Zobrazeno 1 - 10
of 617
pro vyhledávání: '"Ohad, S"'
Autor:
Darrell White, Gary J. Schiller, Sumit Madan, Suzanne Lentzsch, Evgeni Chubar, Noa Lavi, Dane R. Van Domelen, Ohad S. Bentur, Muhamed Baljevic
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
ObjectiveTo identify the optimal dose of selinexor in combination with pomalidomide and dexamethasone (SPd).MethodsAn analysis of efficacy and safety of 2 once-weekly selinexor regimens (60 mg and 40 mg) with pomalidomide and dexamethasone (SPd-60 an
Externí odkaz:
https://doaj.org/article/faf3645ed4d642638bc528022e510fa6
Autor:
Rips, Jonathan, Halstuk, Orli, Fuchs, Adina, Lang, Ziv, Sido, Tal, Gershon-Naamat, Shiri, Abu-Libdeh, Bassam, Edvardson, Simon, Salah, Somaya, Breuer, Oded, Hadhud, Mohamad, Eden, Sharon, Simon, Itamar, Slae, Mordechai, Damseh, Nadirah S., Abu-Libdeh, Abdulsalam, Eskin-Schwartz, Marina, Birk, Ohad S., Varga, Julia, Schueler-Furman, Ora, Rosenbluh, Chaggai, Elpeleg, Orly, Yanovsky-Dagan, Shira, Mor-Shaked, Hagar, Harel, Tamar
Publikováno v:
In Genetics in Medicine April 2024 26(4)
IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and coloboma
Autor:
Ohad Wormser, Yonatan Perez, Vadim Dolgin, Bahman Kamali, Jared A. Tangeman, Libe Gradstein, Yuval Yogev, Noam Hadar, Ofek Freund, Max Drabkin, Daniel Halperin, Inbar Irron, Erika Grajales-Esquivel, Katia Del Rio-Tsonis, Ramon Y. Birnbaum, Gidon Akler, Ohad S. Birk
Publikováno v:
npj Genomic Medicine, Vol 8, Iss 1, Pp 1-11 (2023)
Abstract Genomic sequences residing within introns of few genes have been shown to act as enhancers affecting expression of neighboring genes. We studied an autosomal recessive phenotypic continuum of microphthalmia, anophthalmia and ocular coloboma,
Externí odkaz:
https://doaj.org/article/a8c8b36507974d6a83c24a422501bd60
Autor:
Anat Bahat Dinur, Ortal Buchbut, Libe Gradstein, Baker Elsana, Ofek Freund, Ohad S. Birk, Erez Tsumi
Publikováno v:
Rambam Maimonides Medical Journal, Vol 15, Iss 1, p e0005 (2024)
Late-onset nasolacrimal duct obstruction (NLDO) as a result of inflammatory processes causing dacryo-stenosis is a common entity affecting mostly women. While a few mechanisms have been suggested as contributors to the expression of NLDO, the trigger
Externí odkaz:
https://doaj.org/article/37956adb61884ad3b3180446ca7881df
Autor:
Jagannath, Sundar, Delimpasi, Sosana, Grosicki, Sebastian, Van Domelen, Dane R., Bentur, Ohad S., Špička, Ivan, Dimopoulos, Meletios A.
Publikováno v:
In Clinical Lymphoma, Myeloma and Leukemia December 2023 23(12):917-923
Autor:
Rikken, Sem A.O.F., Bor, Willem L., Selvarajah, Abi, Zheng, Kai L., Hack, Amy P., Gibson, C. Michael, Granger, Christopher B., Bentur, Ohad S., Coller, Barry S., van ’t Hof, Arnoud W.J., ten Berg, Jurriën M.
Publikováno v:
In American Heart Journal August 2023 262:75-82
Autor:
David Shaki, Marina Eskin-Schwartz, Noam Hadar, Emily Bosin, Lior Carmon, Samuel Refetoff, Eli Hershkovitz, Ohad S Birk, Alon Haim
Publikováno v:
European Thyroid Journal, Vol 11, Iss 1, Pp 1-6 (2023)
Objective: Bi-allelic loss-of-function mutations in TSHB, encoding the beta subunit of thyroid-stimulating hormone (TSH), cause congenital hypothyroidism. Homozygosity for the TSHB p.R75G variant, previously described in South Asian individuals, does
Externí odkaz:
https://doaj.org/article/4d2799ea23084429a95d73bf5e191201
Autor:
Schiller, Gary J., Lipe, Brea C., Bahlis, Nizar J., Tuchman, Sascha A., Bensinger, William I., Sutherland, Heather J., Lentzsch, Suzanne, Baljevic, Muhamed, White, Darrell, Kotb, Rami, Chen, Christine I., Rossi, Adriana, Biran, Noa, LeBlanc, Richard, Grosicki, Sebastian, Martelli, Maurizio, Gunsilius, Eberhard, Špička, Ivan, Stevens, Don Ambrose, Facon, Thierry, Mesa, Mercedes Gironella, Zhang, Chris, Van Domelen, Dane R., Bentur, Ohad S., Gasparetto, Cristina
Publikováno v:
In Clinical Lymphoma, Myeloma and Leukemia June 2023
Autor:
Muhamed Baljevic, Cristina Gasparetto, Gary J. Schiller, Sascha A. Tuchman, Natalie S. Callander, Suzanne Lentzsch, Jorge Monge, Rami Kotb, Nizar J. Bahlis, Darrell White, Christine I. Chen, Heather J. Sutherland, Sumit Madan, Richard LeBlanc, Michael Sebag, Christopher P. Venner, William I. Bensinger, Noa Biran, Andrew DeCastro, Dane R. Van Domelen, Chris Zhang, Jatin J. Shah, Sharon Shacham, Michael G. Kauffman, Ohad S. Bentur, Brea Lipe
Publikováno v:
eJHaem, Vol 3, Iss 4, Pp 1270-1276 (2022)
Abstract There is a lack of consensus on therapy sequencing in previously treated multiple myeloma, particularly after anti‐B‐cell maturation antigen (BCMA) therapy. Earlier reports on selinexor (X) regimens demonstrated considerable efficacy in
Externí odkaz:
https://doaj.org/article/cc625c53f2e041649d56e52c14f79586
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