Claudia B. Hanna

The Lowe syndrome protein OCRL1 is involved in primary cilia assembly

Brian G. Coon, Víctor Hernández-Hernández, Kayalvizhi Madhivanan et al. · Human Molecular Genetics · 2012 · 96 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Lowe syndrome patient fibroblasts display Ocrl1-specific cell migration defects that cannot be rescued by the homologous Inpp5b phosphatase

Brian G. Coon, Debarati Mukherjee, Claudia B. Hanna et al. · Human Molecular Genetics · 2009 · 51 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +9

The yeast endocytic protein Epsin 2 functions in a cell-division signaling pathway

Debarati Mukherjee, Brian G. Coon, Claudia B. Hanna et al. · Journal of Cell Science · 2009 · 26 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +15

Genotype &amp; phenotype in Lowe Syndrome: specific <i>OCRL1</i> patient mutations differentially impact cellular phenotypes

Swetha Ramadesikan, Lisette Skiba, Jennifer Lee et al. · Human Molecular Genetics · 2021 · 18 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Lowe syndrome patient cells display mTOR- and RhoGTPase-dependent phenotypes alleviated by rapamycin and statins

Kayalvizhi Madhivanan, Swetha Ramadesikan, W.‐C. Hsieh et al. · Human Molecular Genetics · 2020 · 13 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17