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alanine and Spherocytosis, Hereditary

alanine has been researched along with Spherocytosis, Hereditary in 2 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.

Spherocytosis, Hereditary: A group of familial congenital hemolytic anemias characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boivin, P1
Galand, C1
Devaux, I1
Lecomte, MC1
Garbarz, M1
Dhermy, D1
Iwase, S1
Ideguchi, H1
Takao, M1
Horiguchi-Yamada, J1
Iwasaki, M1
Takahara, S1
Sekikawa, T1
Mochizuki, S1
Yamada, H1

Other Studies

2 other studies available for alanine and Spherocytosis, Hereditary

ArticleYear
Spectrin alpha IIa variant in dominant and non-dominant spherocytosis.
    Human genetics, 1993, Volume: 92, Issue:2

    Topics: Adult; Alanine; Aspartic Acid; Base Sequence; Child; Electrophoresis, Gel, Two-Dimensional; Female;

1993
Band 3 Tokyo: Thr837-->Ala837 substitution in erythrocyte band 3 protein associated with spherocytic hemolysis.
    Acta haematologica, 1998, Volume: 100, Issue:4

    Topics: Adult; Alanine; Amino Acid Substitution; Anion Exchange Protein 1, Erythrocyte; Humans; Male; Point

1998