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alanine and Deficiency, Protein C

alanine has been researched along with Deficiency, Protein C 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.

Research Excerpts

ExcerptRelevanceReference
"The role of two protein C gamma-carboxyglutamic acid domain mutations in familial thrombosis, protein CVermont (Bovill, E."3.69Molecular mechanism for familial protein C deficiency and thrombosis in protein CVermont (Glu20-->Ala and Val34-->Met). ( Bovill, EG; Long, GL; Lu, D, 1994)

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
Lu, D1
Bovill, EG1
Long, GL1
Kemahli, S1
Alhenc-Gelas, M1
Gandrille, S1
Aiach, M1
Akar, N1
Cin, S1

Other Studies

2 other studies available for alanine and Deficiency, Protein C

ArticleYear
Molecular mechanism for familial protein C deficiency and thrombosis in protein CVermont (Glu20-->Ala and Val34-->Met).
    The Journal of biological chemistry, 1994, Nov-18, Volume: 269, Issue:46

    Topics: Alanine; Base Sequence; DNA Primers; Glutamic Acid; Humans; Methionine; Molecular Sequence Data; Mut

1994
Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to Thr.
    Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1998, Volume: 9, Issue:4

    Topics: Alanine; Amino Acid Substitution; Base Sequence; Consanguinity; Genetic Variation; Histidine; Homozy

1998