Lista de obras - Zoubida Karim - Dominio Público Uruguay

A Variant of Peptide Transporter 2 Predicts the Severity of Porphyria-Associated Kidney Disease

artículo científico publicado en 2016

A variant erythroferrone disrupts iron homeostasis in SF3B1-mutated myelodysplastic syndrome

scientific article published on 01 July 2019

Acid pH increases the stability of BSC1/NKCC2 mRNA in the medullary thick ascending limb

artículo científico publicado en 2003

Acute intermittent porphyria causes hepatic mitochondrial energetic failure in a mouse model

artículo científico publicado en 2014

Antisense oligonucleotide-based therapy in human erythropoietic protoporphyria

artículo científico publicado en 2014

Cardiac iron overload in chronically transfused patients with thalassemia, sickle cell anemia, or myelodysplastic syndrome

artículo científico publicado en 2017

Dyserythropoiesis evaluated by RED score and hepcidin/ferritin levels predicts response to erythropoietin in lower risk myelodysplastic syndromes

scientific article published on 04 October 2018

Epistasis in iron metabolism: complex interactions between Cp, Mon1a, and Slc40a1 loci and tissue iron in mice.

artículo científico publicado en 2013

Erythroid-Progenitor-Targeted Gene Therapy Using Bifunctional TFR1 Ligand-Peptides in Human Erythropoietic Protoporphyria

scientific article published on 31 January 2019

Erythropoietin stimulates spleen BMP4-dependent stress erythropoiesis and partially corrects anemia in a mouse model of generalized inflammation.

artículo científico publicado en 2010

Exploring the role of galectin 3 in kidney function: a genetic approach.

artículo científico publicado en 2005

Extrahepatic hepcidin production: The intriguing outcomes of recent years

artículo científico publicado en 2019

From a dominant to an oligogenic model of inheritance with environmental modifiers in acute intermittent porphyria

artículo científico publicado en 2018

Functional EPO-Hepcidin axis in Recombinant human EPO independent hemodialysis patients

artículo científico publicado en 2019

GLRX5 mutations impair heme biosynthetic enzymes ALA synthase 2 and ferrochelatase in Human congenital sideroblastic anemia

artículo científico publicado en 2019

Genetic background influences hepcidin response to iron imbalance in a mouse model of hemolytic anemia (Congenital erythropoietic porphyria)

scientific article published on 07 October 2019

Hemolytic anemia repressed hepcidin level without hepatocyte iron overload: lesson from Günther disease model

artículo científico publicado en 2016

Hepatocellular carcinoma in acute hepatic porphyrias: A Damocles Sword

artículo científico publicado en 2018

Hepcidin as a Major Component of Renal Antibacterial Defenses against Uropathogenic Escherichia coli

artículo científico publicado en 2015

Hepcidin regulates intrarenal iron handling at the distal nephron.

artículo científico publicado en 2013

Heterozygous Mutations in BMP6 Pro-peptide Lead to Inappropriate Hepcidin Synthesis and Moderate Iron Overload in Humans

artículo científico publicado en 2015

High prevalence of and potential mechanisms for chronic kidney disease in patients with acute intermittent porphyria

artículo científico publicado en 2015

High urinary ferritin reflects myoglobin iron evacuation in DMD patients

artículo científico publicado en 2018

Intestinal DMT1 cotransporter is down-regulated by hepcidin via proteasome internalization and degradation.

artículo científico publicado en 2011

Iron is a substrate of the Plasmodium falciparum chloroquine resistance transporter PfCRT in Xenopus oocytes

artículo científico publicado en 2017

Iron metabolism and the role of the iron-regulating hormone hepcidin in health and disease.

artículo científico publicado en 2017

Iron metabolism: State of the art.

artículo científico publicado en 2017

Iron regulatory protein 1 sustains mitochondrial iron loading and function in frataxin deficiency.

artículo científico publicado en 2015

Iron status and inflammatory biomarkers in patients with acutely decompensated heart failure: early in-hospital phase and 30-day follow-up

artículo científico publicado en 2017

LC-MS/MS method for hepcidin-25 measurement in human and mouse serum: clinical and research implications in iron disorders.

artículo científico publicado en 2015

Management of iron overload in hemoglobinopathies.

artículo científico publicado en 2017

Mitochondrial energetic defects in muscle and brain of a Hmbs-/- mouse model of acute intermittent porphyria

artículo científico publicado en 2015

Mutation in human CLPX elevates levels of δ-aminolevulinate synthase and protoporphyrin IX to promote erythropoietic protoporphyria

artículo científico publicado en 2017

Porphyria and kidney diseases.

artículo científico publicado en 2018

Porphyrias: A 2015 update

artículo científico

Predominant role of microglia in brain iron retention in Sanfilippo syndrome, a pediatric neurodegenerative disease

artículo científico publicado en 2018

Protein kinase C isoforms in rat kidney proximal tubule: acute effect of angiotensin II

artículo científico publicado en 1995

Protoporphyrin retention in hepatocytes and Kupffer cells prevents sclerosing cholangitis in erythropoietic protoporphyria mouse model

artículo científico publicado en 2011

Recent concepts concerning the renal handling of NH3/NH4+.

artículo científico publicado en 2006

Recurrent attacks of acute hepatic porphyria: major role of the chronic inflammatory response in the liver

artículo científico publicado en 2018

Regulation and tissue-specific expression of δ-aminolevulinic acid synthases in non-syndromic sideroblastic anemias and porphyrias

artículo científico publicado en 2019

Regulation by PKC isoforms of Na(+)/H(+) exchanger in luminal membrane vesicles isolated from cortical tubules.

artículo científico publicado en 1999

Regulation of ROMK (Kir 1.1) channel expression in kidney thick ascending limb by hypertonicity: role of TonEBP and MAPK pathways

artículo científico publicado en 2006

Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1

scientific article published on 30 January 2019

Renal handling of NH3/NH4+: recent concepts

artículo científico publicado en 2005

Reply

artículo científico publicado en 2016

The microbiota shifts the iron sensing of intestinal cells.

artículo científico publicado en 2015

Zeta-crystallin mediates the acid pH-induced increase of BSC1 cotransporter mRNA stability

artículo científico publicado en 2009

[Effect of angiotensin ii on Na+/H+ exchangers of the renal tubule]

artículo científico publicado en 1998

[Role of the Na(+)-K+(NH4+)-2Cl cotransporter of the medullary ascending limb in the regulation of renal acid-base equilibrium]

artículo científico publicado en 2002

Lista de obras de Zoubida Karim

A Variant of Peptide Transporter 2 Predicts the Severity of Porphyria-Associated Kidney Disease

A variant erythroferrone disrupts iron homeostasis in SF3B1-mutated myelodysplastic syndrome

Acid pH increases the stability of BSC1/NKCC2 mRNA in the medullary thick ascending limb

Acute intermittent porphyria causes hepatic mitochondrial energetic failure in a mouse model

Antisense oligonucleotide-based therapy in human erythropoietic protoporphyria

Cardiac iron overload in chronically transfused patients with thalassemia, sickle cell anemia, or myelodysplastic syndrome

Dyserythropoiesis evaluated by RED score and hepcidin/ferritin levels predicts response to erythropoietin in lower risk myelodysplastic syndromes

Epistasis in iron metabolism: complex interactions between Cp, Mon1a, and Slc40a1 loci and tissue iron in mice.

Erythroid-Progenitor-Targeted Gene Therapy Using Bifunctional TFR1 Ligand-Peptides in Human Erythropoietic Protoporphyria

Erythropoietin stimulates spleen BMP4-dependent stress erythropoiesis and partially corrects anemia in a mouse model of generalized inflammation.

Exploring the role of galectin 3 in kidney function: a genetic approach.

Extrahepatic hepcidin production: The intriguing outcomes of recent years

From a dominant to an oligogenic model of inheritance with environmental modifiers in acute intermittent porphyria

Functional EPO-Hepcidin axis in Recombinant human EPO independent hemodialysis patients

GLRX5 mutations impair heme biosynthetic enzymes ALA synthase 2 and ferrochelatase in Human congenital sideroblastic anemia

Genetic background influences hepcidin response to iron imbalance in a mouse model of hemolytic anemia (Congenital erythropoietic porphyria)

Hemolytic anemia repressed hepcidin level without hepatocyte iron overload: lesson from Günther disease model

Hepatocellular carcinoma in acute hepatic porphyrias: A Damocles Sword

Hepcidin as a Major Component of Renal Antibacterial Defenses against Uropathogenic Escherichia coli

Hepcidin regulates intrarenal iron handling at the distal nephron.

Heterozygous Mutations in BMP6 Pro-peptide Lead to Inappropriate Hepcidin Synthesis and Moderate Iron Overload in Humans

High prevalence of and potential mechanisms for chronic kidney disease in patients with acute intermittent porphyria

High urinary ferritin reflects myoglobin iron evacuation in DMD patients

Intestinal DMT1 cotransporter is down-regulated by hepcidin via proteasome internalization and degradation.

Iron is a substrate of the Plasmodium falciparum chloroquine resistance transporter PfCRT in Xenopus oocytes

Iron metabolism and the role of the iron-regulating hormone hepcidin in health and disease.

Iron metabolism: State of the art.

Iron regulatory protein 1 sustains mitochondrial iron loading and function in frataxin deficiency.

Iron status and inflammatory biomarkers in patients with acutely decompensated heart failure: early in-hospital phase and 30-day follow-up

LC-MS/MS method for hepcidin-25 measurement in human and mouse serum: clinical and research implications in iron disorders.

Management of iron overload in hemoglobinopathies.

Mitochondrial energetic defects in muscle and brain of a Hmbs-/- mouse model of acute intermittent porphyria

Mutation in human CLPX elevates levels of δ-aminolevulinate synthase and protoporphyrin IX to promote erythropoietic protoporphyria

Porphyria and kidney diseases.

Porphyrias: A 2015 update

Predominant role of microglia in brain iron retention in Sanfilippo syndrome, a pediatric neurodegenerative disease

Protein kinase C isoforms in rat kidney proximal tubule: acute effect of angiotensin II

Protoporphyrin retention in hepatocytes and Kupffer cells prevents sclerosing cholangitis in erythropoietic protoporphyria mouse model

Recent concepts concerning the renal handling of NH3/NH4+.

Recurrent attacks of acute hepatic porphyria: major role of the chronic inflammatory response in the liver

Regulation and tissue-specific expression of δ-aminolevulinic acid synthases in non-syndromic sideroblastic anemias and porphyrias

Regulation by PKC isoforms of Na(+)/H(+) exchanger in luminal membrane vesicles isolated from cortical tubules.

Regulation of ROMK (Kir 1.1) channel expression in kidney thick ascending limb by hypertonicity: role of TonEBP and MAPK pathways

Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1

Renal handling of NH3/NH4+: recent concepts

Reply

The microbiota shifts the iron sensing of intestinal cells.

Zeta-crystallin mediates the acid pH-induced increase of BSC1 cotransporter mRNA stability

[Effect of angiotensin ii on Na+/H+ exchangers of the renal tubule]

[Role of the Na(+)-K+(NH4+)-2Cl cotransporter of the medullary ascending limb in the regulation of renal acid-base equilibrium]