Understanding the multiple functions of Nramp1

Cloning and characterization of a mammalian proton-coupled metal-ion transporter

Gunshin, H., Mackenzie, B., Berger, U. V., Gunshin, Y., Romero, M. F., Boron, W. F., Nussberger, S., Gollan, J. L., & Hediger, M. A. (1997) · Nature · doi:10.1038/41343 · Cited by 3,166 · see citing works

Lack of Acidification in <i>Mycobacterium</i> Phagosomes Produced by Exclusion of the Vesicular Proton-ATPase

Sturgill-Koszycki, S., Schlesinger, P. H., Chakraborty, P., Haddix, P. L., Collins, H. L., Fok, A. K., Allen, R. D., Gluck, S. L., Heuser, J., & Russell, D. G. (1994) · Science · doi:10.1126/science.8303277 · Cited by 1,302 · see citing works

Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene

Fleming, M. D., Trenor, C. C., Su, M. A., Foernzler, D., Beier, D. R., Dietrich, W. F., & Andrews, N. C. (1997) · Nature Genetics · doi:10.1038/ng0897-383 · Cited by 1,159 · see citing works

Natural resistance to infection with intracellular parasites: isolation of a candidate for Bcg

Vidal, S. M., Malo, D., Vogan, K., Skamene, E., & Gros, P. (1993) · Cell · doi:10.1016/0092-8674(93)90135-d · Cited by 1,104 · see citing works

<i>Nramp</i> <i>2</i> is mutated in the anemic Belgrade ( <i>b</i> ) rat: Evidence of a role for Nramp2 in endosomal iron transport

Fleming, M. D., Romano, M. A., Su, M. A., Garrick, L. M., Garrick, M. D., & Andrews, N. C. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.3.1148 · Cited by 936 · see citing works

Variations in the NRAMP1 Gene and Susceptibility to Tuberculosis in West Africans

Bellamy, R., Ruwende, C., Corrah, T., McAdam, K. P. W. J., Whittle, H. C., & Hill, A. V. S. (1998) · New England Journal of Medicine · doi:10.1056/nejm199803053381002 · Cited by 731 · see citing works

The Ity/Lsh/Bcg locus: natural resistance to infection with intracellular parasites is abrogated by disruption of the Nramp1 gene

Vidal, S., Tremblay, M. L., Govoni, G., Gauthier, S., Sebastiani, G., Malo, D., Skamene, E., Olivier, M., Jothy, S., & Gros, P. (1995) · The Journal of experimental medicine · doi:10.1084/jem.182.3.655 · Cited by 603 · see citing works

Natural Resistance to Infection with Intracellular Pathogens: The <i>Nramp1</i> Protein Is Recruited to the Membrane of the Phagosome

Gruenheid, S., Pinner, E., Desjardins, M., & Gros, P. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.185.4.717 · Cited by 428 · see citing works

Nramp2 is mutated in the anemic Belgrade (b) rat : evidence of a role for Nramp2 in endosomal iron transport

Flemming (1998) · Medical Entomology and Zoology · Cited by 412 · see citing works

Mycobacterium‐containing phagosomes are accessible to early endosomes and reflect a transitional state in normal phagosome biogenesis.

Sturgill‐Koszycki, S., Schaible, U. E., & Russell, D. G. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb01088.x · Cited by 356 · see citing works

A yeast manganese transporter related to the macrophage protein involved in conferring resistance to mycobacteria.

Supek, F., Supekova, L., Nelson, H., & Nelson, N. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.10.5105 · Cited by 325 · see citing works

The Iron Transport Protein NRAMP2 Is an Integral Membrane Glycoprotein That Colocalizes with Transferrin in Recycling Endosomes

Gruenheid, S., Canonne‐Hergaux, F., Gauthier, S., Hackam, D. J., Grinstein, S., & Gros, P. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.189.5.831 · Cited by 302 · see citing works

Identification and characterization of a second mouse Nramp gene

Gruenheid, S., Cellier, M. F., Vidal, S. M., & Gros, P. (1995) · Genomics · doi:10.1016/0888-7543(95)80053-o · Cited by 287 · see citing works

Susceptibility to Leprosy Is Linked to the HumanNRAMP1Gene

Abel, L., Sánchez, F. O. N., Oberti, J., Thuc, N. V., Hoa, L. V., Lap, V. D., Skamene, E., Lagrange, P. H., & Schurr, E. (1998) · The Journal of Infectious Diseases · doi:10.1086/513830 · Cited by 267 · see citing works

Evidence for a functional repeat polymorphism in the promoter of the human NRAMP1 gene that correlates with autoimmune versus infectious disease susceptibility

Searle, S., & Blackwell, J. M. (1999) · Journal of Medical Genetics · doi:10.1136/jmg.36.4.295 · Cited by 220 · see citing works

Host Resistance to Intracellular Infection: Mutation of Natural Resistance-associated Macrophage Protein 1 (<i>Nramp1</i>) Impairs Phagosomal Acidification

Hackam, D. J., Rotstein, O. D., Zhang, W.-J., Gruenheid, S., Gros, P., & Grinstein, S. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.188.2.351 · Cited by 202 · see citing works

Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene.

Liu, J., Fujiwara, T., Buu, N., Sánchez, F. O. N., Cellier, M. F., Paradis, A. J., Frappier, D., Skamene, E., Gros, P., & Morgan, K. (1995) · PubMed Central · Cited by 171 · see citing works

The Bcg/Ity/Lsh locus: genetic transfer of resistance to infections in C57BL/6J mice transgenic for the Nramp1 Gly169 allele

Govoni, G., Vidal, S., Gauthier, S., Skamene, E., Malo, D., & Gros, P. (1996) · Infection and Immunity · doi:10.1128/iai.64.8.2923-2929.1996 · Cited by 167 · see citing works

Localisation of Nramp1 in macrophages: Modulation with activation and infection

Searle, S., Bright, N. A., Roach, T. I. A., Atkinson, P. G. P., Barton, C. H., Meloen, R. H., & Blackwell, J. M. (1998) · Journal of Cell Science · doi:10.1242/jcs.111.19.2855 · Cited by 158 · see citing works

Role of Iron in<i>Nramp1</i>-Mediated Inhibition of Mycobacterial Growth

Zwilling, B. S., Kuhn, D. E., Wikoff, L., Brown, D., & Lafuse, W. (1999) · Infection and Immunity · doi:10.1128/iai.67.3.1386-1392.1999 · Cited by 155 · see citing works

Genomic Organization and Sequence of the Human NRAMP Gene: Identification and Mapping of a Promoter Region Polymorphism

Blackwell, J. M., Barton, C. H., White, J. K., Searle, S., Baker, A.-M., Williams, H. P., & Shaw, M. (1995) · Molecular Medicine · doi:10.1007/bf03401567 · Cited by 143 · see citing works

Malvolio, the Drosophila homologue of mouse NRAMP-1 (Bcg), is expressed in macrophages and in the nervous system and is required for normal taste behaviour.

Rodrigues, V., Cheah, P. Y., Ray, K., & Chia, W. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb07303.x · Cited by 136 · see citing works

Evidence that genetic susceptibility to Mycobacterium tuberculosis in a brazilian population is under oligogenic control: Linkage study of the candidate genes NRAMP1 and TBFA

Shaw, M., Collins, A. R., Peacock, C. S., Miller, E. N., Black, G. F., Sibthorpe, D., Lins-Lainson, Z., Shaw, J. J., Ramos, F., Sílveira, F. T., et al. (1997) · Tubercle and Lung Disease · doi:10.1016/s0962-8479(97)90014-9 · Cited by 135 · see citing works

Nramp Transfection Transfers Ity/Lsh/Bcg-Related Pleiotropic Effects on Macrophage Activation: Influence on Oxidative Burst and Nitric Oxide Pathways

Barton, C. H., Whitehead, S. H., & Blackwell, J. M. (1995) · Molecular Medicine · doi:10.1007/bf03401551 · Cited by 129 · see citing works

Resistance to intracellular infections: comparative genomic analysis of Nramp

Cellier, M. F., Belouchi, A., & Gros, P. (1996) · Trends in Genetics · doi:10.1016/0168-9525(96)30042-5 · Cited by 124 · see citing works

Functional Complementation of the Yeast Divalent Cation Transporter Family SMF by NRAMP2, a Member of the Mammalian Natural Resistance-associated Macrophage Protein Family

Pinner, E., Gruenheid, S., Raymond, M., & Gros, P. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.46.28933 · Cited by 115 · see citing works

Implication of phagosome-lysosome fusion in restriction of Mycobacterium avium growth in bone marrow macrophages from genetically resistant mice

de Chastellier, C., Fréhel, C., Offredo, C., & Skamene, E. (1993) · Infection and Immunity · doi:10.1128/iai.61.9.3775-3784.1993 · Cited by 115 · see citing works

Differential iron transport into phagosomes isolated from the RAW264.7 macrophage cell lines transfected with Nramp1Gly169 or Nramp1Asp169

Kuhn, D. E., Baker, B. D., Lafuse, W. P., & Zwilling, B. S. (1999) · Journal of Leukocyte Biology · doi:10.1002/jlb.66.1.113 · Cited by 113 · see citing works

Genetic regulation of macrophage activation: understanding the function of Nramp1 (=Ity/Lsh/Bcg)

Blackwell, J. M., & Searle, S. (1999) · Immunology Letters · doi:10.1016/s0165-2478(98)00127-8 · Cited by 102 · see citing works

Genetic regulation of leishmanial and mycobacterial infections: the Lsh / Ity / Bcg gene story continues

Blackwell, J. M., Barton, C. H., White, J. K., Roach, T. I. A., Shaw, M., Whitehead, S. H., Mock, B. A., Searle, S., Williams, H. P., & Baker, A.-M. (1994) · Immunology Letters · doi:10.1016/0165-2478(94)00161-8 · Cited by 98 · see citing works

Structure and function of the natural-resistance-associated macrophage protein (Nramp1), a candidate protein for infectious and autoimmune disease susceptibility

Blackwell, J. M. (1996) · Molecular Medicine Today · doi:10.1016/1357-4310(96)88773-9 · Cited by 97 · see citing works

Immunogenetics of leishmanial and mycobacterial infections: the Belem Family Study

Blackwell, J. M., Black, G. F., Peacock, C. S., Miller, E. N., Sibthorpe, D., Gnananandha, D., Shaw, J. J., Sílveira, F. T., Lins-Lainson, Z., Ramos, F., et al. (1997) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1997.0118 · Cited by 96 · see citing works

NH2-terminal sequence of macrophage-expressed natural resistance-associated macrophage protein (Nramp) encodes a proline/serine-rich putative Src homology 3-binding domain.

Barton, C. H., White, J. K., Roach, T. I. A., & Blackwell, J. M. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.179.5.1683 · Cited by 92 · see citing works

Metal Ions Suppress the Abnormal Taste Behavior of the Drosophila Mutant malvolio

Orgad, S., Nelson, H. R., Segal, D., & Nelson, N. (1998) · Journal of Experimental Biology · doi:10.1242/jeb.201.1.115 · Cited by 90 · see citing works

Linkage of rheumatoid arthritis to the candidate gene NRAMP1 on 2q35.

Shaw, M., Clayton, D. G., Atkinson, S. E., Williams, H. B., Miller, N., Sibthorpe, D., & Blackwell, J. M. (1996) · Journal of Medical Genetics · doi:10.1136/jmg.33.8.672 · Cited by 86 · see citing works

Nramp1 locus encodes a 65 kDa interferon-γ-inducible protein in murine macrophages

ATKINSON, P. G. P., BLACKWELL, J. M., & BARTON, C. H. (1997) · Biochemical Journal · doi:10.1042/bj3250779 · Cited by 81 · see citing works

The macrophage resistance gene Lsh/Ity/Bcg

Blackwell, J. M. (1989) · Research in Immunology · doi:10.1016/0923-2494(89)90029-1 · Cited by 81 · see citing works

Nramp1 transfection transfers Ity/Lsh/Bcg-related pleiotropic effects on macrophage activation: influence on antigen processing and presentation

Lang, T., Prina, E., Sibthorpe, D., & Blackwell, J. M. (1997) · Infection and Immunity · doi:10.1128/iai.65.2.380-386.1997 · Cited by 75 · see citing works

Genetic regulation of macrophage priming/activation: the Lsh gene story

Blackwell, J. M., Roach, T. I. A., Atkinson, S. E., Ajioka, J. W., Barton, C. H., & Shaw, M. (1991) · Immunology Letters · doi:10.1016/0165-2478(91)90032-6 · Cited by 74 · see citing works

The natural resistance-associated macrophage protein gene is associated with Crohn's disease

Hofmeister, A., Neibergs, H. L., Pokorny, R. M., & Galandiuk, S. (1997) · Surgery · doi:10.1016/s0039-6060(97)90006-4 · Cited by 72 · see citing works

Genetic Control of Immune Response to Recombinant Antigens Carried by an AttenuatedSalmonella typhimuriumVaccine Strain:Nramp1Influences T-Helper Subset Responses and Protection against Leishmanial Challenge

Soo, S.-S., Villarreal‐Ramos, B., Khan, C. M. A., Hormaeche, C. E., & Blackwell, J. M. (1998) · Infection and Immunity · doi:10.1128/iai.66.5.1910-1917.1998 · Cited by 68 · see citing works

Genetic analysis of chromosome 2 in type 1 diabetes: analysis of putative loci IDDM7, IDDM12, and IDDM13 and candidate genes NRAMP1 and IA-2 and the interleukin-1 gene cluster. IMDIAB Group.

Esposito, L., Hill, N. J., Pritchard, L. E., Cucca, F., Muxworthy, C., Merriman, M. E., Wilson, A., Julier, C., Délepine, M., Tuomilehto, J., et al. (1998) · Diabetes · doi:10.2337/diabetes.47.11.1797 · Cited by 63 · see citing works

The Bcg Gene Story

Skamene, E. (1994) · Immunobiology · doi:10.1016/s0171-2985(11)80451-1 · Cited by 62 · see citing works

Genetic and Physical Mapping of 2q35 in the Region of the NRAMP and IL8R Genes: Identification of a Polymorphic Repeat in Exon 2 of NRAMP

White, J. K., Shaw, M., Barton, C. H., Cerretti, D. P., Williams, H. P., Mock, B. A., Carter, N. P., Peacock, C. S., & Blackwell, J. M. (1994) · Genomics · doi:10.1006/geno.1994.1619 · Cited by 55 · see citing works

Cytokine-mediated activation of macrophages from Mycobacterium bovis BCG-resistant and -susceptible mice: differential effects of corticosterone on antimycobacterial activity and expression of the Bcg gene (Candidate Nramp)

Brown, D., Lafuse, W. P., & Zwilling, B. S. (1995) · Infection and Immunity · doi:10.1128/iai.63.8.2983-2988.1995 · Cited by 50 · see citing works

Identification of a highly polymorphic length variant in the 3'UTR of NRAMP1

Buu, N., Cellier, M. F., Gros, P., & Schurr, E. (1995) · Immunogenetics · doi:10.1007/bf00179408 · Cited by 43 · see citing works

Zn2+ depletion blocks endosome fusion

Aballay, A., Sarrouf, M. N., Colombo, M. I., Stahl, P. D., & Mayorga, L. S. (1995) · Biochemical Journal · doi:10.1042/bj3120919 · Cited by 37 · see citing works

T-helper 1-like subset selection in Mycobacterium bovis bacillus Calmette-Guérin-infected resistant and susceptible mice.

Kramnik, I., Radzioch, D., & Skamene, E. (1994) · PubMed · Cited by 35 · see citing works

Lsh, Antigen presentation and the development of CMI

Kaye, P. M., & Blackwell, J. M. (1989) · Research in Immunology · doi:10.1016/0923-2494(89)90038-2 · Cited by 32 · see citing works

Molecular mechanisms of natural resistance to mycobacterial infections.

Radzioch, D., Kramnik, I., & Skamene, E. (1994) · PubMed · Cited by 27 · see citing works

A Factor with a Zinc- and Phorbol Ester-Binding Domain Is Necessary for Endosome Fusion

Aballay, A., Arenas, N. G., Quest, A. F. G., & Mayorga, L. S. (1997) · Experimental Cell Research · doi:10.1006/excr.1997.3643 · Cited by 6 · see citing works

Macrophage defense mechanisms against intracellular bacteria

Weiss, G., & Schaible, U. E. (2015) · Immunological Reviews · doi:10.1111/imr.12266 · Cited by 989 · see citing works

The Continuing Challenges of Leprosy

Scollard, D. M., Adams, L. B., Gillis, T., Krahenbuhl, J. L., Truman, R. W., & Williams, D. L. (2006) · Clinical Microbiology Reviews · doi:10.1128/cmr.19.2.338-381.2006 · Cited by 930 · see citing works

Mycobacterium tuberculosis: here today, and here tomorrow

Russell, D. G. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35085034 · Cited by 781 · see citing works

Innate Immunity toMycobacterium tuberculosis

van Crevel, R., Ottenhoff, T. H. M., & van der Meer, J. W. M. (2002) · Clinical Microbiology Reviews · doi:10.1128/cmr.15.2.294-309.2002 · Cited by 602 · see citing works

Iron, anaemia, and inflammatory bowel diseases

Gasché, C., Lomer, M. C. E., Cavill, I., & Weiss, G. (2004) · Gut · doi:10.1136/gut.2003.035758 · Cited by 496 · see citing works

Elemental Analysis of Mycobacterium avium -, Mycobacterium tuberculosis -, and Mycobacterium smegmatis -Containing Phagosomes Indicates Pathogen-Induced Microenvironments within the Host Cell’s Endosomal System

Wagner, D., Maser, J. M., Lai, B. C. H., Cai, Z., Barry, C. E., zu Bentrup, K. H., Russell, D. G., & Bermudez, L. E. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.3.1491 · Cited by 430 · see citing works

Iron at the interface of immunity and infection

Nairz, M., Haschka, D., Demetz, E., & Weiss, G. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00152 · Cited by 325 · see citing works

Iron metabolism in the anemia of chronic disease

Weiss, G. (2009) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2008.08.006 · Cited by 322 · see citing works

Emerging themes in manganese transport, biochemistry and pathogenesis in bacteria

Kehres, D. G., & Maguire, M. E. (2003) · FEMS Microbiology Reviews · doi:10.1016/s0168-6445(03)00052-4 · Cited by 284 · see citing works

Pathogenesis and treatment of anaemia of chronic disease

Weiß, G. (2002) · Blood Reviews · doi:10.1054/blre.2002.0193 · Cited by 276 · see citing works

The Genomics and Genetics of Human Infectious Disease Susceptibility

Hill, A. V. S. (2001) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.2.1.373 · Cited by 264 · see citing works

SLC11A1 (formerly NRAMP1) and disease resistance. Microreview

Blackwell, J. M., Goswami, T., Evans, C. A., Sibthorpe, D., Papo, N., White, J. K., Searle, S., Miller, E. N., Peacock, C. S., Mohammed, H., et al. (2001) · Cellular Microbiology · doi:10.1046/j.1462-5822.2001.00150.x · Cited by 242 · see citing works

Genetic susceptibility to infectious diseases: big is beautiful (and will bigger be even better?)

Burgner, D., Jamieson, S., & Blackwell, J. (2006) · Lancet. Infectious Diseases (Print) · doi:10.1016/s1473-3099(06)70601-6 · Cited by 234 · see citing works

Natural-resistance-associated macrophage protein 1 is an H+/bivalent cation antiporter

GOSWAMI, T., BHATTACHARJEE, A., BABAL, P., SEARLE, S., MOORE, E., LI, M., & BLACKWELL, J. M. (2001) · Biochemical Journal · doi:10.1042/bj3540511 · Cited by 218 · see citing works

Life in vacuoles – nutrient acquisition by Leishmania amastigotes

Burchmore, R., & Barrett, M. P. (2001) · International Journal for Parasitology · doi:10.1016/s0020-7519(01)00259-4 · Cited by 211 · see citing works

Iron in immune cell function and host defense

Haschka, D., Hoffmann, A., & Weiss, G. (2021) · Seminars in Cell &amp; Developmental Biology · doi:10.1016/j.semcdb.2020.12.005 · Cited by 188 · see citing works

Divalent cation transport and susceptibility to infectious and autoimmune disease: continuation of the Ity/Lsh/Bcg/Nramp1/Slc11a1 gene story

Blackwell, J. M., Searle, S., Mohamed, H., & White, J. K. (2003) · Immunology Letters · doi:10.1016/s0165-2478(02)00231-6 · Cited by 169 · see citing works

Role of apoptosis and autophagy in tuberculosis

Lam, A., Prabhu, R., Groß, C., Riesenberg, L. A., Singh, V., & Aggarwal, S. (2017) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00162.2017 · Cited by 175 · see citing works

Modification of iron regulation by the inflammatory response

WEISS, G. (2005) · Best Practice &amp; Research Clinical Haematology · doi:10.1016/j.beha.2004.09.001 · Cited by 161 · see citing works

Role of Iron in<i>Nramp1</i>-Mediated Inhibition of Mycobacterial Growth

Zwilling, B. S., Kuhn, D. E., Wikoff, L., Brown, D., & Lafuse, W. (1999) · Infection and Immunity · doi:10.1128/iai.67.3.1386-1392.1999 · Cited by 155 · see citing works

Interleukin‐10, Polymorphism in<i>SLC11A1</i>(formerly<i>NRAMP1</i>), and Susceptibility to Tuberculosis

Awomoyi, A. A., Marchant, A., Howson, J. M. M., McAdam, K. P. W. J., Blackwell, J. M., & Newport, M. J. (2002) · The Journal of Infectious Diseases · doi:10.1086/345920 · Cited by 153 · see citing works

Innate Immunity to Mycobacterium Tuberculosis

van Crevel, R., Ottenhoff, T. H. M., & van der Meer, J. W. M. (2003) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-0059-9_20 · Cited by 141 · see citing works

C‐reactive protein collaborates with plasma lectins to boost immune response against bacteria

Ng, P. M. L., Saux, A. L., Lee, C. M., Tan, N. S., Lu, J., Thiel, S., Ho, B., & Ding, J. L. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601762 · Cited by 122 · see citing works

Differential iron transport into phagosomes isolated from the RAW264.7 macrophage cell lines transfected with Nramp1Gly169 or Nramp1Asp169

Kuhn, D. E., Baker, B. D., Lafuse, W. P., & Zwilling, B. S. (1999) · Journal of Leukocyte Biology · doi:10.1002/jlb.66.1.113 · Cited by 113 · see citing works

Genetics of susceptibility to leprosy

Fitness, J., Tosh, K., & Hill, A. V. S. (2002) · Genes and Immunity · doi:10.1038/sj.gene.6363926 · Cited by 113 · see citing works

Molecular Mechanisms of Salmonella Virulence and Host Resistance

Valdez, Y., Ferreira, R. B. R., & Finlay, B. B. (2009) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-01846-6_4 · Cited by 111 · see citing works

SLC11A1 (formerly NRAMP1) and susceptibility to visceral leishmaniasis in The Sudan

Mohamed, H. S., Ibrahim, M. E., Miller, E. N., White, J. K., Cordell, H. J., Howson, J. M. M., Peacock, C. S., Khalil, E. A. G., Hassan, A. M. E., & Blackwell, J. M. (2003) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5201089 · Cited by 107 · see citing works

Function and Mechanism of Action of <i>Dictyostelium</i> Nramp1 (Slc11a1) in Bacterial Infection

Peracino, B., Wagner, C., Balest, A., Balbo, A., Pergolizzi, B., Noegel, A. A., Steinert, M., & Bozzaro, S. (2006) · Traffic · doi:10.1111/j.1600-0854.2005.00356.x · Cited by 96 · see citing works

Mitigating the Impact of Antibacterial Drug Resistance through Host-Directed Therapies: Current Progress, Outlook, and Challenges

Chiang, C.-Y., Uzoma, I., Moore, R. T., Gilbert, M., Duplantier, A. J., & Panchal, R. G. (2018) · mBio · doi:10.1128/mbio.01932-17 · Cited by 95 · see citing works

Genetic susceptibility to mycobacterial disease in humans

Fernando, S. L., & Britton, W. J. (2006) · Immunology and Cell Biology · doi:10.1111/j.1440-1711.2006.01420.x · Cited by 94 · see citing works

Antimicrobial responses of teleost phagocytes and innate immune evasion strategies of intracellular bacteria

Grayfer, L., Hodgkinson, J. W., & Belosevic, M. (2013) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2013.08.003 · Cited by 93 · see citing works

Nramp1 Functionality Increases Inducible Nitric Oxide Synthase Transcription Via Stimulation of IFN Regulatory Factor 1 Expression

Fritsche, G., Dlaska, M., Barton, H., Theurl, I., Garimorth, K., & Weiss, G. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.4.1994 · Cited by 86 · see citing works

Iron transport into<i>Mycobacterium avium</i>-containing phagosomes from an<i>Nramp1</i><i>Gly169</i>-transfected RAW264.7 macrophage cell line

Kuhn, D. E., Lafuse, W. P., & Zwilling, B. S. (2001) · Journal of Leukocyte Biology · doi:10.1189/jlb.69.1.43 · Cited by 79 · see citing works

SLC11A1 (NRAMP1) but not SLC11A2 (NRAMP2) polymorphisms are associated with susceptibility to tuberculosis in a high-incidence community in South Africa.

Hoal, E. G., Lewis, L., Jamieson, S., Tanzer, F., Rossouw, M., Victor, T., Hillerman, R., Beyers, N., Blackwell, J. M., & van Helden, P. D. (2004) · PubMed · Cited by 77 · see citing works

High level expression of Nramp1G169 in RAW264.7 cell transfectants: analysis of intracellular iron transport

ATKINSON, & Barton (1999) · Immunology · doi:10.1046/j.1365-2567.1999.00672.x · Cited by 74 · see citing works

Slc11a1 (Nramp1) impairs growth of <i>Salmonella enterica</i> serovar <i>typhimurium</i> in macrophages via stimulation of lipocalin-2 expression

Fritsche, G., Nairz, M., Libby, S. J., Fang, F. C., & Weiss, G. (2012) · Journal of Leukocyte Biology · doi:10.1189/jlb.1111554 · Cited by 72 · see citing works

Key players in the regulation of iron homeostasis at the host-pathogen interface

Ullah, I., & Lang, M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1279826 · Cited by 76 · see citing works

Nramp1 drives an accelerated inflammatory response duringSalmonella-induced colitis in mice

Valdez, Y., Graßl, G. A., Guttman, J. A., Coburn, B. A., Gros, P., Vallance, B. A., & Finlay, B. B. (2008) · Cellular Microbiology · doi:10.1111/j.1462-5822.2008.01258.x · Cited by 74 · see citing works

Mycobacterium avium subsp. paratuberculosis as a trigger of type-1 diabetes: destination Sardinia, or beyond?

Rani, P. S., Sechi, L. A., & Ahmed, N. (2010) · Gut Pathogens · doi:10.1186/1757-4749-2-1 · Cited by 74 · see citing works

The Macrophage: A Cellular Factory at the Interphase Between Iron and Immunity for the Control of Infections

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Natural resistance-associated macrophage protein 1 gene polymorphisms and response to vaccine against or challenge with Salmonella enteritidis in young chicks

Liu, W., Kaiser, M., & Lamont, S. J. (2003) · Poultry Science · doi:10.1093/ps/82.2.259 · Cited by 67 · see citing works

A review of the immunopathogenesis of Brucellosis

Amjadi, O., Rafiei, A., Mardani, M., Zafari, P., & Zarifian, A. (2019) · Scandinavian Journal of Infectious Diseases · doi:10.1080/23744235.2019.1568545 · Cited by 60 · see citing works

Benefits and risks of iron therapy for chronic anaemias

Weiss, G., & Gordeuk, V. R. (2005) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2005.01529.x · Cited by 54 · see citing works

Breeding for Disease Resistance in Farm Animals (2nd edition)

Axford, R. F. E., Bishop, S., Nicholas, F. W., & Owen, J. (2000) · Cited by 53 · see citing works

Paratuberculosis and Type I diabetes Is this the trigger?

Dow, C. T. (2006) · Medical Hypotheses · doi:10.1016/j.mehy.2006.04.029 · Cited by 48 · see citing works

Expression of the SLC11A1 (NRAMP1) 5′-(GT) repeat: Opposite effect in the presence of −237C→T

Zaahl, M. G., Robson, K., Warnich, L., & Kotze, M. J. (2004) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2004.04.003 · Cited by 48 · see citing works

Inflammatory bowel disease is associated with a novel promoter polymorphism of natural resistance‐associated macrophage protein 1 (NRAMP1) gene

Kojima, Y., Kinouchi, Y., Takahashi, S., Negoro, K., Hiwatashi, N., & Shimosegawa, T. (2001) · Tissue Antigens · doi:10.1034/j.1399-0039.2001.580606.x · Cited by 48 · see citing works

The interplay between Salmonella typhimurium and its macrophage host—what can it teach us about innate immunity?

Linehan, S. A., & Holden, D. W. (2003) · Immunology Letters · doi:10.1016/s0165-2478(02)00227-4 · Cited by 47 · see citing works

Ion Transporters Involved in Acidification of the Resorption Lacuna in Osteoclasts

Henriksen, K., Sørensen, M. G., Jensen, V. K., Dziegiel, M. H., Nosjean, O., & Karsdal, M. A. (2008) · Calcified Tissue International · doi:10.1007/s00223-008-9168-8 · Cited by 44 · see citing works

Pro-efferocytic nanotherapies reduce vascular inflammation without inducing anemia in a large animal model of atherosclerosis

Bamezai, S., Zhang, Y., Kumari, M., Lotfi, M., Alsaigh, T., Luo, L., Kumar, G. S., Wang, F., Ye, J., Puri, M., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-52005-1 · Cited by 43 · see citing works

The Reduced Bactericidal Function of Complement C5-Deficient Murine Macrophages Is Associated with Defects in the Synthesis and Delivery of Reactive Oxygen Radicals to Mycobacterial Phagosomes

Daniel, D., Dai, G., Singh, C. R., Lindsey, D. R., Smith, A. K., Dhandayuthapani, S., Hunter, R. L., & Jagannath, C. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.7.4688 · Cited by 38 · see citing works

Dual RNA-Seq Analysis of Trichophyton rubrum and HaCat Keratinocyte Co-Culture Highlights Important Genes for Fungal-Host Interaction

Petrucelli, M. F., Peronni, K. C., Sanches, P. R., Komoto, T. T., Matsuda, J. B., Silva, W. A., Beleboni, R. O., Martinez-Rossi, N. M., Marins, M., & Fachin, A. L. (2018) · Genes · doi:10.3390/genes9070362 · Cited by 37 · see citing works

Polymorphisms of the Human NRAMP1 Gene are Associated With Response to Bacillus Calmette-Guerin Immunotherapy for Superficial Bladder Cancer

Decobert, M., LaRue, H., Bergeron, A., Harel, F., Pfister, C., Rousseau, F., Lacombe, L., & Fradet, Y. (2006) · The Journal of Urology · doi:10.1016/s0022-5347(05)00653-1 · Cited by 36 · see citing works

Induction, binding specificity and function of human ICOS

Beier, K. C., Hutloff, A., Dittrich, A., Heuck, C. J., Rauch, A. M., Büchner, K., Ludewig, B., Ochs, H. D., Mages, H. W., & Kroczek, R. A. (2000) · European Journal of Immunology · doi:10.1002/1521-4141(200012)30:12 · Cited by 179 · see citing works

Transition Metal Homeostasis in Streptococcus pyogenes and Streptococcus pneumoniae

Turner, A. G., Ong, C. Y., Walker, M. J., Djoko, K. Y., & McEwan, A. G. (2017) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/bs.ampbs.2017.01.002 · Cited by 34 · see citing works

Atopy in children in relation to BCG vaccination and genetic polymorphisms at SLC11A1 (formerly NRAMP1) and D2S1471

Alm, J. S., Sanjeevi, C. B., Miller, E. N., Dabadghao, P., Lilja, G., Pershagen, G., Blackwell, J. M., & Scheynius, A. (2002) · Genes and Immunity · doi:10.1038/sj.gene.6363834 · Cited by 34 · see citing works

Infection withMycobacterium aviumDifferentially Regulates the Expression of Iron Transport Protein mRNA in Murine Peritoneal Macrophages

Zhong, W., Lafuse, W. P., & Zwilling, B. S. (2001) · Infection and Immunity · doi:10.1128/iai.69.11.6618-6624.2001 · Cited by 35 · see citing works

Nrf2 Regulates Granuloma Formation and Macrophage Activation during Mycobacterium avium Infection via Mediating Nramp1 and HO-1 Expressions

Nakajima, M., Matsuyama, M., Kawaguchi, M., Kiwamoto, T., Matsuno, Y., Morishima, Y., Yoshida, K., SHERPA, M. T., Yazaki, K., Osawa, H., et al. (2021) · mBio · doi:10.1128/mbio.01947-20 · Cited by 32 · see citing works

Evidence of association with type 1 diabetes in the SLC11A1 gene region

Yang, J. H. M., Downes, K., Howson, J. M. M., Nutland, S. L., Stevens, H. E., Walker, N. M., & Todd, J. A. (2011) · BMC Medical Genetics · doi:10.1186/1471-2350-12-59 · Cited by 33 · see citing works

Role of functional polymorphisms of NRAMP1 gene for the development of Crohnʼs disease

Gazouli, M., Atsaves, V., Mantzaris, G. J., Economou, M., Nasioulas, G., Evangelou, K., Archimandritis, A. J., & Anagnou, N. P. (2008) · Inflammatory Bowel Diseases · doi:10.1002/ibd.20488 · Cited by 30 · see citing works

Novel single nucleotide polymorphisms and haplotypes within the bovine CXCR2 gene

Youngerman, S. M., Saxton, A. M., & Pighetti, G. M. (2004) · Immunogenetics · doi:10.1007/s00251-004-0699-5 · Cited by 29 · see citing works

Incomplete glycosylation and defective intracellular targeting of mutant solute carrier family 11 member 1 (Slc11a1)

White, J. K., Stewart, A., Popoff, J.-F., Wilson, S., & Blackwell, J. M. (2004) · Biochemical Journal · doi:10.1042/bj20040808 · Cited by 29 · see citing works

Effect of polymorphisms in the Slc11a1 coding region on resistance to brucellosis by macrophages in vitro and after challenge in two Bos breeds (Blanco Orejinegro and Zebu)

Martínez, R. A., Dunner, S., Toro, R., Tobón, J., Gallego, J. L., & Cañón, J. (2010) · Genetics and Molecular Biology · doi:10.1590/s1415-47572010000300014 · Cited by 29 · see citing works

The −237C→T promoter polymorphism of the SLC11A1 gene is associated with a protective effect in relation to inflammatory bowel disease in the South African population

Zaahl, M. G., Winter, T. A., Warnich, L., & Kotze, M. J. (2005) · International Journal of Colorectal Disease · doi:10.1007/s00384-005-0019-z · Cited by 29 · see citing works

Genetic Control of Disease Resistance and Immunoresponsiveness

Keirn, S. C., Freeman, A. E., & Kehrli, M. E. (2001) · Veterinary Clinics of North America Food Animal Practice · doi:10.1016/s0749-0720(15)30002-5 · Cited by 27 · see citing works

Analysis of Genetic Variation in the Bovine SLC11A1 Gene, Its Influence on the Expression of NRAMP1 and Potential Association With Resistance to Bovine Tuberculosis

Holder, A. L., Garty, R., Elder, C., Mesnard, P., Laquerbe, C., Bartens, M.-C., Salavati, M., Shabbir, M. Z., Tzelos, T., Connelly, T., et al. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01420 · Cited by 26 · see citing works

Association of Mycobacterium avium subsp. paratuberculosis and SLC11A1 polymorphisms in Sardinian multiple sclerosis patients

Cossu, D., Masala, S., Cocco, E. E., Paccagnini, D., Tranquilli, S., Frau, J., Marrosu, M. G., & Sechi, L. A. (2013) · The Journal of Infection in Developing Countries · doi:10.3855/jidc.2737 · Cited by 25 · see citing works

Molecular Interfaces of the Galactose-binding Protein Tectonin Domains in Host-Pathogen Interaction

Low, D. H. P., Frecer, V., Saux, A. L., Anand, G. S., Ho, B., Chen, J., & Ding, J. L. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.059774 · Cited by 25 · see citing works

Nramp1 Is Not a Major Determinant in the Control ofBrucella melitensisInfection in Mice

Guilloteau, L. L. A., Dornand, J., Gross, A., Olivier, M., Cortade, F., Vern, Y. L., & Kerbœuf, D. (2003) · Infection and Immunity · doi:10.1128/iai.71.2.621-628.2003 · Cited by 25 · see citing works

Genetic polymorphisms in lung disease: bandwagon or breakthrough?

Iannuzzi, M., Maliarik, M., & Rybicki, B. (2002) · Respiratory Research · doi:10.1186/rr164 · Cited by 29 · see citing works

Association of SLC11A1 (NRAMP1) polymorphisms with pulmonary Mycobacterium avium complex infection

Sapkota, B. R., Hijikata, M., Matsushita, I., Tanaka, G., Ieki, R., Kobayashi, N., Toyota, E., Nagai, H., Kurashima, A., Tokunaga, K., et al. (2012) · Human Immunology · doi:10.1016/j.humimm.2012.02.008 · Cited by 24 · see citing works

Effect of the mouse genotype on the expression of IFN-γ gene in early response to infection

Lalmanach, A.-C., Montagne, A., Menanteau, P., & Lantier, F. (2001) · Microbes and Infection · doi:10.1016/s1286-4579(01)01419-8 · Cited by 24 · see citing works

c-Myc Represses and Miz-1 Activates the Murine Natural Resistance-associated Protein 1 Promoter

Bowen, H., Biggs, T. E., Phillips, E. S., Baker, S. T., Perry, V. H., Mann, D. A., & Barton, C. H. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m204232200 · Cited by 23 · see citing works

Hypoxia inducible factor 1α: A critical factor for the immune response to pathogens and Leishmania

Charpentier, T., Hammami, A., & Stäger, S. (2016) · Cellular Immunology · doi:10.1016/j.cellimm.2016.06.002 · Cited by 21 · see citing works

Association of NRAMP1 gene polymorphism with the productive traits of the Ukrainian Large White pig

Ващенко, П. А., Саєнко, А. М., Сухно, В. В., Церенюк, О., Babicz, M., SHKAVRO, N., Smołucha, G., & Łuszczewska‐Sierakowska, I. (2022) · Medycyna Weterynaryjna · doi:10.21521/mw.6698 · Cited by 22 · see citing works

Polymorphism, Expression of Natural Resistance-associated Macrophage Protein 1 Encoding Gene (NRAMP1) and Its Association with Immune Traits in Pigs

Ding, X., Zhang, X., Yang, Y., Ding, Y., Xue, W., Meng, Y., Zhu, W., & Yin, Z. (2014) · Asian-Australasian Journal of Animal Sciences · doi:10.5713/ajas.2014.14017 · Cited by 21 · see citing works

HFIP‐induced structures and assemblies of the peptides from the transmembrane domain 4 of membrane protein Nramp1

Xue, R., Wang, S., Wang, C., Zhu, T., Li, F., & Sun, H. (2006) · Biopolymers · doi:10.1002/bip.20478 · Cited by 21 · see citing works

Disruption of the Nramp1 (also known as Slc11a1) gene in Kupffer cells attenuates early-phase, warm ischemia-reperfusion injury in the mouse liver

Wyllie, S., Seu, P., Gao, F., Gros, P., & Goss, J. A. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.72.5.885 · Cited by 20 · see citing works

Induction of Nramp2 in activated mouse macrophages is dissociated from regulation of the Nramp1, classical inflammatory genes, and genes involved in iron metabolism

Wardrop, S. L., Wells, C. A., Ravasi, T., Hume, D. A., & Richardson, D. R. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.71.1.99 · Cited by 19 · see citing works

Salmonella Typhimurium undergoes distinct genetic adaption during chronic infections of mice

Søndberg, E., & Jelsbak, L. (2016) · BMC Microbiology · doi:10.1186/s12866-016-0646-2 · Cited by 19 · see citing works

Association of functional polymorphisms of SLC11A1 with risk of esophageal cancer in the South African Colored population

Zaahl, M. G., Warnich, L., Victor, T. C., & Kotze, M. J. (2005) · Cancer Genetics and Cytogenetics · doi:10.1016/j.cancergencyto.2004.09.017 · Cited by 19 · see citing works

Mycobacterium tuberculosis: Macrophage Takeover and Modulation of Innate Effector Responses

Bhat, K. H., & Yaseen, I. (2018) · InTech eBooks · doi:10.5772/intechopen.75003 · Cited by 18 · see citing works

Polimorfismos do gene NRAMP1 em indivíduos com reações hansênicas, atendidos em dois Centros de Referência no Recife, nordeste do Brasil

Teixeira, M. A. G., Silva, N. L., Ramos, A. D. L., Hatagima, A., & Magalhães, V. (2010) · Revista da Sociedade Brasileira de Medicina Tropical · doi:10.1590/s0037-86822010000300014 · Cited by 18 · see citing works

Variations in Equid SLC11A1 (NRAMP1) Genes and Associations with Rhodococcus equi Pneumonia in Horses

Halbert, N. D., Cohen, N. D., Slovis, N. M., Faircloth, J., & Martens, R. J. (2006) · Journal of Veterinary Internal Medicine · doi:10.1111/j.1939-1676.2006.tb01814.x · Cited by 18 · see citing works

Removal of the phage-shock protein PspB causes reduction of virulence in Salmonella enterica serovar Typhimurium independently of NRAMP1

Wallrodt, I., Jelsbak, L., Thomsen, L. E., Brix, L., Lemire, S., Gautier, L., Nielsen, D. S., Jovanović, G., Buck, M., & Olsen, J. E. (2014) · Journal of Medical Microbiology · doi:10.1099/jmm.0.072223-0 · Cited by 17 · see citing works

Genetic Susceptibility to Rhodococcus equi

McQueen, C. M., Dindot, S. V., Foster, M., & Cohen, N. D. (2015) · Journal of Veterinary Internal Medicine · doi:10.1111/jvim.13616 · Cited by 16 · see citing works

Variations in Equid SLC11A1 (NRAMP1) Genes and Associations with Rhodococcus Equi Pneumonia in Horses

Halbert, N. D., Cohen, N. D., Slovis, N. M., Faircloth, J., & Martens, R. J. (2006) · Journal of Veterinary Internal Medicine · doi:10.1892/0891-6640(2006)20[974:viesng]2.0.co;2 · Cited by 16 · see citing works

Structure analysis of the fourth transmembrane domain of Nramp1 in model membranes

Xue, R., Wang, S., Qi, H., Song, Y., Wang, C., & Li, F. (2008) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2008.02.005 · Cited by 15 · see citing works

Characterization of chicken natural resistance-associated macrophage protein encoding genes (Nramp1 and Nramp2) and association with salmonellosis resistance

He, X., Fang, M.-M., Zhang, Z. T., Hu, Y., Jia, X. Z., He, D. L., Liang, S. D., Nie, Q. H., & Zhang, X. Q. (2013) · Genetics and Molecular Research · doi:10.4238/2013.january.30.5 · Cited by 14 · see citing works

A study on IL8RB gene polymorphism as a potential immuno-compromised adherent in exaggeration of parenteral and mammo-crine oxidative stress during mastitis in buffalo

Nahas, S. M. E., kasas, A. H. E., Mossallem, A. A. A., Abdelhamid, M., & Warda, M. (2017) · Journal of Advanced Research · doi:10.1016/j.jare.2017.07.002 · Cited by 13 · see citing works

In vitro response of the striped bass natural resistance-associated macrophage protein, Nramp, to LPS and Mycobacterium marinum exposure

Burge, E. J., Gauthier, D. T., & Veld, P. A. V. (2004) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cca.2004.03.007 · Cited by 13 · see citing works

Iron and the Reticuloendothelial System

Weiß, G. (2011) · Humana Press eBooks · doi:10.1007/978-1-60327-485-2_11 · Cited by 13 · see citing works

Association of the solute carrier family 11 member 1 gene polymorphisms with susceptibility to leprosy in a Brazilian sample

Brochado, M. J. F., Gatti, M. F. C., Zago, M. A., & Roselino, A. M. F. (2016) · Memórias do Instituto Oswaldo Cruz · doi:10.1590/0074-02760150326 · Cited by 12 · see citing works

SLC11A1 gene polymorphisms in Korean patients with Behçet's disease

Kim, S., Jang, W., Park, S. B., Park, D. Y., Bang, K. T., Lee, S. S., Jun, J., Yoo, D. H., & Chang, H. K. (2006) · Scandinavian Journal of Rheumatology · doi:10.1080/03009740600704221 · Cited by 12 · see citing works

Influence ofSlc11a1(formerlyNramp1) on DSS-induced colitis in mice

Jiang, H., Gilchrist, D. S., Popoff, J.-F., Jamieson, S. E., Truscott, M., White, J. K., & Blackwell, J. M. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.0708397 · Cited by 11 · see citing works

NRAMP1 Polymorphisms like Susceptibility Marker in Mexican Focus of Cutaneous Leishmaniasis

Hernández-Rivera, M. P., Ramírez-Ramírez, A., Chiñas-Pérez, A., Monroy-Ostria, A., Cancino-Diaz, M. E., & Hernández-Montes, O. (2016) · BioMed Research International · doi:10.1155/2016/7951285 · Cited by 11 · see citing works

A new model of outbred genetically selected mice which present a strong acute inflammatory response in the absence of complement component C5

Amano, M. T., Carneiro, A. S., Ribeiro, O. G., Cabrera, W. K., Franco, M. D., Ibañez, O. M., Isaac, L., & Starobinas, N. (2009) · Inflammation Research · doi:10.1007/s00011-008-8132-4 · Cited by 11 · see citing works

Expressed Sequence Tag Analysis of Blood Cells in the Vanadium-Rich Ascidian, Ascidia sydneiensis samea–A Survey of Genes for Metal Accumulation

Yamaguchi, N., Togi, A., Ueki, T., Uyama, T., & Michibata, H. (2002) · ZOOLOGICAL SCIENCE · doi:10.2108/zsj.19.1001 · Cited by 11 · see citing works

Regulation of phagosomal iron release from murine macrophages by nitric oxide

Mulero, V., Wei, X., Liew, F. Y., & Brock, J. H. (2002) · Biochemical Journal · doi:10.1042/bj20011875 · Cited by 11 · see citing works

Quantitative PCR-Based Competitive Index for High-Throughput Screening of Salmonella Virulence Factors

Yoon, H., Gros, P., & Heffron, F. (2010) · Infection and Immunity · doi:10.1128/iai.00873-10 · Cited by 10 · see citing works

Nramp1 phagocyte intracellular metal withdrawal defense

Cellier, M. F., Courville, P., & Campion, C. (2007) · Microbes and Infection · doi:10.1016/j.micinf.2007.09.006 · Cited by 203 · see citing works

Nramp1

Gruenheid, S., Skamene, E., & Gros, P. (1999) · Advances in cellular and molecular biology of membranes and organelles · doi:10.1016/s1874-5172(99)80039-x · Cited by 3 · see citing works

Divalent-metal transport by NRAMP proteins at the interface of host–pathogen interactions

Forbes, J. R., & Gros, P. (2001) · Trends in Microbiology · doi:10.1016/s0966-842x(01)02098-4 · Cited by 424 · see citing works

Induction of Nramp2 in activated mouse macrophages is dissociated from regulation of the Nramp1, classical inflammatory genes, and genes involved in iron metabolism

Wardrop, S. L., Wells, C. A., Ravasi, T., Hume, D. A., & Richardson, D. R. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.71.1.99 · Cited by 19 · see citing works

SLC11 family of H + -coupled metal-ion transporters NRAMP1 and DMT1

Mackenzie, B., & Hediger, M. A. (2004) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-003-1141-9 · Cited by 123 · see citing works