Compounds > threonine

threonine and Deficiency, Protein C

threonine has been researched along with Deficiency, Protein C in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	3 (75.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (25.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Haugbro, K; Sandset, PM; Skretting, G; Tjeldhorn, L	1
Cooper, DN; Hallam, PJ; Kakkar, VV; Krawczak, M; Kühnau, W; Legnani, C; Mannucci, PM; Wacey, AI	1
Choi, CR; Kim, HK; Kim, HS; Park, Q; Park, YS; Song, KS	1
Aiach, M; Akar, N; Alhenc-Gelas, M; Cin, S; Gandrille, S; Kemahli, S	1

Other Studies

4 other study(ies) available for threonine and Deficiency, Protein C

Article	Year
Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis. Thrombosis research, 2010, Volume: 125, Issue:3 Topics: Activated Protein C Resistance; Adult; Amino Acid Substitution; Anticoagulants; Consanguinity; DNA; Family Health; Female; Heterozygote; Homozygote; Humans; Pedigree; Protein C; Protein C Deficiency; Threonine; Venous Thrombosis	2010
A novel missense mutation (Thr176-->Ile) at the putative hinge of the neo N-terminus of activated protein C. Human genetics, 1995, Volume: 95, Issue:4 Topics: Adult; Amino Acid Sequence; Base Sequence; Enzyme Activation; Female; Humans; Isoleucine; Models, Molecular; Molecular Sequence Data; Point Mutation; Polymerase Chain Reaction; Pregnancy; Protein C; Protein C Deficiency; Protein Folding; Threonine	1995
Hereditary protein C deficiency with recurrent thrombosis: identification of a missense mutation (C6218T). Journal of Korean medical science, 1998, Volume: 13, Issue:2 Topics: Adult; Cysteine; Female; Genetic Diseases, Inborn; Humans; Male; Pedigree; Point Mutation; Protein C; Protein C Deficiency; Recurrence; Threonine; Thrombosis	1998
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; Homozygote; Humans; Infant, Newborn; Male; Mutation; Pedigree; Protein C; Protein C Deficiency; Threonine; Tyrosine	1998