Lista de obras - Nathan V Subramaniam - Dominio Público Uruguay

A 29-Kilodalton Golgi SolubleN-Ethylmaleimide-sensitive Factor Attachment Protein Receptor (Vti1-rp2) Implicated in Protein Trafficking in the Secretory Pathway ⬇️

artículo científico publicado el 21 de agosto de 1998

A SNARE involved in protein transport through the Golgi apparatus ⬇️

artículo científico publicado el 23 de octubre de 1997

A corn oil-based diet protects against combined ethanol and iron-induced liver injury in a mouse model of hemochromatosis.

artículo científico publicado en 2013

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

article

A novel mouse model of veno-occlusive disease provides strategies to prevent thioguanine-induced hepatic toxicity

artículo científico publicado en 2013

A novel mutation in ferroportin implicated in iron overload

scientific article published on 28 February 2007

Altered lipid metabolism in Hfe-knockout mice promotes severe NAFLD and early fibrosis

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

artículo científico publicado en 2004

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

artículo científico publicado en 2011

Carrier-mediated thyroid hormone transport into placenta by placental transthyretin.

artículo científico publicado en 2009

Cirrhosis in Hemochromatosis: Independent Risk Factors in 368 HFE p.C282Y Homozygotes.

artículo científico publicado en 2018

Clinical expression of C282Y homozygous HFE haemochromatosis at 14 years of age

artículo científico publicado en 2006

Combination curcumin and vitamin E treatment attenuates diet-induced steatosis in Hfe-/- mice.

artículo científico publicado en 2017

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

artículo científico publicado en 2009

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

artículo científico publicado en 2007

Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis.

artículo científico publicado en 2003

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

artículo científico publicado en 2015

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

artículo científico publicado en 2018

Excess iron modulates endoplasmic reticulum stress-associated pathways in a mouse model of alcohol and high-fat diet-induced liver injury.

artículo científico publicado en 2013

Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload.

artículo científico publicado en 2015

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

artículo científico publicado en 2018

Ferroportin disease due to the A77D mutation in Australia.

artículo científico publicado en 2005

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

artículo científico publicado en 2005

Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y

scientific article published on 01 April 2002

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

artículo científico publicado en 2009

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

artículo científico publicado en 2015

G80S-linked ferroportin disease: Classical ferroportin disease in an Asian family and reclassification of the mutant as iron transport defective ⬇️

artículo científico publicado el 1 de octubre de 2010

GNPAT p.D519G is independently associated with markedly increased iron stores in HFE p.C282Y homozygotes.

artículo científico publicado en 2016

GS15, a 15-kilodalton Golgi soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) homologous to rbet1

scientific journal article

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

artículo científico publicado en 2016

HFE gene and hemochromatosis.

artículo científico publicado en 2004

Haemochromatosis in the new millennium.

artículo científico publicado en 2000

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

artículo científico publicado en 2016

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

article

Hepatic iron concentration correlates with insulin sensitivity in nonalcoholic fatty liver disease.

artículo científico publicado en 2018

Hepcidin regulation by HFE and TFR2: is it enough to give a hepatocyte a complex?

artículo científico publicado en 2009

Heterozygous Hfe gene deletion leads to impaired glucose homeostasis, but not liver injury in mice fed a high-calorie diet.

artículo científico publicado en 2016

How much iron is too much?

artículo científico publicado en 2008

Identification of ferritin receptors: their role in iron homeostasis, hepatic injury, and inflammation

artículo científico publicado en 2009

Identification of ferroportin disease in the Indian subcontinent.

artículo científico publicado en 2005

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

artículo científico publicado en 2013

Inactivation of the murine Transferrin Receptor 2 gene using the Cre recombinase: loxP system.

artículo científico publicado en 2004

Inconsistent hepatic antifibrotic effects with the iron chelator deferasirox

artículo científico publicado en 2015

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

artículo científico publicado en 2010

Iron Inhibits the Secretion of Apolipoprotein E in Cultured Human Adipocytes

artículo científico publicado en 2018

Iron and non-alcoholic fatty liver disease

artículo científico publicado en 2016

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

artículo científico publicado en 2011

Iron predicts tolerance in liver transplantation

scientific article published on 25 July 2012

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

artículo científico

Ironing out steatohepatitis

artículo científico publicado en 2017

Juvenile iron overload--advances, but no answers

artículo científico publicado en 2008

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

artículo científico publicado en 2014

Mammalian Bet3 functions as a cytosolic factor participating in transport from the ER to the Golgi apparatus

scientific journal article

N-Ethylmaleimide-sensitive factor (NSF) and alpha-soluble NSF attachment proteins (SNAP) mediate dissociation of GS28-syntaxin 5 Golgi SNAP receptors (SNARE) complex

artículo científico publicado en 1997

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

artículo científico

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

artículo científico publicado en 2015

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

artículo científico publicado en 2002

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

artículo científico publicado en 2013

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

artículo científico publicado en 2018

Pocket-sized iron regulators: one size fits all?

artículo científico publicado en 2016

Probiotics modify tight-junction proteins in an animal model of nonalcoholic fatty liver disease.

artículo científico publicado en 2016

Prohepcidin localises to the Golgi compartment and secretory pathway in hepatocytes

artículo científico publicado en 2005

Purification and partial characterisation of recombinant human hepcidin

artículo científico publicado en 2005

Redox cycling metals: Pedaling their roles in metabolism and their use in the development of novel therapeutics

artículo científico publicado en 2016

Regulation of Iron Homeostasis: Is It All in the HBD?

artículo científico publicado en 2009

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artículo científico publicado en 2017

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artículo científico publicado en 2015

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scientific article published on 15 March 2016

Reply: To PMID 25605615.

artículo científico publicado en 2015

Reversal of end-stage heart failure in juvenile hemochromatosis with iron chelation therapy: a case report.

artículo científico publicado en 2018

Role of p97 and syntaxin 5 in the assembly of transitional endoplasmic reticulum.

artículo científico

Serum hyaluronic acid with serum ferritin accurately predicts cirrhosis and reduces the need for liver biopsy in C282Y hemochromatosis.

artículo científico publicado en 2009

Syntaxin 5 is required for copper homeostasis in Drosophila and mammals

artículo científico publicado en 2010

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

artículo científico publicado en 2006

The Mammalian Protein (rbet1) Homologous to Yeast Bet1p Is Primarily Associated with the Pre-Golgi Intermediate Compartment and Is Involved in Vesicular Transport from the Endoplasmic Reticulum to the Golgi Apparatus ⬇️

artículo científico publicado el 1 de diciembre de 1997

The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis

artículo científico publicado en 2006

The control of iron homeostasis: microRNAS join the party

artículo científico publicado en 2011

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

artículo científico publicado en 2017

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

artículo científico publicado en 2015

The liver in regulation of iron homeostasis

artículo científico publicado en 2017

The relationship between systemic iron homeostasis and erythropoiesis.

artículo científico publicado en 2017

Transferrin receptor 1: a ferritin receptor as well?

artículo científico publicado en 2010

Transforming growth factor-β and toll-like receptor-4 polymorphisms are not associated with fibrosis in haemochromatosis

artículo científico publicado en 2013

Transthyretin-thyroid hormone internalization by trophoblasts.

artículo científico publicado en 2013

Lista de obras de Nathan V Subramaniam

A 29-Kilodalton Golgi SolubleN-Ethylmaleimide-sensitive Factor Attachment Protein Receptor (Vti1-rp2) Implicated in Protein Trafficking in the Secretory Pathway ⬇️

A SNARE involved in protein transport through the Golgi apparatus ⬇️

A corn oil-based diet protects against combined ethanol and iron-induced liver injury in a mouse model of hemochromatosis.

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

A novel mouse model of veno-occlusive disease provides strategies to prevent thioguanine-induced hepatic toxicity

A novel mutation in ferroportin implicated in iron overload

Altered lipid metabolism in Hfe-knockout mice promotes severe NAFLD and early fibrosis

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.

Carrier-mediated thyroid hormone transport into placenta by placental transthyretin.

Cirrhosis in Hemochromatosis: Independent Risk Factors in 368 HFE p.C282Y Homozygotes.

Clinical expression of C282Y homozygous HFE haemochromatosis at 14 years of age

Combination curcumin and vitamin E treatment attenuates diet-induced steatosis in Hfe-/- mice.

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.

Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis.

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.

Excess iron modulates endoplasmic reticulum stress-associated pathways in a mouse model of alcohol and high-fat diet-induced liver injury.

Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload.

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.

Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y

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

G80S-linked ferroportin disease: Classical ferroportin disease in an Asian family and reclassification of the mutant as iron transport defective ⬇️

GNPAT p.D519G is independently associated with markedly increased iron stores in HFE p.C282Y homozygotes.

GS15, a 15-kilodalton Golgi soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) homologous to rbet1

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

HFE gene and hemochromatosis.

Haemochromatosis in the new millennium.

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

Hepatic iron concentration correlates with insulin sensitivity in nonalcoholic fatty liver disease.

Hepcidin regulation by HFE and TFR2: is it enough to give a hepatocyte a complex?

Heterozygous Hfe gene deletion leads to impaired glucose homeostasis, but not liver injury in mice fed a high-calorie diet.

How much iron is too much?

Identification of ferritin receptors: their role in iron homeostasis, hepatic injury, and inflammation

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.

Inactivation of the murine Transferrin Receptor 2 gene using the Cre recombinase: loxP system.

Inconsistent hepatic antifibrotic effects with the iron chelator deferasirox

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

Iron Inhibits the Secretion of Apolipoprotein E in Cultured Human Adipocytes

Iron and non-alcoholic fatty liver disease

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

Iron predicts tolerance in liver transplantation

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

Ironing out steatohepatitis

Juvenile iron overload--advances, but no answers

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

Mammalian Bet3 functions as a cytosolic factor participating in transport from the ER to the Golgi apparatus

N-Ethylmaleimide-sensitive factor (NSF) and alpha-soluble NSF attachment proteins (SNAP) mediate dissociation of GS28-syntaxin 5 Golgi SNAP receptors (SNARE) complex

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

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

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

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

Pocket-sized iron regulators: one size fits all?

Probiotics modify tight-junction proteins in an animal model of nonalcoholic fatty liver disease.

Prohepcidin localises to the Golgi compartment and secretory pathway in hepatocytes

Purification and partial characterisation of recombinant human hepcidin

Redox cycling metals: Pedaling their roles in metabolism and their use in the development of novel therapeutics

Regulation of Iron Homeostasis: Is It All in the HBD?

Reply

Reply

Reply

Reply: To PMID 25605615.

Reversal of end-stage heart failure in juvenile hemochromatosis with iron chelation therapy: a case report.

Role of p97 and syntaxin 5 in the assembly of transitional endoplasmic reticulum.

Serum hyaluronic acid with serum ferritin accurately predicts cirrhosis and reduces the need for liver biopsy in C282Y hemochromatosis.

Syntaxin 5 is required for copper homeostasis in Drosophila and mammals

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

The Mammalian Protein (rbet1) Homologous to Yeast Bet1p Is Primarily Associated with the Pre-Golgi Intermediate Compartment and Is Involved in Vesicular Transport from the Endoplasmic Reticulum to the Golgi Apparatus ⬇️

The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis

The control of iron homeostasis: microRNAS join the party

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