Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hengjuan Sun"'
Autor:
Yi Huang, Xi Chen, Liming Bao, Ling Lu, Hengjuan Sun, Lan Yuan, Yongchen Yang, Xingjuan Wang, Lin Zou
Publikováno v:
Annals of hematology. 94(11)
T cell acute lymphoblastic leukemia (T-ALL) is an aggressive neoplasm for which there are currently no adequate biomarkers for developing risk-adapted therapeutic regimens to improve the treatment outcome. In this prospective study of 83 Chinese pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99bc85c5d9035e0ba82b4f30eea34528
https://pubmed.ncbi.nlm.nih.gov/26341754
https://pubmed.ncbi.nlm.nih.gov/26341754
Autor:
Yan Hu, Yongchen Yang, Liming Bao, Zhibao Lv, Yi Huang, Qian Cheng, Jing Yang, Hengjuan Sun, Xi Chen
Publikováno v:
BMC Medical Genetics
Background The proximal chromosome 15q is prone to unequal crossover, leading to rearrangements. Although 15q11q13 duplications are common in patients with developmental delays and mental impairment, 15q aneusomies resulting in greater or equal to 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::253ed00f1bf967df53e1db2e059d488d
https://doi.org/10.1186/1471-2350-14-9
https://doi.org/10.1186/1471-2350-14-9
Autor:
Pengjun Zhao, Liming Bao, Jian Wang, Xike Wang, Yuejuan Xu, Fen Li, Hengjuan Sun, Qi-Hua Fu, Jie Shen, Rang Xu, Kun Sun
Publikováno v:
BMC Medical Genetics, Vol 12, Iss 1, p 169 (2011)
BMC Medical Genetics
BMC Medical Genetics
Background Conotruncal heart defects (CTDs) are present in 75-85% of patients suffering from the 22q11.2 deletion syndrome. To date, no consistent phenotype has been consistently correlated with the 22q11.2 deletions. Genetic studies have implicated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2922a0a7e49bcd082d296496689b283
https://doi.org/10.1186/1471-2350-12-169
https://doi.org/10.1186/1471-2350-12-169
Autor:
Junmin Dai, Cuie Wu, Hejian Zou, Yongchen Yang, Minghua Gu, Hengjuan Sun, Guowei Lin, Hua Fu, Ling Lv, Xi Chen, Liming Bao, Xiang Gao
Publikováno v:
American journal of hematology. 86(2)
Risk factors of mydelodysplastic syndromes (MDS) remain largely unknown. We conducted a hospital-based case-control study consisting of 403 newly diagnosed MDS patients according to World Health Organization classification and 806 individually gender
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7683298b38a076ed4873162f793b443f
https://pubmed.ncbi.nlm.nih.gov/21264898
https://pubmed.ncbi.nlm.nih.gov/21264898
Autor:
Patrick J. Kerzic, Sherilyn A. Gross, Meirong Ji, Ling Lv, Guowei Lin, Yan Chen, Xinyu Du, Lihong Yao, Hui Chen, Hengjuan Sun, Richard D. Irons, Liming Bao, Yongchen Yang, Xiaoqin Wang, Hua Fu, John Ryder
Publikováno v:
European journal of haematology. 77(1)
We report a prospective study of 174 unselected adult de novo acute myeloid leukemia (AML) cases diagnosed using the WHO classification. Of those, 57 (33%) were AML with recurrent cytogenetic abnormalities, 41 were (24%) AML with multilineage dysplas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee9a742efee218fbc045bfb7095dd4c1
https://pubmed.ncbi.nlm.nih.gov/16573742
https://pubmed.ncbi.nlm.nih.gov/16573742
Publikováno v:
BMC Dermatology; 2014, Vol. 14 Issue 1, p1-15, 15p
Autor:
Richard D. Irons, Liming Bao, Xinyu Du, Guowei Lin, Yan Chen, Xiaoqin Wang, Jue Zhou, Sherilyn A. Gross, John Ryder, Hui Chen, Meirong Ji, Hengjuan Sun, Hua Fu
Publikováno v:
Leukemia research. 30(7)
The prevalence of subtypes of the myelodysplastic syndromes (MDS) was determined in a prospective series of 176 patients presenting at 28 Shanghai hospitals. Diagnosis was established in a single laboratory, analyzing morphologic, immunophenotypic, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f05cec38cb2c889dc19c51f0702f1209
https://pubmed.ncbi.nlm.nih.gov/16337268
https://pubmed.ncbi.nlm.nih.gov/16337268
Autor:
Jing Yang, Yongchen Yang, Yi Huang, Yan Hu, Xi Chen, Hengjuan Sun, Zhibao Lv, Qian Cheng, Liming Bao
Publikováno v:
BMC Medical Genetics; 2013, Vol. 14 Issue 1, p1-8, 8p, 2 Color Photographs, 2 Diagrams, 1 Chart
Autor:
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.
Publikováno v:
European Journal of Haematology; Jul2006, Vol. 77 Issue 1, p35-45, 11p, 7 Charts