About: Treatment of Crigler-Najjar Syndrome type 1 by hepatic progenitor cell transplantation: a simple procedure for management of hyperbilirubinemia

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About: Treatment of Crigler-Najjar Syndrome type 1 by hepatic progenitor cell transplantation: a simple procedure for management of hyperbilirubinemia Goto Sponge NotDistinct Permalink

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scientific article published on 01 May 2008

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2008 (fr) наукова стаття, опублікована в травні 2008 (uk) im Mai 2008 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en mayu de 2008 (ast) scientific article published on 01 May 2008 (en)
publication date	wds:Q81458559-D215038F-571C-4390-94A0-C47C3BD33950
publication date	2008-05-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q81458559-057FC9F4-1718-4CAC-BE83-E0A8F98A4B59 wds:Q81458559-0A6FD81B-4093-4E16-A85C-FD61DF3255EC wds:Q81458559-0D27F9C7-3C53-48C6-9A20-BA4C9F20FDDB wds:Q81458559-122E6FBE-B3D6-4005-9657-A85641552BA6 wds:Q81458559-2FB8C4EA-4D91-4F60-9C4E-A848C29F4DF6 wds:Q81458559-4F9C8400-0528-4EA8-AA7A-5AAE545BA593 wds:Q81458559-966233C2-A97D-4B30-9B1D-E2D4F791E161 wds:Q81458559-99462AB1-BCC7-4041-A163-98F82782BFFB wds:Q81458559-AD8EEC8A-81EC-4932-B4CA-5B586D3FD064 wds:Q81458559-C7BA6136-DDD8-46CD-9135-1C6CE28B224B
cites work	Hepatocytes corrected by gene therapy are selected in vivo in a murine model of hereditary tyrosinaemia type I. Treatment of the Crigler-Najjar syndrome type I with hepatocyte transplantation Hepatocyte transplantation as a treatment for glycogen storage disease type 1a. Isolated hepatocyte transplantation in an infant with a severe urea cycle disorder. Long-term amelioration of bilirubin glucuronidation defect in Gunn rats by transplanting genetically modified immortalized autologous hepatocytes Crigler-Najjar syndrome types I and II. Clinical experience--King's College Hospital 1972-1978. Phenobarbitone, phototherapy and liver transplantation Characterization of hepatic progenitors from human fetal liver using CD34 as a hepatic progenitor marker Hepatocellular transplantation for metabolic deficiencies: decrease of plasms bilirubin in Gunn rats Hepatocyte transplantation for the low-density lipoprotein receptor-deficient state. A study in the Watanabe rabbit Repeated intraportal hepatocyte transplantation in analbuminemic rats
author name string	wds:Q81458559-08C0A2F7-B8F4-41A4-9717-AA93000F2184 wds:Q81458559-359B06CA-BABA-40BF-BE71-C970EFCBB5EB wds:Q81458559-4ECD9E51-E88B-4776-BC3E-5A02074826EF wds:Q81458559-566772F8-8923-4C83-8F22-D6BFC66D838E wds:Q81458559-633AAAAC-F553-430A-AD58-22C67BC1F289 wds:Q81458559-6CCFE517-19A7-472C-A663-D2236F5E4A1B wds:Q81458559-6FCC9531-45F5-4A02-9339-8CB644A6A57D wds:Q81458559-A3552F42-FEB6-4438-BCEF-A456E11C86DB wds:Q81458559-A788A73E-E760-4768-934A-2F30217A46FF wds:Q81458559-B3ED58E0-34B8-4B89-A667-6A1B29E28814 wds:Q81458559-B589E1F5-B002-485D-B4EF-06A8816FADC6 wds:Q81458559-DC6C5054-CB43-4830-91C3-41AE51B8ADF7
author name string	P Rao A A Khan A Habeeb A Rajendraprasad C M Habibullah H R Ravindraprakash J Venkateswarlu M Lakshmi Narusu M N Khaja N Parveen R Pramila V S Mahaboob
rdfs:label	Treatment of Crigler-Najjar Syndrome type 1 by hepatic progenitor cell transplantation: a simple procedure for management of hyperbilirubinemia (en) Treatment of Crigler-Najjar Syndrome type 1 by hepatic progenitor cell transplantation: a simple procedure for management of hyperbilirubinemia (nl)
skos:prefLabel	Treatment of Crigler-Najjar Syndrome type 1 by hepatic progenitor cell transplantation: a simple procedure for management of hyperbilirubinemia (en) Treatment of Crigler-Najjar Syndrome type 1 by hepatic progenitor cell transplantation: a simple procedure for management of hyperbilirubinemia (nl)
name	Treatment of Crigler-Najjar Syndrome type 1 by hepatic progenitor cell transplantation: a simple procedure for management of hyperbilirubinemia (en) Treatment of Crigler-Najjar Syndrome type 1 by hepatic progenitor cell transplantation: a simple procedure for management of hyperbilirubinemia (nl)
author	wds:Q81458559-A1ACDC20-0DEA-4401-90CB-62667021DC35
author	Gopal Pande
title	wds:Q81458559-E3F94FBD-EDD5-4316-9B58-E38116818FC9
title	Treatment of Crigler-Najjar Syndrome type 1 by hepatic progenitor cell transplantation: a simple procedure for management of hyperbilirubinemia (en)
page(s)	wds:Q81458559-10AFB044-5910-4B07-A876-036522EFDF2A
page(s)	1148-1150
instance of	wds:Q81458559-14A4468A-AAAF-410E-8AB1-6BADA89BB03B
instance of	scholarly article
main subject	wds:Q81458559-85B15B30-1A91-4D1E-B677-E7E0BD287031 wds:Q81458559-A2279DA2-B448-48F2-8C6E-056799B5A74B
main subject	bilirubin metabolic disorder Crigler-Najjar syndrome
PubMed ID	wds:Q81458559-77684276-6003-4262-8210-B49D54E28C70
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18555136
PubMed ID	18555136
published in	wds:Q81458559-27013543-42CB-482F-9ADA-ECEEF3727694
published in	Transplantation Proceedings
issue	wds:Q81458559-DCA09C90-0099-4AFF-B151-52D54F0EFFA4
volume	wds:Q81458559-EC703F77-2E10-4BC6-A669-42818356C785
issue	4
volume	40
DOI	wds:Q81458559-61E4A3A1-FD56-4497-8C70-A782DD00C9BB
DOI	http://dx.doi.org/10.1016/J.TRANSPROCEED.2008.03.022
DOI	10.1016/J.TRANSPROCEED.2008.03.022
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q81458559
is cites work of	The history and use of human hepatocytes for the treatment of liver diseases: the first 100 patients. Towards a therapy for phosphomannomutase 2 deficiency, the defect in CDG-Ia patients Concise review: clinical programs of stem cell therapies for liver and pancreas Bottom-up signaling from HGF-containing surfaces promotes hepatic differentiation of mesenchymal stem cells Improvement of Infusion Process in Cell Transplantation: Effect of Shear Stress on Hepatocyte Viability Under Horizontal and Vertical Syringe Orientation Tissue-derived stem and progenitor cells Liver, liver cell and stem cell transplantation for the treatment of urea cycle defects Hepatocyte transplantation Stem cells for liver repopulation Implications of the immunoregulatory functions of mesenchymal stem cells in the treatment of human liver diseases Living related liver transplantation in Crigler-Najjar syndrome type 1. Cell Therapy for Acute Liver Failure - Ideal source of cell Bioengineered humanized livers as better three-dimensional drug testing model system. The fetal liver as cell source for the regenerative medicine of liver and pancreas Synergistic modulation of signaling pathways to expand and maintain the bipotency of human hepatoblasts Hepatocyte transplantation: past efforts, current technology, and future expansion of therapeutic potential.

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