Liver cell transplantation leads to repopulation and functional correction in a mouse model of Wilson's disease

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Liver cell transplantation leads to repopulation and functional correction in a mouse model of Wilson's disease is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1111/J.1440-1746.2004.03451.X
P698PubMed publication ID15482536

P50authorKatie AllenQ38589865
P F WrightQ67808153
P2093author name stringSophie Gazeas
Robert Williamson
Nicole E Pettigrew-Buck
Daphne My Cheah
Julian Fb Mercer
Yolanda H Deal
P2860cites workTreatment of the Crigler-Najjar syndrome type I with hepatocyte transplantationQ28270302
Effect of the toxic milk mutation (tx) on the function and intracellular localization of Wnd, the murine homologue of the Wilson copper ATPaseQ31830057
Liver cell transplantation: the road to clinical application.Q34440059
Long-term, near-total liver replacement by transplantation of isolated hepatocytes in rats treated with retrorsineQ35753154
Isolated hepatocyte transplantation in an infant with a severe urea cycle disorder.Q39394474
Correction of liver disease following transplantation of normal rat hepatocytes into Long-Evans Cinnamon rats modeling Wilson's diseaseQ43556283
Hepatocytes corrected by gene therapy are selected in vivo in a murine model of hereditary tyrosinaemia type I.Q45876212
The toxic milk mouse is a murine model of Wilson diseaseQ48059534
Defective localization of the Wilson disease protein (ATP7B) in the mammary gland of the toxic milk mouse and the effects of copper supplementationQ59154486
P433issue11
P921main subjectgastroenterologyQ120569
P304page(s)1283-1290
P577publication date2004-11-01
P1433published inJournal of Gastroenterology and HepatologyQ15764401
P1476titleLiver cell transplantation leads to repopulation and functional correction in a mouse model of Wilson's disease
P478volume19

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cites work (P2860)
Q36084471AAV-mediated gene targeting is significantly enhanced by transient inhibition of nonhomologous end joining or the proteasome in vivo
Q35105022Adeno-associated virus gene repair corrects a mouse model of hereditary tyrosinemia in vivo.
Q33752265Cell therapy to remove excess copper in Wilson's disease
Q37221342Cell-based therapies for metabolic liver disease
Q51650805Copper comes of age in Melbourne.
Q37278160Correction of copper metabolism is not sustained long term in Wilson's disease mice post bone marrow transplantation.
Q36980068Embryonic and induced pluripotent stem cells as a model for liver disease
Q42571919Hepatocyte transplantation (HTx) corrects selected neurometabolic abnormalities in murine intermediate maple syrup urine disease (iMSUD).
Q38025743Hepatocyte transplantation for inherited metabolic diseases of the liver.
Q53186451Hepatogenic differentiation from human adipose-derived stem cells and application for mouse acute liver injury.
Q35776326In Situ Transplantation of Alginate Bioencapsulated Adipose Tissues Derived Stem Cells (ADSCs) via Hepatic Injection in a Mouse Model
Q36298651In vivo selection of transplanted hepatocytes by pharmacological inhibition of fumarylacetoacetate hydrolase in wild-type mice
Q42226193Longitudinal analysis of serum miR-122 in a rat model of Wilson's disease.
Q39896527Magnetic targeting of iron-oxide-labeled fluorescent hepatoma cells to the liver
Q35990789New Tools in Experimental Cellular Therapy for the Treatment of Liver Diseases
Q36368243Stem cells for the treatment of liver disease
Q42974100Transplantation of immortalized human fetal hepatocytes prevents acute liver failure in 90% hepatectomized mice

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