Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Blair R Anderson"'
Autor:
Joseph L Bundy, Blair R Anderson, Ludmila Francescatto, Melanie E Garrett, Karen L Soldano, Marilyn J Telen, Erica E Davis, Allison E Ashley-Koch
Publikováno v:
PLoS ONE, Vol 14, Iss 6, p e0217042 (2019)
Kidney failure occurs in 5-13% of individuals with sickle cell disease and is associated with early mortality. Two APOL1 alleles (G1 and G2) have been identified as risk factors for sickle cell disease nephropathy. Both risk alleles are prevalent in
Externí odkaz:
https://doaj.org/article/ef5f0f7699e041f1847316ab35c51e5d
Autor:
Blair R Anderson, David N Howell, Karen Soldano, Melanie E Garrett, Nicholas Katsanis, Marilyn J Telen, Erica E Davis, Allison E Ashley-Koch
Publikováno v:
PLoS Genetics, Vol 11, Iss 9, p e1005459 (2015)
Externí odkaz:
https://doaj.org/article/5fadc95a5a46473e9de08ae7479730e8
Autor:
Blair R Anderson, David N Howell, Karen Soldano, Melanie E Garrett, Nicholas Katsanis, Marilyn J Telen, Erica E Davis, Allison E Ashley-Koch
Publikováno v:
PLoS Genetics, Vol 11, Iss 7, p e1005349 (2015)
African Americans have a disproportionate risk for developing nephropathy. This disparity has been attributed to coding variants (G1 and G2) in apolipoprotein L1 (APOL1); however, there is little functional evidence supporting the role of this protei
Externí odkaz:
https://doaj.org/article/47fd9d600d314115b8742e42b3168e6e
Autor:
Anna Mae Diehl, Albert S. Baldwin, Steve S. Choi, Thiago A. Pereira, Blair R. Anderson, Wing-Kin Syn, Leandi Krüger, Guanhua Xie, Gamze Karaca, Gregory A. Michelotti, Marzena Swiderska-Syn, Jiuyi Lu, Yuping Chen, Cynthia D. Guy, Isaac S. Chan
PDF file - 54K, Related primer sequences
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05b8d2ec0b2169b14befff350b31cf6d
https://doi.org/10.1158/0008-5472.22395345
https://doi.org/10.1158/0008-5472.22395345
Autor:
Anna Mae Diehl, Albert S. Baldwin, Steve S. Choi, Thiago A. Pereira, Blair R. Anderson, Wing-Kin Syn, Leandi Krüger, Guanhua Xie, Gamze Karaca, Gregory A. Michelotti, Marzena Swiderska-Syn, Jiuyi Lu, Yuping Chen, Cynthia D. Guy, Isaac S. Chan
PDF file - 82K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3304070a7fc7230316683cf540b13403
https://doi.org/10.1158/0008-5472.22395348.v1
https://doi.org/10.1158/0008-5472.22395348.v1
Autor:
Anna Mae Diehl, Albert S. Baldwin, Steve S. Choi, Thiago A. Pereira, Blair R. Anderson, Wing-Kin Syn, Leandi Krüger, Guanhua Xie, Gamze Karaca, Gregory A. Michelotti, Marzena Swiderska-Syn, Jiuyi Lu, Yuping Chen, Cynthia D. Guy, Isaac S. Chan
PDF file - 127K, S1. Panc 10.05 cells do not generate functional Hh ligands. S2. Other malignant hepatoma lines can increase MF Hh and glycolytic activity. S3. Summary of glycolytic metabolism. S4. MF-derived lactate provides energy source for lipoge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f58c258ea1f64c97b029fe142a172ee
https://doi.org/10.1158/0008-5472.22395351.v1
https://doi.org/10.1158/0008-5472.22395351.v1
Autor:
Marilyn J. Telen, Erica E. Davis, Karen Soldano, Melanie E. Garrett, Joseph L. Bundy, Blair R. Anderson, Allison E. Ashley-Koch, Ludmila Francescatto
Publikováno v:
PLoS ONE, Vol 14, Iss 6, p e0217042 (2019)
PLoS ONE
PLoS ONE
Kidney failure occurs in 5-13% of individuals with sickle cell disease and is associated with early mortality. Two APOL1 alleles (G1 and G2) have been identified as risk factors for sickle cell disease nephropathy. Both risk alleles are prevalent in
Autor:
Hana Flögelová, Marijan Saraga, Maria Szczepańska, John M Darlow, Nicholas Katsanis, Barry Honig, Donald Petrey, Ali Samii, Akira Imamoto, Adele Mitrotti, Vladimir J Lozanovski, Bradley A. Warady, Max Werth, Qingxue Liu, Susan L. Furth, Mirna Saraga-Babić, Silvia E. Racedo, Grażyna Krzemień, Yangfan P. Liu, Rik Westland, Christopher E. Gillies, Iain A. Drummond, Alba Carrea, Matthew G. Sampson, Nicholas J Steers, Rémi Salomon, Rong Deng, Valentina P Capone, V. D’Agati, Virginia E. Papaioannou, Richard P. Lifton, Katarina Vukojević, Claudia Izzi, Małgorzata Mizerska-Wasiak, Francesco Scolari, Marcin Tkaczyk, Joanna A.E. van Wijk, Gabriel Makar, Prem Puri, Esther Lopez-Rivera, Loreto Gesualdo, Bernice E. Morrow, Jonathan Barasch, Velibor Tasic, Marcin Zaniew, Cécile Jeanpierre, Adela Arapović, Asaf Vivante, Donna M. McDonald-McGinn, Terrence B. Crowley, Monica Bodria, Daniele Cusi, Wassila Carpentier, Craig S. Wong, Ali G. Gharavi, Miguel Verbitsky, David Fasel, Zhonghai Yan, Edgar A. Otto, David E. Barton, Zoran Gucev, Monika Miklaszewska, Virginia Vega-Warner, Dorota Drozdz, Jeremiah Martino, Elaine H. Zackai, Agnieszka Szmigielska, Anna Latos-Bielenska, Mariarosa Maiorana, Anna Materna-Kiryluk, Landino Allegri, Dominique Gaillard, Laurence Heidet, Friedhelm Hildebrandt, Hakon Hakonarson, Gian Marco Ghiggeri, Simone Sanna-Cherchi, Nenad Kunac, Przemysław Sikora, Emilio Casolari, Krzysztof Kiryluk, Blair R. Anderson
Publikováno v:
New England Journal of Medicine, 376(8), 742-754. Massachussetts Medical Society
Lopez-Rivera, E, Liu, Y P, Verbitsky, M, Anderson, B R, Capone, V P, Otto, E A, Yan, Z, Mitrotti, A, Martino, J, Steers, N J, Fasel, D A, Vukojevic, K, Deng, R, Racedo, S E, Liu, Q, Werth, M, Westland, R, Vivante, A, Makar, G S, Bodria, M, Sampson, M G, Gillies, C E, Vega-Warner, V, Maiorana, M, Petrey, D S, Honig, B, Lozanovski, V J, Salomon, R, Heidet, L, Carpentier, W, Gaillard, D, Carrea, A, Gesualdo, L, Cusi, D, Izzi, C, Scolari, F, Van Wijk, J A E, Arapovic, A, Saraga-Babic, M, Saraga, M, Kunac, N, Samii, A, McDonald-McGinn, D M, Crowley, T B, Zackai, E H, Drozdz, D, Miklaszewska, M, Tkaczyk, M, Sikora, P, Szczepanska, M, Mizerska-Wasiak, M, Krzemien, G, Szmigielska, A, Zaniew, M, Darlow, J M, Puri, P, Barton, D, Casolari, E, Furth, S L, Warady, B A, Gucev, Z, Hakonarson, H, Flogelova, H, Tasic, V, Latos-Bielenska, A, Materna-Kiryluk, A, Allegri, L, Wong, C S, Drummond, I A, D'Agati, V, Imamoto, A, Barasch, J M, Hildebrandt, F, Kiryluk, K, Lifton, R P, Morrow, B E, Jeanpierre, C, Papaioannou, V E, Ghiggeri, G M, Gharavi, A G, Katsanis, N & Sanna-Cherchi, S 2017, ' Genetic drivers of kidney defects in the digeorge syndrome ', New England Journal of Medicine, vol. 376, no. 8, pp. 742-754 . https://doi.org/10.1056/NEJMoa1609009
New England Journal of Medicine
New England Journal of Medicine, 2017, 376 (8), pp.742-754. ⟨10.1056/NEJMoa1609009⟩
New England Journal of Medicine, Massachusetts Medical Society, 2017, 376 (8), pp.742-754. ⟨10.1056/NEJMoa1609009⟩
The New England journal of medicine
376 (2017): 742–754. doi:10.1056/NEJMoa1609009
info:cnr-pdr/source/autori:Lopez-Rivera, E.; Liu, Y. P.; Verbitsky, M.; Anderson, B. R.; Capone, V. P.; Otto, E. A.; Yan, Z.; Mitrotti, A.; Martino, J.; Steers, N. J.; Fasel, D. A.; Vukojevic, K.; Deng, R.; Racedo, S. E.; Liu, Q.; Werth, M.; Westland, R.; Vivante, A.; Makar, G. S.; Bodria, M.; Sampson, M. G.; Gillies, C. E.; Vega-Warner, V.; Maiorana, M.; Petrey, D. S.; Honig, B.; Lozanovski, V. J.; Salomon, R.; Heidet, L.; Carpentier, W.; Gaillard, D.; Carrea, A.; Gesualdo, L.; Cusi, D.; Izzi, C.; Scolari, F.; van Wijk, J. A. E.; Arapovic, A.; Saraga-Babic, M.; Saraga, M.; Kunac, N.; Samii, A.; McDonald-McGinn, D. M.; Crowley, T. B.; Zackai, E. H.; Drozdz, D.; Miklaszewska, M.; Tkaczyk, M.; Sikora, P.; Szczepanska, M.; Mizerska-Wasiak, M.; Krzemien, G.; Szmigielska, A.; Zaniew, M.; Darlow, J. M.; Puri, P.; Barton, D.; Casolari, E.; Furth, S. L.; Warady, B. A.; Gucev, Z.; Hakonarson, H.; Flogelova, H.; Tasic, V.; Latos-Bielenska, A.; Materna-Kiryluk, A.; Allegri, L.; Wong, C. S.; Drummond, I. A.; D'Agati, V.; Imamoto, A.; Barasch, J. M.; Hildebrandt, F.; Kiryluk, K.; Lifton, R. P.; Morrow, B. E.; Jeanpierre, C.; Papaioannou, V. E.; Ghiggeri, G. M.; Gharavi, A. G.; Katsanis, N.; Sanna-Cherchi, S./titolo:Genetic Drivers of Kidney Defects in the DiGeorge Syndrome/doi:10.1056%2FNEJMoa1609009/rivista:The New England journal of medicine (Print)/anno:2017/pagina_da:742/pagina_a:754/intervallo_pagine:742–754/volume:376
Lopez-Rivera, E, Liu, Y P, Verbitsky, M, Anderson, B R, Capone, V P, Otto, E A, Yan, Z, Mitrotti, A, Martino, J, Steers, N J, Fasel, D A, Vukojevic, K, Deng, R, Racedo, S E, Liu, Q, Werth, M, Westland, R, Vivante, A, Makar, G S, Bodria, M, Sampson, M G, Gillies, C E, Vega-Warner, V, Maiorana, M, Petrey, D S, Honig, B, Lozanovski, V J, Salomon, R, Heidet, L, Carpentier, W, Gaillard, D, Carrea, A, Gesualdo, L, Cusi, D, Izzi, C, Scolari, F, Van Wijk, J A E, Arapovic, A, Saraga-Babic, M, Saraga, M, Kunac, N, Samii, A, McDonald-McGinn, D M, Crowley, T B, Zackai, E H, Drozdz, D, Miklaszewska, M, Tkaczyk, M, Sikora, P, Szczepanska, M, Mizerska-Wasiak, M, Krzemien, G, Szmigielska, A, Zaniew, M, Darlow, J M, Puri, P, Barton, D, Casolari, E, Furth, S L, Warady, B A, Gucev, Z, Hakonarson, H, Flogelova, H, Tasic, V, Latos-Bielenska, A, Materna-Kiryluk, A, Allegri, L, Wong, C S, Drummond, I A, D'Agati, V, Imamoto, A, Barasch, J M, Hildebrandt, F, Kiryluk, K, Lifton, R P, Morrow, B E, Jeanpierre, C, Papaioannou, V E, Ghiggeri, G M, Gharavi, A G, Katsanis, N & Sanna-Cherchi, S 2017, ' Genetic drivers of kidney defects in the digeorge syndrome ', New England Journal of Medicine, vol. 376, no. 8, pp. 742-754 . https://doi.org/10.1056/NEJMoa1609009
New England Journal of Medicine
New England Journal of Medicine, 2017, 376 (8), pp.742-754. ⟨10.1056/NEJMoa1609009⟩
New England Journal of Medicine, Massachusetts Medical Society, 2017, 376 (8), pp.742-754. ⟨10.1056/NEJMoa1609009⟩
The New England journal of medicine
376 (2017): 742–754. doi:10.1056/NEJMoa1609009
info:cnr-pdr/source/autori:Lopez-Rivera, E.; Liu, Y. P.; Verbitsky, M.; Anderson, B. R.; Capone, V. P.; Otto, E. A.; Yan, Z.; Mitrotti, A.; Martino, J.; Steers, N. J.; Fasel, D. A.; Vukojevic, K.; Deng, R.; Racedo, S. E.; Liu, Q.; Werth, M.; Westland, R.; Vivante, A.; Makar, G. S.; Bodria, M.; Sampson, M. G.; Gillies, C. E.; Vega-Warner, V.; Maiorana, M.; Petrey, D. S.; Honig, B.; Lozanovski, V. J.; Salomon, R.; Heidet, L.; Carpentier, W.; Gaillard, D.; Carrea, A.; Gesualdo, L.; Cusi, D.; Izzi, C.; Scolari, F.; van Wijk, J. A. E.; Arapovic, A.; Saraga-Babic, M.; Saraga, M.; Kunac, N.; Samii, A.; McDonald-McGinn, D. M.; Crowley, T. B.; Zackai, E. H.; Drozdz, D.; Miklaszewska, M.; Tkaczyk, M.; Sikora, P.; Szczepanska, M.; Mizerska-Wasiak, M.; Krzemien, G.; Szmigielska, A.; Zaniew, M.; Darlow, J. M.; Puri, P.; Barton, D.; Casolari, E.; Furth, S. L.; Warady, B. A.; Gucev, Z.; Hakonarson, H.; Flogelova, H.; Tasic, V.; Latos-Bielenska, A.; Materna-Kiryluk, A.; Allegri, L.; Wong, C. S.; Drummond, I. A.; D'Agati, V.; Imamoto, A.; Barasch, J. M.; Hildebrandt, F.; Kiryluk, K.; Lifton, R. P.; Morrow, B. E.; Jeanpierre, C.; Papaioannou, V. E.; Ghiggeri, G. M.; Gharavi, A. G.; Katsanis, N.; Sanna-Cherchi, S./titolo:Genetic Drivers of Kidney Defects in the DiGeorge Syndrome/doi:10.1056%2FNEJMoa1609009/rivista:The New England journal of medicine (Print)/anno:2017/pagina_da:742/pagina_a:754/intervallo_pagine:742–754/volume:376
International audience; Background: The DiGeorge syndrome, the most common of the microdeletion syndromes, affects multiple organs, including the heart, the nervous system, and the kidney. It is caused by deletions on chromosome 22q11.2; the genetic
Autor:
Thiago A. Pereira, Yuping Chen, Albert S. Baldwin, Wing-Kin Syn, Jiuyi Lu, Guanhua Xie, Blair R. Anderson, Gregory A. Michelotti, Cynthia D. Guy, Gamze Karaca, Anna Mae Diehl, Isaac S. Chan, Leandi Krüger, Marzena Swiderska-Syn, Steve S. Choi
Publikováno v:
Cancer Research. 72:6344-6350
Hepatocellular carcinoma (HCC) typically develops in cirrhosis, a condition characterized by Hedgehog (Hh) pathway activation and accumulation of Hh-responsive myofibroblasts. Although Hh signaling generally regulates stromal–epithelial interaction
Autor:
David N. Howell, Erica E. Davis, Blair R. Anderson, Nicholas Katsanis, Marilyn J. Telen, Allison E. Ashley-Koch, Karen Soldano, Melanie E. Garrett
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 11, Iss 7, p e1005349 (2015)
PLoS Genetics, Vol 11, Iss 7, p e1005349 (2015)
African Americans have a disproportionate risk for developing nephropathy. This disparity has been attributed to coding variants (G1 and G2) in apolipoprotein L1 (APOL1); however, there is little functional evidence supporting the role of this protei