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Experimental and Therapeutic Medicine
|
December 2, 2015
Microgranular variant of acute promyelocytic leukemia with der(17) ins(17;15): A case report and review of the literature
Hongzai Guan, Jing Liu, Xiaofang Guo, et al.
International Journal of Oncology
|
May 17, 2024
Investigating the molecular mechanisms of microRNA‑409‑3p in tumor progression: Towards targeted therapeutics (Review)
Wenjie Xie, Zhichao Wang, Junke Wang, et al.
Neuroscience Letters
|
August 24, 2017
Lack of association between SLC5A7 polymorphisms and Tourette syndrome in a Chinese Han population
Wenmiao Liu, Shiyan Qiu, Chuanping Gao, et al.
Experimental and Therapeutic Medicine
|
October 19, 2017
Overexpression of dominant-negative Ikaros 6 isoform is associated with resistance to TKIs in patients with Philadelphia chromosome positive acute lymphoblastic leukemia
Changfeng Shao, Jie Yang, Yirong Kong, et al.
Hematology (Amsterdam, Netherlands)
|
November 4, 2017
Identification of a de novo ANK1 mutation in a Chinese family with hereditary spherocytosis
Hongzai Guan, Xinping Liang, Rong Zhang, et al.
Genetic Testing and Molecular Biomarkers
|
April 29, 2014
Evaluation of MYOC, ACAN, HGF, and MET as candidate genes for high myopia in a Han Chinese population
Xian Yang, Xiaoqi Liu, Jie Peng, et al.
Pregnancy Hypertension
|
September 6, 2019
Value of ABCG2 Q141K and Q126X genotyping in predicting risk of preeclampsia in Chinese Han women population
Huabin Hou, Meiyun Geng, Ru Zhang, et al.
Frontiers of Medicine
|
May 28, 2017
Philadelphia chromosome-positive acute myeloid leukemia with masses and osteolytic lesions: finding of 18F-FDG PET/CT
Zhan Su, Fengyu Wu, Weiyu Hu, et al.
Molecular Vision
|
November 3, 2010
KIF21A mutations in two Chinese families with congenital fibrosis of the extraocular muscles (CFEOM)
Xian Yang, Koki Yamada, Bradley Katz, et al.
Molecular Psychiatry
|
November 2, 2019
Mutations in ASH1L confer susceptibility to Tourette syndrome
Shiguo Liu, Miaomiao Tian, Fan He, et al.
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Showing results (11-20 of 20) with videos related to
Sort By:
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You have reached the last page of results.
This site can display upto 20 results.
Experimental and Therapeutic Medicine
|
December 2, 2015
Microgranular variant of acute promyelocytic leukemia with der(17) ins(17;15): A case report and review of the literature
Hongzai Guan, Jing Liu, Xiaofang Guo, et al.
International Journal of Oncology
|
May 17, 2024
Investigating the molecular mechanisms of microRNA‑409‑3p in tumor progression: Towards targeted therapeutics (Review)
Wenjie Xie, Zhichao Wang, Junke Wang, et al.
Neuroscience Letters
|
August 24, 2017
Lack of association between SLC5A7 polymorphisms and Tourette syndrome in a Chinese Han population
Wenmiao Liu, Shiyan Qiu, Chuanping Gao, et al.
Experimental and Therapeutic Medicine
|
October 19, 2017
Overexpression of dominant-negative Ikaros 6 isoform is associated with resistance to TKIs in patients with Philadelphia chromosome positive acute lymphoblastic leukemia
Changfeng Shao, Jie Yang, Yirong Kong, et al.
Hematology (Amsterdam, Netherlands)
|
November 4, 2017
Identification of a de novo ANK1 mutation in a Chinese family with hereditary spherocytosis
Hongzai Guan, Xinping Liang, Rong Zhang, et al.
Genetic Testing and Molecular Biomarkers
|
April 29, 2014
Evaluation of MYOC, ACAN, HGF, and MET as candidate genes for high myopia in a Han Chinese population
Xian Yang, Xiaoqi Liu, Jie Peng, et al.
Pregnancy Hypertension
|
September 6, 2019
Value of ABCG2 Q141K and Q126X genotyping in predicting risk of preeclampsia in Chinese Han women population
Huabin Hou, Meiyun Geng, Ru Zhang, et al.
Frontiers of Medicine
|
May 28, 2017
Philadelphia chromosome-positive acute myeloid leukemia with masses and osteolytic lesions: finding of 18F-FDG PET/CT
Zhan Su, Fengyu Wu, Weiyu Hu, et al.
Molecular Vision
|
November 3, 2010
KIF21A mutations in two Chinese families with congenital fibrosis of the extraocular muscles (CFEOM)
Xian Yang, Koki Yamada, Bradley Katz, et al.
Molecular Psychiatry
|
November 2, 2019
Mutations in ASH1L confer susceptibility to Tourette syndrome
Shiguo Liu, Miaomiao Tian, Fan He, et al.
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of 2