Pesquisa | Biblioteca Virtual em Saúde

1.

Integrin-Linked Kinase Deficiency in Collecting Duct Principal Cell Promotes Necroptosis of Principal Cell and Contributes to Kidney Inflammation and Fibrosis.

Huang, Ming; Zhu, Shuai; Huang, Huihui; He, Jinzhao; Tsuji, Kenji; Jin, William W; Xie, Dongping; Ham, Onju; Capen, Diane E; Lu, Weining; Paunescu, Teodor G; Yang, Baoxue; Lu, Hua A Jenny.

J Am Soc Nephrol; 30(11): 2073-2090, 2019 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-31653783

2.

Identification of direct negative cross-talk between the SLIT2 and bone morphogenetic protein-Gremlin signaling pathways.

Tumelty, Kathleen E; Higginson-Scott, Nathan; Fan, Xueping; Bajaj, Piyush; Knowlton, Kelly M; Shamashkin, Michael; Coyle, Anthony J; Lu, Weining; Berasi, Stephen P.

J Biol Chem; 293(9): 3039-3055, 2018 03 02.

Artigo em Inglês | MEDLINE | ID: mdl-29317497

3.

Crim1 regulates integrin signaling in murine lens development.

Zhang, Ying; Fan, Jieqing; Ho, Joshua W K; Hu, Tommy; Kneeland, Stephen C; Fan, Xueping; Xi, Qiongchao; Sellarole, Michael A; de Vries, Wilhelmine N; Lu, Weining; Lachke, Salil A; Lang, Richard A; John, Simon W M; Maas, Richard L.

Development; 143(2): 356-66, 2016 Jan 15.

Artigo em Inglês | MEDLINE | ID: mdl-26681494

4.

Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development.

Vivante, Asaf; Kleppa, Marc-Jens; Schulz, Julian; Kohl, Stefan; Sharma, Amita; Chen, Jing; Shril, Shirlee; Hwang, Daw-Yang; Weiss, Anna-Carina; Kaminski, Michael M; Shukrun, Rachel; Kemper, Markus J; Lehnhardt, Anja; Beetz, Rolf; Sanna-Cherchi, Simone; Verbitsky, Miguel; Gharavi, Ali G; Stuart, Helen M; Feather, Sally A; Goodship, Judith A; Goodship, Timothy H J; Woolf, Adrian S; Westra, Sjirk J; Doody, Daniel P; Bauer, Stuart B; Lee, Richard S; Adam, Rosalyn M; Lu, Weining; Reutter, Heiko M; Kehinde, Elijah O; Mancini, Erika J; Lifton, Richard P; Tasic, Velibor; Lienkamp, Soeren S; Jüppner, Harald; Kispert, Andreas; Hildebrandt, Friedhelm.

Am J Hum Genet; 97(2): 291-301, 2015 Aug 06.

Artigo em Inglês | MEDLINE | ID: mdl-26235987

5.

A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations via Dysregulation of Retinoic Acid Signaling.

Vivante, Asaf; Mann, Nina; Yonath, Hagith; Weiss, Anna-Carina; Getwan, Maike; Kaminski, Michael M; Bohnenpoll, Tobias; Teyssier, Catherine; Chen, Jing; Shril, Shirlee; van der Ven, Amelie T; Ityel, Hadas; Schmidt, Johanna Magdalena; Widmeier, Eugen; Bauer, Stuart B; Sanna-Cherchi, Simone; Gharavi, Ali G; Lu, Weining; Magen, Daniella; Shukrun, Rachel; Lifton, Richard P; Tasic, Velibor; Stanescu, Horia C; Cavaillès, Vincent; Kleta, Robert; Anikster, Yair; Dekel, Benjamin; Kispert, Andreas; Lienkamp, Soeren S; Hildebrandt, Friedhelm.

J Am Soc Nephrol; 28(8): 2364-2376, 2017 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-28381549

6.

Blocking peptides and molecular mimicry as treatment for kidney disease.

Havasi, Andrea; Lu, Weining; Cohen, Herbert T; Beck, Laurence; Wang, Zhiyong; Igwebuike, Chinaemare; Borkan, Steven C.

Am J Physiol Renal Physiol; 312(6): F1016-F1025, 2017 06 01.

Artigo em Inglês | MEDLINE | ID: mdl-27654896

7.

MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus.

Quintero-Rivera, Fabiola; Xi, Qiongchao J; Keppler-Noreuil, Kim M; Lee, Ji Hyun; Higgins, Anne W; Anchan, Raymond M; Roberts, Amy E; Seong, Ihn Sik; Fan, Xueping; Lage, Kasper; Lu, Lily Y; Tao, Joanna; Hu, Xuchen; Berezney, Ronald; Gelb, Bruce D; Kamp, Anna; Moskowitz, Ivan P; Lacro, Ronald V; Lu, Weining; Morton, Cynthia C; Gusella, James F; Maas, Richard L.

Hum Mol Genet; 24(8): 2375-89, 2015 Apr 15.

Artigo em Inglês | MEDLINE | ID: mdl-25574029

8.

Loss of Zeb2 in mesenchyme-derived nephrons causes primary glomerulocystic disease.

Rasouly, Hila Milo; Kumar, Sudhir; Chan, Stefanie; Pisarek-Horowitz, Anna; Sharma, Richa; Xi, Qiongchao J; Nishizaki, Yuriko; Higashi, Yujiro; Salant, David J; Maas, Richard L; Lu, Weining.

Kidney Int; 90(6): 1262-1273, 2016 12.

Artigo em Inglês | MEDLINE | ID: mdl-27591083

9.

Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract.

Hwang, Daw-Yang; Kohl, Stefan; Fan, Xueping; Vivante, Asaf; Chan, Stefanie; Dworschak, Gabriel C; Schulz, Julian; van Eerde, Albertien M; Hilger, Alina C; Gee, Heon Yung; Pennimpede, Tracie; Herrmann, Bernhard G; van de Hoek, Glenn; Renkema, Kirsten Y; Schell, Christoph; Huber, Tobias B; Reutter, Heiko M; Soliman, Neveen A; Stajic, Natasa; Bogdanovic, Radovan; Kehinde, Elijah O; Lifton, Richard P; Tasic, Velibor; Lu, Weining; Hildebrandt, Friedhelm.

Hum Genet; 134(8): 905-16, 2015 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-26026792

10.

Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells.

Nauli, Surya M; Alenghat, Francis J; Luo, Ying; Williams, Eric; Vassilev, Peter; Li, Xiaogang; Elia, Andrew E H; Lu, Weining; Brown, Edward M; Quinn, Stephen J; Ingber, Donald E; Zhou, Jing.

Nat Genet; 33(2): 129-37, 2003 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-12514735

11.

Assessing vesicoureteral reflux in live inbred mice via ultrasound with a microbubble contrast agent.

Paredes, Jose; Sims-Lucas, Sunder; Wang, Hang; Lu, Weining; Coley, Brian; Gittes, George K; Bates, Carlton M.

Am J Physiol Renal Physiol; 300(5): F1262-5, 2011 May.

Artigo em Inglês | MEDLINE | ID: mdl-21325495

12.

The fate of Notch-deficient nephrogenic progenitor cells during metanephric kidney development.

Bonegio, Ramon G B; Beck, Laurence H; Kahlon, Roopkiranjot K; Lu, Weining; Salant, David J.

Kidney Int; 79(10): 1099-112, 2011 May.

Artigo em Inglês | MEDLINE | ID: mdl-21270765

13.

Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project.

Higgins, Anne W; Alkuraya, Fowzan S; Bosco, Amy F; Brown, Kerry K; Bruns, Gail A P; Donovan, Diana J; Eisenman, Robert; Fan, Yanli; Farra, Chantal G; Ferguson, Heather L; Gusella, James F; Harris, David J; Herrick, Steven R; Kelly, Chantal; Kim, Hyung-Goo; Kishikawa, Shotaro; Korf, Bruce R; Kulkarni, Shashikant; Lally, Eric; Leach, Natalia T; Lemyre, Emma; Lewis, Janine; Ligon, Azra H; Lu, Weining; Maas, Richard L; MacDonald, Marcy E; Moore, Steven D P; Peters, Roxanna E; Quade, Bradley J; Quintero-Rivera, Fabiola; Saadi, Irfan; Shen, Yiping; Shendure, Jay; Williamson, Robin E; Morton, Cynthia C.

Am J Hum Genet; 82(3): 712-22, 2008 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-18319076

14.

Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis.

Herron, Bruce J; Lu, Weining; Rao, Cherie; Liu, Shanming; Peters, Heiko; Bronson, Roderick T; Justice, Monica J; McDonald, J David; Beier, David R.

Nat Genet; 30(2): 185-9, 2002 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-11818962

15.

NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.

Lu, Weining; Quintero-Rivera, Fabiola; Fan, Yanli; Alkuraya, Fowzan S; Donovan, Diana J; Xi, Qiongchao; Turbe-Doan, Annick; Li, Qing-Gang; Campbell, Craig G; Shanske, Alan L; Sherr, Elliott H; Ahmad, Ayesha; Peters, Roxana; Rilliet, Benedict; Parvex, Paloma; Bassuk, Alexander G; Harris, David J; Ferguson, Heather; Kelly, Chantal; Walsh, Christopher A; Gronostajski, Richard M; Devriendt, Koenraad; Higgins, Anne; Ligon, Azra H; Quade, Bradley J; Morton, Cynthia C; Gusella, James F; Maas, Richard L.

PLoS Genet; 3(5): e80, 2007 May 25.

Artigo em Inglês | MEDLINE | ID: mdl-17530927

16.

A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux.

van der Ven, Amelie T; Kobbe, Birgit; Kohl, Stefan; Shril, Shirlee; Pogoda, Hans-Martin; Imhof, Thomas; Ityel, Hadas; Vivante, Asaf; Chen, Jing; Hwang, Daw-Yang; Connaughton, Dervla M; Mann, Nina; Widmeier, Eugen; Taglienti, Mary; Schmidt, Johanna Magdalena; Nakayama, Makiko; Senguttuvan, Prabha; Kumar, Selvin; Tasic, Velibor; Kehinde, Elijah O; Mane, Shrikant M; Lifton, Richard P; Soliman, Neveen; Lu, Weining; Bauer, Stuart B; Hammerschmidt, Matthias; Wagener, Raimund; Hildebrandt, Friedhelm.

PLoS One; 13(1): e0191224, 2018.

Artigo em Inglês | MEDLINE | ID: mdl-29351342

17.

Inhibition of HER-2(neu/ErbB2) restores normal function and structure to polycystic kidney disease (PKD) epithelia.

Wilson, Samantha J; Amsler, Kurt; Hyink, Deborah P; Li, Xiaohong; Lu, Weining; Zhou, Jing; Burrow, Christopher R; Wilson, Patricia D.

Biochim Biophys Acta; 1762(7): 647-55, 2006 Jul.

Artigo em Inglês | MEDLINE | ID: mdl-16797938

18.

Unsupervised Sequential Outlier Detection With Deep Architectures.

Lu, Weining; Cheng, Yu; Xiao, Cao; Chang, Shiyu; Huang, Shuai; Liang, Bin; Huang, Thomas.

IEEE Trans Image Process; 26(9): 4321-4330, 2017 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-28600248

19.

Roundabout receptor 2 maintains inhibitory control of the adult midbrain.

Gore, Bryan B; Miller, Samara M; Jo, Yong Sang; Baird, Madison A; Hoon, Mrinalini; Sanford, Christina A; Hunker, Avery; Lu, Weining; Wong, Rachel O; Zweifel, Larry S.

Elife; 62017 04 10.

Artigo em Inglês | MEDLINE | ID: mdl-28394253

20.

SLIT2/ROBO2 signaling pathway inhibits nonmuscle myosin IIA activity and destabilizes kidney podocyte adhesion.

Fan, Xueping; Yang, Hongying; Kumar, Sudhir; Tumelty, Kathleen E; Pisarek-Horowitz, Anna; Rasouly, Hila Milo; Sharma, Richa; Chan, Stefanie; Tyminski, Edyta; Shamashkin, Michael; Belghasem, Mostafa; Henderson, Joel M; Coyle, Anthony J; Salant, David J; Berasi, Stephen P; Lu, Weining.

JCI Insight; 1(19): e86934, 2016 11 17.

Artigo em Inglês | MEDLINE | ID: mdl-27882344

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