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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Disease and RASSF1[original query]
Rectal cancer profiling identifies distinct subtypes in India based on age at onset, genetic, epigenetic and clinicopathological characteristics.
Molecular carcinogenesis 2014 Nov .
Laskar Ruhina Shirin, Ghosh Sankar Kumar, Talukdar Fazlur Rahm
Aberrant DNA methylation is associated with aggressive clinicopathological features and poor survival in cutaneous melanoma.
The British journal of dermatology 2017 Dec .
de Unamuno Bustos B, Murria Estal R, Pérez Simó G, Simarro Farinos J, Pujol Marco C, Navarro Mira M, Alegre de Miquel V, Ballester Sánchez R, Sabater Marco V, Llavador Ros M, Palanca Suela S, Botella Estrada
Mutations of candidate tumor suppressor genes at chromosome 3p in intrahepatic cholangiocarcinoma.
Experimental and molecular pathology 2017 Nov 103 (3): 249-254.
You Huey-Ling, Huang Wan-Ting, Liu Ting-Ting, Weng Shao-Wen, Eng Hock-Li
Genomic alterations of plasma cell-free DNAs in small cell lung cancer and their clinical relevance.
Lung cancer (Amsterdam, Netherlands) 2018 Jun 120 113-121.
Du Meijun, Thompson Jonathan, Fisher Hannah, Zhang Peng, Huang Chiang-Ching, Wang Lia
Investigation of the relationship between CTLA4 and the tumor suppressor RASSF1A and the possible mediating role of STAT4 in a cohort of Egyptian patients infected with hepatitis C virus with and without hepatocellular carcinoma.
Archives of virology 2021 Apr .
Ali Nermin A, Hamdy Nadia M, Gibriel Abdullah A, El Mesallamy Hala
Association of Variants in COMT, RASSF1 and GPM6A with the Risk of Paranoid Schizophrenia Patients in Prof HB Saanin Psychiatric Hospital, West Sumatra, Indonesia.
The Malaysian journal of medical sciences : MJMS 2022 Apr 29 (2): 31-42.
Yunaini Luluk, Khairat Edwi
Exome sequencing identifies RASSF1 and KLK3 germline variants in an Iranian multiple-case breast cancer family.
European journal of medical genetics 2022 1 65 (3): 104425.
Radmanesh Hoda, Liu Di, Geffers Robert, Shandiz Fatemeh Homaei, Sadr-Nabavi Ariane, Hillemanns Peter, Park-Simon Tjoung-Won, Dörk Thi
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