Page last updated: 2024-11-08

alanine and Hypoventilation

alanine has been researched along with Hypoventilation 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.

Hypoventilation: A reduction in the amount of air entering the pulmonary alveoli.

Research Excerpts

ExcerptRelevanceReference
"Heterozygous in frame trinucleotide duplications within the PHOX2B gene, leading to poly-alanine expansions, cause Congenital Central Hypoventilation Syndrome."3.80Recurrence of CCHS associated PHOX2B poly-alanine expansion mutation due to maternal mosaicism. ( Bachetti, T; Ceccherini, I; Della Monica, M; Di Duca, M; Grappone, L; Scarano, G, 2014)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bachetti, T1
Di Duca, M2
Della Monica, M1
Grappone, L1
Scarano, G1
Ceccherini, I2
Wang, Y1
He, XY1
Yang, Y1
Chen, XC1
Parodi, S1
Vollono, C1
Baglietto, MP1
Balestri, M1
Landri, PA1
Ottonello, G1
Cilio, MR1

Other Studies

3 other studies available for alanine and Hypoventilation

ArticleYear
Recurrence of CCHS associated PHOX2B poly-alanine expansion mutation due to maternal mosaicism.
    Pediatric pulmonology, 2014, Volume: 49, Issue:3

    Topics: Abortion, Spontaneous; Alanine; Electrophoresis, Capillary; Female; Genetic Counseling; Germ-Line Mu

2014
[Congenital central hypoventilation syndrome, report of three cases].
    Zhonghua er ke za zhi = Chinese journal of pediatrics, 2013, Volume: 51, Issue:11

    Topics: Alanine; Blood Gas Analysis; Carbon Dioxide; DNA Mutational Analysis; Exons; Female; Homeodomain Pro

2013
Congenital central hypoventilation syndrome: genotype-phenotype correlation in parents of affected children carrying a PHOX2B expansion mutation.
    Clinical genetics, 2010, Volume: 78, Issue:3

    Topics: Adult; Alanine; Child; Child, Preschool; Family Health; Female; Genetic Association Studies; Homeodo

2010