Two different genes encode delta-aminolevulinate synthase in humans: nucleotide sequences of cDNAs for the housekeeping and erythroid genes

Uroporphyrinogen III synthase erythroid promoter mutations in adjacent GATA1 and CP2 elements cause congenital erythropoietic porphyria.

The Journal of clinical investigation·2001

Human uroporphyrinogen-III synthase: genomic organization, alternative promoters, and erythroid-specific expression.

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Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females.

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Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation.

Blood·2000

Uroporphyrinogen III synthase. An alternative promoter controls erythroid-specific expression in the murine gene.

The Journal of biological chemistry·2000

Four new mutations in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia: increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis.

Blood·1999

The MODNAP benchmark set for modeling ribose-based modified nucleic acid and nucleic acid-protein complexes: a case study with AlphaFold 3.

Nucleic acids research·2026

Chemically stabilized long antisense oligonucleotides perturb RNA exosome function.

Nucleic acids research·2026

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DRAMP 5.0: an update integrating sequence and structure in a novel FASTS format for AI-driven design of antimicrobial peptides.

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Science progress·2026

Genetic, Phenotypic, and Quantitative Analysis of Myoblast Fusion in Drosophila Embryos.

Journal of visualized experiments : JoVE·2026

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Tremor and other hyperkinetic movements (New York, N.Y.)·2026

Stage-specific transcriptional atlas of goose satellite cells uncovers sex-biased molecular dynamics associated with embryonic skeletal muscle development.

Frontiers in cell and developmental biology·2026

Growth hormone therapy in Turner syndrome: Do cytogenetic subtypes influence outcomes?

Endocrinologia, diabetes y nutricion·2026

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FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2026

Related Experiment Videos

Two different genes encode delta-aminolevulinate synthase in humans: nucleotide sequences of cDNAs for the

Related Concept Videos

Uroporphyrinogen III synthase erythroid promoter mutations in adjacent GATA1 and CP2 elements cause congenital erythropoietic porphyria.

Human uroporphyrinogen-III synthase: genomic organization, alternative promoters, and erythroid-specific expression.

Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females.

Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation.

Uroporphyrinogen III synthase. An alternative promoter controls erythroid-specific expression in the murine gene.

Four new mutations in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia: increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis.

The MODNAP benchmark set for modeling ribose-based modified nucleic acid and nucleic acid-protein complexes: a case study with AlphaFold 3.

Chemically stabilized long antisense oligonucleotides perturb RNA exosome function.

CLEAN Database: providing enzyme function coverage for over 55 million sequences.

DRAMP 5.0: an update integrating sequence and structure in a novel FASTS format for AI-driven design of antimicrobial peptides.

OAS-nano: the Observed VHH Space Database.

Structural basis of assembly-dependent activation of the MAD3-MAD4 nuclease in the Pseudomonas aeruginosa MADS defense system.

Genetically proxied sex hormones, Sjögren's disease, and broad dry eye disease: A bidirectional two-sample mendelian randomization study.

Genetic, Phenotypic, and Quantitative Analysis of Myoblast Fusion in Drosophila Embryos.

Clinical and Genetic Spectrum of VPS13A Disease Across India: A Retrospective Multicentre Genetically Confirmed Cohort.

Stage-specific transcriptional atlas of goose satellite cells uncovers sex-biased molecular dynamics associated with embryonic skeletal muscle development.

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Related Experiment Videos

Two different genes encode delta-aminolevulinate synthase in humans: nucleotide sequences of cDNAs for the...

Related Concept Videos

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Two different genes encode delta-aminolevulinate synthase in humans: nucleotide sequences of cDNAs for the