Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Sindhuri Prakash"'
Autor:
Yifu Li, Emily E. Groopman, Vivette D’Agati, Sindhuri Prakash, Junying Zhang, Malgorzata Mizerska-Wasiak, Yasar Caliskan, David Fasel, Hussein H. Karnib, Luisa Bono, Sadek Al Omran, Essam Al Sabban, Krzysztof Kiryluk, Gianluca Caridi, Gian Marco Ghiggeri, Simone Sanna-Cherchi, Francesco Scolari, Ali G. Gharavi
Publikováno v:
Kidney International Reports, Vol 5, Iss 7, Pp 1075-1078 (2020)
Externí odkaz:
https://doaj.org/article/616de8107c424b09b01c04830b17999d
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
Publikováno v:
Kidney International. 102:673-674
Autor:
Sindhuri Prakash, Jordan G. Nestor
Publikováno v:
Technological Advances in Care of Patients with Kidney Diseases ISBN: 9783031119415
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5694de7c15beff7d0ac11a4f598dde61
https://doi.org/10.1007/978-3-031-11942-2_1
https://doi.org/10.1007/978-3-031-11942-2_1
Autor:
Gian Marco Ghiggeri, Hussein H. Karnib, Małgorzata Mizerska-Wasiak, Vivette D. D'Agati, Sindhuri Prakash, Krzysztof Kiryluk, Sadek A.Ai. Omran, Gianluca Caridi, David Fasel, Luisa Bono, Junying Zhang, Ali G. Gharavi, Essam Ai. Sabban, Francesco Scolari, Yasar Caliskan, Simone Sanna-Cherchi, Emily E. Groopman, Yifu Li
Publikováno v:
Kidney International Reports, Vol 5, Iss 7, Pp 1075-1078 (2020)
Kidney International Reports
Kidney International Reports
Autor:
Sindhuri Prakash, Ali G. Gharavi
Publikováno v:
Clin J Am Soc Nephrol
BACKGROUND AND OBJECTIVES: IgA nephropathy is the most common form of primary GN worldwide. The evidence of geographic and ethnic differences, as well as familial aggregation of the disease, supports a strong genetic contribution to IgA nephropathy.
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
Publikováno v:
Leukemia Research and Treatment
Common blood disorders include hematopoietic cell malignancies or leukemias and plasma cell dyscrasia, all of which have associated microRNA abnormalities. In this paper, we discuss several leukemias including acute myeloid leukemia (AML) and chronic
Autor:
Leslie A. Bruggeman, Vivette D. D'Agati, Zhenzhen Wu, Zongyu Zheng, Robert L. Thomas, Ali G. Gharavi, Roel Sterken, Sindhuri Prakash, Natalia Papeta, John R. Sedor
Publikováno v:
Journal of the American Society of Nephrology. 22:1497-1504
HIVAN1, HIVAN2, and HIVAN3 are nephropathy-susceptibility loci previously identified in the HIV-1 transgenic mouse, a model of collapsing glomerulopathy. The HIVAN1 and HIVAN2 loci modulate expression of Nphs2, which encodes podocin and several other
Autor:
Sindhuri Prakash, Ali G. Gharavi
Publikováno v:
Current opinion in nephrology and hypertension. 24(4)
Recent technological improvements have increased the use of genetic testing in the clinic. This review serves to summarize the many practical benefits of genetic testing, discusses various methodologies that can be used clinically, and exemplifies wa