Results 121 to 130 of about 1,366 (166)
Regulation of erythroid-specific 5-aminolevulinate synthase (ALAS2) by hypoxia [PDF]
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British Journal of Pharmacology
Despite breakthroughs in immunotherapy and targeted therapies, chemotherapy remains indispensable in oncology.
Jing Chen, Hai-Yan Wu
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Despite breakthroughs in immunotherapy and targeted therapies, chemotherapy remains indispensable in oncology.
Jing Chen, Hai-Yan Wu
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Tissue and Cell, 2023
Polycystic ovary syndrome (PCOS) is a heterogeneous endocrine disorder affecting women at reproductive age. The therapeutic effect of electroacupuncture (EA) on PCOS has been revealed, while the anti-PCOS mechanisms of EA have not been fully explored. In
Jing Cong, Jingshu Gao, Hongli Ma
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Polycystic ovary syndrome (PCOS) is a heterogeneous endocrine disorder affecting women at reproductive age. The therapeutic effect of electroacupuncture (EA) on PCOS has been revealed, while the anti-PCOS mechanisms of EA have not been fully explored. In
Jing Cong, Jingshu Gao, Hongli Ma
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Forensic Science International: Genetics
A rapid, sensitive and specific test for blood is reported based on a novel application of recombinase polymerase amplification integrated with CRISPR-Cas and lateral flow assay (LFA).
Adrian Linacre +2 more
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A rapid, sensitive and specific test for blood is reported based on a novel application of recombinase polymerase amplification integrated with CRISPR-Cas and lateral flow assay (LFA).
Adrian Linacre +2 more
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Blood
Introduction. Many genes relevant to iron metabolism include a transcribed cis-regulatory element called iron-responsive element (IRE) that couples their expression to the availability of intracellular iron. Canonical IREs consist of a conserved stem-
Sarah Ducamp +3 more
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Introduction. Many genes relevant to iron metabolism include a transcribed cis-regulatory element called iron-responsive element (IRE) that couples their expression to the availability of intracellular iron. Canonical IREs consist of a conserved stem-
Sarah Ducamp +3 more
semanticscholar +2 more sources
A synonymous coding variant that alters ALAS2 splicing and causes X‐linked sideroblastic anemia
Pediatric Blood & Cancer, 2021To the Editor: X-linkedsideroblastic anemia (XLSA) is the most common form of congenital sideroblastic anemia (CSA). Approximately 70 different mutations have been described.
Jamie Oakley +7 more
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Clinical and Experimental Dermatology
Erythropoietic protoporphyria (EPP) is usually caused by autosomal dominant mutations in the ferrochelatase gene (FECH), blocking the conversion of protoporphyrin to haem.
S. Srinivas, C. Moss
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Erythropoietic protoporphyria (EPP) is usually caused by autosomal dominant mutations in the ferrochelatase gene (FECH), blocking the conversion of protoporphyrin to haem.
S. Srinivas, C. Moss
semanticscholar +3 more sources
microRNAs (miRNAs) are involved in a variety of biological processes. The regulatory function and potential role of miRNAs targeting the mRNA of the 5′-aminolevulinate synthase 2 (ALAS2) in erythropoiesis were investigated in order to identify miRNAs ...
Hongzhu Qu, Yanming Li, Hongying Sun
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R411C Mutation of the ALAS2 Gene Encodes a Pyridoxine-Responsive Enzyme With Low Activity [PDF]
A R411C missense mutation of the erythroid‐specific δ‐aminolaevulinate synthase (ALAS2) gene was identified in a pedigree with X‐linked pyridoxine‐responsive sideroblastic anaemia (XLSA). The normal and the mutant cDNAs were expressed in E. coli, and the enzyme protein was purified.
Kazumichi Furuyama +2 more
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