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Jane L Hartley

Showing results (1-10 of 11) with videos related to

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Clinics in Liver Disease|April 2, 2013
Alagille syndrome and other hereditary causes of cholestasisJane L Hartley, Paul Gissen, Deirdre A Kelly
Lancet (London, England)|November 17, 2009
Biliary atresiaJane L Hartley, Mark Davenport, Deirdre A Kelly
BMJ Case Reports|January 9, 2014
Dent's disease complicated by an acute Budd-Chiari syndromeCaroline Platt, Lyda Jadresic, Jan Dudley, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 1, 2006
Hyaluronic acid predicts hepatic fibrosis in children with hepatic diseaseJane L Hartley, Rachel M Brown, Aniela Tybulewicz, et al.
Journal of Clinical and Experimental Hepatology|March 11, 2015
Polymorphisms in ABCB11 and ATP8B1 Associated with Development of Severe Intrahepatic Cholestasis in Hodgkin's LymphomaLaura Blackmore, A S Knisely, Jane L Hartley, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 17, 2011
Investigation of primary cilia in the pathogenesis of biliary atresiaJane L Hartley, Christopher O'Callaghan, Sandro Rossetti, et al.
Nature Immunology|July 28, 2014
The SKIV2L RNA exosome limits activation of the RIG-I-like receptorsSterling C Eckard, Gillian I Rice, Alexandre Fabre, et al.
F1000Research|March 18, 2014
Mutation detection in cholestatic patients using microarray resequencing of ATP8B1 and ABCB11Kirsten E McKay, Christopher K Bruce, Jane L Hartley, et al.
Orphanet Journal of Rare Diseases|May 18, 2013
A combination of mutations in AKR1D1 and SKIV2L in a family with severe infantile liver diseaseNeil V Morgan, Jane L Hartley, Kenneth D R Setchell, et al.
Human Mutation|February 19, 2013
Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney DiseaseMiriam Schmidts, Valeska Frank, Tobias Eisenberger, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Clinics in Liver Disease|April 2, 2013
Alagille syndrome and other hereditary causes of cholestasisJane L Hartley, Paul Gissen, Deirdre A Kelly
Lancet (London, England)|November 17, 2009
Biliary atresiaJane L Hartley, Mark Davenport, Deirdre A Kelly
BMJ Case Reports|January 9, 2014
Dent's disease complicated by an acute Budd-Chiari syndromeCaroline Platt, Lyda Jadresic, Jan Dudley, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 1, 2006
Hyaluronic acid predicts hepatic fibrosis in children with hepatic diseaseJane L Hartley, Rachel M Brown, Aniela Tybulewicz, et al.
Journal of Clinical and Experimental Hepatology|March 11, 2015
Polymorphisms in ABCB11 and ATP8B1 Associated with Development of Severe Intrahepatic Cholestasis in Hodgkin's LymphomaLaura Blackmore, A S Knisely, Jane L Hartley, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 17, 2011
Investigation of primary cilia in the pathogenesis of biliary atresiaJane L Hartley, Christopher O'Callaghan, Sandro Rossetti, et al.
Nature Immunology|July 28, 2014
The SKIV2L RNA exosome limits activation of the RIG-I-like receptorsSterling C Eckard, Gillian I Rice, Alexandre Fabre, et al.
F1000Research|March 18, 2014
Mutation detection in cholestatic patients using microarray resequencing of ATP8B1 and ABCB11Kirsten E McKay, Christopher K Bruce, Jane L Hartley, et al.
Orphanet Journal of Rare Diseases|May 18, 2013
A combination of mutations in AKR1D1 and SKIV2L in a family with severe infantile liver diseaseNeil V Morgan, Jane L Hartley, Kenneth D R Setchell, et al.
Human Mutation|February 19, 2013
Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney DiseaseMiriam Schmidts, Valeska Frank, Tobias Eisenberger, et al.
Pageof 2