Vrk1 partial Knockdown in Mice Results in Reduced Brain Weight and Mild Motor Dysfunction, and Indicates Neuronal VRK1 Target Pathways

por Vinograd-Byk, Hadar, Renbaum, Paul, Levy-Lahad, Ephrat
Publicado 2018

Israeli Position Paper: Triage Decisions for Severely Ill Patients During the COVID-19 Pandemic

por Steinberg, Avraham, Levy-Lahad, Ephrat, Karni, Tami, Sprung, Charles L.
Publicado 2020

Prenatal Isolated Ventricular Septal Defect May Not Be Associated with Trisomy 21

por Shen, Ori, Lieberman, Sari, Farber, Benjamin, Terner, Daniel, Lahad, Amnon, Levy-Lahad, Ephrat
Publicado 2014

Israeli Position Paper: Triage Decisions for Severely Ill Patients During the COVID-19 Pandemic. Joint Commission of the Israel National Bioethics Council, the Ethics Bureau of the...

por Steinberg, Avraham, Levy-Lahad, Ephrat, Karni, Tami, Zohar, Noam, Siegal, Gil, Sprung, Charles L.
Publicado 2020

VRK1 regulates Cajal body dynamics and protects coilin from proteasomal degradation in cell cycle

por Cantarero, Lara, Sanz-García, Marta, Vinograd-Byk, Hadar, Renbaum, Paul, Levy-Lahad, Ephrat, Lazo, Pedro A.
Publicado 2015

Analysis of the genetic basis of height in large Jewish nuclear families

por Zeevi, Danny, Bloom, Joshua S., Sadhu, Meru J., Ben Yehuda, Adi, Zangen, David, Levy-Lahad, Ephrat, Kruglyak, Leonid
Publicado 2019

Real World Cost-Effectiveness Analysis of Population Screening for BRCA Variants among Ashkenazi Jews Compared with Family History-Based Strategies

por Michaelson-Cohen, Rachel, Cohen, Matan J., Cohen, Carmit, Greenberg, Dan, Shmueli, Amir, Lieberman, Sari, Tomer, Ariela, Levy-Lahad, Ephrat, Lahad, Amnon
Publicado 2022

Prevention of Lysosomal Storage Diseases and Derivation of Mutant Stem Cell Lines by Preimplantation Genetic Diagnosis

por Altarescu, Gheona, Beeri, Rachel, Eiges, Rachel, Epsztejn-Litman, Silvina, Eldar-Geva, Talia, Elstein, Deborah, Zimran, Ari, Margalioth, Ehud J., Levy-Lahad, Ephrat, Renbaum, Paul
Publicado 2012

TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) Repair

por Gazy, Inbal, Zeevi, David A., Renbaum, Paul, Zeligson, Sharon, Eini, Lital, Bashari, Dana, Smith, Yoav, Lahad, Amnon, Goldberg, Michal, Ginsberg, Doron, Levy-Lahad, Ephrat
Publicado 2015

Establishment of Homozygote Mutant Human Embryonic Stem Cells by Parthenogenesis

por Epsztejn-Litman, Silvina, Cohen-Hadad, Yaara, Aharoni, Shira, Altarescu, Gheona, Renbaum, Paul, Levy-Lahad, Ephrat, Schonberger, Oshrat, Eldar-Geva, Talia, Zeligson, Sharon, Eiges, Rachel
Publicado 2015

Snord 3A: A Molecular Marker and Modulator of Prion Disease Progression

por Cohen, Eran, Avrahami, Dana, Frid, Kati, Canello, Tamar, Levy Lahad, Ephrat, Zeligson, Sharon, Perlberg, Shira, Chapman, Joab, Cohen, Oren S., Kahana, Esther, Lavon, Iris, Gabizon, Ruth
Publicado 2013

Noninvasive paternal exclusion testing for cystic fibrosis in the first five to eight weeks of gestation

por Zeevi, David A., Zahdeh, Fouad, Kling, Yehuda, Rosen, Tzvia, Renbaum, Paul, Ron-El, Raphael, Eldar-Geva, Talia, Holzer, Hananel E. G., Levy-Lahad, Ephrat, Altarescu, Gheona
Publicado 2018

FMR1 Epigenetic Silencing Commonly Occurs in Undifferentiated Fragile X-Affected Embryonic Stem Cells

por Avitzour, Michal, Mor-Shaked, Hagar, Yanovsky-Dagan, Shira, Aharoni, Shira, Altarescu, Gheona, Renbaum, Paul, Eldar-Geva, Talia, Schonberger, Oshrat, Levy-Lahad, Ephrat, Epsztejn-Litman, Silvina, Eiges, Rachel
Publicado 2014

Parkin acts as a transcription factor modulating presenilin-1 and presenilin-2 promoter transactivations

por Duplan, Eric, Sévalle, Jean, Viotti, Julien, Goiran, Thomas, Bauer, Charlotte, Renbaum, Paul, Levy-Lahad, Ephrat, Gautier, Clément A, Corti, Olga, Leroudier, Nathalie, Checler, Frédéric, da Costa, Cristine Alves
Publicado 2013

Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells

por Yanovsky-Dagan, Shira, Avitzour, Michal, Altarescu, Gheona, Renbaum, Paul, Eldar-Geva, Talia, Schonberger, Oshrat, Mitrani-Rosenbaum, Stella, Levy-Lahad, Ephrat, Birnbaum, Ramon Y., Gepstein, Lior, Epsztejn-Litman, Silvina, Eiges, Rachel
Publicado 2015

Helicase-inactivating BRIP1 mutation yields Fanconi anemia with microcephaly and other congenital abnormalities

por Kamal, Lara, Pierce, Sarah B., Canavati, Christina, Rayyan, Amal Abu, Jaraysa, Tamara, Lobel, Orit, Lolas, Suhair, Norquist, Barbara M., Rabie, Grace, Zahdeh, Fouad, Levy-Lahad, Ephrat, King, Mary-Claire, Kanaan, Moien N.
Publicado 2020

Clinical testing of BRCA1 and BRCA2: a worldwide snapshot of technological practices

por Toland, Amanda Ewart, Forman, Andrea, Couch, Fergus J., Culver, Julie O., Eccles, Diana M., Foulkes, William D., Hogervorst, Frans B. L., Houdayer, Claude, Levy-Lahad, Ephrat, Monteiro, Alvaro N., Neuhausen, Susan L., Plon, Sharon E., Sharan, Shyam K., Spurdle, Amanda B., Szabo, Csilla, Brody, Lawrence C.
Publicado 2018

Variable Features of Juvenile Polyposis Syndrome With Gastric Involvement Among Patients With a Large Genomic Deletion of BMPR1A

por Lieberman, Sari, Beeri, Rachel, Walsh, Tom, Schechter, Menachem, Keret, Dan, Half, Elizabet, Gulsuner, Suleyman, Tomer, Ariela, Jacob, Harold, Cohen, Shlomi, Basel-Salmon, Lina, Mansur, Mahmud, Berger, Rachel, Katz, Lior H., Golomb, Eliahu, Peretz, Tamar, Levy, Zohar, Kedar, Inbal, King, Mary-Claire, Levy-Lahad, Ephrat, Goldberg, Yael
Publicado 2019

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families

por Brownstein, Zippora, Friedman, Lilach M, Shahin, Hashem, Oron-Karni, Varda, Kol, Nitzan, Rayyan, Amal Abu, Parzefall, Thomas, Lev, Dorit, Shalev, Stavit, Frydman, Moshe, Davidov, Bella, Shohat, Mordechai, Rahile, Michele, Lieberman, Sari, Levy-Lahad, Ephrat, Lee, Ming K, Shomron, Noam, King, Mary-Claire, Walsh, Tom, Kanaan, Moien, Avraham, Karen B
Publicado 2011

Brain calcifications and PCDH12 variants

por Nicolas, Gaël, Sanchez-Contreras, Monica, Ramos, Eliana Marisa, Lemos, Roberta R., Ferreira, Joana, Moura, Denis, Sobrido, Maria J., Richard, Anne-Claire, Lopez, Alma Rosa, Legati, Andrea, Deleuze, Jean-François, Boland, Anne, Quenez, Olivier, Krystkowiak, Pierre, Favrole, Pascal, Geschwind, Daniel H., Aran, Adi, Segel, Reeval, Levy-Lahad, Ephrat, Dickson, Dennis W., Coppola, Giovanni, Rademakers, Rosa, de Oliveira, João R.M.
Publicado 2017