Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis

Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis

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Bibliografski detalji
Glavni autori:	Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A
Format:	Journal article
Izdano:	1998

Slični predmeti

Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis.
od: Bastin, J, i dr.
Izdano: (1998)

HFE-Associated Hereditary Haemochromatosis
od: Emmeke J Eijkelkamp, i dr.
Izdano: (2000-01-01)

Identification of new ligands for the haemochromatosis protein HFE
od: Drakesmith, H, i dr.
Izdano: (2007)

Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload.
od: Townsend, A, i dr.
Izdano: (2002)

Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload
od: Townsend, A, i dr.
Izdano: (2002)

Clinical haemochromatosis in HFE mutation carriers.
od: Cox, T, i dr.
Izdano: (2002)

Best practice guidelines for the molecular genetic diagnosis of Type 1 (HFE-related) hereditary haemochromatosis
od: Barton David E, i dr.
Izdano: (2006-11-01)

Factors influencing disease phenotype and penetrance in HFE haemochromatosis.
od: Rochette, J, i dr.
Izdano: (2010)

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
od: Merryweather-Clarke, A, i dr.
Izdano: (2003)

Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience
od: Robson, K, i dr.
Izdano: (2000)

Non HFE-related haemochromatosis: exclusion of the 1q21 zinc-iron regulated transporter-like (ZIRTL) gene in juvenile haemochromatosis.
od: Sebastiani, G, i dr.
Izdano: (2003)

RECRUITMENT OF PATIENTS WITH HEREDITARY HAEMOCHROMATOSIS AS BLOOD DONORS
od: Marko Cukjati, i dr.
Izdano: (2004-12-01)

Hereditary haemochromatosis, haemophagocytic lymphohistiocytosis and COVID-19
od: Matthew J. Riley, i dr.
Izdano: (2020-10-01)

Penetrancia familiar del gen HFE: los cuatro hermanos de una familia afectados por hemocromatosis hereditaria Familiar penetrancy of HFE gene: four brothers of the same family affected by hereditary haemochromatosis
od: M. Vázquez Romero, i dr.
Izdano: (2005-08-01)

The hemochromatosis protein HFE inhibits iron export from macrophages.
od: Drakesmith, H, i dr.
Izdano: (2002)

Public health aspects of genetic screening for hereditary haemochromatosis in Australia
od: Dorota M. Gertig, i dr.
Izdano: (2002-12-01)

The development of polycythemia vera after phlebotomy treatment for hereditary haemochromatosis
od: Erik JM vanBommel, i dr.
Izdano: (2021-08-01)

Genetic mutations, diagnostic methods, and therapies related to hereditary haemochromatosis
od: Karina Marini Aguiar, i dr.
Izdano: (2014-03-01)

HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank
od: Luke C Pilling, i dr.
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In vitro binding of HFE to the cation-independent mannose-6 phosphate receptor.
od: Schimanski, L, i dr.
Izdano: (2009)

Ultrasound verified inflammation and structural damage in patients with hereditary haemochromatosis-related arthropathy
od: Christian Dejaco, i dr.
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Primary Biliary Cirrhosis-Specific Antimitochondrial Antibodies in Neonatal Haemochromatosis
od: Daniel S. Smyk, i dr.
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Inflammation can increase hepcidin in HFE‐hereditary hemochromatosis
od: Wenke Moris, i dr.
Izdano: (2021-05-01)

Hereditary haemochromatosis: pilot study of case-finding approach to early diagnosis in primary care.
od: Emery, J, i dr.
Izdano: (2001)

Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.
od: Robson, K, i dr.
Izdano: (2004)

Infertility: Consider haemochromatosis?
od: Lok, C, i dr.
Izdano: (2007)

The molecular genetics of haemochromatosis
od: Shearman, J, i dr.
Izdano: (1996)

The structure and function of HFE.
od: Drakesmith, H, i dr.
Izdano: (2000)

Pilot study of early diagnosis of hereditary haemochromatosis through systematic case finding in primary care.
od: Emery, J, i dr.
Izdano: (2002)

Pathogenesis Diagnostics and Treatment of Hereditary Haemochromatosis: A 150 Year-Long Understanding of an Iron Overload Disorder
od: Anastasia Asimakopoulou, i dr.
Izdano: (2017-11-01)

Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis
od: Wei Zhang, i dr.
Izdano: (2022-06-01)

Hereditary Hemochromatosis <it>(HFE) </it>genotypes in heart failure: Relation to etiology and prognosis
od: Torp-Pedersen Christian, i dr.
Izdano: (2010-07-01)

JUVENILE HAEMOCHROMATOSIS MUTATIONS ARE NOT THAT SIMPLE
od: Bignell, P, i dr.
Izdano: (2013)

Juvenile haemochromatosis in the Bangladeshi community
od: Lok, C, i dr.
Izdano: (2007)

Therapeutic monoclonal antibodies with a focus on hereditary angioedema
od: Bruce L. Zuraw, i dr.
Izdano: (2023-01-01)

Clinical applications of monoclonal antibodies.
od: Mcmichael, A, i dr.
Izdano: (1980)

Erratum: Role of HFE in iron metabolism, hereditary haemochomatosis, anaemia of chronic disease and secondary iron overload (Lancet (March 2) (786))
od: Townsend, A, i dr.
Izdano: (2002)

Role of HFE in iron metabolism, hereditary haemochomatosis, anaemia of chronic disease, and secondary iron overload (vol 359, pg 786, 2002)
od: Townsend, A, i dr.
Izdano: (2002)

Diagnostic strategies using DNA testing for hereditary haemochromatosis in at-risk populations: a systematic review and economic evaluation
od: J Bryant, i dr.
Izdano: (2009-04-01)

Screening for hereditary haemochromatosis in patients undergoing knee arthroplasty: a retrospective cohort study of 2,035 patients
od: Elisha Krasin, i dr.
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