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Lancet, The, ISSN 0140-6736, 2010, Volume 375, Issue 9725, pp. 1525 - 1535
Journal Article
Journal Article
World Journal of Gastroenterology, ISSN 1007-9327, 11/2013, Volume 19, Issue 41, pp. 6969 - 6978
The 148 Isoleucine to Methionine protein variant (I148M) of patatin-like phospholipase domain-containing 3 (PNPLA3), a protein is expressed in the liver and is... 
Liver disease | Patatin-like phospholipase domain-containing 3 | Chronic hepatitis C virus hepatitis | Genetics | Hepatocellular carcinoma | Nonalcoholic fatty liver disease | Single nucleotide polymorphism | Fibrogenesis | Alcoholic liver disease | Steatosis | CHRONIC HEPATITIS-C | NONALCOHOLIC STEATOHEPATITIS | GREATER-THAN-G | B-VIRUS INFECTION | HEPATOCELLULAR-CARCINOMA | INSULIN-RESISTANCE | FATTY LIVER | DOMAIN-CONTAINING 3 | GENETIC VARIANT | GASTROENTEROLOGY & HEPATOLOGY | GENOME-WIDE ASSOCIATION | Cholangitis, Sclerosing - enzymology | Hepatitis C, Chronic - pathology | Fatty Liver - pathology | Humans | Cholangitis, Sclerosing - genetics | Fatty Liver - complications | Hepatitis B, Chronic - enzymology | Hepatitis C, Chronic - complications | Liver Cirrhosis - enzymology | Hemochromatosis - pathology | Fatty Liver, Alcoholic - genetics | Hepatitis B, Chronic - genetics | Liver Cirrhosis, Alcoholic - enzymology | Hepatitis C, Chronic - enzymology | Fatty Liver - enzymology | Non-alcoholic Fatty Liver Disease | Liver Neoplasms - pathology | Fatty Liver, Alcoholic - pathology | Liver Neoplasms - enzymology | Fatty Liver, Alcoholic - enzymology | Hepatitis B, Chronic - pathology | Liver Cirrhosis - genetics | Hemochromatosis - genetics | Fatty Liver - genetics | Genetic Predisposition to Disease | Liver Neoplasms - genetics | Liver Cirrhosis, Alcoholic - pathology | Membrane Proteins - genetics | Risk Factors | Hemochromatosis - enzymology | Disease Progression | Polymorphism, Genetic | Cholangitis, Sclerosing - pathology | Fatty Liver, Alcoholic - complications | Liver Cirrhosis, Alcoholic - genetics | Phenotype | Liver Cirrhosis - pathology | Carcinoma, Hepatocellular | Hepatitis C, Chronic - genetics | Lipase - genetics | Review | Gastroenterologi | Hepatocellular | Gastroenterology and Hepatology
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2012, Volume 7, Issue 6, p. e38339
The existence of multiple inherited disorders of iron metabolism suggests genetic contributions to iron deficiency. We previously performed a genome-wide... 
OVERLOAD SCREENING HEIRS | HOMEOSTASIS | ASSAY | TRANSFERRIN RECEPTOR | BIOLOGY | TMPRSS6 GENE | ANEMIA | MUTATIONS | HEREDITARY HEMOCHROMATOSIS | DEFICIENCY | GENOME-WIDE ASSOCIATION | Prognosis | Follow-Up Studies | Humans | Middle Aged | Asian Continental Ancestry Group - genetics | Hemochromatosis - blood | Hispanic Americans - statistics & numerical data | Male | Iron Overload - blood | Ethnic Groups - genetics | Serine Endopeptidases - genetics | Adult | Female | Hemochromatosis - genetics | Iron - blood | European Continental Ancestry Group - genetics | Hispanic Americans - genetics | Iron Overload - genetics | Membrane Proteins - genetics | California - epidemiology | Biomarkers - analysis | African Americans - genetics | European Continental Ancestry Group - statistics & numerical data | Genotype | African Americans - statistics & numerical data | Iron Overload - epidemiology | Polymorphism, Single Nucleotide - genetics | Hemochromatosis - epidemiology | Asian Continental Ancestry Group - statistics & numerical data | Receptors, Cell Surface - genetics | Analysis | Iron deficiency anemia | Genes | Genomics | Hispanic Americans | Ferritin | African Americans | Physiological aspects | Genetic research | Genetic aspects | Single nucleotide polymorphisms | Health sciences | Biomedical research | Populations | Laboratories | Iron | Genomes | Single-nucleotide polymorphism | Epidemiology | Toxicology | Chromosome 10 | Hemoglobin | Physiology | Public health | Deoxyribonucleic acid--DNA | Chromosome 18 | CUBN gene | Nutrient deficiency | Hemochromatosis | Anemia | Whites | Metabolism | Minority & ethnic groups | Hereditary diseases | Medicine | Studies | Mutation | Deoxyribonucleic acid | DNA
Journal Article
2008, Critical care nursing clinics of North America, ISBN 9781416057734, Volume 20, no. 2., x, p. 139-243
Book
Journal of Hepatology, ISSN 0168-8278, 2009, Volume 52, Issue 2, pp. 252 - 257
Hepatocellular carcinoma (HCC) is a common form of cancer that arises from hepatocytes and whose risk may be affected by several known environmental factors,... 
Gastroenterology and Hepatology | Cirrhosis | Hepatitis | Porphyrias | Hemochromatosis | Tyrosinemia type I | Glycogen storage disease | Non-alcoholic steatohepatitis | PRIMARY HEPATOCELLULAR-CARCINOMA | PORPHYRIA-CUTANEA-TARDA | FOLLOW-UP | NONALCOHOLIC STEATOHEPATITIS | HEREDITARY HEMOCHROMATOSIS | DIABETES-MELLITUS | GLYCOGEN-STORAGE-DISEASE | PRIMARY LIVER-CANCER | Tyrosinemia type 1 | HEPATITIS-B | GASTROENTEROLOGY & HEPATOLOGY | VIRAL-HEPATITIS | Humans | Hypothyroidism - complications | Fatty Liver - complications | Male | Porphyrias, Hepatic - genetics | Glycogen Storage Disease Type I - complications | Liver Neoplasms - etiology | Hemochromatosis - complications | Carcinoma, Hepatocellular - genetics | Female | Carcinoma, Hepatocellular - etiology | Diabetes Complications - genetics | Hepatitis, Autoimmune - genetics | Hemochromatosis - genetics | Fatty Liver - genetics | alpha 1-Antitrypsin Deficiency - genetics | Genetic Predisposition to Disease | Liver Neoplasms - genetics | Risk Factors | Tyrosinemias - genetics | Diabetes Complications - etiology | Tyrosinemias - complications | Hepatitis, Autoimmune - complications | Glycogen Storage Disease Type I - genetics | alpha 1-Antitrypsin Deficiency - complications | Models, Genetic | Porphyrias, Hepatic - complications | Type 2 diabetes | Liver cancer | Histocompatibility antigens | Glycogen | Glutathione transferase | HLA histocompatibility antigens | Genetic research | Genetics | Hepatitis C
Journal Article
PLoS Genetics, ISSN 1553-7390, 07/2017, Volume 13, Issue 7, pp. e1006907 - e1006907
Journal Article
Lancet, The, ISSN 0140-6736, 2016, Volume 388, Issue 10045, pp. 706 - 716
Journal Article
Hepatology, ISSN 0270-9139, 08/2015, Volume 62, Issue 2, pp. 429 - 439
Journal Article