Found: 10
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Sequence Analysis of the UGT1A1 Gene Untranslated Region in Chinese Han Population.
- Published in:
- Journal of Experimental Hematology / Zhongguo Shiyan Xueyexue Zazhi, 2015, v. 23, n. 2, p. 522, doi. 10.7534/j.issn.1009-2137.2015.02.044
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- Publication type:
- Article
Effect of BCLllA Gene on Transcription of γglobin Gene.
- Published in:
- Journal of Experimental Hematology / Zhongguo Shiyan Xueyexue Zazhi, 2013, v. 21, n. 3, p. 628, doi. 10.7534/j.issn.1009-2137.2013.03.018
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- Publication type:
- Article
Correlation Between Hemoglobin F Levels and Single Nucleotide Polymorphism at BCL11A Gene rs11886868 Locus in β-thalassemia Patients.
- Published in:
- Journal of Experimental Hematology / Zhongguo Shiyan Xueyexue Zazhi, 2012, v. 20, n. 3, p. 650
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- Publication type:
- Article
A Novel Mutation in β-Globin Gene of a Patient with β-thalassemia.
- Published in:
- Journal of Experimental Hematology / Zhongguo Shiyan Xueyexue Zazhi, 2012, v. 20, n. 2, p. 398
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- Publication type:
- Article
Polymorphism in BP1 Binding Site Upstream of β-Globin Gene in Chinese Han Population.
- Published in:
- Journal of Experimental Hematology / Zhongguo Shiyan Xueyexue Zazhi, 2011, v. 19, n. 5, p. 1246
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- Publication type:
- Article
Single Nucleotide Polymorphisms of β-globin Gene in β-Thalassaemia Patients.
- Published in:
- Journal of Experimental Hematology / Zhongguo Shiyan Xueyexue Zazhi, 2010, v. 18, n. 5, p. 1220
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- Publication type:
- Article
Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease.
- Published in:
- 2019
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- Publication type:
- journal article
Serum miR-126 and miR-146a levels in patients with acute cerebral infarction and their relationship with severity of the disease.
- Published in:
- Journal of Acute Disease, 2016, v. 5, n. 5, p. 393, doi. 10.1016/j.joad.2016.08.005
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- Publication type:
- Article
Identification of the ataxin-1 interaction network and its impact on spinocerebellar ataxia type 1.
- Published in:
- Human Genomics, 2022, v. 16, n. 1, p. 1, doi. 10.1186/s40246-022-00404-0
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- Publication type:
- Article
C1orf194 deficiency leads to incomplete early embryonic lethality and dominant intermediate Charcot–Marie–Tooth disease in a knockout mouse model.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 15, p. 2471, doi. 10.1093/hmg/ddaa129
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- Publication type:
- Article