Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Drew Bradbury"'
Autor:
Krzysztof Kiryluk, Yifu Li, Zina Moldoveanu, Hitoshi Suzuki, Colin Reily, Ping Hou, Jingyuan Xie, Nikol Mladkova, Sindhuri Prakash, Clara Fischman, Samantha Shapiro, Robert A LeDesma, Drew Bradbury, Iuliana Ionita-Laza, Frank Eitner, Thomas Rauen, Nicolas Maillard, Francois Berthoux, Jürgen Floege, Nan Chen, Hong Zhang, Francesco Scolari, Robert J Wyatt, Bruce A Julian, Ali G Gharavi, Jan Novak
Publikováno v:
PLoS Genetics, Vol 13, Iss 2, p e1006609 (2017)
Aberrant O-glycosylation of serum immunoglobulin A1 (IgA1) represents a heritable pathogenic defect in IgA nephropathy, the most common form of glomerulonephritis worldwide, but specific genetic factors involved in its determination are not known. We
Externí odkaz:
https://doaj.org/article/a1383fb1ffad4d53aeb9cfe36dabf45f
Autor:
Hila Milo-Rasouly, Sophia R. Cameron-Christie, Vimla Aggarwal, Carolina Haefliger, Byum Hee Kil, Adam Platt, Brett Copeland, Andrew S. Bomback, Wan Yee Lam, Natalie S Uy, Simone Sanna-Cherchi, Junying Zhang, Rachel Reingold, Zhong Ren, Stacy Piva, Adele Mitrotti, David J. Cohen, Debanjana Chatterjee, Ruth March, Emily E. Groopman, Maddalena Marasa, Drew Bradbury, Sumit Mohan, Michael DiVecchia, David Goldstein, Shumyle Alam, Colin D. Malone, Jordan G. Nestor, Jan Fleckner, Chunhua Weng, Gerald B. Appel, Yifu Li, Priya Krithivasan, Russell J. Crew, Neha Dagaonkar, Olivia Balderes, Karla Mehl, David Fasel, Holly J. Snyder, Maya K. Rao, Joshua Bridgers, Geoffrey K. Dube, Krzysztof Kiryluk, Pietro A. Canetta, Bengt Fellström, Ali G. Gharavi, Jai Radhakrishnan, Wooin Ahn, Caroline Mebane, Slavé Petrovski, Xueru Mu, Sitharthan Kamalakaran
Publikováno v:
New England Journal of Medicine. 380:142-151
BACKGROUND: Exome sequencing is emerging as a first-line diagnostic method in some clinical disciplines, but its usefulness has yet to be examined for most constitutional disorders in adults, including chronic kidney disease, which affects more than
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1e8c8b3cbd348e504a27d334077dccd
https://doi.org/10.1056/nejmoa1806891
https://doi.org/10.1056/nejmoa1806891
Autor:
Nicholas J, Steers, Yifu, Li, Zahida, Drace, Justin A, D'Addario, Clara, Fischman, Lili, Liu, Katherine, Xu, Young-Ji, Na, Y Dana, Neugut, Jun Y, Zhang, Roel, Sterken, Olivia, Balderes, Drew, Bradbury, Nilgun, Ozturk, Fatih, Ozay, Sanya, Goswami, Karla, Mehl, Jaclyn, Wold, Fatima Z, Jelloul, Mersedeh, Rohanizadegan, Christopher E, Gillies, Elena-Rodica M, Vasilescu, George, Vlad, Yi-An, Ko, Sumit, Mohan, Jai, Radhakrishnan, David J, Cohen, Lloyd E, Ratner, Francesco, Scolari, Katalin, Susztak, Matthew G, Sampson, Silvia, Deaglio, Yasar, Caliskan, Jonathan, Barasch, Aisling E, Courtney, Alexander P, Maxwell, Amy J, McKnight, Iuliana, Ionita-Laza, Stephan J L, Bakker, Harold, Snieder, Martin H, de Borst, Vivette, D'Agati, Antonio, Amoroso, Ali G, Gharavi, Krzysztof, Kiryluk
Publikováno v:
The New England journal of medicine. 380(20)
In the context of kidney transplantation, genomic incompatibilities between donor and recipient may lead to allosensitization against new antigens. We hypothesized that recessive inheritance of gene-disrupting variants may represent a risk factor for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fd96c9afaf150d8060f6271fd0e7ff87
https://pubmed.ncbi.nlm.nih.gov/31461605
https://pubmed.ncbi.nlm.nih.gov/31461605
Autor:
Clara Fischman, Silvia Deaglio, Sanya Goswami, F. Scolari, Jun Zhang, Roel Sterken, Fatima Z. Jelloul, Jonathan Barasch, Katherine Xu, Drew Bradbury, Martin H. de Borst, Karla Mehl, Nilgun Ozturk, Alexander P. Maxwell, Mersedeh Rohanizadegan, Dana Neugut, Yasar Caliskan, Olivia Balderes, Vivette D. D'Agati, Krzysztof Kiryluk, Yifu Li, Lloyd E. Ratner, Ali G. Gharavi, Elena R. Vasilescu, Aisling E. Courtney, David J. Cohen, Fatih Ozay, Iuliana Ionita-Laza, Katalin Susztak, Sumit Mohan, Zahida Drace, Matthew G. Sampson, Young Ji Na, Yi-An Ko, Harold Snieder, Jaclyn Wold, Antonio Amoroso, Jai Radhakrishnan, Christopher E. Gillies, Amy Jayne McKnight, George Vlad, Lili Liu, Stephan J.L. Bakker, Nicholas J Steers, Justin A. D'Addario
Publikováno v:
New England Journal of Medicine, 380(20), 1918-1928. MASSACHUSETTS MEDICAL SOC
Background In the context of kidney transplantation, genomic incompatibilities between donor and recipient may lead to allosensitization against new antigens. We hypothesized that recessive inheritance of gene-disrupting variants may represent a risk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8f7a2f188b4a06b629dc19fb27fbecb
http://hdl.handle.net/11379/516619
http://hdl.handle.net/11379/516619
Autor:
Jan Novak, Hong Zhang, Colin Reily, Krzysztof Kiryluk, Sindhuri Prakash, Iuliana Ionita-Laza, Robert J. Wyatt, Ali G. Gharavi, Drew Bradbury, Nikol Mladkova, Nicolas Maillard, Frank Eitner, Nan Chen, Ping Hou, François Berthoux, Yifu Li, Clara Fischman, Jürgen Floege, Jingyuan Xie, Samantha Shapiro, Robert A. LeDesma, Bruce A. Julian, Zina Moldoveanu, Hitoshi Suzuki, Thomas Rauen, Francesco Scolari
Publikováno v:
PLoS Genetics
PLoS Genetics 13(2), e1006609 (2017). doi:10.1371/journal.pgen.1006609
PLoS Genetics, Vol 13, Iss 2, p e1006609 (2017)
PLoS Genetics 13(2), e1006609 (2017). doi:10.1371/journal.pgen.1006609
PLoS Genetics, Vol 13, Iss 2, p e1006609 (2017)
Aberrant O-glycosylation of serum immunoglobulin A1 (IgA1) represents a heritable pathogenic defect in IgA nephropathy, the most common form of glomerulonephritis worldwide, but specific genetic factors involved in its determination are not known. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc12063608a881d239200e0a4c896bc6
http://europepmc.org/articles/PMC5328405
http://europepmc.org/articles/PMC5328405