Hepatoblastoma
What's New
Last Posted: Sep 16, 2024
- TRMT10C gene polymorphisms confer hepatoblastoma susceptibility: evidence from a seven-center case-control study.
Yanfei Liu, et al. Journal of Cancer 2024 0 (16) 5396-5402 - Nucleotide excision repair gene polymorphisms and hepatoblastoma susceptibility in Eastern Chinese children: A five-center case-control study.
Huimin Yin, et al. Chinese journal of cancer research = Chung-kuo yen cheng yen chiu 2024 0 (3) 298-305 - Comparative Clinicopathological and Genomic Analysis of Hepatocellular Neoplasm, NOS and Hepatoblastoma.
Shengmei Zhou, et al. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2023 0 100385 - Whole-genome Sequencing and RNA Sequencing Analysis Reveals Novel Risk Genes and Differential Expression Patterns in Hepatoblastoma.
Wuqian Wang, et al. Gene 2023 0 147991 - Identification of hepatoblastoma susceptibility loci in the TRMT6 gene from a seven-center case-control study.
Lin Ma, et al. Journal of cellular and molecular medicine 2023 0 - NTHL1 Gene Mutations in Polish Polyposis Patients-Weighty Player or Vague Background?
Natalia Grot, et al. International journal of molecular sciences 2023 0 (19) - TRMT61B rs4563180 G>C variant reduces hepatoblastoma risk: a case-control study of seven medical centers.
Dingyuan Zeng, et al. Aging 2023 0 - Outcomes of Patients Treated for Hepatoblastoma with Low Alpha-Fetoprotein and/or Small Cell Undifferentiated Histology: A Report from the Children's Hepatic Tumors International Collaboration (CHIC).
Trobaugh-Lotrario Angela D, et al. Cancers 2023 0 (2) - Germline APC mutations in hepatoblastoma.
Yang Adeline, et al. Pediatric blood & cancer 2017 0 (4) - A novel tissue-based ß-catenin gene and immunohistochemical analysis to exclude familial adenomatous polyposis among children with hepatoblastoma tumors.
Dubbink Hendrikus J, et al. Pediatric blood & cancer 2018 0 (6) e26991
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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