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Showing 1 to 12 of 302 entries
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Role of flow cytometry in multiple myeloma and the prognostic significance of CD87 (uPAR) expression.

Turkish journal of haematology : official journal of Turkish Society of Haematology

Albayrak M, Şahin Balçık Ö, Dağdaş S, Yılmaz M, Ceran F, Yokuş O, Özet G.
PMID: 27263603
Turk J Haematol. 2010 Sep 05;27(3):182-9. doi: 10.5152/tjh.2010.26.

OBJECTIVE: The plasminogen activator system consists of the serine protease urokinase plasminogen activator (uPA), two endogenous inhibitors of PAI-1 (plasminogen activator inhibitor-1) as well as the PAI-2 and uPA receptor (uPAR or CD87). The aim of this study was...

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Albayrak M, Şahin Balçık Ö, Dağdaş S, et al. Multipl miyelomda akım sitometrinin rolü ve CD87 (uPAR) ekspresyonunun prognostik önemi. Role of flow cytometry in multiple myeloma and the prognostic significance of CD87 (uPAR) expression. Turk J Haematol. 2010;27(3):182-9doi: 10.5152/tjh.2010.26.
Albayrak, M., Şahin Balçık, �. �., Dağdaş, S., Yılmaz, M., Ceran, F., Yokuş, O., & Özet, G. (2010). Multipl miyelomda akım sitometrinin rolü ve CD87 (uPAR) ekspresyonunun prognostik önemi. Role of flow cytometry in multiple myeloma and the prognostic significance of CD87 (uPAR) expression. Turkish journal of haematology : official journal of Turkish Society of Haematology, 27(3), 182-9. https://doi.org/10.5152/tjh.2010.26
Albayrak, Murat, et al. "Multipl miyelomda akım sitometrinin rolü ve CD87 (uPAR) ekspresyonunun prognostik önemi." Role of flow cytometry in multiple myeloma and the prognostic significance of CD87 (uPAR) expression. Turkish journal of haematology : official journal of Turkish Society of Haematology vol. 27,3 (2010): 182-9. doi: https://doi.org/10.5152/tjh.2010.26
Albayrak M, Şahin Balçık Ö, Dağdaş S, Yılmaz M, Ceran F, Yokuş O, Özet G. Multipl miyelomda akım sitometrinin rolü ve CD87 (uPAR) ekspresyonunun prognostik önemi. Role of flow cytometry in multiple myeloma and the prognostic significance of CD87 (uPAR) expression. Turk J Haematol. 2010 Sep 05;27(3):182-9. doi: 10.5152/tjh.2010.26. PMID: 27263603.
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Quantitative testing of the methodology for genome size estimation in plants using flow cytometry: a case study of the Primulina genus.

Frontiers in plant science

Wang J, Liu J, Kang M.
PMID: 26042140
Front Plant Sci. 2015 May 19;6:354. doi: 10.3389/fpls.2015.00354. eCollection 2015.

Flow cytometry (FCM) is a commonly used method for estimating genome size in many organisms. The use of FCM in plants is influenced by endogenous fluorescence inhibitors and may cause an inaccurate estimation of genome size; thus, falsifying the...

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Wang J, Liu J, Kang M. Quantitative testing of the methodology for genome size estimation in plants using flow cytometry: a case study of the Primulina genus. Front Plant Sci. 2015;6:354doi: 10.3389/fpls.2015.00354.
Wang, J., Liu, J., & Kang, M. (2015). Quantitative testing of the methodology for genome size estimation in plants using flow cytometry: a case study of the Primulina genus. Frontiers in plant science, 6354. https://doi.org/10.3389/fpls.2015.00354
Wang, Jing, et al. "Quantitative testing of the methodology for genome size estimation in plants using flow cytometry: a case study of the Primulina genus." Frontiers in plant science vol. 6 (2015): 354. doi: https://doi.org/10.3389/fpls.2015.00354
Wang J, Liu J, Kang M. Quantitative testing of the methodology for genome size estimation in plants using flow cytometry: a case study of the Primulina genus. Front Plant Sci. 2015 May 19;6:354. doi: 10.3389/fpls.2015.00354. eCollection 2015. PMID: 26042140; PMCID: PMC4436564.
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Analysis of subsets of B cells, Breg, CD4Treg and CD8Treg cells in adult patients with primary selective IgM deficiency.

American journal of clinical and experimental immunology

Louis AG, Agrawal S, Gupta S.
PMID: 27168952
Am J Clin Exp Immunol. 2016 Mar 23;5(1):21-32. eCollection 2016.

Primary selective IgM deficiency (SIGMD) is a rare and recently IUIS-recognized primary immunodeficiency disease with increased susceptibility to infections, allergy, and autoimmune diseases. The pathogenesis of selective IgM remains unclear. The objective of the study was to understand the...

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Louis AG, Agrawal S, Gupta S. Analysis of subsets of B cells, Breg, CD4Treg and CD8Treg cells in adult patients with primary selective IgM deficiency. Am J Clin Exp Immunol. 2016;5(1):21-32
Louis, A. G., Agrawal, S., & Gupta, S. (2016). Analysis of subsets of B cells, Breg, CD4Treg and CD8Treg cells in adult patients with primary selective IgM deficiency. American journal of clinical and experimental immunology, 5(1), 21-32.
Louis, Ankmalika Gupta, et al. "Analysis of subsets of B cells, Breg, CD4Treg and CD8Treg cells in adult patients with primary selective IgM deficiency." American journal of clinical and experimental immunology vol. 5,1 (2016): 21-32.
Louis AG, Agrawal S, Gupta S. Analysis of subsets of B cells, Breg, CD4Treg and CD8Treg cells in adult patients with primary selective IgM deficiency. Am J Clin Exp Immunol. 2016 Mar 23;5(1):21-32. eCollection 2016. PMID: 27168952; PMCID: PMC4858603.
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Flow cytometry: a rapid and robust adjuvant technique for pathological diagnosis.

Turkish journal of haematology : official journal of Turkish Society of Haematology

Jain M, Handoo A, Choudhary DR, Bhasin A.
PMID: 24744630
Turk J Haematol. 2012 Mar;29(1):82-4. doi: 10.5505/tjh.2012.62533. Epub 2012 Mar 05.

No abstract available.

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Jain M, Handoo A, Choudhary DR, et al. Flow cytometry: a rapid and robust adjuvant technique for pathological diagnosis. Turk J Haematol. 2012;29(1):82-4doi: 10.5505/tjh.2012.62533.
Jain, M., Handoo, A., Choudhary, D. R., & Bhasin, A. (2012). Flow cytometry: a rapid and robust adjuvant technique for pathological diagnosis. Turkish journal of haematology : official journal of Turkish Society of Haematology, 29(1), 82-4. https://doi.org/10.5505/tjh.2012.62533
Jain, Monica, et al. "Flow cytometry: a rapid and robust adjuvant technique for pathological diagnosis." Turkish journal of haematology : official journal of Turkish Society of Haematology vol. 29,1 (2012): 82-4. doi: https://doi.org/10.5505/tjh.2012.62533
Jain M, Handoo A, Choudhary DR, Bhasin A. Flow cytometry: a rapid and robust adjuvant technique for pathological diagnosis. Turk J Haematol. 2012 Mar;29(1):82-4. doi: 10.5505/tjh.2012.62533. Epub 2012 Mar 05. PMID: 24744630; PMCID: PMC3986775.
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An Unusual Cause of Epistaxis: Paranasal Sinus Myeloid Sarcoma.

Case reports in hematology

Dewan K, Baird JH, Shires CB.
PMID: 30891319
Case Rep Hematol. 2019 Feb 12;2019:1312630. doi: 10.1155/2019/1312630. eCollection 2019.

We report a case of a 65-year-old female who presented with right-sided headaches, blurring of vision in the right eye, cold-induced epistaxis, and facial numbness in the trigeminal nerve distribution. Laboratory studies revealed a significant number of myeloblasts on...

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Dewan K, Baird JH, Shires CB. An Unusual Cause of Epistaxis: Paranasal Sinus Myeloid Sarcoma. Case Rep Hematol. 2019;2019:1312630doi: 10.1155/2019/1312630.
Dewan, K., Baird, J. H., & Shires, C. B. (2019). An Unusual Cause of Epistaxis: Paranasal Sinus Myeloid Sarcoma. Case reports in hematology, 20191312630. https://doi.org/10.1155/2019/1312630
Dewan, Karuna, et al. "An Unusual Cause of Epistaxis: Paranasal Sinus Myeloid Sarcoma." Case reports in hematology vol. 2019 (2019): 1312630. doi: https://doi.org/10.1155/2019/1312630
Dewan K, Baird JH, Shires CB. An Unusual Cause of Epistaxis: Paranasal Sinus Myeloid Sarcoma. Case Rep Hematol. 2019 Feb 12;2019:1312630. doi: 10.1155/2019/1312630. eCollection 2019. PMID: 30891319; PMCID: PMC6390259.
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Numerical Model of Streaming DEP for Stem Cell Sorting.

Micromachines

Natu R, Martinez-Duarte R.
PMID: 30404388
Micromachines (Basel). 2016 Nov 30;7(12). doi: 10.3390/mi7120217.

Neural stem cells are of special interest due to their potential in neurogenesis to treat spinal cord injuries and other nervous disorders. Flow cytometry, a common technique used for cell sorting, is limited due to the lack of antigens...

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Natu R, Martinez-Duarte R. Numerical Model of Streaming DEP for Stem Cell Sorting. Micromachines (Basel). 2016;7(12)doi: 10.3390/mi7120217.
Natu, R., & Martinez-Duarte, R. (2016). Numerical Model of Streaming DEP for Stem Cell Sorting. Micromachines, 7(12), . https://doi.org/10.3390/mi7120217
Natu, Rucha, and Martinez-Duarte, Rodrigo. "Numerical Model of Streaming DEP for Stem Cell Sorting." Micromachines vol. 7,12 (2016). doi: https://doi.org/10.3390/mi7120217
Natu R, Martinez-Duarte R. Numerical Model of Streaming DEP for Stem Cell Sorting. Micromachines (Basel). 2016 Nov 30;7(12). doi: 10.3390/mi7120217. PMID: 30404388; PMCID: PMC6190341.
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Differences in Intercellular Communication During Clinical Relapse and Gadolinium-Enhanced MRI in Patients With Relapsing Remitting Multiple Sclerosis: A Study of the Composition of Extracellular Vesicles in Cerebrospinal Fluid.

Frontiers in cellular neuroscience

Geraci F, Ragonese P, Barreca MM, Aliotta E, Mazzola MA, Realmuto S, Vazzoler G, Savettieri G, Sconzo G, Salemi G.
PMID: 30498433
Front Cell Neurosci. 2018 Nov 15;12:418. doi: 10.3389/fncel.2018.00418. eCollection 2018.

This study was designed based on the hypothesis that changes in both the levels and surface marker expression of extracellular vesicles (EVs) isolated from the cerebrospinal fluid (CSF) may be associated with the clinical form, disease activity, and severity...

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Geraci F, Ragonese P, Barreca MM, et al. Differences in Intercellular Communication During Clinical Relapse and Gadolinium-Enhanced MRI in Patients With Relapsing Remitting Multiple Sclerosis: A Study of the Composition of Extracellular Vesicles in Cerebrospinal Fluid. Front Cell Neurosci. 2018;12:418doi: 10.3389/fncel.2018.00418.
Geraci, F., Ragonese, P., Barreca, M. M., Aliotta, E., Mazzola, M. A., Realmuto, S., Vazzoler, G., Savettieri, G., Sconzo, G., & Salemi, G. (2018). Differences in Intercellular Communication During Clinical Relapse and Gadolinium-Enhanced MRI in Patients With Relapsing Remitting Multiple Sclerosis: A Study of the Composition of Extracellular Vesicles in Cerebrospinal Fluid. Frontiers in cellular neuroscience, 12418. https://doi.org/10.3389/fncel.2018.00418
Geraci, Fabiana, et al. "Differences in Intercellular Communication During Clinical Relapse and Gadolinium-Enhanced MRI in Patients With Relapsing Remitting Multiple Sclerosis: A Study of the Composition of Extracellular Vesicles in Cerebrospinal Fluid." Frontiers in cellular neuroscience vol. 12 (2018): 418. doi: https://doi.org/10.3389/fncel.2018.00418
Geraci F, Ragonese P, Barreca MM, Aliotta E, Mazzola MA, Realmuto S, Vazzoler G, Savettieri G, Sconzo G, Salemi G. Differences in Intercellular Communication During Clinical Relapse and Gadolinium-Enhanced MRI in Patients With Relapsing Remitting Multiple Sclerosis: A Study of the Composition of Extracellular Vesicles in Cerebrospinal Fluid. Front Cell Neurosci. 2018 Nov 15;12:418. doi: 10.3389/fncel.2018.00418. eCollection 2018. PMID: 30498433; PMCID: PMC6249419.
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Something old, something new, something borrowed, something green.

Cytometry. Part A : the journal of the International Society for Analytical Cytology

Polancec D, Zenic L.
PMID: 28494117
Cytometry A. 2017 Jul;91(7):659-661. doi: 10.1002/cyto.a.23125. Epub 2017 May 11.

No abstract available.

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Polancec D, Zenic L. Something old, something new, something borrowed, something green. Cytometry A. 2017;91(7):659-661doi: 10.1002/cyto.a.23125.
Polancec, D., & Zenic, L. (2017). Something old, something new, something borrowed, something green. Cytometry. Part A : the journal of the International Society for Analytical Cytology, 91(7), 659-661. https://doi.org/10.1002/cyto.a.23125
Polancec, Denis, and Zenic, Lucija. "Something old, something new, something borrowed, something green." Cytometry. Part A : the journal of the International Society for Analytical Cytology vol. 91,7 (2017): 659-661. doi: https://doi.org/10.1002/cyto.a.23125
Polancec D, Zenic L. Something old, something new, something borrowed, something green. Cytometry A. 2017 Jul;91(7):659-661. doi: 10.1002/cyto.a.23125. Epub 2017 May 11. PMID: 28494117.
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MicroRNA-433 targets AKT3 and inhibits cell proliferation and viability in breast cancer.

Oncology letters

Hu X, Wang J, He W, Zhao P, Ye C.
PMID: 29556282
Oncol Lett. 2018 Mar;15(3):3998-4004. doi: 10.3892/ol.2018.7803. Epub 2018 Jan 16.

Breast cancer is the most frequently diagnosed malignancy in women. However, the molecular mechanisms underlying breast cancer pathogenesis are not fully understood. The present study examined the role of miR-433 in breast cancer and investigated its underlying molecular mechanisms...

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Hu X, Wang J, He W, et al. MicroRNA-433 targets AKT3 and inhibits cell proliferation and viability in breast cancer. Oncol Lett. 2018;15(3):3998-4004doi: 10.3892/ol.2018.7803.
Hu, X., Wang, J., He, W., Zhao, P., & Ye, C. (2018). MicroRNA-433 targets AKT3 and inhibits cell proliferation and viability in breast cancer. Oncology letters, 15(3), 3998-4004. https://doi.org/10.3892/ol.2018.7803
Hu, Xiaolei, et al. "MicroRNA-433 targets AKT3 and inhibits cell proliferation and viability in breast cancer." Oncology letters vol. 15,3 (2018): 3998-4004. doi: https://doi.org/10.3892/ol.2018.7803
Hu X, Wang J, He W, Zhao P, Ye C. MicroRNA-433 targets AKT3 and inhibits cell proliferation and viability in breast cancer. Oncol Lett. 2018 Mar;15(3):3998-4004. doi: 10.3892/ol.2018.7803. Epub 2018 Jan 16. PMID: 29556282; PMCID: PMC5844142.
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Analysis of procoagulant phosphatidylserine-exposing platelets by imaging flow cytometry.

Research and practice in thrombosis and haemostasis

Reddy EC, Wang H, Christensen H, McMillan-Ward E, Israels SJ, Bang KWA, Rand ML.
PMID: 30349893
Res Pract Thromb Haemost. 2018 Aug 23;2(4):736-750. doi: 10.1002/rth2.12144. eCollection 2018 Oct.

BACKGROUND: Upon platelet activation, a subpopulation of procoagulant platelets is formed, characterized by the exposure of the anionic aminophospholipid phosphatidylserine (PS) on the surface membrane.OBJECTIVE: To evaluate procoagulant PS-exposing platelets by imaging flow cytometry.METHODS: Platelet ultrastructure was examined by...

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Reddy EC, Wang H, Christensen H, et al. Analysis of procoagulant phosphatidylserine-exposing platelets by imaging flow cytometry. Res Pract Thromb Haemost. 2018;2(4):736-750doi: 10.1002/rth2.12144.
Reddy, E. C., Wang, H., Christensen, H., McMillan-Ward, E., Israels, S. J., Bang, K. W. A., & Rand, M. L. (2018). Analysis of procoagulant phosphatidylserine-exposing platelets by imaging flow cytometry. Research and practice in thrombosis and haemostasis, 2(4), 736-750. https://doi.org/10.1002/rth2.12144
Reddy, Emily C, et al. "Analysis of procoagulant phosphatidylserine-exposing platelets by imaging flow cytometry." Research and practice in thrombosis and haemostasis vol. 2,4 (2018): 736-750. doi: https://doi.org/10.1002/rth2.12144
Reddy EC, Wang H, Christensen H, McMillan-Ward E, Israels SJ, Bang KWA, Rand ML. Analysis of procoagulant phosphatidylserine-exposing platelets by imaging flow cytometry. Res Pract Thromb Haemost. 2018 Aug 23;2(4):736-750. doi: 10.1002/rth2.12144. eCollection 2018 Oct. PMID: 30349893; PMCID: PMC6178738.
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New Year Note 2019: Welcome to the Year of the Pig.

Cytometry. Part A : the journal of the International Society for Analytical Cytology

Tárnok A.
PMID: 30633458
Cytometry A. 2019 Jan;95(1):9. doi: 10.1002/cyto.a.23714.

No abstract available.

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Tárnok A. New Year Note 2019: Welcome to the Year of the Pig. Cytometry A. 2019;95(1):9doi: 10.1002/cyto.a.23714.
Tárnok, A. (2019). New Year Note 2019: Welcome to the Year of the Pig. Cytometry. Part A : the journal of the International Society for Analytical Cytology, 95(1), 9. https://doi.org/10.1002/cyto.a.23714
Tárnok, Attila. "New Year Note 2019: Welcome to the Year of the Pig." Cytometry. Part A : the journal of the International Society for Analytical Cytology vol. 95,1 (2019): 9. doi: https://doi.org/10.1002/cyto.a.23714
Tárnok A. New Year Note 2019: Welcome to the Year of the Pig. Cytometry A. 2019 Jan;95(1):9. doi: 10.1002/cyto.a.23714. PMID: 30633458.
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Flow based single cell analysis of the immune landscape distinguishes Barrett's esophagus from adjacent normal tissue.

Oncotarget

Sen M, Hahn F, Black TA, DeMarshall M, Porter W, Snowden E, Yee SS, Tong F, Ferguson M, Fleshman EN, Nakagawa H, Falk GW, Ginsberg GG, Kochman ML, Blaesius R, Rustgi AK, Carpenter EL.
PMID: 31217895
Oncotarget. 2019 Jun 04;10(38):3592-3604. doi: 10.18632/oncotarget.26911. eCollection 2019 Jun 04.

Barrett's esophagus (BE) is metaplasia of the squamous epithelium to a specialized columnar epithelium. BE progresses through low- and high-grade dysplasia before developing into esophageal adenocarcinoma. The BE microenvironment is not well defined. We compare 12 human clinical BE...

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Sen M, Hahn F, Black TA, et al. Flow based single cell analysis of the immune landscape distinguishes Barrett's esophagus from adjacent normal tissue. Oncotarget. 2019;10(38):3592-3604doi: 10.18632/oncotarget.26911.
Sen, M., Hahn, F., Black, T. A., DeMarshall, M., Porter, W., Snowden, E., Yee, S. S., Tong, F., Ferguson, M., Fleshman, E. N., Nakagawa, H., Falk, G. W., Ginsberg, G. G., Kochman, M. L., Blaesius, R., Rustgi, A. K., & Carpenter, E. L. (2019). Flow based single cell analysis of the immune landscape distinguishes Barrett's esophagus from adjacent normal tissue. Oncotarget, 10(38), 3592-3604. https://doi.org/10.18632/oncotarget.26911
Sen, Moen, et al. "Flow based single cell analysis of the immune landscape distinguishes Barrett's esophagus from adjacent normal tissue." Oncotarget vol. 10,38 (2019): 3592-3604. doi: https://doi.org/10.18632/oncotarget.26911
Sen M, Hahn F, Black TA, DeMarshall M, Porter W, Snowden E, Yee SS, Tong F, Ferguson M, Fleshman EN, Nakagawa H, Falk GW, Ginsberg GG, Kochman ML, Blaesius R, Rustgi AK, Carpenter EL. Flow based single cell analysis of the immune landscape distinguishes Barrett's esophagus from adjacent normal tissue. Oncotarget. 2019 Jun 04;10(38):3592-3604. doi: 10.18632/oncotarget.26911. eCollection 2019 Jun 04. PMID: 31217895; PMCID: PMC6557213.
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Showing 1 to 12 of 302 entries