Rabbit β-Globin Is Extended Beyond Its UGA Stop Codon by Multiple Suppressions and Translational Reading Gaps von Chittum, Harold S, Lane, William S, Carlson, Bradley A, Roller, Peter P, Lung, Feng-Di T, Lee, Byeong Jae, Hatfield, Dolph Lee

Volltext

Functional preference of the constituent amino acid residues in a phage-library-based nonphosphorylated inhibitor of the Grb2-SH2 domain von Lung, F.-D. T., Long, Y.-Q., Roller, Peter P., King, C. R., Varady, J., Wu, X.-W., Wang, S.

Volltext

Novel peptide inhibitors for Grb2 SH2 domain and their detection by surface plasmon resonance von Lung, F.-D. T., Tsai, J.-Y., Wei, S.-Y., Cheng, J.-W., Chen, C., Li, P., Roller, P. P.

Volltext

A p21(Waf1/Cip1)carboxyl-terminal peptide exhibited cyclin-dependent kinase-inhibitory activity and cytotoxicity when introduced into human cells von Mutoh, M, Lung, F D, Long, Y Q, Roller, P P, Sikorski, R S, O'Connor, P M

Volltext

Stability and peptide binding specificity of Btk SH2 domain: Molecular basis for X-linked agammaglobulinemia von TZENG, SHIOU-RU, PAI, MING-TAO, LUNG, FENG-DI T., WU, CHIH-WEI, ROLLER, PETER P., LEI, BENFANG, WEI, CHIH-JEN, TU, SHIAO-CHUN, CHEN, SHI-HAN, SOONG, WEN-JUE, CHENG, JYA-WEI

Volltext

Significant compensatory role of position Y-2 conferring high affinity to non-phosphorylated inhibitors of Grb2-SH2 domain von Long, Ya-Qiu, Voigt, Johannes H., Lung, Feng-Di T., King, C.Richter, Roller, Peter P.

Volltext

The GADD45 Inhibition of Cdc2 Kinase Correlates with GADD45-mediated Growth Suppression von Jin, Shunqian, Antinore, Michael J., Lung, Feng-Di T., Dong, Xin, Zhao, Hongcheng, Fan, Feiyue, Colchagie, Amy B., Blanck, Patricia, Roller, Peter P., Fornace, Albert J., Zhan, Qimin

Volltext

Effects of Modifications of Residues in Position 3 of Dynorphin A(1−11)-NH2 on κ Receptor Selectivity and Potency von Lung, Feng-Di T, Meyer, J.-P, Lou, Bih-Show, Xiang, Li, Li, Guigen, Davis, Peg, De Leon, Irene A, Yamamura, Henry I, Porreca, Frank, Hruby, Victor J

Volltext

Highly .kappa. receptor-selective dynorphin A analogs with modifications in position 3 of dynorphin A(1-11)-NH2 von Lung, Feng-Di T, Meyer, J.-Ph, Li, Guigen, Lou, B.-S, Stropova, Dagmar, Davis, Peg, Yamamura, Henry I, Porreca, Frank, Hruby, Victor J

Volltext

Oligomerization of Human Gadd45a Protein von Kovalsky, Oleg, Lung, Feng-Di T., Roller, Peter P., Fornace, Albert J.

Volltext

Nonphosphorylated Peptide Ligands for the Grb2 Src Homology 2 Domain von Oligino, Lyn, Lung, Feng-Di T., Sastry, Lakshmi, Bigelow, James, Cao, Tin, Curran, Michael, Burke, Terrence R., Wang, Shaomeng, Krag, David, Roller, Peter P., King, C. Richter

Volltext

The Central Region of Gadd45 Is Required for Its Interaction with p21/WAF1 von Zhao, Hongcheng, Jin, Shunqian, Antinore, Michael J, Lung, Feng-Di T, Fan, Feiyue, Blanck, Patricia, Roller, Peter, Fornace, Albert J, Zhan, Qimin

Volltext

Design of peptides and peptidomimetics for delta and kappa opioid receptor subtypes von Hruby, Victor J., Collins, N., Lung, F.-D., Meyer, J.-P., Davis, T.P., Yamamura, H.I., Porreca, F.

Volltext

Structural Requirements for Tyr in the Consensus Sequence Y-E-N of a Novel Nonphosphorylated Inhibitor to the Grb2-SH2 Domain von Long, Ya-Qiu, Yao, Zhu-Jun, Voigt, Johannes H., Lung, Feng-Di T., Luo, Juliet H., Burke, Terrence R., King, C.Richter, Yang, Dajun, Roller, Peter P.

Volltext

Design, synthesis, and biological activities of cyclic lactam peptide analogues of dynorphin A(1-11)-NH21 von LUNG, F.-D. T, COLLINS, N, STROPOVA, D, DAVIS, P, YAMAMURA, H. I, PORRECA, F, HRUBY, V. J

Volltext

Solution Structure and Dynamics of G1TE, a Nonphosphorylated Cyclic Peptide Inhibitor for the Grb2 SH2 Domain von Lou, Yuan-Chao, Lung, Feng-Di T., Pai, Ming-Tao, Tzeng, Shiou-Ru, Wei, Sue-Yee, Roller, Peter P., Cheng, Jya-Wei

Volltext

Surface plasmon resonance detection of interactions between peptide fragments of N-telopeptide and its monoclonal antibodies von Lung, F.-D.T., Chen, C.-H., Liou, C.-C., Chen, H.-Y.

Volltext

Development of highly potent and selective dynorphin A analogues as new medicines von Lung, F-D T, Chen, C-H, Liu, J-H

Volltext

Design, Synthesis, and Biological Properties of highly Potent Cyclic Dynorphin A Analogs. Analogs Cyclized between Positions 5 and 11 von Meyer, Jean-Philippe, Collins, Nathan, Lung, Feng-Di, Davis, Peg, Zalewska, Teresa, Porreca, Frank, Yamamura, Henry I., Hruby, Victor J.

Volltext

A p21Waf1/Cip1 carboxyl-terminal peptide exhibited cyclin-dependent kinase-inhibitory activity and cytotoxicity when introduced into human cells von MUTOH, M, LUNG, F.-D. T, LONG, Y.-Q, ROLLER, P. P, SIKORSKI, R. S, O'CONNOR, P. M

Volltext