Chunbao X. Rao
Dongguan, China
Last Updated: 09/26/2026
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Found 23 publications
The Ednrb-Aim2-AKT axis regulates neural crest-derived melanoblast proliferation during early development.
Journal: Development (Cambridge, England)
Published: October 26, 2023
Case Report: A Novel Intronic Mutation in AIFM1 Associated With Fatal Encephalomyopathy and Mitochondrial Disease in Infant.
Journal: Frontiers in pediatrics
Published: March 03, 2022
BVVLS2 overlooked for 3 years in a pediatric patient caused by novel compound heterozygous mutations in SLC52A2 gene.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: September 01, 2021
Raised SPINK1 levels play a role in angiogenesis and the transendothelial migration of ALL cells.
Journal: Scientific reports
Published: August 11, 2021
A Novel IRF6 Frameshift Mutation in a Large Chinese Pedigree With Van der Woude syndrome.
Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
Published: April 28, 2021
A targeted gene capture next-generation sequencing panel for genetic screening of newborns.
Journal: JPMA. The Journal of the Pakistan Medical Association
Published: November 07, 2020
Molecular epidemiological and hematological profile of thalassemia in the Dongguan Region of Guangdong Province, Southern China.
Journal: Journal of clinical laboratory analysis
Published: May 21, 2020
A novel nonsense mutation of ZEB2 gene in a Chinese patient with Mowat-Wilson syndrome.
Journal: Journal of clinical laboratory analysis
Published: March 25, 2020
A molecular-beacon-based asymmetric PCR assay for detecting polymorphisms related to folate metabolism.
Journal: Journal of clinical laboratory analysis
Published: January 30, 2020
Differential expression of peptides serves as an indicator of IgA nephropathy in pediatric patients.
Differential expression of peptides serves as an indicator of IgA nephropathy in pediatric patients.
Journal: Experimental and therapeutic medicine
Published: March 15, 2019
A novel homozygous initiation codon variant associated with infantile alpha-Bcrystallinopathy in a Chinese family.
Journal: Molecular genetics & genomic medicine
Published: February 28, 2019
Last Updated: 09/26/2026