Robert A Kesterson

6PUBLICATIONS
18CO-AUTHORS
Neurology and neuromuscular diseasesCancer diagnosis
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Publications (6)

|Dec 24, 2021
Restoration of Normal NF1 Function with Antisense Morpholino Treatment of Recurrent Pathogenic Patient-Specific Variant c.1466A>G; p.Y489C.

Elias K Awad, Marc Moore, Hui Liu

|Jan 07, 2021
Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy.

Yuliya Voskobiynyk, Gopal Battu, Stephanie A Felker

|Aug 31, 2019
Affinity Purification of NF1 Protein-Protein Interactors Identifies Keratins and Neurofibromin Itself as Binding Partners.

Rachel M Carnes, Robert A Kesterson, Bruce R Korf

|Mar 10, 2018
Neurofibromin (NF1) genetic variant structure-function analyses using a full-length mouse cDNA.

Deeann Wallis, Kairong Li, Hui Lui

|Aug 03, 2016
Mice with missense and nonsense NF1 mutations display divergent phenotypes compared with human neurofibromatosis type I.

Kairong Li, Ashley N Turner, Min Chen

|Jul 30, 2016
Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease.

Wesley R Lewis, Erik B Malarkey, Douglas Tritschler

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Frequent Collaborators

3 joint publications

Deeann Wallis

1 joint publications

Michael R Knowles

1 joint publications

Anil K Challa

1 joint publications

Steven M Rowe