Lista de obras - Piotr Rieske - Dominio Público Uruguay

16q heterozygosity loss in Wilms' tumour in children and its clinical importance

artículo científico publicado en 2000

A comparative study of P53/MDM2 genes alterations and P53/MDM2 proteins immunoreactivity in soft-tissue sarcomas

scientific article published on 01 September 1999

A comparative study of epidermal growth factor receptor (EGFR) and MDM2 gene amplification and protein immunoreactivity in human glioblastomas.

artículo científico publicado en 1998

A population of human brain cells expressing phenotypic markers of more than one lineage can be induced in vitro to differentiate into mesenchymal cells.

artículo científico publicado en 2008

A population of human brain parenchymal cells express markers of glial, neuronal and early neural cells and differentiate into cells of neuronal and glial lineages.

artículo científico publicado en 2007

A way to understand idiopathic senescence and apoptosis in primary glioblastoma cells - possible approaches to circumvent these phenomena

scientific article published on 14 September 2019

Abnormalities of the P53, MDM2, BCL2 and BAX genes in acute leukemias.

artículo científico publicado en 2005

Arrested neural and advanced mesenchymal differentiation of glioblastoma cells-comparative study with neural progenitors

artículo científico publicado en 2009

Assessment of OPG/RANK/RANKL gene expression levels in peripheral blood mononuclear cells (PBMC) after treatment with strontium ranelate and ibandronate in patients with postmenopausal osteoporosis

scientific article published on 29 March 2013

Atypical molecular background of glioblastoma and meningioma developed in a patient with Li-Fraumeni syndrome

artículo científico publicado en 2005

BCR expression is decreased in meningiomas showing loss of heterozygosity of 22q within a new minimal deletion region.

artículo científico publicado en 2008

CYP46: a risk factor for Alzheimer's disease or a coincidence?

artículo científico publicado en 2005

Cell line with endogenous EGFRvIII expression is a suitable model for research and drug development purposes.

artículo científico publicado en 2016

Chitin dipentanoate as the new technologically usable biomaterial.

artículo científico publicado en 2015

Cyclic trans-phosphorylation in a homodimer as the predominant mechanism of EGFRvIII action and regulation

artículo científico publicado en 2018

Detection of P53 mutations in different cancer types is improved by cDNA sequencing.

artículo científico publicado en 2010

Detection of lymph node metastases of papillary thyroid cancer-comparison of the results of histopathology, immunohistochemistry and reverse transcription-polymerase chain reaction-a preliminary report

artículo científico publicado en 2005

Different mutational characteristics of TSG in cell lines and surgical specimens

artículo científico publicado en 2014

Directed differentiation of human iPSC into insulin producing cells is improved by induced expression of PDX1 and NKX6.1 factors in IPC progenitors

artículo científico publicado en 2016

Diverse molecular pattern in a bihemispheric glioblastoma (butterfly glioma) in a 16-year-old boy

scientific article published on 01 September 2007

EGFR Activation Leads to Cell Death Independent of PI3K/AKT/mTOR in an AD293 Cell Line

artículo científico publicado en 2016

EGFRvIII--a stable target for anti-EGFRvIII therapy.

artículo científico publicado en 2013

EGFRvIII: An Oncogene with Ambiguous Role

artículo científico publicado en 2019

Efficient and simple approach to in vitro culture of primary epithelial cancer cells

artículo científico publicado en 2016

Elimination of wild-type P53 mRNA in glioblastomas showing heterozygous mutations of P53.

artículo científico publicado en 2008

GADD45A and EPB41 as tumor suppressor genes in meningioma pathogenesis.

artículo científico publicado en 2005

Gaps and Doubts in Search to Recognize Glioblastoma Cellular Origin and Tumor Initiating Cells

artículo científico publicado en 2020

Generation of human iPSCs from cells of fibroblastic and epithelial origin by means of the oriP/EBNA-1 episomal reprogramming system

artículo científico publicado en 2015

Generation of induced neural stem cells with inducible IDH1R132H for analysis of glioma development and drug testing

scientific article published on 18 September 2020

Genetic heterogeneity of RPMI-8402, a T-acute lymphoblastic leukemia cell line

artículo científico publicado en 2015

Glioblastoma specimens with TP53 mutations do not show EGFRvIII amplification.

artículo científico publicado en 2011

Glioblastoma-derived spheroid cultures as an experimental model for analysis of EGFR anomalies.

artículo científico publicado en 2010

Glioma cells showing IDH1 mutation cannot be propagated in standard cell culture conditions.

artículo científico

Gliomas: association of histology and molecular genetic analysis of chromosomes 1p, 10q, and 19q.

artículo científico publicado en 2007

High incidence of MGMT promoter methylation in primary glioblastomas without correlation with TP53 gene mutations

artículo científico publicado en 2009

Human fibroblast-derived cell lines have characteristics of embryonic stem cells and cells of neuro-ectodermal origin.

artículo científico publicado en 2005

IDH1R132H in Neural Stem Cells: Differentiation Impaired by Increased Apoptosis.

artículo científico publicado en 2016

Imperfect oligodendrocytic and neuronal differentiation of glioblastoma cells.

artículo científico publicado en 2010

KCTD11 expression in medulloblastoma is lower than in adult cerebellum and higher than in neural stem cells

artículo científico publicado en 2006

Limited importance of the dominant-negative effect of TP53 missense mutations

artículo científico publicado en 2011

Loss of heterozygosity for Rb locus and pRb immunostaining in laryngeal cancer: a clinicopathologic, molecular and immunohistochemical study.

artículo científico publicado en 2008

Loss of heterozygosity of WT1 gene in the prognosis of sporadic Wilms' tumour in children

artículo científico publicado en 1999

Low Incidence along with Low mRNA Levels of EGFRvIII in Prostate and Colorectal Cancers Compared to Glioblastoma

artículo científico publicado en 2017

Molecular abnormalities in pediatric embryonal brain tumors--analysis of loss of heterozygosity on chromosomes 1, 5, 9, 10, 11, 16, 17 and 22

scientific article published on 01 September 2004

Molecular alterations in meningiomas: association with clinical data

artículo científico publicado en 2013

Molecular analysis of chromosome 1, 10 and 19 abnormalities in human oligodendroglial tumors: relationship between frequency of LOH grade, age and gender

artículo científico publicado en 2006

Molecular heterogeneity of meningioma with INI1 mutation

artículo científico publicado en 2003

Multiomic analysis on human cell model of wolfram syndrome reveals changes in mitochondrial morphology and function

artículo científico publicado en 2021

Multiple myeloma in a patient with systemic lupus erythematosus, myasthenia gravis and non-familial diffuse palmoplantar keratoderma.

artículo científico publicado en 2004

Mutational analysis of hSNF5/INI1 and TP53 genes in choroid plexus carcinomas

artículo científico publicado en 2005

Neuronal and astrocytic cells, obtained after differentiation of human neural GFAP-positive progenitors, present heterogeneous expression of PrPc

artículo científico publicado en 2007

PIN3 duplication may be partially responsible for TP53 haploinsufficiency

artículo científico publicado en 2014

Phenotypical Flexibility of the EGFRvIII-Positive Glioblastoma Cell Line and the Multidirectional Influence of TGFβ and EGF on These Cells—EGFRvIII Appears as a Weak Oncogene

artículo científico publicado en 2022

Platelet activation by mercuric compounds

scientific article published on 01 January 1997

Prevalence of mutated TP53 on cDNA (but not on DNA template) in pleomorphic xanthoastrocytoma with positive TP53 immunohistochemistry.

artículo científico publicado en 2009

Reduced expression of ELAVL4 in male meningioma patients.

artículo científico publicado en 2012

Regulation of PrPC expression: nerve growth factor (NGF) activates the prion gene promoter through the MEK1 pathway in PC12 cells.

artículo científico publicado en 2006

Richter's syndrome in the brain first manifested as an ischaemic stroke

artículo científico publicado en 2004

SOX2 and SOX2-MYC Reprogramming Process of Fibroblasts to the Neural Stem Cells Compromised by Senescence

artículo científico publicado en 2015

Screening for EGFR amplifications with a novel method and their significance for the outcome of glioblastoma patients

artículo científico publicado en 2013

Sensitivity of neoplastic cells to senescence unveiled under standard cell culture conditions

artículo científico publicado en 2015

Simultaneous occurrence of medullary and papillary carcinomas of the thyroid gland with metastases of papillary carcinoma to the cervical lymph nodes and the coinciding small B-cell lymphocytic lymphoma of the lymph nodes--a case report.

artículo científico publicado en 2004

Spontaneous in vitro senescence of glioma cells confirmed by an antibody against IDH1R132H.

artículo científico publicado en 2014

Successful elimination of non-neural cells and unachievable elimination of glial cells by means of commonly used cell culture manipulations during differentiation of GFAP and SOX2 positive neural progenitors (NHA) to neuronal cells

artículo científico publicado en 2008

Synthesis and physicochemical characterization of chitin dihexanoate--A new biocompatible chitin derivative--In comparison to chitin dibutyrate.

artículo científico publicado en 2015

The failure in the stabilization of glioblastoma-derived cell lines: spontaneous in vitro senescence as the main culprit

artículo científico publicado en 2014

The infrequent simultaneous genetic alterations in glioblastoma multiforme (LOH 10, 17, 19q, TP53 mutation and EGFR amplification) with short clinical course.

artículo científico publicado en 2007

[Expression of p16 gene and protein in the evaluation of dynamics of laryngeal cancer growth]

artículo científico publicado en 2004

[Familial occurrence of nephroblastoma]

artículo científico publicado en 2001

[Glioblastoma with BRAFV600E mutation and numerous metastatic foci: a case report]

scientific article published on 01 January 2019

cDNA sequencing improves the detection of P53 missense mutations in colorectal cancer

artículo científico publicado en 2009

Lista de obras de Piotr Rieske

16q heterozygosity loss in Wilms' tumour in children and its clinical importance

A comparative study of P53/MDM2 genes alterations and P53/MDM2 proteins immunoreactivity in soft-tissue sarcomas

A comparative study of epidermal growth factor receptor (EGFR) and MDM2 gene amplification and protein immunoreactivity in human glioblastomas.

A population of human brain cells expressing phenotypic markers of more than one lineage can be induced in vitro to differentiate into mesenchymal cells.

A population of human brain parenchymal cells express markers of glial, neuronal and early neural cells and differentiate into cells of neuronal and glial lineages.

A way to understand idiopathic senescence and apoptosis in primary glioblastoma cells - possible approaches to circumvent these phenomena

Abnormalities of the P53, MDM2, BCL2 and BAX genes in acute leukemias.

Arrested neural and advanced mesenchymal differentiation of glioblastoma cells-comparative study with neural progenitors

Assessment of OPG/RANK/RANKL gene expression levels in peripheral blood mononuclear cells (PBMC) after treatment with strontium ranelate and ibandronate in patients with postmenopausal osteoporosis

Atypical molecular background of glioblastoma and meningioma developed in a patient with Li-Fraumeni syndrome

BCR expression is decreased in meningiomas showing loss of heterozygosity of 22q within a new minimal deletion region.

CYP46: a risk factor for Alzheimer's disease or a coincidence?

Cell line with endogenous EGFRvIII expression is a suitable model for research and drug development purposes.

Chitin dipentanoate as the new technologically usable biomaterial.

Cyclic trans-phosphorylation in a homodimer as the predominant mechanism of EGFRvIII action and regulation

Detection of P53 mutations in different cancer types is improved by cDNA sequencing.

Detection of lymph node metastases of papillary thyroid cancer-comparison of the results of histopathology, immunohistochemistry and reverse transcription-polymerase chain reaction-a preliminary report

Different mutational characteristics of TSG in cell lines and surgical specimens

Directed differentiation of human iPSC into insulin producing cells is improved by induced expression of PDX1 and NKX6.1 factors in IPC progenitors

Diverse molecular pattern in a bihemispheric glioblastoma (butterfly glioma) in a 16-year-old boy

EGFR Activation Leads to Cell Death Independent of PI3K/AKT/mTOR in an AD293 Cell Line

EGFRvIII--a stable target for anti-EGFRvIII therapy.

EGFRvIII: An Oncogene with Ambiguous Role

Efficient and simple approach to in vitro culture of primary epithelial cancer cells

Elimination of wild-type P53 mRNA in glioblastomas showing heterozygous mutations of P53.

GADD45A and EPB41 as tumor suppressor genes in meningioma pathogenesis.

Gaps and Doubts in Search to Recognize Glioblastoma Cellular Origin and Tumor Initiating Cells

Generation of human iPSCs from cells of fibroblastic and epithelial origin by means of the oriP/EBNA-1 episomal reprogramming system

Generation of induced neural stem cells with inducible IDH1R132H for analysis of glioma development and drug testing

Genetic heterogeneity of RPMI-8402, a T-acute lymphoblastic leukemia cell line

Glioblastoma specimens with TP53 mutations do not show EGFRvIII amplification.

Glioblastoma-derived spheroid cultures as an experimental model for analysis of EGFR anomalies.

Glioma cells showing IDH1 mutation cannot be propagated in standard cell culture conditions.

Gliomas: association of histology and molecular genetic analysis of chromosomes 1p, 10q, and 19q.

High incidence of MGMT promoter methylation in primary glioblastomas without correlation with TP53 gene mutations

Human fibroblast-derived cell lines have characteristics of embryonic stem cells and cells of neuro-ectodermal origin.

IDH1R132H in Neural Stem Cells: Differentiation Impaired by Increased Apoptosis.

Imperfect oligodendrocytic and neuronal differentiation of glioblastoma cells.

KCTD11 expression in medulloblastoma is lower than in adult cerebellum and higher than in neural stem cells

Limited importance of the dominant-negative effect of TP53 missense mutations

Loss of heterozygosity for Rb locus and pRb immunostaining in laryngeal cancer: a clinicopathologic, molecular and immunohistochemical study.

Loss of heterozygosity of WT1 gene in the prognosis of sporadic Wilms' tumour in children

Low Incidence along with Low mRNA Levels of EGFRvIII in Prostate and Colorectal Cancers Compared to Glioblastoma

Molecular abnormalities in pediatric embryonal brain tumors--analysis of loss of heterozygosity on chromosomes 1, 5, 9, 10, 11, 16, 17 and 22

Molecular alterations in meningiomas: association with clinical data

Molecular analysis of chromosome 1, 10 and 19 abnormalities in human oligodendroglial tumors: relationship between frequency of LOH grade, age and gender

Molecular heterogeneity of meningioma with INI1 mutation

Multiomic analysis on human cell model of wolfram syndrome reveals changes in mitochondrial morphology and function

Multiple myeloma in a patient with systemic lupus erythematosus, myasthenia gravis and non-familial diffuse palmoplantar keratoderma.

Mutational analysis of hSNF5/INI1 and TP53 genes in choroid plexus carcinomas

Neuronal and astrocytic cells, obtained after differentiation of human neural GFAP-positive progenitors, present heterogeneous expression of PrPc

PIN3 duplication may be partially responsible for TP53 haploinsufficiency

Phenotypical Flexibility of the EGFRvIII-Positive Glioblastoma Cell Line and the Multidirectional Influence of TGFβ and EGF on These Cells—EGFRvIII Appears as a Weak Oncogene

Platelet activation by mercuric compounds

Prevalence of mutated TP53 on cDNA (but not on DNA template) in pleomorphic xanthoastrocytoma with positive TP53 immunohistochemistry.

Reduced expression of ELAVL4 in male meningioma patients.

Regulation of PrPC expression: nerve growth factor (NGF) activates the prion gene promoter through the MEK1 pathway in PC12 cells.

Richter's syndrome in the brain first manifested as an ischaemic stroke

SOX2 and SOX2-MYC Reprogramming Process of Fibroblasts to the Neural Stem Cells Compromised by Senescence

Screening for EGFR amplifications with a novel method and their significance for the outcome of glioblastoma patients

Sensitivity of neoplastic cells to senescence unveiled under standard cell culture conditions

Simultaneous occurrence of medullary and papillary carcinomas of the thyroid gland with metastases of papillary carcinoma to the cervical lymph nodes and the coinciding small B-cell lymphocytic lymphoma of the lymph nodes--a case report.

Spontaneous in vitro senescence of glioma cells confirmed by an antibody against IDH1R132H.

Successful elimination of non-neural cells and unachievable elimination of glial cells by means of commonly used cell culture manipulations during differentiation of GFAP and SOX2 positive neural progenitors (NHA) to neuronal cells

Synthesis and physicochemical characterization of chitin dihexanoate--A new biocompatible chitin derivative--In comparison to chitin dibutyrate.

The failure in the stabilization of glioblastoma-derived cell lines: spontaneous in vitro senescence as the main culprit

The infrequent simultaneous genetic alterations in glioblastoma multiforme (LOH 10, 17, 19q, TP53 mutation and EGFR amplification) with short clinical course.

[Expression of p16 gene and protein in the evaluation of dynamics of laryngeal cancer growth]

[Familial occurrence of nephroblastoma]

[Glioblastoma with BRAFV600E mutation and numerous metastatic foci: a case report]

cDNA sequencing improves the detection of P53 missense mutations in colorectal cancer