located within the thyroid gland, is the most common endocrine cancer. It is one of the few cancers whereby incidence rates have increased in recent years. It occurs in all age
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95a64c4755b02c2758548be883dd8b33
https://www.mdpi.com/2073-4425/10/11/913/pdf?version=1574326824
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9
Dnmt3b knock-down in enteric precursors reveals a possible mechanism by which this de novo methyltransferase is involved in the enteric nervous system development and the onset of Hirschsprung disease
Autor: Raquel M. Fernández, Guillermo Antiñolo, Salud Borrego, María José Moya-Jiménez, Leticia Villalba-Benito, Ana Torroglosa
Publikováno v: Digital.CSIC. Repositorio Institucional del CSIC
instname
Oncotarget
idUS. Depósito de Investigación de la Universidad de Sevilla
idUS: Depósito de Investigación de la Universidad de Sevilla
Universidad de Sevilla (US)
Hirschsprung disease (HSCR, OMIM 142623) is a pathology that shows a lack of enteric ganglia along of the distal gastrointestinal tract. This aganglionosis is attributed to an abnormal proliferation, migration, differentiation and/or survival of ente
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af640172eedbd82207b2869cb0040e75
http://hdl.handle.net/10261/197763
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10
Overexpression of DNMT3b target genes during Enteric Nervous System development contribute to the onset of Hirschsprung disease
Autor: María José Moya-Jiménez, Raquel M. Fernández, Leticia Villalba-Benito, Ana Torroglosa, Salud Borrego, Macarena Ruiz-Ferrer, Guillermo Antiñolo
Publikováno v: Digital.CSIC. Repositorio Institucional del CSIC
instname
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
Scientific Reports
Hirschsprung disease (HSCR) is attributed to a failure of neural crest cells (NCCs) to migrate, proliferate, differentiate and/or survive in the bowel wall during embryonic Enteric Nervous System (ENS) development. ENS formation is the result from a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b62ab2e3d035e40f598760defac4e98f
https://hdl.handle.net/10668/11433
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