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The place of the surgical specialties in the training of the general surgeon.

Journal of the Royal College of Surgeons of Edinburgh

Dennis C.
PMID: 5073904
J R Coll Surg Edinb. 1972 Jul;17(4):209-16.

No abstract available.

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Dennis C. The place of the surgical specialties in the training of the general surgeon. J R Coll Surg Edinb. 1972;17(4):209-16
Dennis, C. (1972). The place of the surgical specialties in the training of the general surgeon. Journal of the Royal College of Surgeons of Edinburgh, 17(4), 209-16.
Dennis, C. "The place of the surgical specialties in the training of the general surgeon." Journal of the Royal College of Surgeons of Edinburgh vol. 17,4 (1972): 209-16.
Dennis C. The place of the surgical specialties in the training of the general surgeon. J R Coll Surg Edinb. 1972 Jul;17(4):209-16. PMID: 5073904.
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Efficient hydroxymethylation reactions of iodoarenes using CO and 1,3-dimethylimidazol-2-ylidene borane.

Organic letters

Kawamoto T, Okada T, Curran DP, Ryu I.
PMID: 23590524
Org Lett. 2013 May 03;15(9):2144-7. doi: 10.1021/ol4006294. Epub 2013 Apr 16.

A hydroxymethylation reaction of a variety of iodoarenes proceeded effectively in the presence of CO, NHC-borane, diMeImd-BH3 (2) as a radical mediator, and a catalytic amount of AIBN. The reaction took place chemoselectively at the aryl-iodine bond but not...

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Kawamoto T, Okada T, Curran DP, et al. Efficient hydroxymethylation reactions of iodoarenes using CO and 1,3-dimethylimidazol-2-ylidene borane. Org Lett. 2013;15(9):2144-7doi: 10.1021/ol4006294.
Kawamoto, T., Okada, T., Curran, D. P., & Ryu, I. (2013). Efficient hydroxymethylation reactions of iodoarenes using CO and 1,3-dimethylimidazol-2-ylidene borane. Organic letters, 15(9), 2144-7. https://doi.org/10.1021/ol4006294
Kawamoto, Takuji, et al. "Efficient hydroxymethylation reactions of iodoarenes using CO and 1,3-dimethylimidazol-2-ylidene borane." Organic letters vol. 15,9 (2013): 2144-7. doi: https://doi.org/10.1021/ol4006294
Kawamoto T, Okada T, Curran DP, Ryu I. Efficient hydroxymethylation reactions of iodoarenes using CO and 1,3-dimethylimidazol-2-ylidene borane. Org Lett. 2013 May 03;15(9):2144-7. doi: 10.1021/ol4006294. Epub 2013 Apr 16. PMID: 23590524.
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GapMap: Enabling Comprehensive Autism Resource Epidemiology.

JMIR public health and surveillance

Albert N, Daniels J, Schwartz J, Du M, Wall DP.
PMID: 28473303
JMIR Public Health Surveill. 2017 May 04;3(2):e27. doi: 10.2196/publichealth.7150.

BACKGROUND: For individuals with autism spectrum disorder (ASD), finding resources can be a lengthy and difficult process. The difficulty in obtaining global, fine-grained autism epidemiological data hinders researchers from quickly and efficiently studying large-scale correlations among ASD, environmental factors,...

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Albert N, Daniels J, Schwartz J, et al. GapMap: Enabling Comprehensive Autism Resource Epidemiology. JMIR Public Health Surveill. 2017;3(2):e27doi: 10.2196/publichealth.7150.
Albert, N., Daniels, J., Schwartz, J., Du, M., & Wall, D. P. (2017). GapMap: Enabling Comprehensive Autism Resource Epidemiology. JMIR public health and surveillance, 3(2), e27. https://doi.org/10.2196/publichealth.7150
Albert, Nikhila, et al. "GapMap: Enabling Comprehensive Autism Resource Epidemiology." JMIR public health and surveillance vol. 3,2 (2017): e27. doi: https://doi.org/10.2196/publichealth.7150
Albert N, Daniels J, Schwartz J, Du M, Wall DP. GapMap: Enabling Comprehensive Autism Resource Epidemiology. JMIR Public Health Surveill. 2017 May 04;3(2):e27. doi: 10.2196/publichealth.7150. PMID: 28473303; PMCID: PMC5438459.
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A Simplified Strategy for Introducing Genetic Variants into .

G3 (Bethesda, Md.)

Gilliland WD, May DP, Colwell EM, Kennison JA.
PMID: 27672111
G3 (Bethesda). 2016 Nov 08;6(11):3749-3755. doi: 10.1534/g3.116.035634.

No abstract available.

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Gilliland WD, May DP, Colwell EM, et al. A Simplified Strategy for Introducing Genetic Variants into . G3 (Bethesda). 2016;6(11):3749-3755doi: 10.1534/g3.116.035634.
Gilliland, W. D., May, D. P., Colwell, E. M., & Kennison, J. A. (2016). A Simplified Strategy for Introducing Genetic Variants into . G3 (Bethesda, Md.), 6(11), 3749-3755. https://doi.org/10.1534/g3.116.035634
Gilliland, William D, et al. "A Simplified Strategy for Introducing Genetic Variants into ." G3 (Bethesda, Md.) vol. 6,11 (2016): 3749-3755. doi: https://doi.org/10.1534/g3.116.035634
Gilliland WD, May DP, Colwell EM, Kennison JA. A Simplified Strategy for Introducing Genetic Variants into . G3 (Bethesda). 2016 Nov 08;6(11):3749-3755. doi: 10.1534/g3.116.035634. PMID: 27672111; PMCID: PMC5100873.
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Philosophy and efficacy of multidisciplinary approach to chronic pain management.

Journal of anesthesia

Okifuji A, Turk DC.
PMID: 28921182
J Anesth. 1998 Sep;12(3):142-152. doi: 10.1007/BF02480093.

No abstract available.

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Okifuji A, Turk DC. Philosophy and efficacy of multidisciplinary approach to chronic pain management. J Anesth. 1998;12(3):142-152doi: 10.1007/BF02480093.
Okifuji, A., & Turk, D. C. (1998). Philosophy and efficacy of multidisciplinary approach to chronic pain management. Journal of anesthesia, 12(3), 142-152. https://doi.org/10.1007/BF02480093
Okifuji, Akiko, and Turk, Dennis C. "Philosophy and efficacy of multidisciplinary approach to chronic pain management." Journal of anesthesia vol. 12,3 (1998): 142-152. doi: https://doi.org/10.1007/BF02480093
Okifuji A, Turk DC. Philosophy and efficacy of multidisciplinary approach to chronic pain management. J Anesth. 1998 Sep;12(3):142-152. doi: 10.1007/BF02480093. PMID: 28921182.
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Development of Non-C2-symmetric ProPhenol Ligands. The Asymmetric Vinylation of N-Boc Imines.

Organic letters

Trost BM, Hung CI, Koester DC, Miller Y.
PMID: 26200769
Org Lett. 2015 Aug 07;17(15):3778-81. doi: 10.1021/acs.orglett.5b01755. Epub 2015 Jul 22.

The development and application of a new generation of non-C2-symmetric ProPhenol ligands is reported herein. Rational design of the ProPhenol ligand paved the way to the first catalytic and asymmetric vinylation of N-Boc imines via hydrozirconation giving rise to...

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Trost BM, Hung CI, Koester DC, et al. Development of Non-C2-symmetric ProPhenol Ligands. The Asymmetric Vinylation of N-Boc Imines. Org Lett. 2015;17(15):3778-81doi: 10.1021/acs.orglett.5b01755.
Trost, B. M., Hung, C. I., Koester, D. C., & Miller, Y. (2015). Development of Non-C2-symmetric ProPhenol Ligands. The Asymmetric Vinylation of N-Boc Imines. Organic letters, 17(15), 3778-81. https://doi.org/10.1021/acs.orglett.5b01755
Trost, Barry M, et al. "Development of Non-C2-symmetric ProPhenol Ligands. The Asymmetric Vinylation of N-Boc Imines." Organic letters vol. 17,15 (2015): 3778-81. doi: https://doi.org/10.1021/acs.orglett.5b01755
Trost BM, Hung CI, Koester DC, Miller Y. Development of Non-C2-symmetric ProPhenol Ligands. The Asymmetric Vinylation of N-Boc Imines. Org Lett. 2015 Aug 07;17(15):3778-81. doi: 10.1021/acs.orglett.5b01755. Epub 2015 Jul 22. PMID: 26200769.
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Correction to "Design, synthesis, and structure-activity relationship of a novel series of GluN2C-selective potentiators".

Journal of medicinal chemistry

Zimmerman SS, Khatri A, Garnier-Amblard EC, Mullasseril P, Kurtkaya NL, Gyoneva S, Hansen KB, Traynelis SF, Liotta DC.
PMID: 25738634
J Med Chem. 2015 Mar 26;58(6):2862. doi: 10.1021/acs.jmedchem.5b00199. Epub 2015 Mar 04.

No abstract available.

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Zimmerman SS, Khatri A, Garnier-Amblard EC, et al. Correction to "Design, synthesis, and structure-activity relationship of a novel series of GluN2C-selective potentiators". J Med Chem. 2015;58(6):2862doi: 10.1021/acs.jmedchem.5b00199.
Zimmerman, S. S., Khatri, A., Garnier-Amblard, E. C., Mullasseril, P., Kurtkaya, N. L., Gyoneva, S., Hansen, K. B., Traynelis, S. F., & Liotta, D. C. (2015). Correction to "Design, synthesis, and structure-activity relationship of a novel series of GluN2C-selective potentiators". Journal of medicinal chemistry, 58(6), 2862. https://doi.org/10.1021/acs.jmedchem.5b00199
Zimmerman, Sommer S, et al. "Correction to "Design, synthesis, and structure-activity relationship of a novel series of GluN2C-selective potentiators"." Journal of medicinal chemistry vol. 58,6 (2015): 2862. doi: https://doi.org/10.1021/acs.jmedchem.5b00199
Zimmerman SS, Khatri A, Garnier-Amblard EC, Mullasseril P, Kurtkaya NL, Gyoneva S, Hansen KB, Traynelis SF, Liotta DC. Correction to "Design, synthesis, and structure-activity relationship of a novel series of GluN2C-selective potentiators". J Med Chem. 2015 Mar 26;58(6):2862. doi: 10.1021/acs.jmedchem.5b00199. Epub 2015 Mar 04. PMID: 25738634; PMCID: PMC4415028.
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Saproamanita, a new name for both Lepidella E.-J. Gilbert and Aspidella E.-J. Gilbert (Amaniteae, Amanitaceae).

IMA fungus

Redhead SA, Vizzini A, Drehmel DC, Contu M.
PMID: 27433443
IMA Fungus. 2016 Jun;7(1):119-29. doi: 10.5598/imafungus.2016.07.01.07. Epub 2016 Jun 01.

The genus Amanita has been divided into two monophyletic taxa, Amanita, an ectomycorrhizal genus, and Aspidella, a saprotrophic genus. The controversies and histories about recognition of the two genera based on trophic status are discussed. The name Aspidella E.-J....

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Redhead SA, Vizzini A, Drehmel DC, et al. Saproamanita, a new name for both Lepidella E.-J. Gilbert and Aspidella E.-J. Gilbert (Amaniteae, Amanitaceae). IMA Fungus. 2016;7(1):119-29doi: 10.5598/imafungus.2016.07.01.07.
Redhead, S. A., Vizzini, A., Drehmel, D. C., & Contu, M. (2016). Saproamanita, a new name for both Lepidella E.-J. Gilbert and Aspidella E.-J. Gilbert (Amaniteae, Amanitaceae). IMA fungus, 7(1), 119-29. https://doi.org/10.5598/imafungus.2016.07.01.07
Redhead, Scott A, et al. "Saproamanita, a new name for both Lepidella E.-J. Gilbert and Aspidella E.-J. Gilbert (Amaniteae, Amanitaceae)." IMA fungus vol. 7,1 (2016): 119-29. doi: https://doi.org/10.5598/imafungus.2016.07.01.07
Redhead SA, Vizzini A, Drehmel DC, Contu M. Saproamanita, a new name for both Lepidella E.-J. Gilbert and Aspidella E.-J. Gilbert (Amaniteae, Amanitaceae). IMA Fungus. 2016 Jun;7(1):119-29. doi: 10.5598/imafungus.2016.07.01.07. Epub 2016 Jun 01. PMID: 27433443; PMCID: PMC4941681.
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Relative Reactivity of Stable Ligated Boranes and a Borohydride Salt in Rhodium(II)-Catalyzed Boron-Hydrogen Insertion Reactions.

The Journal of organic chemistry

Allen TH, Curran DP.
PMID: 26871613
J Org Chem. 2016 Mar 04;81(5):2094-8. doi: 10.1021/acs.joc.6b00091. Epub 2016 Feb 23.

Relative reactivities of a series of neutral ligated boranes L-BH3 (where L is NHC, amine, pyridine, or phosphine) and the cyanoborohydride anion have been assessed in Rh(II)-catalyzed B-H insertion reactions with methyl 2-phenyl-2-diazoacetate. Stable α-boryl ester products were isolated...

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Allen TH, Curran DP. Relative Reactivity of Stable Ligated Boranes and a Borohydride Salt in Rhodium(II)-Catalyzed Boron-Hydrogen Insertion Reactions. J Org Chem. 2016;81(5):2094-8doi: 10.1021/acs.joc.6b00091.
Allen, T. H., & Curran, D. P. (2016). Relative Reactivity of Stable Ligated Boranes and a Borohydride Salt in Rhodium(II)-Catalyzed Boron-Hydrogen Insertion Reactions. The Journal of organic chemistry, 81(5), 2094-8. https://doi.org/10.1021/acs.joc.6b00091
Allen, Thomas H, and Curran, Dennis P. "Relative Reactivity of Stable Ligated Boranes and a Borohydride Salt in Rhodium(II)-Catalyzed Boron-Hydrogen Insertion Reactions." The Journal of organic chemistry vol. 81,5 (2016): 2094-8. doi: https://doi.org/10.1021/acs.joc.6b00091
Allen TH, Curran DP. Relative Reactivity of Stable Ligated Boranes and a Borohydride Salt in Rhodium(II)-Catalyzed Boron-Hydrogen Insertion Reactions. J Org Chem. 2016 Mar 04;81(5):2094-8. doi: 10.1021/acs.joc.6b00091. Epub 2016 Feb 23. PMID: 26871613.
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Dermatopathology quiz: Keratotic papules of the palms.

Indian dermatology online journal

Flamm A, Xie Q, Polley DC, Vanstory L, Elston DM.
PMID: 27990395
Indian Dermatol Online J. 2016 Nov-Dec;7(6):536-537. doi: 10.4103/2229-5178.193904.

No abstract available.

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Flamm A, Xie Q, Polley DC, et al. Dermatopathology quiz: Keratotic papules of the palms. Indian Dermatol Online J. 2016;7(6):536-537doi: 10.4103/2229-5178.193904.
Flamm, A., Xie, Q., Polley, D. C., Vanstory, L., & Elston, D. M. (2016). Dermatopathology quiz: Keratotic papules of the palms. Indian dermatology online journal, 7(6), 536-537. https://doi.org/10.4103/2229-5178.193904
Flamm, Alex, et al. "Dermatopathology quiz: Keratotic papules of the palms." Indian dermatology online journal vol. 7,6 (2016): 536-537. doi: https://doi.org/10.4103/2229-5178.193904
Flamm A, Xie Q, Polley DC, Vanstory L, Elston DM. Dermatopathology quiz: Keratotic papules of the palms. Indian Dermatol Online J. 2016 Nov-Dec;7(6):536-537. doi: 10.4103/2229-5178.193904. PMID: 27990395; PMCID: PMC5134174.
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N-Heterocyclic Carbene Boryl Iodides Catalyze Insertion Reactions of N-Heterocyclic Carbene Boranes and Diazoesters.

Organic letters

Allen TH, Kawamoto T, Gardner S, Geib SJ, Curran DP.
PMID: 28641014
Org Lett. 2017 Jul 07;19(13):3680-3683. doi: 10.1021/acs.orglett.7b01777. Epub 2017 Jun 22.

Boron-hydrogen bond insertion reactions of N-heterocyclic carbene (NHC) boranes and diazoesters can be catalyzed by NHC-boryl iodides and produce stable α-NHC-boryl esters. The conditions of the reaction resemble the previous rhodium-catalyzed transformations (only the catalyst is different); however, the...

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Allen TH, Kawamoto T, Gardner S, et al. N-Heterocyclic Carbene Boryl Iodides Catalyze Insertion Reactions of N-Heterocyclic Carbene Boranes and Diazoesters. Org Lett. 2017;19(13):3680-3683doi: 10.1021/acs.orglett.7b01777.
Allen, T. H., Kawamoto, T., Gardner, S., Geib, S. J., & Curran, D. P. (2017). N-Heterocyclic Carbene Boryl Iodides Catalyze Insertion Reactions of N-Heterocyclic Carbene Boranes and Diazoesters. Organic letters, 19(13), 3680-3683. https://doi.org/10.1021/acs.orglett.7b01777
Allen, Thomas H, et al. "N-Heterocyclic Carbene Boryl Iodides Catalyze Insertion Reactions of N-Heterocyclic Carbene Boranes and Diazoesters." Organic letters vol. 19,13 (2017): 3680-3683. doi: https://doi.org/10.1021/acs.orglett.7b01777
Allen TH, Kawamoto T, Gardner S, Geib SJ, Curran DP. N-Heterocyclic Carbene Boryl Iodides Catalyze Insertion Reactions of N-Heterocyclic Carbene Boranes and Diazoesters. Org Lett. 2017 Jul 07;19(13):3680-3683. doi: 10.1021/acs.orglett.7b01777. Epub 2017 Jun 22. PMID: 28641014.
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Modulation of Chemical Composition and Other Parameters of the Cell at Different Exponential Growth Rates.

EcoSal Plus

Bremer H, Dennis PP.
PMID: 26443740
EcoSal Plus. 2008 Sep;3(1). doi: 10.1128/ecosal.5.2.3.

This review begins by briefly presenting the history of research on the chemical composition and other parameters of cells of E. coli and S. enterica at different exponential growth rates. Studies have allowed us to determine the in vivo...

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Bremer H, Dennis PP. Modulation of Chemical Composition and Other Parameters of the Cell at Different Exponential Growth Rates. EcoSal Plus. 2008;3(1)doi: 10.1128/ecosal.5.2.3.
Bremer, H., & Dennis, P. P. (2008). Modulation of Chemical Composition and Other Parameters of the Cell at Different Exponential Growth Rates. EcoSal Plus, 3(1), . https://doi.org/10.1128/ecosal.5.2.3
Bremer, Hans, and Dennis, Patrick P. "Modulation of Chemical Composition and Other Parameters of the Cell at Different Exponential Growth Rates." EcoSal Plus vol. 3,1 (2008). doi: https://doi.org/10.1128/ecosal.5.2.3
Bremer H, Dennis PP. Modulation of Chemical Composition and Other Parameters of the Cell at Different Exponential Growth Rates. EcoSal Plus. 2008 Sep;3(1). doi: 10.1128/ecosal.5.2.3. PMID: 26443740.
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Showing 1 to 12 of 812 entries