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Ayelet Erez

Showing results (41-50 of 77) with videos related to

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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 3, 2017
Recommendations for Surveillance for Children with Leukemia-Predisposing ConditionsChristopher C Porter, Todd E Druley, Ayelet Erez, et al.
Developmental Cell|March 27, 2021
BCKDK regulates the TCA cycle through PDC in the absence of PDK family during embryonic developmentLia Heinemann-Yerushalmi, Lital Bentovim, Neta Felsenthal, et al.
Nature|November 13, 2015
Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesisShiran Rabinovich, Lital Adler, Keren Yizhak, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 17, 2017
Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in ChildhoodSurya P Rednam, Ayelet Erez, Harriet Druker, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12Sandesh Chakravarthy Sreenath Nagamani, Ayelet Erez, Joseph Shen, et al.
Cancers|December 11, 2022
Sex Biases in Cancer and Autoimmune Disease Incidence Are Strongly Positively Correlated with Mitochondrial Gene Expression across Human TissuesDavid R Crawford, Sanju Sinha, Nishanth Ulhas Nair, et al.
Nature Medicine|October 13, 2015
PAR1 signaling regulates the retention and recruitment of EPCR-expressing bone marrow hematopoietic stem cellsShiri Gur-Cohen, Tomer Itkin, Sagarika Chakrabarty, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 10, 2025
Oncogenic IDH1<sup>mut</sup> drives robust loss of histone acetylation and increases chromatin heterogeneityNoa Furth, Niv Cohen, Avishay Spitzer, et al.
Human Molecular Genetics|April 25, 2015
Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3Shen Gu, Bo Yuan, Ian M Campbell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 5, 2011
Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two femalesMagdalena Bartnik, Katarzyna Derwińska, Monika Gos, et al.
Pageof 8

Showing results (41-50 of 77) with videos related to

Sort By:
Pageof 8
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 3, 2017
Recommendations for Surveillance for Children with Leukemia-Predisposing ConditionsChristopher C Porter, Todd E Druley, Ayelet Erez, et al.
Developmental Cell|March 27, 2021
BCKDK regulates the TCA cycle through PDC in the absence of PDK family during embryonic developmentLia Heinemann-Yerushalmi, Lital Bentovim, Neta Felsenthal, et al.
Nature|November 13, 2015
Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesisShiran Rabinovich, Lital Adler, Keren Yizhak, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 17, 2017
Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in ChildhoodSurya P Rednam, Ayelet Erez, Harriet Druker, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12Sandesh Chakravarthy Sreenath Nagamani, Ayelet Erez, Joseph Shen, et al.
Cancers|December 11, 2022
Sex Biases in Cancer and Autoimmune Disease Incidence Are Strongly Positively Correlated with Mitochondrial Gene Expression across Human TissuesDavid R Crawford, Sanju Sinha, Nishanth Ulhas Nair, et al.
Nature Medicine|October 13, 2015
PAR1 signaling regulates the retention and recruitment of EPCR-expressing bone marrow hematopoietic stem cellsShiri Gur-Cohen, Tomer Itkin, Sagarika Chakrabarty, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 10, 2025
Oncogenic IDH1<sup>mut</sup> drives robust loss of histone acetylation and increases chromatin heterogeneityNoa Furth, Niv Cohen, Avishay Spitzer, et al.
Human Molecular Genetics|April 25, 2015
Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3Shen Gu, Bo Yuan, Ian M Campbell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 5, 2011
Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two femalesMagdalena Bartnik, Katarzyna Derwińska, Monika Gos, et al.
Pageof 8