List of works - Daniel F. Wallace

A critical role for murine transferrin receptor 2 in erythropoiesis during iron restriction

article

A novel mutation in ferroportin implicated in iron overload

scientific article published on 28 February 2007

ATP7B variant penetrance explains differences between genetic and clinical prevalence estimates for Wilson disease

scientific article published on 04 April 2020

Analysis of IL-22 contribution to hepcidin induction and hypoferremia during the response to LPS in vivo.

scientific article published on 7 January 2015

Autosomal dominant iron overload due to a novel mutation of ferroportin1 associated with parenchymal iron loading and cirrhosis.

scientific article published in April 2004

Blunted hepcidin response to inflammation in the absence of Hfe and transferrin receptor 2.

scientific article published on 18 January 2011

Combined deletion of Hfe and transferrin receptor 2 in mice leads to marked dysregulation of hepcidin and iron overload.

scientific article

Defective trafficking and localization of mutated transferrin receptor 2: implications for type 3 hereditary hemochromatosis.

scientific article

Endofin, a novel BMP-SMAD regulator of the iron-regulatory hormone, hepcidin

scientific article

Evaluation of a bone morphogenetic protein 6 variant as a cause of iron loading.

scientific article

Ferroportin Expression in Adipocytes Does Not Contribute to Iron Homeostasis or Metabolic Responses to a High Calorie Diet.

scientific article

Ferroportin disease due to the A77D mutation in Australia.

scientific article published in July 2005

First phenotypic description of transferrin receptor 2 knockout mouse, and the role of hepcidin.

scientific article published on July 2005

Functional analysis and theoretical modeling of ferroportin reveals clustering of mutations according to phenotype.

scientific article published on 21 October 2009

Functional analysis of matriptase-2 mutations and domains: insights into the molecular basis of iron-refractory iron deficiency anemia

scientific article published on 14 January 2015

Genetic Variants in the BMP6 Pro-Peptide May Not Cause Iron Loading and Should Be Interpreted With Caution

scientific article published on 31 August 2016

Hematopoietic deletion of transferrin receptor 2 in mice leads to a block in erythroid differentiation during iron-deficient anemia.

scientific article

Hepatic Iron Deposition Does Not Predict Extrahepatic Iron Loading in Mouse Models of Hereditary Hemochromatosis

article

Hepcidin: regulation of the master iron regulator

scientific article (publication date: 2015)

Identification of ferroportin disease in the Indian subcontinent.

scientific article published on April 2005

In situ proximity ligation assays indicate that hemochromatosis proteins Hfe and transferrin receptor 2 (Tfr2) do not interact.

scientific article

Increased iron stores correlate with worse disease outcomes in a mouse model of schistosomiasis infection

scientific article

Iron loading and oxidative stress in the Atm-/- mouse liver.

scientific article

Iron storage disease in Asia-Pacific populations: the importance of non-HFE mutations.

scientific article published on July 2013

Juvenile iron overload--advances, but no answers

scientific article published on 01 October 2008

Linking hypoxia and iron homeostasis: a 'plate' full of factors

scientific article published on 04 April 2014

Next-generation sequencing: Application of a novel platform to analyze atypical iron disorders.

scientific article published on 04 July 2015

Non HFE-related haemochromatosis: exclusion of the 1q21 zinc-iron regulated transporter-like (ZIRTL) gene in juvenile haemochromatosis

scientific article published on 01 March 2003

Normal systemic iron homeostasis in mice with macrophage-specific deletion of transferrin receptor 2

scientific article published on 25 November 2015

Parenteral vs. oral iron: influence on hepcidin signaling pathways through analysis of Hfe/Tfr2-null mice.

scientific article published on 27 November 2013

Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease

scientific article published on 09 May 2018

Prohepcidin localises to the Golgi compartment and secretory pathway in hepatocytes

scientific article published on 01 October 2005

Purification and partial characterisation of recombinant human hepcidin

scientific article published on 18 August 2005

Targeted disruption of the hepatic transferrin receptor 2 gene in mice leads to iron overload.

scientific article published on 18 November 2006

The Regulation of Iron Absorption and Homeostasis

scientific article published on May 2016

The dynamics of hepcidin-ferroportin internalization and consequences of a novel ferroportin disease mutation.

scientific article

The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data.

scientific article

Therapeutic Advances in Regulating the Hepcidin/Ferroportin Axis

scientific article published on 25 November 2019

Transferrin receptor 1: a ferritin receptor as well?

scientific article published on 27 July 2010

List of works by Daniel F. Wallace

A critical role for murine transferrin receptor 2 in erythropoiesis during iron restriction

A novel mutation in ferroportin implicated in iron overload

ATP7B variant penetrance explains differences between genetic and clinical prevalence estimates for Wilson disease

Analysis of IL-22 contribution to hepcidin induction and hypoferremia during the response to LPS in vivo.

Autosomal dominant iron overload due to a novel mutation of ferroportin1 associated with parenchymal iron loading and cirrhosis.

Blunted hepcidin response to inflammation in the absence of Hfe and transferrin receptor 2.

Combined deletion of Hfe and transferrin receptor 2 in mice leads to marked dysregulation of hepcidin and iron overload.

Defective trafficking and localization of mutated transferrin receptor 2: implications for type 3 hereditary hemochromatosis.

Endofin, a novel BMP-SMAD regulator of the iron-regulatory hormone, hepcidin

Evaluation of a bone morphogenetic protein 6 variant as a cause of iron loading.

Ferroportin Expression in Adipocytes Does Not Contribute to Iron Homeostasis or Metabolic Responses to a High Calorie Diet.

Ferroportin disease due to the A77D mutation in Australia.

First phenotypic description of transferrin receptor 2 knockout mouse, and the role of hepcidin.

Functional analysis and theoretical modeling of ferroportin reveals clustering of mutations according to phenotype.

Functional analysis of matriptase-2 mutations and domains: insights into the molecular basis of iron-refractory iron deficiency anemia

Genetic Variants in the BMP6 Pro-Peptide May Not Cause Iron Loading and Should Be Interpreted With Caution

Hematopoietic deletion of transferrin receptor 2 in mice leads to a block in erythroid differentiation during iron-deficient anemia.

Hepatic Iron Deposition Does Not Predict Extrahepatic Iron Loading in Mouse Models of Hereditary Hemochromatosis

Hepcidin: regulation of the master iron regulator

Identification of ferroportin disease in the Indian subcontinent.

In situ proximity ligation assays indicate that hemochromatosis proteins Hfe and transferrin receptor 2 (Tfr2) do not interact.

Increased iron stores correlate with worse disease outcomes in a mouse model of schistosomiasis infection

Iron loading and oxidative stress in the Atm-/- mouse liver.

Iron storage disease in Asia-Pacific populations: the importance of non-HFE mutations.

Juvenile iron overload--advances, but no answers

Linking hypoxia and iron homeostasis: a 'plate' full of factors

Next-generation sequencing: Application of a novel platform to analyze atypical iron disorders.

Non HFE-related haemochromatosis: exclusion of the 1q21 zinc-iron regulated transporter-like (ZIRTL) gene in juvenile haemochromatosis

Normal systemic iron homeostasis in mice with macrophage-specific deletion of transferrin receptor 2

Parenteral vs. oral iron: influence on hepcidin signaling pathways through analysis of Hfe/Tfr2-null mice.

Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease

Prohepcidin localises to the Golgi compartment and secretory pathway in hepatocytes

Purification and partial characterisation of recombinant human hepcidin

Targeted disruption of the hepatic transferrin receptor 2 gene in mice leads to iron overload.

The Regulation of Iron Absorption and Homeostasis

The dynamics of hepcidin-ferroportin internalization and consequences of a novel ferroportin disease mutation.

The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data.

Therapeutic Advances in Regulating the Hepcidin/Ferroportin Axis

Transferrin receptor 1: a ferritin receptor as well?