Decheng Cai

Guangzhou, China

Last Updated: 09/26/2026

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Found 14 publications

Relationship between interleukin-37 genetic polymorphisms and HBV-related liver disease in a Chinese Han cohort.

Relationship between interleukin-37 genetic polymorphisms and HBV-related liver disease in a Chinese Han cohort.

Journal: Journal of applied biomedicine
Published: January 24, 2025

Relationship Between Polymorphism of Thrombin-Activatable Fibrinolysis Inhibitor Gene +1040C/T and a Cohort of Chinese Women With Recurrent Spontaneous Abortion.

Relationship Between Polymorphism of Thrombin-Activatable Fibrinolysis Inhibitor Gene +1040C/T and a Cohort of Chinese Women With Recurrent Spontaneous Abortion.

Journal: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
Published: June 30, 2021

VPS4B deficiency causes early embryonic lethality and induces signal transduction disorders of cell endocytosis.

VPS4B deficiency causes early embryonic lethality and induces signal transduction disorders of cell endocytosis.

Journal: Genesis (New York, N.Y. : 2000)
Published: November 12, 2020

Unusual survival of a twin with homozygous α0-thalassemia due to Chimerism.

Unusual survival of a twin with homozygous α0-thalassemia due to Chimerism.

Journal: Haematologica
Published: June 29, 2020

APC c.4621C>T variant causing Gardner's syndrome in a Han Chinese family may be inherited through maternal mosaicism.

APC c.4621C>T variant causing Gardner's syndrome in a Han Chinese family may be inherited through maternal mosaicism.

Journal: Experimental and therapeutic medicine
Published: June 20, 2020

Evaluation of plasma D-dimer for the diagnosis in Chinese patients with hepatocellular carcinoma: A meta-analysis.

Evaluation of plasma D-dimer for the diagnosis in Chinese patients with hepatocellular carcinoma: A meta-analysis.

Journal: Medicine
Published: March 21, 2020

A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis.

A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis.

Journal: Gene
Published: September 02, 2019

A combination of the (αα)GZ and --SEA deletions causing a severe form of hemoglobin H disease.

A combination of the (αα)GZ and --SEA deletions causing a severe form of hemoglobin H disease.

Journal: International journal of laboratory hematology
Published: June 10, 2019

A novel 223 kb deletion in the beta-globin gene cluster was identified in a Chinese thalassemia major patient.

A novel 223 kb deletion in the beta-globin gene cluster was identified in a Chinese thalassemia major patient.

Journal: International journal of laboratory hematology
Published: January 24, 2019

Thalassaemia intermedia caused by coinheritance of a β-thalassaemia mutation and a de novo duplication of α-globin genes in the paternal allele.

Thalassaemia intermedia caused by coinheritance of a β-thalassaemia mutation and a de novo duplication of α-globin genes in the paternal allele.

Journal: British journal of haematology
Published: January 01, 2019

A case report of heterozygous TINF2 gene mutation associated with pulmonary fibrosis in a patient with dyskeratosis congenita.

A case report of heterozygous TINF2 gene mutation associated with pulmonary fibrosis in a patient with dyskeratosis congenita.

Journal: Medicine
Published: May 10, 2018

Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders.

Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders.

Journal: International journal of oral science
Published: January 18, 2018
Showing 1-12 of 14

Last Updated: 09/26/2026