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alanine and Hamartoma Syndrome, Multiple

alanine has been researched along with Hamartoma Syndrome, Multiple 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.

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.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Rodríguez-Escudero, I1
Oliver, MD1
Andrés-Pons, A1
Molina, M1
Cid, VJ1
Pulido, R1

Other Studies

1 other study available for alanine and Hamartoma Syndrome, Multiple

ArticleYear
A comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromes.
    Human molecular genetics, 2011, Nov-01, Volume: 20, Issue:21

    Topics: Alanine; Amino Acid Sequence; Aspartic Acid; Autistic Disorder; Catalytic Domain; DNA Mutational Ana

2011