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Metabolic dysfunction-associated steatotic liver disease: pathogenesis and novel treatment options. [PDF]
Ren R, Liang X, Wei X.
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The role of circulating cytokines in eosinophilic esophagitis: A Mendelian randomization and gene expression analysis study. [PDF]
Jiang L +5 more
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Hepatocyte nuclear factor 1 beta induces transformation and epithelial‐to‐mesenchymal transition
FEBS Letters, 2016Gene amplification can be a cause of cancer, and driver oncogenes have been often identified in amplified regions. However, comprehensive analysis of other genes coamplified with an oncogene is rarely performed. We focused on the 17q12–21 amplicon, which contains ERBB2.
Kosuke Ishikawa
exaly +3 more sources
Deletion of Hepatocyte Nuclear Factor-1-Beta in an Infant with Prune Belly Syndrome
American Journal of Perinatology, 2010Prune belly syndrome is a rare congenital disorder characterized by deficiency of abdominal wall muscles, cryptorchidism, and urinary tract anomalies. We have had the opportunity to study a baby with prune belly syndrome associated with an apparently de novo 1.3-megabase interstitial 17q12 microdeletion that includes the hepatocyte nuclear factor-1 ...
Sina Haeri, Honor Wolfe, Honor M Wolfe
exaly +3 more sources
Pathology, 2015
Napsin A and α-methylacyl-coenzyme A racemase (AMACR, P504S) have recently been described as being frequently expressed in clear cell carcinomas (CCC) of the gynecological tract. The present study was conducted to assess the test performance of these newer markers relative to the more traditional marker, hepatocyte nuclear factor 1β (HNF1β), in a large
Chengquan Zhao +2 more
exaly +3 more sources
Napsin A and α-methylacyl-coenzyme A racemase (AMACR, P504S) have recently been described as being frequently expressed in clear cell carcinomas (CCC) of the gynecological tract. The present study was conducted to assess the test performance of these newer markers relative to the more traditional marker, hepatocyte nuclear factor 1β (HNF1β), in a large
Chengquan Zhao +2 more
exaly +3 more sources
Practical Diabetes, 2017
AbstractThe HNF1B gene plays an important role in endodermal development, and mutations of HNF1B are associated with the renal cysts and diabetes (RCAD) syndrome. Other than renal cystic malformations and monogenic diabetes, various other abnormalities have been described depending on HNF1β expression.
Pallavi Hegde +4 more
openaire +1 more source
AbstractThe HNF1B gene plays an important role in endodermal development, and mutations of HNF1B are associated with the renal cysts and diabetes (RCAD) syndrome. Other than renal cystic malformations and monogenic diabetes, various other abnormalities have been described depending on HNF1β expression.
Pallavi Hegde +4 more
openaire +1 more source

