Found: 19
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Application and research progress of single cell sequencing technology in leukemia.
- Published in:
- Frontiers in Oncology, 2024, p. 1, doi. 10.3389/fonc.2024.1389468
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- Article
Differential expression of microRNAs in plasma of patients with prediabetes and newly diagnosed type 2 diabetes.
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- Acta Diabetologica, 2016, v. 53, n. 5, p. 693, doi. 10.1007/s00592-016-0837-1
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- Article
A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia.
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- American Journal of Hematology, 2016, v. 91, n. 11, p. 1118, doi. 10.1002/ajh.24527
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- Article
Transmembrane Protein ANTXR1 Regulates -Globin Expression by Targeting the Wnt/ -Catenin Signaling Pathway.
- Published in:
- 2022
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- Publication type:
- journal article
Effect of Emi1 gene silencing on the proliferation and invasion of human breast cancer cells.
- Published in:
- BMC Molecular & Cell Biology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12860-023-00494-1
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- Article
Correlations between Multiple SNPs and HbF Levels in ß-Thalassemia Carriers.
- Published in:
- Clinical Laboratory, 2023, v. 69, n. 9, p. 1875, doi. 10.7754/Clin.Lab.2023.230220
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- Article
Two novel mutations in PADI6 and TLE6 genes cause female infertility due to arrest in embryonic development.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 6, p. 1551, doi. 10.1007/s10815-021-02194-1
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- Article
LncRNA VPS9D1-AS1 promotes cell proliferation in acute lymphoblastic leukemia through modulating GPX1 expression by miR-491-5p and miR-214-3p evasion.
- Published in:
- Bioscience Reports, 2020, v. 40, n. 10, p. 1, doi. 10.1042/BSR20193461
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- Publication type:
- Article
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.1069453
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- Publication type:
- Article
Data Imputation for Detected Traffic Volume of Freeway Using Regression of Multilayer Perceptron.
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- Journal of Advanced Transportation, 2022, p. 1, doi. 10.1155/2022/4840021
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- Publication type:
- Article
The genetic basis of asymptomatic codon 8 frame-shift ( HBB:c25_26del AA) β<sup>0</sup>-thalassaemia homozygotes.
- Published in:
- British Journal of Haematology, 2016, v. 172, n. 6, p. 958, doi. 10.1111/bjh.13909
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- Publication type:
- Article
Whole-exome sequencing identified five novel de novo variants in patients with unexplained intellectual disability.
- Published in:
- 2022
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- Publication type:
- journal article
Identification of two CUL7 variants in two Chinese families with 3-M syndrome by whole-exome sequencing.
- Published in:
- 2020
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- Publication type:
- journal article
Association of polymorphisms in the HBG1-HBD intergenic region with HbF levels.
- Published in:
- 2020
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- Publication type:
- journal article
Evaluating the Clinical Utility of a Long-Read Sequencing-Based Approach in Prenatal Diagnosis of Thalassemia.
- Published in:
- Clinical Chemistry, 2023, v. 69, n. 3, p. 239, doi. 10.1093/clinchem/hvac200
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- Publication type:
- Article
ANTXR1 Regulates Erythroid Cell Proliferation and Differentiation through wnt/β-Catenin Signaling Pathway In Vitro and in Hematopoietic Stem Cell.
- Published in:
- Disease Markers, 2022, p. 1, doi. 10.1155/2022/1226697
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- Publication type:
- Article
A Three-Year Prospective Study Assessing the Application of Chromosomal Microarray Analysis in 576 High-Risk Pregnant Women.
- Published in:
- Evidence-based Complementary & Alternative Medicine (eCAM), 2022, p. 1, doi. 10.1155/2022/1533346
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- Publication type:
- Article
Adenosine monophosphate-activated protein kinase attenuates cardiomyocyte hypertrophy through regulation of FOXO3a/MAFbx signaling pathway.
- Published in:
- Acta Biochimica et Biophysica Sinica, 2016, v. 48, n. 9, p. 827, doi. 10.1093/abbs/gmw076
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- Publication type:
- Article
A novel variant c.902C>A (p. A301D) in KCNQ4 associated with non‐syndromic deafness 2A in a Chinese family.
- Published in:
- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 7, p. 1, doi. 10.1002/mgg3.2446
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- Article