Lista de obras - Inga Vater - Dominio Público Uruguay

A comprehensive microarray-based DNA methylation study of 367 hematological neoplasms

artículo científico publicado en 2009

A de novo 1.1Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformation

artículo científico publicado en 2011

A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma

artículo científico publicado en 2014

A summary of molecular genetic findings in fructose-1,6-bisphosphatase deficiency with a focus on a common long-range deletion and the role of MLPA analysis

artículo científico publicado en 2016

DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional control

artículo científico publicado en 2015

Detection of genomic aberrations in molecularly defined Burkitt's lymphoma by array-based, high resolution, single nucleotide polymorphism analysis

artículo científico publicado en 2010

Frequency and characterization of DNA methylation defects in children born SGA.

artículo científico publicado en 2012

GeneChip analyses point to novel pathogenetic mechanisms in mantle cell lymphoma

artículo científico publicado en 2008

Genetic characteristics of the human hepatic stellate cell line LX-2.

artículo científico publicado en 2013

Genetic lesions of the TRAF3 and MAP3K14 genes in classical Hodgkin lymphoma

artículo científico publicado en 2012

Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome

artículo científico publicado en 2010

Hunting for the 5th base: Techniques for analyzing DNA methylation

artículo científico publicado en 2009

Immunoglobulin heavy chain locus chromosomal translocations in B-cell precursor acute lymphoblastic leukemia: rare clinical curios or potent genetic drivers?

artículo científico publicado en 2009

Inhibition of anaplastic lymphoma kinase (ALK) activity provides a therapeutic approach for CLTC-ALK-positive human diffuse large B cell lymphomas

artículo científico publicado en 2011

Janus--a comprehensive tool investigating the two faces of transcription

artículo científico publicado en 2013

Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance

artículo científico publicado en 2014

New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3).

artículo científico publicado en 2015

Rare occurrence of biallelic CYLD gene mutations in classical Hodgkin lymphoma

artículo científico publicado en 2010

Recurrent deletions of the TNFSF7 and TNFSF9 genes in 19p13.3 in diffuse large B-cell and Burkitt lymphomas

artículo científico publicado en 2012

Statistical inference of allelic imbalance from transcriptome data

artículo científico publicado en 2011

TNFAIP3 (A20) is a tumor suppressor gene in Hodgkin lymphoma and primary mediastinal B cell lymphoma

artículo científico publicado en 2009

Lista de obras de Inga Vater

A comprehensive microarray-based DNA methylation study of 367 hematological neoplasms

A de novo 1.1Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformation

A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma

A summary of molecular genetic findings in fructose-1,6-bisphosphatase deficiency with a focus on a common long-range deletion and the role of MLPA analysis

DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional control

Detection of genomic aberrations in molecularly defined Burkitt's lymphoma by array-based, high resolution, single nucleotide polymorphism analysis

Frequency and characterization of DNA methylation defects in children born SGA.

GeneChip analyses point to novel pathogenetic mechanisms in mantle cell lymphoma

Genetic characteristics of the human hepatic stellate cell line LX-2.

Genetic lesions of the TRAF3 and MAP3K14 genes in classical Hodgkin lymphoma

Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome

Hunting for the 5th base: Techniques for analyzing DNA methylation

Immunoglobulin heavy chain locus chromosomal translocations in B-cell precursor acute lymphoblastic leukemia: rare clinical curios or potent genetic drivers?

Inhibition of anaplastic lymphoma kinase (ALK) activity provides a therapeutic approach for CLTC-ALK-positive human diffuse large B cell lymphomas

Janus--a comprehensive tool investigating the two faces of transcription

Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance

New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3).

Rare occurrence of biallelic CYLD gene mutations in classical Hodgkin lymphoma

Recurrent deletions of the TNFSF7 and TNFSF9 genes in 19p13.3 in diffuse large B-cell and Burkitt lymphomas

Statistical inference of allelic imbalance from transcriptome data

TNFAIP3 (A20) is a tumor suppressor gene in Hodgkin lymphoma and primary mediastinal B cell lymphoma