Lista de obras -

Caspase recruitment domain (CARD) family (CARD9, CARD10, CARD11, CARD14 and CARD15) are increased during active inflammation in patients with inflammatory bowel disease.

artículo científico publicado en 2018

Differential Expression of IL-36 Family Members and IL-38 by Immune and Nonimmune Cells in Patients with Active Inflammatory Bowel Disease

artículo científico publicado en 2018

Differential Expression of MUC12, MUC16, and MUC20 in Patients with Active and Remission Ulcerative Colitis.

artículo científico publicado en 2015

Expression of interleukin (IL)-19 and IL-24 in inflammatory bowel disease patients: a cross-sectional study

artículo científico publicado en 2014

Gene Expression Profiling of Mediators Associated with the Inflammatory Pathways in the Intestinal Tissue from Patients with Ulcerative Colitis

artículo científico publicado en 2020

Gene and protein expression of centaurin beta 1 (CENTB1) are up-regulated in patients with ulcerative colitis ⬇️

artículo científico publicado el 11 de enero de 2013

Gene expression of carnitine organic cation transporters 1 and 2 (OCTN) is downregulated in patients with ulcerative colitis.

artículo científico publicado en 2010

Genetic Markers Associated with Clinical Outcomes in Patients with Inflammatory Bowel Disease.

artículo científico

High gene expression of MDR1 (ABCB1) is associated with medical treatment response and long-term remission in patients with ulcerative colitis.

artículo científico publicado en 2010

IL-10-- and IL-20--expressing epithelial and inflammatory cells are increased in patients with ulcerative colitis.

artículo científico publicado en 2012

Immunoregulatory Pathways Involved in Inflammatory Bowel Disease.

artículo científico

Increased expression of discs large homolog 5 gene (DLG5) in ulcerative colitis patients compared to healthy individuals.

artículo científico publicado en 2010

Indoleamine 2,3-dioxygenase: expressing cells in inflammatory bowel disease-a cross-sectional study.

artículo científico publicado en 2013

Interleukin 17 gene and protein expression are increased in patients with ulcerative colitis

artículo científico publicado el 14 de julio de 2011

Interleukin 21 expression is increased in rectal biopsies from patients with ulcerative colitis.

artículo científico publicado en 2010

Interleukin 27 is up-regulated in patients with active inflammatory bowel disease

artículo científico publicado en 2016

Interleukin 35 (IL-35) and IL-37: Intestinal and peripheral expression by T and B regulatory cells in patients with Inflammatory Bowel Disease

artículo científico publicado en 2015

Peroxisome proliferator-activated receptors family is involved in the response to treatment and mild clinical course in patients with ulcerative colitis

artículo científico publicado en 2014

Synthesis of Interleukin-10 in Patients with Ulcerative Colitis and Helicobacter pylori Infection

artículo científico publicado en 2020

TLR9 mRNA expression is upregulated in patients with active ulcerative colitis

article

TRPV Subfamily (TRPV2, TRPV3, TRPV4, TRPV5, and TRPV6) Gene and Protein Expression in Patients with Ulcerative Colitis

artículo científico publicado en 2020

The Transient Receptor Potential Vanilloid 1 Is Associated with Active Inflammation in Ulcerative Colitis

artículo científico publicado en 2018

TβRIII is induced by TCR signaling and downregulated in FoxP3+ regulatory T cells.

artículo científico publicado en 2017

Lista de obras de

Caspase recruitment domain (CARD) family (CARD9, CARD10, CARD11, CARD14 and CARD15) are increased during active inflammation in patients with inflammatory bowel disease.

Differential Expression of IL-36 Family Members and IL-38 by Immune and Nonimmune Cells in Patients with Active Inflammatory Bowel Disease

Differential Expression of MUC12, MUC16, and MUC20 in Patients with Active and Remission Ulcerative Colitis.

Expression of interleukin (IL)-19 and IL-24 in inflammatory bowel disease patients: a cross-sectional study

Gene Expression Profiling of Mediators Associated with the Inflammatory Pathways in the Intestinal Tissue from Patients with Ulcerative Colitis

Gene and protein expression of centaurin beta 1 (CENTB1) are up-regulated in patients with ulcerative colitis ⬇️

Gene expression of carnitine organic cation transporters 1 and 2 (OCTN) is downregulated in patients with ulcerative colitis.

Genetic Markers Associated with Clinical Outcomes in Patients with Inflammatory Bowel Disease.

High gene expression of MDR1 (ABCB1) is associated with medical treatment response and long-term remission in patients with ulcerative colitis.

IL-10-- and IL-20--expressing epithelial and inflammatory cells are increased in patients with ulcerative colitis.

Immunoregulatory Pathways Involved in Inflammatory Bowel Disease.

Increased expression of discs large homolog 5 gene (DLG5) in ulcerative colitis patients compared to healthy individuals.

Indoleamine 2,3-dioxygenase: expressing cells in inflammatory bowel disease-a cross-sectional study.

Interleukin 17 gene and protein expression are increased in patients with ulcerative colitis

Interleukin 21 expression is increased in rectal biopsies from patients with ulcerative colitis.

Interleukin 27 is up-regulated in patients with active inflammatory bowel disease

Interleukin 35 (IL-35) and IL-37: Intestinal and peripheral expression by T and B regulatory cells in patients with Inflammatory Bowel Disease

Peroxisome proliferator-activated receptors family is involved in the response to treatment and mild clinical course in patients with ulcerative colitis

Synthesis of Interleukin-10 in Patients with Ulcerative Colitis and Helicobacter pylori Infection

TLR9 mRNA expression is upregulated in patients with active ulcerative colitis

TRPV Subfamily (TRPV2, TRPV3, TRPV4, TRPV5, and TRPV6) Gene and Protein Expression in Patients with Ulcerative Colitis

The Transient Receptor Potential Vanilloid 1 Is Associated with Active Inflammation in Ulcerative Colitis

TβRIII is induced by TCR signaling and downregulated in FoxP3+ regulatory T cells.