ArticleNature communications2019
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions.
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Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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10citing papers in PubMed
1.2field-weighted citation impact, top 24% of its field
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Who cites it
10 citing papers in PubMed, 21 citations in OpenAlex.
- Role of Endogenous Myoglobin in Anthracycline Response in Breast Cancer.Biomolecules · 2026Article
- Mutation-induced heme pocket destabilization in myoglobinopathy.Frontiers in bioinformatics · 2026Article
- Sex-specific response to A1BG loss results in female dilated cardiomyopathy.Biology of sex differences · 2025Article
- Dominantly inherited muscle disorders: understanding their complexity and exploring therapeutic approaches.Disease models & mechanisms · 2024Review
- Pseudoperoxidase activity, conformational stability, and aggregation propensity of the His98Tyr myoglobin variant: implications for the onset of myoglobinopathy.The FEBS journal · 2022Article
- Article
- Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients.Genome medicine · 2021Article
- Panorama of the distal myopathies.Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2020Review
- Targeted gene panel use in 2249 neuromuscular patients: the Australasian referral center experience.Annals of clinical and translational neurology · 2020Article
- Top ten discoveries of the year: Neuromuscular disease.Free neuropathology · 2020Article
Corrections and comments
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Authors and funding
44 authors at 19 institutions in 12 countries.
Montse OlivéNeuropathology Unit, Department of Pathology and Neuromuscular Unit, Department of Neurology, IDIBELL-Hospital de Bellvitge, Hospitalet de Llobregat, Barcelona, 08907, Spain. montseolivep@gmail.com.ORCID http://orcid.org/0000-0001-5727-0165
Martin EngvallDepartment of Molecular Medicine and Surgery, Science for Life Laboratory, Karolinska Institutet, Stockholm, SE-17176, Sweden.
Gianina RavenscroftCentre for Medical Research, University of Western Australia, Harry Perkins Institute of Medical Research, Perth, 6000, WA, Australia.
Macarena Cabrera-SerranoNeurology Department and Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío, Seville, 41013, Spain.
Hong JiaoDepartment of Biosciences and Nutrition, Science for Life Laboratory, Karolinska Institutet, Stockholm, SE-14157, Sweden.
Carlo Augusto BortolottiDepartment of Life Sciences, University of Modena and Reggio Emilia, Modena, 41121, Italy.ORCID http://orcid.org/0000-0002-5701-5727
Marcello PignataroDepartment of Chemical and Geological Sciences, University of Modena and Reggio Emilia, Modena, 41121, Italy.ORCID http://orcid.org/0000-0003-0058-3659
Matteo LambrughiDepartment of Life Sciences, University of Modena and Reggio Emilia, Modena, 41121, Italy.
Haibo JiangSchool of Molecular Sciences, The University of Western Australia, 35 Stirling Highway, Crawley, 6009, WA, Australia.
Alistair R R ForrestCentre for Medical Research, University of Western Australia, Harry Perkins Institute of Medical Research, Perth, 6000, WA, Australia.
Núria Benseny-CasesALBA Synchrotron Light Source, Cerdanyola del Vallès, Barcelona, 08290, Spain.
Stefan HofbauerDivision of Biochemistry, Department of Chemistry, Vienna Institute of BioTechnology, BOKU-University of Natural Resources and Life Sciences, Vienna, A-1180, Austria.ORCID http://orcid.org/0000-0003-3375-7715
Christian ObingerDivision of Biochemistry, Department of Chemistry, Vienna Institute of BioTechnology, BOKU-University of Natural Resources and Life Sciences, Vienna, A-1180, Austria.ORCID http://orcid.org/0000-0002-7133-3430
Gianantonio BattistuzziDepartment of Chemical and Geological Sciences, University of Modena and Reggio Emilia, Modena, 41121, Italy.
Marzia BelleiDepartment of Life Sciences, University of Modena and Reggio Emilia, Modena, 41121, Italy.
Marco BorsariDepartment of Chemical and Geological Sciences, University of Modena and Reggio Emilia, Modena, 41121, Italy.ORCID http://orcid.org/0000-0002-3612-4764
Giulia Di RoccoDepartment of Life Sciences, University of Modena and Reggio Emilia, Modena, 41121, Italy.
Helena M ViolaSchool of Human Sciences, The University of Western Australia, Perth, 6000, Western Australia, Australia.
Livia C HoolSchool of Human Sciences, The University of Western Australia, Perth, 6000, Western Australia, Australia.
Josep CladeraUnitat de Biofísica, Departament de Bioquímica i de Biologia Molecular, Facultat de Medicina, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain.
Kristina Lagerstedt-RobinsonDepartment of Molecular Medicine and Surgery, Karolinska Institutet, and Department of Clinical Genetics, Karolinska University Hospital, Solna, Stockholm, SE-17176, Sweden.
Fengqing XiangDepartment of Women's and Children's Health, Karolinska Institutet, Stockholm, SE-17177, Sweden.
Anna WredenbergCentre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, SE-17177, Sweden.
Francesc MirallesNeurology Department, Hospital Son Espases, Palma de Mallorca, 07120, Spain.
Juan José BaigesNeurology Department, Hospital Verge de la Cinta, Tortosa, 43500, Spain.
Edoardo MalfattiUniversité Sorbonne, UPMC Univ Paris 06, INSERM; UMRS974, CNRS FRE3617, Center for Research in Myology, GH Pitié-Salpêtrière, 47 Boulevard de l'hôpital, 75013, Paris, France.
Norma B RomeroUniversité Sorbonne, UPMC Univ Paris 06, INSERM; UMRS974, CNRS FRE3617, Center for Research in Myology, GH Pitié-Salpêtrière, 47 Boulevard de l'hôpital, 75013, Paris, France.
Nathalie StreichenbergerCentre de Pathologie et Neuropathologie Est, Hospices Civils de Lyon; Université Claude Bernard Lyon1, Institut NeuroMyogène CNRS UMR 5310-INSERM U1217; Institut NeuroMyogène, Villeurbanne, 69677, France.
Christophe VialElectromyographie-Groupement Hospitalier Est, Hospices Civils de Lyon, 69677, France.
Kristl G ClaeysDepartment of Neurology, University Hospitals Leuven, Leuven, 2333, Belgium.
Chiara S M StraathofDepartment of Neurology, Leiden University Medical Center, Leiden, 2333, The Netherlands.
An GorisKU Leuven-University of Leuven, Laboratory for Neuroimmunology, Department of Neurosciences, Experimental Neurology, Leuven, 2333, Belgium.
Christoph FreyerCentre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, SE-17177, Sweden.ORCID http://orcid.org/0000-0003-0418-1673
Martin LammensDepartment of Pathology, Antwerp University Hospital, Edegem, 2650, Belgium.
Guillaume BassezNeuromuscular Reference Center, Henri Mondor University Hospital AP-HP, INSERM U955, Team 10, Biology of the Neuromuscular System, East-Paris University (UPEC), Paris, 94010, France.
Juha KereDepartment of Biosciences and Nutrition, Science for Life Laboratory, Karolinska Institutet, Stockholm, SE-14157, Sweden.ORCID http://orcid.org/0000-0003-1974-0271
Paula ClementeDepartment of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, SE-17177, Sweden.
Thomas SejersenDepartment of Women's and Children's Health, Karolinska Institutet, Stockholm, SE-17177, Sweden.ORCID http://orcid.org/0000-0001-5961-7097
Bjarne UddNeuromuscular Research Center, Tampere University Hospital, University of Tampere, Tampere, 33521, Finland.
Noemí VidalNeuropathology Unit, Department of Pathology and Neuromuscular Unit, Department of Neurology, IDIBELL-Hospital de Bellvitge, Hospitalet de Llobregat, Barcelona, 08907, Spain.
Isidre FerrerNeuropathology Unit, Department of Pathology and Neuromuscular Unit, Department of Neurology, IDIBELL-Hospital de Bellvitge, Hospitalet de Llobregat, Barcelona, 08907, Spain.
Lars EdströmCenter for Molecular Medicine, Karolinska Institutet, Stockolm, 17177, Sweden.
Anna WedellDepartment of Molecular Medicine and Surgery, Science for Life Laboratory, Karolinska Institutet, Stockholm, SE-17176, Sweden.
Nigel G LaingCentre for Medical Research, University of Western Australia, Harry Perkins Institute of Medical Research, Perth, 6000, WA, Australia. nigel.laing@uwa.edu.au.
Karolinska University Hospital · SEUniversity of Modena and Reggio Emilia · ITThe University of Western Australia · AUKarolinska Institutet · SEBellvitge University Hospital · ESBOKU University · ATCentre National de la Recherche Scientifique · FRKU Leuven · BEALBA Synchrotron (Spain) · ESHospices Civils de Lyon · FRHospital Universitari de Tortosa Verge de la Cinta · ESHospital Universitario Son Espases · ESInserm · FRInstituto de Biomedicina de Sevilla · ESLeiden University Medical Center · NLRadboud University Nijmegen · NLUniversitat Autònoma de Barcelona · ESUniversité Claude Bernard Lyon 1 · FRUniversity of Helsinki · FI
Funding
No grant is acknowledged in the PubMed record.
Abstract
Myoglobin, encoded by MB, is a small cytoplasmic globular hemoprotein highly expressed in cardiac myocytes and oxidative skeletal myofibers. Myoglobin binds O
Indexed as
AdultFemaleHeart FailureHemeHumansInclusion BodiesMaleMiddle AgedMuscle Fibers, SkeletalMuscle, SkeletalMuscle WeaknessMuscular DiseasesMutationMyocytes, CardiacMyoglobinOxygenHemeMyoglobinOxygenSuperoxides
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