-
1
-
-
0027478912
-
Peptidomimetics derived from natural products
-
Rich DH, Wiley RA: Peptidomimetics derived from natural products. Med Res Rev 1993, 13:327-384.
-
(1993)
Med Res Rev
, vol.13
, pp. 327-384
-
-
Rich, D.H.1
Wiley, R.A.2
-
2
-
-
0029065615
-
Combinatorial synthesis - The design of compound libraries and their application to drug discovery
-
Terrett NK, Gardner M, Gordon D, Kobylecki RJ, Steele J: Combinatorial synthesis - the design of compound libraries and their application to drug discovery. Tetrahedron 1995, 51:8135-8173. An excellent paper reviewing the pioneering concepts and fundamentals in the field of combinatorial and high speed synthesis.
-
(1995)
Tetrahedron
, vol.51
, pp. 8135-8173
-
-
Terrett, N.K.1
Gardner, M.2
Gordon, D.3
Kobylecki, R.J.4
Steele, J.5
-
3
-
-
0030477258
-
Combinatorial synthesis of small organic molecules
-
Balkenhohl F, Bussche-Hunnefeld C, Lansky A, Zechel C: Combinatorial synthesis of small organic molecules. Angew Chem Int Ed 1996, 35:2288-2337. A comprehensive review of methodologies to prepare compound libraries.
-
(1996)
Angew Chem Int Ed
, vol.35
, pp. 2288-2337
-
-
Balkenhohl, F.1
Bussche-Hunnefeld, C.2
Lansky, A.3
Zechel, C.4
-
4
-
-
0029930278
-
Solid-phase organic reactions: A review of the recent literature
-
Hermkens PHH, Ottenheijm HCJ, Rees D: Solid-phase organic reactions: a review of the recent literature. Tetrahedron 1996, 52:4527-4554. A comprehensive and tabulated review of solid-phase chemical reactions.
-
(1996)
Tetrahedron
, vol.52
, pp. 4527-4554
-
-
Hermkens, P.1
Ottenheijm, H.2
Rees, D.3
-
5
-
-
7044263277
-
Synthesis and applications of small molecule libraries
-
Thompson LA, Ellman JA: Synthesis and applications of small molecule libraries. Chem Rev 1996, 96:555-600.
-
(1996)
Chem Rev
, vol.96
, pp. 555-600
-
-
Thompson, L.A.1
Ellman, J.A.2
-
6
-
-
33748237769
-
Organic chemistry on solid supports
-
Fruchtel JS, Jung G: Organic chemistry on solid supports. Angew Chem Int Ed 1996, 35:17-42.
-
(1996)
Angew Chem Int Ed
, vol.35
, pp. 17-42
-
-
Fruchtel, J.S.1
Jung, G.2
-
8
-
-
0004337068
-
-
On the World Wide Web URL
-
Dynamic database of references in molecular diversity. On the World Wide Web URL: http://vesta.pd.com A popular (at least amongst the staff at Oxford Diversity) means of keeping up to date with the ever expanding rate of publications in the subject area.
-
Dynamic Database of References in Molecular Diversity
-
-
-
10
-
-
85030035729
-
-
MDL Information Systems, 14600 Catalina Street, San Leandro, CA 94577 (USA). On the World Wide Web URL
-
Solid phase organic reaction database (SPORE), MDL Information Systems, 14600 Catalina Street, San Leandro, CA 94577 (USA). On the World Wide Web URL: http://www mdli.com
-
Solid Phase Organic Reaction Database (SPORE)
-
-
-
11
-
-
0029991217
-
A novel linker strategy for solid-phase synthesis
-
Morphy JR, Rankovic Z, Rees DC: A novel linker strategy for solid-phase synthesis. Tetrahedron Lett 1996, 37:3209-3212. Of note in this process are the mildness of the conditions employed and the fact that the REM resin is reusable at the end of the process.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 3209-3212
-
-
Morphy, J.R.1
Rankovic, Z.2
Rees, D.C.3
-
12
-
-
0030605136
-
A method for the synthesis of hydroxamic acids on solid phase
-
Floyd CD, Lewis CN, Patel RP, Whittaker M: A method for the synthesis of hydroxamic acids on solid phase. Tetrahedron Lett 1996, 37:8045-8048.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 8045-8048
-
-
Floyd, C.D.1
Lewis, C.N.2
Patel, R.P.3
Whittaker, M.4
-
13
-
-
33751156625
-
A silicon-based linker for traceless solid-phase synthesis
-
Plunkett MJ, Ellman JA: A silicon-based linker for traceless solid-phase synthesis. J Org Chem 1995, 60:6006-6007. This first example of a silane linker suffers from the fact that a multistep synthesis is required to prepare an appropriate linker for each class of library compound and therefore lacks generality in synthetic use.
-
(1995)
J Org Chem
, vol.60
, pp. 6006-6007
-
-
Plunkett, M.J.1
Ellman, J.A.2
-
14
-
-
0013249477
-
Protodetachable arylsilane polymer linkages for use in solid phase organic synthesis
-
Chenera B, Finkelstein JA, Veber DF: Protodetachable arylsilane polymer linkages for use in solid phase organic synthesis. J Am Chem Soc 1995, 117:11999-12000. This linker requires quite forcing conditions (CsF in aqueous dimethylfluoride at 100°C) to liberate the product biaryl derivatives.
-
(1995)
J Am Chem Soc
, vol.117
, pp. 11999-12000
-
-
Chenera, B.1
Finkelstein, J.A.2
Veber, D.F.3
-
16
-
-
0029865824
-
Silicon directed ipso-substitution of polymer bound arylsilanes: Preparation of biaryls via the Suzuki cross-coupling reaction
-
Han Y, Walker SD, Young RN: Silicon directed ipso-substitution of polymer bound arylsilanes: preparation of biaryls via the Suzuki cross-coupling reaction. Tetrahedron Lett 1996, 37:2703-2706. The yields quoted for ipso-substitution with chlorine and bromine are excellent and therefore this is the method of choice for preparing halogenated compounds in library format.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 2703-2706
-
-
Han, Y.1
Walker, S.D.2
Young, R.N.3
-
17
-
-
0030583495
-
Application of polymer-bound phosphonium salts as traceless supports for solid phase synthesis
-
Hughes I: Application of polymer-bound phosphonium salts as traceless supports for solid phase synthesis. Tetrahedron Lett 1996, 37:7579-7598. A potentially very valuable linker as it can be cleaved under a variety of conditions to afford a diverse set of products from common intermediates.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 7579-7598
-
-
Hughes, I.1
-
18
-
-
0030041813
-
Synthesis of ketones and aldehydes via reactions of Weinreb-type amides on solid support
-
Dinh TQ, Armstrong RW: Synthesis of ketones and aldehydes via reactions of Weinreb-type amides on solid support. Tetrahedron Lett 1996, 37:1161-1164.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 1161-1164
-
-
Dinh, T.Q.1
Armstrong, R.W.2
-
19
-
-
37049089078
-
A novel lysine-protecting procedure for continuous flow solid phase synthesis of branched peptides
-
Bycroft BW, Chan WC, Chhabra SR, Hone ND: A novel lysine-protecting procedure for continuous flow solid phase synthesis of branched peptides. J Chem Soc Chem Commun 1993, 778-779.
-
(1993)
J Chem Soc Chem Commun
, pp. 778-779
-
-
Bycroft, B.W.1
Chan, W.C.2
Chhabra, S.R.3
Hone, N.D.4
-
20
-
-
0030576321
-
A new linker for primary amines applicable to combinatorial approaches
-
Bannwarth W, Huebscher J, Barner R: A new linker for primary amines applicable to combinatorial approaches. Bioorg Med Chem Lett 1996, 6:1525-1528. Cleavage of products from this resin is accomplished with 2% hydrazine and is generally very specific, which permits a wide degree of structural diversity to be placed in the library. Structural diversity is not consistent with the more usual acid or base cleavage.
-
(1996)
Bioorg Med Chem Lett
, vol.6
, pp. 1525-1528
-
-
Bannwarth, W.1
Huebscher, J.2
Barner, R.3
-
21
-
-
0029937132
-
The design and synthesis of substituted biphenyl libraries
-
Pavia MR, Cohen MP, Dilley GJ, Dubuc GR, Durgin TL, Forman FW, Hediger ME, Milot G, Powers TS, Sucholeiki I et al.: The design and synthesis of substituted biphenyl libraries. Bioorg Med Chem 1996, 4:659-666. A review of synthetic approaches to the biaryl privileged structure - the pharmacophore of the 1990s.
-
(1996)
Bioorg Med Chem
, vol.4
, pp. 659-666
-
-
Pavia, M.R.1
Cohen, M.P.2
Dilley, G.J.3
Dubuc, G.R.4
Durgin, T.L.5
Forman, F.W.6
Hediger, M.E.7
Milot, G.8
Powers, T.S.9
Sucholeiki, I.10
-
22
-
-
0001644755
-
Solid phase Suzuki coupling for C-C bond formation
-
Guiles JW, Johnson SG, Murray WV: Solid phase Suzuki coupling for C-C bond formation. J Org Chem 1996, 61:5169-5171. An approach to biaryls that involves reaction of resin-bound aryl boronates with aryl iodides. This reaction is usually carried out the other way round and is thus limited to the range of the relatively few commercial aryl boronates.
-
(1996)
J Org Chem
, vol.61
, pp. 5169-5171
-
-
Guiles, J.W.1
Johnson, S.G.2
Murray, W.V.3
-
23
-
-
0029011229
-
Solid phase synthesis of aryl ethers via the Mitsunobu reaction
-
Rano TA, Chapman KT: Solid phase synthesis of aryl ethers via the Mitsunobu reaction. Tetrahedron Lett 1996, 36:3789-3792.
-
(1996)
Tetrahedron Lett
, vol.36
, pp. 3789-3792
-
-
Rano, T.A.1
Chapman, K.T.2
-
24
-
-
0030599273
-
Solid phase synthesis of aryl amines via Palladium catalysed amination of resin bound aromatic bromides
-
Ward YD, Farina V: Solid phase synthesis of aryl amines via Palladium catalysed amination of resin bound aromatic bromides. Tetrahedron Lett 1996, 37:6993-6996.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 6993-6996
-
-
Ward, Y.D.1
Farina, V.2
-
25
-
-
0030607186
-
Solid phase synthesis of aryl amines
-
Willoughby CA, Chapman KT: Solid phase synthesis of aryl amines. Tetrahedron Lett 1996, 37:7181-7184. This paper highlights the route development that frequently needs to be performed before library synthesis can take place. In this case, screening of phosphine ligands to assist palladium catalyzed amine insertion identified BINAP as the optimum ligand.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 7181-7184
-
-
Willoughby, C.A.1
Chapman, K.T.2
-
26
-
-
0029042575
-
Combinatorial organic synthesis of highly functionalized pyrrolidines: Identification of a potent angiotensin converting enzyme inhibitor from a mercaptoacyl proline library
-
Murphy MM, Schullek JR, Gordon EM, Gallop MA: Combinatorial organic synthesis of highly functionalized pyrrolidines: identification of a potent angiotensin converting enzyme inhibitor from a mercaptoacyl proline library. J Am Chem Soc 1995, 117:7029-7030. This first paper on 1,3-dipolar cycloaddition approaches to pyrrolidines exemplifies the power of libraries for lead discovery. In this case, a pyrrolidine compound was identified that was three-fold more potent than Captopril® in ACE inhibition.
-
(1995)
J Am Chem Soc
, vol.117
, pp. 7029-7030
-
-
Murphy, M.M.1
Schullek, J.R.2
Gordon, E.M.3
Ma, G.4
-
27
-
-
0029944026
-
Solid-phase synthesis of proline analogs via a three component 1,3-dipolar cycloaddition
-
Hamper BC, Dukesherer DR, South MS: Solid-phase synthesis of proline analogs via a three component 1,3-dipolar cycloaddition. Tetrahedron Lett 1996, 37:3671-3674.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 3671-3674
-
-
Hamper, B.C.1
Dukesherer, D.R.2
South, M.S.3
-
28
-
-
0030598197
-
Synthesis of a highly functionalized rigid template by solid phase azomethine ylide cycloaddition
-
Bicknell AJ, Hird NW: Synthesis of a highly functionalized rigid template by solid phase azomethine ylide cycloaddition. Bioorg Med Chem Lett 1996, 6:2441-2444.
-
(1996)
Bioorg Med Chem Lett
, vol.6
, pp. 2441-2444
-
-
Bicknell, A.J.1
Hird, N.W.2
-
29
-
-
0030590979
-
Stereoselective synthesis of highly functionalised pyrrolidines via 1,3-dipolar cycloaddition reactions on a solid support
-
Hollinshead SP: Stereoselective synthesis of highly functionalised pyrrolidines via 1,3-dipolar cycloaddition reactions on a solid support. Tetrahedron Lett 1996, 37:9157-9160.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 9157-9160
-
-
Hollinshead, S.P.1
-
30
-
-
0030064961
-
Solid supported combinatorial synthesis of structurally diverse β-lactams
-
Ruhland B, Bhandari A, Gordon EM, Gallop MA: Solid supported combinatorial synthesis of structurally diverse β-lactams. J Am Chem Soc 1996, 118:253-254. This paper from the Affymax group covers an efficient synthesis of β-lactams using either a super acid labile linker, Sasrin, or a phototabile linker attached to Tentagel™ resin. Release of the sensitive products is facilitated using these methods.
-
(1996)
J Am Chem Soc
, vol.118
, pp. 253-254
-
-
Ruhland, B.1
Bhandari, A.2
Gordon, E.M.3
Gallop, Ma.4
-
31
-
-
0030034999
-
Solid phase synthesis of hydantoins using a carbamate linker and a novel cyclisation/ cleavage step
-
Dressman BA, Spangle LA, Kaldor SW: Solid phase synthesis of hydantoins using a carbamate linker and a novel cyclisation/ cleavage step. Tetrahedron Lett 1996, 37:937-940.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 937-940
-
-
Dressman, B.A.1
Spangle, L.A.2
Kaldor, S.W.3
-
32
-
-
0030599228
-
Solid phase synthesis of chiral 3-substituted quinazoline-2,4-diones
-
Gouilleux L, Fehrentz J, Winternitz F, Martinez J: Solid phase synthesis of chiral 3-substituted quinazoline-2,4-diones. Tetrahedron Lett 1996, 37:7031-7034.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 7031-7034
-
-
Gouilleux, L.1
Fehrentz, J.2
Winternitz, F.3
Martinez, J.4
-
33
-
-
0029681546
-
Solid phase synthesis of 5,6-dihydropyrimidine-2,4-diones
-
Kolodziej SA, Hamper BC: Solid phase synthesis of 5,6-dihydropyrimidine-2,4-diones. Tetrahedron Lett 1996, 37:5277-5280.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 5277-5280
-
-
Kolodziej, S.A.1
Hamper, B.C.2
-
34
-
-
0030569368
-
Solid phase synthesis of 1,4-benzodiazepine-2,5-diones
-
Mayer JP, Zhang J, Bjergarde K, Lenz DM, Gaudino JJ: Solid phase synthesis of 1,4-benzodiazepine-2,5-diones. Tetrahedron Lett 1996, 37:8081-8084. This paper provides a method to prepare the benzodiazepine template very efficiently. However, the diversity of the substituants is rather limited and the compounds prepared appear structurally similar. This is a relatively common feature with SPOC papers currently.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 8081-8084
-
-
Mayer, J.P.1
Zhang, J.2
Bjergarde, K.3
Lenz, D.M.4
Gaudino, J.J.5
-
35
-
-
0001791986
-
A general and expedient method for the solid phase synthesis of structurally diverse 1-phenyl-pyrazolone derivatives
-
Tietze LF. Steinmetz: A general and expedient method for the solid phase synthesis of structurally diverse 1-phenyl-pyrazolone derivatives. SynLett 1996, 667-668.
-
(1996)
SynLett
, pp. 667-668
-
-
Steinmetz, T.L.F.1
-
36
-
-
0028834658
-
Solid phase synthesis of 1,2,3,4-tetrahydro-β-carbolines: Implications for combinatorial chemistry
-
Kaljuste K, Unden A: Solid phase synthesis of 1,2,3,4-tetrahydro-β-carbolines: implications for combinatorial chemistry. Tetrahedron Lett 1995, 36:9211-9214.
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 9211-9214
-
-
Kaljuste, K.1
Unden, A.2
-
37
-
-
0029891295
-
Pictet-Spengler reaction on solid support: Synthesis of 1,2,3,4-tetrahydro-b-carboline libraries
-
Mohan R, Chou Y-L, Morrissey M: Pictet-Spengler reaction on solid support: synthesis of 1,2,3,4-tetrahydro-b-carboline libraries. Tetrahedron Lett 1996, 37:3963-3966.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 3963-3966
-
-
Mohan, R.1
Chou, Y.-L.2
Morrissey, M.3
-
38
-
-
0030586143
-
Pictet-Spengler reaction on solid support
-
Yang L, Guo L: Pictet-Spengler reaction on solid support. Tetrahedron Lett 1996, 37:5041-5044.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 5041-5044
-
-
Yang, L.1
Guo, L.2
-
39
-
-
0342371152
-
1,2,6-trisubstituted tetrahydroisoquinoline derivatives by solid phase synthesis
-
Rolfing K, Thiel M, Kunzer H: 1,2,6-trisubstituted tetrahydroisoquinoline derivatives by solid phase synthesis. SynLett 1996, 1036-1038.
-
(1996)
SynLett
, pp. 1036-1038
-
-
Rolfing, K.1
Thiel, M.2
Kunzer, H.3
-
40
-
-
0028784613
-
The solid phase synthesis of dihydro- And tetrahydroisoquinolines
-
Meutermans WDF, Alewood PF: The solid phase synthesis of dihydro- and tetrahydroisoquinolines. Tetrahedron Lett 1995, 36:7709-7712.
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 7709-7712
-
-
Meutermans, W.1
Alewood, P.F.2
-
41
-
-
0030575349
-
Solid phase synthesis of tetrahydroisoquinolines and tetrahydroimidazopyridines
-
Hutchins SM, Chapman KT: Solid phase synthesis of tetrahydroisoquinolines and tetrahydroimidazopyridines. Tetrahedron Lett 1996, 37:4865-4868. A very effective route to tetrahydroisoquinolines and tetrahydroimidazopyridines using mild conditions. It is amenable to automation.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 4865-4868
-
-
Hutchins, S.M.1
Chapman, K.T.2
-
42
-
-
0030575421
-
Fischer indole synthesis on a solid support
-
Hutchins SM, Chapman KT: Fischer indole synthesis on a solid support. Tetrahedron Lett 1996, 37:4869-4872. A practical example of how reaction conditions should be tailored to resin type to afford the highest yields and purities of products.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 4869-4872
-
-
Hutchins, S.M.1
Chapman, K.T.2
-
43
-
-
0030607199
-
Heck reaction on solid support: Synthesis of indole analogs
-
Yun W, Mohan R: Heck reaction on solid support: synthesis of indole analogs. Tetrahedron Lett 1996, 37:7189-7192.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 7189-7192
-
-
Yun, W.1
Mohan, R.2
-
44
-
-
0030038838
-
Approaches to combinatorial synthesis of heterocycles: A solid phase synthesis of 1,4-dihydropyridines
-
Gordeev MF, Patel DV, Gordon EM: Approaches to combinatorial synthesis of heterocycles: A solid phase synthesis of 1,4-dihydropyridines. J Org Chem 1996, 61:924-928. A detailed account of the preparation of 1,4-dihydropyridines on solid phase including synthesis of the potent cardiovascular drugs, Nifedipine, Nitrendipine and Nimodipine.
-
(1996)
J Org Chem
, vol.61
, pp. 924-928
-
-
Gordeev, M.F.1
Patel, D.V.2
Gordon, E.M.3
-
45
-
-
0027423674
-
Polymer bound EDC (P-EDC): A convenient reagent for formation of an amide bond
-
Desai MC, Stephens Stramiello LM: Polymer bound EDC (P-EDC): A convenient reagent for formation of an amide bond. Tetrahedron Lett 1993, 34:7685-7688.
-
(1993)
Tetrahedron Lett
, vol.34
, pp. 7685-7688
-
-
Desai, M.C.1
Stephens Stramiello, L.M.2
-
46
-
-
0031021840
-
Ion-exchange resins for solution phase parallel synthesis of chemical libraries
-
Gayo LM, Suto MJ: Ion-exchange resins for solution phase parallel synthesis of chemical libraries. Tetrahedron Lett 1997, 38:513-516.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 513-516
-
-
Gayo, L.M.1
Suto, M.J.2
-
47
-
-
0030598016
-
The use of anion exchange resins for the synthesis of combinatorial libraries containing aryl and heteroaryl ethers
-
Parlow JJ: The use of anion exchange resins for the synthesis of combinatorial libraries containing aryl and heteroaryl ethers. Tetrahedron Lett 1996, 37:5257-5260.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 5257-5260
-
-
Parlow, J.J.1
-
48
-
-
0030607141
-
Use of solid supported nucleophiles and electrophiles for the purification of non-peptide small molecule libraries
-
Kaldor SW, Siegel MG, Fritz JE, Dressman BA, Hahn PJ: Use of solid supported nucleophiles and electrophiles for the purification of non-peptide small molecule libraries. Tetrahedron Lett 1996, 37:7193-7196. An excellent paper covering the latest uses of polymer-bound functional groups to facilitate the preparation and purification of chemical libraries containing a wide range of molecular diversity and that can start to be considered as 'privileged'. It is unlikely that these compounds would be accessible using solution phase methodologies alone.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 7193-7196
-
-
Kaldor, S.W.1
Siegel, M.G.2
Fritz, J.E.3
Dressman, B.A.4
Hahn, P.J.5
-
49
-
-
0029963887
-
Post-condensation modifications of Ugi four-component condensation products: 1-isocyanocyclohexene as a convertible isocyanide, Mechanism of conversion, synthesis of diverse structures, and demonstration of resin capture
-
Keating TA, Armstrong RW: Post-condensation modifications of Ugi four-component condensation products: 1-isocyanocyclohexene as a convertible isocyanide, Mechanism of conversion, synthesis of diverse structures, and demonstration of resin capture. J Am Chem Soc 1996, 118:2574-2583. Conceptually, this approach to library generation offers the best that solid-phase and solution-phase have to offer and will no doubt be developed to make privileged structure libraries in the near future.
-
(1996)
J Am Chem Soc
, vol.118
, pp. 2574-2583
-
-
Keating, T.A.1
Armstrong, R.W.2
-
50
-
-
0030062225
-
Synthesis of tetrasubstituted ethylenes on solid support via resin capture
-
Brown SD, Armstrong RW: Synthesis of tetrasubstituted ethylenes on solid support via resin capture. J Am Chem Soc 1996, 118:6331-6332.
-
(1996)
J Am Chem Soc
, vol.118
, pp. 6331-6332
-
-
Brown, S.D.1
Armstrong, R.W.2
-
51
-
-
0028881514
-
Interaction of Tamoxifen with the multidrug-resistant p-glycoprotein
-
Callaghan R, Higgins CF: Interaction of Tamoxifen with the multidrug-resistant p-glycoprotein. Br J Cancer 1995, 71:294-299.
-
(1995)
Br J Cancer
, vol.71
, pp. 294-299
-
-
Callaghan, R.1
Higgins, C.F.2
-
52
-
-
0030038898
-
Tamoxifen induced protooncogene expression persists in uterine endometrial epithelium
-
Nephew KP, Polek TC, Khan SA: Tamoxifen induced protooncogene expression persists in uterine endometrial epithelium. Endocrinology 1996, 137:219-244.
-
(1996)
Endocrinology
, vol.137
, pp. 219-244
-
-
Nephew, K.P.1
Polek, T.C.2
Khan, S.A.3
|