Hannah H. Chen

Oxford, ENG OX39DS, United Kingdom

Last Updated: 09/26/2026

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Found 9 publications

Tracking in situ checkpoint inhibitor-bound target T cells in patients with checkpoint-induced colitis.

Tracking in situ checkpoint inhibitor-bound target T cells in patients with checkpoint-induced colitis.

Journal: Cancer cell
Published: May 23, 2023

BCG Vaccine-Associated Complications in Patients with PTEN Hamartoma Tumor Syndrome.

BCG Vaccine-Associated Complications in Patients with PTEN Hamartoma Tumor Syndrome.

Journal: Journal of clinical immunology
Published: February 23, 2021

Use of synthesized double-stranded gene fragments as qPCR standards for the quantification of antibiotic resistance genes.

Use of synthesized double-stranded gene fragments as qPCR standards for the quantification of antibiotic resistance genes.

Journal: Journal of microbiological methods
Published: May 07, 2019

Becalming Type 17 Inflammation in Ulcerative Colitis.

Becalming Type 17 Inflammation in Ulcerative Colitis.

Journal: Immunity
Published: April 18, 2019

Colonic epithelial cell diversity in health and inflammatory bowel disease.

Colonic epithelial cell diversity in health and inflammatory bowel disease.

Journal: Nature
Published: July 07, 2018

Structural Remodeling of the Human Colonic Mesenchyme in Inflammatory Bowel Disease.

Structural Remodeling of the Human Colonic Mesenchyme in Inflammatory Bowel Disease.

Journal: Cell
Published: November 23, 2017

Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells.

Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells.

Journal: The Journal of allergy and clinical immunology
Published: July 17, 2015

A recessive form of extreme macrocephaly and mild intellectual disability complements the spectrum of PTEN hamartoma tumour syndrome.

A recessive form of extreme macrocephaly and mild intellectual disability complements the spectrum of PTEN hamartoma tumour syndrome.

Journal: European journal of human genetics : EJHG
Published: October 09, 2014

Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease.

Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease.

Journal: Gastroenterology
Published: October 02, 2013
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Last Updated: 09/26/2026