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Monoclonal antibody 10A5 recognizes an antigen unique to the water-insoluble 25/45 membrane fraction of the rat ocular lens.

SpringerPlus

Whitman JK, Alviar AF, Fleschner CR, Stuart MK.
PMID: 24109564
Springerplus. 2013 Oct 02;2:500. doi: 10.1186/2193-1801-2-500. eCollection 2013.

The water-insoluble 25/45 fraction and non-sedimenting membrane fraction (NSMF) are two membrane preparations isolated from the ocular lens. The fractions are postulated to represent distinct subdomains of the lens with unique functions. However, attempts to distinguish between the two...

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Whitman JK, Alviar AF, Fleschner CR, et al. Monoclonal antibody 10A5 recognizes an antigen unique to the water-insoluble 25/45 membrane fraction of the rat ocular lens. Springerplus. 2013;2:500doi: 10.1186/2193-1801-2-500.
Whitman, J. K., Alviar, A. F., Fleschner, C. R., & Stuart, M. K. (2013). Monoclonal antibody 10A5 recognizes an antigen unique to the water-insoluble 25/45 membrane fraction of the rat ocular lens. SpringerPlus, 2500. https://doi.org/10.1186/2193-1801-2-500
Whitman, Joseph K, et al. "Monoclonal antibody 10A5 recognizes an antigen unique to the water-insoluble 25/45 membrane fraction of the rat ocular lens." SpringerPlus vol. 2 (2013): 500. doi: https://doi.org/10.1186/2193-1801-2-500
Whitman JK, Alviar AF, Fleschner CR, Stuart MK. Monoclonal antibody 10A5 recognizes an antigen unique to the water-insoluble 25/45 membrane fraction of the rat ocular lens. Springerplus. 2013 Oct 02;2:500. doi: 10.1186/2193-1801-2-500. eCollection 2013. PMID: 24109564; PMCID: PMC3793078.
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Prevalence of IgG Autoantibodies against GD3 Ganglioside in Acute Zika Virus Infection.

Frontiers in medicine

Nico D, Conde L, Rivera-Correa JL, Vasconcelos-Dos-Santos A, Mesentier-Louro L, Freire-de-Lima L, Arruda MB, Freire-de-Lima CG, Ferreira ODC, Lopes Moreira ME, Zin AA, Vasconcelos ZFM, Otero RM, Palatnik-de-Sousa CB, Tanuri A, Todeschini AR, Savino W, Rodriguez A, Morrot A.
PMID: 29594116
Front Med (Lausanne). 2018 Mar 09;5:25. doi: 10.3389/fmed.2018.00025. eCollection 2018.

Zika virus (ZIKV) disease has become a global health emergency with devastating effects on public health. Recent evidences implicate the virus as an emergent neuropathological agent promoting serious pathologies of the human nervous system, that include destructive and malformation...

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Nico D, Conde L, Rivera-Correa JL, et al. Prevalence of IgG Autoantibodies against GD3 Ganglioside in Acute Zika Virus Infection. Front Med (Lausanne). 2018;5:25doi: 10.3389/fmed.2018.00025.
Nico, D., Conde, L., Rivera-Correa, J. L., Vasconcelos-Dos-Santos, A., Mesentier-Louro, L., Freire-de-Lima, L., Arruda, M. B., Freire-de-Lima, C. G., Ferreira, O. D. C., Lopes Moreira, M. E., Zin, A. A., Vasconcelos, Z. F. M., Otero, R. M., Palatnik-de-Sousa, C. B., Tanuri, A., Todeschini, A. R., Savino, W., Rodriguez, A., & Morrot, A. (2018). Prevalence of IgG Autoantibodies against GD3 Ganglioside in Acute Zika Virus Infection. Frontiers in medicine, 525. https://doi.org/10.3389/fmed.2018.00025
Nico, Dirlei, et al. "Prevalence of IgG Autoantibodies against GD3 Ganglioside in Acute Zika Virus Infection." Frontiers in medicine vol. 5 (2018): 25. doi: https://doi.org/10.3389/fmed.2018.00025
Nico D, Conde L, Rivera-Correa JL, Vasconcelos-Dos-Santos A, Mesentier-Louro L, Freire-de-Lima L, Arruda MB, Freire-de-Lima CG, Ferreira ODC, Lopes Moreira ME, Zin AA, Vasconcelos ZFM, Otero RM, Palatnik-de-Sousa CB, Tanuri A, Todeschini AR, Savino W, Rodriguez A, Morrot A. Prevalence of IgG Autoantibodies against GD3 Ganglioside in Acute Zika Virus Infection. Front Med (Lausanne). 2018 Mar 09;5:25. doi: 10.3389/fmed.2018.00025. eCollection 2018. PMID: 29594116; PMCID: PMC5854646.
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AP-MALDI Mass Spectrometry Imaging of Gangliosides Using 2,6-Dihydroxyacetophenone.

Journal of the American Society for Mass Spectrometry

Jackson SN, Muller L, Roux A, Oktem B, Moskovets E, Doroshenko VM, Woods AS.
PMID: 29549666
J Am Soc Mass Spectrom. 2018 Jul;29(7):1463-1472. doi: 10.1007/s13361-018-1928-8. Epub 2018 Mar 16.

Matrix-assisted laser/desorption ionization (MALDI) mass spectrometry imaging (MSI) is widely used as a unique tool to record the distribution of a large range of biomolecules in tissues. 2,6-Dihydroxyacetophenone (DHA) matrix has been shown to provide efficient ionization of lipids,...

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Jackson SN, Muller L, Roux A, et al. AP-MALDI Mass Spectrometry Imaging of Gangliosides Using 2,6-Dihydroxyacetophenone. J Am Soc Mass Spectrom. 2018;29(7):1463-1472doi: 10.1007/s13361-018-1928-8.
Jackson, S. N., Muller, L., Roux, A., Oktem, B., Moskovets, E., Doroshenko, V. M., & Woods, A. S. (2018). AP-MALDI Mass Spectrometry Imaging of Gangliosides Using 2,6-Dihydroxyacetophenone. Journal of the American Society for Mass Spectrometry, 29(7), 1463-1472. https://doi.org/10.1007/s13361-018-1928-8
Jackson, Shelley N, et al. "AP-MALDI Mass Spectrometry Imaging of Gangliosides Using 2,6-Dihydroxyacetophenone." Journal of the American Society for Mass Spectrometry vol. 29,7 (2018): 1463-1472. doi: https://doi.org/10.1007/s13361-018-1928-8
Jackson SN, Muller L, Roux A, Oktem B, Moskovets E, Doroshenko VM, Woods AS. AP-MALDI Mass Spectrometry Imaging of Gangliosides Using 2,6-Dihydroxyacetophenone. J Am Soc Mass Spectrom. 2018 Jul;29(7):1463-1472. doi: 10.1007/s13361-018-1928-8. Epub 2018 Mar 16. PMID: 29549666; PMCID: PMC7549319.
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Lipidomic Evaluation of Feline Neurologic Disease after AAV Gene Therapy.

Molecular therapy. Methods & clinical development

Gray-Edwards HL, Jiang X, Randle AN, Taylor AR, Voss TL, Johnson AK, McCurdy VJ, Sena-Esteves M, Ory DS, Martin DR.
PMID: 28808666
Mol Ther Methods Clin Dev. 2017 Jul 26;6:135-142. doi: 10.1016/j.omtm.2017.07.005. eCollection 2017 Sep 15.

GM1 gangliosidosis is a fatal lysosomal disorder, for which there is no effective treatment. Adeno-associated virus (AAV) gene therapy in GM1 cats has resulted in a greater than 6-fold increase in lifespan, with many cats remaining alive at >5.7...

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Gray-Edwards HL, Jiang X, Randle AN, et al. Lipidomic Evaluation of Feline Neurologic Disease after AAV Gene Therapy. Mol Ther Methods Clin Dev. 2017;6:135-142doi: 10.1016/j.omtm.2017.07.005.
Gray-Edwards, H. L., Jiang, X., Randle, A. N., Taylor, A. R., Voss, T. L., Johnson, A. K., McCurdy, V. J., Sena-Esteves, M., Ory, D. S., & Martin, D. R. (2017). Lipidomic Evaluation of Feline Neurologic Disease after AAV Gene Therapy. Molecular therapy. Methods & clinical development, 6135-142. https://doi.org/10.1016/j.omtm.2017.07.005
Gray-Edwards, Heather L, et al. "Lipidomic Evaluation of Feline Neurologic Disease after AAV Gene Therapy." Molecular therapy. Methods & clinical development vol. 6 (2017): 135-142. doi: https://doi.org/10.1016/j.omtm.2017.07.005
Gray-Edwards HL, Jiang X, Randle AN, Taylor AR, Voss TL, Johnson AK, McCurdy VJ, Sena-Esteves M, Ory DS, Martin DR. Lipidomic Evaluation of Feline Neurologic Disease after AAV Gene Therapy. Mol Ther Methods Clin Dev. 2017 Jul 26;6:135-142. doi: 10.1016/j.omtm.2017.07.005. eCollection 2017 Sep 15. PMID: 28808666; PMCID: PMC5545771.
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Dysarthria and Stutter as Presenting Symptoms of Late-Onset Tay-Sachs Disease in Three Siblings.

Movement disorders clinical practice

Grim KK, Phillips GD, Renner DR.
PMID: 30363497
Mov Disord Clin Pract. 2015 Jun 30;2(3):289-290. doi: 10.1002/mdc3.12194. eCollection 2015 Sep.

Late-onset Tay-Sachs disease (LOTS) is a rare autosomal-recessive genetic disorder caused by insufficient activity of the lysosomal enzyme, beta-hexosaminidase A, resulting in intracellular accumulation of gangliosides in the central nervous system. Clinical manifestations can include unsteadiness in gait, muscle...

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Grim KK, Phillips GD, Renner DR. Dysarthria and Stutter as Presenting Symptoms of Late-Onset Tay-Sachs Disease in Three Siblings. Mov Disord Clin Pract. 2015;2(3):289-290doi: 10.1002/mdc3.12194.
Grim, K. K., Phillips, G. D., & Renner, D. R. (2015). Dysarthria and Stutter as Presenting Symptoms of Late-Onset Tay-Sachs Disease in Three Siblings. Movement disorders clinical practice, 2(3), 289-290. https://doi.org/10.1002/mdc3.12194
Grim, Kristina K, et al. "Dysarthria and Stutter as Presenting Symptoms of Late-Onset Tay-Sachs Disease in Three Siblings." Movement disorders clinical practice vol. 2,3 (2015): 289-290. doi: https://doi.org/10.1002/mdc3.12194
Grim KK, Phillips GD, Renner DR. Dysarthria and Stutter as Presenting Symptoms of Late-Onset Tay-Sachs Disease in Three Siblings. Mov Disord Clin Pract. 2015 Jun 30;2(3):289-290. doi: 10.1002/mdc3.12194. eCollection 2015 Sep. PMID: 30363497; PMCID: PMC6178690.
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Anomalies in Dopamine Transporter Expression and Primary Cilium Distribution in the Dorsal Striatum of a Mouse Model of Niemann-Pick C1 Disease.

Frontiers in cellular neuroscience

Lucarelli M, Di Pietro C, La Sala G, Fiorenza MT, Marazziti D, Canterini S.
PMID: 31178699
Front Cell Neurosci. 2019 May 24;13:226. doi: 10.3389/fncel.2019.00226. eCollection 2019.

The Niemann-Pick type C1 (NPC1) is a rare genetic disease characterized by the accumulation of endocytosed cholesterol and other lipids in the endosome/lysosome compartments. In the brain, the accumulation/mislocalization of unesterified cholesterol, gangliosides and sphingolipids is responsible for the...

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Lucarelli M, Di Pietro C, La Sala G, et al. Anomalies in Dopamine Transporter Expression and Primary Cilium Distribution in the Dorsal Striatum of a Mouse Model of Niemann-Pick C1 Disease. Front Cell Neurosci. 2019;13:226doi: 10.3389/fncel.2019.00226.
Lucarelli, M., Di Pietro, C., La Sala, G., Fiorenza, M. T., Marazziti, D., & Canterini, S. (2019). Anomalies in Dopamine Transporter Expression and Primary Cilium Distribution in the Dorsal Striatum of a Mouse Model of Niemann-Pick C1 Disease. Frontiers in cellular neuroscience, 13226. https://doi.org/10.3389/fncel.2019.00226
Lucarelli, Micaela, et al. "Anomalies in Dopamine Transporter Expression and Primary Cilium Distribution in the Dorsal Striatum of a Mouse Model of Niemann-Pick C1 Disease." Frontiers in cellular neuroscience vol. 13 (2019): 226. doi: https://doi.org/10.3389/fncel.2019.00226
Lucarelli M, Di Pietro C, La Sala G, Fiorenza MT, Marazziti D, Canterini S. Anomalies in Dopamine Transporter Expression and Primary Cilium Distribution in the Dorsal Striatum of a Mouse Model of Niemann-Pick C1 Disease. Front Cell Neurosci. 2019 May 24;13:226. doi: 10.3389/fncel.2019.00226. eCollection 2019. PMID: 31178699; PMCID: PMC6544041.
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Disialoganglioside GD2 Expression in Solid Tumors and Role as a Target for Cancer Therapy.

Frontiers in oncology

Nazha B, Inal C, Owonikoko TK.
PMID: 32733795
Front Oncol. 2020 Jul 07;10:1000. doi: 10.3389/fonc.2020.01000. eCollection 2020.

Gangliosides are carbohydrate-containing sphingolipids that are widely expressed in normal tissues, making most subtypes unsuitable as targets for cancer therapy. However, the disialoganglioside GD2 subtype has limited expression in normal tissues but is overexpressed across a wide range of...

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Nazha B, Inal C, Owonikoko TK. Disialoganglioside GD2 Expression in Solid Tumors and Role as a Target for Cancer Therapy. Front Oncol. 2020;10:1000doi: 10.3389/fonc.2020.01000.
Nazha, B., Inal, C., & Owonikoko, T. K. (2020). Disialoganglioside GD2 Expression in Solid Tumors and Role as a Target for Cancer Therapy. Frontiers in oncology, 101000. https://doi.org/10.3389/fonc.2020.01000
Nazha, Bassel, et al. "Disialoganglioside GD2 Expression in Solid Tumors and Role as a Target for Cancer Therapy." Frontiers in oncology vol. 10 (2020): 1000. doi: https://doi.org/10.3389/fonc.2020.01000
Nazha B, Inal C, Owonikoko TK. Disialoganglioside GD2 Expression in Solid Tumors and Role as a Target for Cancer Therapy. Front Oncol. 2020 Jul 07;10:1000. doi: 10.3389/fonc.2020.01000. eCollection 2020. PMID: 32733795; PMCID: PMC7358363.
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Detection of Ganglioside-Specific Toxin Binding with Biomembrane-Based Bioelectronic Sensors.

ACS applied bio materials

Bint E Naser SF, Su H, Liu HY, Manzer ZA, Chao Z, Roy A, Pappa AM, Salleo A, Owens RM, Daniel S.
PMID: 35006775
ACS Appl Bio Mater. 2021 Nov 15;4(11):7942-7950. doi: 10.1021/acsabm.1c00878. Epub 2021 Oct 22.

Gangliosides, glycolipids that are abundant in the plasma membrane outer leaflet, play an integral role in cellular recognition, adhesion, and infection by interacting with different endogenous molecules, viruses, and toxins. Model membrane systems, such as ganglioside-enriched supported lipid bilayers...

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Bint E Naser SF, Su H, Liu HY, et al. Detection of Ganglioside-Specific Toxin Binding with Biomembrane-Based Bioelectronic Sensors. ACS Appl Bio Mater. 2021;4(11):7942-7950doi: 10.1021/acsabm.1c00878.
Bint E Naser, S. F., Su, H., Liu, H. Y., Manzer, Z. A., Chao, Z., Roy, A., Pappa, A. M., Salleo, A., Owens, R. M., & Daniel, S. (2021). Detection of Ganglioside-Specific Toxin Binding with Biomembrane-Based Bioelectronic Sensors. ACS applied bio materials, 4(11), 7942-7950. https://doi.org/10.1021/acsabm.1c00878
Bint E Naser, Samavi Farnush, et al. "Detection of Ganglioside-Specific Toxin Binding with Biomembrane-Based Bioelectronic Sensors." ACS applied bio materials vol. 4,11 (2021): 7942-7950. doi: https://doi.org/10.1021/acsabm.1c00878
Bint E Naser SF, Su H, Liu HY, Manzer ZA, Chao Z, Roy A, Pappa AM, Salleo A, Owens RM, Daniel S. Detection of Ganglioside-Specific Toxin Binding with Biomembrane-Based Bioelectronic Sensors. ACS Appl Bio Mater. 2021 Nov 15;4(11):7942-7950. doi: 10.1021/acsabm.1c00878. Epub 2021 Oct 22. PMID: 35006775.
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Innovative treatment targeting gangliosides aimed at blocking the formation of neurotoxic α-synuclein oligomers in Parkinson's disease.

Glycoconjugate journal

Yahi N, Di Scala C, Chahinian H, Fantini J.
PMID: 34328594
Glycoconj J. 2021 Jul 30; doi: 10.1007/s10719-021-10012-0. Epub 2021 Jul 30.

Parkinson's disease (PD) is a major neurodegenerative disorder which exhibits many of the characteristics of a pandemic. Current therapeutic strategies are centered on the dopaminergic system, with limited efficacy, so that a treatment that has a direct impact on...

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Yahi N, Di Scala C, Chahinian H, et al. Innovative treatment targeting gangliosides aimed at blocking the formation of neurotoxic α-synuclein oligomers in Parkinson's disease. Glycoconj J. 2021;doi: 10.1007/s10719-021-10012-0.
Yahi, N., Di Scala, C., Chahinian, H., & Fantini, J. (2021). Innovative treatment targeting gangliosides aimed at blocking the formation of neurotoxic α-synuclein oligomers in Parkinson's disease. Glycoconjugate journal, . https://doi.org/10.1007/s10719-021-10012-0
Yahi, Nouara, et al. "Innovative treatment targeting gangliosides aimed at blocking the formation of neurotoxic α-synuclein oligomers in Parkinson's disease." Glycoconjugate journal vol. (2021). doi: https://doi.org/10.1007/s10719-021-10012-0
Yahi N, Di Scala C, Chahinian H, Fantini J. Innovative treatment targeting gangliosides aimed at blocking the formation of neurotoxic α-synuclein oligomers in Parkinson's disease. Glycoconj J. 2021 Jul 30; doi: 10.1007/s10719-021-10012-0. Epub 2021 Jul 30. PMID: 34328594.
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Burkholderia cenocepacia BCAM2418-induced antibody inhibits bacterial adhesion, confers protection to infection and enables identification of host glycans as adhesin targets.

Cellular microbiology

Pimenta AI, Kilcoyne M, Bernardes N, Mil-Homens D, Joshi L, Fialho AM.
PMID: 33822465
Cell Microbiol. 2021 Aug;23(8):e13340. doi: 10.1111/cmi.13340. Epub 2021 Apr 20.

Trimeric Autotransporter Adhesins (TAA) found in Gram-negative bacteria play a key role in virulence. This is the case of Burkholderia cepacia complex (Bcc), a group of related bacteria able to cause infections in patients with cystic fibrosis. These bacteria...

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Pimenta AI, Kilcoyne M, Bernardes N, et al. Burkholderia cenocepacia BCAM2418-induced antibody inhibits bacterial adhesion, confers protection to infection and enables identification of host glycans as adhesin targets. Cell Microbiol. 2021;23(8):e13340doi: 10.1111/cmi.13340.
Pimenta, A. I., Kilcoyne, M., Bernardes, N., Mil-Homens, D., Joshi, L., & Fialho, A. M. (2021). Burkholderia cenocepacia BCAM2418-induced antibody inhibits bacterial adhesion, confers protection to infection and enables identification of host glycans as adhesin targets. Cellular microbiology, 23(8), e13340. https://doi.org/10.1111/cmi.13340
Pimenta, Andreia I, et al. "Burkholderia cenocepacia BCAM2418-induced antibody inhibits bacterial adhesion, confers protection to infection and enables identification of host glycans as adhesin targets." Cellular microbiology vol. 23,8 (2021): e13340. doi: https://doi.org/10.1111/cmi.13340
Pimenta AI, Kilcoyne M, Bernardes N, Mil-Homens D, Joshi L, Fialho AM. Burkholderia cenocepacia BCAM2418-induced antibody inhibits bacterial adhesion, confers protection to infection and enables identification of host glycans as adhesin targets. Cell Microbiol. 2021 Aug;23(8):e13340. doi: 10.1111/cmi.13340. Epub 2021 Apr 20. PMID: 33822465.
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Specificity in protein-membrane associations: the interaction of gangliosides with Escherichia coli heat-labile enterotoxin and choleragen.

Biophysical journal

Osborne JC, Moss J, Fishman PH, Nakaya S, Robertson DC.
PMID: 19431461
Biophys J. 1982 Jan;37(1):168-9. doi: 10.1016/s0006-3495(82)84654-7.

No abstract available.

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Osborne JC, Moss J, Fishman PH, et al. Specificity in protein-membrane associations: the interaction of gangliosides with Escherichia coli heat-labile enterotoxin and choleragen. Biophys J. 1982;37(1):168-9doi: 10.1016/s0006-3495(82)84654-7.
Osborne, J. C., Moss, J., Fishman, P. H., Nakaya, S., & Robertson, D. C. (1982). Specificity in protein-membrane associations: the interaction of gangliosides with Escherichia coli heat-labile enterotoxin and choleragen. Biophysical journal, 37(1), 168-9. https://doi.org/10.1016/s0006-3495(82)84654-7
Osborne, J C, et al. "Specificity in protein-membrane associations: the interaction of gangliosides with Escherichia coli heat-labile enterotoxin and choleragen." Biophysical journal vol. 37,1 (1982): 168-9. doi: https://doi.org/10.1016/s0006-3495(82)84654-7
Osborne JC, Moss J, Fishman PH, Nakaya S, Robertson DC. Specificity in protein-membrane associations: the interaction of gangliosides with Escherichia coli heat-labile enterotoxin and choleragen. Biophys J. 1982 Jan;37(1):168-9. doi: 10.1016/s0006-3495(82)84654-7. PMID: 19431461; PMCID: PMC1329109.
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Sequence analysis of the .

Veterinary world

Neov B, Krastanov J, Angelova T, Palova N, Laleva S, Hristov P.
PMID: 33642786
Vet World. 2021 Jan;14(1):56-60. doi: 10.14202/vetworld.2021.56-60. Epub 2021 Jan 08.

BACKGROUND AND AIM: Jacob sheep are a rare ancient breed of sheep believed to have originated from the Mediterranean area but which are now kept throughout the world. These sheep have recently attracted medical interest due to the observation...

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Neov B, Krastanov J, Angelova T, et al. Sequence analysis of the . Vet World. 2021;14(1):56-60doi: 10.14202/vetworld.2021.56-60.
Neov, B., Krastanov, J., Angelova, T., Palova, N., Laleva, S., & Hristov, P. (2021). Sequence analysis of the . Veterinary world, 14(1), 56-60. https://doi.org/10.14202/vetworld.2021.56-60
Neov, Boyko, et al. "Sequence analysis of the ." Veterinary world vol. 14,1 (2021): 56-60. doi: https://doi.org/10.14202/vetworld.2021.56-60
Neov B, Krastanov J, Angelova T, Palova N, Laleva S, Hristov P. Sequence analysis of the . Vet World. 2021 Jan;14(1):56-60. doi: 10.14202/vetworld.2021.56-60. Epub 2021 Jan 08. PMID: 33642786; PMCID: PMC7896910.
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Showing 25 to 36 of 325 entries