Yangyang Wu

Key Laboratory Of Clinical Laboratory Medicine Of Guangxi Department Of Education
Nanning, China

Last Updated: 09/26/2026

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Found 16 publications

Congenital hypofibrinogenemia with bleeding risk: mutations in the FGA, FGB, and FGG genes.

Congenital hypofibrinogenemia with bleeding risk: mutations in the FGA, FGB, and FGG genes.

Journal: Laboratory medicine

Published: November 14, 2025

Direct and indirect regulation of bone metabolism by lactoferrin.

Direct and indirect regulation of bone metabolism by lactoferrin.

Journal: Frontiers in endocrinology

Published: July 09, 2025

Responses of the mud snail Cipangopaludina cathayensis to thermal stress: Insights from metabolism, oxidative stress damage, and hepatopancreas transcriptional modulation.

Responses of the mud snail Cipangopaludina cathayensis to thermal stress: Insights from metabolism, oxidative stress damage, and hepatopancreas transcriptional modulation.

Journal: Comparative biochemistry and physiology. Part D, Genomics & proteomics

Published: October 30, 2024

The β-Chain Mutation p.Arg17Stop Impairs Fibrinogen Synthesis and Secretion: A Nonsense Mutation Associated With Hypofibrinogenemia.

The β-Chain Mutation p.Arg17Stop Impairs Fibrinogen Synthesis and Secretion: A Nonsense Mutation Associated With Hypofibrinogenemia.

Journal: Journal of clinical laboratory analysis

Published: September 05, 2024

Genetic mutation analysis of hereditary spherocytosis in Guangxi Zhuang Autonomous Region.

Genetic mutation analysis of hereditary spherocytosis in Guangxi Zhuang Autonomous Region.

Journal: Journal of hematopathology

Published: September 21, 2022

Adaptive Responses of the Sea Anemone Heteractis crispa to the Interaction of Acidification and Global Warming.

Adaptive Responses of the Sea Anemone Heteractis crispa to the Interaction of Acidification and Global Warming.

Journal: Animals : an open access journal from MDPI

Published: August 09, 2022

Congenital dysfibrinogenemia in major surgery: A description of four cases and review of the literature.

Congenital dysfibrinogenemia in major surgery: A description of four cases and review of the literature.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: December 14, 2021

The diagnostic protocol for hereditary spherocytosis-2021 update.

The diagnostic protocol for hereditary spherocytosis-2021 update.

Journal: Journal of clinical laboratory analysis

Published: June 27, 2021

A novel fibrinogen γ-chain frameshift mutation, p. Cys365Phefs*41, causing hypofibrinogenemia with bleeding phenotype in a Chinese family.

A novel fibrinogen γ-chain frameshift mutation, p. Cys365Phefs*41, causing hypofibrinogenemia with bleeding phenotype in a Chinese family.

Journal: Annals of translational medicine

Published: June 02, 2021

Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D region.

Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D region.

Journal: Hematology (Amsterdam, Netherlands)

Published: March 05, 2021

Ameliorative effect and mechanism of Yi-Suan-Cha against hyperuricemia in rats.

Ameliorative effect and mechanism of Yi-Suan-Cha against hyperuricemia in rats.

Journal: Journal of clinical laboratory analysis

Published: February 06, 2021

The β-chain mutation p.Trp433Stop impairs fibrinogen secretion: A novel nonsense mutation associated with hypofibrinogenemia.

The β-chain mutation p.Trp433Stop impairs fibrinogen secretion: A novel nonsense mutation associated with hypofibrinogenemia.

Journal: International journal of laboratory hematology

Published: December 08, 2020

Showing 1-12 of 16

Last Updated: 09/26/2026