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.

Mostrar otras versiones (1)

Hereditary haemochromatosis is an inherited disorder of iron absorption that leads to excessive iron storage in the liver and other organs. A candidate disease gene HFE has been identified that encodes a novel MHC class I like protein. We report the development of a monoclonal antibody (HFE-JB1) spe...

Descripción completa

Detalles Bibliográficos
Autores principales:	Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A
Formato:	Journal article
Lenguaje:	English
Publicado:	1998

Ejemplares similares

Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis
por: Bastin, J, et al.
Publicado: (1998)

HFE-Associated Hereditary Haemochromatosis
por: Emmeke J Eijkelkamp, et al.
Publicado: (2000-01-01)

Identification of new ligands for the haemochromatosis protein HFE
por: Drakesmith, H, et al.
Publicado: (2007)

Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload.
por: Townsend, A, et al.
Publicado: (2002)

Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload
por: Townsend, A, et al.
Publicado: (2002)

Clinical haemochromatosis in HFE mutation carriers.
por: Cox, T, et al.
Publicado: (2002)

Best practice guidelines for the molecular genetic diagnosis of Type 1 (HFE-related) hereditary haemochromatosis
por: Barton David E, et al.
Publicado: (2006-11-01)

Factors influencing disease phenotype and penetrance in HFE haemochromatosis.
por: Rochette, J, et al.
Publicado: (2010)

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
por: Merryweather-Clarke, A, et al.
Publicado: (2003)

Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience
por: Robson, K, et al.
Publicado: (2000)

Non HFE-related haemochromatosis: exclusion of the 1q21 zinc-iron regulated transporter-like (ZIRTL) gene in juvenile haemochromatosis.
por: Sebastiani, G, et al.
Publicado: (2003)

RECRUITMENT OF PATIENTS WITH HEREDITARY HAEMOCHROMATOSIS AS BLOOD DONORS
por: Marko Cukjati, et al.
Publicado: (2004-12-01)

Hereditary haemochromatosis, haemophagocytic lymphohistiocytosis and COVID-19
por: Matthew J. Riley, et al.
Publicado: (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
por: M. Vázquez Romero, et al.
Publicado: (2005-08-01)

The hemochromatosis protein HFE inhibits iron export from macrophages.
por: Drakesmith, H, et al.
Publicado: (2002)

Public health aspects of genetic screening for hereditary haemochromatosis in Australia
por: Dorota M. Gertig, et al.
Publicado: (2002-12-01)

The development of polycythemia vera after phlebotomy treatment for hereditary haemochromatosis
por: Erik JM vanBommel, et al.
Publicado: (2021-08-01)

Genetic mutations, diagnostic methods, and therapies related to hereditary haemochromatosis
por: Karina Marini Aguiar, et al.
Publicado: (2014-03-01)

HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank
por: Luke C Pilling, et al.
Publicado: (2024-03-01)

In vitro binding of HFE to the cation-independent mannose-6 phosphate receptor.
por: Schimanski, L, et al.
Publicado: (2009)

Ultrasound verified inflammation and structural damage in patients with hereditary haemochromatosis-related arthropathy
por: Christian Dejaco, et al.
Publicado: (2017-10-01)

Primary Biliary Cirrhosis-Specific Antimitochondrial Antibodies in Neonatal Haemochromatosis
por: Daniel S. Smyk, et al.
Publicado: (2013-01-01)

Inflammation can increase hepcidin in HFE‐hereditary hemochromatosis
por: Wenke Moris, et al.
Publicado: (2021-05-01)

Hereditary haemochromatosis: pilot study of case-finding approach to early diagnosis in primary care.
por: Emery, J, et al.
Publicado: (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.
por: Robson, K, et al.
Publicado: (2004)

Infertility: Consider haemochromatosis?
por: Lok, C, et al.
Publicado: (2007)

The molecular genetics of haemochromatosis
por: Shearman, J, et al.
Publicado: (1996)

The structure and function of HFE.
por: Drakesmith, H, et al.
Publicado: (2000)

Pilot study of early diagnosis of hereditary haemochromatosis through systematic case finding in primary care.
por: Emery, J, et al.
Publicado: (2002)

Pathogenesis Diagnostics and Treatment of Hereditary Haemochromatosis: A 150 Year-Long Understanding of an Iron Overload Disorder
por: Anastasia Asimakopoulou, et al.
Publicado: (2017-11-01)

Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis
por: Wei Zhang, et al.
Publicado: (2022-06-01)

Hereditary Hemochromatosis <it>(HFE) </it>genotypes in heart failure: Relation to etiology and prognosis
por: Torp-Pedersen Christian, et al.
Publicado: (2010-07-01)

JUVENILE HAEMOCHROMATOSIS MUTATIONS ARE NOT THAT SIMPLE
por: Bignell, P, et al.
Publicado: (2013)

Juvenile haemochromatosis in the Bangladeshi community
por: Lok, C, et al.
Publicado: (2007)

Therapeutic monoclonal antibodies with a focus on hereditary angioedema
por: Bruce L. Zuraw, et al.
Publicado: (2023-01-01)

Clinical applications of monoclonal antibodies.
por: Mcmichael, A, et al.
Publicado: (1980)

Erratum: Role of HFE in iron metabolism, hereditary haemochomatosis, anaemia of chronic disease and secondary iron overload (Lancet (March 2) (786))
por: Townsend, A, et al.
Publicado: (2002)

Role of HFE in iron metabolism, hereditary haemochomatosis, anaemia of chronic disease, and secondary iron overload (vol 359, pg 786, 2002)
por: Townsend, A, et al.
Publicado: (2002)

Diagnostic strategies using DNA testing for hereditary haemochromatosis in at-risk populations: a systematic review and economic evaluation
por: J Bryant, et al.
Publicado: (2009-04-01)

Screening for hereditary haemochromatosis in patients undergoing knee arthroplasty: a retrospective cohort study of 2,035 patients
por: Elisha Krasin, et al.
Publicado: (2021-12-01)