-
1
-
-
0028912561
-
The clot thickens; clues provided by thrombin structure
-
Stubbs, M. T.; Bode, W. The clot thickens; clues provided by thrombin structure. Trends Biochem. 1995, 20, 23-28.
-
(1995)
Trends Biochem.
, vol.20
, pp. 23-28
-
-
Stubbs, M.T.1
Bode, W.2
-
2
-
-
0027304964
-
Structure of human des(1-45) factor Xa at 2,2 Å resolution
-
Padmanabhan, K.; Padmanabhan, K. P.; Tulinsky, A.; Park, C. H.; Bode, W.; Huber, R.; Blankenship, D. T.; Cardin, A. D.; Kiaiel, W. Structure of human des(1-45) factor Xa at 2,2 Å resolution. J. Mol. Biol. 1993, 232, 947-966.
-
(1993)
J. Mol. Biol.
, vol.232
, pp. 947-966
-
-
Padmanabhan, K.1
Padmanabhan, K.P.2
Tulinsky, A.3
Park, C.H.4
Bode, W.5
Huber, R.6
Blankenship, D.T.7
Cardin, A.D.8
Kiaiel, W.9
-
3
-
-
0024431034
-
The refined 1.9 Å crystal structure of human β-thrombin: Interaction with D-Phe-Pro-Arg chloromethyl ketone and significance of the Tyr-Pro-Pro-Trp insertion segment
-
Bode, W.; Mayr, I.; Baumann, U.; Huber, R.; Stone, S. R.; Hofsteenge, J. The refined 1.9 Å crystal structure of human β-thrombin: interaction with D-Phe-Pro-Arg chloromethyl ketone and significance of the Tyr-Pro-Pro-Trp insertion segment. EMBO J. 1989, 8, 3467-3475.
-
(1989)
EMBO J.
, vol.8
, pp. 3467-3475
-
-
Bode, W.1
Mayr, I.2
Baumann, U.3
Huber, R.4
Stone, S.R.5
Hofsteenge, J.6
-
4
-
-
0027050807
-
The refined 1,9 Å X-ray crystal structure of D-Phe-Pro-Arg chloromethyl ketone-inhibited human β-thrombin: Structure analysis, overall structure, electrostatic properties, detailed active-site geometry, and structure-function relationships
-
Bode, W.; Turk, D.; Karshikov, A. The refined 1,9 Å X-ray crystal structure of D-Phe-Pro-Arg chloromethyl ketone-inhibited human β-thrombin: structure analysis, overall structure, electrostatic properties, detailed active-site geometry, and structure-function relationships. Protein Sci. 1992, 1, 426-471.
-
(1992)
Protein Sci.
, vol.1
, pp. 426-471
-
-
Bode, W.1
Turk, D.2
Karshikov, A.3
-
5
-
-
0028801352
-
X-ray structure of clotting factor IXa: Active site and module structure related to Xase activity and hemophilia B
-
Brandstetter, H.; Bauer, M.; Huber, R.; Lollar, P.; Bode, W. X-ray structure of clotting factor IXa: active site and module structure related to Xase activity and hemophilia B. Proc. Natl. Acad. Sci. U.S.A. 1995, 2, 9796-9800.
-
(1995)
Proc. Natl. Acad. Sci. U.S.A.
, vol.2
, pp. 9796-9800
-
-
Brandstetter, H.1
Bauer, M.2
Huber, R.3
Lollar, P.4
Bode, W.5
-
6
-
-
0029926396
-
The crystal structure of the complex of blood coagulation factor VIIa with soluble tissue factor
-
Banner, D. W.; D'Arcy, A.; Chène, C.; Winkler, F. K.; Guha, A.; Konigsberg, W. H.; Nemerson, Y.; Kirchhofer, D. The crystal structure of the complex of blood coagulation factor VIIa with soluble tissue factor. Nature 1996, 380, 41-46.
-
(1996)
Nature
, vol.380
, pp. 41-46
-
-
Banner, D.W.1
D'Arcy, A.2
Chène, C.3
Winkler, F.K.4
Guha, A.5
Konigsberg, W.H.6
Nemerson, Y.7
Kirchhofer, D.8
-
7
-
-
0030468098
-
The 2.8 Å crystal structure of Gladomainless activated protein C
-
Mather, T.; Oganessyan, V.; Hof, P.; Huber, R.; Foundling, S.; Esmon, C.; Bode, W. The 2.8 Å crystal structure of Gladomainless activated protein C. EMBO J. 1996, 15, 6822-6831.
-
(1996)
EMBO J.
, vol.15
, pp. 6822-6831
-
-
Mather, T.1
Oganessyan, V.2
Hof, P.3
Huber, R.4
Foundling, S.5
Esmon, C.6
Bode, W.7
-
8
-
-
0027751754
-
A novel factor Xa inhibitor: Structure-activity relationships and selectivity between factor Xa and thrombin
-
Katakura, S.; Nagahara, T.; Hara, T.; Iwamoto, M. A novel factor Xa inhibitor: structure-activity relationships and selectivity between factor Xa and thrombin. Biochem. Biophys. Res. Commun. 1993, 197, 965-972.
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.197
, pp. 965-972
-
-
Katakura, S.1
Nagahara, T.2
Hara, T.3
Iwamoto, M.4
-
9
-
-
14444288877
-
-
Patent No. WO9616940, June 6, 1996
-
Hirayama, F.; Koshio, H.; Matsumoto, Y.; Kawasaki, T.; Kaku, S.; Yanagisawa, I. Patent No. WO9616940, June 6, 1996.
-
-
-
Hirayama, F.1
Koshio, H.2
Matsumoto, Y.3
Kawasaki, T.4
Kaku, S.5
Yanagisawa, I.6
-
10
-
-
0024328497
-
Synthetic inhibitors of bovine factor Xa and thrombin: Comparison of their anticoagulant efficiency
-
Stürzebecher, J.; Stürzebecher, U.; Vieweg, H.; Wagner, G.; Hauptmann, J.; Markwardt, F. Synthetic inhibitors of bovine factor Xa and thrombin: comparison of their anticoagulant efficiency. Thromb. Res. 1989, 54, 245-252.
-
(1989)
Thromb. Res.
, vol.54
, pp. 245-252
-
-
Stürzebecher, J.1
Stürzebecher, U.2
Vieweg, H.3
Wagner, G.4
Hauptmann, J.5
Markwardt, F.6
-
11
-
-
0029923976
-
X-ray structure of active site-inhibited clotting factor Xa
-
Brandstetter, H.; Kühne, A.; Bode, W.; Huber, R.; von der Saal, W.; Wirthensohn, K.; Engh, R. A. X-ray structure of active site-inhibited clotting factor Xa. J. Biol. Chem. 1996, 271, 29988-29992.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 29988-29992
-
-
Brandstetter, H.1
Kühne, A.2
Bode, W.3
Huber, R.4
Von der Saal, W.5
Wirthensohn, K.6
Engh, R.A.7
-
12
-
-
0028824422
-
Crystal structures of factor Xa specific inhibitors in complex with trypsin: Structural grounds for inhibition of factor Xa and selectivity against thrombin
-
Stubbs, M. T.; Huber, R.; Bode, W. Crystal structures of factor Xa specific inhibitors in complex with trypsin: structural grounds for inhibition of factor Xa and selectivity against thrombin. FEBS Lett. 1995, 375, 103-107.
-
(1995)
FEBS Lett.
, vol.375
, pp. 103-107
-
-
Stubbs, M.T.1
Huber, R.2
Bode, W.3
-
13
-
-
0024321257
-
X-ray analysis of a thrombin inhibitor-trypsin complex
-
Matsuzaki, T.; Sasaki, C.; Okumura, C.; Umeyama, H. X-ray analysis of a thrombin inhibitor-trypsin complex. J. Biochem. 1989, 105, 949-952.
-
(1989)
J. Biochem.
, vol.105
, pp. 949-952
-
-
Matsuzaki, T.1
Sasaki, C.2
Okumura, C.3
Umeyama, H.4
-
14
-
-
0025175641
-
α-(3-methyl-1,2,3,4-tetra-hydro-8-qumolinesulphonyl)-L-arginyl] -2-piperidine carboxylic acid (MQPA) to human β-thrombin
-
α-(3-methyl-1,2,3,4-tetra-hydro-8-qumolinesulphonyl)-L-arginyl] -2-piperidine carboxylic acid (MQPA) to human β-thrombin. Eur. J. Biochem. 1990, 193,175-182.
-
(1990)
Eur. J. Biochem.
, vol.193
, pp. 175-182
-
-
Bode, W.1
Turk, D.2
Stürzebecher, J.3
-
15
-
-
0025851272
-
α-tosylated piperidides of m-amidino-, p-amidino- and p-guanidino phenylalanine to thrombin and trypsin
-
α-tosylated piperidides of m-amidino-, p-amidino- and p-guanidino phenylalanine to thrombin and trypsin. FEES Lett. 1991, 287, 133-138.
-
(1991)
FEES Lett.
, vol.287
, pp. 133-138
-
-
Turk, D.1
Stürzebecher, J.2
Bode, W.3
-
16
-
-
0025837452
-
Crystallographic analysis at 3.0-Å resolution of the binding to human thrombin of four active site-directed inhibitors
-
Banner, D. W.; Hadváry, P. Crystallographic analysis at 3.0-Å resolution of the binding to human thrombin of four active site-directed inhibitors. J. Biol. Chem. 1991, 266, 20085-20093.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 20085-20093
-
-
Banner, D.W.1
Hadváry, P.2
-
17
-
-
0026465007
-
Refined 2.3 Å X-ray crystal structure of bovine thrombin complexes formed with the benzamidine and arginine-based thrombin inhibitors NAPAP, 4-TAPAP and MQPA
-
Brandstetter, H.; Turk, D.; Hoeffken, W.; Grosse, D.; Stürzebecher, J.; Martin, P. D.; Edwards, B. F. P.; Bode, W. Refined 2.3 Å X-ray crystal structure of bovine thrombin complexes formed with the benzamidine and arginine-based thrombin inhibitors NAPAP, 4-TAPAP and MQPA. J. Mol Biol. 1992, 226, 1085-1099.
-
(1992)
J. Mol Biol.
, vol.226
, pp. 1085-1099
-
-
Brandstetter, H.1
Turk, D.2
Hoeffken, W.3
Grosse, D.4
Stürzebecher, J.5
Martin, P.D.6
Edwards, B.F.P.7
Bode, W.8
-
18
-
-
14444281871
-
-
Manuscript in preparation
-
Renatus, M.; Bode, W.; Huber, R.; Stürzebecher, J.; Stubbs, M. T. Structural and functional analyses of benzamidine-based inhibitors in complex with trypsin: implications for the inhibition of factor Xa, tPA and urokinase. Manuscript in preparation.
-
Structural and Functional Analyses of Benzamidine-based Inhibitors in Complex with Trypsin: Implications for the Inhibition of Factor Xa, TPA and Urokinase
-
-
Renatus, M.1
Bode, W.2
Huber, R.3
Stürzebecher, J.4
Stubbs, M.T.5
-
19
-
-
0021235491
-
α-(Arylsulfonylglycy)amidino-phenyl-alaninamiden als hochaktive Inhibitoren des Thrombins
-
α-(Arylsulfonylglycy)amidino-phenyl-alaninamiden als hochaktive Inhibitoren des Thrombins. Pharmazie 1984, 39, 226-230.
-
(1984)
Pharmazie
, vol.39
, pp. 226-230
-
-
Wagner, G.1
Voigt, B.2
Vieweg, H.3
-
20
-
-
0000673837
-
The synthesis of amino acids by reaction of an electrophilic glycine cation equivalent with neutral carbon nucleophiles
-
O'Donnell, M. J.; Bennett, W. D. The synthesis of amino acids by reaction of an electrophilic glycine cation equivalent with neutral carbon nucleophiles. Tetrahedron 1988, 44, 5389-5401.
-
(1988)
Tetrahedron
, vol.44
, pp. 5389-5401
-
-
O'Donnell, M.J.1
Bennett, W.D.2
-
22
-
-
0002943240
-
Synthetic substrates and inhibitors of thrombin
-
Berliner, L. J., Ed.; Plenum Press: New York
-
Powers, J. C.; Kam, C.-M. Synthetic substrates and inhibitors of thrombin. In Thrombin. Structure and Function; Berliner, L. J., Ed.; Plenum Press: New York, 1992; pp 117-158.
-
(1992)
Thrombin. Structure and Function
, pp. 117-158
-
-
Powers, J.C.1
Kam, C.-M.2
-
23
-
-
0029147936
-
Challenges in the development of orally bioavailable thrombin active site inhibitors
-
Kimball, S. D. Challenges in the development of orally bioavailable thrombin active site inhibitors. Blood Coagul. Fibrinol. 1995, 6, 511-519.
-
(1995)
Blood Coagul. Fibrinol.
, vol.6
, pp. 511-519
-
-
Kimball, S.D.1
-
24
-
-
0028905557
-
Characterization of a class of peptide boronates with neutral P1 side-chains as highly selective inhibitors of thrombin
-
Deadman, J. J.; Elgendy, S.; Goodwin, C. A.; Green, D.; Baban, J. A.; Patel, G.; Skordalakes, E.; Chino, N.; Claeson, G.; Kakkar, V. V.; Scully, M. F. Characterization of a class of peptide boronates with neutral P1 side-chains as highly selective inhibitors of thrombin. J. Med. Chem. 1995, 38, 1511-1522.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1511-1522
-
-
Deadman, J.J.1
Elgendy, S.2
Goodwin, C.A.3
Green, D.4
Baban, J.A.5
Patel, G.6
Skordalakes, E.7
Chino, N.8
Claeson, G.9
Kakkar, V.V.10
Scully, M.F.11
-
25
-
-
0025811857
-
Degradation of a benzamidine-type synthetic inhibitor of coagulation enzymes in plasma of various species
-
Hauptmann, J. Degradation of a benzamidine-type synthetic inhibitor of coagulation enzymes in plasma of various species. Thromb. Res. 1991, 61, 279-284.
-
(1991)
Thromb. Res.
, vol.61
, pp. 279-284
-
-
Hauptmann, J.1
-
26
-
-
0024500788
-
Pharmacological characterization of a new structural variant of 4-amidinophenylalanine amide-type synthetic thrombin inhibitor
-
Hauptmann, J.; Kaiser, B.; Paintz, M.; Markwardt, F. Pharmacological characterization of a new structural variant of 4-amidinophenylalanine amide-type synthetic thrombin inhibitor. Pharmazie 1989, 44, 282-284.
-
(1989)
Pharmazie
, vol.44
, pp. 282-284
-
-
Hauptmann, J.1
Kaiser, B.2
Paintz, M.3
Markwardt, F.4
-
27
-
-
0030768740
-
Synthesis and structure-activity relationships of potent thrombin inhibitors: Piperazides of 3-amidinophenylalanine
-
Stürzebecher, J.; Prasa, D.; Hauptmann, J.; Vieweg, H.; Wikström, P. Synthesis and structure-activity relationships of potent thrombin inhibitors: piperazides of 3-amidinophenylalanine. J. Med. Chem. 1997, 40, 3091-3099.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 3091-3099
-
-
Stürzebecher, J.1
Prasa, D.2
Hauptmann, J.3
Vieweg, H.4
Wikström, P.5
-
28
-
-
15144344269
-
Rational design and synthesis of novel, potent bis-phenylamidine carboxylate factor Xa inhibitors
-
Maduskuie, T. P., Jr.; McNamara, K. J.; Ru, Y.; Knabb, R. M.; Stouten, P. F. W. Rational design and synthesis of novel, potent bis-phenylamidine carboxylate factor Xa inhibitors. J. Med. Chem. 1998, 41, 53-62.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 53-62
-
-
Maduskuie Jr., T.P.1
McNamara, K.J.2
Ru, Y.3
Knabb, R.M.4
Stouten, P.F.W.5
-
29
-
-
0025329390
-
The structure of a complex of recombinant hirudin and human β-thrombin
-
Rydel, T. J.; Ravichandran, K. G.; Tulinsky, A.; Bode, W.; Huber, R.; Roitsch, C.; Fenton, J. W. The structure of a complex of recombinant hirudin and human β-thrombin. Science 1990, 249, 277-280.
-
(1990)
Science
, vol.249
, pp. 277-280
-
-
Rydel, T.J.1
Ravichandran, K.G.2
Tulinsky, A.3
Bode, W.4
Huber, R.5
Roitsch, C.6
Fenton, J.W.7
-
30
-
-
0025866812
-
Refined structure of the hirudin-thrombin complex
-
Rydel, T. J.; Tulinsky, A.; Bode, W.; Huber, R. Refined structure of the hirudin-thrombin complex. J. Mol. Biol. 1991, 221, 583-601.
-
(1991)
J. Mol. Biol.
, vol.221
, pp. 583-601
-
-
Rydel, T.J.1
Tulinsky, A.2
Bode, W.3
Huber, R.4
-
31
-
-
0026646203
-
The structure of a complex of bovine β-thrombin and recombinant hirudin at 2.8 Å resolution
-
Vitali, J.; Martin, P. D.; Malkowski, M. G.; Robertson, W. D.; Lazar, J. B.; Winant, R. C.; Johnson, P. H.; Edwards, B. F. The structure of a complex of bovine β-thrombin and recombinant hirudin at 2.8 Å resolution. J. Biol. Chem. 1992, 267, 17670-17678.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 17670-17678
-
-
Vitali, J.1
Martin, P.D.2
Malkowski, M.G.3
Robertson, W.D.4
Lazar, J.B.5
Winant, R.C.6
Johnson, P.H.7
Edwards, B.F.8
-
32
-
-
0029957955
-
The ornithodorin-thrombin crystal structure, a key to the TAP enigma?
-
van de Locht, A.; Stubbs, M. T.; Bode, W.; Friedrich, T.; Bollschweiler, C.; Höffken, W.; Huber, R. The ornithodorin-thrombin crystal structure, a key to the TAP enigma? EMBO J. 1996, 15, 6011-6017.
-
(1996)
EMBO J.
, vol.15
, pp. 6011-6017
-
-
Van de Locht, A.1
Stubbs, M.T.2
Bode, W.3
Friedrich, T.4
Bollschweiler, C.5
Höffken, W.6
Huber, R.7
-
33
-
-
0029895694
-
A noncleavable retro-binding peptide that spans the substrate binding cleft of serine proteases - Atomic structure of Nazumamide A-human thrombin
-
Nienaber, V. L. A noncleavable retro-binding peptide that spans the substrate binding cleft of serine proteases - Atomic structure of Nazumamide A-human thrombin. J. Am. Chem. Soc. 1996, 118, 6807-6810.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 6807-6810
-
-
Nienaber, V.L.1
-
34
-
-
0028276982
-
Retro-binding tripeptide thrombin active-site inhibitors: Discovery, synthesis, and molecular modeling
-
Iwanowicz, E. J.; Lau, W. F.; Lin, J.; Roberts, D. G.; Seiler, S. M. Retro-binding tripeptide thrombin active-site inhibitors: discovery, synthesis, and molecular modeling. J. Med. Chem. 1994, 37, 2122-2124.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 2122-2124
-
-
Iwanowicz, E.J.1
Lau, W.F.2
Lin, J.3
Roberts, D.G.4
Seiler, S.M.5
-
35
-
-
0028930131
-
Structure of a retro-binding peptide inhibitor complexed with human β-thrombin
-
Tabernero, L.; Chang, C. Y.; Ohringer, S. L.; Lau, W. F.; Iwanowicz, E. J.; Han, W. C.; Wang, T. C.; Seiler, S. M.; Roberts, D. G.; Sack, J. S. Structure of a retro-binding peptide inhibitor complexed with human β-thrombin. J. Mol. Biol. 1995, 246, 14-20.
-
(1995)
J. Mol. Biol.
, vol.246
, pp. 14-20
-
-
Tabernero, L.1
Chang, C.Y.2
Ohringer, S.L.3
Lau, W.F.4
Iwanowicz, E.J.5
Han, W.C.6
Wang, T.C.7
Seiler, S.M.8
Roberts, D.G.9
Sack, J.S.10
-
36
-
-
0031890648
-
Hirunorms are true hirudin mimetics. the crystal structure of human β-thrombin-hirunorm V complex
-
De Simone, G.; Lombardi, A.; Galdiero, S.; Nastri, F.; Della Morte, R.; Staiano, N.; Pedone, C.; Bolognesi, M.; Pavone, V. Hirunorms are true hirudin mimetics. The crystal structure of human β-thrombin-hirunorm V complex. Protein. Sci. 1998, 7, 243-253
-
(1998)
Protein. Sci.
, vol.7
, pp. 243-253
-
-
De Simone, G.1
Lombardi, A.2
Galdiero, S.3
Nastri, F.4
Della Morte, R.5
Staiano, N.6
Pedone, C.7
Bolognesi, M.8
Pavone, V.9
-
37
-
-
0028821564
-
Pharmacological characterization of a new 4-amidinophenylalanine thrombin-inhibitor (CRC 220)
-
Dickneite, G.; Seiffge, D.; Diehl, K.-H.; Reers, M.; Czech, J.; Weinmann, E.; Hoffmann, D.; Stüber, W. Pharmacological characterization of a new 4-amidinophenylalanine thrombin-inhibitor (CRC 220). Thromb. Res. 1995, 77, 357-368.
-
(1995)
Thromb. Res.
, vol.77
, pp. 357-368
-
-
Dickneite, G.1
Seiffge, D.2
Diehl, K.-H.3
Reers, M.4
Czech, J.5
Weinmann, E.6
Hoffmann, D.7
Stüber, W.8
-
38
-
-
33845555590
-
A mild and efficient route to Schiff base derivatives of amino acids
-
O'Donnell, M. J.; Polt, R. L. A mild and efficient route to Schiff base derivatives of amino acids. J. Org. Chem. 1982, 47, 2663-2666.
-
(1982)
J. Org. Chem.
, vol.47
, pp. 2663-2666
-
-
O'Donnell, M.J.1
Polt, R.L.2
-
39
-
-
77049143386
-
Determination of enzyme inhibitor constants
-
Dixon, M. Determination of enzyme inhibitor constants. Biochem. J. 1953, 55, 170-171.
-
(1953)
Biochem. J.
, vol.55
, pp. 170-171
-
-
Dixon, M.1
-
40
-
-
0028920221
-
Evidence for multiple interacting binding sites in bovine tryptase
-
Fiorucci, L.; Erba, F.; Coletta, M.; Ascoli, F. Evidence for multiple interacting binding sites in bovine tryptase. FEBS Lett. 1995, 363, 81-84.
-
(1995)
FEBS Lett.
, vol.363
, pp. 81-84
-
-
Fiorucci, L.1
Erba, F.2
Coletta, M.3
Ascoli, F.4
-
41
-
-
0014308079
-
Über die Reinigung von Thrombinpräparaten
-
Walsmann, P. Über die Reinigung von Thrombinpräparaten. Pharmazie 1968, 23, 401-402.
-
(1968)
Pharmazie
, vol.23
, pp. 401-402
-
-
Walsmann, P.1
-
42
-
-
0027081333
-
Mapping of the catalytic site of CHO-t-PA and the t-PA variant BM 06.022 by synthetic inhibitors and substrates
-
Stürzebecher, J.; Neumann, U.; Kohnert, U.; Kresse, G.-B.; Fischer, S. Mapping of the catalytic site of CHO-t-PA and the t-PA variant BM 06.022 by synthetic inhibitors and substrates. Protein Sci. 1992, 1, 1007-1013.
-
(1992)
Protein Sci.
, vol.1
, pp. 1007-1013
-
-
Stürzebecher, J.1
Neumann, U.2
Kohnert, U.3
Kresse, G.-B.4
Fischer, S.5
-
43
-
-
0026940256
-
Inhibition of human mast cell tryptase by benzamidine derivatives
-
Stürzebecher, J.; Prasa, D.; Sommerhoff, C. P. Inhibition of human mast cell tryptase by benzamidine derivatives. Biol. Chem. Hoppe-Seyler 1992, 373, 1025-1030.
-
(1992)
Biol. Chem. Hoppe-Seyler
, vol.373
, pp. 1025-1030
-
-
Stürzebecher, J.1
Prasa, D.2
Sommerhoff, C.P.3
-
44
-
-
85046526624
-
Evalution of single-crystal X-ray diffraction data from a position-sensitive detector
-
Kabsch, W. Evalution of single-crystal X-ray diffraction data from a position-sensitive detector. J. Appl. Crystallogr. 1988, 21, 916-924.
-
(1988)
J. Appl. Crystallogr.
, vol.21
, pp. 916-924
-
-
Kabsch, W.1
-
46
-
-
0003838966
-
-
Silicon Graphics: Mountain View, CA
-
Roussel, A.; Cambilleau, C. Turbo-Frodo in Silicon Graphics Geometrry, Partners Directory, Silicon Graphics: Mountain View, CA, 1989.
-
(1989)
Turbo-Frodo in Silicon Graphics Geometrry, Partners Directory
-
-
Roussel, A.1
Cambilleau, C.2
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