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Guillain-Barré syndrome.

Expert review of neurotherapeutics

Wakerley BR, Yuki N.
PMID: 26154996
Expert Rev Neurother. 2015;15(8):847-9. doi: 10.1586/14737175.2015.1065732. Epub 2015 Jul 08.

Over the past three decades much has been elucidated about the pathogenesis and clinical manifestations of Guillain-Barré syndrome, the most common cause of acute flaccid paralysis worldwide. Cross-reactivity between surface epitopes on the bacterium Campylobacter jejuni and peripheral nerve...

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Wakerley BR, Yuki N. Guillain-Barré syndrome. Expert Rev Neurother. 2015;15(8):847-9doi: 10.1586/14737175.2015.1065732.
Wakerley, B. R., & Yuki, N. (2015). Guillain-Barré syndrome. Expert review of neurotherapeutics, 15(8), 847-9. https://doi.org/10.1586/14737175.2015.1065732
Wakerley, Benjamin R, and Yuki, Nobuhiro. "Guillain-Barré syndrome." Expert review of neurotherapeutics vol. 15,8 (2015): 847-9. doi: https://doi.org/10.1586/14737175.2015.1065732
Wakerley BR, Yuki N. Guillain-Barré syndrome. Expert Rev Neurother. 2015;15(8):847-9. doi: 10.1586/14737175.2015.1065732. Epub 2015 Jul 08. PMID: 26154996.
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Efficient Presentation of Multiple Endogenous Epitopes to Both CD4.

Molecular therapy. Methods & clinical development

Dastagir SR, Postigo-Fernandez J, Xu C, Stoeckle JH, Firdessa-Fite R, Creusot RJ.
PMID: 28344989
Mol Ther Methods Clin Dev. 2016 Dec 24;4:27-38. doi: 10.1016/j.omtm.2016.12.002. eCollection 2017 Mar 17.

Antigen-specific immunotherapy of type 1 diabetes, typically via delivery of a single native β cell antigen, has had little clinical benefit to date. With increasing evidence that diabetogenic T cells react against multiple β cell antigens, including previously unappreciated...

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Dastagir SR, Postigo-Fernandez J, Xu C, et al. Efficient Presentation of Multiple Endogenous Epitopes to Both CD4. Mol Ther Methods Clin Dev. 2016;4:27-38doi: 10.1016/j.omtm.2016.12.002.
Dastagir, S. R., Postigo-Fernandez, J., Xu, C., Stoeckle, J. H., Firdessa-Fite, R., & Creusot, R. J. (2017). Efficient Presentation of Multiple Endogenous Epitopes to Both CD4. Molecular therapy. Methods & clinical development, 427-38. https://doi.org/10.1016/j.omtm.2016.12.002
Dastagir, Shamael R, et al. "Efficient Presentation of Multiple Endogenous Epitopes to Both CD4." Molecular therapy. Methods & clinical development vol. 4 (2017): 27-38. doi: https://doi.org/10.1016/j.omtm.2016.12.002
Dastagir SR, Postigo-Fernandez J, Xu C, Stoeckle JH, Firdessa-Fite R, Creusot RJ. Efficient Presentation of Multiple Endogenous Epitopes to Both CD4. Mol Ther Methods Clin Dev. 2016 Dec 24;4:27-38. doi: 10.1016/j.omtm.2016.12.002. eCollection 2017 Mar 17. PMID: 28344989; PMCID: PMC5363322.
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Immunogenicity of a Multi-Epitope DNA Vaccine Encoding Epitopes from Cu-Zn Superoxide Dismutase and Open Reading Frames of .

Frontiers in immunology

Escalona E, Sáez D, Oñate A.
PMID: 28232837
Front Immunol. 2017 Feb 09;8:125. doi: 10.3389/fimmu.2017.00125. eCollection 2017.

Brucellosis is a bacterial zoonotic disease affecting several mammalian species that is transmitted to humans by direct or indirect contact with infected animals or their products. In cattle, brucellosis is almost invariably caused by

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Escalona E, Sáez D, Oñate A. Immunogenicity of a Multi-Epitope DNA Vaccine Encoding Epitopes from Cu-Zn Superoxide Dismutase and Open Reading Frames of . Front Immunol. 2017;8:125doi: 10.3389/fimmu.2017.00125.
Escalona, E., Sáez, D., & Oñate, A. (2017). Immunogenicity of a Multi-Epitope DNA Vaccine Encoding Epitopes from Cu-Zn Superoxide Dismutase and Open Reading Frames of . Frontiers in immunology, 8125. https://doi.org/10.3389/fimmu.2017.00125
Escalona, Emilia, et al. "Immunogenicity of a Multi-Epitope DNA Vaccine Encoding Epitopes from Cu-Zn Superoxide Dismutase and Open Reading Frames of ." Frontiers in immunology vol. 8 (2017): 125. doi: https://doi.org/10.3389/fimmu.2017.00125
Escalona E, Sáez D, Oñate A. Immunogenicity of a Multi-Epitope DNA Vaccine Encoding Epitopes from Cu-Zn Superoxide Dismutase and Open Reading Frames of . Front Immunol. 2017 Feb 09;8:125. doi: 10.3389/fimmu.2017.00125. eCollection 2017. PMID: 28232837; PMCID: PMC5298974.
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Alloantibody Generation and Effector Function Following Sensitization to Human Leukocyte Antigen.

Frontiers in immunology

Hickey MJ, Valenzuela NM, Reed EF.
PMID: 26870045
Front Immunol. 2016 Feb 04;7:30. doi: 10.3389/fimmu.2016.00030. eCollection 2016.

Allorecognition is the activation of the adaptive immune system to foreign human leukocyte antigen (HLA) resulting in the generation of alloantibodies. Due to a high polymorphism, foreign HLA is recognized by the immune system following transplant, transfusion, or pregnancy...

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Hickey MJ, Valenzuela NM, Reed EF. Alloantibody Generation and Effector Function Following Sensitization to Human Leukocyte Antigen. Front Immunol. 2016;7:30doi: 10.3389/fimmu.2016.00030.
Hickey, M. J., Valenzuela, N. M., & Reed, E. F. (2016). Alloantibody Generation and Effector Function Following Sensitization to Human Leukocyte Antigen. Frontiers in immunology, 730. https://doi.org/10.3389/fimmu.2016.00030
Hickey, Michelle J, et al. "Alloantibody Generation and Effector Function Following Sensitization to Human Leukocyte Antigen." Frontiers in immunology vol. 7 (2016): 30. doi: https://doi.org/10.3389/fimmu.2016.00030
Hickey MJ, Valenzuela NM, Reed EF. Alloantibody Generation and Effector Function Following Sensitization to Human Leukocyte Antigen. Front Immunol. 2016 Feb 04;7:30. doi: 10.3389/fimmu.2016.00030. eCollection 2016. PMID: 26870045; PMCID: PMC4740371.
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In Silico Design of a Chimeric Protein Containing Antigenic Fragments of Helicobacter pylori; A Bioinformatic Approach.

The open microbiology journal

Mohammad N, Karsabet MT, Amani J, Ardjmand A, Zadeh MR, Gholi MK, Saffari M, Ghasemi A.
PMID: 27335622
Open Microbiol J. 2016 May 20;10:97-112. doi: 10.2174/1874285801610010097. eCollection 2016.

Helicobacter pylori is a global health problem which has encouraged scientists to find new ways to diagnose, immunize and eradicate the H. pylori infection. In silico studies are a promising approach to design new chimeric antigen having the immunogenic...

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Mohammad N, Karsabet MT, Amani J, et al. In Silico Design of a Chimeric Protein Containing Antigenic Fragments of Helicobacter pylori; A Bioinformatic Approach. Open Microbiol J. 2016;10:97-112doi: 10.2174/1874285801610010097.
Mohammad, N., Karsabet, M. T., Amani, J., Ardjmand, A., Zadeh, M. R., Gholi, M. K., Saffari, M., & Ghasemi, A. (2016). In Silico Design of a Chimeric Protein Containing Antigenic Fragments of Helicobacter pylori; A Bioinformatic Approach. The open microbiology journal, 1097-112. https://doi.org/10.2174/1874285801610010097
Mohammad, Nazanin, et al. "In Silico Design of a Chimeric Protein Containing Antigenic Fragments of Helicobacter pylori; A Bioinformatic Approach." The open microbiology journal vol. 10 (2016): 97-112. doi: https://doi.org/10.2174/1874285801610010097
Mohammad N, Karsabet MT, Amani J, Ardjmand A, Zadeh MR, Gholi MK, Saffari M, Ghasemi A. In Silico Design of a Chimeric Protein Containing Antigenic Fragments of Helicobacter pylori; A Bioinformatic Approach. Open Microbiol J. 2016 May 20;10:97-112. doi: 10.2174/1874285801610010097. eCollection 2016. PMID: 27335622; PMCID: PMC4899534.
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Automated glycan assembly of branched β-(1,3)-glucans to identify antibody epitopes.

Chemical communications (Cambridge, England)

Weishaupt MW, Hahm HS, Geissner A, Seeberger PH.
PMID: 28291272
Chem Commun (Camb). 2017 Mar 23;53(25):3591-3594. doi: 10.1039/c7cc00520b.

β-(1,3)-Glucans exhibit immunomodulatory and anti-tumor effects. Since the isolation of pure β-(1,3)-glucan oligosaccharides from natural sources is complicated, especially when certain branching patterns are desired, chemical synthesis is frequently the only means of accessing these molecules. We report the...

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Weishaupt MW, Hahm HS, Geissner A, et al. Automated glycan assembly of branched β-(1,3)-glucans to identify antibody epitopes. Chem Commun (Camb). 2017;53(25):3591-3594doi: 10.1039/c7cc00520b.
Weishaupt, M. W., Hahm, H. S., Geissner, A., & Seeberger, P. H. (2017). Automated glycan assembly of branched β-(1,3)-glucans to identify antibody epitopes. Chemical communications (Cambridge, England), 53(25), 3591-3594. https://doi.org/10.1039/c7cc00520b
Weishaupt, M W, et al. "Automated glycan assembly of branched β-(1,3)-glucans to identify antibody epitopes." Chemical communications (Cambridge, England) vol. 53,25 (2017): 3591-3594. doi: https://doi.org/10.1039/c7cc00520b
Weishaupt MW, Hahm HS, Geissner A, Seeberger PH. Automated glycan assembly of branched β-(1,3)-glucans to identify antibody epitopes. Chem Commun (Camb). 2017 Mar 23;53(25):3591-3594. doi: 10.1039/c7cc00520b. PMID: 28291272.
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Structural and Functional Characterization of Recombinant Isoforms of the Lentil Lipid Transfer Protein.

Acta naturae

Bogdanov IV, Finkina EI, Balandin SV, Melnikova DN, Stukacheva EA, Ovchinnikova TV.
PMID: 26483961
Acta Naturae. 2015 Jul-Sep;7(3):65-73.

The recombinant isoforms Lc-LTP1 and Lc-LTP3 of the lentil lipid transfer protein were overexpressed in E. coli cells. It was confirmed that both proteins are stabilized by four disulfide bonds and characterized by a high proportion of the α-helical...

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Bogdanov IV, Finkina EI, Balandin SV, et al. Structural and Functional Characterization of Recombinant Isoforms of the Lentil Lipid Transfer Protein. Acta Naturae. 2015;7(3):65-73
Bogdanov, I. V., Finkina, E. I., Balandin, S. V., Melnikova, D. N., Stukacheva, E. A., & Ovchinnikova, T. V. (2015). Structural and Functional Characterization of Recombinant Isoforms of the Lentil Lipid Transfer Protein. Acta naturae, 7(3), 65-73.
Bogdanov, I V, et al. "Structural and Functional Characterization of Recombinant Isoforms of the Lentil Lipid Transfer Protein." Acta naturae vol. 7,3 (2015): 65-73.
Bogdanov IV, Finkina EI, Balandin SV, Melnikova DN, Stukacheva EA, Ovchinnikova TV. Structural and Functional Characterization of Recombinant Isoforms of the Lentil Lipid Transfer Protein. Acta Naturae. 2015 Jul-Sep;7(3):65-73. PMID: 26483961; PMCID: PMC4610166.
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Why Oats Are Safe and Healthy for Celiac Disease Patients.

Medical sciences (Basel, Switzerland)

Gilissen LJWJ, van der Meer IM, Smulders MJM.
PMID: 29083384
Med Sci (Basel). 2016 Nov 26;4(4). doi: 10.3390/medsci4040021.

The water-insoluble storage proteins of cereals (prolamins) are called "gluten" in wheat, barley, and rye, and "avenins" in oat. Gluten can provoke celiac disease (CD) in genetically susceptible individuals (those with human leukocyte antigen (HLA)-DQ2 or HLA-DQ8 serotypes). Avenins...

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Gilissen LJWJ, van der Meer IM, Smulders MJM. Why Oats Are Safe and Healthy for Celiac Disease Patients. Med Sci (Basel). 2016;4(4)doi: 10.3390/medsci4040021.
Gilissen, L. J. W. J., van der Meer, I. M., & Smulders, M. J. M. (2016). Why Oats Are Safe and Healthy for Celiac Disease Patients. Medical sciences (Basel, Switzerland), 4(4), . https://doi.org/10.3390/medsci4040021
Gilissen, Luud J W J, et al. "Why Oats Are Safe and Healthy for Celiac Disease Patients." Medical sciences (Basel, Switzerland) vol. 4,4 (2016). doi: https://doi.org/10.3390/medsci4040021
Gilissen LJWJ, van der Meer IM, Smulders MJM. Why Oats Are Safe and Healthy for Celiac Disease Patients. Med Sci (Basel). 2016 Nov 26;4(4). doi: 10.3390/medsci4040021. PMID: 29083384; PMCID: PMC5635790.
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A Brief Review of Computer-Assisted Approaches to Rational Design of Peptide Vaccines.

International journal of molecular sciences

Nandy A, Basak SC.
PMID: 27153063
Int J Mol Sci. 2016 May 04;17(5). doi: 10.3390/ijms17050666.

The growing incidences of new viral diseases and increasingly frequent viral epidemics have strained therapeutic and preventive measures; the high mutability of viral genes puts additional strains on developmental efforts. Given the high cost and time requirements for new...

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Nandy A, Basak SC. A Brief Review of Computer-Assisted Approaches to Rational Design of Peptide Vaccines. Int J Mol Sci. 2016;17(5)doi: 10.3390/ijms17050666.
Nandy, A., & Basak, S. C. (2016). A Brief Review of Computer-Assisted Approaches to Rational Design of Peptide Vaccines. International journal of molecular sciences, 17(5), . https://doi.org/10.3390/ijms17050666
Nandy, Ashesh, and Basak, Subhash C. "A Brief Review of Computer-Assisted Approaches to Rational Design of Peptide Vaccines." International journal of molecular sciences vol. 17,5 (2016). doi: https://doi.org/10.3390/ijms17050666
Nandy A, Basak SC. A Brief Review of Computer-Assisted Approaches to Rational Design of Peptide Vaccines. Int J Mol Sci. 2016 May 04;17(5). doi: 10.3390/ijms17050666. PMID: 27153063; PMCID: PMC4881492.
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Commercially available glutenases: a potential hazard in coeliac disease.

Therapeutic advances in gastroenterology

Krishnareddy S, Stier K, Recanati M, Lebwohl B, Green PH.
PMID: 28567117
Therap Adv Gastroenterol. 2017 Jun;10(6):473-481. doi: 10.1177/1756283X17690991. Epub 2017 Apr 02.

BACKGROUND: The only treatment for celiac disease (CD) is a gluten-free diet (GFD). However, there is interest among patients in a medical therapy to replace or help with a GFD. Therapies include gluten-degrading enzymes (glutenases). There are glutenases available...

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Krishnareddy S, Stier K, Recanati M, et al. Commercially available glutenases: a potential hazard in coeliac disease. Therap Adv Gastroenterol. 2017;10(6):473-481doi: 10.1177/1756283X17690991.
Krishnareddy, S., Stier, K., Recanati, M., Lebwohl, B., & Green, P. H. (2017). Commercially available glutenases: a potential hazard in coeliac disease. Therapeutic advances in gastroenterology, 10(6), 473-481. https://doi.org/10.1177/1756283X17690991
Krishnareddy, Suneeta, et al. "Commercially available glutenases: a potential hazard in coeliac disease." Therapeutic advances in gastroenterology vol. 10,6 (2017): 473-481. doi: https://doi.org/10.1177/1756283X17690991
Krishnareddy S, Stier K, Recanati M, Lebwohl B, Green PH. Commercially available glutenases: a potential hazard in coeliac disease. Therap Adv Gastroenterol. 2017 Jun;10(6):473-481. doi: 10.1177/1756283X17690991. Epub 2017 Apr 02. PMID: 28567117; PMCID: PMC5424869.
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Antibody Immunity Induced by H7N9 Avian Influenza Vaccines: Evaluation Criteria, Affecting Factors, and Implications for Rational Vaccine Design.

Frontiers in microbiology

Hu Z, Jiao X, Liu X.
PMID: 29018438
Front Microbiol. 2017 Sep 26;8:1898. doi: 10.3389/fmicb.2017.01898. eCollection 2017.

Severe H7N9 avian influenza virus (AIV) infections in humans have public health authorities around the world on high alert for the potential development of a human influenza pandemic. Currently, the newly-emerged highly pathogenic avian influenza A (H7N9) virus poses...

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Hu Z, Jiao X, Liu X. Antibody Immunity Induced by H7N9 Avian Influenza Vaccines: Evaluation Criteria, Affecting Factors, and Implications for Rational Vaccine Design. Front Microbiol. 2017;8:1898doi: 10.3389/fmicb.2017.01898.
Hu, Z., Jiao, X., & Liu, X. (2017). Antibody Immunity Induced by H7N9 Avian Influenza Vaccines: Evaluation Criteria, Affecting Factors, and Implications for Rational Vaccine Design. Frontiers in microbiology, 81898. https://doi.org/10.3389/fmicb.2017.01898
Hu, Zenglei, et al. "Antibody Immunity Induced by H7N9 Avian Influenza Vaccines: Evaluation Criteria, Affecting Factors, and Implications for Rational Vaccine Design." Frontiers in microbiology vol. 8 (2017): 1898. doi: https://doi.org/10.3389/fmicb.2017.01898
Hu Z, Jiao X, Liu X. Antibody Immunity Induced by H7N9 Avian Influenza Vaccines: Evaluation Criteria, Affecting Factors, and Implications for Rational Vaccine Design. Front Microbiol. 2017 Sep 26;8:1898. doi: 10.3389/fmicb.2017.01898. eCollection 2017. PMID: 29018438; PMCID: PMC5622983.
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Generation of HLA-Universal iPSC-Derived Megakaryocytes and Platelets for Survival Under Refractoriness Conditions.

Molecular medicine (Cambridge, Mass.)

Börger AK, Eicke D, Wolf C, Gras C, Aufderbeck S, Schulze K, Engels L, Eiz-Vesper B, Schambach A, Guzman CA, Lachmann N, Moritz T, Martin U, Blasczyk R, Figueiredo C.
PMID: 27262025
Mol Med. 2016 Sep;22:274-285. doi: 10.2119/molmed.2015.00235. Epub 2016 May 16.

Platelet (PLT) transfusion is indispensable to maintain homeostasis in thrombocytopenic patients. However, PLT transfusion refractoriness is a common life-threatening condition observed in multitransfused patients. The most frequent immune cause for PLT transfusion refractoriness is the presence of alloantibodies specific...

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Börger AK, Eicke D, Wolf C, et al. Generation of HLA-Universal iPSC-Derived Megakaryocytes and Platelets for Survival Under Refractoriness Conditions. Mol Med. 2016;22:274-285doi: 10.2119/molmed.2015.00235.
Börger, A. K., Eicke, D., Wolf, C., Gras, C., Aufderbeck, S., Schulze, K., Engels, L., Eiz-Vesper, B., Schambach, A., Guzman, C. A., Lachmann, N., Moritz, T., Martin, U., Blasczyk, R., & Figueiredo, C. (2016). Generation of HLA-Universal iPSC-Derived Megakaryocytes and Platelets for Survival Under Refractoriness Conditions. Molecular medicine (Cambridge, Mass.), 22274-285. https://doi.org/10.2119/molmed.2015.00235
Börger, Ann-Kathrin, et al. "Generation of HLA-Universal iPSC-Derived Megakaryocytes and Platelets for Survival Under Refractoriness Conditions." Molecular medicine (Cambridge, Mass.) vol. 22 (2016): 274-285. doi: https://doi.org/10.2119/molmed.2015.00235
Börger AK, Eicke D, Wolf C, Gras C, Aufderbeck S, Schulze K, Engels L, Eiz-Vesper B, Schambach A, Guzman CA, Lachmann N, Moritz T, Martin U, Blasczyk R, Figueiredo C. Generation of HLA-Universal iPSC-Derived Megakaryocytes and Platelets for Survival Under Refractoriness Conditions. Mol Med. 2016 Sep;22:274-285. doi: 10.2119/molmed.2015.00235. Epub 2016 May 16. PMID: 27262025; PMCID: PMC5023513.
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Showing 13 to 24 of 3774 entries