Ming-yang Deng

Changsha, 410011, China

Last Updated: 09/26/2026

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Found 8 publications

Xenopax for the treatment of steroid-refractory acute graft-versus-host disease: the RELAX study.

Xenopax for the treatment of steroid-refractory acute graft-versus-host disease: the RELAX study.

Journal: Military Medical Research

Published: December 02, 2024

The novel HLA-B*48:01:11 allele, identified by Sanger dideoxy nucleotide sequencing in a Chinese individual.

The novel HLA-B*48:01:11 allele, identified by Sanger dideoxy nucleotide sequencing in a Chinese individual.

Journal: HLA

Published: November 30, 2022

Relationship between TET2 Gene SNP rs3733609 C/T and JAK2V617F Allele Burden in Patients with Myeloproliferative Neoplasms

Relationship between TET2 Gene SNP rs3733609 C/T and JAK2V617F Allele Burden in Patients with Myeloproliferative Neoplasms

Journal: Zhongguo shi yan xue ye xue za zhi

Published: October 15, 2019

Two novel compound heterozygous mutations associated with types I and II protein C deficiency with unusual phenotypes.

Two novel compound heterozygous mutations associated with types I and II protein C deficiency with unusual phenotypes.

Journal: Thrombosis research

Published: April 26, 2016

A TET2 rs3733609 C/T genotype is associated with predisposition to the myeloproliferative neoplasms harboring JAK2(V617F) and confers a proliferative potential on erythroid lineages.

A TET2 rs3733609 C/T genotype is associated with predisposition to the myeloproliferative neoplasms harboring JAK2(V617F) and confers a proliferative potential on erythroid lineages.

Journal: Oncotarget

Published: August 19, 2015

Thrombotic thrombocytopenic purpura as initial and major presentation of multiple myeloma.

Thrombotic thrombocytopenic purpura as initial and major presentation of multiple myeloma.

Journal: Journal of thrombosis and thrombolysis

Published: February 12, 2013

Analysis of clinical and laboratory characteristics in 42 patients with thrombotic thrombocytopenic purpura from a single center in China.

Analysis of clinical and laboratory characteristics in 42 patients with thrombotic thrombocytopenic purpura from a single center in China.

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: April 30, 2012

An intron mutation in the ACVRL1 may be associated with a transcriptional regulation defect in a Chinese family with hereditary hemorrhagic telangiectasia.

An intron mutation in the ACVRL1 may be associated with a transcriptional regulation defect in a Chinese family with hereditary hemorrhagic telangiectasia.

Journal: PloS one

Published: November 27, 2011

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Last Updated: 09/26/2026