Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Roel, Sterken"'
Autor:
Francesca Lugani, Ripla Arora, Natalia Papeta, Ami Patel, Zongyu Zheng, Roel Sterken, Ruth A Singer, Gianluca Caridi, Cathy Mendelsohn, Lori Sussel, Virginia E Papaioannou, Ali G Gharavi
Publikováno v:
PLoS Genetics, Vol 9, Iss 2, p e1003206 (2013)
Danforth's short tail mutant (Sd) mouse, first described in 1930, is a classic spontaneous mutant exhibiting defects of the axial skeleton, hindgut, and urogenital system. We used meiotic mapping in 1,497 segregants to localize the mutation to a 42.8
Externí odkaz:
https://doaj.org/article/5f4f2d23e14d4828a4b401726b1aba27
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
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:
Michael W. Ross, Jonathan A. Winston, Mary E. Klotman, Robert J. Wyatt, Holly J. Snyder, Vivette D. D'Agati, Nilgun Kacak, Jan Novak, Roel Sterken, Ali G. Gharavi, Anand N. Mhatre, Gerald B. Appel, Natalia Papeta, Bruce A. Julian, Christina M. Wyatt, Phil H. Imus, Ami Patel, Anil K. Lawani, David J. Cohen, Paul E. Klotman, Krzysztof Kiryluk
Publikováno v:
Journal of the American Society of Nephrology. 22:1991-1996
A chromosome 22q13 locus strongly associates with increased risk for idiopathic focal segmental glomerulosclerosis (FSGS), HIV-1-associated nephropathy (HIVAN), and hypertensive ESRD among individuals of African descent. Although initial studies impl
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:
Gianluca Caridi, Ami Patel, Ruth A. Singer, Virginia E. Papaioannou, Ripla Arora, Zongyu Zheng, Francesca Lugani, Roel Sterken, Lori Sussel, Ali G. Gharavi, Natalia Papeta, Cathy Mendelsohn
Publikováno v:
PLoS Genetics, Vol 9, Iss 2, p e1003206 (2013)
Danforth's short tail mutant (Sd) mouse, first described in 1930, is a classic spontaneous mutant exhibiting defects of the axial skeleton, hindgut, and urogenital system. We used meiotic mapping in 1,497 segregants to localize the mutation to a 42.8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f17154aad349de2ecb0c964325cfc684
Autor:
Ilse Vercauteren, Marnik Vuylsteke, Fanghong Zhang, Annelies Vercauteren, Raphaël Kiekens, Joanna Boruc, Lien De Smet, Dirk Inzé, Eugenia Russinova, Roel Sterken, Stijn Dhondt, Lieven De Veylder
Endoreduplication is the process where a cell replicates its genome without mitosis and cytokinesis, often followed by cell differentiation. This alternative cell cycle results in various levels of endoploidy, reaching 4× or higher one haploid set o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cb53fd338133282e1a8ed5152d8adf6
https://biblio.vub.ac.be/vubir/combined-linkage-and-association-mapping-reveals-cycd51-as-a-quantitative-trait-gene-for-endoreduplication-in-arabidopsis(70754e0c-776c-465e-90fe-5531a369aafe).html
https://biblio.vub.ac.be/vubir/combined-linkage-and-association-mapping-reveals-cycd51-as-a-quantitative-trait-gene-for-endoreduplication-in-arabidopsis(70754e0c-776c-465e-90fe-5531a369aafe).html
Autor:
Francesca, Lugani, Ripla, Arora, Natalia, Papeta, Ami, Patel, Zongyu, Zheng, Roel, Sterken, Ruth A, Singer, Gianluca, Caridi, Cathy, Mendelsohn, Lori, Sussel, Virginia E, Papaioannou, Ali G, Gharavi
Publikováno v:
PLoS Genetics
Danforth's short tail mutant (Sd) mouse, first described in 1930, is a classic spontaneous mutant exhibiting defects of the axial skeleton, hindgut, and urogenital system. We used meiotic mapping in 1,497 segregants to localize the mutation to a 42.8
Autor:
Roel Sterken, Krzysztof Kiryluk
Publikováno v:
Kidney international. 77(3)
Aging is a physiological process involving both genetic factors and environmental agents that can lead to function loss in organs. In the kidney, aging can cause leakage of proteins in urine, starting with albumin. Discovering molecular mechanisms re
Autor:
Emmy Coppens, Jonathan M. Flowers, Dirk Inzé, Marc Zabeau, Raphaël Kiekens, Ilse Vercauteren, Marnik Vuylsteke, Roel Sterken
Publikováno v:
PLANT CELL
Large-scale comparison of sequence polymorphism and divergence at numerous genomic loci within and between closely related species can reveal signatures of natural selection. Here, we present a population genomics study based on direct sequencing of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46827a6614e0affca6b467188ceb32cf
https://hdl.handle.net/1854/LU-815094
https://hdl.handle.net/1854/LU-815094