CRYβA3/A1-Crystallin Knockout Develops Nuclear Cataract and Causes Impaired Lysosomal Cargo Clearance and Calpain Activation

por Hegde, Shylaja, Kesterson, Robert A., Srivastava, Om P.
Publicado 2016

Updated nomenclature for human and mouse neurofibromatosis type 1 genes

por Anastasaki, Corina, Le, Lu Q., Kesterson, Robert A., Gutmann, David H.
Publicado 2017

Partial duplication of the APBA2 gene in chromosome 15q13 corresponds to duplicon structures

por Sutcliffe, James S, Han, Michael K, Amin, Taneem, Kesterson, Robert A, Nurmi, Erika L
Publicado 2003

Genetic Ablation of CD68 Results in Mice with Increased Bone and Dysfunctional Osteoclasts

por Ashley, Jason W., Shi, Zhenqi, Zhao, Haibo, Li, Xingsheng, Kesterson, Robert A., Feng, Xu
Publicado 2011

Affinity Purification of NF1 Protein–Protein Interactors Identifies Keratins and Neurofibromin Itself as Binding Partners

por Carnes, Rachel M., Kesterson, Robert A., Korf, Bruce R., Mobley, James A., Wallis, Deeann
Publicado 2019

Mammalian Clusterin associated protein 1 is an evolutionarily conserved protein required for ciliogenesis

por Pasek, Raymond C, Berbari, Nicolas F, Lewis, Wesley R, Kesterson, Robert A, Yoder, Bradley K
Publicado 2012

Effects of risperidone on energy balance in female C57BL/6J mice

por Li, Xingsheng, Johnson, Maria S., Smith, Daniel L., Li, Yan, Kesterson, Robert A., Allison, David B., Nagy, Tim R.
Publicado 2013

BBSome Component BBS5 Is Required for Cone Photoreceptor Protein Trafficking and Outer Segment Maintenance

por Bales, Katie L., Bentley, Melissa R., Croyle, Mandy J., Kesterson, Robert A., Yoder, Bradley K., Gross, Alecia K.
Publicado 2020

Humanized GPRC6A(KGKY) is a gain-of-function polymorphism in mice

por Pi, Min, Xu, Fuyi, Ye, Ruisong, Nishimoto, Satoru K., Kesterson, Robert A., Williams, Robert W., Lu, Lu, Quarles, L. Darryl
Publicado 2020

Conditional knockout of N-Myc and STAT interactor disrupts normal mammary development and enhances metastatic ability of mammary tumors

por Pruitt, Hawley C., Metge, Brandon J., Weeks, Shannon E., Chen, Dongquan, Wei, Shi, Kesterson, Robert A., Shevde, Lalita A., Samant, Rajeev S.
Publicado 2018

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

por Awad, Elias K., Moore, Marc, Liu, Hui, Ciszewski, Lukasz, Lambert, Laura, Korf, Bruce R., Popplewell, Linda, Kesterson, Robert A., Wallis, Deeann
Publicado 2021

A CreER mouse to study melanin concentrating hormone signaling in the developing brain

por Engle, Staci E., Antonellis, Patrick J., Whitehouse, Logan S., Bansal, Ruchi, Emond, Michelle R., Jontes, James D., Kesterson, Robert A., Mykytyn, Kirk, Berbari, Nicolas F.
Publicado 2018

Novel Hypomorphic Alleles of the Mouse Tyrosinase Gene Induced by CRISPR-Cas9 Nucleases Cause Non-Albino Pigmentation Phenotypes

por Challa, Anil K., Boitet, Evan R., Turner, Ashley N., Johnson, Larry W., Kennedy, Daniel, Downs, Ethan R., Hymel, Katherine M., Gross, Alecia K., Kesterson, Robert A.
Publicado 2016

An inducible CiliaGFP mouse model for in vivo visualization and analysis of cilia in live tissue

por O’Connor, Amber K, Malarkey, Erik B, Berbari, Nicolas F, Croyle, Mandy J, Haycraft, Courtney J, Bell, P Darwin, Hohenstein, Peter, Kesterson, Robert A, Yoder, Bradley K
Publicado 2013

Increased trabecular bone and improved biomechanics in an osteocalcin-null rat model created by CRISPR/Cas9 technology

por Lambert, Laura J., Challa, Anil K., Niu, Aidi, Zhou, Lihua, Tucholski, Janusz, Johnson, Maria S., Nagy, Tim R., Eberhardt, Alan W., Estep, Patrick N., Kesterson, Robert A., Grams, Jayleen M.
Publicado 2016

Mutation-Directed Therapeutics for Neurofibromatosis Type I

por Leier, Andre, Bedwell, David M., Chen, Ann T., Dickson, George, Keeling, Kim M., Kesterson, Robert A., Korf, Bruce R., Marquez Lago, Tatiana T., Müller, Ulrich F., Popplewell, Linda, Zhou, Jiangbing, Wallis, Deeann
Publicado 2020

Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy

por Voskobiynyk, Yuliya, Battu, Gopal, Felker, Stephanie A., Cochran, J. Nicholas, Newton, Megan P., Lambert, Laura J., Kesterson, Robert A., Myers, Richard M., Cooper, Gregory M., Roberson, Erik D., Barsh, Gregory S.
Publicado 2021

Mice with missense and nonsense NF1 mutations display divergent phenotypes compared with human neurofibromatosis type I

por Li, Kairong, Turner, Ashley N., Chen, Min, Brosius, Stephanie N., Schoeb, Trenton R., Messiaen, Ludwine M., Bedwell, David M., Zinn, Kurt R., Anastasaki, Corina, Gutmann, David H., Korf, Bruce R., Kesterson, Robert A.
Publicado 2016

Targeted exon skipping of NF1 exon 17 as a therapeutic for neurofibromatosis type I

por Leier, André, Moore, Marc, Liu, Hui, Daniel, Michael, Hyde, Alexis M., Messiaen, Ludwine, Korf, Bruce R., Selvakumaran, Jamuna, Ciszewski, Lukasz, Lambert, Laura, Foote, Jeremy, Wallace, Margaret R., Kesterson, Robert A., Dickson, George, Popplewell, Linda, Wallis, Deeann
Publicado 2022

Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expression

por Yang, Chaozhe, Harafuji, Naoe, O’Connor, Amber K., Kesterson, Robert A., Watts, Jacob A., Majmundar, Amar J., Braun, Daniela A., Lek, Monkol, Laricchia, Kristen M., Fathy, Hanan M., Mane, Shrikant, Shril, Shirlee, Hildebrandt, Friedhelm, Guay-Woodford, Lisa M.
Publicado 2021