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1.
Integrin-Linked Kinase Deficiency in Collecting Duct Principal Cell Promotes Necroptosis of Principal Cell and Contributes to Kidney Inflammation and Fibrosis.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Biochim Biophys Acta;
1762(7): 647-55, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16797938
18.
Unsupervised Sequential Outlier Detection With Deep Architectures.
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.
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.
JCI Insight;
1(19): e86934, 2016 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27882344