Page last updated: 2024-11-08

alanine and Alobar Holoprosencephaly

alanine has been researched along with Alobar Holoprosencephaly in 3 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.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Brown, L1
Paraso, M1
Arkell, R1
Brown, S1
Roessler, E1
Belloni, E1
Gaudenz, K1
Vargas, F1
Scherer, SW1
Tsui, LC1
Muenke, M2
Brown, LY1
Odent, S1
David, V1
Blayau, M1
Dubourg, C1
Apacik, C1
Delgado, MA1
Hall, BD1
Reynolds, JF1
Sommer, A1
Wieczorek, D1
Brown, SA1

Other Studies

3 other studies available for alanine and Alobar Holoprosencephaly

ArticleYear
In vitro analysis of partial loss-of-function ZIC2 mutations in holoprosencephaly: alanine tract expansion modulates DNA binding and transactivation.
    Human molecular genetics, 2005, Feb-01, Volume: 14, Issue:3

    Topics: Alanine; Amino Acid Sequence; Animals; CHO Cells; Cloning, Molecular; Cricetinae; Cricetulus; DNA; D

2005
Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly.
    Human molecular genetics, 1997, Volume: 6, Issue:11

    Topics: Alanine; Amino Acid Sequence; Animals; Cell Line, Transformed; DNA Mutational Analysis; Exons; Femal

1997
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination.
    Human molecular genetics, 2001, Apr-01, Volume: 10, Issue:8

    Topics: Alanine; Amino Acid Sequence; Female; Genomic Imprinting; Holoprosencephaly; Humans; Male; Molecular

2001