review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Oleh Khalimonchuk | |
Amit R Reddi | |||
Courtney M Moore | |||
Amy E Medlock | |||
Jason R Marcero | |||
Samantha A Swenson | |||
P2860 | cites work | Iterative orthology prediction uncovers new mitochondrial proteins and identifies C12orf62 as the human ortholog of COX14, a protein involved in the assembly of cytochrome c oxidase | Q21184006 |
SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome | Q22008476 | ||
Interaction between succinyl CoA synthetase and the heme-biosynthetic enzyme ALAS-E is disrupted in sideroblastic anemia | Q22253368 | ||
A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency | Q22253915 | ||
The stem cell marker Bcrp/ABCG2 enhances hypoxic cell survival through interactions with heme | Q42830333 | ||
Measurement of heme concentration | Q42856098 | ||
Functional expression of human mitochondrial CYP11B2 in fission yeast and identification of a new internal electron transfer protein, etp1. | Q43883487 | ||
Intravenous heme-albumin in acute intermittent porphyria: evidence for repletion of hepatic hemoproteins and regulatory heme pools | Q43898909 | ||
Regulation of the heme A biosynthetic pathway in Saccharomyces cerevisiae | Q43962955 | ||
Identification of novel hemes generated by heme A synthase: evidence for two successive monooxygenase reactions | Q44121782 | ||
Why heme needs to be degraded to iron, biliverdin IXalpha, and carbon monoxide? | Q45042106 | ||
Nutritional regulation of hepatic heme biosynthesis and porphyria through PGC-1alpha | Q46669140 | ||
Mitochondrial cytochrome c oxidase biogenesis: Recent developments. | Q47783506 | ||
Mutation in human CLPX elevates levels of δ-aminolevulinate synthase and protoporphyrin IX to promote erythropoietic protoporphyria | Q47851870 | ||
Spatial distribution of heme species in erythrocytes infected with Plasmodium falciparum by use of resonance Raman imaging and multivariate analysis | Q47879703 | ||
Measurement of heme efflux and heme content in isolated developing chloroplasts | Q47920900 | ||
Molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome | Q48054632 | ||
Endocytosis of Red Blood Cell Microparticles by Pulmonary Endothelial Cells is Mediated By Rab5. | Q50042263 | ||
Identification of the receptor scavenging hemopexin-heme complexes. | Q50337480 | ||
The Fowler syndrome-associated protein FLVCR2 is an importer of heme | Q24298998 | ||
The DGCR8 RNA-binding heme domain recognizes primary microRNAs by clamping the hairpin | Q24299093 | ||
Mitochondrial Atpif1 regulates haem synthesis in developing erythroblasts | Q24302493 | ||
Identification of a human heme exporter that is essential for erythropoiesis | Q24304121 | ||
Identification of a mammalian mitochondrial porphyrin transporter | Q24305008 | ||
The mitochondrial heme exporter FLVCR1b mediates erythroid differentiation | Q24305046 | ||
Site-directed mutagenesis and spectroscopic characterization of human ferrochelatase: identification of residues coordinating the [2Fe-2S] cluster | Q24308804 | ||
HRG1 is essential for heme transport from the phagolysosome of macrophages during erythrophagocytosis | Q24315610 | ||
Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency | Q24317097 | ||
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia | Q24321734 | ||
Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy | Q24328756 | ||
Kinetics and specificity of feline leukemia virus subgroup C receptor (FLVCR) export function and its dependence on hemopexin | Q24338112 | ||
Erythroid-specific 5-aminolevulinate synthase protein is stabilized by low oxygen and proteasomal inhibition | Q24338581 | ||
Crystal structure of 5-aminolevulinate synthase, the first enzyme of heme biosynthesis, and its link to XLSA in humans. | Q24531335 | ||
C-terminal deletions in the ALAS2 gene lead to gain of function and cause X-linked dominant protoporphyria without anemia or iron overload | Q24642289 | ||
Spectroscopic and biochemical characterization of heme binding to yeast Dap1p and mouse PGRMC1p | Q24645476 | ||
Noninvasive molecular imaging of small living subjects using Raman spectroscopy | Q24653843 | ||
Identification of heme as the ligand for the orphan nuclear receptors REV-ERBalpha and REV-ERBbeta | Q24655134 | ||
Measurement of the heme affinity for yeast dap1p, and its importance in cellular function | Q24658256 | ||
Functional and genetic studies demonstrate that mutation in the COX15 gene can cause Leigh syndrome | Q24675204 | ||
The role of mitochondria in cellular iron-sulfur protein biogenesis: mechanisms, connected processes, and diseases | Q26865882 | ||
The 2.0 A structure of human ferrochelatase, the terminal enzyme of heme biosynthesis | Q27629543 | ||
Architecture of succinate dehydrogenase and reactive oxygen species generation | Q27640410 | ||
Structural Insights into Ubiquinone Biosynthesis in Membranes | Q27681854 | ||
Solution structure of apocytochrome b562 | Q27729836 | ||
Redox-coupled crystal structural changes in bovine heart cytochrome c oxidase | Q27758647 | ||
Heme dynamics and trafficking factors revealed by genetically encoded fluorescent heme sensors. | Q27929826 | ||
Sequence and chromosomal localization of two PET genes required for cytochrome c oxidase assembly in Saccharomyces cerevisiae | Q27930995 | ||
Analysis of Oligomerization Properties of Heme a Synthase Provides Insights into Its Function in Eukaryotes. | Q27931313 | ||
Identification of rate-limiting steps in yeast heme biosynthesis | Q27931650 | ||
Overlapping Specificities of the Mitochondrial Cytochrome c and c1 Heme Lyases | Q27931671 | ||
Yeast flavohemoglobin, a nitric oxide oxidoreductase, is located in both the cytosol and the mitochondrial matrix: effects of respiration, anoxia, and the mitochondrial genome on its intracellular level and distribution | Q27932410 | ||
Regulation of iron homeostasis mediated by the heme-binding protein Dap1 (damage resistance protein 1) via the P450 protein Erg11/Cyp51. | Q27933369 | ||
Analysis of Leigh syndrome mutations in the yeast SURF1 homolog reveals a new member of the cytochrome oxidase assembly factor family | Q27933372 | ||
Adenine nucleotide translocator transports haem precursors into mitochondria | Q27933402 | ||
Structure, expression and regulation of a nuclear gene encoding a mitochondrial protein: the yeast L(+)-lactate cytochrome c oxidoreductase (cytochrome b2) | Q27933413 | ||
Mitochondrial ferredoxin is required for heme A synthesis in Saccharomyces cerevisiae | Q27935174 | ||
Yeast mutants deficient in heme biosynthesis and a heme mutant additionally blocked in cyclization of 2,3-oxidosqualene | Q27936429 | ||
Glycine and Folate Ameliorate Models of Congenital Sideroblastic Anemia | Q27936634 | ||
Involvement of mitochondrial ferredoxin and Cox15p in hydroxylation of heme O. | Q27937032 | ||
Role of PUG1 in inducible porphyrin and heme transport in Saccharomyces cerevisiae | Q27937165 | ||
Cyc2p, a membrane-bound flavoprotein involved in the maturation of mitochondrial c-type cytochromes | Q27937225 | ||
Coa2 is an assembly factor for yeast cytochrome c oxidase biogenesis that facilitates the maturation of Cox1. | Q27937418 | ||
Plasma membrane microdomains regulate turnover of transport proteins in yeast | Q27939761 | ||
Cellular iron uptake, trafficking and metabolism: Key molecules and mechanisms and their roles in disease | Q28087521 | ||
Haem homeostasis is regulated by the conserved and concerted functions of HRG-1 proteins | Q28115078 | ||
A Novel Role for Progesterone Receptor Membrane Component 1 (PGRMC1): A Partner and Regulator of Ferrochelatase | Q28118692 | ||
Human delta-aminolevulinate synthase: assignment of the housekeeping gene to 3p21 and the erythroid-specific gene to the X chromosome | Q28119035 | ||
Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients | Q28140418 | ||
Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency | Q28143304 | ||
Cytochrome c oxidase deficiency | Q28189586 | ||
Conserved residues of the human mitochondrial holocytochrome c synthase mediate interactions with heme | Q28244549 | ||
Mechanisms of mitochondrial holocytochrome c synthase and the key roles played by cysteines and histidine of the heme attachment site, Cys-XX-Cys-His | Q28246920 | ||
The role of succinyl-CoA synthetase in the control of heme biosynthesis | Q28256911 | ||
ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis | Q28257493 | ||
Sequential regulation of ferroportin expression after erythrophagocytosis in murine macrophages: early mRNA induction by haem, followed by iron-dependent protein expression | Q28260693 | ||
Discovering hematopoietic mechanisms through genome-wide analysis of GATA factor chromatin occupancy | Q28265885 | ||
Heme is involved in microRNA processing | Q28278198 | ||
TMEM14C is required for erythroid mitochondrial heme metabolism | Q28505553 | ||
Role of the heme regulatory motif in the heme-mediated inhibition of mitochondrial import of 5-aminolevulinate synthase | Q28572054 | ||
Heme Assimilation in Schizosaccharomyces pombe Requires Cell-surface-anchored Protein Shu1 and Vacuolar Transporter Abc3. | Q51139086 | ||
A missing metabolic pathway in the cattle tick Boophilus microplus. | Q52571343 | ||
Structure of the Mitochondrial Aminolevulinic Acid Synthase, a Key Heme Biosynthetic Enzyme. | Q52650168 | ||
Label-Free Imaging of Heme Dynamics in Living Organisms by Transient Absorption Microscopy. | Q52699580 | ||
Transfer of heme from ferrihemoglobin and ferrihemoglobin isolated chains to hemopexin. | Q52913136 | ||
Lessons from bloodless worms: heme homeostasis in C. elegans. | Q53232578 | ||
Pro-oxidant and cytotoxic effects of circulating heme. | Q53854957 | ||
Human ferrochelatase is an iron-sulfur protein. | Q54642721 | ||
Dap1/PGRMC1 binds and regulates cytochrome P450 enzymes. | Q55043047 | ||
Infantile cardioencephalopathy due to a COX15 gene defect: report and review. | Q55054069 | ||
Immune-modulating enzyme indoleamine 2,3-dioxygenase is effectively inhibited by targeting its apo-form. | Q55333337 | ||
Glyceraldehyde-3-phosphate dehydrogenase is a chaperone that allocates labile heme in cells | Q57255599 | ||
Crystal structure of heme A synthase from | Q58612169 | ||
Glutamine via α-ketoglutarate dehydrogenase provides succinyl-CoA for heme synthesis during erythropoiesis | Q58761708 | ||
Epitope mapping of anti-PGRMC1 antibodies reveals the non-conventional membrane topology of PGRMC1 on the cell surface | Q61444636 | ||
A scavenger receptor B (CD36)-like protein is a potential mediator of intestinal heme absorption in the hematophagous ectoparasite Lepeophtheirus salmonis | Q64105702 | ||
Heme regulates hepatic 5-aminolevulinate synthase mRNA expression by decreasing mRNA half-life and not by altering its rate of transcription | Q67981471 | ||
Assignment of the histidine axial ligands to the cytochrome bH and cytochrome bL components of the bcl complex from Rhodobacter sphaeroides by site-directed mutagenesis | Q68243533 | ||
Induction of hepatic delta-amino-levulinic acid synthetase by oral contraceptive steroids | Q70127385 | ||
Analysis of the affinity of each haptoglobin polymer for hemoglobin by two-dimensional affinity electrophoresis | Q73165134 | ||
Phylogenetic analysis of the 5-aminolevulinate synthase gene | Q73924669 | ||
The mechanism of porphyrin formation; the formation of a succinyl intermediate from succinate | Q74049700 | ||
Photothermal imaging of nanometer-sized metal particles among scatterers | Q74620784 | ||
ACETONE EXTRACTION OF HEME FROM MYOGLOBIN AND HEMOGLOBIN AT ACID PH | Q76639066 | ||
Evaluating the roles of the heme a side chains in cytochrome c oxidase using designed heme proteins | Q79212543 | ||
Porphyrias | Q83185413 | ||
The flavoprotein Cyc2p, a mitochondrial cytochrome c assembly factor, is a NAD(P)H-dependent haem reductase | Q83274084 | ||
HPLC methods for analysis of porphyrins in biological media | Q87417881 | ||
Recurrent attacks of acute hepatic porphyria: major role of the chronic inflammatory response in the liver | Q87937480 | ||
The major facilitator transporter Str3 is required for low-affinity heme acquisition in Schizosaccharomyces pombe | Q88084786 | ||
Heme bioavailability and signaling in response to stress in yeast cells | Q89157346 | ||
Handling heme: The mechanisms underlying the movement of heme within and between cells | Q90854530 | ||
PGRMC2 is an intracellular haem chaperone critical for adipocyte function | Q91362753 | ||
Dimeric ferrochelatase bridges ABCB7 and ABCB10 homodimers in an architecturally defined molecular complex required for heme biosynthesis | Q91594557 | ||
Heme biosynthesis and the porphyrias | Q92046226 | ||
Enasidenib drives human erythroid differentiation independently of isocitrate dehydrogenase 2 | Q92374458 | ||
Heme acquisition by Shu1 requires Nbr1 and proteins of the ESCRT complex in Schizosaccharomyces pombe | Q92816966 | ||
Mechanistic study of PpIX accumulation using the JFCR39 cell panel revealed a role for dynamin 2-mediated exocytosis | Q92826130 | ||
The Molar Light Absorption of Pyridine Ferroprotoporphrin (Pyridine Haemochromogen) | Q100807771 | ||
ABCG2 transports and transfers heme to albumin through its large extracellular loop | Q34236666 | ||
GAPDH regulates cellular heme insertion into inducible nitric oxide synthase | Q34241252 | ||
Structure, function, and assembly of heme centers in mitochondrial respiratory complexes | Q34272542 | ||
Heme protein assemblies | Q34296929 | ||
Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene. | Q34354144 | ||
The heme a synthase Cox15 associates with cytochrome c oxidase assembly intermediates during Cox1 maturation | Q34366873 | ||
Heme deficiency may be a factor in the mitochondrial and neuronal decay of aging | Q34379668 | ||
Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency | Q34388122 | ||
The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMT1A-REPs. | Q34438070 | ||
Iron metabolism regulates p53 signaling through direct heme-p53 interaction and modulation of p53 localization, stability, and function | Q34449959 | ||
Biogenesis of cytochrome c oxidase | Q34455978 | ||
Molecular identification of adrenal inner zone antigen as a heme-binding protein | Q34466405 | ||
Identification of the Mitochondrial Heme Metabolism Complex | Q34490149 | ||
Iron-sulfur protein biogenesis in eukaryotes: components and mechanisms | Q34545190 | ||
Cytochrome P450 regulation: the interplay between its heme and apoprotein moieties in synthesis, assembly, repair, and disposal | Q34555359 | ||
Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency | Q34650518 | ||
Regulation of the heme A biosynthetic pathway: differential regulation of heme A synthase and heme O synthase in Saccharomyces cerevisiae | Q34866183 | ||
Molecular enzymology of 5-aminolevulinate synthase, the gatekeeper of heme biosynthesis | Q34958839 | ||
An intercellular heme-trafficking protein delivers maternal heme to the embryo during development in C. elegans | Q35014184 | ||
ABCG2: a perspective. | Q35016817 | ||
ApoHRP-based assay to measure intracellular regulatory heme | Q35079585 | ||
Lon peptidase 1 (LONP1)-dependent breakdown of mitochondrial 5-aminolevulinic acid synthase protein by heme in human liver cells | Q35128157 | ||
Heme oxygenase-1 in inflammation and cardiovascular disease | Q35660128 | ||
Selective Oma1 protease-mediated proteolysis of Cox1 subunit of cytochrome oxidase in assembly mutants | Q35801928 | ||
Circulating cell membrane microparticles transfer heme to endothelial cells and trigger vasoocclusions in sickle cell disease | Q35813199 | ||
Mitochondrial cytochrome c biogenesis: no longer an enigma. | Q35875522 | ||
In situ Spectroscopy on Intact Leptospirillum ferrooxidans Reveals that Reduced Cytochrome 579 is an Obligatory Intermediate in the Aerobic Iron Respiratory Chain | Q35884542 | ||
ATP-dependent mitochondrial porphyrin importer ABCB6 protects against phenylhydrazine toxicity. | Q35921685 | ||
Cellular and mitochondrial iron homeostasis in vertebrates | Q35954736 | ||
Human Erythroid 5-Aminolevulinate Synthase Mutations Associated with X-Linked Protoporphyria Disrupt the Conformational Equilibrium and Enhance Product Release. | Q36068952 | ||
Oligomerization of heme o synthase in cytochrome oxidase biogenesis is mediated by cytochrome oxidase assembly factor Coa2. | Q36137383 | ||
Free heme toxicity and its detoxification systems in human | Q36139710 | ||
One ring to rule them all: trafficking of heme and heme synthesis intermediates in the metazoans | Q36143730 | ||
CO as a cellular signaling molecule | Q36364694 | ||
The heme-Bach1 pathway in the regulation of oxidative stress response and erythroid differentiation | Q36399771 | ||
Heme as key regulator of major mammalian cellular functions: molecular, cellular, and pharmacological aspects. | Q36411963 | ||
Biosynthesis of heme in mammals | Q36535259 | ||
Heme: a versatile signaling molecule controlling the activities of diverse regulators ranging from transcription factors to MAP kinases | Q36559262 | ||
The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyes | Q36602142 | ||
Heme and FLVCR-related transporter families SLC48 and SLC49. | Q36700191 | ||
Interdomain lateral gene transfer of an essential ferrochelatase gene in human parasitic nematodes | Q36835654 | ||
Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior | Q36843054 | ||
Heme as a magnificent molecule with multiple missions: heme determines its own fate and governs cellular homeostasis | Q36929292 | ||
Mitochondrial and cellular heme-dependent proteins as targets for the bioactive function of the heme oxygenase/carbon monoxide system | Q36940024 | ||
The severity of hereditary porphyria is modulated by the porphyrin exporter and Lan antigen ABCB6. | Q37181184 | ||
Regulation of intracellular heme trafficking revealed by subcellular reporters | Q37258637 | ||
A role for heme in Alzheimer's disease: heme binds amyloid beta and has altered metabolism | Q37285877 | ||
Discovery of genes essential for heme biosynthesis through large-scale gene expression analysis. | Q37350017 | ||
Surf1, associated with Leigh syndrome in humans, is a heme-binding protein in bacterial oxidase biogenesis | Q37377668 | ||
Trafficking of heme and porphyrins in metazoa. | Q37403265 | ||
Heme oxygenase-1 and neurodegeneration: expanding frontiers of engagement | Q37490200 | ||
The heme groups of cytochrome o from Escherichia coli | Q37546856 | ||
Cytochrome c biogenesis: mechanisms for covalent modifications and trafficking of heme and for heme-iron redox control. | Q37590030 | ||
Iron regulatory protein-1 protects against mitoferrin-1-deficient porphyria | Q37635844 | ||
Quantification of labile heme in live malaria parasites using a genetically encoded biosensor | Q37711617 | ||
Inventory control: cytochrome c oxidase assembly regulates mitochondrial translation | Q37823208 | ||
Role of Surf1 in heme recruitment for bacterial COX biogenesis | Q37938429 | ||
Heme A biosynthesis | Q38000881 | ||
MAM (mitochondria-associated membranes) in mammalian cells: lipids and beyond | Q38169449 | ||
Heme in pathophysiology: a matter of scavenging, metabolism and trafficking across cell membranes | Q38208296 | ||
Heme on innate immunity and inflammation | Q38218093 | ||
Human mitochondrial COX1 assembly into cytochrome c oxidase at a glance | Q38348706 | ||
Proteomic analysis of lipid raft-enriched membranes isolated from internal organelles | Q38500174 | ||
Regulation of heme biosynthesis and transport in metazoa | Q38534629 | ||
Compartmentalization of iron between mitochondria and the cytosol and its regulation | Q38538795 | ||
Porphyrias: A 2015 update | Q38542777 | ||
Heme Mobilization in Animals: A Metallolipid's Journey. | Q38559870 | ||
Direct measurement of metal ion chelation in the active site of human ferrochelatase | Q38621097 | ||
Heme Gazing: Illuminating Eukaryotic Heme Trafficking, Dynamics, and Signaling with Fluorescent Heme Sensors. | Q38711615 | ||
A Genetically Encoded FRET Sensor for Intracellular Heme | Q38888959 | ||
Prokaryotic Heme Biosynthesis: Multiple Pathways to a Common Essential Product. | Q39103477 | ||
Trans-regulation of RNA-binding protein motifs by microRNA. | Q39105795 | ||
Iron regulatory protein-1 and -2: transcriptome-wide definition of binding mRNAs and shaping of the cellular proteome by iron regulatory proteins | Q39469494 | ||
There is blood in the water: hemolysis, hemoglobin, and heme in acute lung injury | Q39472367 | ||
Rapid and sensitive quantitation of heme in hemoglobinized cells | Q39487515 | ||
Shu1 is a cell-surface protein involved in iron acquisition from heme in Schizosaccharomyces pombe. | Q39715525 | ||
Heme-binding protein HRG-1 is induced by insulin-like growth factor I and associates with the vacuolar H+-ATPase to control endosomal pH and receptor trafficking. | Q39781832 | ||
Identification of enzymically inactive apocytochrome c peroxidase in anaerobically grown Saccharomyces cerevisiae | Q40152375 | ||
Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions. | Q40261041 | ||
Involvement of heme regulatory motif in heme-mediated ubiquitination and degradation of IRP2. | Q40394197 | ||
Molecular regulation of heme biosynthesis in higher vertebrates. | Q40473960 | ||
Biosynthesis and functional role of haem O and haem A. | Q40609423 | ||
Absorbance and redox based approaches for measuring free heme and free hemoglobin in biological matrices | Q40990649 | ||
The Plasma Membrane Protein Nce102 Implicated in Eisosome Formation Rescues a Heme Defect in Mitochondria | Q41045936 | ||
Transient absorption imaging of hemes with 2-color, independently tunable visible-wavelength ultrafast source | Q41069821 | ||
The free heme concentration in healthy human erythrocytes | Q41140605 | ||
Spectroscopic and mutagenesis studies of human PGRMC1. | Q41445077 | ||
Special delivery from mitochondria to peroxisomes | Q41452491 | ||
Identification of a novel erythroid-specific enhancer for the ALAS2 gene and its loss-of-function mutation which is associated with congenital sideroblastic anemia | Q41813591 | ||
Measurement of cytochrome P450 and NADPH-cytochrome P450 reductase | Q41840629 | ||
Proteomic mapping of mitochondria in living cells via spatially restricted enzymatic tagging. | Q41927329 | ||
Correction for Khalimonchuk et al., "Formation of the Redox Cofactor Centers during Cox1 Maturation in Yeast Cytochrome Oxidase". | Q42251082 | ||
Translational inhibition by heme of the synthesis of hepatic delta-aminolevulinate synthase in a cell-free system | Q42253065 | ||
Evidence for the transcriptional inhibition by heme of the synthesis of delta-aminolevulinate synthase in rat liver | Q42264149 | ||
Ascorbate peroxidase proximity labeling coupled with biochemical fractionation identifies promoters of endoplasmic reticulum-mitochondrial contacts | Q42285856 | ||
A heme-sensing mechanism in the translational regulation of mitochondrial cytochrome c oxidase biogenesis | Q42412712 | ||
The Assembly Factor Pet117 Couples Heme a Synthase Activity to Cytochrome Oxidase Assembly | Q42427959 | ||
Pyridine Hemochromagen Assay for Determining the Concentration of Heme in Purified Protein Solutions. | Q42432474 | ||
SURF1 missense mutations promote a mild Leigh phenotype. | Q42460422 | ||
Storage lesion: role of red blood cell breakdown | Q42720111 | ||
Hemopexin prevents endothelial damage and liver congestion in a mouse model of heme overload | Q28585150 | ||
Mitoferrin is essential for erythroid iron assimilation | Q28587125 | ||
Examination of mitochondrial protein targeting of haem synthetic enzymes: in vivo identification of three functional haem-responsive motifs in 5-aminolaevulinate synthase | Q28589533 | ||
A heme export protein is required for red blood cell differentiation and iron homeostasis | Q28592039 | ||
Characterization of Human and Yeast Mitochondrial Glycine Carriers with Implications for Heme Biosynthesis and Anemia. | Q29568201 | ||
Regulation by heme of mitochondrial protein transport through a conserved amino acid motif | Q30467462 | ||
Topologically conserved residues direct heme transport in HRG-1-related proteins. | Q30505390 | ||
Drugs mediate the transcriptional activation of the 5-aminolevulinic acid synthase (ALAS1) gene via the chicken xenobiotic-sensing nuclear receptor (CXR). | Q30711956 | ||
Heme A synthase does not incorporate molecular oxygen into the formyl group of heme A. | Q30941319 | ||
Imaging chromophores with undetectable fluorescence by stimulated emission microscopy | Q33511745 | ||
The role of Coa2 in hemylation of yeast Cox1 revealed by its genetic interaction with Cox10 | Q33558128 | ||
Heme-mediated SPI-C induction promotes monocyte differentiation into iron-recycling macrophages | Q33570011 | ||
Investigations of heme distortion, low-frequency vibrational excitations, and electron transfer in cytochrome c | Q33607085 | ||
Formation of the redox cofactor centers during Cox1 maturation in yeast cytochrome oxidase. | Q33627236 | ||
Assembly factors monitor sequential hemylation of cytochrome b to regulate mitochondrial translation. | Q33663212 | ||
Induction of -aminolevulinic acid synthetase in chick embryo liver cells in cluture | Q33704586 | ||
Like iron in the blood of the people: the requirement for heme trafficking in iron metabolism. | Q33709768 | ||
Control of metazoan heme homeostasis by a conserved multidrug resistance protein | Q33737434 | ||
Progesterone inhibits apoptosis in part by PGRMC1-regulated gene expression. | Q33749200 | ||
Cell biology of heme | Q33752149 | ||
5-aminolevulinate synthase: catalysis of the first step of heme biosynthesis | Q33830495 | ||
Mutation of the heme axial ligand of Escherichia coli succinate-quinone reductase: implications for heme ligation in mitochondrial complex II from yeast | Q33926010 | ||
Lack of heme synthesis in a free-living eukaryote | Q33934583 | ||
Nitric oxide scavenging by red blood cell microparticles and cell-free hemoglobin as a mechanism for the red cell storage lesion | Q33957600 | ||
Humans possess two mitochondrial ferredoxins, Fdx1 and Fdx2, with distinct roles in steroidogenesis, heme, and Fe/S cluster biosynthesis | Q33977876 | ||
Structure--function relationships of rat hepatic tryptophan 2,3-dioxygenase: identification of the putative heme-ligating histidine residues | Q34084855 | ||
Ferrochelatase forms an oligomeric complex with mitoferrin-1 and Abcb10 for erythroid heme biosynthesis | Q34112735 | ||
CD163: a signal receptor scavenging haptoglobin-hemoglobin complexes from plasma | Q34114924 | ||
Molecular mechanism of heme signaling in yeast: the transcriptional activator Hap1 serves as the key mediator. | Q34158451 | ||
Involvement of ABC7 in the biosynthesis of heme in erythroid cells: interaction of ABC7 with ferrochelatase | Q34164494 | ||
Pump-probe optical microscopy for imaging nonfluorescent chromophores | Q34192555 | ||
Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core | Q34220248 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 3 | |
P577 | publication date | 2020-02-29 | |
P1433 | published in | Cells | Q27724621 |
P1476 | title | From Synthesis to Utilization: The Ins and Outs of Mitochondrial Heme | |
P478 | volume | 9 |
Q99557050 | Relationships between hyperinsulinaemia, magnesium, vitamin D, thrombosis and COVID-19: rationale for clinical management | cites work | P2860 |
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