Lista de obras - Dan Andrews - Dominio Público Uruguay

A high-resolution survey of deletion polymorphism in the human genome

2005 scientific article

Absence of mucosal-associated invariant T cells in a person with a homozygous point mutation in MR1

artículo científico publicado en 2020

An overview of Ensembl

artículo científico publicado en 2004

Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.

artículo científico publicado en 2007

Brief Report: Identification of a Pathogenic Variant in TREX1 in Early-Onset Cerebral Systemic Lupus Erythematosus by Whole-Exome Sequencing

artículo científico publicado en 2014

Comparison of predicted and actual consequences of missense mutations

artículo científico publicado en 2015

DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project

artículo científico publicado en 2004

DNA sequence and analysis of human chromosome 9

artículo científico publicado en 2004

Finding new immune regulatory genes by ENU mutagenesis

artículo científico publicado en 2012

Genome-wide dFOXO targets and topology of the transcriptomic response to stress and insulin signalling

artículo científico publicado en 2011

Interplay of dFOXO and two ETS-family transcription factors determines lifespan in Drosophila melanogaster

artículo científico publicado en 2014

Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models.

artículo científico publicado en 2012

Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren's syndrome

artículo científico publicado en 2015

Rasgrp1 mutation increases naive T-cell CD44 expression and drives mTOR-dependent accumulation of Helios⁺ T cells and autoantibodies.

artículo científico publicado en 2013

TLR7 gain-of-function genetic variation causes human lupus

artículo científico publicado en 2022

The DNA sequence and analysis of human chromosome 6

artículo científico publicado en 2003

The DNA sequence and biological annotation of human chromosome

artículo científico publicado en 2006

The RNA-binding protein hnRNPLL induces a T cell alternative splicing program delineated by differential intron retention in polyadenylated RNA.

artículo científico publicado en 2014

Understanding the immunological impact of the human mutation explosion ⬇️

artículo científico publicado el 16 de enero de 2013

Zinc-finger protein ZFP318 is essential for expression of IgD, the alternatively spliced Igh product made by mature B lymphocytes.

artículo científico publicado en 2014

Lista de obras de Dan Andrews

A high-resolution survey of deletion polymorphism in the human genome

Absence of mucosal-associated invariant T cells in a person with a homozygous point mutation in MR1

An overview of Ensembl

Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.

Brief Report: Identification of a Pathogenic Variant in TREX1 in Early-Onset Cerebral Systemic Lupus Erythematosus by Whole-Exome Sequencing

Comparison of predicted and actual consequences of missense mutations

DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project

DNA sequence and analysis of human chromosome 9

Finding new immune regulatory genes by ENU mutagenesis

Genome-wide dFOXO targets and topology of the transcriptomic response to stress and insulin signalling

Interplay of dFOXO and two ETS-family transcription factors determines lifespan in Drosophila melanogaster

Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models.

Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren's syndrome

Rasgrp1 mutation increases naive T-cell CD44 expression and drives mTOR-dependent accumulation of Helios⁺ T cells and autoantibodies.

TLR7 gain-of-function genetic variation causes human lupus

The DNA sequence and analysis of human chromosome 6

The DNA sequence and biological annotation of human chromosome

The RNA-binding protein hnRNPLL induces a T cell alternative splicing program delineated by differential intron retention in polyadenylated RNA.

Understanding the immunological impact of the human mutation explosion ⬇️

Zinc-finger protein ZFP318 is essential for expression of IgD, the alternatively spliced Igh product made by mature B lymphocytes.