Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 203 entries
Sorted by: Best Match Show Resources per page
Short-read, high-throughput sequencing technology for STR genotyping.

BioTechniques. Rapid dispatches

Bornman DM, Hester ME, Schuetter JM, Kasoji MD, Minard-Smith A, Barden CA, Nelson SC, Godbold GD, Baker CH, Yang B, Walther JE, Tornes IE, Yan PS, Rodriguez B, Bundschuh R, Dickens ML, Young BA, Faith SA.
PMID: 25621315
Biotech Rapid Dispatches. 2012 Apr;2012:1-6.

DNA-based methods for human identification principally rely upon genotyping of short tandem repeat (STR) loci. Electrophoretic-based techniques for variable-length classification of STRs are universally utilized, but are limited in that they have relatively low throughput and do not yield...

Cite
Bornman DM, Hester ME, Schuetter JM, et al. Short-read, high-throughput sequencing technology for STR genotyping. Biotech Rapid Dispatches. 2012;2012:1-6
Bornman, D. M., Hester, M. E., Schuetter, J. M., Kasoji, M. D., Minard-Smith, A., Barden, C. A., Nelson, S. C., Godbold, G. D., Baker, C. H., Yang, B., Walther, J. E., Tornes, I. E., Yan, P. S., Rodriguez, B., Bundschuh, R., Dickens, M. L., Young, B. A., & Faith, S. A. (2012). Short-read, high-throughput sequencing technology for STR genotyping. BioTechniques. Rapid dispatches, 20121-6.
Bornman, Daniel M, et al. "Short-read, high-throughput sequencing technology for STR genotyping." BioTechniques. Rapid dispatches vol. 2012 (2012): 1-6.
Bornman DM, Hester ME, Schuetter JM, Kasoji MD, Minard-Smith A, Barden CA, Nelson SC, Godbold GD, Baker CH, Yang B, Walther JE, Tornes IE, Yan PS, Rodriguez B, Bundschuh R, Dickens ML, Young BA, Faith SA. Short-read, high-throughput sequencing technology for STR genotyping. Biotech Rapid Dispatches. 2012 Apr;2012:1-6. PMID: 25621315; PMCID: PMC4301848.
Copy Download .nbib Format: NLM
The Fab Fragment of a Human Anti-Siglec-9 Monoclonal Antibody Suppresses LPS-Induced Inflammatory Responses in Human Macrophages.

Frontiers in immunology

Chu S, Zhu X, You N, Zhang W, Zheng F, Cai B, Zhou T, Wang Y, Sun Q, Yang Z, Zhang X, Wang C, Nie S, Zhu J, Wang M.
PMID: 28082984
Front Immunol. 2016 Dec 26;7:649. doi: 10.3389/fimmu.2016.00649. eCollection 2016.

Sepsis is a major cause of death for hospitalized patients and is characterized by massive overreaction of immune responses to invading pathogens which is mediated by cytokines. For decades, there has been no effective treatment for sepsis. Sialic acid-binding,...

Cite
Chu S, Zhu X, You N, et al. The Fab Fragment of a Human Anti-Siglec-9 Monoclonal Antibody Suppresses LPS-Induced Inflammatory Responses in Human Macrophages. Front Immunol. 2016;7:649doi: 10.3389/fimmu.2016.00649.
Chu, S., Zhu, X., You, N., Zhang, W., Zheng, F., Cai, B., Zhou, T., Wang, Y., Sun, Q., Yang, Z., Zhang, X., Wang, C., Nie, S., Zhu, J., & Wang, M. (2016). The Fab Fragment of a Human Anti-Siglec-9 Monoclonal Antibody Suppresses LPS-Induced Inflammatory Responses in Human Macrophages. Frontiers in immunology, 7649. https://doi.org/10.3389/fimmu.2016.00649
Chu, Sasa, et al. "The Fab Fragment of a Human Anti-Siglec-9 Monoclonal Antibody Suppresses LPS-Induced Inflammatory Responses in Human Macrophages." Frontiers in immunology vol. 7 (2016): 649. doi: https://doi.org/10.3389/fimmu.2016.00649
Chu S, Zhu X, You N, Zhang W, Zheng F, Cai B, Zhou T, Wang Y, Sun Q, Yang Z, Zhang X, Wang C, Nie S, Zhu J, Wang M. The Fab Fragment of a Human Anti-Siglec-9 Monoclonal Antibody Suppresses LPS-Induced Inflammatory Responses in Human Macrophages. Front Immunol. 2016 Dec 26;7:649. doi: 10.3389/fimmu.2016.00649. eCollection 2016. PMID: 28082984; PMCID: PMC5183739.
Copy Download .nbib Format: NLM
Biotechniques for improving acid aluminum tolerance in alfalfa.

Plant cell reports

Kamp-Glass M, Powell D, Reddy GB, Baligar VC, Wright RJ.
PMID: 24201792
Plant Cell Rep. 1993 Aug;12(10):590-2. doi: 10.1007/BF00233067.

Alfalfa (Medicago sativa L.), cultivars ARC, Regen Y and Saranac were selected in vitro in a recently developed acid/aluminum toxic media. The new media produced higher initiation rates and higher fresh callus weights than those obtainable with the media...

Cite
Kamp-Glass M, Powell D, Reddy GB, et al. Biotechniques for improving acid aluminum tolerance in alfalfa. Plant Cell Rep. 1993;12(10):590-2doi: 10.1007/BF00233067.
Kamp-Glass, M., Powell, D., Reddy, G. B., Baligar, V. C., & Wright, R. J. (1993). Biotechniques for improving acid aluminum tolerance in alfalfa. Plant cell reports, 12(10), 590-2. https://doi.org/10.1007/BF00233067
Kamp-Glass, M, et al. "Biotechniques for improving acid aluminum tolerance in alfalfa." Plant cell reports vol. 12,10 (1993): 590-2. doi: https://doi.org/10.1007/BF00233067
Kamp-Glass M, Powell D, Reddy GB, Baligar VC, Wright RJ. Biotechniques for improving acid aluminum tolerance in alfalfa. Plant Cell Rep. 1993 Aug;12(10):590-2. doi: 10.1007/BF00233067. PMID: 24201792.
Copy Download .nbib Format: NLM
Impossible problems.

BioTechniques

Webb WW.
PMID: 15884665
Biotechniques. 2005 Apr;38(4):515. doi: 10.2144/05384sp01.

No abstract available.

Cite
Webb WW. Impossible problems. Biotechniques. 2005;38(4):515doi: 10.2144/05384sp01.
Webb, W. W. (2005). Impossible problems. BioTechniques, 38(4), 515. https://doi.org/10.2144/05384sp01
Webb, Watt W. "Impossible problems." BioTechniques vol. 38,4 (2005): 515. doi: https://doi.org/10.2144/05384sp01
Webb WW. Impossible problems. Biotechniques. 2005 Apr;38(4):515. doi: 10.2144/05384sp01. PMID: 15884665.
Copy Download .nbib Format: NLM
Returning to diagnostic basics.

BioTechniques

Webb SA.
PMID: 20629269
Biotechniques. 2010 Jul;49(1):491-3. doi: 10.2144/000113461.

No abstract available.

Cite
Webb SA. Returning to diagnostic basics. Biotechniques. 2010;49(1):491-3doi: 10.2144/000113461.
Webb, S. A. (2010). Returning to diagnostic basics. BioTechniques, 49(1), 491-3. https://doi.org/10.2144/000113461
Webb, Sarah A. "Returning to diagnostic basics." BioTechniques vol. 49,1 (2010): 491-3. doi: https://doi.org/10.2144/000113461
Webb SA. Returning to diagnostic basics. Biotechniques. 2010 Jul;49(1):491-3. doi: 10.2144/000113461. PMID: 20629269.
Copy Download .nbib Format: NLM
Antitumor activity of a newly developed monoclonal antibody against ROR1 in ovarian cancer cells.

Oncotarget

Yin Z, Gao M, Chu S, Su Y, Ye C, Wang Y, Pan Z, Wang Z, Zhang H, Tong H, Zhu J.
PMID: 29212222
Oncotarget. 2017 Oct 07;8(55):94210-94222. doi: 10.18632/oncotarget.21618. eCollection 2017 Nov 07.

Receptor-tyrosine-kinase-like Orphan Receptor 1 (ROR1) is a tyrosine-protein kinase transmembrane receptor and ROR1 overexpression is associated with a poor prognosis in various cancers, including ovarian cancer. Targeting of ROR1 has been evaluated as a novel cancer therapy strategy. This...

Cite
Yin Z, Gao M, Chu S, et al. Antitumor activity of a newly developed monoclonal antibody against ROR1 in ovarian cancer cells. Oncotarget. 2017;8(55):94210-94222doi: 10.18632/oncotarget.21618.
Yin, Z., Gao, M., Chu, S., Su, Y., Ye, C., Wang, Y., Pan, Z., Wang, Z., Zhang, H., Tong, H., & Zhu, J. (2017). Antitumor activity of a newly developed monoclonal antibody against ROR1 in ovarian cancer cells. Oncotarget, 8(55), 94210-94222. https://doi.org/10.18632/oncotarget.21618
Yin, Zhengna, et al. "Antitumor activity of a newly developed monoclonal antibody against ROR1 in ovarian cancer cells." Oncotarget vol. 8,55 (2017): 94210-94222. doi: https://doi.org/10.18632/oncotarget.21618
Yin Z, Gao M, Chu S, Su Y, Ye C, Wang Y, Pan Z, Wang Z, Zhang H, Tong H, Zhu J. Antitumor activity of a newly developed monoclonal antibody against ROR1 in ovarian cancer cells. Oncotarget. 2017 Oct 07;8(55):94210-94222. doi: 10.18632/oncotarget.21618. eCollection 2017 Nov 07. PMID: 29212222; PMCID: PMC5706868.
Copy Download .nbib Format: NLM
The killing effect of novel bi-specific Trop2/PD-L1 CAR-T cell targeted gastric cancer.

American journal of cancer research

Zhao W, Jia L, Zhang M, Huang X, Qian P, Tang Q, Zhu J, Feng Z.
PMID: 31497363
Am J Cancer Res. 2019 Aug 01;9(8):1846-1856. eCollection 2019.

Due to their high heterogeneity and complex tumor microenvironment, the treatment of solid tumors by CAR-T cell technology is limited. This study developed bi-specific Trop2/PD-L1 specific third-generation CAR-T cells by lentiviral infection. The specific killing ability of the bi-specific...

Cite
Zhao W, Jia L, Zhang M, et al. The killing effect of novel bi-specific Trop2/PD-L1 CAR-T cell targeted gastric cancer. Am J Cancer Res. 2019;9(8):1846-1856
Zhao, W., Jia, L., Zhang, M., Huang, X., Qian, P., Tang, Q., Zhu, J., & Feng, Z. (2019). The killing effect of novel bi-specific Trop2/PD-L1 CAR-T cell targeted gastric cancer. American journal of cancer research, 9(8), 1846-1856.
Zhao, Wei, et al. "The killing effect of novel bi-specific Trop2/PD-L1 CAR-T cell targeted gastric cancer." American journal of cancer research vol. 9,8 (2019): 1846-1856.
Zhao W, Jia L, Zhang M, Huang X, Qian P, Tang Q, Zhu J, Feng Z. The killing effect of novel bi-specific Trop2/PD-L1 CAR-T cell targeted gastric cancer. Am J Cancer Res. 2019 Aug 01;9(8):1846-1856. eCollection 2019. PMID: 31497363; PMCID: PMC6726977.
Copy Download .nbib Format: NLM
Opening up to open access.

BioTechniques

[No authors listed]
PMID: 30987441
Biotechniques. 2019 Apr;66(4):107. doi: 10.2144/btn-2019-0028.

No abstract available.

Cite
Opening up to open access. Biotechniques. 2019;66(4):107doi: 10.2144/btn-2019-0028.
(2019). Opening up to open access. BioTechniques, 66(4), 107. https://doi.org/10.2144/btn-2019-0028
"Opening up to open access." BioTechniques vol. 66,4 (2019): 107. doi: https://doi.org/10.2144/btn-2019-0028
Opening up to open access. Biotechniques. 2019 Apr;66(4):107. doi: 10.2144/btn-2019-0028. PMID: 30987441.
Copy Download .nbib Format: NLM
Simple, inexpensive and RNase-free purification of plasmid DNA by fractional precipitation with isopropanol.

BioTechniques

Paalme V, Speek M.
PMID: 34392702
Biotechniques. 2021 Sep;71(3):490-494. doi: 10.2144/btn-2021-0018. Epub 2021 Aug 16.

We present a modified alkaline lysis method for purification of plasmid DNA (pDNA) from bacterial extract using fractional precipitation with isopropanol (FPI). This method includes two successive precipitations with 0.33 and 0.36 volumes of isopropanol and separates pDNA from...

Cite
Paalme V, Speek M. Simple, inexpensive and RNase-free purification of plasmid DNA by fractional precipitation with isopropanol. Biotechniques. 2021;71(3):490-494doi: 10.2144/btn-2021-0018.
Paalme, V., & Speek, M. (2021). Simple, inexpensive and RNase-free purification of plasmid DNA by fractional precipitation with isopropanol. BioTechniques, 71(3), 490-494. https://doi.org/10.2144/btn-2021-0018
Paalme, Viiu, and Speek, Mart. "Simple, inexpensive and RNase-free purification of plasmid DNA by fractional precipitation with isopropanol." BioTechniques vol. 71,3 (2021): 490-494. doi: https://doi.org/10.2144/btn-2021-0018
Paalme V, Speek M. Simple, inexpensive and RNase-free purification of plasmid DNA by fractional precipitation with isopropanol. Biotechniques. 2021 Sep;71(3):490-494. doi: 10.2144/btn-2021-0018. Epub 2021 Aug 16. PMID: 34392702.
Copy Download .nbib Format: NLM
Comparative Analysis of Blood-Derived Endothelial Cells for Designing Next-Generation Personalized Organ-on-Chips.

Journal of the American Heart Association

Mathur T, Tronolone JJ, Jain A.
PMID: 34743553
J Am Heart Assoc. 2021 Nov 16;10(22):e022795. doi: 10.1161/JAHA.121.022795. Epub 2021 Nov 06.

Background Organ-on-chip technology has accelerated in vitro preclinical research of the vascular system, and a key strength of this platform is its promise to impact personalized medicine by providing a primary human cell-culture environment where endothelial cells are directly...

Cite
Mathur T, Tronolone JJ, Jain A. Comparative Analysis of Blood-Derived Endothelial Cells for Designing Next-Generation Personalized Organ-on-Chips. J Am Heart Assoc. 2021;10(22):e022795doi: 10.1161/JAHA.121.022795.
Mathur, T., Tronolone, J. J., & Jain, A. (2021). Comparative Analysis of Blood-Derived Endothelial Cells for Designing Next-Generation Personalized Organ-on-Chips. Journal of the American Heart Association, 10(22), e022795. https://doi.org/10.1161/JAHA.121.022795
Mathur, Tanmay, et al. "Comparative Analysis of Blood-Derived Endothelial Cells for Designing Next-Generation Personalized Organ-on-Chips." Journal of the American Heart Association vol. 10,22 (2021): e022795. doi: https://doi.org/10.1161/JAHA.121.022795
Mathur T, Tronolone JJ, Jain A. Comparative Analysis of Blood-Derived Endothelial Cells for Designing Next-Generation Personalized Organ-on-Chips. J Am Heart Assoc. 2021 Nov 16;10(22):e022795. doi: 10.1161/JAHA.121.022795. Epub 2021 Nov 06. PMID: 34743553; PMCID: PMC8751908.
Copy Download .nbib Format: NLM
High-yield expression of periplasmic single-chain variable fragments by solid .

BioTechniques

Hanyu Y, Kato M.
PMID: 34841891
Biotechniques. 2022 Jan;72(1):29-32. doi: 10.2144/btn-2021-0093. Epub 2021 Nov 29.

High-yield expression of quality antibody fragments is indispensable for research and diagnosis. Most recombinant antibody fragments are expressed in

Cite
Hanyu Y, Kato M. High-yield expression of periplasmic single-chain variable fragments by solid . Biotechniques. 2021;72(1):29-32doi: 10.2144/btn-2021-0093.
Hanyu, Y., & Kato, M. (2022). High-yield expression of periplasmic single-chain variable fragments by solid . BioTechniques, 72(1), 29-32. https://doi.org/10.2144/btn-2021-0093
Hanyu, Yoshiro, and Kato, Mieko. "High-yield expression of periplasmic single-chain variable fragments by solid ." BioTechniques vol. 72,1 (2022): 29-32. doi: https://doi.org/10.2144/btn-2021-0093
Hanyu Y, Kato M. High-yield expression of periplasmic single-chain variable fragments by solid . Biotechniques. 2022 Jan;72(1):29-32. doi: 10.2144/btn-2021-0093. Epub 2021 Nov 29. PMID: 34841891.
Copy Download .nbib Format: NLM
Inside the brain of a killer: the ethics of neuroimaging in a criminal conviction.

BioTechniques

Straiton J, Lake F.
PMID: 33567884
Biotechniques. 2021 Feb;70(2):69-71. doi: 10.2144/btn-2020-0171. Epub 2021 Feb 11.

With neuroimaging techniques being taken out of the lab and into the court, we ask whether brain scans can - or should - be used to explain a criminal act.

Cite
Straiton J, Lake F. Inside the brain of a killer: the ethics of neuroimaging in a criminal conviction. Biotechniques. 2021;70(2):69-71doi: 10.2144/btn-2020-0171.
Straiton, J., & Lake, F. (2021). Inside the brain of a killer: the ethics of neuroimaging in a criminal conviction. BioTechniques, 70(2), 69-71. https://doi.org/10.2144/btn-2020-0171
Straiton, Jenny, and Lake, Francesca. "Inside the brain of a killer: the ethics of neuroimaging in a criminal conviction." BioTechniques vol. 70,2 (2021): 69-71. doi: https://doi.org/10.2144/btn-2020-0171
Straiton J, Lake F. Inside the brain of a killer: the ethics of neuroimaging in a criminal conviction. Biotechniques. 2021 Feb;70(2):69-71. doi: 10.2144/btn-2020-0171. Epub 2021 Feb 11. PMID: 33567884.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 203 entries