alanine has been researched along with Colon Cancer, Familial Nonpolyposis in 1 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
Excerpt | Relevance | Reference |
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"Hereditary nonpolyposis colorectal cancer (HNPCC) is caused by mutations in the mismatch-repair genes." | 1.31 | The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population. ( Bonner, JD; Boyd, J; Chong, G; De La Chapelle, A; Ellis, NA; Farber, D; Figer, A; Foulkes, WD; Friedman, E; Gaff, CL; Gebert, J; Gordon, PH; Greenwood, CM; Gregersen, PK; Gruber, SB; Hamel, N; Hampel, H; Horwitz, M; King, MC; Lee, C; MacNamara, E; Macrae, FA; Marcus, V; Markowitz, A; Nafa, K; Offit, K; Paillerets, BB; Rennert, G; Shia, J; Thiffault, I; Tomsho, L; Walsh, T; Weitzel, JN, 2002) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Foulkes, WD | 1 |
Thiffault, I | 1 |
Gruber, SB | 1 |
Horwitz, M | 1 |
Hamel, N | 1 |
Lee, C | 1 |
Shia, J | 1 |
Markowitz, A | 1 |
Figer, A | 1 |
Friedman, E | 1 |
Farber, D | 1 |
Greenwood, CM | 1 |
Bonner, JD | 1 |
Nafa, K | 1 |
Walsh, T | 1 |
Marcus, V | 1 |
Tomsho, L | 1 |
Gebert, J | 1 |
Macrae, FA | 1 |
Gaff, CL | 1 |
Paillerets, BB | 1 |
Gregersen, PK | 1 |
Weitzel, JN | 1 |
Gordon, PH | 1 |
MacNamara, E | 1 |
King, MC | 1 |
Hampel, H | 1 |
De La Chapelle, A | 1 |
Boyd, J | 1 |
Offit, K | 1 |
Rennert, G | 1 |
Chong, G | 1 |
Ellis, NA | 1 |
1 other study available for alanine and Colon Cancer, Familial Nonpolyposis
Article | Year |
---|---|
The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.
Topics: Alanine; Case-Control Studies; Chromosomes, Human, Pair 2; Colorectal Neoplasms, Hereditary Nonpolyp | 2002 |