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Showing 1 to 12 of 65 entries
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Values clarification--where does it belong?.

Health education

Goodlett DE.
PMID: 815207
Health Educ. 1976 Mar-Apr;7(2):10-1.

No abstract available.

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Goodlett DE. Values clarification--where does it belong?. Health Educ. 1976;7(2):10-1
Goodlett, D. E. (1976). Values clarification--where does it belong?. Health education, 7(2), 10-1.
Goodlett, D E. "Values clarification--where does it belong?." Health education vol. 7,2 (1976): 10-1.
Goodlett DE. Values clarification--where does it belong?. Health Educ. 1976 Mar-Apr;7(2):10-1. PMID: 815207.
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Detection of Carbofuran-Protein Adducts in Serum of Occupationally Exposed Pesticide Factory Workers in Pakistan.

Chemical research in toxicology

Rehman T, Khan MM, Shad MA, Hussain M, Oyler BL, Goo YA, Goodlett DR.
PMID: 27657490
Chem Res Toxicol. 2016 Oct 17;29(10):1720-1728. doi: 10.1021/acs.chemrestox.6b00222. Epub 2016 Oct 06.

This study was conducted to investigate the protein adducts with pesticides in a cohort of 172 factory workers that were exposed to a mixture of pesticides. The 35 samples showing considerable variation in biochemical parameters, i.e., butyrylcholinestrase (BChE), serum...

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Rehman T, Khan MM, Shad MA, et al. Detection of Carbofuran-Protein Adducts in Serum of Occupationally Exposed Pesticide Factory Workers in Pakistan. Chem Res Toxicol. 2016;29(10):1720-1728doi: 10.1021/acs.chemrestox.6b00222.
Rehman, T., Khan, M. M., Shad, M. A., Hussain, M., Oyler, B. L., Goo, Y. A., & Goodlett, D. R. (2016). Detection of Carbofuran-Protein Adducts in Serum of Occupationally Exposed Pesticide Factory Workers in Pakistan. Chemical research in toxicology, 29(10), 1720-1728. https://doi.org/10.1021/acs.chemrestox.6b00222
Rehman, Tanzila, et al. "Detection of Carbofuran-Protein Adducts in Serum of Occupationally Exposed Pesticide Factory Workers in Pakistan." Chemical research in toxicology vol. 29,10 (2016): 1720-1728. doi: https://doi.org/10.1021/acs.chemrestox.6b00222
Rehman T, Khan MM, Shad MA, Hussain M, Oyler BL, Goo YA, Goodlett DR. Detection of Carbofuran-Protein Adducts in Serum of Occupationally Exposed Pesticide Factory Workers in Pakistan. Chem Res Toxicol. 2016 Oct 17;29(10):1720-1728. doi: 10.1021/acs.chemrestox.6b00222. Epub 2016 Oct 06. PMID: 27657490.
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Targeting trisomic treatments: optimizing Dyrk1a inhibition to improve Down syndrome deficits.

Molecular genetics & genomic medicine

Stringer M, Goodlett CR, Roper RJ.
PMID: 28944229
Mol Genet Genomic Med. 2017 Sep 20;5(5):451-465. doi: 10.1002/mgg3.334. eCollection 2017 Sep.

Overexpression of

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Stringer M, Goodlett CR, Roper RJ. Targeting trisomic treatments: optimizing Dyrk1a inhibition to improve Down syndrome deficits. Mol Genet Genomic Med. 2017;5(5):451-465doi: 10.1002/mgg3.334.
Stringer, M., Goodlett, C. R., & Roper, R. J. (2017). Targeting trisomic treatments: optimizing Dyrk1a inhibition to improve Down syndrome deficits. Molecular genetics & genomic medicine, 5(5), 451-465. https://doi.org/10.1002/mgg3.334
Stringer, Megan, et al. "Targeting trisomic treatments: optimizing Dyrk1a inhibition to improve Down syndrome deficits." Molecular genetics & genomic medicine vol. 5,5 (2017): 451-465. doi: https://doi.org/10.1002/mgg3.334
Stringer M, Goodlett CR, Roper RJ. Targeting trisomic treatments: optimizing Dyrk1a inhibition to improve Down syndrome deficits. Mol Genet Genomic Med. 2017 Sep 20;5(5):451-465. doi: 10.1002/mgg3.334. eCollection 2017 Sep. PMID: 28944229; PMCID: PMC5606891.
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Forward models for extending the mechanical damage evaluation capability of resonant ultrasound spectroscopy.

Ultrasonics

Goodlet BR, Torbet CJ, Biedermann EJ, Jauriqui LM, Aldrin JC, Pollock TM.
PMID: 28254563
Ultrasonics. 2017 May;77:183-196. doi: 10.1016/j.ultras.2017.02.002. Epub 2017 Feb 08.

Finite element (FE) modeling has been coupled with resonant ultrasound spectroscopy (RUS) for nondestructive evaluation (NDE) of high temperature damage induced by mechanical loading. Forward FE models predict mode-specific changes in resonance frequencies (Δf

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Goodlet BR, Torbet CJ, Biedermann EJ, et al. Forward models for extending the mechanical damage evaluation capability of resonant ultrasound spectroscopy. Ultrasonics. 2017;77:183-196doi: 10.1016/j.ultras.2017.02.002.
Goodlet, B. R., Torbet, C. J., Biedermann, E. J., Jauriqui, L. M., Aldrin, J. C., & Pollock, T. M. (2017). Forward models for extending the mechanical damage evaluation capability of resonant ultrasound spectroscopy. Ultrasonics, 77183-196. https://doi.org/10.1016/j.ultras.2017.02.002
Goodlet, B R, et al. "Forward models for extending the mechanical damage evaluation capability of resonant ultrasound spectroscopy." Ultrasonics vol. 77 (2017): 183-196. doi: https://doi.org/10.1016/j.ultras.2017.02.002
Goodlet BR, Torbet CJ, Biedermann EJ, Jauriqui LM, Aldrin JC, Pollock TM. Forward models for extending the mechanical damage evaluation capability of resonant ultrasound spectroscopy. Ultrasonics. 2017 May;77:183-196. doi: 10.1016/j.ultras.2017.02.002. Epub 2017 Feb 08. PMID: 28254563.
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Shotgun proteomics as a viable approach for biological discovery in the Pacific oyster.

Conservation physiology

Timmins-Schiffman E, Nunn BL, Goodlett DR, Roberts SB.
PMID: 27293593
Conserv Physiol. 2013 May 17;1(1):cot009. doi: 10.1093/conphys/cot009. eCollection 2013.

Shotgun proteomics offers an efficient means to characterize proteins in a complex mixture, particularly when sufficient genomic resources are available. In order to assess the practical application of shotgun proteomics in the Pacific oyster (Crassostrea gigas), liquid chromatography coupled...

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Timmins-Schiffman E, Nunn BL, Goodlett DR, et al. Shotgun proteomics as a viable approach for biological discovery in the Pacific oyster. Conserv Physiol. 2013;1(1):cot009doi: 10.1093/conphys/cot009.
Timmins-Schiffman, E., Nunn, B. L., Goodlett, D. R., & Roberts, S. B. (2013). Shotgun proteomics as a viable approach for biological discovery in the Pacific oyster. Conservation physiology, 1(1), cot009. https://doi.org/10.1093/conphys/cot009
Timmins-Schiffman, Emma, et al. "Shotgun proteomics as a viable approach for biological discovery in the Pacific oyster." Conservation physiology vol. 1,1 (2013): cot009. doi: https://doi.org/10.1093/conphys/cot009
Timmins-Schiffman E, Nunn BL, Goodlett DR, Roberts SB. Shotgun proteomics as a viable approach for biological discovery in the Pacific oyster. Conserv Physiol. 2013 May 17;1(1):cot009. doi: 10.1093/conphys/cot009. eCollection 2013. PMID: 27293593; PMCID: PMC4732435.
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Deviations in brain early serotonergic development as a result of fetal alcohol exposure.

Neurotoxicity research

Zhou FC, Sari Y, Li TK, Goodlett C, Azmitia EC.
PMID: 12829423
Neurotox Res. 2002 Jun;4(4):337-42. doi: 10.1080/10298420290030532.

Serotonin (5-HT) has specific roles not only as a transmitter but also as a signal for differentiation. We recently found that alcohol drinking during pregnancy resulted in incomplete-neural-tube-fusion which hindered the development of midline cells such as 5-HT neurons...

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Zhou FC, Sari Y, Li TK, et al. Deviations in brain early serotonergic development as a result of fetal alcohol exposure. Neurotox Res. 2002;4(4):337-42doi: 10.1080/10298420290030532.
Zhou, F. C., Sari, Y., Li, T. K., Goodlett, C., & Azmitia, E. C. (2002). Deviations in brain early serotonergic development as a result of fetal alcohol exposure. Neurotoxicity research, 4(4), 337-42. https://doi.org/10.1080/10298420290030532
Zhou, Feng C, et al. "Deviations in brain early serotonergic development as a result of fetal alcohol exposure." Neurotoxicity research vol. 4,4 (2002): 337-42. doi: https://doi.org/10.1080/10298420290030532
Zhou FC, Sari Y, Li TK, Goodlett C, Azmitia EC. Deviations in brain early serotonergic development as a result of fetal alcohol exposure. Neurotox Res. 2002 Jun;4(4):337-42. doi: 10.1080/10298420290030532. PMID: 12829423.
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Comparison of a label-free quantitative proteomic method based on peptide ion current area to the isotope coded affinity tag method.

Cancer informatics

Ryu S, Gallis B, Goo YA, Shaffer SA, Radulovic D, Goodlett DR.
PMID: 19259412
Cancer Inform. 2008;6:243-55. doi: 10.4137/cin.s385. Epub 2008 Apr 17.

Recently, several research groups have published methods for the determination of proteomic expression profiling by mass spectrometry without the use of exogenously added stable isotopes or stable isotope dilution theory. These so-called label-free, methods have the advantage of allowing...

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Ryu S, Gallis B, Goo YA, et al. Comparison of a label-free quantitative proteomic method based on peptide ion current area to the isotope coded affinity tag method. Cancer Inform. 2008;6:243-55doi: 10.4137/cin.s385.
Ryu, S., Gallis, B., Goo, Y. A., Shaffer, S. A., Radulovic, D., & Goodlett, D. R. (2008). Comparison of a label-free quantitative proteomic method based on peptide ion current area to the isotope coded affinity tag method. Cancer informatics, 6243-55. https://doi.org/10.4137/cin.s385
Ryu, Soyoung, et al. "Comparison of a label-free quantitative proteomic method based on peptide ion current area to the isotope coded affinity tag method." Cancer informatics vol. 6 (2008): 243-55. doi: https://doi.org/10.4137/cin.s385
Ryu S, Gallis B, Goo YA, Shaffer SA, Radulovic D, Goodlett DR. Comparison of a label-free quantitative proteomic method based on peptide ion current area to the isotope coded affinity tag method. Cancer Inform. 2008;6:243-55. doi: 10.4137/cin.s385. Epub 2008 Apr 17. PMID: 19259412; PMCID: PMC2623286.
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Proteomics on Fixed Tissue Specimens - A Review.

Current proteomics

Reimel BA, Pan S, May DH, Shaffer SA, Goodlett DR, McIntosh MW, Yerian LM, Bronner MP, Chen R, Brentnall TA.
PMID: 19829741
Curr Proteomics. 2009 Apr 01;6(1):63-69. doi: 10.2174/157016409787847420.

The vast majority of clinical tissue samples are formalin-fixed and paraffin-preserved. This type of preservation has been considered an obstacle to protein extraction from these tissues. However, these are the very tissue samples that have associated patient histories, diagnoses...

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Reimel BA, Pan S, May DH, et al. Proteomics on Fixed Tissue Specimens - A Review. Curr Proteomics. 2009;6(1):63-69doi: 10.2174/157016409787847420.
Reimel, B. A., Pan, S., May, D. H., Shaffer, S. A., Goodlett, D. R., McIntosh, M. W., Yerian, L. M., Bronner, M. P., Chen, R., & Brentnall, T. A. (2009). Proteomics on Fixed Tissue Specimens - A Review. Current proteomics, 6(1), 63-69. https://doi.org/10.2174/157016409787847420
Reimel, Beth Ann, et al. "Proteomics on Fixed Tissue Specimens - A Review." Current proteomics vol. 6,1 (2009): 63-69. doi: https://doi.org/10.2174/157016409787847420
Reimel BA, Pan S, May DH, Shaffer SA, Goodlett DR, McIntosh MW, Yerian LM, Bronner MP, Chen R, Brentnall TA. Proteomics on Fixed Tissue Specimens - A Review. Curr Proteomics. 2009 Apr 01;6(1):63-69. doi: 10.2174/157016409787847420. PMID: 19829741; PMCID: PMC2760948.
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Systematic investigation of lycopene effects in LNCaP cells by use of novel large-scale proteomic analysis software.

Proteomics. Clinical applications

Goo YA, Li Z, Pajkovic N, Shaffer S, Taylor G, Chen J, Campbell D, Arnstein L, Goodlett DR, van Breemen RB.
PMID: 20740054
Proteomics Clin Appl. 2007 May 01;1(5):513-523. doi: 10.1002/prca.200600511.

Lycopene, the red pigment of tomatoes, is a carotenoid with potent antioxidant properties. Although lycopene might function as a prostate cancer chemoprevention agent, little is known about its effects at the cellular level. To define general changes induced by...

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Goo YA, Li Z, Pajkovic N, et al. Systematic investigation of lycopene effects in LNCaP cells by use of novel large-scale proteomic analysis software. Proteomics Clin Appl. 2007;1(5):513-523doi: 10.1002/prca.200600511.
Goo, Y. A., Li, Z., Pajkovic, N., Shaffer, S., Taylor, G., Chen, J., Campbell, D., Arnstein, L., Goodlett, D. R., & van Breemen, R. B. (2007). Systematic investigation of lycopene effects in LNCaP cells by use of novel large-scale proteomic analysis software. Proteomics. Clinical applications, 1(5), 513-523. https://doi.org/10.1002/prca.200600511
Goo, Young Ah, et al. "Systematic investigation of lycopene effects in LNCaP cells by use of novel large-scale proteomic analysis software." Proteomics. Clinical applications vol. 1,5 (2007): 513-523. doi: https://doi.org/10.1002/prca.200600511
Goo YA, Li Z, Pajkovic N, Shaffer S, Taylor G, Chen J, Campbell D, Arnstein L, Goodlett DR, van Breemen RB. Systematic investigation of lycopene effects in LNCaP cells by use of novel large-scale proteomic analysis software. Proteomics Clin Appl. 2007 May 01;1(5):513-523. doi: 10.1002/prca.200600511. PMID: 20740054; PMCID: PMC2926987.
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Proteins That Underlie Neoplastic Progression of Ulcerative Colitis.

Proteomics. Clinical applications

Brentnall TA, Pan S, Bronner MP, Crispin DA, Mirzaei H, Cooke K, Tamura Y, Nikolskaya T, Jebailey L, Goodlett DR, McIntosh M, Aebersold R, Rabinovitch PS, Chen R.
PMID: 20098637
Proteomics Clin Appl. 2009 Sep 14;3(11):1326. doi: 10.1002/prca.200900061.

Patients with ulcerative colitis (UC) have an increased risk for developing colorectal cancer. Because UC tumorigenesis is associated with genomic field defects that can extend throughout the entire colon, including the non-dysplastic mucosa; we hypothesized that the same field...

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Brentnall TA, Pan S, Bronner MP, et al. Proteins That Underlie Neoplastic Progression of Ulcerative Colitis. Proteomics Clin Appl. 2009;3(11):1326doi: 10.1002/prca.200900061.
Brentnall, T. A., Pan, S., Bronner, M. P., Crispin, D. A., Mirzaei, H., Cooke, K., Tamura, Y., Nikolskaya, T., Jebailey, L., Goodlett, D. R., McIntosh, M., Aebersold, R., Rabinovitch, P. S., & Chen, R. (2009). Proteins That Underlie Neoplastic Progression of Ulcerative Colitis. Proteomics. Clinical applications, 3(11), 1326. https://doi.org/10.1002/prca.200900061
Brentnall, Teresa A, et al. "Proteins That Underlie Neoplastic Progression of Ulcerative Colitis." Proteomics. Clinical applications vol. 3,11 (2009): 1326. doi: https://doi.org/10.1002/prca.200900061
Brentnall TA, Pan S, Bronner MP, Crispin DA, Mirzaei H, Cooke K, Tamura Y, Nikolskaya T, Jebailey L, Goodlett DR, McIntosh M, Aebersold R, Rabinovitch PS, Chen R. Proteins That Underlie Neoplastic Progression of Ulcerative Colitis. Proteomics Clin Appl. 2009 Sep 14;3(11):1326. doi: 10.1002/prca.200900061. PMID: 20098637; PMCID: PMC2809935.
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VOXEL-WISE GROUP ANALYSIS OF DTI.

Proceedings. IEEE International Symposium on Biomedical Imaging

Liu Z, Zhu H, Marks BL, Katz LM, Goodlett CB, Gerig G, Styner M.
PMID: 23703686
Proc IEEE Int Symp Biomed Imaging. 2009;807-810. doi: 10.1109/isbi.2009.5193172.

Diffusion tensor MRI (DTI) is now a widely used modality to investigate the fiber tissues in vivo, especially the white matter in brain. An automatic pipeline is described in this paper to conduct a localized voxel-wise multiple-subject group comparison...

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Liu Z, Zhu H, Marks BL, et al. VOXEL-WISE GROUP ANALYSIS OF DTI. Proc IEEE Int Symp Biomed Imaging. 2009;807-810doi: 10.1109/isbi.2009.5193172.
Liu, Z., Zhu, H., Marks, B. L., Katz, L. M., Goodlett, C. B., Gerig, G., & Styner, M. (2009). VOXEL-WISE GROUP ANALYSIS OF DTI. Proceedings. IEEE International Symposium on Biomedical Imaging, 807-810. https://doi.org/10.1109/isbi.2009.5193172
Liu, Zhexing, et al. "VOXEL-WISE GROUP ANALYSIS OF DTI." Proceedings. IEEE International Symposium on Biomedical Imaging vol. (2009): 807-810. doi: https://doi.org/10.1109/isbi.2009.5193172
Liu Z, Zhu H, Marks BL, Katz LM, Goodlett CB, Gerig G, Styner M. VOXEL-WISE GROUP ANALYSIS OF DTI. Proc IEEE Int Symp Biomed Imaging. 2009;807-810. doi: 10.1109/isbi.2009.5193172. PMID: 23703686; PMCID: PMC3660096.
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Preparation and Use of an Integrated Microcapillary HPLC Column and ESI Device for Proteomic Analysis.

CSH protocols

Goodlett DR, Yi EC, Mottay P.
PMID: 21357072
CSH Protoc. 2007 May 01;2007:pdb.prot4617. doi: 10.1101/pdb.prot4617.

INTRODUCTIONImplementation of separation techniques in miniaturized formats on-line with high-performance mass spectrometers and the development of miniaturized sprayers as electrospray ionization (ESI) ion sources have reduced the amount of peptide required for complete and routine sequence characterization from several...

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Goodlett DR, Yi EC, Mottay P. Preparation and Use of an Integrated Microcapillary HPLC Column and ESI Device for Proteomic Analysis. CSH Protoc. 2007;2007:pdb.prot4617doi: 10.1101/pdb.prot4617.
Goodlett, D. R., Yi, E. C., & Mottay, P. (2007). Preparation and Use of an Integrated Microcapillary HPLC Column and ESI Device for Proteomic Analysis. CSH protocols, 2007pdb.prot4617. https://doi.org/10.1101/pdb.prot4617
Goodlett, David R, et al. "Preparation and Use of an Integrated Microcapillary HPLC Column and ESI Device for Proteomic Analysis." CSH protocols vol. 2007 (2007): pdb.prot4617. doi: https://doi.org/10.1101/pdb.prot4617
Goodlett DR, Yi EC, Mottay P. Preparation and Use of an Integrated Microcapillary HPLC Column and ESI Device for Proteomic Analysis. CSH Protoc. 2007 May 01;2007:pdb.prot4617. doi: 10.1101/pdb.prot4617. PMID: 21357072.
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Showing 1 to 12 of 65 entries