Lista de obras - Judith Favier - Dominio Público Uruguay

A MEN1 syndrome with a paraganglioma.

artículo científico publicado en 2013

A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma

artículo científico publicado en 2012

A novel TMEM127 mutation in a patient with familial bilateral pheochromocytoma

artículo científico publicado en 2010

Achievements of the COMETE program in the genetics of pheochromocytoma

artículo científico publicado en 2008

An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis

artículo científico publicado en 2009

Angiogenesis and vascular architecture in pheochromocytomas: distinctive traits in malignant tumors

artículo científico publicado en 2002

Angiopoietin-like 4 is a proangiogenic factor produced during ischemia and in conventional renal cell carcinoma

artículo científico publicado en 2003

Angiopoietins can directly activate endothelial cells and neutrophils to promote proinflammatory responses

artículo científico publicado en 2004

Carbonic anhydrase 9 immunohistochemistry as a tool to predict or validate germline and somatic VHL mutations in pheochromocytoma and paraganglioma-a retrospective and prospective study

artículo científico publicado en 2019

Cloning and expression pattern of EPAS1 in the chicken embryo. Colocalization with tyrosine hydroxylase

artículo científico publicado en 1999

Coexpression of endothelial PAS protein 1 with essential angiogenic factors suggests its involvement in human vascular development

article

Critical overexpression of thrombospondin 1 in chronic leg ischaemia

artículo científico publicado en 2005

DNA Methylation Profiling in Pheochromocytoma and Paraganglioma Reveals Diagnostic and Prognostic Markers

artículo científico publicado en 2015

Deciphering the molecular basis of invasiveness in Sdhb-deficient cells

artículo científico publicado en 2015

Dosage-dependent regulation of VAV2 expression by steroidogenic factor-1 drives adrenocortical carcinoma cell invasion.

artículo científico publicado en 2017

Epithelial to mesenchymal transition is activated in metastatic pheochromocytomas and paragangliomas caused by SDHB gene mutations

artículo científico publicado en 2012

Establishment of a mouse xenograft model of metastatic adrenocortical carcinoma

artículo científico publicado en 2017

From Nf1 to Sdhb knockout: Successes and failures in the quest for animal models of pheochromocytoma.

artículo científico

Functional and in silico assessment of MAX variants of unknown significance

artículo científico publicado en 2015

Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma

artículo científico publicado en 2002

Genetics of paragangliomas and pheochromocytomas

artículo científico publicado en 2012

Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas

artículo científico publicado en 2013

Germline mutations in the mitochondrial 2-oxoglutarate/malate carrier SLC25A11 gene confer a predisposition to metastatic paragangliomas.

artículo científico publicado en 2018

HIF2 alpha reduces growth rate but promotes angiogenesis in a mouse model of neuroblastoma

artículo científico publicado en 2007

HIF2AMutations in Paraganglioma with Polycythemia

artículo científico publicado en 2012

Hereditary paraganglioma/pheochromocytoma and inherited succinate dehydrogenase deficiency

artículo científico publicado en 2005

IN SITU HYBRIDIZATION AND IMMUNOGOLD LOCALIZATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR-2 ON THE PERICYTES OF THE CHICK CHORIOALLANTOIC MEMBRANE

scientific article published on 01 March 2002

In Vivo Detection of Succinate by Magnetic Resonance Spectroscopy as a Hallmark of SDHx Mutations in Paraganglioma

scientific article published on 21 October 2015

Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma

article

Loss of succinate dehydrogenase activity results in dependency on pyruvate carboxylation for cellular anabolism

artículo científico publicado en 2015

Mitochondrial Deficiencies in the Predisposition to Paraganglioma

artículo científico publicado en 2017

Mitochondrial succinate is instrumental for HIF1alpha nuclear translocation in SDHA-mutant fibroblasts under normoxic conditions

artículo científico publicado en 2005

Mosaicism in HIF2A-related polycythemia-paraganglioma syndrome.

artículo científico publicado en 2013

Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas

artículo científico publicado en 2015

Mutations in succinate dehydrogenase and DNA methylation

artículo científico publicado en 2013

Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.

artículo científico publicado en 2003

Oncometabolites-driven tumorigenesis: From genetics to targeted therapy

artículo científico publicado en 2014

Paraganglioma and phaeochromocytoma: from genetics to personalized medicine

artículo científico publicado en 2014

Peritoneal Implantation of Pheochromocytoma Following Tumor Capsule Rupture During Surgery

Persistent Properties of a Subpopulation of Cancer Cells Overexpressing the Hedgehog Receptor Patched

artículo científico publicado en 2022

Pheochromocytomas: the (pseudo)-hypoxia hypothesis.

artículo científico publicado en 2010

Rapid determination of tricarboxylic acid cycle enzyme activities in biological samples

artículo científico publicado en 2010

Rationale for anti-angiogenic therapy in pheochromocytoma and paraganglioma

artículo científico publicado en 2012

Recent advances in the genetics of phaeochromocytoma and functional paraganglioma

artículo científico publicado en 2008

Rethinking pheochromocytomas and paragangliomas from a genomic perspective.

artículo científico

Risk assessment of maternally inherited SDHD paraganglioma and phaeochromocytoma

artículo científico publicado en 2016

Rodent models of pheochromocytoma, parallels in rodent and human tumorigenesis

artículo científico publicado en 2018

Role of MSK1 in the signaling pathway leading to VEGF-mediated PAF synthesis in endothelial cells.

artículo científico publicado en 2006

Role of the renin-angiotensin system in primitive erythropoiesis in the chick embryo

artículo científico publicado en 2004

SDH mutations establish a hypermethylator phenotype in paraganglioma.

artículo científico publicado en 2013

SDHA Immunohistochemistry Detects GermlineSDHAGene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas

artículo científico publicado en 2011

SDHA is a tumor suppressor gene causing paraganglioma

artículo científico publicado en 2010

SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T).

artículo científico publicado en 2015

SDHBmutations are associated with response to temozolomide in patients with metastatic pheochromocytoma or paraganglioma

article

SDHD Immunohistochemistry: A New Tool to ValidateSDHxMutations in Pheochromocytoma/Paraganglioma

artículo científico publicado en 2014

Simultaneous positron emission tomography and ultrafast ultrasound for hybrid molecular, anatomical and functional imaging

artículo científico publicado en 2018

Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma

article

Succinate dehydrogenase deficiency in human

artículo científico publicado en 2005

The MITF, p.E318K Variant, as a Risk Factor for Pheochromocytoma and Paraganglioma

artículo científico publicado en 2016

The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway

artículo científico publicado en 2001

The Warburg effect is genetically determined in inherited pheochromocytomas

artículo científico publicado en 2009

The genetics of paragangliomas.

artículo científico publicado en 2012

The mTORC1 Complex Is Significantly Overactivated in SDHX-Mutated Paragangliomas

artículo científico publicado en 2017

Tricarboxylic acid cycle dysfunction as a cause of human diseases and tumor formation.

artículo científico publicado en 2006

Unsuspected task for an old team: succinate, fumarate and other Krebs cycle acids in metabolic remodeling

artículo científico

VEGF-mediated endothelial P-selectin translocation: role of VEGF receptors and endogenous PAF synthesis.

artículo científico publicado en 2004

Vascular endothelial growth factor-A is associated with chronic mountain sickness in the Andean population.

artículo científico publicado en 2014

Vascular pattern analysis for the prediction of clinical behaviour in pheochromocytomas and paragangliomas

artículo científico publicado en 2015

[Fundamentals of angiogenesis]

scientific article published on 01 January 2005

Lista de obras de Judith Favier

A MEN1 syndrome with a paraganglioma.

A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma

A novel TMEM127 mutation in a patient with familial bilateral pheochromocytoma

Achievements of the COMETE program in the genetics of pheochromocytoma

An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis

Angiogenesis and vascular architecture in pheochromocytomas: distinctive traits in malignant tumors

Angiopoietin-like 4 is a proangiogenic factor produced during ischemia and in conventional renal cell carcinoma

Angiopoietins can directly activate endothelial cells and neutrophils to promote proinflammatory responses

Carbonic anhydrase 9 immunohistochemistry as a tool to predict or validate germline and somatic VHL mutations in pheochromocytoma and paraganglioma-a retrospective and prospective study

Cloning and expression pattern of EPAS1 in the chicken embryo. Colocalization with tyrosine hydroxylase

Coexpression of endothelial PAS protein 1 with essential angiogenic factors suggests its involvement in human vascular development

Critical overexpression of thrombospondin 1 in chronic leg ischaemia

DNA Methylation Profiling in Pheochromocytoma and Paraganglioma Reveals Diagnostic and Prognostic Markers

Deciphering the molecular basis of invasiveness in Sdhb-deficient cells

Dosage-dependent regulation of VAV2 expression by steroidogenic factor-1 drives adrenocortical carcinoma cell invasion.

Epithelial to mesenchymal transition is activated in metastatic pheochromocytomas and paragangliomas caused by SDHB gene mutations

Establishment of a mouse xenograft model of metastatic adrenocortical carcinoma

From Nf1 to Sdhb knockout: Successes and failures in the quest for animal models of pheochromocytoma.

Functional and in silico assessment of MAX variants of unknown significance

Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma

Genetics of paragangliomas and pheochromocytomas

Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas

Germline mutations in the mitochondrial 2-oxoglutarate/malate carrier SLC25A11 gene confer a predisposition to metastatic paragangliomas.

HIF2 alpha reduces growth rate but promotes angiogenesis in a mouse model of neuroblastoma

HIF2AMutations in Paraganglioma with Polycythemia

Hereditary paraganglioma/pheochromocytoma and inherited succinate dehydrogenase deficiency

IN SITU HYBRIDIZATION AND IMMUNOGOLD LOCALIZATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR-2 ON THE PERICYTES OF THE CHICK CHORIOALLANTOIC MEMBRANE

In Vivo Detection of Succinate by Magnetic Resonance Spectroscopy as a Hallmark of SDHx Mutations in Paraganglioma

Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma

Loss of succinate dehydrogenase activity results in dependency on pyruvate carboxylation for cellular anabolism

Mitochondrial Deficiencies in the Predisposition to Paraganglioma

Mitochondrial succinate is instrumental for HIF1alpha nuclear translocation in SDHA-mutant fibroblasts under normoxic conditions

Mosaicism in HIF2A-related polycythemia-paraganglioma syndrome.

Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas

Mutations in succinate dehydrogenase and DNA methylation

Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.

Oncometabolites-driven tumorigenesis: From genetics to targeted therapy

Paraganglioma and phaeochromocytoma: from genetics to personalized medicine

Peritoneal Implantation of Pheochromocytoma Following Tumor Capsule Rupture During Surgery

Persistent Properties of a Subpopulation of Cancer Cells Overexpressing the Hedgehog Receptor Patched

Pheochromocytomas: the (pseudo)-hypoxia hypothesis.

Rapid determination of tricarboxylic acid cycle enzyme activities in biological samples

Rationale for anti-angiogenic therapy in pheochromocytoma and paraganglioma

Recent advances in the genetics of phaeochromocytoma and functional paraganglioma

Rethinking pheochromocytomas and paragangliomas from a genomic perspective.

Risk assessment of maternally inherited SDHD paraganglioma and phaeochromocytoma

Rodent models of pheochromocytoma, parallels in rodent and human tumorigenesis

Role of MSK1 in the signaling pathway leading to VEGF-mediated PAF synthesis in endothelial cells.

Role of the renin-angiotensin system in primitive erythropoiesis in the chick embryo

SDH mutations establish a hypermethylator phenotype in paraganglioma.

SDHA Immunohistochemistry Detects GermlineSDHAGene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas

SDHA is a tumor suppressor gene causing paraganglioma

SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T).

SDHBmutations are associated with response to temozolomide in patients with metastatic pheochromocytoma or paraganglioma

SDHD Immunohistochemistry: A New Tool to ValidateSDHxMutations in Pheochromocytoma/Paraganglioma

Simultaneous positron emission tomography and ultrafast ultrasound for hybrid molecular, anatomical and functional imaging

Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma

Succinate dehydrogenase deficiency in human

The MITF, p.E318K Variant, as a Risk Factor for Pheochromocytoma and Paraganglioma

The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway

The Warburg effect is genetically determined in inherited pheochromocytomas

The genetics of paragangliomas.

The mTORC1 Complex Is Significantly Overactivated in SDHX-Mutated Paragangliomas

Tricarboxylic acid cycle dysfunction as a cause of human diseases and tumor formation.

Unsuspected task for an old team: succinate, fumarate and other Krebs cycle acids in metabolic remodeling

VEGF-mediated endothelial P-selectin translocation: role of VEGF receptors and endogenous PAF synthesis.

Vascular endothelial growth factor-A is associated with chronic mountain sickness in the Andean population.

Vascular pattern analysis for the prediction of clinical behaviour in pheochromocytomas and paragangliomas

[Fundamentals of angiogenesis]