Search research articles
Contact Us
Filters
Showing results (41-50 of 77) with videos related to
Page
of 8
Sort By:
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 3, 2017
Recommendations for Surveillance for Children with Leukemia-Predisposing Conditions
Christopher 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 development
Lia Heinemann-Yerushalmi, Lital Bentovim, Neta Felsenthal, et al.
Nature
|
November 13, 2015
Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesis
Shiran 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 Childhood
Surya 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 17q12
Sandesh 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 Tissues
David 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 cells
Shiri 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 heterogeneity
Noa 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 p13.3
Shen 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 females
Magdalena Bartnik, Katarzyna Derwińska, Monika Gos, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 77) with videos related to
Sort By:
Page
of 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 Conditions
Christopher 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 development
Lia Heinemann-Yerushalmi, Lital Bentovim, Neta Felsenthal, et al.
Nature
|
November 13, 2015
Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesis
Shiran 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 Childhood
Surya 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 17q12
Sandesh 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 Tissues
David 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 cells
Shiri 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 heterogeneity
Noa 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 p13.3
Shen 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 females
Magdalena Bartnik, Katarzyna Derwińska, Monika Gos, et al.
Page
of 8