Lista de obras - Ryan D Morin - Dominio Público Uruguay

<i>BCL10</i> Mutations Define Distinct Dependencies Guiding Precision Therapy for DLBCL

artículo científico publicado en 2022

ALEXA: a microarray design platform for alternative expression analysis

article

Acquired TNFRSF14 mutations in follicular lymphoma are associated with worse prognosis.

artículo científico publicado en 2010

Activating mutations in genes related to TCR signaling in angioimmunoblastic and other follicular helper T-cell-derived lymphomas.

artículo científico publicado en 2016

An RCOR1 loss-associated gene expression signature identifies a prognostically significant DLBCL subgroup

artículo científico publicado en 2014

Analysis of FOXO1 mutations in diffuse large B-cell lymphoma

artículo científico publicado en 2013

BCL6 repression of EP300 in human diffuse large B cell lymphoma cells provides a basis for rational combinatorial therapy

artículo científico publicado en 2010

Cell-free DNA (cfDNA): Clinical Significance and Utility in Cancer Shaped By Emerging Technologies

artículo científico

Circulating Tumor Cells (CTC) and Cell-Free DNA (cfDNA) Workshop 2016: Scientific Opportunities and Logistics for Cancer Clinical Trial Incorporation

artículo científico publicado en 2016

Comprehensive characterization of programmed death ligand structural rearrangements in B-cell non-Hodgkin lymphomas.

artículo científico publicado en 2016

Comprehensive miRNA sequence analysis reveals survival differences in diffuse large B-cell lymphoma patients

artículo científico publicado en 2015

Cross-cancer profiling of molecular alterations within the human autophagy interaction network

artículo científico publicado en 2015

De novo transcriptome assembly with ABySS.

artículo científico publicado en 2009

Enhancing knowledge discovery from cancer genomics data with Galaxy.

artículo científico publicado en 2017

Evaluating the quantity, quality and size distribution of cell-free DNA by multiplex droplet digital PCR

artículo científico publicado en 2020

Evolution of an adenocarcinoma in response to selection by targeted kinase inhibitors

artículo científico publicado en 2010

FOXL2 402C>G Mutation Can Be Identified in the Circulating Tumor DNA of Patients with Adult-Type Granulosa Cell Tumor.

artículo científico publicado en 2016

Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma

artículo científico publicado en 2011

Frequent mutations of FBXO11 highlight BCL6 as a therapeutic target in Burkitt lymphoma

scientific article published on 01 December 2021

Genetic Landscapes of Relapsed and Refractory Diffuse Large B-Cell Lymphomas.

artículo científico publicado en 2015

Genetic heterogeneity in primary and relapsed mantle cell lymphomas: Impact of recurrent CARD11 mutations.

artículo científico publicado en 2016

Genetic inactivation of TRAF3 in canine and human B-cell lymphoma

artículo científico publicado en 2014

Genetic profiling of MYC and BCL2 in diffuse large B-cell lymphoma determines cell-of-origin-specific clinical impact.

artículo científico publicado en 2017

Genome-wide chemical mapping of O-GlcNAcylated proteins in Drosophila melanogaster

artículo científico publicado en 2016

Genome-wide discovery of somatic coding and noncoding mutations in pediatric endemic and sporadic Burkitt lymphoma

artículo científico publicado en 2019

Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma

Genome-wide discovery of somatic regulatory variants in diffuse large B-cell lymphoma

artículo científico publicado en 2018

Genomic analysis of a rare human tumor

artículo científico publicado en 2010

High-resolution architecture and partner genes of rearrangements in lymphoma with DLBCL morphology

artículo científico

Histological Transformation and Progression in Follicular Lymphoma: A Clonal Evolution Study

artículo científico publicado en 2016

Identification of miR-145 and miR-146a as mediators of the 5q- syndrome phenotype

artículo científico publicado en 2009

IgCaller for reconstructing immunoglobulin gene rearrangements and oncogenic translocations from whole-genome sequencing in lymphoid neoplasms

artículo científico publicado en 2020

Immunogenicity of recurrent mutations in MYD88 and EZH2 in non-Hodgkin lymphomas.

artículo científico publicado en 2015

LongSAGE profiling of nine human embryonic stem cell lines.

artículo científico publicado en 2007

Management and visualization of whole genome shotgun assemblies using SAM.

artículo científico publicado en 2005

Mapping the human T cell repertoire to recurrent driver mutations in MYD88 and EZH2 in lymphoma

artículo científico publicado en 2017

Methods for sample acquisition and processing of serial blood and tumor biopsies for multicenter diffuse large B-cell lymphoma clinical trials

artículo científico publicado en 2014

Multiplex Droplet Digital PCR Quantification of Recurrent Somatic Mutations in Diffuse Large B-Cell and Follicular Lymphoma

artículo científico publicado en 2016

Mutation ofFOXL2in Granulosa-Cell Tumors of the Ovary

scientific article published on 10 June 2009

Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencing

scientific article published on 22 May 2013

Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution

artículo científico publicado en 2009

Newly identified mechanisms in B-cell non-Hodgkin lymphomas uncovered by next-generation sequencing.

artículo científico

Pediatric-type nodal follicular lymphoma: a biologically distinct lymphoma with frequent MAPK pathway mutations

artículo científico publicado en 2016

Phase 2 study of panobinostat with or without rituximab in relapsed diffuse large B-cell lymphoma

artículo científico publicado en 2016

Preparation and analysis of microRNA libraries using the Illumina massively parallel sequencing technology.

artículo científico publicado en 2010

Profiling the HeLa S3 transcriptome using randomly primed cDNA and massively parallel short-read sequencing

artículo científico publicado en 2008

Recurrent genomic rearrangements in primary testicular lymphoma.

artículo científico

Recurrent targets of aberrant somatic hypermutation in lymphoma

artículo científico publicado en 2012

Sequencing and analysis of 10,967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis reveals post-tetraploidization transcriptome remodeling

artículo científico publicado en 2006

Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin

artículo científico publicado en 2010

TBL1XR1/TP63: a novel recurrent gene fusion in B-cell non-Hodgkin lymphoma

artículo científico publicado en 2012

TMEM30A loss-of-function mutations drive lymphomagenesis and confer therapeutically exploitable vulnerability in B-cell lymphoma

scientific article published on 24 February 2020

The completion of the Mammalian Gene Collection (MGC).

artículo científico publicado en 2009

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)

artículo científico publicado en 2004

Toward Personalized Lymphoma Immunotherapy: Identification of Common Driver Mutations Recognized by Patient CD8+ T Cells

artículo científico publicado en 2015

Variability in DNA methylation defines novel epigenetic subgroups of DLBCL associated with different clinical outcomes.

scientific article published on 02 January 2014

Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma.

artículo científico publicado en 2012

Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport

artículo científico publicado en 2016

Lista de obras de Ryan D Morin

<i>BCL10</i> Mutations Define Distinct Dependencies Guiding Precision Therapy for DLBCL

ALEXA: a microarray design platform for alternative expression analysis

Acquired TNFRSF14 mutations in follicular lymphoma are associated with worse prognosis.

Activating mutations in genes related to TCR signaling in angioimmunoblastic and other follicular helper T-cell-derived lymphomas.

An RCOR1 loss-associated gene expression signature identifies a prognostically significant DLBCL subgroup

Analysis of FOXO1 mutations in diffuse large B-cell lymphoma

BCL6 repression of EP300 in human diffuse large B cell lymphoma cells provides a basis for rational combinatorial therapy

Cell-free DNA (cfDNA): Clinical Significance and Utility in Cancer Shaped By Emerging Technologies

Circulating Tumor Cells (CTC) and Cell-Free DNA (cfDNA) Workshop 2016: Scientific Opportunities and Logistics for Cancer Clinical Trial Incorporation

Comprehensive characterization of programmed death ligand structural rearrangements in B-cell non-Hodgkin lymphomas.

Comprehensive miRNA sequence analysis reveals survival differences in diffuse large B-cell lymphoma patients

Cross-cancer profiling of molecular alterations within the human autophagy interaction network

De novo transcriptome assembly with ABySS.

Enhancing knowledge discovery from cancer genomics data with Galaxy.

Evaluating the quantity, quality and size distribution of cell-free DNA by multiplex droplet digital PCR

Evolution of an adenocarcinoma in response to selection by targeted kinase inhibitors

FOXL2 402C>G Mutation Can Be Identified in the Circulating Tumor DNA of Patients with Adult-Type Granulosa Cell Tumor.

Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma

Frequent mutations of FBXO11 highlight BCL6 as a therapeutic target in Burkitt lymphoma

Genetic Landscapes of Relapsed and Refractory Diffuse Large B-Cell Lymphomas.

Genetic heterogeneity in primary and relapsed mantle cell lymphomas: Impact of recurrent CARD11 mutations.

Genetic inactivation of TRAF3 in canine and human B-cell lymphoma

Genetic profiling of MYC and BCL2 in diffuse large B-cell lymphoma determines cell-of-origin-specific clinical impact.

Genome-wide chemical mapping of O-GlcNAcylated proteins in Drosophila melanogaster

Genome-wide discovery of somatic coding and noncoding mutations in pediatric endemic and sporadic Burkitt lymphoma

Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma

Genome-wide discovery of somatic regulatory variants in diffuse large B-cell lymphoma

Genomic analysis of a rare human tumor

High-resolution architecture and partner genes of rearrangements in lymphoma with DLBCL morphology

Histological Transformation and Progression in Follicular Lymphoma: A Clonal Evolution Study

Identification of miR-145 and miR-146a as mediators of the 5q- syndrome phenotype

IgCaller for reconstructing immunoglobulin gene rearrangements and oncogenic translocations from whole-genome sequencing in lymphoid neoplasms

Immunogenicity of recurrent mutations in MYD88 and EZH2 in non-Hodgkin lymphomas.

LongSAGE profiling of nine human embryonic stem cell lines.

Management and visualization of whole genome shotgun assemblies using SAM.

Mapping the human T cell repertoire to recurrent driver mutations in MYD88 and EZH2 in lymphoma

Methods for sample acquisition and processing of serial blood and tumor biopsies for multicenter diffuse large B-cell lymphoma clinical trials

Multiplex Droplet Digital PCR Quantification of Recurrent Somatic Mutations in Diffuse Large B-Cell and Follicular Lymphoma

Mutation ofFOXL2in Granulosa-Cell Tumors of the Ovary

Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencing

Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution

Newly identified mechanisms in B-cell non-Hodgkin lymphomas uncovered by next-generation sequencing.

Pediatric-type nodal follicular lymphoma: a biologically distinct lymphoma with frequent MAPK pathway mutations

Phase 2 study of panobinostat with or without rituximab in relapsed diffuse large B-cell lymphoma

Preparation and analysis of microRNA libraries using the Illumina massively parallel sequencing technology.

Profiling the HeLa S3 transcriptome using randomly primed cDNA and massively parallel short-read sequencing

Recurrent genomic rearrangements in primary testicular lymphoma.

Recurrent targets of aberrant somatic hypermutation in lymphoma

Sequencing and analysis of 10,967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis reveals post-tetraploidization transcriptome remodeling

Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin

TBL1XR1/TP63: a novel recurrent gene fusion in B-cell non-Hodgkin lymphoma

TMEM30A loss-of-function mutations drive lymphomagenesis and confer therapeutically exploitable vulnerability in B-cell lymphoma

The completion of the Mammalian Gene Collection (MGC).

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)

Toward Personalized Lymphoma Immunotherapy: Identification of Common Driver Mutations Recognized by Patient CD8+ T Cells

Variability in DNA methylation defines novel epigenetic subgroups of DLBCL associated with different clinical outcomes.

Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma.

Whole-Organism Developmental Expression Profiling Identifies RAB-28 as a Novel Ciliary GTPase Associated with the BBSome and Intraflagellar Transport