Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 140 entries
Sorted by: Best Match Show Resources per page
trans-6-Hexadecenoic acid in the Atlantic leatherbackDermochelys coriacea coriacea L. and other marine turtles.

Lipids

Hooper SN, Ackman RG.
PMID: 27520952
Lipids. 1970 Mar;5(3):288-92. doi: 10.1007/BF02531459.

Depot fat from the Atlantic leatherback turtle (Dermochelys coriacea coriacea L.) was shown to contain ≈3% oftrans-6-hexadecenoic acid. Structural details were elucidated through comparative aspects of isolation techniques, NMR, IR, hydrogenation, oxidative fission, etc., and confirmed by similarity of...

Cite
Hooper SN, Ackman RG. trans-6-Hexadecenoic acid in the Atlantic leatherbackDermochelys coriacea coriacea L. and other marine turtles. Lipids. 1970;5(3):288-92doi: 10.1007/BF02531459.
Hooper, S. N., & Ackman, R. G. (1970). trans-6-Hexadecenoic acid in the Atlantic leatherbackDermochelys coriacea coriacea L. and other marine turtles. Lipids, 5(3), 288-92. https://doi.org/10.1007/BF02531459
Hooper, S N, and Ackman, R G. "trans-6-Hexadecenoic acid in the Atlantic leatherbackDermochelys coriacea coriacea L. and other marine turtles." Lipids vol. 5,3 (1970): 288-92. doi: https://doi.org/10.1007/BF02531459
Hooper SN, Ackman RG. trans-6-Hexadecenoic acid in the Atlantic leatherbackDermochelys coriacea coriacea L. and other marine turtles. Lipids. 1970 Mar;5(3):288-92. doi: 10.1007/BF02531459. PMID: 27520952.
Copy Download .nbib Format: NLM
Isolation of xestosterol esters of brominated acetylenic fatty acids from the marine sponge xestospongia testudinaria.

Journal of natural products

Pham NB, Butler MS, Hooper JN, Moni RW, Quinn RJ.
PMID: 10543913
J Nat Prod. 1999 Oct;62(10):1439-42. doi: 10.1021/np9901635.

The CH(2)Cl(2) extract of the marine sponge Xestospongia testudinaria inhibited [(3)H]DPCPX binding to rat-brain adenosine A(1) receptors. Bioassay-guided fractionation led to the isolation of a known brominated acetylenic fatty acid 1 as the active component. Also isolated were two...

Cite
Pham NB, Butler MS, Hooper JN, et al. Isolation of xestosterol esters of brominated acetylenic fatty acids from the marine sponge xestospongia testudinaria. J Nat Prod. 1999;62(10):1439-42doi: 10.1021/np9901635.
Pham, N. B., Butler, M. S., Hooper, J. N., Moni, R. W., & Quinn, R. J. (1999). Isolation of xestosterol esters of brominated acetylenic fatty acids from the marine sponge xestospongia testudinaria. Journal of natural products, 62(10), 1439-42. https://doi.org/10.1021/np9901635
Pham, et al. "Isolation of xestosterol esters of brominated acetylenic fatty acids from the marine sponge xestospongia testudinaria." Journal of natural products vol. 62,10 (1999): 1439-42. doi: https://doi.org/10.1021/np9901635
Pham NB, Butler MS, Hooper JN, Moni RW, Quinn RJ. Isolation of xestosterol esters of brominated acetylenic fatty acids from the marine sponge xestospongia testudinaria. J Nat Prod. 1999 Oct;62(10):1439-42. doi: 10.1021/np9901635. PMID: 10543913.
Copy Download .nbib Format: NLM
Estrogen-progestin replacement and risk of breast cancer.

JAMA

Schairer C, Lubin J, Troisi R, Sturgeon S, Brinton L, Hoover R.
PMID: 10927819
JAMA. 2000 Aug 09;284(6):691-4.

No abstract available.

Cite
Schairer C, Lubin J, Troisi R, et al. Estrogen-progestin replacement and risk of breast cancer. JAMA. 2000;284(6):691-4
Schairer, C., Lubin, J., Troisi, R., Sturgeon, S., Brinton, L., & Hoover, R. (2000). Estrogen-progestin replacement and risk of breast cancer. JAMA, 284(6), 691-4.
Schairer, et al. "Estrogen-progestin replacement and risk of breast cancer." JAMA vol. 284,6 (2000): 691-4.
Schairer C, Lubin J, Troisi R, Sturgeon S, Brinton L, Hoover R. Estrogen-progestin replacement and risk of breast cancer. JAMA. 2000 Aug 09;284(6):691-4. PMID: 10927819.
Copy Download .nbib Format: NLM
Molar Refractivity and Connectivity Index Correlations for Henry's Law Virial Coefficients of Odorous Sulfur Compounds on Carbon and for Gas-Chromatographic Retention Indices.

Journal of colloid and interface science

Rybolt TR, Hooper DN, Stensby JB, Thomas HE, Baker ML.
PMID: 11161504
J Colloid Interface Sci. 2001 Feb 01;234(1):168-177. doi: 10.1006/jcis.2000.7202.

Gas-solid chromatography was used to obtain values of the second gas-solid virial coefficient, B(2s), in the temperature range from 392 to 511 K for 10 volatile, malodorous organic sulfur compounds; ethanethiol, 1-propanethiol, methyl sulfide, 2-propanethiol, 1-methyl-1-propanethiol, 2-methyl-1-propanethiol, 2-methyl-2-propanethiol, ethyl...

Cite
Rybolt TR, Hooper DN, Stensby JB, et al. Molar Refractivity and Connectivity Index Correlations for Henry's Law Virial Coefficients of Odorous Sulfur Compounds on Carbon and for Gas-Chromatographic Retention Indices. J Colloid Interface Sci. 2001;234(1):168-177doi: 10.1006/jcis.2000.7202.
Rybolt, T. R., Hooper, D. N., Stensby, J. B., Thomas, H. E., & Baker, M. L. (2001). Molar Refractivity and Connectivity Index Correlations for Henry's Law Virial Coefficients of Odorous Sulfur Compounds on Carbon and for Gas-Chromatographic Retention Indices. Journal of colloid and interface science, 234(1), 168-177. https://doi.org/10.1006/jcis.2000.7202
Rybolt, Thomas R., et al. "Molar Refractivity and Connectivity Index Correlations for Henry's Law Virial Coefficients of Odorous Sulfur Compounds on Carbon and for Gas-Chromatographic Retention Indices." Journal of colloid and interface science vol. 234,1 (2001): 168-177. doi: https://doi.org/10.1006/jcis.2000.7202
Rybolt TR, Hooper DN, Stensby JB, Thomas HE, Baker ML. Molar Refractivity and Connectivity Index Correlations for Henry's Law Virial Coefficients of Odorous Sulfur Compounds on Carbon and for Gas-Chromatographic Retention Indices. J Colloid Interface Sci. 2001 Feb 01;234(1):168-177. doi: 10.1006/jcis.2000.7202. PMID: 11161504.
Copy Download .nbib Format: NLM
Axinellamines A-D, Novel Imidazo-Azolo-Imidazole Alkaloids from the Australian Marine Sponge Axinella sp. .

The Journal of organic chemistry

Urban S, de Almeida Leone P, Carroll AR, Fechner GA, Smith J, Hooper JN, Quinn RJ.
PMID: 11674140
J Org Chem. 1999 Feb 05;64(3):731-735. doi: 10.1021/jo981034g.

Four imidazo-azolo-imidazole alkaloids, axinellamines A-D, have been isolated from an Australian marine sponge, Axinella sp. (order: Halichondrida: family: Axinellidae). These compounds contain a unique perhydrocyclopenta-imidazo-azolo-imidazole carbon skeleton. Three of these compounds had bactericidal activity against Helicobacter pylori at 1000...

Cite
Urban S, de Almeida Leone P, Carroll AR, et al. Axinellamines A-D, Novel Imidazo-Azolo-Imidazole Alkaloids from the Australian Marine Sponge Axinella sp. . J Org Chem. 1999;64(3):731-735doi: 10.1021/jo981034g.
Urban, S., de Almeida Leone, P., Carroll, A. R., Fechner, G. A., Smith, J., Hooper, J. N., & Quinn, R. J. (1999). Axinellamines A-D, Novel Imidazo-Azolo-Imidazole Alkaloids from the Australian Marine Sponge Axinella sp. . The Journal of organic chemistry, 64(3), 731-735. https://doi.org/10.1021/jo981034g
Urban, Sylvia, et al. "Axinellamines A-D, Novel Imidazo-Azolo-Imidazole Alkaloids from the Australian Marine Sponge Axinella sp. ." The Journal of organic chemistry vol. 64,3 (1999): 731-735. doi: https://doi.org/10.1021/jo981034g
Urban S, de Almeida Leone P, Carroll AR, Fechner GA, Smith J, Hooper JN, Quinn RJ. Axinellamines A-D, Novel Imidazo-Azolo-Imidazole Alkaloids from the Australian Marine Sponge Axinella sp. . J Org Chem. 1999 Feb 05;64(3):731-735. doi: 10.1021/jo981034g. PMID: 11674140.
Copy Download .nbib Format: NLM
Variable-addressability electronic binocular system.

Applied optics

Kubala K, Hooker RB.
PMID: 11993917
Appl Opt. 2002 Feb 01;41(4):707-16. doi: 10.1364/ao.41.000707.

The eye's acuity varies across its field of view (FOV), decreasing to 10% of its axial value at only 20 degrees. We describe an optical system that radially remaps the pixels of a miniature display or sensor to match...

Cite
Kubala K, Hooker RB. Variable-addressability electronic binocular system. Appl Opt. 2002;41(4):707-16doi: 10.1364/ao.41.000707.
Kubala, K., & Hooker, R. B. (2002). Variable-addressability electronic binocular system. Applied optics, 41(4), 707-16. https://doi.org/10.1364/ao.41.000707
Kubala, Kenneth, and Hooker, R Brian. "Variable-addressability electronic binocular system." Applied optics vol. 41,4 (2002): 707-16. doi: https://doi.org/10.1364/ao.41.000707
Kubala K, Hooker RB. Variable-addressability electronic binocular system. Appl Opt. 2002 Feb 01;41(4):707-16. doi: 10.1364/ao.41.000707. PMID: 11993917.
Copy Download .nbib Format: NLM
Realistic mitigation options for global warming.

Science (New York, N.Y.)

Rubin ES, Cooper RN, Frosch RA, Lee TH, Marland G, Rosenfeld AH, Stine DD.
PMID: 17794735
Science. 1992 Jul 10;257(5067):148-266. doi: 10.1126/science.257.5067.148.

No abstract available.

Cite
Rubin ES, Cooper RN, Frosch RA, et al. Realistic mitigation options for global warming. Science. 1992;257(5067):148-266doi: 10.1126/science.257.5067.148.
Rubin, E. S., Cooper, R. N., Frosch, R. A., Lee, T. H., Marland, G., Rosenfeld, A. H., & Stine, D. D. (1992). Realistic mitigation options for global warming. Science (New York, N.Y.), 257(5067), 148-266. https://doi.org/10.1126/science.257.5067.148
Rubin, E S, et al. "Realistic mitigation options for global warming." Science (New York, N.Y.) vol. 257,5067 (1992): 148-266. doi: https://doi.org/10.1126/science.257.5067.148
Rubin ES, Cooper RN, Frosch RA, Lee TH, Marland G, Rosenfeld AH, Stine DD. Realistic mitigation options for global warming. Science. 1992 Jul 10;257(5067):148-266. doi: 10.1126/science.257.5067.148. PMID: 17794735.
Copy Download .nbib Format: NLM
1,2-Diphosphinobenzene as a synthon for the 1,2,3-triphospha- and 2-arsa-1,3-diphosphaindenyl anions and a stable organo derivative of the P8 unit of Hittorf's phosphorus.

Chemical communications (Cambridge, England)

Butts CP, Green M, Hooper TN, Kilby RJ, McGrady JE, Pantazis DA, Russell CA.
PMID: 18253527
Chem Commun (Camb). 2008 Feb 21;(7):856-8. doi: 10.1039/b717204d. Epub 2008 Jan 15.

The electronic structure of the 1,2,3-triphosphaindenyl ligand suggests that it should exhibit enhanced pi-acceptor properties when compared to the eta(5)-indenyl system; this insight encouraged us to develop a simple synthetic pathway from 1,2-diphosphinobenzene to the 1,2,3-C(6)H(4)P(3) and 2-As-1,3-C(6)H(4)P(2) anions,...

Cite
Butts CP, Green M, Hooper TN, et al. 1,2-Diphosphinobenzene as a synthon for the 1,2,3-triphospha- and 2-arsa-1,3-diphosphaindenyl anions and a stable organo derivative of the P8 unit of Hittorf's phosphorus. Chem Commun (Camb). 2008;(7):856-8doi: 10.1039/b717204d.
Butts, C. P., Green, M., Hooper, T. N., Kilby, R. J., McGrady, J. E., Pantazis, D. A., & Russell, C. A. (2008). 1,2-Diphosphinobenzene as a synthon for the 1,2,3-triphospha- and 2-arsa-1,3-diphosphaindenyl anions and a stable organo derivative of the P8 unit of Hittorf's phosphorus. Chemical communications (Cambridge, England), (7), 856-8. https://doi.org/10.1039/b717204d
Butts, Craig P, et al. "1,2-Diphosphinobenzene as a synthon for the 1,2,3-triphospha- and 2-arsa-1,3-diphosphaindenyl anions and a stable organo derivative of the P8 unit of Hittorf's phosphorus." Chemical communications (Cambridge, England) vol. ,7 (2008): 856-8. doi: https://doi.org/10.1039/b717204d
Butts CP, Green M, Hooper TN, Kilby RJ, McGrady JE, Pantazis DA, Russell CA. 1,2-Diphosphinobenzene as a synthon for the 1,2,3-triphospha- and 2-arsa-1,3-diphosphaindenyl anions and a stable organo derivative of the P8 unit of Hittorf's phosphorus. Chem Commun (Camb). 2008 Feb 21;(7):856-8. doi: 10.1039/b717204d. Epub 2008 Jan 15. PMID: 18253527.
Copy Download .nbib Format: NLM
Synthesis and structural characterisation of stable cationic gold(I) alkene complexes.

Chemical communications (Cambridge, England)

Hooper TN, Green M, McGrady JE, Patel JR, Russell CA.
PMID: 19662238
Chem Commun (Camb). 2009 Jul 14;(26):3877-9. doi: 10.1039/b908109g. Epub 2009 Jun 05.

Treatment of [AuCl(PBu(t)(3))] with AgSbF(6) in CH(2)Cl(2) at room temperature in the presence of the alkenes norbornene, norbornadiene, trans-cyclooctene, and also interestingly, isobutylene, leads to the formation of stable crystalline complexes [Au(PBu(t)(3))(alkene)][SbF(6)], characterised by NMR spectroscopy and X-ray crystallography.

Cite
Hooper TN, Green M, McGrady JE, et al. Synthesis and structural characterisation of stable cationic gold(I) alkene complexes. Chem Commun (Camb). 2009;(26):3877-9doi: 10.1039/b908109g.
Hooper, T. N., Green, M., McGrady, J. E., Patel, J. R., & Russell, C. A. (2009). Synthesis and structural characterisation of stable cationic gold(I) alkene complexes. Chemical communications (Cambridge, England), (26), 3877-9. https://doi.org/10.1039/b908109g
Hooper, Thomas N, et al. "Synthesis and structural characterisation of stable cationic gold(I) alkene complexes." Chemical communications (Cambridge, England) vol. ,26 (2009): 3877-9. doi: https://doi.org/10.1039/b908109g
Hooper TN, Green M, McGrady JE, Patel JR, Russell CA. Synthesis and structural characterisation of stable cationic gold(I) alkene complexes. Chem Commun (Camb). 2009 Jul 14;(26):3877-9. doi: 10.1039/b908109g. Epub 2009 Jun 05. PMID: 19662238.
Copy Download .nbib Format: NLM
A Ship Surgeon's Log.

California and western medicine

Hooker RW.
PMID: 18743373
Cal West Med. 1935 Sep;43(3):209-12.

No abstract available.

Cite
Hooker RW. A Ship Surgeon's Log. Cal West Med. 1935;43(3):209-12
Hooker, R. W. (1935). A Ship Surgeon's Log. California and western medicine, 43(3), 209-12.
Hooker, R W. "A Ship Surgeon's Log." California and western medicine vol. 43,3 (1935): 209-12.
Hooker RW. A Ship Surgeon's Log. Cal West Med. 1935 Sep;43(3):209-12. PMID: 18743373; PMCID: PMC1753782.
Copy Download .nbib Format: NLM
Study of UV-bleached channel-waveguide performance in nonlinear optical polymer films.

Applied optics

Feng W, Lin S, Hooker RB, Mickelson AR.
PMID: 21060549
Appl Opt. 1995 Oct 20;34(30):6885-91. doi: 10.1364/AO.34.006885.

We report studies on UV-photobleached optical channel waveguides in nonlinear optical polymer films. The nonlinear optical polymer used is poly(methyl methacrylate)/DR1 side-chain polymer. The effective indices of the channel waveguides are measured with the prism-coupling technique, along with the...

Cite
Feng W, Lin S, Hooker RB, et al. Study of UV-bleached channel-waveguide performance in nonlinear optical polymer films. Appl Opt. 1995;34(30):6885-91doi: 10.1364/AO.34.006885.
Feng, W., Lin, S., Hooker, R. B., & Mickelson, A. R. (1995). Study of UV-bleached channel-waveguide performance in nonlinear optical polymer films. Applied optics, 34(30), 6885-91. https://doi.org/10.1364/AO.34.006885
Feng, W, et al. "Study of UV-bleached channel-waveguide performance in nonlinear optical polymer films." Applied optics vol. 34,30 (1995): 6885-91. doi: https://doi.org/10.1364/AO.34.006885
Feng W, Lin S, Hooker RB, Mickelson AR. Study of UV-bleached channel-waveguide performance in nonlinear optical polymer films. Appl Opt. 1995 Oct 20;34(30):6885-91. doi: 10.1364/AO.34.006885. PMID: 21060549.
Copy Download .nbib Format: NLM
Design of a normal incidence multilayer imaging x-ray microscope.

Journal of X-ray science and technology

Shealy DL, Gabardi DR, Hoover RB, Walker AB, Lindblom JF, Barbee TW.
PMID: 21307411
J Xray Sci Technol. 1989 Jan 01;1(2):190-206. doi: 10.3233/XST-1989-1207.

Normal incidence multilayer Cassegrain x-ray telescopes were flown on the Stanford/MSFC Rocket X-Ray Spectroheliograph. These instruments produced high spatial resolution images of the Sun and conclusively demonstrated that doubly reflecting multilayer x-ray optical systems are feasible. The images indicated...

Cite
Shealy DL, Gabardi DR, Hoover RB, et al. Design of a normal incidence multilayer imaging x-ray microscope. J Xray Sci Technol. 1989;1(2):190-206doi: 10.3233/XST-1989-1207.
Shealy, D. L., Gabardi, D. R., Hoover, R. B., Walker, A. B., Lindblom, J. F., & Barbee, T. W. (1989). Design of a normal incidence multilayer imaging x-ray microscope. Journal of X-ray science and technology, 1(2), 190-206. https://doi.org/10.3233/XST-1989-1207
Shealy, D L, et al. "Design of a normal incidence multilayer imaging x-ray microscope." Journal of X-ray science and technology vol. 1,2 (1989): 190-206. doi: https://doi.org/10.3233/XST-1989-1207
Shealy DL, Gabardi DR, Hoover RB, Walker AB, Lindblom JF, Barbee TW. Design of a normal incidence multilayer imaging x-ray microscope. J Xray Sci Technol. 1989 Jan 01;1(2):190-206. doi: 10.3233/XST-1989-1207. PMID: 21307411.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 140 entries