Xiaoning Liu

Kunming, China

Last Updated: 09/26/2026

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Found 9 publications

ICF Syndrome in Chinese Children: Four Case Reports with Novel Mutations.

ICF Syndrome in Chinese Children: Four Case Reports with Novel Mutations.

Journal: Genetic testing and molecular biomarkers

Published: June 24, 2026

A novel mutation in the STK4 gene (Serine/threonine kinase 4) in a Chinese Blang child.

A novel mutation in the STK4 gene (Serine/threonine kinase 4) in a Chinese Blang child.

Journal: Immunology letters

Published: November 06, 2025

LC3B as a potential serum biomarker for screening high-risk neuroblastoma patients.

LC3B as a potential serum biomarker for screening high-risk neuroblastoma patients.

Journal: Acta neurologica Belgica

Published: October 30, 2025

β2-Microglobulin: A potential novel prognostic indicator for neuroblastoma.

β2-Microglobulin: A potential novel prognostic indicator for neuroblastoma.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: April 29, 2025

Epstein-Barr virus downregulates the α7 nicotinic acetylcholine receptor of CD8+ T lymphocytes might associate with coronary artery lesions in Kawasaki disease patients.

Epstein-Barr virus downregulates the α7 nicotinic acetylcholine receptor of CD8+ T lymphocytes might associate with coronary artery lesions in Kawasaki disease patients.

Journal: Microbes and infection

Published: March 07, 2023

Clinical and genetic analysis of 2 rare cases of Wiskott-Aldrich syndrome from Chinese minorities: Two case reports.

Clinical and genetic analysis of 2 rare cases of Wiskott-Aldrich syndrome from Chinese minorities: Two case reports.

Journal: Medicine

Published: January 23, 2021

Two novel mutations of the LPL gene in two Chinese family cases with familial chylomicronemia syndrome.

Two novel mutations of the LPL gene in two Chinese family cases with familial chylomicronemia syndrome.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: January 05, 2021

A novel homozygous mutation of the PCNT gene in a Chinese patient with microcephalic osteodysplastic primordial dwarfism type II.

A novel homozygous mutation of the PCNT gene in a Chinese patient with microcephalic osteodysplastic primordial dwarfism type II.

Journal: Molecular genetics & genomic medicine

Published: June 27, 2020

A novel mutation of the ITGB2 gene in a Chinese Zhuang minority patient with leukocyte adhesion deficiency type 1 and glucose-6-phosphate dehydrogenase deficiency.

A novel mutation of the ITGB2 gene in a Chinese Zhuang minority patient with leukocyte adhesion deficiency type 1 and glucose-6-phosphate dehydrogenase deficiency.

Journal: Gene

Published: May 28, 2019

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Last Updated: 09/26/2026