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The copy number variation landscape of congenital anomalies of the kidney and urinary tract (vol 51, pg 117, 2018) Verbitsky, Miguel; Westland, Rik; Perez, Alejandra; Kiryluk, Krzysztof; Liu, Qingxue; Krithivasan, Priya; Mitrotti, Adele; Fasel, David A.; Batourina, Ekaterina; Sampson, Matthew G.; Bodria, Monica; Werth, Max; Kao, Charlly; Martino, Jeremiah; Capone, Valentina P.; Vivante, Asaf; Shril, Shirlee; Kil, Byum Hee; Marasa, Maddalena; Zhang, Jun Y.; Na, Young-Ji; Lim, Tze Y.; Ahram, Dina; Weng, Patricia L.; Heinzen, Erin L.; Carrea, Alba; Piaggio, Giorgio; Gesualdo, Loreto; Manca, Valeria; Masnata, Giuseppe; Gigante, Maddalena; Cusi, Daniele; Izzi, Claudia; Scolari, Francesco; van Wijk, Joanna A. E.; Saraga, Marijan; Santoro, Domenico; Conti, Giovanni; Zamboli, Pasquale; White, Hope; Drozdz, Dorota; Zachwieja, Katarzyna; Miklaszewska, Monika; Tkaczyk, Marcin; Tomczyk, Daria; Krakowska, Anna; Sikora, Przemyslaw; Jarmolinski, Tomasz; Borszewska-Kornacka, Maria K.; Pawluch, Robert; Szczepanska, Maria; Adamczyk, Piotr; Mizerska-Wasiak, Malgorzata; Krzemien, Grazyna; Szmigielska, Agnieszka; Zaniew, Marcin; Dobson, Mark G.; Darlow, John M.; Puri, Prem; Barton, David E.; Furth, Susan L.; Warady, Bradley A.; Gucev, Zoran; Lozanovski, Vladimir J.; Tasic, Velibor; Pisani, Isabella; Allegri, Landino; Rodas, Lida M.; Campistol, Josep M.; Jeanpierre, Cecile; Alam, Shumyle; Casale, Pasquale; Wong, Craig S.; Lin, Fangming; Miranda, Debora M.; Oliveira, Eduardo A.; Simoes-e-Silva, Ana Cristina; Barasch, Jonathan M.; Levy, Brynn; Wu, Nan; Hildebrandt, Friedhelm; Ghiggeri, Gian Marco; Latos-Bielenska, Anna; Materna-Kiryluk, Anna; Zhang, Feng; Hakonarson, Hakon; Papaioannou, Virginia E.; Mendelsohn, Cathy L.; Gharavi, Ali G.; Sanna-Cherchi, Simone 分享 收藏
The copy number variation landscape of congenital anomalies of the kidney and urinary tract Verbitsky, Miguel; Westland, Rik; Perez, Alejandra; Kiryluk, Krzysztof; Liu, Qingxue; Krithivasan, Priya; Mitrotti, Adele; Fasel, David A.; Batourina, Ekaterina; Sampson, Matthew G.; Bodria, Monica; Werth, Max; Kao, Charlly; Martino, Jeremiah; Capone, Valentina P.; Vivante, Asaf; Shril, Shirlee; Kil, Byum Hee; Marasa, Maddalena; Zhang, Jun Y.; Na, Young-Ji; Lim, Tze Y.; Ahram, Dina; Weng, Patricia L.; Heinzen, Erin L.; Carrea, Alba; Piaggio, Giorgio; Gesualdo, Loreto; Manca, Valeria; Masnata, Giuseppe; Gigante, Maddalena; Cusi, Daniele; Izzi, Claudia; Scolari, Francesco; van Wijk, Joanna A. E.; Saraga, Marijan; Santoro, Domenico; Conti, Giovanni; Zamboli, Pasquale; White, Hope; Drozdz, Dorota; Zachwieja, Katarzyna; Miklaszewska, Monika; Tkaczyk, Marcin; Tomczyk, Daria; Krakowska, Anna; Sikora, Przemyslaw; Jarmolinski, Tomasz; Borszewska-Kornacka, Maria K.; Pawluch, Robert; Szczepanska, Maria; Adamczyk, Piotr; Mizerska-Wasiak, Malgorzata; Krzemien, Grazyna; Szmigielska, Agnieszka; Zaniew, Marcin; Dobson, Mark G.; Darlow, John M.; Puri, Prem; Barton, David E.; Furth, Susan L.; Warady, Bradley A.; Gucev, Zoran; Lozanovski, Vladimir J.; Tasic, Velibor; Pisani, Isabella; Allegri, Landino; Rodas, Lida M.; Campistol, Josep M.; Jeanpierre, Cecile; Alam, Shumyle; Casale, Pasquale; Wong, Craig S.; Lin, Fangming; Miranda, Debora M.; Oliveira, Eduardo A.; Simoes-e-Silva, Ana Cristina; Barasch, Jonathan M.; Levy, Brynn; Wu, Nan; Hildebrandt, Friedhelm; Ghiggeri, Gian Marco; Latos-Bielenska, Anna; Materna-Kiryluk, Anna; Zhang, Feng; Hakonarson, Hakon; Papaioannou, Virginia E.; Mendelsohn, Cathy L.; Gharavi, Ali G.; Sanna-Cherchi, Simone 分享 收藏
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Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux (vol 7, 2017) Darlow, John M.; Darlay, Rebecca; Dobson, Mark G.; Stewart, Aisling; Charoen, Pimphen; Southgate, Jennifer; Baker, Simon C.; Xu, Yaobo; Hunziker, Manuela; Lambert, Heather J.; Green, Andrew J.; Santibanez-Koref, Mauro; Sayer, John A.; Goodship, Timothy H. J.; Puri, Prem; Woolf, Adrian S.; Kenda, Rajko B.; Barton, David E.; Cordell, Heather J. 分享 收藏
Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux 全基因组连锁和关联研究表明10q26区域是原发性非综合征性膀胱输尿管反流的主要遗传因素 Darlow, John M.; Darlay, Rebecca; Dobson, Mark G.; Stewart, Aisling; Charoen, Pimphen; Southgate, Jennifer; Baker, Simon C.; Xu, Yaobo; Hunziker, Manuela; Lambert, Heather J.; Green, Andrew J.; Santibanez-Koref, Mauro; Sayer, John A.; Goodship, Timothy H. J.; Puri, Prem; Woolf, Adrian S.; Kenda, Rajko B.; Barton, David E.; Cordell, Heather J. 分享 收藏
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Genetic Drivers of Kidney Defects in the DiGeorge Syndrome 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. 分享 收藏
Autophagy regulates satellite cell ability to regenerate normal and dystrophic muscles Fiacco, E.; Castagnetti, F.; Bianconi, V.; Madaro, L.; De Bardi, M.; Nazio, F.; D'Amico, A.; Bertini, E.; Cecconi, F.; Puri, P. L.; Latella, L. 分享 收藏
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OMEGA-3 CARBOXYLIC ACIDS, EPANOVA®, AND THE SODIUM-GLUCOSE CO-TRANSPORTER 2 INHIBITOR, DAPAGLIFLOZIN®, IMPROVE STEATOHEPATITIS AND FIBROSIS SCORING IN A MOUSE MODEL OF NON-ALCOHOLIC STEATOHEPATITIS Cazanave, S.; Banini, B.; Asgharpour, A.; Vincent, R.; Seneshaw, M.; Kumar, D. Prassana; Mirshahi, F.; Daita, K.; Puri, P.; Oscarsson, J.; Bedossa, P.; Sanyal, A. 分享 收藏
ELDERLY CIRRHOTIC PATIENTS WITH PRE-DEMENTIA MILD COGNITIVE IMPAIRMENT AND MINIMAL HEPATIC ENCEPHALOPATHY HAVE A DISTINCT COGNITIVE AND BRAIN MR PROFILE Ahluwahlia, V.; Wade, J.; Moeller, F.; Steinberg, J.; White, M.; Unser, A.; Fagan, A.; Ganapathy, D.; Sterling, R.; Stravitz, R. T.; Matherly, S.; Luketic, V.; Sanyal, A.; Siddiqui, M.; Puri, P.; Fuchs, M.; Heuman, D.; Bajaj, J. S. S. 分享 收藏
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PATIENT-REPORTED HEALTH-RELATED QUALITY OF LIFE OUTCOMES INDEPENDENTLY PREDICT DEATH, TRANSPLANT, HOSPITALIZATION AND HEPATIC ENCEPHALOPATHY IN CIRRHOSIS Patidar, K.; Thacker, L.; Wade, J.; White, M.; Unser, A.; Gavis, E.; Hovermale, J.; Sterling, R. K.; Fuchs, M.; Siddiqui, M. S.; Matherly, S.; Stravitz, R. T.; Sanyal, A.; Puri, P.; Luketic, V.; Bajaj, J. S. 分享 收藏
DISTINCT FECAL AND PLASMA BILE ACID METABOLOME OF MICROBIAL ORIGIN CHARACTERIZES HUMAN NONALCOHOLIC FATTY LIVER DISEASE (NAFLD) Puri, P.; Siddiqui, S. M.; Boyette, S.; Sargeant, C.; White, L. D.; Walker, S.; Daita, K.; Ammons, C.; Cazanave, S.; Asgharpour, A.; Mirshahi, F.; Joyce, A.; Sanyal, A. J. 分享 收藏
A DIET-INDUCED MOUSE MODEL OF NONALCOHOLIC FATTY LIVER DISEASE WITH PROGRESSION TO ADVANCED FIBROSIS AND HEPATOCELLULAR CARCINOMA WITH A GENE EXPRESSION SIGNATURE MIMICKING HUMAN DISEASE Asgharpour, A.; Bedossa, P.; Hoshida, Y.; Cazanave, S.; Vincent, R.; Pacana, T.; Mirshahi, F.; Sheneshaw, M.; Daita, K.; Puri, P.; Sanyal, A. 分享 收藏
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