| scholarly article | Q13442814 |
| P50 | author | Peter Rotwein | Q56013910 |
| P2093 | author name string | Peter Rotwein | |
| P2860 | cites work | Hemojuvelin and bone morphogenetic protein (BMP) signaling in iron homeostasis | Q21129271 |
| Pro-protein convertases control the maturation and processing of the iron-regulatory protein, RGMc/hemojuvelin | Q21284382 | ||
| DRAGON, a bone morphogenetic protein co-receptor | Q24292739 | ||
| Furin-mediated release of soluble hemojuvelin: a new link between hypoxia and iron homeostasis | Q24297889 | ||
| Neogenin interacts with hemojuvelin through its two membrane-proximal fibronectin type III domains | Q24310451 | ||
| Hemojuvelin is essential for dietary iron sensing, and its mutation leads to severe iron overload | Q24312272 | ||
| Deleted in Colorectal Cancer (DCC) encodes a netrin receptor | Q24313278 | ||
| Hemojuvelin regulates hepcidin expression via a selective subset of BMP ligands and receptors independently of neogenin | Q24321923 | ||
| A mouse model of juvenile hemochromatosis | Q24532268 | ||
| Analysis of protein-coding genetic variation in 60,706 humans | Q26831376 | ||
| Understanding rare and common diseases in the context of human evolution | Q28067740 | ||
| New insights into the generation and role of de novo mutations in health and disease | Q28073446 | ||
| The serine protease matriptase-2 (TMPRSS6) inhibits hepcidin activation by cleaving membrane hemojuvelin | Q28115763 | ||
| Vertebrate homologues of C. elegans UNC-5 are candidate netrin receptors | Q28118661 | ||
| RGMs: Structural Insights, Molecular Regulation, and Downstream Signaling | Q39050838 | ||
| Targeting repulsive guidance molecule A to promote regeneration and neuroprotection in multiple sclerosis. | Q41175140 | ||
| A high-coverage Neandertal genome from Vindija Cave in Croatia. | Q46270621 | ||
| Genetic effects on gene expression across human tissues | Q46285732 | ||
| The Contribution of Neanderthals to Phenotypic Variation in Modern Humans | Q47189890 | ||
| Repulsive guidance molecule plays multiple roles in neuronal differentiation and axon guidance. | Q48515205 | ||
| Enhancing GTEx by bridging the gaps between genotype, gene expression, and disease. | Q50093911 | ||
| Gene discovery by microarray: identification of novel genes induced during growth factor-mediated muscle cell survival and differentiation. | Q52086790 | ||
| Levodopa increases oxidative stress and repulsive guidance molecule A levels: a pilot study in patients with Parkinson's disease. | Q52855994 | ||
| Repulsive guidance molecule-a is involved in Th17-cell-induced neurodegeneration in autoimmune encephalomyelitis. | Q55069657 | ||
| RGMa modulates T cell responses and is involved in autoimmune encephalomyelitis | Q56771929 | ||
| Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry | Q57463053 | ||
| Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations | Q57910661 | ||
| Genetic variation: ExAC boosts clinical variant interpretation in rare diseases | Q64047944 | ||
| Neogenin-RGMa signaling at the growth cone is bone morphogenetic protein-independent and involves RhoA, ROCK, and PKC | Q80050476 | ||
| HJV gene mutations in European patients with juvenile hemochromatosis | Q81614831 | ||
| Organization of GPI-anchored proteins at the cell surface and its physiopathological relevance | Q90440775 | ||
| Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis | Q28188379 | ||
| Isolation and expression pattern of three mouse homologues of chick Rgm | Q28191703 | ||
| RGM is a repulsive guidance molecule for retinal axons | Q28204359 | ||
| DRAGON: a member of the repulsive guidance molecule-related family of neuronal- and muscle-expressed membrane proteins is regulated by DRG11 and has neuronal adhesive properties | Q28246971 | ||
| Complex biosynthesis of the muscle-enriched iron regulator RGMc | Q28254101 | ||
| Molecular biology, genetics and biochemistry of the repulsive guidance molecule family | Q28255922 | ||
| The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data | Q28266682 | ||
| Selective binding of RGMc/hemojuvelin, a key protein in systemic iron metabolism, to BMP-2 and neogenin | Q28269309 | ||
| Neogenin mediates the action of repulsive guidance molecule | Q28272500 | ||
| RGM and its receptor neogenin regulate neuronal survival | Q28272510 | ||
| Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal | Q28288215 | ||
| Dependence receptors: when apoptosis controls tumor progression | Q28298762 | ||
| Repulsive guidance molecule (RGM) gene function is required for neural tube closure but not retinal topography in the mouse visual system | Q28506752 | ||
| Repulsive guidance molecule (RGMa), a DRAGON homologue, is a bone morphogenetic protein co-receptor | Q28510682 | ||
| RGMa inhibition promotes axonal growth and recovery after spinal cord injury. | Q28571215 | ||
| Upper Palaeolithic genomes reveal deep roots of modern Eurasians | Q29544409 | ||
| New fossils from Jebel Irhoud, Morocco and the pan-African origin of Homo sapiens | Q30156627 | ||
| Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis. | Q30339036 | ||
| HFE gene: Structure, function, mutations, and associated iron abnormalities. | Q30380172 | ||
| The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data. | Q31030085 | ||
| The ExAC browser: displaying reference data information from over 60 000 exomes | Q31145461 | ||
| Small Amounts of Archaic Admixture Provide Big Insights into Human History | Q34045116 | ||
| The dependence receptors DCC and UNC5H as a link between neuronal guidance and survival | Q35575340 | ||
| Dragon (repulsive guidance molecule b, RGMb) is a novel gene that promotes colorectal cancer growth | Q36299749 | ||
| The RGM/DRAGON family of BMP co-receptors | Q37026226 | ||
| Repulsive guidance molecule B inhibits metastasis and is associated with decreased mortality in non-small cell lung cancer | Q37085857 | ||
| Patterns of genic intolerance of rare copy number variation in 59,898 human exomes | Q37297685 | ||
| The continuum of causality in human genetic disorders | Q37422176 | ||
| The neurophysiology of the esophagus | Q38151803 | ||
| Human occupation of northern Australia by 65,000 years ago. | Q38369079 | ||
| The New Genomics: What Molecular Databases Can Tell us About Human Population Variation and Endocrine Disease | Q38789207 | ||
| TGF-β and the TGF-β Family: Context-Dependent Roles in Cell and Tissue Physiology | Q38824306 | ||
| Large-scale analysis of variation in the insulin-like growth factor family in humans reveals rare disease links and common polymorphisms. | Q38847165 | ||
| TGF-β Signaling from Receptors to Smads | Q38906099 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Hemojuvelin | Q24766888 |
| Hemochromatosis | Q61508171 | ||
| P304 | page(s) | e13959 | |
| P577 | publication date | 2019-02-01 | |
| P1433 | published in | Physiological Reports | Q15716763 |
| P1476 | title | Variation in the repulsive guidance molecule family in human populations | |
| P478 | volume | 7 |
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