Megha Desai

发表

Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability.

Stephan J Sanders, R. Redon, J. Rosenfeld, 2019, American journal of human genetics.

A role of cellular translation regulation associated with toxic Huntingtin protein

A. Majumdar, Tania Bose, Megha Desai, 2019, Cellular and Molecular Life Sciences.

A role of cellular translation regulation associated with toxic Huntingtin protein

A. Majumdar, Tania Bose, Megha Desai, 2019, Cellular and Molecular Life Sciences.

RED CELLS , IRON , AND ERYTHROPOIESIS Mi 2 b-mediated silencing of the fetal g-globin gene in adult erythroid cells

David C Williams, David C. Williams, M. Gnanapragasam, 2013 .

Mi2β-mediated silencing of the fetal γ-globin gene in adult erythroid cells.

David C Williams, David C. Williams, M. Gnanapragasam, 2012, Blood.

An intrinsically disordered region of methyl-CpG binding domain protein 2 (MBD2) recruits the histone deacetylase core of the NuRD complex

Leander M. Sinanan, J. N. Scarsdale, Ninad M Walavalkar, 2015, Nucleic acids research.

Structural and Functional Characterization of the MBD2-NuRD Co-Repressor Complex

Megha Desai, 2014 .

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

R. Pfundt, B. D. de Vries, M. Bamshad, 2021, medRxiv.

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females.

Meghan C Towne, Carol J. Saunders, B. V. van Bon, 2021, American journal of human genetics.

p66α–MBD2 coiled-coil interaction and recruitment of Mi-2 are critical for globin gene silencing by the MBD2–NuRD complex

Ninad M Walavalkar, David C. Williams, M. Gnanapragasam, 2011, Proceedings of the National Academy of Sciences.