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CUBN gene
Known as:
INTRINSIC FACTOR-COBALAMIN RECEPTOR
, gp280
, CUBILIN
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National Institutes of Health
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Related topics
Related topics
1 relation
intrinsic factor-cobalamin receptor
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Amelioration of Albuminuria in ROCK1 Knockout Mice with Streptozotocin-Induced Diabetic Kidney Disease
Li Zhou
,
Fei Liu
,
+7 authors
P. Fu
American Journal of Nephrology
2011
Corpus ID: 35352595
Background: Although blockade of Rho kinase with pharmacologic inhibitors ameliorates renal fibrosis and diabetic kidney disease…
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Review
2010
Review
2010
Molecular-targeted approaches to reduce renal accumulation of nephrotoxic drugs
J. Nagai
,
M. Takano
Expert Opinion on Drug Metabolism & Toxicology
2010
Corpus ID: 24388678
Importance of the field: Nephrotoxicity limits the clinical use of some antibiotics, cancer chemotherapeutics and diagnostic…
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Highly Cited
2009
Highly Cited
2009
Cubilin and Megalin Co-Localize in the Neonatal Inner Ear
Jacob Tauris
,
E. Christensen
,
A. Nykjær
,
C. Jacobsen
,
C. Petersen
,
T. Ovesen
Audiology and Neurotology
2009
Corpus ID: 39727364
Cubilin and megalin are multifunctional endocytotic receptors expressed in many absorptive epithelia. The receptors have separate…
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Highly Cited
2008
Highly Cited
2008
Silencing megalin and cubilin genes inhibits myeloma light chain endocytosis and ameliorates toxicity in human renal proximal tubule epithelial cells.
Min Li
,
S. Balamuthusamy
,
E. Simon
,
V. Batuman
AJP - Renal Physiology
2008
Corpus ID: 42810872
Using target-specific short interfering (si) RNAs, we silenced the tandem endocytic receptors megalin and cubilin genes in…
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Highly Cited
2008
Highly Cited
2008
Urinary protein excretion pattern and renal expression of megalin and cubilin in nephropathic cystinosis.
M. Wilmer
,
E. Christensen
,
L. P. Van den Heuvel
,
L. Monnens
,
E. Levtchenko
American Journal of Kidney Diseases
2008
Corpus ID: 1552552
BACKGROUND Nephropathic cystinosis is the most common cause of inherited renal Fanconi syndrome, caused by mutations in lysosomal…
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Review
2007
Review
2007
Multiligand endocytosis and congenital defects: roles of cubilin, megalin and amnionless.
R. Kozyraki
,
F. Gofflot
Current pharmaceutical design
2007
Corpus ID: 43048398
Cubilin and megalin are multiligand receptors that mediate uptake of extracellular ligands. Their function has extensively been…
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Highly Cited
2006
Highly Cited
2006
Application of a fluorescent cobalamin analogue for analysis of the binding kinetics
S. Fedosov
,
C. Grissom
,
N. Fedosova
,
S. Moestrup
,
E. Nexo
,
T. Petersen
The FEBS Journal
2006
Corpus ID: 18807948
Fluorescent probe rhodamine was appended to 5′ OH‐ribose of cobalamin (Cbl). The prepared conjugate, CBC, bound to the…
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Highly Cited
2005
Highly Cited
2005
Light chains are a ligand for megalin.
R. B. Klassen
,
P. Allen
,
V. Batuman
,
Kimberly Crenshaw
,
T. Hammond
Journal of applied physiology
2005
Corpus ID: 10070688
Cubilin and megalin are giant glycoprotein receptors abundant on the luminal surface of proximal tubular cells of the kidney. We…
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Highly Cited
2003
Highly Cited
2003
Rat enterocytes secrete SLPs containing alkaline phosphatase and cubilin in response to corn oil feeding.
A. Mahmood
,
J. Shao
,
D. Alpers
American Journal of Physiology - Gastrointestinal…
2003
Corpus ID: 30731288
Surfactant-like particles (SLP) are unilamellar secreted membranes associated with the process of lipid absorption and isolated…
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Highly Cited
2000
Highly Cited
2000
Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor–vitamin B12 by cubilin
M. Kristiansen
,
M. Aminoff
,
+4 authors
S. Moestrup
2000
Corpus ID: 208531087
Megaloblastic anemia 1 (MGA1) is an autosomal recessive disorder caused by the selective intestinal malabsorption of intrinsic…
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