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Diabetes mellitus.

Clinical pediatrics

Laron Z.
PMID: 679589
Clin Pediatr (Phila). 1978 Sep;17(9):727. doi: 10.1177/000992287801700913.

No abstract available.

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Laron Z. Diabetes mellitus. Clin Pediatr (Phila). 1978;17(9):727doi: 10.1177/000992287801700913.
Laron, Z. (1978). Diabetes mellitus. Clinical pediatrics, 17(9), 727. https://doi.org/10.1177/000992287801700913
Laron, Z. "Diabetes mellitus." Clinical pediatrics vol. 17,9 (1978): 727. doi: https://doi.org/10.1177/000992287801700913
Laron Z. Diabetes mellitus. Clin Pediatr (Phila). 1978 Sep;17(9):727. doi: 10.1177/000992287801700913. PMID: 679589.
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Training and Consultation in Evidence-Based Psychosocial Treatments in Public Mental Health Settings: The ACCESS Model.

Professional psychology, research and practice

Stirman SW, Spokas M, Creed TA, Farabaugh DT, Bhar SS, Brown GK, Perivoliotis D, Grant PM, Beck AT.
PMID: 22872783
Prof Psychol Res Pr. 2010 Feb;41(1):48-56. doi: 10.1037/a0018099.

We present a model of training in evidence-based psychosocial treatments (EBTs). The ACCESS (assess and adapt, convey basics, consult, evaluate, study outcomes, sustain) model integrates principles and findings from adult education and training literatures, research, and practical suggestions based...

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Stirman SW, Spokas M, Creed TA, et al. Training and Consultation in Evidence-Based Psychosocial Treatments in Public Mental Health Settings: The ACCESS Model. Prof Psychol Res Pr. 2010;41(1):48-56doi: 10.1037/a0018099.
Stirman, S. W., Spokas, M., Creed, T. A., Farabaugh, D. T., Bhar, S. S., Brown, G. K., Perivoliotis, D., Grant, P. M., & Beck, A. T. (2010). Training and Consultation in Evidence-Based Psychosocial Treatments in Public Mental Health Settings: The ACCESS Model. Professional psychology, research and practice, 41(1), 48-56. https://doi.org/10.1037/a0018099
Stirman, Shannon Wiltsey, et al. "Training and Consultation in Evidence-Based Psychosocial Treatments in Public Mental Health Settings: The ACCESS Model." Professional psychology, research and practice vol. 41,1 (2010): 48-56. doi: https://doi.org/10.1037/a0018099
Stirman SW, Spokas M, Creed TA, Farabaugh DT, Bhar SS, Brown GK, Perivoliotis D, Grant PM, Beck AT. Training and Consultation in Evidence-Based Psychosocial Treatments in Public Mental Health Settings: The ACCESS Model. Prof Psychol Res Pr. 2010 Feb;41(1):48-56. doi: 10.1037/a0018099. PMID: 22872783; PMCID: PMC3412177.
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Synthesis, structural characterization, aromatic characteristics, and metalation of neo-confused porphyrins, a newly discovered class of porphyrin isomers.

The Journal of organic chemistry

Li R, Lammer AD, Ferrence GM, Lash TD.
PMID: 24697282
J Org Chem. 2014 May 02;79(9):4078-93. doi: 10.1021/jo500580e. Epub 2014 Apr 18.

Neo-confused porphyrins represent a unique family of porphyrin isomers that retain overall aromatic characteristics by virtue of a 17-atom 18π electron delocalization pathway. These porphyrin analogues have a pyrrolic subunit linked in a 1,3-fashion so that a nitrogen atom...

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Li R, Lammer AD, Ferrence GM, et al. Synthesis, structural characterization, aromatic characteristics, and metalation of neo-confused porphyrins, a newly discovered class of porphyrin isomers. J Org Chem. 2014;79(9):4078-93doi: 10.1021/jo500580e.
Li, R., Lammer, A. D., Ferrence, G. M., & Lash, T. D. (2014). Synthesis, structural characterization, aromatic characteristics, and metalation of neo-confused porphyrins, a newly discovered class of porphyrin isomers. The Journal of organic chemistry, 79(9), 4078-93. https://doi.org/10.1021/jo500580e
Li, Ruoshi, et al. "Synthesis, structural characterization, aromatic characteristics, and metalation of neo-confused porphyrins, a newly discovered class of porphyrin isomers." The Journal of organic chemistry vol. 79,9 (2014): 4078-93. doi: https://doi.org/10.1021/jo500580e
Li R, Lammer AD, Ferrence GM, Lash TD. Synthesis, structural characterization, aromatic characteristics, and metalation of neo-confused porphyrins, a newly discovered class of porphyrin isomers. J Org Chem. 2014 May 02;79(9):4078-93. doi: 10.1021/jo500580e. Epub 2014 Apr 18. PMID: 24697282.
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Unraveling the core-shell structure of ligand-capped Sn/SnOx nanoparticles by surface-enhanced nuclear magnetic resonance, Mössbauer, and X-ray absorption spectroscopies.

ACS nano

Protesescu L, Rossini AJ, Kriegner D, Valla M, de Kergommeaux A, Walter M, Kravchyk KV, Nachtegaal M, Stangl J, Malaman B, Reiss P, Lesage A, Emsley L, Copéret C, Kovalenko MV.
PMID: 24494636
ACS Nano. 2014 Mar 25;8(3):2639-48. doi: 10.1021/nn406344n. Epub 2014 Feb 04.

A particularly difficult challenge in the chemistry of nanomaterials is the detailed structural and chemical analysis of multicomponent nano-objects. This is especially true for the determination of spatially resolved information. In this study, we demonstrate that dynamic nuclear polarization...

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Protesescu L, Rossini AJ, Kriegner D, et al. Unraveling the core-shell structure of ligand-capped Sn/SnOx nanoparticles by surface-enhanced nuclear magnetic resonance, Mössbauer, and X-ray absorption spectroscopies. ACS Nano. 2014;8(3):2639-48doi: 10.1021/nn406344n.
Protesescu, L., Rossini, A. J., Kriegner, D., Valla, M., de Kergommeaux, A., Walter, M., Kravchyk, K. V., Nachtegaal, M., Stangl, J., Malaman, B., Reiss, P., Lesage, A., Emsley, L., Copéret, C., & Kovalenko, M. V. (2014). Unraveling the core-shell structure of ligand-capped Sn/SnOx nanoparticles by surface-enhanced nuclear magnetic resonance, Mössbauer, and X-ray absorption spectroscopies. ACS nano, 8(3), 2639-48. https://doi.org/10.1021/nn406344n
Protesescu, Loredana, et al. "Unraveling the core-shell structure of ligand-capped Sn/SnOx nanoparticles by surface-enhanced nuclear magnetic resonance, Mössbauer, and X-ray absorption spectroscopies." ACS nano vol. 8,3 (2014): 2639-48. doi: https://doi.org/10.1021/nn406344n
Protesescu L, Rossini AJ, Kriegner D, Valla M, de Kergommeaux A, Walter M, Kravchyk KV, Nachtegaal M, Stangl J, Malaman B, Reiss P, Lesage A, Emsley L, Copéret C, Kovalenko MV. Unraveling the core-shell structure of ligand-capped Sn/SnOx nanoparticles by surface-enhanced nuclear magnetic resonance, Mössbauer, and X-ray absorption spectroscopies. ACS Nano. 2014 Mar 25;8(3):2639-48. doi: 10.1021/nn406344n. Epub 2014 Feb 04. PMID: 24494636.
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Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with wiskott-Aldrich syndrome.

Frontiers in immunology

O'Connell AE, Volpi S, Dobbs K, Fiorini C, Tsitsikov E, de Boer H, Barlan IB, Despotovic JM, Espinosa-Rosales FJ, Hanson IC, Kanariou MG, Martínez-Beckerat R, Mayorga-Sirera A, Mejia-Carvajal C, Radwan N, Weiss AR, Pai SY, Lee YN, Notarangelo LD.
PMID: 25101082
Front Immunol. 2014 Jul 18;5:340. doi: 10.3389/fimmu.2014.00340. eCollection 2014.

The Wiskott-Aldrich syndrome (WAS) is due to mutations of the WAS gene encoding for the cytoskeletal WAS protein, leading to abnormal downstream signaling from the T cell and B cell antigen receptors (TCR and BCR). We hypothesized that the...

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O'Connell AE, Volpi S, Dobbs K, et al. Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with wiskott-Aldrich syndrome. Front Immunol. 2014;5:340doi: 10.3389/fimmu.2014.00340.
O'Connell, A. E., Volpi, S., Dobbs, K., Fiorini, C., Tsitsikov, E., de Boer, H., Barlan, I. B., Despotovic, J. M., Espinosa-Rosales, F. J., Hanson, I. C., Kanariou, M. G., Martínez-Beckerat, R., Mayorga-Sirera, A., Mejia-Carvajal, C., Radwan, N., Weiss, A. R., Pai, S. Y., Lee, Y. N., & Notarangelo, L. D. (2014). Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with wiskott-Aldrich syndrome. Frontiers in immunology, 5340. https://doi.org/10.3389/fimmu.2014.00340
O'Connell, Amy E, et al. "Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with wiskott-Aldrich syndrome." Frontiers in immunology vol. 5 (2014): 340. doi: https://doi.org/10.3389/fimmu.2014.00340
O'Connell AE, Volpi S, Dobbs K, Fiorini C, Tsitsikov E, de Boer H, Barlan IB, Despotovic JM, Espinosa-Rosales FJ, Hanson IC, Kanariou MG, Martínez-Beckerat R, Mayorga-Sirera A, Mejia-Carvajal C, Radwan N, Weiss AR, Pai SY, Lee YN, Notarangelo LD. Next generation sequencing reveals skewing of the T and B cell receptor repertoires in patients with wiskott-Aldrich syndrome. Front Immunol. 2014 Jul 18;5:340. doi: 10.3389/fimmu.2014.00340. eCollection 2014. PMID: 25101082; PMCID: PMC4102881.
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Lewis base mediated β-elimination and Lewis acid mediated insertion reactions of disilazido zirconium compounds.

Journal of the American Chemical Society

Yan K, Duchimaza Heredia JJ, Ellern A, Gordon MS, Sadow AD.
PMID: 24067161
J Am Chem Soc. 2013 Oct 09;135(40):15225-37. doi: 10.1021/ja407950e. Epub 2013 Sep 25.

The reactivity of a series of disilazido zirconocene complexes is dominated by the migration of anionic groups (hydrogen, alkyl, halide, OTf) between the zirconium and silicon centers. The direction of these migrations is controlled by the addition of two-electron...

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Yan K, Duchimaza Heredia JJ, Ellern A, et al. Lewis base mediated β-elimination and Lewis acid mediated insertion reactions of disilazido zirconium compounds. J Am Chem Soc. 2013;135(40):15225-37doi: 10.1021/ja407950e.
Yan, K., Duchimaza Heredia, J. J., Ellern, A., Gordon, M. S., & Sadow, A. D. (2013). Lewis base mediated β-elimination and Lewis acid mediated insertion reactions of disilazido zirconium compounds. Journal of the American Chemical Society, 135(40), 15225-37. https://doi.org/10.1021/ja407950e
Yan, KaKing, et al. "Lewis base mediated β-elimination and Lewis acid mediated insertion reactions of disilazido zirconium compounds." Journal of the American Chemical Society vol. 135,40 (2013): 15225-37. doi: https://doi.org/10.1021/ja407950e
Yan K, Duchimaza Heredia JJ, Ellern A, Gordon MS, Sadow AD. Lewis base mediated β-elimination and Lewis acid mediated insertion reactions of disilazido zirconium compounds. J Am Chem Soc. 2013 Oct 09;135(40):15225-37. doi: 10.1021/ja407950e. Epub 2013 Sep 25. PMID: 24067161.
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Arthroscopic repair of the floating posterior-inferior glenohumeral ligament lesion.

Arthroscopy techniques

Baran S, Krych AJ, Dahm DL.
PMID: 24265985
Arthrosc Tech. 2013 Jun 07;2(3):e209-12. doi: 10.1016/j.eats.2013.02.007. eCollection 2013.

We present our technique for diagnosis and arthroscopic repair of a floating posterior-inferior glenohumeral ligament avulsion injury. A high degree of suspicion based on the patient's history, along with careful examination, should alert the surgeon to the existence of...

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Baran S, Krych AJ, Dahm DL. Arthroscopic repair of the floating posterior-inferior glenohumeral ligament lesion. Arthrosc Tech. 2013;2(3):e209-12doi: 10.1016/j.eats.2013.02.007.
Baran, S., Krych, A. J., & Dahm, D. L. (2013). Arthroscopic repair of the floating posterior-inferior glenohumeral ligament lesion. Arthroscopy techniques, 2(3), e209-12. https://doi.org/10.1016/j.eats.2013.02.007
Baran, Sean, et al. "Arthroscopic repair of the floating posterior-inferior glenohumeral ligament lesion." Arthroscopy techniques vol. 2,3 (2013): e209-12. doi: https://doi.org/10.1016/j.eats.2013.02.007
Baran S, Krych AJ, Dahm DL. Arthroscopic repair of the floating posterior-inferior glenohumeral ligament lesion. Arthrosc Tech. 2013 Jun 07;2(3):e209-12. doi: 10.1016/j.eats.2013.02.007. eCollection 2013. PMID: 24265985; PMCID: PMC3834661.
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Atomistic description of thiostannate-capped CdSe nanocrystals: retention of four-coordinate SnS4 motif and preservation of Cd-rich stoichiometry.

Journal of the American Chemical Society

Protesescu L, Nachtegaal M, Voznyy O, Borovinskaya O, Rossini AJ, Emsley L, Copéret C, Günther D, Sargent EH, Kovalenko MV.
PMID: 25597625
J Am Chem Soc. 2015 Feb 11;137(5):1862-74. doi: 10.1021/ja510862c. Epub 2015 Jan 29.

Colloidal semiconductor nanocrystals (NCs) are widely studied as building blocks for novel solid-state materials. Inorganic surface functionalization, used to displace native organic capping ligands from NC surfaces, has been a major enabler of electronic solid-state devices based on colloidal...

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Protesescu L, Nachtegaal M, Voznyy O, et al. Atomistic description of thiostannate-capped CdSe nanocrystals: retention of four-coordinate SnS4 motif and preservation of Cd-rich stoichiometry. J Am Chem Soc. 2015;137(5):1862-74doi: 10.1021/ja510862c.
Protesescu, L., Nachtegaal, M., Voznyy, O., Borovinskaya, O., Rossini, A. J., Emsley, L., Copéret, C., Günther, D., Sargent, E. H., & Kovalenko, M. V. (2015). Atomistic description of thiostannate-capped CdSe nanocrystals: retention of four-coordinate SnS4 motif and preservation of Cd-rich stoichiometry. Journal of the American Chemical Society, 137(5), 1862-74. https://doi.org/10.1021/ja510862c
Protesescu, Loredana, et al. "Atomistic description of thiostannate-capped CdSe nanocrystals: retention of four-coordinate SnS4 motif and preservation of Cd-rich stoichiometry." Journal of the American Chemical Society vol. 137,5 (2015): 1862-74. doi: https://doi.org/10.1021/ja510862c
Protesescu L, Nachtegaal M, Voznyy O, Borovinskaya O, Rossini AJ, Emsley L, Copéret C, Günther D, Sargent EH, Kovalenko MV. Atomistic description of thiostannate-capped CdSe nanocrystals: retention of four-coordinate SnS4 motif and preservation of Cd-rich stoichiometry. J Am Chem Soc. 2015 Feb 11;137(5):1862-74. doi: 10.1021/ja510862c. Epub 2015 Jan 29. PMID: 25597625; PMCID: PMC4525771.
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A Comprehensive Analysis in Terms of Molecule-Intrinsic, Quasi-Atomic Orbitals. II. Strongly Correlated MCSCF Wave Functions.

The journal of physical chemistry. A

West AC, Schmidt MW, Gordon MS, Ruedenberg K.
PMID: 26376320
J Phys Chem A. 2015 Oct 15;119(41):10360-7. doi: 10.1021/acs.jpca.5b03399. Epub 2015 Oct 01.

A methodology is developed for the quantitative identification of the quasi-atomic orbitals that are embedded in a strongly correlated molecular wave function. The wave function is presumed to be generated from configurations in an internal orbital space whose dimension...

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West AC, Schmidt MW, Gordon MS, et al. A Comprehensive Analysis in Terms of Molecule-Intrinsic, Quasi-Atomic Orbitals. II. Strongly Correlated MCSCF Wave Functions. J Phys Chem A. 2015;119(41):10360-7doi: 10.1021/acs.jpca.5b03399.
West, A. C., Schmidt, M. W., Gordon, M. S., & Ruedenberg, K. (2015). A Comprehensive Analysis in Terms of Molecule-Intrinsic, Quasi-Atomic Orbitals. II. Strongly Correlated MCSCF Wave Functions. The journal of physical chemistry. A, 119(41), 10360-7. https://doi.org/10.1021/acs.jpca.5b03399
West, Aaron C, et al. "A Comprehensive Analysis in Terms of Molecule-Intrinsic, Quasi-Atomic Orbitals. II. Strongly Correlated MCSCF Wave Functions." The journal of physical chemistry. A vol. 119,41 (2015): 10360-7. doi: https://doi.org/10.1021/acs.jpca.5b03399
West AC, Schmidt MW, Gordon MS, Ruedenberg K. A Comprehensive Analysis in Terms of Molecule-Intrinsic, Quasi-Atomic Orbitals. II. Strongly Correlated MCSCF Wave Functions. J Phys Chem A. 2015 Oct 15;119(41):10360-7. doi: 10.1021/acs.jpca.5b03399. Epub 2015 Oct 01. PMID: 26376320.
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5α-Reductase Inhibitors for Treatment of Benign Prostatic Hyperplasia: A Systematic Review and Meta-Analysis.

The Canadian journal of hospital pharmacy

Jun JEJ, Kinkade A, Tung ACH, Tejani AM.
PMID: 28487578
Can J Hosp Pharm. 2017 Mar-Apr;70(2):113-119. doi: 10.4212/cjhp.v70i2.1643. Epub 2017 Apr 28.

BACKGROUND: Finasteride and dutasteride are competitive inhibitors of 5α-reductase enzymes and are commonly used to treat symptomatic benign prostatic hyperplasia (BPH).OBJECTIVE: To compare the efficacy and safety of finasteride and dutasteride in terms of clinically important outcomes.DATA SOURCES: A...

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Jun JEJ, Kinkade A, Tung ACH, et al. 5α-Reductase Inhibitors for Treatment of Benign Prostatic Hyperplasia: A Systematic Review and Meta-Analysis. Can J Hosp Pharm. 2017;70(2):113-119doi: 10.4212/cjhp.v70i2.1643.
Jun, J. E. J., Kinkade, A., Tung, A. C. H., & Tejani, A. M. (2017). 5α-Reductase Inhibitors for Treatment of Benign Prostatic Hyperplasia: A Systematic Review and Meta-Analysis. The Canadian journal of hospital pharmacy, 70(2), 113-119. https://doi.org/10.4212/cjhp.v70i2.1643
Jun, Jennifer E J, et al. "5α-Reductase Inhibitors for Treatment of Benign Prostatic Hyperplasia: A Systematic Review and Meta-Analysis." The Canadian journal of hospital pharmacy vol. 70,2 (2017): 113-119. doi: https://doi.org/10.4212/cjhp.v70i2.1643
Jun JEJ, Kinkade A, Tung ACH, Tejani AM. 5α-Reductase Inhibitors for Treatment of Benign Prostatic Hyperplasia: A Systematic Review and Meta-Analysis. Can J Hosp Pharm. 2017 Mar-Apr;70(2):113-119. doi: 10.4212/cjhp.v70i2.1643. Epub 2017 Apr 28. PMID: 28487578; PMCID: PMC5407420.
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Genome Sequence of a .

Genome announcements

Yuan Y, Zhang Y, Fu S, Crippen TL, Visi DK, Benbow ME, Allen MS, Tomberlin JK, Sze SH, Tarone AM.
PMID: 28450516
Genome Announc. 2017 Apr 27;5(17). doi: 10.1128/genomeA.00250-17.

We present here the draft genome sequence of a

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Yuan Y, Zhang Y, Fu S, et al. Genome Sequence of a . Genome Announc. 2017;5(17)doi: 10.1128/genomeA.00250-17.
Yuan, Y., Zhang, Y., Fu, S., Crippen, T. L., Visi, D. K., Benbow, M. E., Allen, M. S., Tomberlin, J. K., Sze, S. H., & Tarone, A. M. (2017). Genome Sequence of a . Genome announcements, 5(17), . https://doi.org/10.1128/genomeA.00250-17
Yuan, Ye, et al. "Genome Sequence of a ." Genome announcements vol. 5,17 (2017). doi: https://doi.org/10.1128/genomeA.00250-17
Yuan Y, Zhang Y, Fu S, Crippen TL, Visi DK, Benbow ME, Allen MS, Tomberlin JK, Sze SH, Tarone AM. Genome Sequence of a . Genome Announc. 2017 Apr 27;5(17). doi: 10.1128/genomeA.00250-17. PMID: 28450516; PMCID: PMC5408114.
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The Synthesis of Methyl-Substituted Spirocyclic Piperidine-Azetidine (2,7-Diazaspiro[3.5]nonane) and Spirocyclic Piperidine-Pyrrolidine (2,8-Diazaspiro[4.5]decane) Ring Systems.

The Journal of organic chemistry

Smith AC, Cabral S, Kung DW, Rose CR, Southers JA, García-Irizarry CN, Damon DB, Bagley SW, Griffith DA.
PMID: 27056793
J Org Chem. 2016 May 06;81(9):3509-19. doi: 10.1021/acs.joc.5b02890. Epub 2016 Apr 25.

The synthesis of a series of pharmaceutically important N-protected methyl-substituted spirocyclic piperidine-azetidine (2,7-diazaspiro[3.5]nonane) and spirocyclic piperidine-pyrrolidine (2,8-diazaspiro[4.5]decane) ring systems was developed. These motifs contain two differentiated sites (protected secondary amines) to allow for further functionalization via reductive amination, amidation,...

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Smith AC, Cabral S, Kung DW, et al. The Synthesis of Methyl-Substituted Spirocyclic Piperidine-Azetidine (2,7-Diazaspiro[3.5]nonane) and Spirocyclic Piperidine-Pyrrolidine (2,8-Diazaspiro[4.5]decane) Ring Systems. J Org Chem. 2016;81(9):3509-19doi: 10.1021/acs.joc.5b02890.
Smith, A. C., Cabral, S., Kung, D. W., Rose, C. R., Southers, J. A., García-Irizarry, C. N., Damon, D. B., Bagley, S. W., & Griffith, D. A. (2016). The Synthesis of Methyl-Substituted Spirocyclic Piperidine-Azetidine (2,7-Diazaspiro[3.5]nonane) and Spirocyclic Piperidine-Pyrrolidine (2,8-Diazaspiro[4.5]decane) Ring Systems. The Journal of organic chemistry, 81(9), 3509-19. https://doi.org/10.1021/acs.joc.5b02890
Smith, Aaron C, et al. "The Synthesis of Methyl-Substituted Spirocyclic Piperidine-Azetidine (2,7-Diazaspiro[3.5]nonane) and Spirocyclic Piperidine-Pyrrolidine (2,8-Diazaspiro[4.5]decane) Ring Systems." The Journal of organic chemistry vol. 81,9 (2016): 3509-19. doi: https://doi.org/10.1021/acs.joc.5b02890
Smith AC, Cabral S, Kung DW, Rose CR, Southers JA, García-Irizarry CN, Damon DB, Bagley SW, Griffith DA. The Synthesis of Methyl-Substituted Spirocyclic Piperidine-Azetidine (2,7-Diazaspiro[3.5]nonane) and Spirocyclic Piperidine-Pyrrolidine (2,8-Diazaspiro[4.5]decane) Ring Systems. J Org Chem. 2016 May 06;81(9):3509-19. doi: 10.1021/acs.joc.5b02890. Epub 2016 Apr 25. PMID: 27056793.
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