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Cell Reports
|
January 15, 2023
Stem cell plasticity, acetylation of H3K14, and de novo gene activation rely on KAT7
Andrew J Kueh, Maria I Bergamasco, Anna Quaglieri, et al.
Haematologica
|
April 23, 2026
Novel <i>KAT6B::NUTM2B</i> fusion oncogene in congenital acute myeloid leukemia and implications for menin inhibitor therapy
Rebecca K Voss, Wenqing Qi, La'Ron Browne, et al.
American Journal of Human Genetics
|
November 15, 2011
Whole-exome-sequencing identifies mutations in histone acetyltransferase gene KAT6B in individuals with the Say-Barber-Biesecker variant of Ohdo syndrome
Jill Clayton-Smith, James O'Sullivan, Sarah Daly, et al.
The Journal of Biological Chemistry
|
April 27, 2012
Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) gene
Dillon W Leong, Jasper C Komen, Chelsee A Hewitt, et al.
Cell Reports
|
April 11, 2019
Loss of p53 Causes Stochastic Aberrant X-Chromosome Inactivation and Female-Specific Neural Tube Defects
Alex R D Delbridge, Andrew J Kueh, Francine Ke, et al.
Elife
|
December 3, 2014
TNFR1-dependent cell death drives inflammation in Sharpin-deficient mice
James A Rickard, Holly Anderton, Nima Etemadi, et al.
Biorxiv : the Preprint Server for Biology
|
September 4, 2024
Functional mapping of epigenetic regulators uncovers coordinated tumor suppression by the HBO1 and MLL1 complexes
Yuning J Tang, Haiqing Xu, Nicholas W Hughes, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
October 28, 2015
Cortical Layer Inversion and Deregulation of Reelin Signaling in the Absence of SOCS6 and SOCS7
Isobel D Lawrenson, Danielle L Krebs, Edmond M Linossi, et al.
American Journal of Human Genetics
|
October 18, 2003
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation
Kathryn P Burdon, James D McKay, Michèle M Sale, et al.
Science Advances
|
June 19, 2026
SIRT2 antagonizes MOF function during mitotic entry
María Espinosa-Alcantud, Núria Sima, Irene Fernández-Duran, et al.
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Search research articles
Search
Showing results (221-230 of 274) with videos related to
Sort By:
Page
of 28
Cell Reports
|
January 15, 2023
Stem cell plasticity, acetylation of H3K14, and de novo gene activation rely on KAT7
Andrew J Kueh, Maria I Bergamasco, Anna Quaglieri, et al.
Haematologica
|
April 23, 2026
Novel <i>KAT6B::NUTM2B</i> fusion oncogene in congenital acute myeloid leukemia and implications for menin inhibitor therapy
Rebecca K Voss, Wenqing Qi, La'Ron Browne, et al.
American Journal of Human Genetics
|
November 15, 2011
Whole-exome-sequencing identifies mutations in histone acetyltransferase gene KAT6B in individuals with the Say-Barber-Biesecker variant of Ohdo syndrome
Jill Clayton-Smith, James O'Sullivan, Sarah Daly, et al.
The Journal of Biological Chemistry
|
April 27, 2012
Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) gene
Dillon W Leong, Jasper C Komen, Chelsee A Hewitt, et al.
Cell Reports
|
April 11, 2019
Loss of p53 Causes Stochastic Aberrant X-Chromosome Inactivation and Female-Specific Neural Tube Defects
Alex R D Delbridge, Andrew J Kueh, Francine Ke, et al.
Elife
|
December 3, 2014
TNFR1-dependent cell death drives inflammation in Sharpin-deficient mice
James A Rickard, Holly Anderton, Nima Etemadi, et al.
Biorxiv : the Preprint Server for Biology
|
September 4, 2024
Functional mapping of epigenetic regulators uncovers coordinated tumor suppression by the HBO1 and MLL1 complexes
Yuning J Tang, Haiqing Xu, Nicholas W Hughes, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
October 28, 2015
Cortical Layer Inversion and Deregulation of Reelin Signaling in the Absence of SOCS6 and SOCS7
Isobel D Lawrenson, Danielle L Krebs, Edmond M Linossi, et al.
American Journal of Human Genetics
|
October 18, 2003
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation
Kathryn P Burdon, James D McKay, Michèle M Sale, et al.
Science Advances
|
June 19, 2026
SIRT2 antagonizes MOF function during mitotic entry
María Espinosa-Alcantud, Núria Sima, Irene Fernández-Duran, et al.
Page
of 28