2 búsqueda de la palabra clave 'DICER1'

DICER1 gene mutations in endocrine tumors / Luis Vicente Syro Moreno  

Público ISBD Título : DICER1 gene mutations in endocrine tumors Tipo de documento : documento electrónico Autores : Luis Vicente Syro Moreno, Fecha de publicación : 2018 Títulos uniformes : Endocrine Related Cancer Idioma : Inglés (eng) Palabras clave : DICER1  endocrine tumors  mutation  neoplasms  pathology Resumen : In this review, the importance of the DICER1 gene in the function of endocrine cells is discussed. There is conclusive evidence that DICER1 mutations play a crucial role in the development, progression, cell proliferation, therapeutic responsiveness and behavior of several endocrine tumors. We review the literature of DICER1 gene mutations in thyroid, parathyroid, pituitary, pineal gland, endocrine pancreas, paragangliomas, medullary, adrenocortical, ovarian and testicular tumors. Although significant progress has been made during the last few years, much more work is needed to fully understand the significance of DICER1 mutations. Mención de responsabilidad : Michael Solarski, Fabio Rotondo, William D Foulkes, John R Priest, Luis V Syro, Henriett Butz, Michael D Cusimano, Kalman Kovacs Referencia : Endocr Relat Cancer. 2018 Mar;25(3):R197-R208. DOI (Digital Object Identifier) : 10.1530/ERC-17-0509 PMID : 29330195 En línea : https://erc.bioscientifica.com/view/journals/erc/25/3/ERC-17-0509.xml Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=4195 DICER1 gene mutations in endocrine tumors [documento electrónico] / Luis Vicente Syro Moreno,  . - 2018. Obra : Endocrine Related Cancer Idioma : Inglés (eng) Palabras clave : DICER1  endocrine tumors  mutation  neoplasms  pathology Resumen : In this review, the importance of the DICER1 gene in the function of endocrine cells is discussed. There is conclusive evidence that DICER1 mutations play a crucial role in the development, progression, cell proliferation, therapeutic responsiveness and behavior of several endocrine tumors. We review the literature of DICER1 gene mutations in thyroid, parathyroid, pituitary, pineal gland, endocrine pancreas, paragangliomas, medullary, adrenocortical, ovarian and testicular tumors. Although significant progress has been made during the last few years, much more work is needed to fully understand the significance of DICER1 mutations. Mención de responsabilidad : Michael Solarski, Fabio Rotondo, William D Foulkes, John R Priest, Luis V Syro, Henriett Butz, Michael D Cusimano, Kalman Kovacs Referencia : Endocr Relat Cancer. 2018 Mar;25(3):R197-R208. DOI (Digital Object Identifier) : 10.1530/ERC-17-0509 PMID : 29330195 En línea : https://erc.bioscientifica.com/view/journals/erc/25/3/ERC-17-0509.xml Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=4195

Reserva

Reservar este documento

Ejemplares(1)

Código de barras	Número de Ubicación	Tipo de medio	Ubicación	Sección	Estado
DD000809	AC-2018-096	Archivo digital	Producción Científica	Artículos científicos	Disponible

Clinicopathologic features of familial pituitary adenomas / Luis Vicente Syro Moreno  

Público ISBD Título : Clinicopathologic features of familial pituitary adenomas Tipo de documento : documento electrónico Autores : Luis Vicente Syro Moreno, Fecha de publicación : 2016 Títulos uniformes : Diagnostic Histopathology Idioma : Inglés (eng) Palabras clave : AIP  Carney complex  classification  diagnosis  DICER1  familial isolated  familial syndromes  genetics  McCune–Albright syndrome  multiple endocrine neoplasia type 1  pathology  pituitary adenoma  pituitary blastoma  X-linked acrogigantism syndrome Resumen : Pituitary adenomas are common neoplasms. Initially considered as sporadic tumours, some of them are associated with familial syndromes such as familial isolated pituitary adenoma, multiple endocrine neoplasia type 1 and type 4, X-linked acrogigantism syndrome, Carney complex, pheochromocytoma/paraganglioma–pituitary adenoma, pituitary blastoma and McCune–Albright syndrome. They represent a group of diseases with different genetic background and variable phenotype. Here, we summarize the clinicopathological features of pituitary adenomas associated with these familial syndromes. Mención de responsabilidad : Luis V. Syro, Fabio Rotondo, Kalman Kovacs, Márta Korbonits Referencia : Diag Histop. 2016;22(3):85-91. DOI (Digital Object Identifier) : 10.1016/j.mpdhp.2016.02.004 En línea : http://www.diagnostichistopathology.co.uk/article/S1756-2317(16)00022-0/fulltext Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3958 Clinicopathologic features of familial pituitary adenomas [documento electrónico] / Luis Vicente Syro Moreno,  . - 2016. Obra : Diagnostic Histopathology Idioma : Inglés (eng) Palabras clave : AIP  Carney complex  classification  diagnosis  DICER1  familial isolated  familial syndromes  genetics  McCune–Albright syndrome  multiple endocrine neoplasia type 1  pathology  pituitary adenoma  pituitary blastoma  X-linked acrogigantism syndrome Resumen : Pituitary adenomas are common neoplasms. Initially considered as sporadic tumours, some of them are associated with familial syndromes such as familial isolated pituitary adenoma, multiple endocrine neoplasia type 1 and type 4, X-linked acrogigantism syndrome, Carney complex, pheochromocytoma/paraganglioma–pituitary adenoma, pituitary blastoma and McCune–Albright syndrome. They represent a group of diseases with different genetic background and variable phenotype. Here, we summarize the clinicopathological features of pituitary adenomas associated with these familial syndromes. Mención de responsabilidad : Luis V. Syro, Fabio Rotondo, Kalman Kovacs, Márta Korbonits Referencia : Diag Histop. 2016;22(3):85-91. DOI (Digital Object Identifier) : 10.1016/j.mpdhp.2016.02.004 En línea : http://www.diagnostichistopathology.co.uk/article/S1756-2317(16)00022-0/fulltext Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3958

Reserva

Reservar este documento

Ejemplares(1)

Código de barras	Número de Ubicación	Tipo de medio	Ubicación	Sección	Estado
DD000544	AC-2016-019	Archivo digital	Producción Científica	Artículos científicos	Disponible