glycine has been researched along with Hamartoma Syndrome, Multiple in 1 studies
Hamartoma Syndrome, Multiple: A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE.
| 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 |
|---|---|
| Xiao, Y | 1 |
| Yeong Chit Chia, J | 1 |
| Gajewski, JE | 1 |
| Sio Seng Lio, D | 1 |
| Mulhern, TD | 1 |
| Zhu, HJ | 1 |
| Nandurkar, H | 1 |
| Cheng, HC | 1 |
1 other study available for glycine and Hamartoma Syndrome, Multiple
| Article | Year |
|---|---|
PTEN catalysis of phospholipid dephosphorylation reaction follows a two-step mechanism in which the conserved aspartate-92 does not function as the general acid--mechanistic analysis of a familial Cowden disease-associated PTEN mutation.
Topics: Animals; Aspartic Acid; Binding Sites; Catalysis; Conserved Sequence; Cysteine; Glycine; Hamartoma S | 2007 |