Global microRNA profiling in human urinary exosomes reveals novel disease biomarkers and cellular pathways for autosomal dominant polycystic kidney disease
Magayr, Tajdida A., Song, Xuewen, Streets, Andrew J., Vergoz, Laura, Chang, Lijun, Valluru, Manoj K., Yap, Hsiu L., Lannoy, Morgane, Haghighi, Amirreza, Simms, Roslyn J., Tam, Frederick W.K., Pei, York, Ong, Albert C.M.
Published in Kidney international (01.08.2020)
Published in Kidney international (01.08.2020)
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MicroRNAs and Their Roles in Breast Cancer Bone Metastasis
Puppo, Margherita, Valluru, Manoj K., Clézardin, Philippe
Published in Current osteoporosis reports (01.06.2021)
Published in Current osteoporosis reports (01.06.2021)
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Journal Article
The positive effect of selective prostaglandin E2 receptor EP2 and EP4 blockade on cystogenesis in vitro is counteracted by increased kidney inflammation in vivo
Lannoy, Morgane, Valluru, Manoj K., Chang, Lijun, Abdela-Ali, Fatima, Peters, Dorien J.M., Streets, Andrew J., Ong, Albert C.M.
Published in Kidney international (01.08.2020)
Published in Kidney international (01.08.2020)
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Journal Article
Combining genotype with height-adjusted kidney length predicts rapid progression of ADPKD
Chen, Eugene W C, Chong, Jiehan, Valluru, Manoj K, Durkie, Miranda, Simms, Roslyn J, Harris, Peter C, Ong, Albert C M
Published in Nephrology, dialysis, transplantation (31.05.2024)
Published in Nephrology, dialysis, transplantation (31.05.2024)
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Debunking the Myth of the Endogenous Antiangiogenic Vegfaxxxb Transcripts
Dardente, Hugues, English, William R., Valluru, Manoj K., Kanthou, Chryso, Simpson, David
Published in Trends in endocrinology and metabolism (01.06.2020)
Published in Trends in endocrinology and metabolism (01.06.2020)
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Journal Article
The Common PKD1 p.(Ile3167Phe) Variant Is Hypomorphic and Associated with Very Early Onset, Biallelic Polycystic Kidney Disease
Durkie, Miranda, Watson, Christopher M., Winship, Peter, Hogg, Anne-Cecile, Nyanhete, Rodney, Cooley, Sharon, Valluru, Manoj K., Shaw-Smith, Charles, Bingham, Coralie, Gilchrist, Mark, Kenny, Janna, Consortium, Genomics England Research, Ong, Albert C. M.
Published in Human mutation (28.07.2023)
Published in Human mutation (28.07.2023)
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A founder UMOD variant is a common cause of hereditary nephropathy in the British population
Valluru, Manoj K, Chung, Noelle KX, Gilchrist, Mark, Butland, Laura, Cook, Jackie, Takou, Anna, Dixit, Abhijit, Weedon, Michael N, Ong, Albert C M, Ambrose, John C, Arumugam, Prabhu, Bevers, Roel, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R, Brittain, Helen, Caulfield, Mark J, Chan, Georgia C, Elgar, Greg, Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J P, Jackson, Rob, Jones, Louise J, Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E A, Leong, Ivonne U S, Lopez, Javier F, MaleadyCrowe, Fiona, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C, O’Donovan, Peter, Odhams, Chris A, Patch, Christine, Pereira, Mariana Buongermino, Perez-Gil, Daniel, Pullinger, John, Rahim, Tahrima, Rendon, Augusto, Rogers, Tim, Savage, Kevin, Sawant, Kushmita, Scott, Richard H, Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C, Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, TaylorTavares, Ana Lisa, Thomas, Ellen R A, Thompson, Simon R, Tucci, Arianna, Welland, Matthew J, Williams, Eleanor, Witkowska, Katarzyna, Wood, Suzanne M
Published in Journal of medical genetics (01.04.2023)
Published in Journal of medical genetics (01.04.2023)
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BICC1 Interacts with PKD1 and PKD2 to Drive Cystogenesis in ADPKD
Tran, Uyen, Streets, Andrew J, Smith, Devon, Decker, Eva, Kirschfink, Annemarie, Izem, Lahoucine, Hassey, Jessie M, Rutland, Briana, Valluru, Manoj K, Bräsen, Jan Hinrich, Ott, Elisabeth, Epting, Daniel, Eisenberger, Tobias, Ong, Albert Cm, Bergmann, Carsten, Wessely, Oliver
Published in bioRxiv (27.08.2024)
Published in bioRxiv (27.08.2024)
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