threonine and Deficiency, Factor II

threonine has been researched along with Deficiency, Factor II in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baidya, S; Chandy, M; Jayandharan, G; Nair, SC; Shaji, RV; Srivastava, A; Viswabandya, A	1

Other Studies

1 other study(ies) available for threonine and Deficiency, Factor II

Article	Year
Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation. Journal of thrombosis and haemostasis : JTH, 2005, Volume: 3, Issue:7 Topics: Adult; Alanine; Alternative Splicing; Child, Preschool; Codon; DNA; DNA Mutational Analysis; DNA Primers; Evolution, Molecular; Female; Gene Deletion; Heterozygote; Homozygote; Humans; Hypoprothrombinemias; India; Male; Middle Aged; Models, Genetic; Models, Molecular; Mutation; Mutation, Missense; Partial Thromboplastin Time; Protein Conformation; Protein Structure, Tertiary; Prothrombin; Prothrombin Time; Sequence Analysis, DNA; Threonine; Thrombin	2005

Article

Year

Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.

Journal of thrombosis and haemostasis : JTH, 2005, Volume: 3, Issue:7

Topics: Adult; Alanine; Alternative Splicing; Child, Preschool; Codon; DNA; DNA Mutational Analysis; DNA Primers; Evolution, Molecular; Female; Gene Deletion; Heterozygote; Homozygote; Humans; Hypoprothrombinemias; India; Male; Middle Aged; Models, Genetic; Models, Molecular; Mutation; Mutation, Missense; Partial Thromboplastin Time; Protein Conformation; Protein Structure, Tertiary; Prothrombin; Prothrombin Time; Sequence Analysis, DNA; Threonine; Thrombin

2005