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ALAS2
Molecular Expression, Characterization and Mechanism of ALAS2 Gain-Of-Function Mutants Vassili Tchaikovskii, Robert J
GATA Transcription Factors Directly Regulate the Parkinson's
Case Reports
REPORT C-Terminal Deletions in the ALAS2 Gene Lead to Gain of Function and Cause X-Linked Dominant Protoporphyria Without Anemia Or Iron Overload
Loss-Of-Function Ferrochelatase and Gain-Of-Function Erythroid-Specific
Mir-218 Inhibits Erythroid Differentiation and Alters Iron Metabolism by Targeting ALAS2 in K562 Cells
Significance of Heme and Heme Degradation in the Pathogenesis Of
Coordinate Expression of Heme and Globin Is Essential for Effective Erythropoiesis
Acute Intermittent Porphyria: an Overview of Therapy Developments and Future Perspectives Focusing on Stabilisation of HMBS and Proteostasis Regulators
Zebrafish Models for Human ALA-Dehydratase-Deficient Porphyria (ADP) And
ALAS2 Gene 5-Aminolevulinate Synthase 2
Circadian Rhythms in Acute Intermittent Porphyria a Pilot Study
Mutation in Human CLPX Elevates Levels of Δ-Aminolevulinate
Biochemical Characterization of Human Heme Oxygenase-2
Leaders Molecular Genetics of Disorders of Haem Biosynthesis
Biology of Heme in Mammalian Erythroid Cells and Related Disorders
© Ferrata Storti Foundation
Influence of Iron Metabolism on Gene Expression in Erythropoietic Protoporphyria
Top View
Heme Biosynthesis Depends on Previously Unrecognized Acquisition of Iron-Sulfur Cofactors in Human Amino-Levulinic Acid Dehydratase
Do Mammalian Cells Really Need to Export and Import Heme?
A Metabolomics Analysis to Define the Source of Heme
Exploration of Mutations in Erythroid 5-Aminolevulinate Synthase That
Function of ALAS2 Gene in Congenital Sideroblastic Anemia
Cystathionine Β-Synthase (CBS) Deficiency Suppresses
Biosynthesis of Heme in Mammals ⁎ Richard S
From Synthesis to Utilization: the Ins and Outs of Mitochondrial Heme
Heme Regulates Exocrine Peptidase Precursor Genes in Zebrafish
Hypoxic Up-Regulation of Erythroid 5-Aminolevulinate Synthase
Muscle Atrophy Induced by Overexpression of ALAS2 Is Related
36 Disorders of Heme Biosynthesis
Molecular Mechanisms Underlying Heme Action in Promoting the Pathogenesis of Alzheimer’S Disease
Iron in Erythropoietic Protoporphyrias: Dr. Jekyll Or Mr. Hyde? Jasmin Barman-Aksoezen1, Xiaoye Schneider-Yin1, Elisabeth I
Role of the Heme Regulatory Motif in the Heme-Mediated Inhibition of Mitochondrial Import of 5-Aminolevulinate Synthase
X-Linked Sideroblastic Anaemia Due to ALAS2 Mutations in the Netherlands: a Disease in Disguise
X-Linked Macrocytic Dyserythropoietic Anemia in Females with an ALAS2 Mutation
Heme Biosynthesis: Structure–Activity Studies of Murine Ferrochelatase
Sideroblastic Anemia: Molecular Analysis of ALAS2 Gene in a Series of 29 Probands and Functional Studies of Ten Missense Mutations
Acute Intermittent Porphyria Causes Hepatic Mitochondrial Energetic
ALAS2) a Target Enabling Package (TEP)
Investigation Into the Rate-Determining Step Of