Zoubida Karim

researcher

Zoubida Karim is …
instance of (P31):
humanQ5

External links are
P269IdRef ID174709374
P496ORCID iD0000-0002-3724-5592
P214VIAF cluster ID305983039

P185doctoral studentRaed DaherQ58393673
P734family nameKarimQ37099341
P735given name???Q74421605
???Q74421605
P106occupationresearcherQ1650915
P21sex or genderfemaleQ6581072

Reverse relations

author (P50)
Q51229898A Variant of Peptide Transporter 2 Predicts the Severity of Porphyria-Associated Kidney Disease
Q91775903A variant erythroferrone disrupts iron homeostasis in SF3B1-mutated myelodysplastic syndrome
Q44560782Acid pH increases the stability of BSC1/NKCC2 mRNA in the medullary thick ascending limb
Q59590280Acute intermittent porphyria causes hepatic mitochondrial energetic failure in a mouse model
Q37693360Antisense oligonucleotide-based therapy in human erythropoietic protoporphyria
Q36296712Cardiac iron overload in chronically transfused patients with thalassemia, sickle cell anemia, or myelodysplastic syndrome
Q57027140Dyserythropoiesis evaluated by RED score and hepcidin/ferritin levels predicts response to erythropoietin in lower risk myelodysplastic syndromes
Q44115012Epistasis in iron metabolism: complex interactions between Cp, Mon1a, and Slc40a1 loci and tissue iron in mice.
Q91321350Erythroid-Progenitor-Targeted Gene Therapy Using Bifunctional TFR1 Ligand-Peptides in Human Erythropoietic Protoporphyria
Q42906357Erythropoietin stimulates spleen BMP4-dependent stress erythropoiesis and partially corrects anemia in a mouse model of generalized inflammation.
Q46706379Exploring the role of galectin 3 in kidney function: a genetic approach.
Q92685570Extrahepatic hepcidin production: The intriguing outcomes of recent years
Q87588017From a dominant to an oligogenic model of inheritance with environmental modifiers in acute intermittent porphyria
Q57161823Functional EPO-Hepcidin axis in Recombinant human EPO independent hemodialysis patients
Q91123013GLRX5 mutations impair heme biosynthetic enzymes ALA synthase 2 and ferrochelatase in Human congenital sideroblastic anemia
Q90636459Genetic background influences hepcidin response to iron imbalance in a mouse model of hemolytic anemia (Congenital erythropoietic porphyria)
Q37618819Hemolytic anemia repressed hepcidin level without hepatocyte iron overload: lesson from Günther disease model
Q58578906Hepatocellular carcinoma in acute hepatic porphyrias: A Damocles Sword
Q36624644Hepcidin as a Major Component of Renal Antibacterial Defenses against Uropathogenic Escherichia coli
Q39161145Hepcidin regulates intrarenal iron handling at the distal nephron.
Q38818590Heterozygous Mutations in BMP6 Pro-peptide Lead to Inappropriate Hepcidin Synthesis and Moderate Iron Overload in Humans
Q41129067High prevalence of and potential mechanisms for chronic kidney disease in patients with acute intermittent porphyria
Q62381824High urinary ferritin reflects myoglobin iron evacuation in DMD patients
Q50529592Intestinal DMT1 cotransporter is down-regulated by hepcidin via proteasome internalization and degradation.
Q38646046Iron is a substrate of the Plasmodium falciparum chloroquine resistance transporter PfCRT in Xenopus oocytes
Q47412147Iron metabolism and the role of the iron-regulating hormone hepcidin in health and disease.
Q40140993Iron metabolism: State of the art.
Q41480174Iron regulatory protein 1 sustains mitochondrial iron loading and function in frataxin deficiency.
Q88093117Iron status and inflammatory biomarkers in patients with acutely decompensated heart failure: early in-hospital phase and 30-day follow-up
Q41203826LC-MS/MS method for hepcidin-25 measurement in human and mouse serum: clinical and research implications in iron disorders.
Q39412094Management of iron overload in hemoglobinopathies.
Q42478276Mitochondrial energetic defects in muscle and brain of a Hmbs-/- mouse model of acute intermittent porphyria
Q47851870Mutation in human CLPX elevates levels of δ-aminolevulinate synthase and protoporphyrin IX to promote erythropoietic protoporphyria
Q52324266Porphyria and kidney diseases.
Q38542777Porphyrias: A 2015 update
Q88291969Predominant role of microglia in brain iron retention in Sanfilippo syndrome, a pediatric neurodegenerative disease
Q71949218Protein kinase C isoforms in rat kidney proximal tubule: acute effect of angiotensin II
Q84564481Protoporphyrin retention in hepatocytes and Kupffer cells prevents sclerosing cholangitis in erythropoietic protoporphyria mouse model
Q36493422Recent concepts concerning the renal handling of NH3/NH4+.
Q87937480Recurrent attacks of acute hepatic porphyria: major role of the chronic inflammatory response in the liver
Q91428293Regulation and tissue-specific expression of δ-aminolevulinic acid synthases in non-syndromic sideroblastic anemias and porphyrias
Q54072280Regulation by PKC isoforms of Na(+)/H(+) exchanger in luminal membrane vesicles isolated from cortical tubules.
Q79144158Regulation of ROMK (Kir 1.1) channel expression in kidney thick ascending limb by hypertonicity: role of TonEBP and MAPK pathways
Q91282530Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1
Q81093664Renal handling of NH3/NH4+: recent concepts
Q88322832Reply
Q35775491The microbiota shifts the iron sensing of intestinal cells.
Q84354621Zeta-crystallin mediates the acid pH-induced increase of BSC1 cotransporter mRNA stability
Q77698003[Effect of angiotensin ii on Na+/H+ exchangers of the renal tubule]
Q74778645[Role of the Na(+)-K+(NH4+)-2Cl cotransporter of the medullary ascending limb in the regulation of renal acid-base equilibrium]

Q58393673Raed Daherdoctoral advisorP184