Optothermal control of the Raman gain enhanced ringing in microresonators von Wang, T., Wang, M., Hu, Y.-Q., Long, G.-L.

Volltext

Theoretically efficient high-capacity quantum-key-distribution scheme von Long, G. L., Liu, X. S.

Volltext

Heritability of plasma concentrations of clotting factors and measures of a prethrombotic state in a protein C‐deficient family von Vossen, C. Y., Hasstedt, S. J., Rosendaal, F. R., Callas, P. W., Bauer, K. A., Broze, G. J., Hoogendoorn, H., Long, G. L., Scott, B. T., Bovill, E. G.

Volltext

Analysis of density matrix reconstruction in NMR quantum computing von Long, G L, Yan, H Y, Sun, Yang

Volltext

Genome scan of venous thrombosis in a pedigree with protein C deficiency von Hasstedt, S. J., Scott, B. T., Callas, P. W., Vossen, C. Y., Rosendaal, F. R., Long, G. L., Bovill, E. G.

Volltext

Genetic Screening of Candidate Genes for a Prothrombotic Interaction with Type I Protein C Deficiency in a Large Kindred von Scott, Bruce T., Bovill, Edwin G., Callas, Peter W., Hasstedt, Sandra J., Leppert, Mark F., Valliere, Julia E., Varvil, Tena S., Long, G. L.

Volltext

A general method of site-specific mutagenesis using a modification of the Thermus aquaticus polymerase chain reaction von Nelson, Richard M., Long, George L.

Volltext

Characterization of the human prostaglandin H synthase 1 gene (PTGS1): exclusion by genetic linkage analysis as a second modifier gene in familial thrombosis von Scott, B T, Hasstedt, S J, Bovill, E G, Callas, P W, Valliere, J E, Wang, L, Wu, K K, Long, G L

Volltext

Chronic venous abnormalities in symptomatic and asymptomatic protein C deficiency von EMMERICH, J., VOSSEN, C. Y., CALLAS, P. W., DEMERS, C., NAUD, S., LONG, G. L., COUTURE, P., ROSENDAAL, F. R., BOVILL, E. G.

Volltext

Quantum Computing von Li, Shu-Shen, Long, Gui-Lu, Bai, Feng-Shan, Feng, Song-Lin, Zheng, Hou-Zhi

Volltext

Structure and Organization of the Human Metaxin Gene (MTX) and Pseudogene von Long, George L., Winfield, Suzanne, Adolph, Kenneth W., Ginns, Edward I., Bornstein, Paul

Volltext

Evolution and Organization of the Human Protein C Gene von Plutzky, Jorge, Hoskins, Jo Ann, Long, George L., Crabtree, Gerald R.

Volltext

An Unknown Genetic Defect Increases Venous Thrombosis Risk, through Interaction with Protein C Deficiency von Hasstedt, Sandra J., Bovill, Edwin G., Callas, Peter W., Long, George L.

Volltext

Proteolytic Events That Regulate Factor V Activity in Whole Plasma From Normal and Activated Protein C (APC)-Resistant Individuals During Clotting: An Insight Into the APC-Resistan... von Kalafatis, Michael, Haley, Paul E., Lu, Deshun, Bertina, Rogier M., Long, George L., Mann, Kenneth G.

Volltext

Grover algorithm with zero theoretical failure rate von Long, G. L.

Volltext

Organization of the human protein S genes von Schmidel, Dyann K, Tatro, Alicia V, Phelps, Lisa G, Tomczak, Jennifer A, Long, George L

Volltext

The G20210A Prothrombin Polymorphism Is not Associated with Increased Thromboembolic Risk in a Large Protein C Deficient Kindred von Bovill, Edwin G., Hasstedt, Sandra J., Callas, Peter W., Valliere, Julia E., Scott, Bruce T., Bauer, Kenneth A., Long, George L.

Volltext

Binding of protein S to C4b-binding protein. Mutagenesis of protein S von NELSON, R. M, LONG, G. L

Volltext

Evidence of a Founder Effect for the Protein C Gene 3363 Inserted C Mutation in Thrombophilic Pedigrees of French Origin von Couture, Patrick, Bovill, Edwin G., Demers, Christine, Delage, Robert, Scott, Bruce T., Valliere, Julia E., Callas, Peter W., Jomphe, Michèle, Rosendaal, Frits R., Aiach, Martine, Long, George L.

Volltext

Creation of entanglement between two electron spins induced by many spin ensemble excitations von Ai, Q., Li, Y., Long, G. L., Sun, C. P.

Volltext