Pesquisa | Biblioteca Virtual em Saúde

1.

Lin28 sustains early renal progenitors and induces Wilms tumor.

Urbach, Achia; Yermalovich, Alena; Zhang, Jin; Spina, Catherine S; Zhu, Hao; Perez-Atayde, Antonio R; Shukrun, Rachel; Charlton, Jocelyn; Sebire, Neil; Mifsud, William; Dekel, Benjamin; Pritchard-Jones, Kathy; Daley, George Q.

Genes Dev; 28(9): 971-82, 2014 May 01.

Artigo em Inglês | MEDLINE | ID: mdl-24732380

2.

Prenatal diagnosis and postnatal outcome of anterior urethral anomalies.

Perlman, Sharon; Borovitz, Yael; Ben-Meir, David; Hazan, Yenon; Nagar, Ran; Bardin, Ron; Brusilov, Michael; Dekel, Benjamin; Achiron, Reuven; Gilboa, Yinon.

Prenat Diagn; 2019 Oct 26.

Artigo em Inglês | MEDLINE | ID: mdl-31654578

3.

Renal lineage cells as a source for renal regeneration.

Pleniceanu, Oren; Omer, Dorit; Harari-Steinberg, Orit; Dekel, Benjamin.

Pediatr Res; 83(1-2): 267-274, 2018 01.

Artigo em Inglês | MEDLINE | ID: mdl-28985199

4.

Severe fetal hydronephrosis: the added value of associated congenital anomalies of the kidneys and urinary tract (CAKUT) in the prediction of postnatal outcome.

Perlman, Sharon; Roitman, Lucia; Lotan, Danny; Kivilevitch, Zvi; Pode-Shakked, Naomi; Pode-Shakked, Ben; Achiron, Reuven; Dekel, Benjamin; Gilboa, Yinon.

Prenat Diagn; 38(3): 179-183, 2018 02.

Artigo em Inglês | MEDLINE | ID: mdl-29314159

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.

Fetal Renal to Abdominal Ratio: A Constant Measurement Throughout Gestation.

Nagar, Ran; Perlman, Sharon; Yariv, Or; Kivilevich, Zvi; Dekel, Benjamin; Achiron, Reuven; Gilboa, Yinon.

Isr Med Assoc J; 20(3): 151-154, 2018 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-29527852

7.

A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism.

Pillar, Nir; Pleniceanu, Oren; Fang, Mingyan; Ziv, Limor; Lahav, Einat; Botchan, Shay; Cheng, Le; Dekel, Benjamin; Shomron, Noam.

Hum Genet; 136(7): 835-845, 2017 07.

Artigo em Inglês | MEDLINE | ID: mdl-28444561

8.

Crossed ectopic kidney: prenatal diagnosis and postnatal follow-up.

Zajicek, Michal; Perlman, Sharon; Dekel, Benjamin; Lahav, Einat; Lotan, Danny; Lotan, Dor; Achiron, Reuven; Gilboa, Yinon.

Prenat Diagn; 37(7): 712-715, 2017 Jul.

Artigo em Inglês | MEDLINE | ID: mdl-28505705

9.

Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia.

Schlingmann, Karl P; Ruminska, Justyna; Kaufmann, Martin; Dursun, Ismail; Patti, Monica; Kranz, Birgitta; Pronicka, Ewa; Ciara, Elzbieta; Akcay, Teoman; Bulus, Derya; Cornelissen, Elisabeth A M; Gawlik, Aneta; Sikora, Przemyslaw; Patzer, Ludwig; Galiano, Matthias; Boyadzhiev, Veselin; Dumic, Miroslav; Vivante, Asaf; Kleta, Robert; Dekel, Benjamin; Levtchenko, Elena; Bindels, René J; Rust, Stephan; Forster, Ian C; Hernando, Nati; Jones, Glenville; Wagner, Carsten A; Konrad, Martin.

J Am Soc Nephrol; 27(2): 604-14, 2016 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-26047794

10.

Kidney stem cells in development, regeneration and cancer.

Dziedzic, Klaudyna; Pleniceanu, Oren; Dekel, Benjamin.

Semin Cell Dev Biol; 36: 57-65, 2014 Dec.

Artigo em Inglês | MEDLINE | ID: mdl-25128731

11.

Prenatal compensatory renal growth in unilateral renal agenesis.

Perlman, Sharon; Lotan, Dani; Dekel, Benjamin; Kivilevitch, Zvi; Hazan, Yinon; Achiron, Reuven; Gilboa, Yinon.

Prenat Diagn; 36(11): 1075-1080, 2016 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-27734512

12.

Prenatal diagnosis of 17q12 deletion syndrome: from fetal hyperechogenic kidneys to high risk for autism.

Gilboa, Yinon; Perlman, Sharon; Pode-Shakked, Naomi; Pode-Shakked, Ben; Shrim, Alon; Azaria-Lahav, Einat; Dekel, Benjamin; Yonath, Hagith; Berkenstadt, Michal; Achiron, Reuven.

Prenat Diagn; 36(11): 1027-1032, 2016 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-27634641

13.

Lack of IL7Rα expression in T cells is a hallmark of T-cell immunodeficiency in Schimke immuno-osseous dysplasia (SIOD).

Sanyal, Mrinmoy; Morimoto, Marie; Baradaran-Heravi, Alireza; Choi, Kunho; Kambham, Neeraja; Jensen, Kent; Dutt, Suparna; Dionis-Petersen, Kira Y; Liu, Lan Xiang; Felix, Katie; Mayfield, Christy; Dekel, Benjamin; Bokenkamp, Arend; Fryssira, Helen; Guillen-Navarro, Encarna; Lama, Giuliana; Brugnara, Milena; Lücke, Thomas; Olney, Ann Haskins; Hunley, Tracy E; Polat, Ayse Ipek; Yis, Uluc; Bogdanovic, Radovan; Mitrovic, Katarina; Berry, Susan; Najera, Lydia; Najafian, Behzad; Gentile, Mattia; Nur Semerci, C; Tsimaratos, Michel; Lewis, David B; Boerkoel, Cornelius F.

Clin Immunol; 161(2): 355-65, 2015 Dec.

Artigo em Inglês | MEDLINE | ID: mdl-26499378

14.

Integrin α3 mutations with kidney, lung, and skin disease.

Has, Cristina; Spartà, Giuseppina; Kiritsi, Dimitra; Weibel, Lisa; Moeller, Alexander; Vega-Warner, Virginia; Waters, Aoife; He, Yinghong; Anikster, Yair; Esser, Philipp; Straub, Beate K; Hausser, Ingrid; Bockenhauer, Detlef; Dekel, Benjamin; Hildebrandt, Friedhelm; Bruckner-Tuderman, Leena; Laube, Guido F.

N Engl J Med; 366(16): 1508-14, 2012 Apr 19.

Artigo em Inglês | MEDLINE | ID: mdl-22512483

15.

Reactivation of NCAM1 defines a subpopulation of human adult kidney epithelial cells with clonogenic and stem/progenitor properties.

Buzhor, Ella; Omer, Dorit; Harari-Steinberg, Orit; Dotan, Zohar; Vax, Einav; Pri-Chen, Sara; Metsuyanim, Sally; Pleniceanu, Oren; Goldstein, Ronald S; Dekel, Benjamin.

Am J Pathol; 183(5): 1621-1633, 2013 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-24055371

16.

Bitterness of glucose/galactose: novel mutations in the SLC5A1 gene.

Pode-Shakked, Ben; Reish, Orit; Aktuglu-Zeybek, Cigdem; Kesselman, Dafna; Dekel, Benjamin; Bujanover, Yoram; Anikster, Yair.

J Pediatr Gastroenterol Nutr; 58(1): 57-60, 2014 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-24048166

17.

Targeted therapy aimed at cancer stem cells: Wilms' tumor as an example.

Shukrun, Rachel; Pode Shakked, Naomi; Dekel, Benjamin.

Pediatr Nephrol; 29(5): 815-23; quiz 821, 2014 May.

Artigo em Inglês | MEDLINE | ID: mdl-23760992

18.

Renal hypodysplasia associates with a WNT4 variant that causes aberrant canonical WNT signaling.

Vivante, Asaf; Mark-Danieli, Michal; Davidovits, Miriam; Harari-Steinberg, Orit; Omer, Dorit; Gnatek, Yehudit; Cleper, Roxana; Landau, Daniel; Kovalski, Yael; Weissman, Irit; Eisenstein, Israel; Soudack, Michalle; Wolf, Haike Reznik; Issler, Naomi; Lotan, Danny; Anikster, Yair; Dekel, Benjamin.

J Am Soc Nephrol; 24(4): 550-8, 2013 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-23520208

19.

The transcription factor grainyhead-like 2 regulates the molecular composition of the epithelial apical junctional complex.

Werth, Max; Walentin, Katharina; Aue, Annekatrin; Schönheit, Jörg; Wuebken, Anne; Pode-Shakked, Naomi; Vilianovitch, Larissa; Erdmann, Bettina; Dekel, Benjamin; Bader, Michael; Barasch, Jonathan; Rosenbauer, Frank; Luft, Friedrich C; Schmidt-Ott, Kai M.

Development; 137(22): 3835-45, 2010 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-20978075

20.

Hyponatremic hypertensive syndrome in pediatric patients: is it really so rare?

Kovalski, Yael; Cleper, Roxana; Krause, Irit; Dekel, Benjamin; Belenky, Alexander; Davidovits, Miriam.

Pediatr Nephrol; 27(6): 1037-40, 2012 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-22366877

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