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An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature.

Clinical case reports

Õunap K, Pajusalu S, Zilina O, Reimand T, Žordania R.
PMID: 27525095
Clin Case Rep. 2016 Jul 22;4(8):824-30. doi: 10.1002/ccr3.632. eCollection 2016 Aug.

3q26.33-3q27.2 microdeletion can be classified as a clinical entity characterized by intrauterine growth retardation, feeding problems in infancy, short stature, intellectual disability, hypotonia, dysmorphic facial features (medially sparse eyebrows, narrow horizontal palpebral fissures, epicanthal folds, flat nasal bridge and...

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Õunap K, Pajusalu S, Zilina O, et al. An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature. Clin Case Rep. 2016;4(8):824-30doi: 10.1002/ccr3.632.
Õunap, K., Pajusalu, S., Zilina, O., Reimand, T., & Žordania, R. (2016). An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature. Clinical case reports, 4(8), 824-30. https://doi.org/10.1002/ccr3.632
Õunap, Katrin, et al. "An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature." Clinical case reports vol. 4,8 (2016): 824-30. doi: https://doi.org/10.1002/ccr3.632
Õunap K, Pajusalu S, Zilina O, Reimand T, Žordania R. An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature. Clin Case Rep. 2016 Jul 22;4(8):824-30. doi: 10.1002/ccr3.632. eCollection 2016 Aug. PMID: 27525095; PMCID: PMC4974439.
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The Biochemical Cascades of the Human Pancreatic .

Journal of bioanalysis & biomedicine

Kim JW, Luo JZ, Luo L.
PMID: 28503255
J Bioanal Biomed. 2015 Dec;7(6). doi: 10.4172/1948-593X.1000e133. Epub 2015 Dec 11.

Diabetes mellitus is a disease that poses a burden to the health care system due to its prevalence and chronic nature. Understanding β cell pathophysiology may lead to future therapeutic options for diabetes mellitus type 1 and 2. MicroRNAs...

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Kim JW, Luo JZ, Luo L. The Biochemical Cascades of the Human Pancreatic . J Bioanal Biomed. 2015;7(6)doi: 10.4172/1948-593X.1000e133.
Kim, J. W., Luo, J. Z., & Luo, L. (2015). The Biochemical Cascades of the Human Pancreatic . Journal of bioanalysis & biomedicine, 7(6), . https://doi.org/10.4172/1948-593X.1000e133
Kim, Joseph W, et al. "The Biochemical Cascades of the Human Pancreatic ." Journal of bioanalysis & biomedicine vol. 7,6 (2015). doi: https://doi.org/10.4172/1948-593X.1000e133
Kim JW, Luo JZ, Luo L. The Biochemical Cascades of the Human Pancreatic . J Bioanal Biomed. 2015 Dec;7(6). doi: 10.4172/1948-593X.1000e133. Epub 2015 Dec 11. PMID: 28503255; PMCID: PMC5426857.
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Expansion size and presence of CCG/CTC/CGG sequence interruptions in the expanded CTG array are independently associated to hypermethylation at the DMPK locus in myotonic dystrophy type 1 (DM1).

Biochimica et biophysica acta

Santoro M, Fontana L, Masciullo M, Bianchi ML, Rossi S, Leoncini E, Novelli G, Botta A, Silvestri G.
PMID: 26391753
Biochim Biophys Acta. 2015 Dec;1852(12):2645-52. doi: 10.1016/j.bbadis.2015.09.007. Epub 2015 Sep 21.

No abstract available.

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Santoro M, Fontana L, Masciullo M, et al. Expansion size and presence of CCG/CTC/CGG sequence interruptions in the expanded CTG array are independently associated to hypermethylation at the DMPK locus in myotonic dystrophy type 1 (DM1). Biochim Biophys Acta. 2015;1852(12):2645-52doi: 10.1016/j.bbadis.2015.09.007.
Santoro, M., Fontana, L., Masciullo, M., Bianchi, M. L., Rossi, S., Leoncini, E., Novelli, G., Botta, A., & Silvestri, G. (2015). Expansion size and presence of CCG/CTC/CGG sequence interruptions in the expanded CTG array are independently associated to hypermethylation at the DMPK locus in myotonic dystrophy type 1 (DM1). Biochimica et biophysica acta, 1852(12), 2645-52. https://doi.org/10.1016/j.bbadis.2015.09.007
Santoro, Massimo, et al. "Expansion size and presence of CCG/CTC/CGG sequence interruptions in the expanded CTG array are independently associated to hypermethylation at the DMPK locus in myotonic dystrophy type 1 (DM1)." Biochimica et biophysica acta vol. 1852,12 (2015): 2645-52. doi: https://doi.org/10.1016/j.bbadis.2015.09.007
Santoro M, Fontana L, Masciullo M, Bianchi ML, Rossi S, Leoncini E, Novelli G, Botta A, Silvestri G. Expansion size and presence of CCG/CTC/CGG sequence interruptions in the expanded CTG array are independently associated to hypermethylation at the DMPK locus in myotonic dystrophy type 1 (DM1). Biochim Biophys Acta. 2015 Dec;1852(12):2645-52. doi: 10.1016/j.bbadis.2015.09.007. Epub 2015 Sep 21. PMID: 26391753.
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DBAASP v.2: an enhanced database of structure and antimicrobial/cytotoxic activity of natural and synthetic peptides.

Nucleic acids research

Pirtskhalava M, Gabrielian A, Cruz P, Griggs HL, Squires RB, Hurt DE, Grigolava M, Chubinidze M, Gogoladze G, Vishnepolsky B, Alekseyev V, Rosenthal A, Tartakovsky M.
PMID: 27060142
Nucleic Acids Res. 2016 Jul 27;44(13):6503. doi: 10.1093/nar/gkw243. Epub 2016 Apr 08.

No abstract available.

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Pirtskhalava M, Gabrielian A, Cruz P, et al. DBAASP v.2: an enhanced database of structure and antimicrobial/cytotoxic activity of natural and synthetic peptides. Nucleic Acids Res. 2016;44(13):6503doi: 10.1093/nar/gkw243.
Pirtskhalava, M., Gabrielian, A., Cruz, P., Griggs, H. L., Squires, R. B., Hurt, D. E., Grigolava, M., Chubinidze, M., Gogoladze, G., Vishnepolsky, B., Alekseyev, V., Rosenthal, A., & Tartakovsky, M. (2016). DBAASP v.2: an enhanced database of structure and antimicrobial/cytotoxic activity of natural and synthetic peptides. Nucleic acids research, 44(13), 6503. https://doi.org/10.1093/nar/gkw243
Pirtskhalava, Malak, et al. "DBAASP v.2: an enhanced database of structure and antimicrobial/cytotoxic activity of natural and synthetic peptides." Nucleic acids research vol. 44,13 (2016): 6503. doi: https://doi.org/10.1093/nar/gkw243
Pirtskhalava M, Gabrielian A, Cruz P, Griggs HL, Squires RB, Hurt DE, Grigolava M, Chubinidze M, Gogoladze G, Vishnepolsky B, Alekseyev V, Rosenthal A, Tartakovsky M. DBAASP v.2: an enhanced database of structure and antimicrobial/cytotoxic activity of natural and synthetic peptides. Nucleic Acids Res. 2016 Jul 27;44(13):6503. doi: 10.1093/nar/gkw243. Epub 2016 Apr 08. PMID: 27060142; PMCID: PMC4994862.
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Experimental factors affecting the robustness of DNA methylation analysis.

Scientific reports

Pharo HD, Honne H, Vedeld HM, Dahl C, Andresen K, Liestøl K, Jeanmougin M, Guldberg P, Lind GE.
PMID: 27671843
Sci Rep. 2016 Sep 27;6:33936. doi: 10.1038/srep33936.

Diverging methylation frequencies are often reported for the same locus in the same disease, underscoring the need for limiting technical variability in DNA methylation analyses. We have investigated seven likely sources of variability at different steps of bisulfite PCR-based...

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Pharo HD, Honne H, Vedeld HM, et al. Experimental factors affecting the robustness of DNA methylation analysis. Sci Rep. 2016;6:33936doi: 10.1038/srep33936.
Pharo, H. D., Honne, H., Vedeld, H. M., Dahl, C., Andresen, K., Liestøl, K., Jeanmougin, M., Guldberg, P., & Lind, G. E. (2016). Experimental factors affecting the robustness of DNA methylation analysis. Scientific reports, 633936. https://doi.org/10.1038/srep33936
Pharo, Heidi D, et al. "Experimental factors affecting the robustness of DNA methylation analysis." Scientific reports vol. 6 (2016): 33936. doi: https://doi.org/10.1038/srep33936
Pharo HD, Honne H, Vedeld HM, Dahl C, Andresen K, Liestøl K, Jeanmougin M, Guldberg P, Lind GE. Experimental factors affecting the robustness of DNA methylation analysis. Sci Rep. 2016 Sep 27;6:33936. doi: 10.1038/srep33936. PMID: 27671843; PMCID: PMC5037394.
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T cell progenitor therapy-facilitated thymopoiesis depends upon thymic input and continued thymic microenvironment interaction.

JCI insight

Smith MJ, Reichenbach DK, Parker SL, Riddle MJ, Mitchell J, Osum KC, Mohtashami M, Stefanski HE, Fife BT, Bhandoola A, Hogquist KA, Holländer GA, Zúñiga-Pflücker JC, Tolar J, Blazar BR.
PMID: 28515359
JCI Insight. 2017 May 18;2(10). doi: 10.1172/jci.insight.92056. eCollection 2017 May 18.

Infusion of in vitro-derived T cell progenitor (proT) therapy with hematopoietic stem cell transplant aids the recovery of the thymus damaged by total body irradiation. To understand the interaction between proTs and the thymic microenvironment, WT mice were lethally...

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Smith MJ, Reichenbach DK, Parker SL, et al. T cell progenitor therapy-facilitated thymopoiesis depends upon thymic input and continued thymic microenvironment interaction. JCI Insight. 2017;2(10)doi: 10.1172/jci.insight.92056.
Smith, M. J., Reichenbach, D. K., Parker, S. L., Riddle, M. J., Mitchell, J., Osum, K. C., Mohtashami, M., Stefanski, H. E., Fife, B. T., Bhandoola, A., Hogquist, K. A., Holländer, G. A., Zúñiga-Pflücker, J. C., Tolar, J., & Blazar, B. R. (2017). T cell progenitor therapy-facilitated thymopoiesis depends upon thymic input and continued thymic microenvironment interaction. JCI insight, 2(10), . https://doi.org/10.1172/jci.insight.92056
Smith, Michelle J, et al. "T cell progenitor therapy-facilitated thymopoiesis depends upon thymic input and continued thymic microenvironment interaction." JCI insight vol. 2,10 (2017). doi: https://doi.org/10.1172/jci.insight.92056
Smith MJ, Reichenbach DK, Parker SL, Riddle MJ, Mitchell J, Osum KC, Mohtashami M, Stefanski HE, Fife BT, Bhandoola A, Hogquist KA, Holländer GA, Zúñiga-Pflücker JC, Tolar J, Blazar BR. T cell progenitor therapy-facilitated thymopoiesis depends upon thymic input and continued thymic microenvironment interaction. JCI Insight. 2017 May 18;2(10). doi: 10.1172/jci.insight.92056. eCollection 2017 May 18. PMID: 28515359; PMCID: PMC5436538.
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Medicinal Product Regulation: Portugal's Framework.

Clinical therapeutics

Herdeiro MT, Bastos PA, Rodrigues AT, Roque F.
PMID: 27673656
Clin Ther. 2016 Oct 06;38(10):e3-e4. doi: 10.1016/j.clinthera.2016.07.021.

No abstract available.

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Herdeiro MT, Bastos PA, Rodrigues AT, et al. Medicinal Product Regulation: Portugal's Framework. Clin Ther. 2016;38(10):e3-e4doi: 10.1016/j.clinthera.2016.07.021.
Herdeiro, M. T., Bastos, P. A., Rodrigues, A. T., & Roque, F. (2016). Medicinal Product Regulation: Portugal's Framework. Clinical therapeutics, 38(10), e3-e4. https://doi.org/10.1016/j.clinthera.2016.07.021
Herdeiro, M T, et al. "Medicinal Product Regulation: Portugal's Framework." Clinical therapeutics vol. 38,10 (2016): e3-e4. doi: https://doi.org/10.1016/j.clinthera.2016.07.021
Herdeiro MT, Bastos PA, Rodrigues AT, Roque F. Medicinal Product Regulation: Portugal's Framework. Clin Ther. 2016 Oct 06;38(10):e3-e4. doi: 10.1016/j.clinthera.2016.07.021. PMID: 27673656.
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De novo transcriptome assembly databases for the butterfly orchid Phalaenopsis equestris.

Scientific data

Niu SC, Xu Q, Zhang GQ, Zhang YQ, Tsai WC, Hsu JL, Liang CK, Luo YB, Liu ZJ.
PMID: 27673730
Sci Data. 2016 Sep 27;3:160083. doi: 10.1038/sdata.2016.83.

Orchids are renowned for their spectacular flowers and ecological adaptations. After the sequencing of the genome of the tropical epiphytic orchid Phalaenopsis equestris, we combined Illumina HiSeq2000 for RNA-Seq and Trinity for de novo assembly to characterize the transcriptomes...

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Niu SC, Xu Q, Zhang GQ, et al. De novo transcriptome assembly databases for the butterfly orchid Phalaenopsis equestris. Sci Data. 2016;3:160083doi: 10.1038/sdata.2016.83.
Niu, S. C., Xu, Q., Zhang, G. Q., Zhang, Y. Q., Tsai, W. C., Hsu, J. L., Liang, C. K., Luo, Y. B., & Liu, Z. J. (2016). De novo transcriptome assembly databases for the butterfly orchid Phalaenopsis equestris. Scientific data, 3160083. https://doi.org/10.1038/sdata.2016.83
Niu, Shan-Ce, et al. "De novo transcriptome assembly databases for the butterfly orchid Phalaenopsis equestris." Scientific data vol. 3 (2016): 160083. doi: https://doi.org/10.1038/sdata.2016.83
Niu SC, Xu Q, Zhang GQ, Zhang YQ, Tsai WC, Hsu JL, Liang CK, Luo YB, Liu ZJ. De novo transcriptome assembly databases for the butterfly orchid Phalaenopsis equestris. Sci Data. 2016 Sep 27;3:160083. doi: 10.1038/sdata.2016.83. PMID: 27673730; PMCID: PMC5037975.
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Correction for Gabai et al., "Heat Shock Transcription Factor Hsf1 Is Involved in Tumor Progression via Regulation of Hypoxia-Inducible Factor 1 and RNA-Binding Protein HuR".

Molecular and cellular biology

Gabai VL, Meng L, Kim G, Mills TA, Benjamin IJ, Sherman MY.
PMID: 28951485
Mol Cell Biol. 2017 Sep 26;37(20). doi: 10.1128/MCB.00415-17. Print 2017 Oct 15.

No abstract available.

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Gabai VL, Meng L, Kim G, et al. Correction for Gabai et al., "Heat Shock Transcription Factor Hsf1 Is Involved in Tumor Progression via Regulation of Hypoxia-Inducible Factor 1 and RNA-Binding Protein HuR". Mol Cell Biol. 2017;37(20)doi: 10.1128/MCB.00415-17.
Gabai, V. L., Meng, L., Kim, G., Mills, T. A., Benjamin, I. J., & Sherman, M. Y. (2017). Correction for Gabai et al., "Heat Shock Transcription Factor Hsf1 Is Involved in Tumor Progression via Regulation of Hypoxia-Inducible Factor 1 and RNA-Binding Protein HuR". Molecular and cellular biology, 37(20), . https://doi.org/10.1128/MCB.00415-17
Gabai, Vladimir L, et al. "Correction for Gabai et al., "Heat Shock Transcription Factor Hsf1 Is Involved in Tumor Progression via Regulation of Hypoxia-Inducible Factor 1 and RNA-Binding Protein HuR"." Molecular and cellular biology vol. 37,20 (2017). doi: https://doi.org/10.1128/MCB.00415-17
Gabai VL, Meng L, Kim G, Mills TA, Benjamin IJ, Sherman MY. Correction for Gabai et al., "Heat Shock Transcription Factor Hsf1 Is Involved in Tumor Progression via Regulation of Hypoxia-Inducible Factor 1 and RNA-Binding Protein HuR". Mol Cell Biol. 2017 Sep 26;37(20). doi: 10.1128/MCB.00415-17. Print 2017 Oct 15. PMID: 28951485; PMCID: PMC5615190.
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Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments.

Nature communications

Becker D, Kaczmarska Z, Arkona C, Schulz R, Tauber C, Wolber G, Hilgenfeld R, Coll M, Rademann J.
PMID: 27677239
Nat Commun. 2016 Sep 28;7:12761. doi: 10.1038/ncomms12761.

Small-molecule fragments binding to biomacromolecules can be starting points for the development of drugs, but are often difficult to detect due to low affinities. Here we present a strategy that identifies protein-binding fragments through their potential to induce the...

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Becker D, Kaczmarska Z, Arkona C, et al. Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments. Nat Commun. 2016;7:12761doi: 10.1038/ncomms12761.
Becker, D., Kaczmarska, Z., Arkona, C., Schulz, R., Tauber, C., Wolber, G., Hilgenfeld, R., Coll, M., & Rademann, J. (2016). Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments. Nature communications, 712761. https://doi.org/10.1038/ncomms12761
Becker, Daniel, et al. "Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments." Nature communications vol. 7 (2016): 12761. doi: https://doi.org/10.1038/ncomms12761
Becker D, Kaczmarska Z, Arkona C, Schulz R, Tauber C, Wolber G, Hilgenfeld R, Coll M, Rademann J. Irreversible inhibitors of the 3C protease of Coxsackie virus through templated assembly of protein-binding fragments. Nat Commun. 2016 Sep 28;7:12761. doi: 10.1038/ncomms12761. PMID: 27677239; PMCID: PMC5052702.
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Deficiency in Calcium-Binding Protein S100A4 Impairs the Adjuvant Action of Cholera Toxin.

Frontiers in immunology

Sun JB, Holmgren J, Larena M, Terrinoni M, Fang Y, Bresnick AR, Xiang Z.
PMID: 28951732
Front Immunol. 2017 Sep 11;8:1119. doi: 10.3389/fimmu.2017.01119. eCollection 2017.

The calcium-binding protein S100A4 has been described to promote pathological inflammation in experimental autoimmune and inflammatory disorders and in allergy and to contribute to antigen presentation and antibody response after parenteral immunization with an alum-adjuvanted antigen. In this study,...

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Sun JB, Holmgren J, Larena M, et al. Deficiency in Calcium-Binding Protein S100A4 Impairs the Adjuvant Action of Cholera Toxin. Front Immunol. 2017;8:1119doi: 10.3389/fimmu.2017.01119.
Sun, J. B., Holmgren, J., Larena, M., Terrinoni, M., Fang, Y., Bresnick, A. R., & Xiang, Z. (2017). Deficiency in Calcium-Binding Protein S100A4 Impairs the Adjuvant Action of Cholera Toxin. Frontiers in immunology, 81119. https://doi.org/10.3389/fimmu.2017.01119
Sun, Jia-Bin, et al. "Deficiency in Calcium-Binding Protein S100A4 Impairs the Adjuvant Action of Cholera Toxin." Frontiers in immunology vol. 8 (2017): 1119. doi: https://doi.org/10.3389/fimmu.2017.01119
Sun JB, Holmgren J, Larena M, Terrinoni M, Fang Y, Bresnick AR, Xiang Z. Deficiency in Calcium-Binding Protein S100A4 Impairs the Adjuvant Action of Cholera Toxin. Front Immunol. 2017 Sep 11;8:1119. doi: 10.3389/fimmu.2017.01119. eCollection 2017. PMID: 28951732; PMCID: PMC5600718.
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Single-cell SNP analyses and interpretations based on RNA-Seq data for colon cancer research.

Scientific reports

Chen J, Zhou Q, Wang Y, Ning K.
PMID: 27677461
Sci Rep. 2016 Sep 28;6:34420. doi: 10.1038/srep34420.

Single-cell sequencing is useful for illustrating the cellular heterogeneities inherent in many intricate biological systems, particularly in human cancer. However, owing to the difficulties in acquiring, amplifying and analyzing single-cell genetic material, obstacles remain for single-cell diversity assessments such...

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Chen J, Zhou Q, Wang Y, et al. Single-cell SNP analyses and interpretations based on RNA-Seq data for colon cancer research. Sci Rep. 2016;6:34420doi: 10.1038/srep34420.
Chen, J., Zhou, Q., Wang, Y., & Ning, K. (2016). Single-cell SNP analyses and interpretations based on RNA-Seq data for colon cancer research. Scientific reports, 634420. https://doi.org/10.1038/srep34420
Chen, Jiahuan, et al. "Single-cell SNP analyses and interpretations based on RNA-Seq data for colon cancer research." Scientific reports vol. 6 (2016): 34420. doi: https://doi.org/10.1038/srep34420
Chen J, Zhou Q, Wang Y, Ning K. Single-cell SNP analyses and interpretations based on RNA-Seq data for colon cancer research. Sci Rep. 2016 Sep 28;6:34420. doi: 10.1038/srep34420. PMID: 27677461; PMCID: PMC5039670.
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Showing 25 to 36 of 30284 entries