Found: 6
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Screening of dystrophin gene deletions in Egyptian patients with DMD/BMD muscular dystrophies.
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- Disease Markers, 2000, v. 16, n. 3-4, p. 125, doi. 10.1155/2000/437372
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- Article
Distribution of CYP2C8 and CYP2C9 amino acid substitution alleles in South Indian diabetes patients: A genotypic and computational protein phenotype study.
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- Clinical & Experimental Pharmacology & Physiology, 2017, v. 44, n. 12, p. 1171, doi. 10.1111/1440-1681.12810
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- Article
Pluripotent Stem Cell-Derived Hematopoietic Progenitors Are Unable to Downregulate Key Epithelial-Mesenchymal Transition-Associated miRNAs.
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- Stem Cells, 2018, v. 36, n. 1, p. 55, doi. 10.1002/stem.2724
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- Article
iPSC modeling of severe aplastic anemia reveals impaired differentiation and telomere shortening in blood progenitors.
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- Cell Death & Disease, 2018, v. 9, n. 2, p. 1, doi. 10.1038/s41419-017-0141-1
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- Article
Identification of miRNA–mRNA–TFs regulatory network and crucial pathways involved in asthma through advanced systems biology approaches.
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- PLoS ONE, 2022, v. 17, n. 10, p. 1, doi. 10.1371/journal.pone.0271262
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- Article
First Comprehensive In Silico Analysis of the Functional and Structural Consequences of SNPs in Human GalNAc-T1 Gene.
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- Computational & Mathematical Methods in Medicine, 2014, p. 1, doi. 10.1155/2014/904052
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- Article