A Human Integrin-α3 Mutation Confers Major Renal Developmental Defects

Tekijä Shukrun, Rachel, Vivante, Asaf, Pleniceanu, Oren, Vax, Einav, Anikster, Yair, Dekel, Benjamin, Lotan, Danny
Julkaistu 2014

Wilms’ Tumor Blastemal Stem Cells Dedifferentiate to Propagate the Tumor Bulk

Tekijä Shukrun, Rachel, Pode-Shakked, Naomi, Pleniceanu, Oren, Omer, Dorit, Vax, Einav, Peer, Eyal, Pri-Chen, Sara, Jacob, Jasmine, Hu, Qianghua, Harari-Steinberg, Orit, Huff, Vicki, Dekel, Benjamin
Julkaistu 2014

Lin28 sustains early renal progenitors and induces Wilms tumor

Tekijä 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.
Julkaistu 2014

Novel homozygous ENPP1 mutation causes generalized arterial calcifications of infancy, thrombocytopenia, and cardiovascular and central nervous system syndrome

Tekijä Staretz-Chacham, Orna, Shukrun, Rachel, Barel, Ortal, Pode-Shakked, Ben, Pleniceanu, Oren, Anikster, Yair, Shalva, Nechama, Ferreira, Carlos R., Kadosh, Admit Ben-Haim, Richardson, Justin, Mane, Shrikant M., Hildebrandt, Friedhelm, Vivante, Asaf
Julkaisussa Am J Med Genet A (2019)

NCAM1/FGF module serves as a putative pleuropulmonary blastoma therapeutic target

Tekijä Shukrun, Rachel, Golan, Hana, Caspi, Revital, Pode-Shakked, Naomi, Pleniceanu, Oren, Vax, Einav, Bar-Lev, Dekel D., Pri-Chen, Sara, Jacob-Hirsch, Jasmine, Schiby, Ginette, Harari-Steinberg, Orit, Mark-Danieli, Michal, Dekel, Benjamin, Toren, Amos
Julkaisussa Oncogenesis (2019)

Dissecting Stages of Human Kidney Development and Tumorigenesis with Surface Markers Affords Simple Prospective Purification of Nephron Stem Cells

Tekijä Pode-Shakked, Naomi, Pleniceanu, Oren, Gershon, Rotem, Shukrun, Rachel, Kanter, Itamar, Bucris, Efrat, Pode-Shakked, Ben, Tam, Gal, Tam, Hadar, Caspi, Revital, Pri-Chen, Sara, Vax, Einav, Katz, Guy, Omer, Dorit, Harari-Steinberg, Orit, Kalisky, Tomer, Dekel, Benjamin
Julkaisussa Sci Rep (2016)

The isolation and characterization of renal cancer initiating cells from human Wilms' tumour xenografts unveils new therapeutic targets†

Tekijä Pode-Shakked, Naomi, Shukrun, Rachel, Mark-Danieli, Michal, Tsvetkov, Peter, Bahar, Sarit, Pri-Chen, Sara, Goldstein, Ronald S, Rom-Gross, Eithan, Mor, Yoram, Fridman, Edward, Meir, Karen, Simon, Amos, Magister, Marcus, Kaminski, Naftali, Goldmacher, Victor S, Harari-Steinberg, Orit, Dekel, Benjamin
Julkaistu 2013

In Vivo Expansion of Cancer Stemness Affords Novel Cancer Stem Cell Targets: Malignant Rhabdoid Tumor as an Example

Tekijä Golan, Hana, Shukrun, Rachel, Caspi, Revital, Vax, Einav, Pode-Shakked, Naomi, Goldberg, Sanja, Pleniceanu, Oren, Bar-Lev, Dekel D., Mark-Danieli, Michal, Pri-Chen, Sara, Jacob-Hirsch, Jasmine, Kanter, Itamar, Trink, Ariel, Schiby, Ginette, Bilik, Ron, Kalisky, Tomer, Harari-Steinberg, Orit, Toren, Amos, Dekel, Benjamin
Julkaisussa Stem Cell Reports (2018)

Whole exome sequencing in childhood-onset lupus frequently detects single gene etiologies

Tekijä Tirosh, Irit, Spielman, Shiri, Barel, Ortal, Ram, Reut, Stauber, Tali, Paret, Gideon, Rubinsthein, Marina, Pessach, Itai M., Gerstein, Maya, Anikster, Yair, Shukrun, Rachel, Dagan, Adi, Adler, Katerina, Pode-Shakked, Ben, Volkov, Alexander, Perelman, Marina, Greenberger, Shoshana, Somech, Raz, Lahav, Einat, Majmundar, Amar J., Padeh, Shai, Hildebrandt, Friedhelm, Vivante, Asaf
Julkaisussa Pediatr Rheumatol Online J (2019)

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

Tekijä 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
Julkaisussa J Am Soc Nephrol (2017)

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

Tekijä 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
Julkaisussa Am J Hum Genet (2015)