Lista de obras - Juan Luis García - Dominio Público Uruguay

A high number of losses in 13q14 chromosome band is associated with a worse outcome and biological differences in patients with B-cell chronic lymphoid leukemia.

artículo científico publicado en 2009

Abnormalities on 1q and 7q are associated with poor outcome in sporadic Burkitt's lymphoma. A cytogenetic and comparative genomic hybridization study

artículo científico publicado en 2003

Analysis of DNA repair gene polymorphisms in glioblastoma.

artículo científico publicado en 2013

Analysis of chromosomal imbalances in an elderly woman with a giant cell tumour

scientific article published on 12 October 2005

Association between trisomy 8 and the immunophenotype of blast cells from acute leukemias secondary to a myelodysplastic syndrome or chronic myeloproliferative disorders

scientific article published on 01 May 1997

Association of Polyps with Early-Onset Colorectal Cancer and Throughout Surveillance: Novel Clinical and Molecular Implications

scientific article published on 29 November 2019

Both expanded and uncultured mesenchymal stem cells from MDS patients are genomically abnormal, showing a specific genetic profile for the 5q- syndrome

artículo científico publicado en 2009

Characterization of breast cancer by array comparative genomic hybridization.

artículo científico publicado en 2007

Chromosomal imbalances identified by comparative genomic hybridization in sporadic parathyroid adenomas

artículo científico publicado en 2002

Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes.

artículo científico publicado en 2016

Classifying early-onset colorectal cancer according to tumor location: new potential subcategories to explore

artículo científico publicado en 2015

Clinical and biological characteristics of myelodysplastic syndromes with nulisomy Y by fish

artículo científico publicado en 1997

Clinical, molecular and biochemical characterization of nine Spanish families with Conradi-Hünermann-Happle syndrome: new insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature.

artículo científico

Comment on 'Wild-type APC prediction of poor prognosis in microsatellite-stable proximal colorectal cancer differs according to the age of onset'.

artículo científico publicado en 2016

Comprehensive conventional and molecular cytogenetic characterization of B-CPAP, a human papillary thyroid carcinoma-derived cell line.

artículo científico publicado en 2004

Correlation between cytogenetic abnormalities and disease characteristics in multiple myeloma: monosomy of chromosome 13 and structural abnormalities of 11q are associated with a high percentage of S-phase plasma cells

artículo científico publicado en 2000

Cutaneous intraneural perineurioma: a case report.

artículo científico publicado en 2013

DNA copy number profiling reveals different patterns of chromosomal instability within colorectal cancer according to the age of onset

artículo científico publicado en 2015

Detection of the Mbcr/abl translocation in chronic myeloid leukemia by fluorescence in situ hybridization: comparison with conventional cytogenetics and implications for minimal residual disease detection

scientific article published on 01 February 1997

Differences in genetic changes between multiple myeloma and plasma cell leukemia demonstrated by comparative genomic hybridization

artículo científico publicado en 2001

Early-onset colorectal cancer: a separate subset of colorectal cancer

artículo científico publicado en 2014

Effects of imatinib mesylate on normal bone marrow cells from chronic myeloid leukemia patients in complete cytogenetic response.

artículo científico publicado en 2008

Epidermal growth factor receptor expression is associated with poor outcome in cutaneous squamous cell carcinoma.

artículo científico publicado en 2016

Expression of VAV1 in the tumour microenvironment of glioblastoma multiforme.

artículo científico publicado en 2012

Factors influencing malignant evolution and long-term survival in solitary fibrous tumours of the pleura

artículo científico publicado en 2014

Frequency and impact of KRAS mutation in early onset colorectal cancer

artículo científico publicado en 2016

Gene expression profile reveals deregulation of genes with relevant functions in the different subclasses of acute myeloid leukemia.

artículo científico publicado en 2005

Genome-Wide DNA Copy Number Analysis of Acute Lymphoblastic Leukemia Identifies New Genetic Markers Associated with Clinical Outcome

artículo científico publicado en 2016

Genome-wide profiling of methylation identifies novel targets with aberrant hypermethylation and reduced expression in low-risk myelodysplastic syndromes.

artículo científico publicado en 2012

Geographic differences in the incidence of cytogenetic abnormalities of acute myelogenous leukemia (AML) in Spain

article

Hematological, immunophenotypic, and cytogenetic characteristics of acute myeloblastic leukemia with trisomy 11

artículo científico publicado en 2005

Heterogeneity of structural abnormalities in the 7q31.3∼q34 region in myeloid malignancies

artículo científico publicado en 2004

IL-4 improves the detection of cytogenetic abnormalities in multiple myeloma and increases the proportion of clonally abnormal metaphases

artículo científico publicado en 1998

Imatinib therapy of chronic myeloid leukemia restores the expression levels of key genes for DNA damage and cell-cycle progression

article

Immunomodulatory effect of 5-azacytidine (5-azaC): potential role in the transplantation setting.

artículo científico publicado en 2009

Integrated analysis of mismatch repair system in malignant astrocytomas.

artículo científico publicado en 2013

Integration of global spectral karyotyping, CGH arrays, and expression arrays reveals important genes in the pathogenesis of glioblastoma multiforme

artículo científico publicado en 2012

Lenalidomide plus dexamethasone versus observation in patients with high-risk smouldering multiple myeloma (QuiRedex): long-term follow-up of a randomised, controlled, phase 3 trial.

artículo científico publicado en 2016

Liquid Biopsy as Novel Tool in Precision Medicine: Origins, Properties, Identification and Clinical Perspective of Cancer's Biomarkers

scientific article published on 13 April 2020

Mesenchymal stem cells from multiple myeloma patients display distinct genomic profile as compared with those from normal donors

scientific article published on 09 April 2009

MicroRNA-223 is a novel negative regulator of HSP90B1 in CLL.

artículo científico publicado en 2015

Molecular analysis of ex-vivo CD133+ GBM cells revealed a common invasive and angiogenic profile but different proliferative signatures among high grade gliomas.

artículo científico publicado en 2010

Molecular characterization of chronic lymphocytic leukemia patients with a high number of losses in 13q14.

artículo científico publicado en 2012

Molecular characterization of the region 7q22.1 in splenic marginal zone lymphomas

artículo científico publicado en 2011

Multicolor fluorescence in situ hybridization studies in multiple myeloma and monoclonal gammopathy of undetermined significance.

artículo científico

Novel Dominant KCNQ2 Exon 7 Partial In-Frame Duplication in a Complex Epileptic and Neurodevelopmental Delay Syndrome

artículo científico publicado en 2020

Novel genomic imbalances in B-cell splenic marginal zone lymphomas revealed by comparative genomic hybridization and cytogenetics.

artículo científico publicado en 2001

Onychomatricoma: genome-wide analyses of a rare nail matrix tumor.

scientific article published on 05 August 2010

Overexpression of the VAV proto-oncogene product is associated with B-cell chronic lymphocytic leukaemia displaying loss on 13q.

artículo científico publicado en 2006

P53deletion may drive the clinical evolution and treatment response in multiple myeloma

artículo científico publicado en 2009

Pathogenic convergence of CNVs in genes functionally associated to a severe neuromotor developmental delay syndrome

artículo científico publicado en 2021

Post-transcriptional Modifications Contribute to the Upregulation of Cyclin D2 in Multiple Myeloma

artículo científico publicado en 2015

Primary cutaneous T-cell lymphoproliferative disorder of donor origin after allogeneic haematopoietic stem-cell transplantation

artículo científico publicado en 2009

Prognostic and biologic significance of chromosomal imbalances assessed by comparative genomic hybridization in multiple myeloma

artículo científico publicado en 2004

TET2 overexpression in chronic lymphocytic leukemia is unrelated to the presence of TET2 variations.

artículo científico publicado en 2014

The presence of genomic imbalances is associated with poor outcome in patients with burkitt lymphoma treated with dose-intensive chemotherapy including rituximab

artículo científico publicado en 2015

The value of cell cultures for the diagnosis of mixed myelodysplastic/myeloproliferative disorders

artículo científico publicado en 1998

The value of fluorescence in situ hybridization for the detection of 11q in multiple myeloma

scientific article published on 01 October 2004

Toward a Molecular Classification of Synchronous Colorectal Cancer: Clinical and Molecular Characterization.

artículo científico publicado en 2016

Two cases of myeloid disorders and a t(8;12) (q12;p13)

scientific article published on 01 January 2000

Uniparental disomy causes deficiencies of vitamin K-dependent proteins

artículo científico publicado en 2016

Unsupervised Analysis of Array Comparative Genomic Hybridization Data from Early-Onset Colorectal Cancer Reveals Equivalence with Molecular Classification and Phenotypes.

artículo científico publicado en 2016

VRK2 identifies a subgroup of primary high-grade astrocytomas with a better prognosis

artículo científico publicado en 2013

[Applications of fluorescence in situ hybridization in the study of hematologic neoplasms]

scientific article published on 01 August 1996

[Comparative genomic hybridization. Methodologic features]

scientific article published on 01 August 1999

[Cytogenetics in the study of malignant blood diseases]

scientific article published on 01 August 1996

Lista de obras de Juan Luis García

A high number of losses in 13q14 chromosome band is associated with a worse outcome and biological differences in patients with B-cell chronic lymphoid leukemia.

Abnormalities on 1q and 7q are associated with poor outcome in sporadic Burkitt's lymphoma. A cytogenetic and comparative genomic hybridization study

Analysis of DNA repair gene polymorphisms in glioblastoma.

Analysis of chromosomal imbalances in an elderly woman with a giant cell tumour

Association between trisomy 8 and the immunophenotype of blast cells from acute leukemias secondary to a myelodysplastic syndrome or chronic myeloproliferative disorders

Association of Polyps with Early-Onset Colorectal Cancer and Throughout Surveillance: Novel Clinical and Molecular Implications

Both expanded and uncultured mesenchymal stem cells from MDS patients are genomically abnormal, showing a specific genetic profile for the 5q- syndrome

Characterization of breast cancer by array comparative genomic hybridization.

Chromosomal imbalances identified by comparative genomic hybridization in sporadic parathyroid adenomas

Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes.

Classifying early-onset colorectal cancer according to tumor location: new potential subcategories to explore

Clinical and biological characteristics of myelodysplastic syndromes with nulisomy Y by fish

Clinical, molecular and biochemical characterization of nine Spanish families with Conradi-Hünermann-Happle syndrome: new insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature.

Comment on 'Wild-type APC prediction of poor prognosis in microsatellite-stable proximal colorectal cancer differs according to the age of onset'.

Comprehensive conventional and molecular cytogenetic characterization of B-CPAP, a human papillary thyroid carcinoma-derived cell line.

Correlation between cytogenetic abnormalities and disease characteristics in multiple myeloma: monosomy of chromosome 13 and structural abnormalities of 11q are associated with a high percentage of S-phase plasma cells

Cutaneous intraneural perineurioma: a case report.

DNA copy number profiling reveals different patterns of chromosomal instability within colorectal cancer according to the age of onset

Detection of the Mbcr/abl translocation in chronic myeloid leukemia by fluorescence in situ hybridization: comparison with conventional cytogenetics and implications for minimal residual disease detection

Differences in genetic changes between multiple myeloma and plasma cell leukemia demonstrated by comparative genomic hybridization

Early-onset colorectal cancer: a separate subset of colorectal cancer

Effects of imatinib mesylate on normal bone marrow cells from chronic myeloid leukemia patients in complete cytogenetic response.

Epidermal growth factor receptor expression is associated with poor outcome in cutaneous squamous cell carcinoma.

Expression of VAV1 in the tumour microenvironment of glioblastoma multiforme.

Factors influencing malignant evolution and long-term survival in solitary fibrous tumours of the pleura

Frequency and impact of KRAS mutation in early onset colorectal cancer

Gene expression profile reveals deregulation of genes with relevant functions in the different subclasses of acute myeloid leukemia.

Genome-Wide DNA Copy Number Analysis of Acute Lymphoblastic Leukemia Identifies New Genetic Markers Associated with Clinical Outcome

Genome-wide profiling of methylation identifies novel targets with aberrant hypermethylation and reduced expression in low-risk myelodysplastic syndromes.

Geographic differences in the incidence of cytogenetic abnormalities of acute myelogenous leukemia (AML) in Spain

Hematological, immunophenotypic, and cytogenetic characteristics of acute myeloblastic leukemia with trisomy 11

Heterogeneity of structural abnormalities in the 7q31.3∼q34 region in myeloid malignancies

IL-4 improves the detection of cytogenetic abnormalities in multiple myeloma and increases the proportion of clonally abnormal metaphases

Imatinib therapy of chronic myeloid leukemia restores the expression levels of key genes for DNA damage and cell-cycle progression

Immunomodulatory effect of 5-azacytidine (5-azaC): potential role in the transplantation setting.

Integrated analysis of mismatch repair system in malignant astrocytomas.

Integration of global spectral karyotyping, CGH arrays, and expression arrays reveals important genes in the pathogenesis of glioblastoma multiforme

Lenalidomide plus dexamethasone versus observation in patients with high-risk smouldering multiple myeloma (QuiRedex): long-term follow-up of a randomised, controlled, phase 3 trial.

Liquid Biopsy as Novel Tool in Precision Medicine: Origins, Properties, Identification and Clinical Perspective of Cancer's Biomarkers

Mesenchymal stem cells from multiple myeloma patients display distinct genomic profile as compared with those from normal donors

MicroRNA-223 is a novel negative regulator of HSP90B1 in CLL.

Molecular analysis of ex-vivo CD133+ GBM cells revealed a common invasive and angiogenic profile but different proliferative signatures among high grade gliomas.

Molecular characterization of chronic lymphocytic leukemia patients with a high number of losses in 13q14.

Molecular characterization of the region 7q22.1 in splenic marginal zone lymphomas

Multicolor fluorescence in situ hybridization studies in multiple myeloma and monoclonal gammopathy of undetermined significance.

Novel Dominant KCNQ2 Exon 7 Partial In-Frame Duplication in a Complex Epileptic and Neurodevelopmental Delay Syndrome

Novel genomic imbalances in B-cell splenic marginal zone lymphomas revealed by comparative genomic hybridization and cytogenetics.

Onychomatricoma: genome-wide analyses of a rare nail matrix tumor.

Overexpression of the VAV proto-oncogene product is associated with B-cell chronic lymphocytic leukaemia displaying loss on 13q.

P53deletion may drive the clinical evolution and treatment response in multiple myeloma

Pathogenic convergence of CNVs in genes functionally associated to a severe neuromotor developmental delay syndrome

Post-transcriptional Modifications Contribute to the Upregulation of Cyclin D2 in Multiple Myeloma

Primary cutaneous T-cell lymphoproliferative disorder of donor origin after allogeneic haematopoietic stem-cell transplantation

Prognostic and biologic significance of chromosomal imbalances assessed by comparative genomic hybridization in multiple myeloma

TET2 overexpression in chronic lymphocytic leukemia is unrelated to the presence of TET2 variations.

The presence of genomic imbalances is associated with poor outcome in patients with burkitt lymphoma treated with dose-intensive chemotherapy including rituximab

The value of cell cultures for the diagnosis of mixed myelodysplastic/myeloproliferative disorders

The value of fluorescence in situ hybridization for the detection of 11q in multiple myeloma

Toward a Molecular Classification of Synchronous Colorectal Cancer: Clinical and Molecular Characterization.

Two cases of myeloid disorders and a t(8;12) (q12;p13)

Uniparental disomy causes deficiencies of vitamin K-dependent proteins

Unsupervised Analysis of Array Comparative Genomic Hybridization Data from Early-Onset Colorectal Cancer Reveals Equivalence with Molecular Classification and Phenotypes.

VRK2 identifies a subgroup of primary high-grade astrocytomas with a better prognosis

[Applications of fluorescence in situ hybridization in the study of hematologic neoplasms]

[Comparative genomic hybridization. Methodologic features]

[Cytogenetics in the study of malignant blood diseases]