Lista de obras - Adam P. Levine - Dominio Público Uruguay

A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSF.

artículo científico publicado en 2016

A New Look at Familial Risk of Inflammatory Bowel Disease in the Ashkenazi Jewish Population

artículo científico publicado en 2018

Alkalinity of neutrophil phagocytic vacuoles is modulated by HVCN1 and has consequences for myeloperoxidase activity

artículo científico publicado en 2015

An Exploration of Charge Compensating Ion Channels across the Phagocytic Vacuole of Neutrophils

artículo científico publicado en 2017

Characterization of expression quantitative trait loci in the human colon

artículo científico publicado en 2015

Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies.

artículo científico publicado en 2015

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

correction of a scientific article; published on 30 May 2019

Corrigendum: An Exploration of Charge Compensating Ion Channels across the Phagocytic Vacuole of Neutrophils.

artículo científico publicado en 2017

Defective tumor necrosis factor release from Crohn's disease macrophages in response to Toll-like receptor activation: relationship to phenotype and genome-wide association susceptibility loci

artículo científico publicado en 2012

Disruption of macrophage pro-inflammatory cytokine release in Crohn's disease is associated with reduced optineurin expression in a subset of patients

artículo científico publicado en 2015

Elevation in Cell Cycle and Protein Metabolism Gene Transcription in Inactive Colonic Tissue From Icelandic Patients With Ulcerative Colitis

article

Endoscopy, but not as we know it

artículo científico publicado en 2011

Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease

artículo científico publicado en 2018

Galactosylation of IgA1 Is Associated with Common Variation in C1GALT1.

artículo científico publicado en 2017

Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families

artículo científico publicado en 2016

Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome

scientific article published on 01 July 2019

Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients

artículo científico publicado en 2023

Imaging the Neutrophil Phagosome and Cytoplasm Using a Ratiometric pH Indicator.

artículo científico publicado en 2017

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

preprint published 25 September 2016

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

artículo científico publicado en 2018

Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy

artículo científico publicado en 2020

Mucosal transcriptomics implicates under expression of BRINP3 in the pathogenesis of ulcerative colitis

artículo científico publicado en 2014

Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease

scientific article published on 22 August 2018

Seqfam: A python package for analysis of Next Generation Sequencing DNA data in families

The Human Salivary Microbiome Is Shaped by Shared Environment Rather than Genetics: Evidence from a Large Family of Closely Related Individuals.

artículo científico publicado en 2017

The LRRC8A Mediated "Swell Activated" Chloride Conductance Is Dispensable for Vacuolar Homeostasis in Neutrophils

artículo científico publicado en 2017

The NADPH Oxidase and Microbial Killing by Neutrophils, With a Particular Emphasis on the Proposed Antimicrobial Role of Myeloperoxidase within the Phagocytic Vacuole

artículo científico publicado en 2016

The human oral microbiome is shaped by shared environment rather than genetics: evidence from a large family of closely-related individuals

article

Using genetic prediction from known complex disease Loci to guide the design of next-generation sequencing experiments

artículo científico publicado en 2013

What is wrong with granulocytes in inflammatory bowel diseases?

artículo científico publicado en 2013

Whole-genome sequencing of patients with rare diseases in a national health system

artículo científico publicado en 2020

ZODET: software for the identification, analysis and visualisation of outlier genes in microarray expression data

artículo científico publicado en 2014

Lista de obras de Adam P. Levine

A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSF.

A New Look at Familial Risk of Inflammatory Bowel Disease in the Ashkenazi Jewish Population

Alkalinity of neutrophil phagocytic vacuoles is modulated by HVCN1 and has consequences for myeloperoxidase activity

An Exploration of Charge Compensating Ion Channels across the Phagocytic Vacuole of Neutrophils

Characterization of expression quantitative trait loci in the human colon

Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies.

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Corrigendum: An Exploration of Charge Compensating Ion Channels across the Phagocytic Vacuole of Neutrophils.

Defective tumor necrosis factor release from Crohn's disease macrophages in response to Toll-like receptor activation: relationship to phenotype and genome-wide association susceptibility loci

Disruption of macrophage pro-inflammatory cytokine release in Crohn's disease is associated with reduced optineurin expression in a subset of patients

Elevation in Cell Cycle and Protein Metabolism Gene Transcription in Inactive Colonic Tissue From Icelandic Patients With Ulcerative Colitis

Endoscopy, but not as we know it

Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease

Galactosylation of IgA1 Is Associated with Common Variation in C1GALT1.

Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families

Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome

Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients

Imaging the Neutrophil Phagosome and Cytoplasm Using a Ratiometric pH Indicator.

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy

Mucosal transcriptomics implicates under expression of BRINP3 in the pathogenesis of ulcerative colitis

Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease

Seqfam: A python package for analysis of Next Generation Sequencing DNA data in families

The Human Salivary Microbiome Is Shaped by Shared Environment Rather than Genetics: Evidence from a Large Family of Closely Related Individuals.

The LRRC8A Mediated "Swell Activated" Chloride Conductance Is Dispensable for Vacuolar Homeostasis in Neutrophils

The NADPH Oxidase and Microbial Killing by Neutrophils, With a Particular Emphasis on the Proposed Antimicrobial Role of Myeloperoxidase within the Phagocytic Vacuole

The human oral microbiome is shaped by shared environment rather than genetics: evidence from a large family of closely-related individuals

Using genetic prediction from known complex disease Loci to guide the design of next-generation sequencing experiments

What is wrong with granulocytes in inflammatory bowel diseases?

Whole-genome sequencing of patients with rare diseases in a national health system

ZODET: software for the identification, analysis and visualisation of outlier genes in microarray expression data