Lista de obras - Beth Coyle - Dominio Público Uruguay

3D hydrogels reveal medulloblastoma subgroup differences and identify extracellular matrix subtypes that predict patient outcome

artículo científico publicado en 2020

A HIF-independent, CD133-mediated mechanism of cisplatin resistance in glioblastoma cells.

artículo científico publicado en 2018

A role for ABCB1 in prognosis, invasion and drug resistance in ependymoma

scientific article published on 16 July 2019

ABCB1 in children's brain tumours.

artículo científico publicado en 2015

An investigation of WNT pathway activation and association with survival in central nervous system primitive neuroectodermal tumours (CNS PNET).

artículo científico publicado en 2009

BM-23Twist1 EXPRESSION CONFIRMS THE ROLE OF AN EMT-LIKE PROCESS IN MEDULLOBLASTOMA METASTASIS

CD105 (Endoglin) exerts prognostic effects via its role in the microvascular niche of paediatric high grade glioma.

artículo científico publicado en 2012

Copy number gain of 1q25 predicts poor progression-free survival for pediatric intracranial ependymomas and enables patient risk stratification: a prospective European clinical trial cohort analysis on behalf of the Children's Cancer Leukaemia Group

artículo científico publicado en 2012

Data on the number and frequency of scientific literature citations for established medulloblastoma cell lines

artículo científico publicado en 2016

Genome-wide molecular characterization of central nervous system primitive neuroectodermal tumor and pineoblastoma

artículo científico publicado en 2011

Homozygous loss of ADAM3A revealed by genome-wide analysis of pediatric high-grade glioma and diffuse intrinsic pontine gliomas

artículo científico publicado en 2010

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images.

artículo científico publicado en 2017

In vitro models of medulloblastoma: Choosing the right tool for the job

artículo científico publicado en 2016

Integrated molecular genetic profiling of pediatric high-grade gliomas reveals key differences with the adult disease

artículo científico publicado en 2010

Investigation of chromosome 1q reveals differential expression of members of the S100 family in clinical subgroups of intracranial paediatric ependymoma

artículo científico publicado en 2008

Long-term exposure to irinotecan reduces cell migration in glioma cells.

artículo científico publicado en 2016

Medulloblastoma and ependymoma cells display increased levels of 5-carboxylcytosine and elevated TET1 expression.

artículo científico publicado en 2017

Minimal information for studies of extracellular vesicles 2018 (MISEV2018): a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines

scientific article published on 23 November 2018

Molecular Analysis of the Pds Gene in Pendred Syndrome (Sensorineural Hearing Loss and Goitre)

article

Multifactorial analysis of predictors of outcome in pediatric intracranial ependymoma

artículo científico publicado en 2008

Overcoming multiple drug resistance mechanisms in medulloblastoma.

artículo científico publicado en 2014

PI3K pathway activation provides a novel therapeutic target for pediatric ependymoma and is an independent marker of progression-free survival

artículo científico publicado en 2013

Pediatric ependymoma: biological perspectives.

artículo científico publicado en 2009

Pediatric high-grade glioma: identification of poly(ADP-ribose) polymerase as a potential therapeutic target.

artículo científico publicado en 2011

Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4

artículo científico publicado en 1996

Pendred syndrome: evidence for genetic homogeneity and further refinement of linkage

artículo científico publicado en 1997

RASSF1A and the BH3-only mimetic ABT-737 promote apoptosis in pediatric medulloblastoma cell lines.

artículo científico publicado en 2011

Regulation of apoptosis by peroxisome proliferators.

artículo científico publicado en 2004

Supratentorial and spinal pediatric ependymomas display a hypermethylated phenotype which includes the loss of tumor suppressor genes involved in the control of cell growth and death

artículo científico publicado en 2011

The role of the WNT/β-catenin pathway in central nervous system primitive neuroectodermal tumours (CNS PNETs).

artículo científico publicado en 2013

Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome

artículo científico publicado en 1996

WNT/β-catenin pathway activation in Myc immortalised cerebellar progenitor cells inhibits neuronal differentiation and generates tumours resembling medulloblastoma.

artículo científico publicado en 2012

Wilms' Tumor Protein 1 and Enzymatic Oxidation of 5-Methylcytosine in Brain Tumors: Potential Perspectives.

artículo científico publicado en 2018

Y-box Binding Protein-1: A Neglected Target in Pediatric Brain Tumors?

artículo científico publicado en 2020

Lista de obras de Beth Coyle

3D hydrogels reveal medulloblastoma subgroup differences and identify extracellular matrix subtypes that predict patient outcome

A HIF-independent, CD133-mediated mechanism of cisplatin resistance in glioblastoma cells.

A role for ABCB1 in prognosis, invasion and drug resistance in ependymoma

ABCB1 in children's brain tumours.

An investigation of WNT pathway activation and association with survival in central nervous system primitive neuroectodermal tumours (CNS PNET).

BM-23Twist1 EXPRESSION CONFIRMS THE ROLE OF AN EMT-LIKE PROCESS IN MEDULLOBLASTOMA METASTASIS

CD105 (Endoglin) exerts prognostic effects via its role in the microvascular niche of paediatric high grade glioma.

Copy number gain of 1q25 predicts poor progression-free survival for pediatric intracranial ependymomas and enables patient risk stratification: a prospective European clinical trial cohort analysis on behalf of the Children's Cancer Leukaemia Group

Data on the number and frequency of scientific literature citations for established medulloblastoma cell lines

Genome-wide molecular characterization of central nervous system primitive neuroectodermal tumor and pineoblastoma

Homozygous loss of ADAM3A revealed by genome-wide analysis of pediatric high-grade glioma and diffuse intrinsic pontine gliomas

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images.

In vitro models of medulloblastoma: Choosing the right tool for the job

Integrated molecular genetic profiling of pediatric high-grade gliomas reveals key differences with the adult disease

Investigation of chromosome 1q reveals differential expression of members of the S100 family in clinical subgroups of intracranial paediatric ependymoma

Long-term exposure to irinotecan reduces cell migration in glioma cells.

Medulloblastoma and ependymoma cells display increased levels of 5-carboxylcytosine and elevated TET1 expression.

Minimal information for studies of extracellular vesicles 2018 (MISEV2018): a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines

Molecular Analysis of the Pds Gene in Pendred Syndrome (Sensorineural Hearing Loss and Goitre)

Multifactorial analysis of predictors of outcome in pediatric intracranial ependymoma

Overcoming multiple drug resistance mechanisms in medulloblastoma.

PI3K pathway activation provides a novel therapeutic target for pediatric ependymoma and is an independent marker of progression-free survival

Pediatric ependymoma: biological perspectives.

Pediatric high-grade glioma: identification of poly(ADP-ribose) polymerase as a potential therapeutic target.

Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4

Pendred syndrome: evidence for genetic homogeneity and further refinement of linkage

RASSF1A and the BH3-only mimetic ABT-737 promote apoptosis in pediatric medulloblastoma cell lines.

Regulation of apoptosis by peroxisome proliferators.

Supratentorial and spinal pediatric ependymomas display a hypermethylated phenotype which includes the loss of tumor suppressor genes involved in the control of cell growth and death

The role of the WNT/β-catenin pathway in central nervous system primitive neuroectodermal tumours (CNS PNETs).

Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome

WNT/β-catenin pathway activation in Myc immortalised cerebellar progenitor cells inhibits neuronal differentiation and generates tumours resembling medulloblastoma.

Wilms' Tumor Protein 1 and Enzymatic Oxidation of 5-Methylcytosine in Brain Tumors: Potential Perspectives.

Y-box Binding Protein-1: A Neglected Target in Pediatric Brain Tumors?