| Iron-regulatory proteins limit hypoxia-inducible factor-2α expression in iron deficiency M Sanchez, B Galy, MU Muckenthaler, MW Hentze Nature structural & molecular biology 14 (5), 420-426, 2007 | 352 | 2007 |
| Iron refractory iron deficiency anemia L De Falco, M Sanchez, L Silvestri, C Kannengiesser, MU Muckenthaler, ... haematologica 98 (6), 845, 2013 | 214 | 2013 |
| An Hfe-dependent pathway mediates hyposideremia in response to lipopolysaccharide-induced inflammation in mice CN Roy, ÁO Custodio, J De Graaf, S Schneider, I Akpan, LK Montross, ... Nature genetics 36 (5), 481-485, 2004 | 145 | 2004 |
| Iron regulation and the cell cycle: identification of an iron-responsive element in the 3′-untranslated region of human cell division cycle 14A mRNA by a refined microarray … M Sanchez, B Galy, T Dandekar, P Bengert, Y Vainshtein, J Stolte, ... Journal of Biological Chemistry 281 (32), 22865-22874, 2006 | 137 | 2006 |
| Iron regulatory protein-1 and-2: transcriptome-wide definition of binding mRNAs and shaping of the cellular proteome by iron regulatory proteins M Sanchez, B Galy, B Schwanhaeusser, J Blake, T Bähr-Ivacevic, ... Blood, The Journal of the American Society of Hematology 118 (22), e168-e179, 2011 | 136 | 2011 |
| Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls M Sánchez, M Bruguera, J Bosch, J Rodés, F Ballesta, R Oliva Journal of hepatology 29 (5), 725-728, 1998 | 126 | 1998 |
| Hemochromatosis classification: update and recommendations by the BIOIRON Society D Girelli, F Busti, P Brissot, I Cabantchik, MU Muckenthaler, G Porto Blood, The Journal of the American Society of Hematology 139 (20), 3018-3029, 2022 | 110 | 2022 |
| SIREs: searching for iron-responsive elements M Campillos, I Cases, MW Hentze, M Sanchez Nucleic acids research 38 (suppl_2), W360-W367, 2010 | 99 | 2010 |
| The European hematology association roadmap for European hematology research: a consensus document A Engert, C Balduini, A Brand, B Coiffier, C Cordonnier, H Döhner, ... haematologica 101 (2), 115, 2016 | 94 | 2016 |
| Matriptase-2 mutations in iron-refractory iron deficiency anemia patients provide new insights into protease activation mechanisms AJ Ramsay, V Quesada, M Sanchez, C Garabaya, MP Sardà, M Baiget, ... Human molecular genetics 18 (19), 3673-3683, 2009 | 80 | 2009 |
| Population screening for hemochromatosis: a study in 5370 Spanish blood donors M Sánchez, M Villa, M Ingelmo, C Sanz, M Bruguera, C Ascaso, R Oliva Journal of hepatology 38 (6), 745-750, 2003 | 73 | 2003 |
| Functional and Clinical Impact of Novel Tmprss6 Variants in Iron‐Refractory Iron‐Deficiency Anemia Patients and Genotype–Phenotype Studies L De Falco, L Silvestri, C Kannengiesser, E Morán, C Oudin, M Rausa, ... Human mutation 35 (11), 1321-1329, 2014 | 72 | 2014 |
| Genética médica R Oliva, J Oriola, F Ballesta, J Clària, L Mengual Edicions Universitat Barcelona, 2013 | 68 | 2013 |
| Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia C Kannengiesser, M Sanchez, M Sweeney, G Hetet, B Kerr, E Moran, ... Haematologica 96 (6), 808, 2011 | 65 | 2011 |
| Identification of conserved potentially regulatory sequences of the SRY gene from 10 different species of mammals E Margarit, A Guillén, C Rebordosa, J Vidal-Taboada, M Sánchez, ... Biochemical and biophysical research communications 245 (2), 370-377, 1998 | 65 | 1998 |
| Contributors and Hemochromatosis International Taskforce. Therapeutic recommendations in HFE hemochromatosis for p. Cys282Tyr (C282Y/C282Y) homozygous genotype P Adams, A Altes, P Brissot, B Butzeck, I Cabantchik, R Cançado, ... | 63* | 2018 |
| Novel mutations in the ferritin-L iron-responsive element that only mildly impair IRP binding cause hereditary hyperferritinaemia cataract syndrome S Luscieti, G Tolle, J Aranda, CB Campos, F Risse, É Morán, ... Orphanet journal of rare diseases 8, 1-10, 2013 | 54 | 2013 |
| Functional consequences of transferrin receptor‐2 mutations causing hereditary hemochromatosis type 3 R Joshi, M Shvartsman, E Morán, S Lois, J Aranda, A Barqué, ... Molecular Genetics & Genomic Medicine 3 (3), 221-232, 2015 | 38 | 2015 |
| Genetic and clinical heterogeneity in thirteen new cases with aceruloplasminemia. Atypical anemia as a clue for an early diagnosis M Vila Cuenca, G Marchi, A Barqué, C Esteban-Jurado, A Marchetto, ... International journal of molecular sciences 21 (7), 2374, 2020 | 35 | 2020 |
| Mycobacteria-induced anaemia revisited: a molecular approach reveals the involvement of NRAMP1 and lipocalin-2, but not of hepcidin PN Rodrigues, SS Gomes, JV Neves, S Gomes-Pereira, M Correia-Neves, ... Immunobiology 216 (10), 1127-1134, 2011 | 35 | 2011 |
martina Muckenthaler在 med.uni-heidelberg.de 的电子邮件经过验证
