Bellus, Gary A.
https://orcid.org/0000-0001-7492-3324
Mayo Clinic
Clinical Genetics and Genomic Medicine, Geisinger, 100 N. Academy Ave., Danville, PA 17822, USA
Citations 2
Deficient histone H3 propionylation by BRPF1-KAT6 complexes in neurodevelopmental disorders and cancer
Yan, Kezhi , Rousseau, Justine , Machol, Keren , Cross, Laura , Agre, Katherine , Gibson, Cynthia Forster, Goverde, Anne , Engleman, Kendra, Verdin, Hannah , Baere, Elfride De, Potocki, Lorraine , Zhou, Dihong , Cadieux‐Dion, Maxime , Wagner, Monisa, Hale, Rebecca J., Esber, Natacha , Solomon, Benjamin D. , Cho, Megan T. , Eyal, Roy , Hainlen, Meagan K., Mendelsohn, Bryce A. , Porter, Hillary M. , Lanpher, Brendan C. , Lewis, Andrea M. , Savatt, Juliann M. , Thiffault, Isabelle, Callewaert, Bert , Campeau, Philippe M. , Yang, Xiang‐Jiao , Agre, Katherine E, Esber, Natacha , Riley, Alan F , McWalter, Kirsty , Eyal, Roy , Mendelsohn, Bryce A , Thiffault, Isabelle , Callewaert, Bert , Campeau, Philippe M , Yang, Xiang-Jiao , Baere, Elfride De, Bellus, Gary A.
Science Advances | January 22, 2020 | Volume: 6 | Issue: 4 | Pages: No page available
Two lysine acyltransferases govern histone H3 propionylation at lysine 23 in normal and pathological conditions.
High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype–Phenotype Correlation
Rojnueangnit, Kitiwan , Xie, Jing , Gomes, Alicia , Sharp, Angela, Callens, Tom, Chen, Yunjia , Liu, Ying , Abbott, Mary‐Alice , Atkin, Joan, Babovic‐Vuksanovic, Dusica , Barnett, Christopher , Crenshaw, Melissa , Bartholomew, Dennis W., Basel, Lina, Bellus, Gary A. , Ben‐Shachar, Shay , Bialer, Martin G., Bick, David , Blumberg, Bruce , Cortés, Fanny, David, Karen L. , Destrèe, Anne , Rodríguez, Anna Duat , Earl, Dawn , Eswara, Marthanda, Ezquieta, Begoña, Frayling, Ian M. , Frydman, Moshe , Gardner, Kathy, Gripp, Karen W. , Hernández‐Chico, Concepción, Heyrman, Kurt, Ibrahim, Jennifer, Janssens, Sandra , Keena, Beth, Llano‐Rivas, Isabel , Leppig, Kathy, McDonald, Marie , Misra, Vinod K. , Mulbury, Jennifer, Narayanan, Vinodh , Orenstein, Naama, Galvin‐Parton, Patricia , Pedro, Hélio , Pivnick, Enikö K., Powell, Cynthia M. , Randolph, Linda M., Raskin, Salmo , Rubin, Karol, Seashore, Margretta R., Schaaf, Christian P. , Schultz, Meredith, Schorry, Elizabeth K. , Schnur, Rhonda E. , Siqveland, Elizabeth, Tkachuk, Amanda , Tonsgard, James H. , Upadhyaya, Meena , Verma, Ishwar C. , Wallace, Stephanie E , Williams, Charles A. , Zackai, Elaine H. , Zonana, Jonathan, Lázaro, Conxi , Claes, Kathleen , Korf, Bruce R. , Messiaen, Ludwine , Babovic-Vuksanovic, Dusica, Cochran, J. Nicholas , Escobar, Luis Fernando , Hernández-Chico, Concepción, Rosell, Jordi , Scheuerle, Angela E. , Martín, Yolanda , Legius, Eric , Claes, Kathleen B M , Lazaro, Conxi
Human Mutation | July 14, 2015 | Volume: 36 | Issue: 11 | Pages: 1052-1063