Metabolic predictors of response to immune checkpoint blockade therapy von Shorer, Ofir, Yizhak, Keren

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561 Targeting CD38-driven T cell dysfunction restores sensitivity to cancer immunotherapy von Revach, Or-Yam, Cicerchia, Angelina, Sade-Feldman, Moshe, Anderson, Seth, Petrova, Boryana, Shorer, Ofir, Bod, Lloyd, Mehta, Arnav, Cattaneo, Giulia, Tiwari, Payal, Sharova, Tatyana, Xie, Hongyan, Michaud, William, Rasmussen, Martin, Fang, Jacy, Ferrone, Soldano, Flaherty, Keith, Boland, Genevieve M, Sen, Debattama R, Yizhak, Keren, Kanarek, Naama, Manguso, Robert T, Hacohen, Nir, Jenkins, Russell

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Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9 von Barel, Ortal, Shalev, Stavit A., Ofir, Rivka, Cohen, Asi, Zlotogora, Joel, Shorer, Zamir, Mazor, Galia, Finer, Gal, Khateeb, Shareef, Zilberberg, Noam, Birk, Ohad S.

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Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel von Yeshareem, Lital, Yacobovich, Joanne, Lebel, Asaf, Noy‐Lotan, Sharon, Dgany, Orly, Krasnov, Tanya, Berger Pinto, Galit, Oniashvili, Nino, Mardoukh, Jacques, Bielorai, Bella, Laor, Ruth, Mandel‐Shorer, Noa, Ben Barak, Ayelet, Levin, Carina, Asleh, Mahdi, Miskin, Hagit, Revel‐Vilk, Shoshana, Levin, Dror, Benish, Marganit, Zuckerman, Tsila, Wolach, Ofir, Pazgal, Idit, Brik Simon, Dafna, Gilad, Oded, Yanir, Asaf David, Goldberg, Tracie Alison, Izraeli, Shai, Tamary, Hannah, Steinberg‐Shemer, Orna

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PLA2G6 Mutation Underlies Infantile Neuroaxonal Dystrophy von Khateeb, Shareef, Flusser, Hagit, Ofir, Rivka, Shelef, Ilan, Narkis, Ginat, Vardi, Gideon, Shorer, Zamir, Levy, Rachel, Galil, Aharon, Elbedour, Khalil, Birk, Ohad S.

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Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ von Barel, Ortal, Shorer, Zamir, Flusser, Hagit, Ofir, Rivka, Narkis, Ginat, Finer, Gal, Shalev, Hanah, Nasasra, Ahmad, Saada, Ann, Birk, Ohad S.

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RSRC1 mutation affects intellect and behaviour through aberrant splicing and transcription, downregulating IGFBP3 von Perez, Yonatan, Menascu, Shay, Cohen, Idan, Kadir, Rotem, Basha, Omer, Shorer, Zamir, Romi, Hila, Meiri, Gal, Rabinski, Tatiana, Ofir, Rivka, Yeger-Lotem, Esti, Birk, Ohad S

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Maternally Inherited Birk Bard Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9 von Barel, Ortal, Shalev, Stavit A, Ofir, Rivka, Cohen, Asi, Ztotogora, Joel, Shorer, Zamir, Mazor, Galia, Finer, Gal, Khateeb, Shareef, Zilberberg, Noam, Birk, Ohad S

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