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MeSH:(Hepatocyte Nuclear Factor 1)

1.Clinicopathological Analysis of Hepatocellular Adenoma According to New Bordeaux Classification: Report of Eight Korean Cases.

Hyunchul KIM ; Ja June JANG ; Dong Sik KIM ; Beom Woo YEOM ; Nam Hee WON

Korean Journal of Pathology 2013;47(5):411-417

2.Expression of β-catenin and HNF-1α and their influence on prognosis in human hepatocellular carcinoma.

Jianfei SHI ; Fei YIN

Chinese Journal of Oncology 2014;36(8):587-591

3.Sortilin-induced lipid accumulation and atherogenesis are suppressed by HNF1b SUMOylation promoted by flavone of Polygonatum odoratum.

Fang LIU ; Shirui CHEN ; Xinyue MING ; Huijuan LI ; Zhaoming ZENG ; Yuncheng LV

Journal of Zhejiang University. Science. B 2023;24(11):998-1013

4.Benign hepatocellular nodules of healthy liver: focal nodular hyperplasia and hepatocellular adenoma.

Massimo RONCALLI ; Amedeo SCIARRA ; Luca Di TOMMASO

Clinical and Molecular Hepatology 2016;22(2):199-211

5.Benign hepatocellular nodules of healthy liver: focal nodular hyperplasia and hepatocellular adenoma.

Massimo RONCALLI ; Amedeo SCIARRA ; Luca Di TOMMASO

Clinical and Molecular Hepatology 2016;22(2):199-211

6.MODY Syndrome.

Jin Soon HWANG

Journal of Korean Society of Pediatric Endocrinology 2010;15(1):1-6

7.Loss of Liver Fatty Acid Binding Protein Expression in Hepatocellular Carcinomas is Associated with a Decreased Recurrence-Free Survival.

Haeryoung KIM ; Hyejung LEE ; Young Nyun PARK

Journal of Liver Cancer 2015;15(1):30-35

8.Systematic review of TCF2 anomalies in renal cysts and diabetes syndrome/maturity onset diabetes of the young type 5.

Yi-Zhi CHEN ; Qing GAO ; Xue-Zhi ZHAO ; Ying-Zhang CHEN ; Craig L BENNETT ; Xi-Shan XIONG ; Chang-Lin MEI ; Yong-Quan SHI ; Xiang-Mei CHEN

Chinese Medical Journal 2010;123(22):3326-3333

10.Clinical phenotype and genetic analysis of three pedigrees with 17q12 microdeletion syndrome.

Qinghua WU ; Saisai YANG ; Can WANG ; Huirong SHI ; Xiangdong KONG ; Shumin REN ; Zhihui JIAO ; Ning LIU ; Panlai SHI

Chinese Journal of Medical Genetics 2020;37(4):397-400

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