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Bonkovsky, Herbert
One or more keywords matched the following items that are connected to
Bonkovsky, Herbert
Item Type
Name
Concept
Mutation
Concept
Mutation, Missense
Academic Article
Chronic leukocytoclastic vasculitis complicating HBV infection. Possible role of mutant forms of HBV in pathogenesis and persistence of disease.
Academic Article
Porphyria cutanea tarda, hepatitis C, and HFE gene mutations in North America.
Academic Article
Non-alcoholic steatohepatitis and iron: increased prevalence of mutations of the HFE gene in non-alcoholic steatohepatitis.
Academic Article
Effects of phenylarsine oxide on expression of heme oxygenase-1 reporter constructs in transiently transfected cultures of chick embryo liver cells.
Academic Article
Role of HFE gene mutations in liver diseases other than hereditary hemochromatosis.
Academic Article
Zebrafish dracula encodes ferrochelatase and its mutation provides a model for erythropoietic protoporphyria.
Academic Article
Ubiquitin as a marker of cell injury in nonalcoholic steatohepatitis.
Academic Article
Iron and HFE or TfR1 mutations as comorbid factors for development and progression of chronic hepatitis C.
Academic Article
Iron as a co-morbid factor in nonhemochromatotic liver disease.
Academic Article
Hemochromatosis mutations in Iranians with hepatitis B virus infection.
Academic Article
Roles of iron and HFE mutations on severity and response to therapy during retreatment of advanced chronic hepatitis C.
Academic Article
Serum measures of iron status and HFE gene mutations in patients with hepatitis B virus infection.
Academic Article
Hereditary hemochromatosis: time for targeted screening.
Academic Article
CTL escape mutations of core protein are more frequent in strains of HBeAg negative patients with low levels of HBV DNA.
Academic Article
The let-7 microRNA enhances heme oxygenase-1 by suppressing Bach1 and attenuates oxidant injury in human hepatocytes.
Academic Article
Loss-of-function ferrochelatase and gain-of-function erythroid-specific 5-aminolevulinate synthase mutations causing erythropoietic protoporphyria and x-linked protoporphyria in North American patients reveal novel mutations and a high prevalence of X-linked protoporphyria.
Academic Article
Hepatitis B and liver transplantation: molecular and clinical features that influence recurrence and outcome.
Grant
Effect of Heme on mRNA and miRNA Profile
Academic Article
Clinical, Biochemical, and Genetic Characterization of North American Patients With Erythropoietic Protoporphyria and X-linked Protoporphyria.
Academic Article
Peripheral Neuropathy and the Ceruloplasmin Gene.
Academic Article
Pathogenesis and clinical features of the acute hepatic porphyrias (AHPs).
Search Criteria
Mutation