Related Experiment Videos
[Gene analysis of congenital platelet disorders]
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
A unique phenotype of acquired Glanzmann thrombasthenia due to non-function-blocking anti-αIIbβ3 autoantibodies.
Journal of thrombosis and haemostasis : JTH·2018
Mcl-1 and Bcl-xL regulate Bak/Bax-dependent apoptosis of the megakaryocytic lineage at multistages.
Cell death and differentiation·2012
A lower starting dose of eltrombopag is efficacious in Japanese patients with previously treated chronic immune thrombocytopenia.
Journal of thrombosis and haemostasis : JTH·2012
Uneven distribution of the luxS gene within the genus Campylobacter.
British journal of biomedical science·2011
Bleeding tendency and impaired platelet function in a patient carrying a heterozygous mutation in the thromboxane A2 receptor.
Journal of thrombosis and haemostasis : JTH·2011
Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.
Journal of genetics and genomics = Yi chuan xue bao·2026
Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.
Clinica chimica acta; international journal of clinical chemistry·2026
High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.
The Journal of heredity·2026
Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.
Pediatrics international : official journal of the Japan Pediatric Society·2026