Works matching AU Yongchen Yang

Results: 14

A multiplex ligation-dependent probe amplification-based next-generation sequencing approach for the detection of copy number variations in the human genome.

Published in:

Molecular Medicine Reports, 2018, v. 18, n. 6, p. 5823, doi. 10.3892/mmr.2018.9581

By:

Yang, Yongchen;
Xia, Chaoran;
Zhou, Zaiwei;
Wei, Dongkai;
Xu, Kangping;
Jia, Jia;
Xu, Wuhen;
Zhang, Hong

Publication type:

Article

Combined 677CC/1298AC genotypes of methylenetetrahydrofolate reductase ( MTHFR ) reduce susceptibility to precursor B lymphoblastic leukemia in a Chinese population.

Published in:

European Journal of Haematology, 2010, v. 84, n. 6, p. 506, doi. 10.1111/j.1600-0609.2010.01430.x

By:

Ling Lv;
Cuie Wu;
Henjuan Sun;
Saijuan Zhu;
Yongchen Yang;
Xi Chen;
Hua Fu;
Liming Bao

Publication type:

Article

Prospective study of 174 de novo acute myelogenous leukemias according to the WHO classification: subtypes, cytogenetic features and FLT3 mutations.

Published in:

European Journal of Haematology, 2006, v. 77, n. 1, p. 35, doi. 10.1111/j.1600-0609.2006.00660.x

By:

Liming Bao;
Xiaoqin Wang;
Ryder, John;
Meirong Ji;
Yan Chen;
Hui Chen;
Hengjuan Sun;
Yongchen Yang;
Xinyu Du;
Kerzic, Patrick;
Gross, Sherilyn A.;
Lihong Yao;
Ling Lv;
Hua Fu;
Guowei Lin;
Irons, Richard D.

Publication type:

Article

Adult precursor B lymphoblastic leukemia in Shanghai, China: characterization of phenotype, cytogenetics and outcome for 137 consecutive cases.

Published in:

2009

By:

Bao, Liming;
Gross, Sherilyn;
Ryder, John;
Wang, Xiaoqin;
Ji, Meirong;
Chen, Yan;
Yang, Yongchen;
Zhu, Saijuan;
Irons, Richard;
Gross, Sherilyn A;
Irons, Richard D

Publication type:

journal article

Case-control study of risk factors of myelodysplastic syndromes according to World Health Organization classification in a Chinese population.

Published in:

American Journal of Hematology, 2011, v. 86, n. 2, p. 163, doi. 10.1002/ajh.21941

By:

Lv, Ling;
Lin, Guowei;
Gao, Xiang;
Wu, Cuie;
Dai, Junmin;
Yang, Yongchen;
Zou, Hejian;
Sun, Hengjuan;
Gu, Minghua;
Chen, Xi;
Fu, Hua;
Bao, Liming

Publication type:

Article

WT1 mutations and single nucleotide polymorphism rs16754 analysis of patients with pediatric acute myeloid leukemia in a Chinese population.

Published in:

Leukemia & Lymphoma, 2012, v. 53, n. 11, p. 2195, doi. 10.3109/10428194.2012.685732

By:

Chen, Xi;
Yang, Yongchen;
Huang, Yi;
Tan, Junjie;
Chen, Yuanyuan;
Yang, Jing;
Dou, Hu;
Zou, Lin;
Yu, Jie;
Bao, Liming

Publication type:

Article

HLA class II alleles may influence susceptibility to adult dermatomyositis and polymyositis in a Han Chinese population.

Published in:

BMC Dermatology, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-5945-14-9

By:

Xiang Gao;
Lei Han;
Lan Yuan;
Yongchen Yang;
Guimei Gou;
Hengjuan Sun;
Ling Lu;
Liming Bao

Publication type:

Article

HLA class II alleles may influence susceptibility to adult dermatomyositis and polymyositis in a Han Chinese population.

Published in:

2014

By:

Gao, Xiang;
Han, Lei;
Yuan, Lan;
Yang, Yongchen;
Gou, Guimei;
Sun, Hengjuan;
Lu, Ling;
Bao, Liming

Publication type:

journal article

Applications of BIM, Cloud Computing and Internet of Things Technology in Full Life Cycle of Bridges.

Published in:

Railway Standard Design, 2022, v. 66, n. 12, p. 78, doi. 10.13238/j.issn.1004-2954.202110090003

By:

WANG Qinghe;
LIU Ruixin;
SUN Liye;
YANG Yongchen

Publication type:

Article

Genetic mutational profiling analysis of T cell acute lymphoblastic leukemia reveal mutant FBXW7 as a prognostic indicator for inferior survival.

Published in:

2015

By:

Yuan, Lan;
Lu, Ling;
Yang, Yongchen;
Sun, Hengjuan;
Chen, Xi;
Huang, Yi;
Wang, Xingjuan;
Zou, Lin;
Bao, Liming

Publication type:

journal article

Diagnostic Utility of Trio–Exome Sequencing for Children With Neurodevelopmental Disorders.

Published in:

JAMA Network Open, 2025, v. 8, n. 3, p. e251807, doi. 10.1001/jamanetworkopen.2025.1807

By:

Lan, Xiaoping;
Tang, Xiaojun;
Weng, Wenhao;
Xu, Wuhen;
Song, Xiaozhen;
Yang, Yongchen;
Sun, Hong;
Ye, Haiyun;
Zhang, Hong;
Yu, Guangjun;
Wu, Shengnan

Publication type:

Article

Origin of the X-chromosome influences the development and treatment outcomes of Turner syndrome.

Published in:

PeerJ, 2021, p. 1, doi. 10.7717/peerj.12354

By:

Ying Zhang;
Yongchen Yang;
Pin Li;
Sheng Guo

Publication type:

Article

A study of two Chinese patients with tetrasomy and pentasomy 15q11q13 including Prader-Willi/ Angelman syndrome critical region present with developmental delays and mental impairment.

Published in:

BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-9

By:

Jing Yang;
Yongchen Yang;
Yi Huang;
Yan Hu;
Xi Chen;
Hengjuan Sun;
Zhibao Lv;
Qian Cheng;
Liming Bao

Publication type:

Article

Application of a Multiplex Ligation-Dependent Probe Amplification-Based Next-Generation Sequencing Approach for the Detection of Pathogenesis of Duchenne Muscular Dystrophy and Spinal Muscular Atrophy Caused by Copy Number Aberrations.

Published in:

Molecular Neurobiology, 2024, v. 61, n. 1, p. 200, doi. 10.1007/s12035-023-03572-9

By:

Yang, Yongchen;
Xia, Chaoran;
Song, Xiaozhen;
Tang, Xiaojun;
Nie, Xueling;
Xu, Wuhen;
Du, Chengkan;
Zhang, Hong;
Luo, Peng

Publication type:

Article