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Sarah J Goodman

Showing results (11-20 of 15) with videos related to

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Leukemia|October 17, 2025
DNA methylation alterations in acute lymphoblastic leukemia survivors with late neurocognitive deficitsSarah 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 KDM5CDaria 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 syndromeEric 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 inhibitionJonathan 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 signatureDmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 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 deficitsSarah 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 KDM5CDaria 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 syndromeEric 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 inhibitionJonathan 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 signatureDmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, et al.
Pageof 2