Claudia B. Hanna - Search Results

Year	Number of Results
2009	2
2012	2
2020	2
2021	1
2023	1
2024	0

1

Genotype & phenotype in Lowe Syndrome: specific OCRL1 patient mutations differentially impact cellular phenotypes.

Ramadesikan S, Skiba L, Lee J, Madhivanan K, Sarkar D, De La Fuente A, Hanna CB, Terashi G, Hazbun T, Kihara D, Aguilar RC. Ramadesikan S, et al. Among authors: hanna cb. Hum Mol Genet. 2021 Apr 26;30(3-4):198-212. doi: 10.1093/hmg/ddab025. Hum Mol Genet. 2021. PMID: 33517444 Free PMC article.

2

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

Madhivanan K, Ramadesikan S, Hsieh WC, Aguilar MC, Hanna CB, Bacallao RL, Aguilar RC. Madhivanan K, et al. Among authors: hanna cb. Hum Mol Genet. 2020 Jun 27;29(10):1700-1715. doi: 10.1093/hmg/ddaa086. Hum Mol Genet. 2020. PMID: 32391547 Free PMC article.

3

Heterogeneity in Lowe Syndrome: Mutations Affecting the Phosphatase Domain of OCRL1 Differ in Impact on Enzymatic Activity and Severity of Cellular Phenotypes.

Lee JJ, Ramadesikan S, Black AF, Christoffer C, Pacheco AFP, Subramanian S, Hanna CB, Barth G, Stauffacher CV, Kihara D, Aguilar RC. Lee JJ, et al. Among authors: hanna cb. Biomolecules. 2023 Mar 29;13(4):615. doi: 10.3390/biom13040615. Biomolecules. 2023. PMID: 37189363 Free PMC article.

4

The Na⁺ pump Ena1 is a yeast epsin-specific cargo requiring its ubiquitylation and phosphorylation sites for internalization.

Sen A, Hsieh WC, Hanna CB, Hsu CC, Pearson M 2nd, Tao WA, Aguilar RC. Sen A, et al. Among authors: hanna cb. J Cell Sci. 2020 Aug 21;133(16):jcs245415. doi: 10.1242/jcs.245415. J Cell Sci. 2020. PMID: 32694166

5

Artificial neural network for the prediction of tyrosine-based sorting signal recognition by adaptor complexes.

Mukherjee D, Hanna CB, Aguilar RC. Mukherjee D, et al. Among authors: hanna cb. J Biomed Biotechnol. 2012;2012:498031. doi: 10.1155/2012/498031. Epub 2012 Mar 11. J Biomed Biotechnol. 2012. PMID: 22505811 Free PMC article.

6

The Lowe syndrome protein OCRL1 is involved in primary cilia assembly.

Coon BG, Hernandez V, Madhivanan K, Mukherjee D, Hanna CB, Barinaga-Rementeria Ramirez I, Lowe M, Beales PL, Aguilar RC. Coon BG, et al. Among authors: hanna cb. Hum Mol Genet. 2012 Apr 15;21(8):1835-47. doi: 10.1093/hmg/ddr615. Epub 2012 Jan 6. Hum Mol Genet. 2012. PMID: 22228094

7

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

Mukherjee D, Coon BG, Edwards DF 3rd, Hanna CB, Longhi SA, McCaffery JM, Wendland B, Retegui LA, Bi E, Aguilar RC. Mukherjee D, et al. Among authors: hanna cb. J Cell Sci. 2009 Jul 15;122(Pt 14):2453-63. doi: 10.1242/jcs.041137. Epub 2009 Jun 16. J Cell Sci. 2009. PMID: 19531587 Free PMC article.

8

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

Coon BG, Mukherjee D, Hanna CB, Riese DJ 2nd, Lowe M, Aguilar RC. Coon BG, et al. Among authors: hanna cb. Hum Mol Genet. 2009 Dec 1;18(23):4478-91. doi: 10.1093/hmg/ddp407. Epub 2009 Aug 21. Hum Mol Genet. 2009. PMID: 19700499 Free PMC article.

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