Activity of Porphyridium sp. polysaccharide against herpes simplex viruses in vitro and in vivo

Angiogenesis Inhibition and Tumor Regression Caused by Heparin or a Heparin Fragment in the Presence of Cortisone

Folkman, J., Langer, R., Linhardt, R. J., Haudenschild, C. C., & Taylor, S. (1983) · Science · doi:10.1126/science.6192498 · Cited by 619 · see citing works

Sulfated Polysaccharides Extracted from Sea Algae as Potential Antiviral Drugs

Witvrouw, M., & Clercq, E. D. (1997) · General Pharmacology The Vascular System · doi:10.1016/s0306-3623(96)00563-0 · Cited by 531 · see citing works

Mechanism of inhibitory effect of dextran sulfate and heparin on replication of human immunodeficiency virus in vitro.

Baba, M., Pauwels, R., Balzarini, J. M., Arnout, J., Desmyter, J., & Clercq, E. D. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.16.6132 · Cited by 465 · see citing works

Marine Algae in pharmaceutical science

Woodhead, H. (1980) · Endeavour · doi:10.1016/0160-9327(80)90084-8 · Cited by 269 · see citing works

Marine algae in pharmaceutical science

Hoppe, H. A., Levring, T., & Tanaka, Y. (1979) · De Gruyter eBooks · Cited by 219 · see citing works

Purification and characterization of an avian myeloblastosis and human immunodeficiency virus reverse transcriptase inhibitor, sulfated polysaccharides extracted from sea algae

Nakashima, H., Kido, Y., Kobayashi, N., Motoki, Y., Neushul, M., & Yamamoto, N. (1987) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.31.10.1524 · Cited by 188 · see citing works

Polysaccharides as antiviral agents: antiviral activity of carrageenan

González, M. E., Alarcón, B., & Carrasco, L. (1987) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.31.9.1388 · Cited by 187 · see citing works

INHIBITORY EFFECT OF HEPARIN ON HERPES SIMPLEX VIRUS

Nahmias, A. J., & Kibrick, S. (1964) · Journal of Bacteriology · doi:10.1128/jb.87.5.1060-1066.1964 · Cited by 175 · see citing works

Protective Effect of Seaweed Extracts for Chicken Embryos Infected with Influenza B or Mumps Virus

Gerber, P. J., Dutcher, J. D., Adams, E. V., & Sherman, J. H. (1958) · Experimental Biology and Medicine · doi:10.3181/00379727-99-24429 · Cited by 161 · see citing works

The extracellular polysaccharides of the red microalgae: Chemistry and rheology

Geresh, S., & Arad, S. M. (1991) · Bioresource Technology · doi:10.1016/0960-8524(91)90154-c · Cited by 145 · see citing works

Antiviral Agents and Viral Diseases of Man

Galasso, G. J., Merigan, T. C., & Buchanan, R. A. (1990) · Medical Entomology and Zoology · Cited by 136 · see citing works

Interferon-stimulating and in vivo antiviral effects of various synthetic anionic polymers

Merigan, T. C., & Finkelstein, M. S. (1968) · Virology · doi:10.1016/0042-6822(68)90215-8 · Cited by 123 · see citing works

Efficacy of phosphonylmethoxyalkyl derivatives of adenine in experimental herpes simplex virus and vaccinia virus infections in vivo

Clercq, E. D., Holý, A., & Rosenberg, I. (1989) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.33.2.185 · Cited by 111 · see citing works

Novel sulfated polymers as highly potent and selective inhibitors of human immunodeficiency virus replication and giant cell formation

Baba, M., Schols, D., Clercq, E. D., Pauwels, R., Nagy, M., Györgyi-Edelényi, J., Löw, M., & Gǒrög, S. (1990) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.34.1.134 · Cited by 108 · see citing works

Inhibition of human immunodeficiency virus type 1 RNase H by sulfated polyanions

Moelling, K., Schulze, T., & Diringer, H. (1989) · Journal of Virology · doi:10.1128/jvi.63.12.5489-5491.1989 · Cited by 82 · see citing works

Antiviral Activity of Polyacrylic and Polymethacrylic Acids

Somer, P. D., Clercq, E. D., Billiau, A., Schonne, E., & Claesen, M. (1968) · Journal of Virology · doi:10.1128/jvi.2.9.886-893.1968 · Cited by 79 · see citing works

Comparative activity of selected antiviral compounds against clinical isolates of human cytomegalovirus

Andreï, G., Snoeck, R., Schols, D., Goubau, P., Desmyter, J., & Clercq, E. D. (1991) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/bf01984924 · Cited by 72 · see citing works

Adsorption, Penetration and Uncoating of Herpes Simplex Virus

Hochberg, E., & Becker, Y. (1968) · Journal of General Virology · doi:10.1099/0022-1317-2-2-231 · Cited by 46 · see citing works

Inhibition of HIV and virus replication by polysulphated polyxylan

BIESERT, L., Suhartono, H., Winkler, I., Meichsner, C., Helsberg, M., Hewlett, G., Klimetzek, V., Moelling, K., Hd, S., Schrinner, E., et al. (1988) · AIDS · doi:10.1097/00002030-198812000-00007 · Cited by 40 · see citing works

Antiviral carbohydrates from marine red algae

Neushul, M. (1990) · Hydrobiologia · doi:10.1007/bf00040220 · Cited by 37 · see citing works

ULTRASTRUCTURE, DEVELOPMENT AND CYTOPLASMIC ROTATION OF SETA‐BEARING CELLS OFCOLEOCHAETE SCUTATA(CHLOROPHYCEAE)1

Marchant, H. J. (1977) · Journal of Phycology · doi:10.1111/j.1529-8817.1977.tb02882.x · Cited by 30 · see citing works

Antiviral Agents and Viral Diseases of Man

Fanning, W. L. (1985) · JAMA · doi:10.1001/jama.1985.03350430114044 · Cited by 24 · see citing works

Antiviral activity of carbopol, a cross-linked polycarboxylate

Clercq, E. D., & Łuczak, M. (1976) · Archives of Virology · doi:10.1007/bf01317874 · Cited by 20 · see citing works

Anti-human immunodeficiency virus (HIV) drug HOE/BAY 946 increases membrane hydrophobicity of human lymphocytes and specifically suppresses HIV-protein synthesis

BIESERT, L., Adamski, M., Zimmer, G., Suhartono, H., Fuchs, J., Unkelbach, U., Mehlhorn, R. J., Hideg, K., Milbradt, R., & Rübsamen‐Waigmann, H. (1990) · Medical Microbiology and Immunology · doi:10.1007/bf00189609 · Cited by 11 · see citing works

Biological activities and potential health benefits of sulfated polysaccharides derived from marine algae

Wijesekara, I., Pangestuti, R., & Kim, S.-K. (2011) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2010.10.062 · Cited by 992 · see citing works

Overview of microalgal extracellular polymeric substances (EPS) and their applications

Xiao, R., & Zheng, Y. (2016) · Biotechnology Advances · doi:10.1016/j.biotechadv.2016.08.004 · Cited by 938 · see citing works

Marine Bioactives as Functional Food Ingredients: Potential to Reduce the Incidence of Chronic Diseases

Lordan, S., Ross, R. P., & Stanton, C. (2011) · Marine Drugs · doi:10.3390/md9061056 · Cited by 756 · see citing works

Microalgae for High-Value Products Towards Human Health and Nutrition

Barkia, I., Saari, N., & Manning, S. R. (2019) · Marine Drugs · doi:10.3390/md17050304 · Cited by 719 · see citing works

Marine Polysaccharides from Algae with Potential Biomedical Applications

Raposo, M. F. D. J., Morais, A. M. M. B., & Morais, R. M. S. C. (2015) · Marine Drugs · doi:10.3390/md13052967 · Cited by 693 · see citing works

Bioactivity and applications of sulphated polysaccharides from marine microalgae

Raposo, M., De Morais, R., & Bernardo de Morais, A. (2013) · Marine Drugs · doi:10.3390/md11010233 · Cited by 594 · see citing works

Innovative natural functional ingredients from microalgae

Plaza, M., Herrero, M., Cifuentes, A., & Ibáñez, E. (2009) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf901070g · Cited by 509 · see citing works

Screening for bioactive compounds from algae

Plaza, M., Santoyo, S., Jaime, L., Reina, G. G.-B., Herrero, M., Señoráns, F. J., & Ibáñez, E. (2009) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2009.03.016 · Cited by 493 · see citing works

Production, extraction and characterization of microalgal and cyanobacterial exopolysaccharides

Delattre, C., Pierre, G., Laroche, C., & Michaud, P. (2016) · Biotechnology Advances · doi:10.1016/j.biotechadv.2016.08.001 · Cited by 486 · see citing works

Health applications of bioactive compounds from marine microalgae

Raposo, M. F. D. J., Morais, R. M. S. C., & Morais, A. M. M. B. (2013) · Life Sciences · doi:10.1016/j.lfs.2013.08.002 · Cited by 412 · see citing works

Microalgae as Healthy Ingredients for Functional Food: A Review

Matos, J., Cardoso, C., Bandarra, N. M., & Afonso, C. (2017) · Food & Function · doi:10.1039/c7fo00409e · Cited by 393 · see citing works

Preparation of different molecular weight polysaccharides from Porphyridium cruentum and their antioxidant activities

Sun, L., Wang, C., Shi, Q., & Ma, C. (2009) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2009.03.013 · Cited by 338 · see citing works

Chemical modifications of polysaccharides and their anti-tumor activities

Xie, L., Shen, M., Hong, Y., Ye, H., Huang, L., & Xie, J. (2019) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2019.115436 · Cited by 314 · see citing works

The Potential of Microalgae for the Production of Bioactive Molecules of Pharmaceutical Interest

Mimouni, V., Ulmann, L., Pasquet, V., Mathieu, M., Picot, L., Bougaran, G., Cadoret, J., Morant-Manceau, A., & Schoefs, B. (2012) · Current Pharmaceutical Biotechnology · doi:10.2174/138920112804724828 · Cited by 274 · see citing works

Red microalgal cell-wall polysaccharides: biotechnological aspects

Arad, S. M., & Levy‐Ontman, O. (2010) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2010.02.008 · Cited by 265 · see citing works

Antimicrobial Compounds from Eukaryotic Microalgae against Human Pathogens and Diseases in Aquaculture

Falaise, C., François, C., Travers, M., Morga, B., Haure, J., Tremblay, R., Turcotte, F., Pasetto, P., Gastineau, R., Hardivillier, Y., et al. (2016) · Marine Drugs · doi:10.3390/md14090159 · Cited by 253 · see citing works

Immunomodulation and antitumor activities of different-molecular-weight polysaccharides from Porphyridium cruentum

Sun, L., Wang, L., & Zhou, Y. (2012) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2011.08.097 · Cited by 249 · see citing works

Defensive effects of a fucoidan from brown alga Undaria pinnatifida against herpes simplex virus infection

Hayashi, K., Nakano, T., Hashimoto, M., Kanekiyo, K., & Hayashi, T. (2008) · International Immunopharmacology · doi:10.1016/j.intimp.2007.10.017 · Cited by 247 · see citing works

Marine Algae-Derived Bioactive Compounds: A New Wave of Nanodrugs?

Menaa, F., Wijesinghe, U., Thiripuranathar, G., Althobaiti, N. A., Albalawi, A. E., Khan, B. A., & Menaa, B. (2021) · Marine Drugs · doi:10.3390/md19090484 · Cited by 247 · see citing works

Neuroprotective Effects of Marine Algae

Pangestuti, R., & Kim, S. (2011) · Marine Drugs · doi:10.3390/md9050803 · Cited by 245 · see citing works

Functional ingredients from microalgae

Buono, S., Langellotti, A. L., Martello, A., Rinna, F., & Fogliano, V. (2014) · Food & Function · doi:10.1039/c4fo00125g · Cited by 241 · see citing works

The structure of a sulfated galactan from Porphyra haitanensis and its in vivo antioxidant activity

Zhang, Q., Li, N., Liu, X., Zhao, Z., Li, Z., & Xu, Z. (2003) · Carbohydrate Research · doi:10.1016/j.carres.2003.09.015 · Cited by 235 · see citing works

The “Cheshire Cat” escape strategy of the coccolithophore Emiliania huxleyi in response to viral infection

Frada, M. J., Probert, I., Allen, M. J., Wilson, W. H., & de Vargas, C. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807707105 · Cited by 228 · see citing works

Overview on the Application of Modern Methods for the Extraction of Bioactive Compounds from Marine Macroalgae

Cikoš, A.-M., Jokić, S., Šubarić, D., & Jerković, I. (2018) · Marine Drugs · doi:10.3390/md16100348 · Cited by 225 · see citing works

Exopolysaccharides from Microalgae and Cyanobacteria: Diversity of Strains, Production Strategies, and Applications

Laroche, C. (2022) · Marine Drugs · doi:10.3390/md20050336 · Cited by 218 · see citing works

BioCO2 – A multidisciplinary, biological approach using solar energy to capture CO2 while producing H2 and high value products

Skjånes, K., Lindblad, P. C., & Muller, J. (2007) · Biomolecular Engineering · doi:10.1016/j.bioeng.2007.06.002 · Cited by 215 · see citing works

The anti-cancer effects of fucoidan: a review of both in vivo and in vitro investigations

Lin, Y., Qi, X., Liu, H.-J., Xue, K., Xu, S., & Tian, Z. (2020) · Cancer Cell International · doi:10.1186/s12935-020-01233-8 · Cited by 214 · see citing works

Phytoplankton defence mechanisms: traits and trade‐offs

Pančić, M., & Kiørboe, T. (2018) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12395 · Cited by 212 · see citing works

Microalgae Encapsulation Systems for Food, Pharmaceutical and Cosmetics Applications

Vieira, M. V., Pastrana, L. M., & Fuciños, P. (2020) · Marine Drugs · doi:10.3390/md18120644 · Cited by 205 · see citing works

Influence of sulphate on the composition and antibacterial and antiviral properties of the exopolysaccharide from Porphyridium cruentum

Raposo, M. F. D. J., Morais, A. M. M. B., & Morais, R. M. S. C. (2014) · Life Sciences · doi:10.1016/j.lfs.2014.02.013 · Cited by 200 · see citing works

Extracellular polysaccharide synthesis by Nostoc strains as affected by N source and light intensity

Otero, A., & Vincenzini, M. (2003) · Journal of Biotechnology · doi:10.1016/s0168-1656(03)00022-1 · Cited by 191 · see citing works

Health Benefits of Algal Polysaccharides in Human Nutrition

Mišurcová, L., Škrovánková, S., Samek, D., Ambrožová, J. V., & Machů, L. (2012) · Advances in food and nutrition research · doi:10.1016/b978-0-12-394597-6.00003-3 · Cited by 157 · see citing works

Antiviral Polymers: Past Approaches and Future Possibilities

Bianculli, R. H., Mase, J. D., & Schulz, M. D. (2020) · Macromolecules · doi:10.1021/acs.macromol.0c01273 · Cited by 147 · see citing works

Natural products against cancer: Review on phytochemicals from marine sources in preventing cancer

Wali, A. F., Majid, S., Rasool, S., Shehada, S. B., Abdulkareem, S. K., Firdous, A., Beigh, S., Shakeel, S., Mushtaq, S., Akbar, I., et al. (2019) · Saudi Pharmaceutical Journal · doi:10.1016/j.jsps.2019.04.013 · Cited by 147 · see citing works

Biotechnological exploitation of microalgae

Gangl, D., Zedler, J. A. Z., Rajakumar, P. D., Ramos‐Martinez, E. M., Riseley, A. S., Włodarczyk, A., Purton, S., Sakuragi, Y., Howe, C. J., Jensen, P. E., et al. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv426 · Cited by 145 · see citing works

Polysaccharides as Potential Anti-tumor Biomacromolecules —A Review

Guo, R., Chen, M., Ding, Y., Pengyao, Y., Wang, M., Zhang, H., He, Y., & Ma, H. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.838179 · Cited by 142 · see citing works

Therapeutic Potentials of Microalgae in the Treatment of Alzheimer’s Disease

Olasehinde, T. A., Olaniran, A. O., & Okoh, A. I. (2017) · Molecules · doi:10.3390/molecules22030480 · Cited by 141 · see citing works

Isolation and antioxidant property of the extracellular polysaccharide from Rhodella reticulata

Chen, B., You, W., Huang, J., Yu, Y., & Chen, W. (2009) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-009-0240-y · Cited by 130 · see citing works

Anti-herpes Simplex Virus Target of an Acidic Polysaccharide, Nostoflan, from the Edible Blue-Green Alga Nostoc flagelliforme

Kanekiyo, K., Hayashi, K., Takenaka, H., Lee, J., & Hayashi, T. (2007) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.30.1573 · Cited by 127 · see citing works

Microalgal Cell Biofactory—Therapeutic, Nutraceutical and Functional Food Applications

Kiran, B. R., & Venkata Mohan, S. (2021) · Plants · doi:10.3390/plants10050836 · Cited by 124 · see citing works

Concomitant extraction of bio-oil and value added polysaccharides from Chlorella sorokiniana using a unique sequential hydrothermal extraction technology

Chakraborty, M., Miao, C., McDonald, A. G., & Chen, S. (2011) · Fuel · doi:10.1016/j.fuel.2011.10.055 · Cited by 118 · see citing works

Green seaweed Enteromorpha compressa ( Chlorophyta , Ulvaceae ) derived sulphated polysaccharides inhibit herpes simplex virus

Lopes, N., Ray, S., Espada, S. F., Bomfim, W. A., Ray, B., Galhardi, L. C. F., Linhares, R. E. C., & Nozawa, C. (2017) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2017.04.043 · Cited by 115 · see citing works

Advances in the production of bioactive substances from marine unicellular microalgae Porphyridium spp.

Li, S., Ji, L., Shi, Q., Wu, H., & Fan, J. (2019) · Bioresource Technology · doi:10.1016/j.biortech.2019.122048 · Cited by 113 · see citing works

Pharmaceutical, Cosmeceutical, and Traditional Applications of Marine Carbohydrates

Ahmed, A. B. A., Adel, M., Karimi, P., & Peidayesh, M. (2014) · Advances in food and nutrition research · doi:10.1016/b978-0-12-800268-1.00010-x · Cited by 112 · see citing works

Medicinal Plants, Phytochemicals, and Herbs to Combat Viral Pathogens Including SARS-CoV-2

Anand, A. V., Balasubramanian, B., Kaviya, M., Kathirvel, B., Parithathvi, A., Meyyazhagan, A., Senthilkumar, N., Velayuthaprabhu, S., Muthukrishnan, S., Al-Dhabi, N. A., et al. (2021) · Molecules · doi:10.3390/molecules26061775 · Cited by 110 · see citing works

Preparation and antiherpetic activities of chemically modified polysaccharides from Polygonatum cyrtonema Hua

Liu, X., Wan, Z.-J., Shi, L., & Lü, X. (2010) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2010.08.044 · Cited by 108 · see citing works

Antiviral compounds obtained from microalgae commonly used as carotenoid sources

Santoyo, S., Jaime, L., Plaza, M., Herrero, M., Rodríguez‐Meizoso, I., Ibáñez, E., & Reglero, G. (2011) · Journal of Applied Phycology · doi:10.1007/s10811-011-9692-1 · Cited by 105 · see citing works

Characterization of Exopolysaccharides Produced by Cyanobacteria Isolated from Polynesian Microbial Mats

Richert, L., Golubić, S., Guédès, R. L., Ratiskol, J., Payri, C. E., & Guézennec, J. (2005) · Current Microbiology · doi:10.1007/s00284-005-0069-z · Cited by 101 · see citing works

Preparation and antihypertensive activity of peptides from Porphyra yezoensis

Qu, W., Ma, H., Pan, Z., Luo, L., Wang, Z., & He, R. (2010) · Food Chemistry · doi:10.1016/j.foodchem.2010.03.091 · Cited by 101 · see citing works

Towards the biorefinery concept: Interaction of light, temperature and nitrogen for optimizing the co-production of high-value compounds in Porphyridium purpureum

Guihéneuf, F., & Stengel, D. B. (2015) · Algal Research · doi:10.1016/j.algal.2015.04.025 · Cited by 101 · see citing works

The urge of algal biomass-based fuels for environmental sustainability against a steady tide of biofuel conflict analysis: Is third-generation algal biorefinery a boon?

Sundaram, T., Sundaram, V. A., Dey, N., Gulothungan, G., Subbaiya, R., Govarthanan, M., Karmegam, N., & Kim, W. (2022) · Fuel · doi:10.1016/j.fuel.2022.123494 · Cited by 96 · see citing works

Antiviral Effect of Guazuma ulmifolia and Stryphnodendron adstringens on Poliovirus and Bovine Herpesvirus

Felipe, A. M. M., Rincão, V. P., Benati, F. J., Linhares, R. E. C., Galina, K. J., de Toledo, C. E. M., Lopes, G. C., de Mello, J. C. P., & Nozawa, C. (2006) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.29.1092 · Cited by 92 · see citing works

Structural Characterization and Antioxidant Activities of 2 Water‐Soluble Polysaccharide Fractions Purified from Tea ( Camellia sinensis ) Flower

Quan, H., Qiong‐Yao, Y., Shi, J. T., Xiong, C., Ze‐Jie, L., & He, P. (2011) · Journal of Food Science · doi:10.1111/j.1750-3841.2011.02063.x · Cited by 91 · see citing works

Microalgae: Fast-Growth Sustainable Green Factories

Forján, E., Navarro, F., Cuaresma, M., Vaquero, I., Ruiz‐Domínguez, M. C., Gojkovic, Ž., Vázquez, M., Márquez, M., Mogedas, B., Bermejo, E., et al. (2014) · Critical Reviews in Environmental Science and Technology · doi:10.1080/10643389.2014.966426 · Cited by 84 · see citing works

Marine organisms as a therapeutic source against herpes simplex virus infection

Vo, T., Ngo, D., Ta, Q. V., & Kim, S. (2011) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2011.07.005 · Cited by 83 · see citing works

Immunomodulatory, Antioxidant Activity and Cytotoxic Effect of Sulfated Polysaccharides from Porphyridium cruentum. (S.F.Gray) Nägeli

Casas-Arrojo, V., Decara, J. M., Arrojo, M. Á., Pérez, C. I., & Abdala‐Díaz, R. (2021) · Biomolecules · doi:10.3390/biom11040488 · Cited by 83 · see citing works

Exopolysaccharides from Marine Microbes: Source, Structure and Application

Qi, M., Zheng, C., Wu, W., Yu, G., & Wang, P. (2022) · Marine Drugs · doi:10.3390/md20080512 · Cited by 81 · see citing works

The Potential of Algal Biotechnology to Produce Antiviral Compounds and Biopharmaceuticals

Rosales‐Mendoza, S., García-Silva, I., González‐Ortega, O., Sandoval-Vargas, J. M., Malla, A., & Vimolmangkang, S. (2020) · Molecules · doi:10.3390/molecules25184049 · Cited by 79 · see citing works

Anticancer, Antiviral, Antibacterial, and Antifungal Properties in Microalgae

Dewi, I. C., Falaise, C., Hellio, C., Bourgougnon, N., & Mouget, J. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811405-6.00012-8 · Cited by 80 · see citing works

Microalgae, Functional Genomics and Biotechnology

Cadoret, J., Garnier, M., & Saint‐Jean, B. (2012) · Advances in botanical research · doi:10.1016/b978-0-12-391499-6.00008-6 · Cited by 79 · see citing works

Cancer Protective Action of Polysaccharide, Derived from Red Microalga<i>Porphyridium Cruentum</i>—A Biological Background

Gardeva, E., Toshkova, R., Minkova, K., & Gigova, L. (2009) · Biotechnology &amp; Biotechnological Equipment · doi:10.1080/13102818.2009.10818540 · Cited by 76 · see citing works

Preparation of the different derivatives of the low-molecular-weight porphyran from Porphyra haitanensis and their antioxidant activities in vitro

Zhang, Z., Zhang, Q., Wang, J., Zhang, H., Niu, X., & Li, P. (2009) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2009.03.009 · Cited by 75 · see citing works

Sulfated polysaccharide of Caesalpinia ferrea inhibits herpes simplex virus and poliovirus

Lopes, N., Galhardi, L. C. F., Espada, S. F., Pacheco, A. C., Ricardo, N. M. P. S., Linhares, R. E. C., & Nozawa, C. (2013) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2013.05.015 · Cited by 73 · see citing works

Bioactivity and Applications of Polysaccharides from Marine Microalgae

Raposo, M. F. D. J., Morais, A. M. M. B., & Morais, R. M. S. C. (2015) · Springer eBooks · doi:10.1007/978-3-319-16298-0_47 · Cited by 67 · see citing works

Potential of Exopolysaccharide from Porphyridium marinum to Contend with Bacterial Proliferation, Biofilm Formation, and Breast Cancer

Gargouch, N., Elleuch, F., Karkouch, I., Tabbene, O., Pichon, C., Gardarin, C., Rihouey, C., Picton, L., Abdelkafi, S., Fendri, I., et al. (2021) · Marine Drugs · doi:10.3390/md19020066 · Cited by 65 · see citing works

Structure of polysaccharide from Polygonatum cyrtonema Hua and the antiherpetic activity of its hydrolyzed fragments

LIU, F., Liu, Y., Meng, Y., Yang, M., & HE, K. (2004) · Antiviral Research · doi:10.1016/j.antiviral.2004.04.006 · Cited by 64 · see citing works

In Vivo Anti-Herpes Simplex Virus Activity of a Sulfated Derivative of Agaricus brasiliensis Mycelial Polysaccharide

Cardozo, F. T. G. S., Larsen, I. V., Carballo, E. V., José, G., Stern, R. A., Brummel, R., Camelini, C. M., Rossi, M. J., Simões, C. M. O., & Brandt, C. R. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02250-12 · Cited by 61 · see citing works

Development of a Green Downstream Process for the Valorization of Porphyridium cruentum Biomass

Gallego, R., Martínez, M., Cifuentes, A., Ibáñez, E., & Herrero, M. (2019) · Molecules · doi:10.3390/molecules24081564 · Cited by 60 · see citing works

A REVIEW ON MARINE ALGAE AND ITS APPLICATIONS

Veluchamy, C., & Palaniswamy, R. (2020) · Asian Journal of Pharmaceutical and Clinical Research · doi:10.22159/ajpcr.2020.v13i3.36130 · Cited by 58 · see citing works

High-added value products from microalgae and prospects of aquaculture wastewaters as microalgae growth media

Dourou, M., Dritsas, P., Baeshen, M. N., Elazzazy, A. M., AL-Farga, A. M., & Aggelis, G. (2020) · FEMS Microbiology Letters · doi:10.1093/femsle/fnaa081 · Cited by 57 · see citing works

Integrated marine microalgae biorefineries for improved bioactive compounds: A review

Cheng, P., Li, Y., Wang, C., Guo, J., Zhou, C., Zhang, R., Ma, Y., Ma, X., Wang, L., Cheng, Y., et al. (2022) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.152895 · Cited by 57 · see citing works

Physicochemical properties, immunomodulation and antitumor activities of polysaccharide from Pavlova viridis

Sun, L., Jinling, C., Sun, Z., & Chen, L. (2015) · Life Sciences · doi:10.1016/j.lfs.2015.11.013 · Cited by 56 · see citing works

Microalgae-derived polysaccharides: Potential building blocks for biomedical applications

Severo, I. A., Dias, R. R., do Nascimento, T. C., Deprá, M. C., Maroneze, M. M., Zepka, L. Q., & Lopes, E. J. (2022) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-022-03342-0 · Cited by 56 · see citing works

The sulfated polysaccharide from a marine red microalga as a platform for the incorporation of zinc ions

Liberman, G. N., Ochbaum, G., Arad, S. M., & Bitton, R. (2016) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2016.07.025 · Cited by 55 · see citing works

The antiviral potential of algal-derived macromolecules

Liu, J., Obaidi, I., Nagar, S., Scalabrino, G., & Sheridan, H. (2021) · Current Research in Biotechnology · doi:10.1016/j.crbiot.2021.04.003 · Cited by 53 · see citing works

Synthesized oversulfated and acetylated derivatives of polysaccharide extracted from Enteromorpha linza and their potential antioxidant activity

Zhang, Z., Wang, X., Shu-chi, Y., Yin, L., Zhao, M., & Han, Z.-P. (2011) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2011.08.023 · Cited by 53 · see citing works

Seaweeds’ nutraceutical and biomedical potential in cancer therapy: a concise review

Cotas, J., Pacheco, D., Gonçalves, A. M. M., silva, P. H. D. S., Carvalho, L. G., & Pereira, L. (2021) · Journal of Cancer Metastasis and Treatment · doi:10.20517/2394-4722.2020.134 · Cited by 50 · see citing works

Characterization and immunostimulating activity of a water-soluble polysaccharide isolated from Haematococcus lacustris

Park, J. K., Kim, Z.-H., Lee, C., Synytsya, A., Jo, H. S., Kim, S. O., Park, J. W., & Park, Y. I. (2011) · Biotechnology and Bioprocess Engineering · doi:10.1007/s12257-011-0173-9 · Cited by 47 · see citing works

Exploring the Diversity of Red Microalgae for Exopolysaccharide Production

Borjas, A., Gardarin, C., & Laroche, C. (2022) · Marine Drugs · doi:10.3390/md20040246 · Cited by 46 · see citing works

Screening, production, optimization and characterization of cyanobacterial polysaccharide

Singh, S., & Das, S. (2011) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-011-0657-y · Cited by 47 · see citing works

Antiviral Activities of Polysaccharides from Natural Sources

Martínez, M. J. A., Bedoya, L. M., & Bermejo, P. (2005) · Studies in natural products chemistry · doi:10.1016/s1572-5995(05)80038-9 · Cited by 46 · see citing works

Sulfated exopolysaccharides from Porphyridium cruentum: A useful strategy to extend the shelf life of minced beef meat

Hlima, H. B., Smaoui, S., Barkallah, M., Elhadef, K., Tounsi, L., Michaud, P., Fendri, I., & Abdelkafi, S. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.10.161 · Cited by 45 · see citing works

Antiviral Properties of Phytochemicals

Liu, A., & Du, G. (2012) · Springer eBooks · doi:10.1007/978-94-007-3926-0_3 · Cited by 43 · see citing works

Microbial Metabolites: The Emerging Hotspot of Antiviral Compounds as Potential Candidates to Avert Viral Pandemic Alike COVID-19

Raihan, T., Rabbee, M. F., Roy, P., Choudhury, S., Baek, K.-H., & Azad, A. K. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.732256 · Cited by 43 · see citing works

Production, isolation and bioactive estimation of extracellular polysaccharides of green microalga Neochloris oleoabundans

Li, Y., Wang, C., Liu, H., Su, J., Lan, C. Q., Zhong, M., & Hu, X. (2020) · Algal Research · doi:10.1016/j.algal.2020.101883 · Cited by 42 · see citing works

Marine Bioactives and Potential Application in Sports

Gammone, M. A., Gemello, E., Riccioni, G., & D’Orazio, N. (2014) · Marine Drugs · doi:10.3390/md12052357 · Cited by 41 · see citing works

Bioactive polysaccharides from microalgae

Prybylski, N., Toucheteau, C., Alaoui, H. E., Bridiau, N., Maugard, T., Abdelkafi, S., Fendri, I., Delattre, C., Dubessay, P., Pierre, G., et al. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818536-0.00020-8 · Cited by 39 · see citing works

Chemical modifications in the structure of seaweed polysaccharides as a viable antimicrobial application: A current overview and future perspectives

Santinon, C., Ochi, D., Beppu, M. M., & Vieira, M. G. A. (2022) · Algal Research · doi:10.1016/j.algal.2022.102796 · Cited by 41 · see citing works

Optimization of culturing conditions of Porphyridium cruentum using uniform design

Wang, J., Chen, B., Rao, X., Huang, J., & Li, M. (2007) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-007-9369-8 · Cited by 39 · see citing works

Feasibility of attached cultivation for polysaccharides production by Porphyridium cruentum

Lutzu, G. A., Zhang, L., Zhang, Z., & Liu, T. (2016) · Bioprocess and Biosystems Engineering · doi:10.1007/s00449-016-1676-8 · Cited by 39 · see citing works

Anticoagulant, Antiherpetic and Antibacterial Activities of Sulphated Polysaccharide from Indian Medicinal Plant Tridax procumbens L. (Asteraceae)

Naqash, S. Y., & Nazeer, R. A. (2011) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-011-9307-y · Cited by 40 · see citing works

Microalgae: A Promising Source of Bioactive Polysaccharides for Biotechnological Applications

Magnabosco, C., Santaniello, G., & Romano, G. (2025) · Molecules · doi:10.3390/molecules30092055 · Cited by 36 · see citing works

Screening for Bioactive Compounds from Algae

Herrero, M., Mendiola, J. A., Plaza, M., & Ibáñez, E. (2012) · Springer eBooks · doi:10.1007/978-1-4614-3348-4_35 · Cited by 39 · see citing works

A Review of Antiviral and Antioxidant Activity of Bioactive Metabolite of Macroalgae within an Optimized Extraction Method

ElShafei, R. A. E. N., Hegazy, H., & Acharya, B. (2021) · Energies · doi:10.3390/en14113092 · Cited by 36 · see citing works

Effects of Light Regime on Extracellular Polysaccharide Production by Porphyridium Cruentum Cultured in Flat Plate Photobioreactors

Liqin, S., Wang, C., & Shi, L. G. (2008) · International Conference on Bioinformatics and Biomedical Engineering · doi:10.1109/icbbe.2008.701 · Cited by 34 · see citing works

Biofiltration of fishpond effluents and accumulation of N-compounds (phycobiliproteins and mycosporine-like amino acids) versus C-compounds (polysaccharides) in Hydropuntia cornea (Rhodophyta)

Figueroa, F. L., Korbee, N., Abdala, R., Jerez, C. G., López-de la Torre, M., Güenaga, L., Larrubia, M. A., & Gómez-Pinchetti, J. L. (2012) · Marine Pollution Bulletin · doi:10.1016/j.marpolbul.2011.11.012 · Cited by 32 · see citing works

Can Algal Derived Bioactive Metabolites Serve as Potential Therapeutics for the Treatment of SARS-CoV-2 Like Viral Infection?

Bhatt, A., Arora, P., & Prajapati, S. K. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.596374 · Cited by 33 · see citing works

Recent Advances in Marine Enzymes for Biotechnological Processes

Lima, R. N., & Porto, A. L. M. (2016) · Advances in food and nutrition research · doi:10.1016/bs.afnr.2016.06.005 · Cited by 33 · see citing works

Antimycobacterial Activity of the Red AlgaPolysiphonia virgata.

Saravanakumar, D. E. M., Folb, P. I., Campbell, B., & Smith, P. (2008) · Pharmaceutical Biology · doi:10.1080/13880200701739413 · Cited by 32 · see citing works

Effects of sulfated lentinan on cellular infectivity of avian infectious bronchitis virus

Wang, D., Guo, Z., Ma, X., Hu, Y., Huang, X., Fan, Y., Yang, S., & Guo, L. (2009) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2009.09.016 · Cited by 30 · see citing works

Antiviral effect of red microalgal polysaccharides on Herpes simplex and Varicella zoster viruses

Huleihel, M., Ishanu, V., Tal, J., & Arad, S. (2001) · Journal of Applied Phycology · doi:10.1023/a:1011178225912 · Cited by 179 · see citing works

A review of studies of Porphyridium sp. and its polysaccharide

Liu, X. (2004) · Guangxi kexue · Cited by 1 · see citing works

Antiviral property and mechanisms of a sulphated polysaccharide from the brown alga Sargassum patens against Herpes simplex virus type 1

Zhu, W., Chiu, L. C. M., Ooi, V. E. C., Chan, P. K. S., & Ang, P. O. (2006) · Phytomedicine · doi:10.1016/j.phymed.2005.11.003 · Cited by 83 · see citing works

Over-sulfation of polysaccharides derived from Porphyridium cruentum: Characterization and antiviral activity against Herpes viruses

Karshan, N., Huliehel, M., & Levy‐Ontman, O. (2026) · Polymer · doi:10.1016/j.polymer.2026.130755

Antiviral Activities of Sulfated Polysaccharides Isolated from Sphaerococcus coronopifolius (Rhodophytha, Gigartinales) and Boergeseniella thuyoides (Rhodophyta, Ceramiales)

Bouhlal, R., Haslin, C., Chermann, J., Colliec‐Jouault, S., Sinquin, C., Simon, G., Cérantola, S., Riadi, H., & Bourgougnon, N. (2011) · Marine Drugs · doi:10.3390/md9071187 · Cited by 188 · see citing works