Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Moumita Barua"'
Autor:
Sarah A. Gagliano Taliun, Ian R. Dinsmore, Tooraj Mirshahi, Alexander R. Chang, Andrew D. Paterson, Moumita Barua
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Our GWAS of hematuria in the UK Biobank identified 6 loci, some of which overlap with loci for albuminuria suggesting pleiotropy. Since clinical syndromes are often defined by combinations of traits, generating a combined phenotype can impro
Externí odkaz:
https://doaj.org/article/2961d97a0ea84df2982656a4fb202606
Autor:
Sarah A. Gagliano Taliun, Ian R. Dinsmore, Tooraj Mirshahi, Alexander R. Chang, Andrew D. Paterson, Moumita Barua
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/47fbc4e88ff44fc7b1bf3fb2c70a986c
Publikováno v:
Kidney Medicine, Vol 5, Iss 5, Pp 100631- (2023)
Alport syndrome is a hereditary disorder characterized by kidney disease, ocular abnormalities, and sensorineural hearing loss. Work in understanding the cause of Alport syndrome and the molecular composition of the glomerular basement membrane ultim
Externí odkaz:
https://doaj.org/article/7d1b10c287494916a24c1f79a923b161
Autor:
Poornima Vijayan, Saidah Hack, Tony Yao, Mohammad Azfar Qureshi, Andrew D. Paterson, Rohan John, Bernard Davenport, Rachel Lennon, York Pei, Moumita Barua
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-6 (2021)
Abstract Background Focal and segmental glomerulosclerosis (FSGS) is a histologic pattern of injury that characterizes a wide spectrum of diseases. Many genetic causes have been identified in FSGS but even in families with comprehensive testing, a si
Externí odkaz:
https://doaj.org/article/1baf9a696e0c489a99934778bbd0a795
Autor:
Cole Shulman, Emerald Liang, Misato Kamura, Khalil Udwan, Tony Yao, Daniel Cattran, Heather Reich, Michelle Hladunewich, York Pei, Judy Savige, Andrew D. Paterson, Mary Ann Suico, Hirofumi Kai, Moumita Barua
Publikováno v:
Kidney Medicine, Vol 3, Iss 2, Pp 257-266 (2021)
Rationale & Objective: Pathogenic variants in type IV collagen have been reported to account for a significant proportion of chronic kidney disease. Accordingly, genetic testing is increasingly used to diagnose kidney diseases, but testing also may r
Externí odkaz:
https://doaj.org/article/ffd8ff3c66d642ec8e6b32efc848dda8
Autor:
Ainslie M. Hildebrand, Moumita Barua, Sean J. Barbour, Karthik K. Tennankore, Daniel C. Cattran, Tomoko Takano, Ping Lam, Sacha A. De Serres, Ratna Samanta, Michelle A. Hladunewich, Todd Fairhead, Penelope Poyah, D. Danielle Bush, Brian MacLaren, Dwight Sparkes, Philip Boll, Arenn Jauhal, Rohan John, Carmen Avila-Casado, Heather N. Reich
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 9 (2022)
Background: Glomerulonephritis (GN) is a leading cause of kidney failure and accounts for 20% of incident cases of end-stage kidney disease (ESKD) in Canada annually. Reversal of kidney injury and prevention of progression to kidney failure is possib
Externí odkaz:
https://doaj.org/article/a7e9b9e8e2954c89a16b956da9e77828
Publikováno v:
Journal of Agrometeorology, Vol 23, Iss 4 (2021)
Externí odkaz:
https://doaj.org/article/79fddde3290b4218944985125fc9a27f
Publikováno v:
The Indian Journal of Agricultural Sciences, Vol 91, Iss 7 (2021)
Field experiment was planned to investigate the integration of establishment methods, variable seed rates and weed control in zero-till wheat (Triticum aestivum L.). The experiment was conducted in split-plot design with four replications. Treatments
Externí odkaz:
https://doaj.org/article/7e421843042144afa84f3ec88fedbf05
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 4 (2017)
Purpose of Review: Patient engagement in research is increasingly recognized as an important component of the research process and may facilitate translation of research findings. To heighten awareness on this important topic, this review presents op
Externí odkaz:
https://doaj.org/article/1b05b231c41d4125812354ac03d7b562
Autor:
Sergio Daga, Jie Ding, Constantinos Deltas, Judy Savige, Beata S. Lipska-Ziętkiewicz, Julia Hoefele, Frances Flinter, Daniel P. Gale, Marina Aksenova, Hirofumi Kai, Laura Perin, Moumita Barua, Roser Torra, Jeff H. Miner, Laura Massella, Danica Galešić Ljubanović, Rachel Lennon, Andrè B. Weinstock, Bertrand Knebelmann, Agne Cerkauskaite, Susie Gear, Oliver Gross, A. Neil Turner, Margherita Baldassarri, Anna Maria Pinto, Alessandra Renieri
Publikováno v:
European Journal of Human Genetics.