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Prediction of positron emission tomography/computed tomography (PET/CT) positivity in patients with high-risk primary melanoma.

American journal of nuclear medicine and molecular imaging

Danielsen M, Kjaer A, Wu M, Martineau L, Nosrati M, Leong SP, Sagebiel RW, Miller JR, Kashani-Sabet M.
PMID: 27766186
Am J Nucl Med Mol Imaging. 2016 Sep 22;6(5):277-285. eCollection 2016.

Positron emission tomography/computed tomography (PET/CT) is an important tool to identify occult melanoma metastasis. To date, it is controversial which patients with primary cutaneous melanoma should have staging PET/CT. In this retrospective analysis of more than 800 consecutive patients...

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Danielsen M, Kjaer A, Wu M, et al. Prediction of positron emission tomography/computed tomography (PET/CT) positivity in patients with high-risk primary melanoma. Am J Nucl Med Mol Imaging. 2016;6(5):277-285
Danielsen, M., Kjaer, A., Wu, M., Martineau, L., Nosrati, M., Leong, S. P., Sagebiel, R. W., Miller, J. R., & Kashani-Sabet, M. (2016). Prediction of positron emission tomography/computed tomography (PET/CT) positivity in patients with high-risk primary melanoma. American journal of nuclear medicine and molecular imaging, 6(5), 277-285.
Danielsen, Maria, et al. "Prediction of positron emission tomography/computed tomography (PET/CT) positivity in patients with high-risk primary melanoma." American journal of nuclear medicine and molecular imaging vol. 6,5 (2016): 277-285.
Danielsen M, Kjaer A, Wu M, Martineau L, Nosrati M, Leong SP, Sagebiel RW, Miller JR, Kashani-Sabet M. Prediction of positron emission tomography/computed tomography (PET/CT) positivity in patients with high-risk primary melanoma. Am J Nucl Med Mol Imaging. 2016 Sep 22;6(5):277-285. eCollection 2016. PMID: 27766186; PMCID: PMC5069280.
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Temporal Trends in Clinical and Pathological Characteristics for Men Undergoing Radical Prostatectomy Between 1995 and 2013 at Rigshospitalet, Copenhagen, Denmark, and Stanford University Hospital, United States.

Clinical genitourinary cancer

Loft MD, Berg KD, Kjaer A, Iversen P, Ferrari M, Zhang CA, Brasso K, Brooks JD, Røder MA.
PMID: 28988695
Clin Genitourin Cancer. 2017 Sep 06; doi: 10.1016/j.clgc.2017.08.014. Epub 2017 Sep 06.

PURPOSE: To analyze how prostate-specific antigen (PSA) screening and practice patterns has affected trends in tumor characteristics in men undergoing radical prostatectomy (RP) in the United States and Denmark. Unlike in the United States, PSA screening has not been...

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Loft MD, Berg KD, Kjaer A, et al. Temporal Trends in Clinical and Pathological Characteristics for Men Undergoing Radical Prostatectomy Between 1995 and 2013 at Rigshospitalet, Copenhagen, Denmark, and Stanford University Hospital, United States. Clin Genitourin Cancer. 2017;doi: 10.1016/j.clgc.2017.08.014.
Loft, M. D., Berg, K. D., Kjaer, A., Iversen, P., Ferrari, M., Zhang, C. A., Brasso, K., Brooks, J. D., & Røder, M. A. (2017). Temporal Trends in Clinical and Pathological Characteristics for Men Undergoing Radical Prostatectomy Between 1995 and 2013 at Rigshospitalet, Copenhagen, Denmark, and Stanford University Hospital, United States. Clinical genitourinary cancer, . https://doi.org/10.1016/j.clgc.2017.08.014
Loft, Mathias Dyrberg, et al. "Temporal Trends in Clinical and Pathological Characteristics for Men Undergoing Radical Prostatectomy Between 1995 and 2013 at Rigshospitalet, Copenhagen, Denmark, and Stanford University Hospital, United States." Clinical genitourinary cancer vol. (2017). doi: https://doi.org/10.1016/j.clgc.2017.08.014
Loft MD, Berg KD, Kjaer A, Iversen P, Ferrari M, Zhang CA, Brasso K, Brooks JD, Røder MA. Temporal Trends in Clinical and Pathological Characteristics for Men Undergoing Radical Prostatectomy Between 1995 and 2013 at Rigshospitalet, Copenhagen, Denmark, and Stanford University Hospital, United States. Clin Genitourin Cancer. 2017 Sep 06; doi: 10.1016/j.clgc.2017.08.014. Epub 2017 Sep 06. PMID: 28988695.
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Efficient regioselective ring opening of activated aziridine-2-carboxylates with [(18)f]fluoride.

ChemistryOpen

Schjoeth-Eskesen C, Hansen PR, Kjaer A, Gillings N.
PMID: 25861572
ChemistryOpen. 2015 Feb;4(1):65-71. doi: 10.1002/open.201402081. Epub 2014 Nov 21.

Aziridines can undergo a range of ring-opening reactions with nucleophiles. The regio- and stereochemistry of the products depend on the substituents on the aziridine. Aziridine ring-opening reactions have rarely been used in radiosynthesis. Herein we report the ring opening...

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Schjoeth-Eskesen C, Hansen PR, Kjaer A, et al. Efficient regioselective ring opening of activated aziridine-2-carboxylates with [(18)f]fluoride. ChemistryOpen. 2014;4(1):65-71doi: 10.1002/open.201402081.
Schjoeth-Eskesen, C., Hansen, P. R., Kjaer, A., & Gillings, N. (2015). Efficient regioselective ring opening of activated aziridine-2-carboxylates with [(18)f]fluoride. ChemistryOpen, 4(1), 65-71. https://doi.org/10.1002/open.201402081
Schjoeth-Eskesen, Christina, et al. "Efficient regioselective ring opening of activated aziridine-2-carboxylates with [(18)f]fluoride." ChemistryOpen vol. 4,1 (2015): 65-71. doi: https://doi.org/10.1002/open.201402081
Schjoeth-Eskesen C, Hansen PR, Kjaer A, Gillings N. Efficient regioselective ring opening of activated aziridine-2-carboxylates with [(18)f]fluoride. ChemistryOpen. 2015 Feb;4(1):65-71. doi: 10.1002/open.201402081. Epub 2014 Nov 21. PMID: 25861572; PMCID: PMC4380955.
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Simulator Study of Driver Responses to Pedestrian Treatments at Multilane Roundabouts.

Transportation research record

Salamati K, Schroeder B, Rouphail NM, Cunningham C, Zhang Y, Kaber D.
PMID: 24353370
Transp Res Rec. 2012;2312(2012). doi: 10.3141/2312-07.

Previous studies have shown that roundabouts - especially multilane roundabouts - pose accessibility challenges to pedestrians with vision impairments, in part due to a lack of yielding by drivers, especially on multilane roundabout exit legs. In this study, three...

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Salamati K, Schroeder B, Rouphail NM, et al. Simulator Study of Driver Responses to Pedestrian Treatments at Multilane Roundabouts. Transp Res Rec. 2012;2312(2012)doi: 10.3141/2312-07.
Salamati, K., Schroeder, B., Rouphail, N. M., Cunningham, C., Zhang, Y., & Kaber, D. (2012). Simulator Study of Driver Responses to Pedestrian Treatments at Multilane Roundabouts. Transportation research record, 2312(2012), . https://doi.org/10.3141/2312-07
Salamati, Katayoun, et al. "Simulator Study of Driver Responses to Pedestrian Treatments at Multilane Roundabouts." Transportation research record vol. 2312,2012 (2012). doi: https://doi.org/10.3141/2312-07
Salamati K, Schroeder B, Rouphail NM, Cunningham C, Zhang Y, Kaber D. Simulator Study of Driver Responses to Pedestrian Treatments at Multilane Roundabouts. Transp Res Rec. 2012;2312(2012). doi: 10.3141/2312-07. PMID: 24353370; PMCID: PMC3863904.
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Crystalline self-assembly into monolayers of folded oligomers at the air-water interface.

Chemistry (Weinheim an der Bergstrasse, Germany)

Lederer K, Godt A, Howes PB, Kjaer K, Als-Nielsen J, Lahav M, Wegner G, Leiserowitz L, Weissbuch I.
PMID: 10926223
Chemistry. 2000 Jun 16;6(12):2173-83. doi: 10.1002/1521-3765(20000616)6:12<2173::aid-chem2173>3.0.co;2-e.

Insertion of the 1,3-bis(ethynylene)benzene unit as a rigid spacer into a linear alkyl chain, thus separating the two resulting stems by 9 A. induces chain folding at the air-water interface. These folded molecules self-assemble into crystalline monolayers at this...

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Lederer K, Godt A, Howes PB, et al. Crystalline self-assembly into monolayers of folded oligomers at the air-water interface. Chemistry. 2000;6(12):2173-83doi: 10.1002/1521-3765(20000616)6:12<2173::aid-chem2173>3.0.co;2-e.
Lederer, K., Godt, A., Howes, P. B., Kjaer, K., Als-Nielsen, J., Lahav, M., Wegner, G., Leiserowitz, L., & Weissbuch, I. (2000). Crystalline self-assembly into monolayers of folded oligomers at the air-water interface. Chemistry (Weinheim an der Bergstrasse, Germany), 6(12), 2173-83. https://doi.org/10.1002/1521-3765(20000616)6:12<2173::aid-chem2173>3.0.co;2-e
Lederer, et al. "Crystalline self-assembly into monolayers of folded oligomers at the air-water interface." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 6,12 (2000): 2173-83. doi: https://doi.org/10.1002/1521-3765(20000616)6:12<2173::aid-chem2173>3.0.co;2-e
Lederer K, Godt A, Howes PB, Kjaer K, Als-Nielsen J, Lahav M, Wegner G, Leiserowitz L, Weissbuch I. Crystalline self-assembly into monolayers of folded oligomers at the air-water interface. Chemistry. 2000 Jun 16;6(12):2173-83. doi: 10.1002/1521-3765(20000616)6:12<2173::aid-chem2173>3.0.co;2-e. PMID: 10926223.
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"On-line or non-line".

Scandinavian journal of medicine & science in sports

Kjaer M.
PMID: 11782262
Scand J Med Sci Sports. 2001 Dec;11(6):319-20. doi: 10.1034/j.1600-0838.2001.110601.x.

No abstract available.

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Kjaer M. "On-line or non-line". Scand J Med Sci Sports. 2001;11(6):319-20doi: 10.1034/j.1600-0838.2001.110601.x.
Kjaer, M. (2001). "On-line or non-line". Scandinavian journal of medicine & science in sports, 11(6), 319-20. https://doi.org/10.1034/j.1600-0838.2001.110601.x
Kjaer, M. ""On-line or non-line"." Scandinavian journal of medicine & science in sports vol. 11,6 (2001): 319-20. doi: https://doi.org/10.1034/j.1600-0838.2001.110601.x
Kjaer M. "On-line or non-line". Scand J Med Sci Sports. 2001 Dec;11(6):319-20. doi: 10.1034/j.1600-0838.2001.110601.x. PMID: 11782262.
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Chirality-Controlling Chelate (CCC) Ligands in Analogues of Platinum Anticancer Agents. Influence of N9 Substituents of Guanine Derivatives (G) on the Distribution of Chiral Conformers of (CCC)PtG(2) with CCC = N,N'-Dimethyl-2,3-diaminobutane.

Inorganic chemistry

Marzilli LG, Intini FP, Kiser D, Wong HC, Ano SO, Marzilli PA, Natile G.
PMID: 11670827
Inorg Chem. 1998 Dec 28;37(26):6898-6905. doi: 10.1021/ic980843f.

Chirality-controlling chelate (CCC) ligands are a class of chiral diamine ligands with one or two chiral secondary amine ligating groups. Analogues of platinum anticancer agents containing CCC ligands exhibit unusual steric and dynamic features. In this study NMR and...

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Marzilli LG, Intini FP, Kiser D, et al. Chirality-Controlling Chelate (CCC) Ligands in Analogues of Platinum Anticancer Agents. Influence of N9 Substituents of Guanine Derivatives (G) on the Distribution of Chiral Conformers of (CCC)PtG(2) with CCC = N,N'-Dimethyl-2,3-diaminobutane. Inorg Chem. 1998;37(26):6898-6905doi: 10.1021/ic980843f.
Marzilli, L. G., Intini, F. P., Kiser, D., Wong, H. C., Ano, S. O., Marzilli, P. A., & Natile, G. (1998). Chirality-Controlling Chelate (CCC) Ligands in Analogues of Platinum Anticancer Agents. Influence of N9 Substituents of Guanine Derivatives (G) on the Distribution of Chiral Conformers of (CCC)PtG(2) with CCC = N,N'-Dimethyl-2,3-diaminobutane. Inorganic chemistry, 37(26), 6898-6905. https://doi.org/10.1021/ic980843f
Marzilli, Luigi G., et al. "Chirality-Controlling Chelate (CCC) Ligands in Analogues of Platinum Anticancer Agents. Influence of N9 Substituents of Guanine Derivatives (G) on the Distribution of Chiral Conformers of (CCC)PtG(2) with CCC = N,N'-Dimethyl-2,3-diaminobutane." Inorganic chemistry vol. 37,26 (1998): 6898-6905. doi: https://doi.org/10.1021/ic980843f
Marzilli LG, Intini FP, Kiser D, Wong HC, Ano SO, Marzilli PA, Natile G. Chirality-Controlling Chelate (CCC) Ligands in Analogues of Platinum Anticancer Agents. Influence of N9 Substituents of Guanine Derivatives (G) on the Distribution of Chiral Conformers of (CCC)PtG(2) with CCC = N,N'-Dimethyl-2,3-diaminobutane. Inorg Chem. 1998 Dec 28;37(26):6898-6905. doi: 10.1021/ic980843f. PMID: 11670827.
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Oriented crystalline monolayers and bilayers of 2 x 2 silver(I) grid architectures at the air-solution interface: their assembly and crystal structure elucidation.

Chemistry (Weinheim an der Bergstrasse, Germany)

Weissbuch I, Baxter PN, Kuzmenko I, Cohen H, Cohen S, Kjaer K, Howes PB, Als-Nielsen J, Lehn JM, Leiserowitz L, Lahav M.
PMID: 10807183
Chemistry. 2000 Feb 18;6(4):725-34. doi: 10.1002/(sici)1521-3765(20000218)6:4<725::aid-chem725>3.0.co;2-e.

Oriented crystalline monolayers, approximately 14 A thick, of a 2 x 2 Ag+ grid complex, self-assembled at the air-solution interface starting from an water-insoluble ligand 3,6-bis[2-(6-phenylpyridine)]pyridazine spread on silver-ion-containing solutions, were examined by grazing-incidence X-ray diffraction and specular X-ray...

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Weissbuch I, Baxter PN, Kuzmenko I, et al. Oriented crystalline monolayers and bilayers of 2 x 2 silver(I) grid architectures at the air-solution interface: their assembly and crystal structure elucidation. Chemistry. 2000;6(4):725-34doi: 10.1002/(sici)1521-3765(20000218)6:4<725::aid-chem725>3.0.co;2-e.
Weissbuch, I., Baxter, P. N., Kuzmenko, I., Cohen, H., Cohen, S., Kjaer, K., Howes, P. B., Als-Nielsen, J., Lehn, J. M., Leiserowitz, L., & Lahav, M. (2000). Oriented crystalline monolayers and bilayers of 2 x 2 silver(I) grid architectures at the air-solution interface: their assembly and crystal structure elucidation. Chemistry (Weinheim an der Bergstrasse, Germany), 6(4), 725-34. https://doi.org/10.1002/(sici)1521-3765(20000218)6:4<725::aid-chem725>3.0.co;2-e
Weissbuch, et al. "Oriented crystalline monolayers and bilayers of 2 x 2 silver(I) grid architectures at the air-solution interface: their assembly and crystal structure elucidation." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 6,4 (2000): 725-34. doi: https://doi.org/10.1002/(sici)1521-3765(20000218)6:4<725::aid-chem725>3.0.co;2-e
Weissbuch I, Baxter PN, Kuzmenko I, Cohen H, Cohen S, Kjaer K, Howes PB, Als-Nielsen J, Lehn JM, Leiserowitz L, Lahav M. Oriented crystalline monolayers and bilayers of 2 x 2 silver(I) grid architectures at the air-solution interface: their assembly and crystal structure elucidation. Chemistry. 2000 Feb 18;6(4):725-34. doi: 10.1002/(sici)1521-3765(20000218)6:4<725::aid-chem725>3.0.co;2-e. PMID: 10807183.
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Tetrathiafulvaleno-Annelated Porphyrins We gratefully acknowledge financial support from Carlsbergfondet and Bengt Lundquists Minnesfond for a post-doctoral position to T. B., the University of Odense for a Ph.D. scholarship to J. O. J. and the French Embassy Copenhagen for a travel grant to J. B. We thank HASYLAB at DESY, Hamburg for beam time at beam line BW1 and DANSYNC for financial support. The gift of Jan Skov Peterson's FORTRAN program LSQREFL is gratefully acknowledged. Finally, we thank.

Angewandte Chemie (International ed. in English)

Becher J, Brimert T, Jeppesen JO, Pedersen JZ, Zubarev R, Bjørnholm T, Reitzel N, Jensen TR, Kjaer K, Levillain E.
PMID: 11443677
Angew Chem Int Ed Engl. 2001 Jul 02;40(13):2497-2500.

No abstract available.

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Becher J, Brimert T, Jeppesen JO, et al. Tetrathiafulvaleno-Annelated Porphyrins We gratefully acknowledge financial support from Carlsbergfondet and Bengt Lundquists Minnesfond for a post-doctoral position to T. B., the University of Odense for a Ph.D. scholarship to J. O. J. and the French Embassy Copenhagen for a travel grant to J. B. We thank HASYLAB at DESY, Hamburg for beam time at beam line BW1 and DANSYNC for financial support. The gift of Jan Skov Peterson's FORTRAN program LSQREFL is gratefully acknowledged. Finally, we thank. Angew Chem Int Ed Engl. 2001;40(13):2497-2500
Becher, J., Brimert, T., Jeppesen, J. O., Pedersen, J. Z., Zubarev, R., Bjørnholm, T., Reitzel, N., Jensen, T. R., Kjaer, K., & Levillain, E. (2001). Tetrathiafulvaleno-Annelated Porphyrins We gratefully acknowledge financial support from Carlsbergfondet and Bengt Lundquists Minnesfond for a post-doctoral position to T. B., the University of Odense for a Ph.D. scholarship to J. O. J. and the French Embassy Copenhagen for a travel grant to J. B. We thank HASYLAB at DESY, Hamburg for beam time at beam line BW1 and DANSYNC for financial support. The gift of Jan Skov Peterson's FORTRAN program LSQREFL is gratefully acknowledged. Finally, we thank. Angewandte Chemie (International ed. in English), 40(13), 2497-2500.
Becher, Jan, et al. "Tetrathiafulvaleno-Annelated Porphyrins We gratefully acknowledge financial support from Carlsbergfondet and Bengt Lundquists Minnesfond for a post-doctoral position to T. B., the University of Odense for a Ph.D. scholarship to J. O. J. and the French Embassy Copenhagen for a travel grant to J. B. We thank HASYLAB at DESY, Hamburg for beam time at beam line BW1 and DANSYNC for financial support. The gift of Jan Skov Peterson's FORTRAN program LSQREFL is gratefully acknowledged. Finally, we thank." Angewandte Chemie (International ed. in English) vol. 40,13 (2001): 2497-2500.
Becher J, Brimert T, Jeppesen JO, Pedersen JZ, Zubarev R, Bjørnholm T, Reitzel N, Jensen TR, Kjaer K, Levillain E. Tetrathiafulvaleno-Annelated Porphyrins We gratefully acknowledge financial support from Carlsbergfondet and Bengt Lundquists Minnesfond for a post-doctoral position to T. B., the University of Odense for a Ph.D. scholarship to J. O. J. and the French Embassy Copenhagen for a travel grant to J. B. We thank HASYLAB at DESY, Hamburg for beam time at beam line BW1 and DANSYNC for financial support. The gift of Jan Skov Peterson's FORTRAN program LSQREFL is gratefully acknowledged. Finally, we thank. Angew Chem Int Ed Engl. 2001 Jul 02;40(13):2497-2500. PMID: 11443677.
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[Progress in results of lung cancer treatment].

Ugeskrift for laeger

HANSEN JL, KJAER T.
PMID: 13078008
Ugeskr Laeger. 1953 May 25;115(22):836-41.

No abstract available.

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HANSEN JL, KJAER T. Fremskridt i resultaterne ved behandlingen af lunge-cancer. [Progress in results of lung cancer treatment]. Ugeskr Laeger. 1953;115(22):836-41
HANSEN, J. L., & KJAER, T. (1953). Fremskridt i resultaterne ved behandlingen af lunge-cancer. [Progress in results of lung cancer treatment]. Ugeskrift for laeger, 115(22), 836-41.
HANSEN, J L, and KJAER, T. "Fremskridt i resultaterne ved behandlingen af lunge-cancer." [Progress in results of lung cancer treatment]. Ugeskrift for laeger vol. 115,22 (1953): 836-41.
HANSEN JL, KJAER T. Fremskridt i resultaterne ved behandlingen af lunge-cancer. [Progress in results of lung cancer treatment]. Ugeskr Laeger. 1953 May 25;115(22):836-41. Undetermined. PMID: 13078008.
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Open comparative trial of formestane versus megestrol acetate in postmenopausal patients with advanced breast cancer previously treated with tamoxifen.

Breast (Edinburgh, Scotland)

Freue M, Kjaer M, Boni C, Joliver J, Jänicke F, Willemse PH, Coombes RC, Van Belle S, Pérez-Carrión R, Zieschang J, Ibarra de Palacios P, Rose C.
PMID: 14731578
Breast. 2000 Feb;9(1):9-16. doi: 10.1054/brst.1999.0118.

The aim of the trial was to compare efficacy and safety of the aromatase inhibitor formestane (250 mg i.m. given every 2 weeks) with the progestin megestrol acetate (160 mg administered orally once daily), as second-line therapy in postmenopausal...

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Freue M, Kjaer M, Boni C, et al. Open comparative trial of formestane versus megestrol acetate in postmenopausal patients with advanced breast cancer previously treated with tamoxifen. Breast. 2000;9(1):9-16doi: 10.1054/brst.1999.0118.
Freue, M., Kjaer, M., Boni, C., Joliver, J., Jänicke, F., Willemse, P. H., Coombes, R. C., Van Belle, S., Pérez-Carrión, R., Zieschang, J., Ibarra de Palacios, P., & Rose, C. (2000). Open comparative trial of formestane versus megestrol acetate in postmenopausal patients with advanced breast cancer previously treated with tamoxifen. Breast (Edinburgh, Scotland), 9(1), 9-16. https://doi.org/10.1054/brst.1999.0118
Freue, M, et al. "Open comparative trial of formestane versus megestrol acetate in postmenopausal patients with advanced breast cancer previously treated with tamoxifen." Breast (Edinburgh, Scotland) vol. 9,1 (2000): 9-16. doi: https://doi.org/10.1054/brst.1999.0118
Freue M, Kjaer M, Boni C, Joliver J, Jänicke F, Willemse PH, Coombes RC, Van Belle S, Pérez-Carrión R, Zieschang J, Ibarra de Palacios P, Rose C. Open comparative trial of formestane versus megestrol acetate in postmenopausal patients with advanced breast cancer previously treated with tamoxifen. Breast. 2000 Feb;9(1):9-16. doi: 10.1054/brst.1999.0118. PMID: 14731578.
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Langmuir-blodgett films of a functionalized molecule with cross-sectional mismatch between head and tail.

Science (New York, N.Y.)

Garnaes J, Larsen NB, Bjørnholm T, Jørgensen M, Kjaer K, Als-Nielsen J, Jørgensen JF, Zasadzinski JA.
PMID: 17780847
Science. 1994 May 27;264(5163):1301-4. doi: 10.1126/science.264.5163.1301.

A functionalized surfactant has been investigated as floating monolayers by synchrotron x-ray diffraction and as bilayers transferred to solid supports by the Langmuir-Blodgett technique through atomic force microscopy. The transfer process is accompanied by an increase of the unit...

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Garnaes J, Larsen NB, Bjørnholm T, et al. Langmuir-blodgett films of a functionalized molecule with cross-sectional mismatch between head and tail. Science. 1994;264(5163):1301-4doi: 10.1126/science.264.5163.1301.
Garnaes, J., Larsen, N. B., Bjørnholm, T., Jørgensen, M., Kjaer, K., Als-Nielsen, J., Jørgensen, J. F., & Zasadzinski, J. A. (1994). Langmuir-blodgett films of a functionalized molecule with cross-sectional mismatch between head and tail. Science (New York, N.Y.), 264(5163), 1301-4. https://doi.org/10.1126/science.264.5163.1301
Garnaes, J, et al. "Langmuir-blodgett films of a functionalized molecule with cross-sectional mismatch between head and tail." Science (New York, N.Y.) vol. 264,5163 (1994): 1301-4. doi: https://doi.org/10.1126/science.264.5163.1301
Garnaes J, Larsen NB, Bjørnholm T, Jørgensen M, Kjaer K, Als-Nielsen J, Jørgensen JF, Zasadzinski JA. Langmuir-blodgett films of a functionalized molecule with cross-sectional mismatch between head and tail. Science. 1994 May 27;264(5163):1301-4. doi: 10.1126/science.264.5163.1301. PMID: 17780847.
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