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Leukemia
|
October 17, 2025
DNA methylation alterations in acute lymphoblastic leukemia survivors with late neurocognitive deficits
Sarah J Goodman, Darci T Butcher, Sharon L Guger, et al.
BMC Medical Genomics
|
January 30, 2013
Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C
Daria Grafodatskaya, Barian H Y Chung, Darci T Butcher, et al.
BMC Medical Genomics
|
July 11, 2019
New insights into DNA methylation signatures: SMARCA2 variants in Nicolaides-Baraitser syndrome
Eric Chater-Diehl, Resham Ejaz, Cheryl Cytrynbaum, et al.
Acta Neuropathologica
|
July 17, 2022
X-linked myotubular myopathy is associated with epigenetic alterations and is ameliorated by HDAC inhibition
Jonathan R Volpatti, Mehdi M Ghahramani-Seno, Mélanie Mansat, et al.
American Journal of Human Genetics
|
April 28, 2021
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
Dmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, et al.
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of 2
Search research articles
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Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
Leukemia
|
October 17, 2025
DNA methylation alterations in acute lymphoblastic leukemia survivors with late neurocognitive deficits
Sarah J Goodman, Darci T Butcher, Sharon L Guger, et al.
BMC Medical Genomics
|
January 30, 2013
Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C
Daria Grafodatskaya, Barian H Y Chung, Darci T Butcher, et al.
BMC Medical Genomics
|
July 11, 2019
New insights into DNA methylation signatures: SMARCA2 variants in Nicolaides-Baraitser syndrome
Eric Chater-Diehl, Resham Ejaz, Cheryl Cytrynbaum, et al.
Acta Neuropathologica
|
July 17, 2022
X-linked myotubular myopathy is associated with epigenetic alterations and is ameliorated by HDAC inhibition
Jonathan R Volpatti, Mehdi M Ghahramani-Seno, Mélanie Mansat, et al.
American Journal of Human Genetics
|
April 28, 2021
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
Dmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, et al.
Page
of 2