Items where the Publication is International journal of molecular sciences
Number of items: 9.
2024
  • Identification of a Clade-Specific HLA-C*03:02 CTL Epitope GY9 Derived from the HIV-1 p17 Matrix Protein. (2024) Kyobe, Samuel; Mwesigwa, Savannah; Nkurunungi, Gyaviira; Retshabile, Gaone; Egesa, Moses; Katagirya, Eric; Amujal, Marion; Mlotshwa, Busisiwe C; Williams, Lesedi; Sendagire, Hakim; On Behalf Of The CAfGEN Consortium; Kiragga, Dithan; Mardon, Graeme; Matshaba, Mogomotsi; Hanchard, Neil A; Kyosiimire-Lugemwa, Jacqueline; Robinson, David
    • 2023
  • Altered Faecal Microbiota Composition and Structure of Ghanaian Children with Acute Gastroenteritis. (2023) Quaye, Emmanuel Kofi; Adjei, Raymond Lovelace; Isawumi, Abiola; Allen, David J; Caporaso, J Gregory; Quaye, Osbourne
  • Meta-Analysis and Multivariate GWAS Analyses in 80,950 Individuals of African Ancestry Identify Novel Variants Associated with Blood Pressure Traits. (2023) Udosen, Brenda; Soremekun, Opeyemi; Kamiza, Abram; Machipisa, Tafadzwa; Cheickna, Cisse; Omotuyi, Olaposi; Soliman, Mahmoud; Wélé, Mamadou; Nashiru, Oyekanmi; Chikowore, Tinashe; Fatumo, Segun
    • 2022
  • Characterization and Involvement of Exosomes Originating from Chikungunya Virus-Infected Epithelial Cells in the Transmission of Infectious Viral Elements. (2022) Le, Bao Chi Thi; Burassakarn, Ati; Tongchai, Panwad; Ekalaksananan, Tipaya; Aromseree, Sirinart; Phanthanawiboon, Supranee; Polsan, Yada; Alexander, Neal; Overgaard, Hans J; Pientong, Chamsai
    • 2021
  • Fatal Attraction: The Case of Toxic Soluble Dimers of Truncated PQBP-1 Mutants in X-Linked Intellectual Disability. (2021) Chen, Yu Wai; Rahman, Shah Kamranur
  • Aflatoxin Exposure during Early Life Is Associated with Differential DNA Methylation in Two-Year-Old Gambian Children. (2021) Ghantous, Akram; Novoloaca, Alexei; Bouaoun, Liacine; Cuenin, Cyrille; Cros, Marie-Pierre; Xu, Ya; Hernandez-Vargas, Hector; Darboe, Momodou K; Prentice, Andrew M; Moore, Sophie E; Gong, Yun Yun; Herceg, Zdenko; Routledge, Michael N
    • 2020
  • Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies. (2020) Nikolic, Ana; Jones, Takako I; Govi, Monica; Mele, Fabiano; Maranda, Louise; Sera, Francesco; Ricci, Giulia; Ruggiero, Lucia; Vercelli, Liliana; Portaro, Simona; Villa, Luisa; Fiorillo, Chiara; Maggi, Lorenzo; Santoro, Lucio; Antonini, Giovanni; Filosto, Massimiliano; Moggio, Maurizio; Angelini, Corrado; Pegoraro, Elena; Berardinelli, Angela; Maioli, Maria Antonetta; D'Angelo, Grazia; Di Muzio, Antonino; Siciliano, Gabriele; Tomelleri, Giuliano; D'Esposito, Maurizio; Della Ragione, Floriana; Brancaccio, Arianna; Piras, Rachele; Rodolico, Carmelo; Mongini, Tiziana; Magdinier, Frederique; Salsi, Valentina; Jones, Peter L; Tupler, Rossella
    • 2019
  • Matrix Metalloproteinases in Pulmonary and Central Nervous System Tuberculosis-A Review. (2019) Rohlwink, Ursula K; Walker, Naomi F; Ordonez, Alvaro A; Li, Yifan J; Tucker, Elizabeth W; Elkington, Paul T; Wilkinson, Robert J; Wilkinson, Katalin A
    • 2017
  • Enhancing the Biological Relevance of Machine Learning Classifiers for Reverse Vaccinology. (2017) Heinson, Ashley I; Gunawardana, Yawwani; Moesker, Bastiaan; Hume, Carmen C Denman; Vataga, Elena; Hall, Yper; Stylianou, Elena; McShane, Helen; Williams, Ann; Niranjan, Mahesan; Woelk, Christopher H