Shuai Guo
Changsha, China
Last Updated: 09/26/2026
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Found 12 publications
Genetic predisposition to immune dysregulation and extracellular matrix remodeling in cardiac arrhythmia reveals potential mediation by SPP1+ macrophages.
Journal: Frontiers in cell and developmental biology
Published: April 14, 2025
Integrated Analysis of WES and scRNA-Seq Data Reveals the Genetic Basis of Immune Dysregulation in Unexplained Recurrent Pregnancy Loss.
Journal: Journal of clinical laboratory analysis
Published: December 23, 2023
Genetic analysis combined with 3D-printing assistant surgery in diagnosis and treatment for an X-linked hypophosphatemia patient.
Journal: Journal of clinical laboratory analysis
Published: October 14, 2021
Effect of Minor Er Additions on the Microstructures and Mechanical Properties of Cast Al-Cu-Mg-Ag Alloys.
Journal: Materials (Basel, Switzerland)
Published: June 21, 2021
Whole Exome Sequencing Identified a 13 Base Pair MYH7 Deletion-mutation in a Patient with Restrictive Cardiomyopathy and Left Ventricle Hypertrophy.
Journal: Annals of clinical and laboratory science
Published: December 29, 2019
Increased Reticulon 3 (RTN3) Leads to Obesity and Hypertriglyceridemia by Interacting With Heat Shock Protein Family A (Hsp70) Member 5 (HSPA5).
Journal: Circulation
Published: May 03, 2018
Whole-exome sequencing identifies a Novel SCN5A mutation (C335R) in a Chinese family with arrhythmia.
Journal: Cardiology in the young
Published: February 07, 2018
Microduplications of 10q24 Detected in Two Chinese Patients with Split-hand/foot Malformation Type 3.
Journal: Annals of clinical and laboratory science
Published: December 22, 2017
A novel proximal 3q29 chromosome microdeletion in a Chinese patient with Chiari malformation type II and Sprengel's deformity.
Journal: Molecular cytogenetics
Published: October 20, 2017
Microduplication of 10q26.3 in a Chinese hypertriglyceridemia patient.
Journal: Molecular and cellular probes
Published: June 09, 2017
Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death.
Journal: Journal of cellular and molecular medicine
Published: May 25, 2017
Showing 1-12 of 12
Last Updated: 09/26/2026