Natalia Gomez-Ospina
Affiliations: | 2002-2008 | Medicine | Stanford University, Palo Alto, CA |
Google:
"Natalia Gomez-Ospina"Mean distance: (not calculated yet)
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Scharenberg SG, Poletto E, Lucot KL, et al. (2020) Author Correction: Engineering monocyte/macrophage-specific glucocerebrosidase expression in human hematopoietic stem cells using genome editing. Nature Communications. 11: 4231 |
| Scharenberg SG, Poletto E, Lucot KL, et al. (2020) Engineering monocyte/macrophage-specific glucocerebrosidase expression in human hematopoietic stem cells using genome editing. Nature Communications. 11: 3327 |
| Gomez-Ospina N, Scharenberg SG, Lucot KL, et al. (2020) Monocyte lineage-specific glucocerebrosidase expression in human hematopoietic stem cells: A universal genome editing strategy for Gaucher disease Molecular Genetics and Metabolism. 129: S64-S65 |
| Gomez-Ospina N, Scharenberg SG, Mostrel N, et al. (2019) Human genome-edited hematopoietic stem cells phenotypically correct Mucopolysaccharidosis type I. Nature Communications. 10: 4045 |
| Dever DP, Scharenberg SG, Camarena J, et al. (2019) CRISPR/Cas9 Genome Engineering in Engraftable Human Brain-Derived Neural Stem Cells. Iscience. 15: 524-535 |
| Vakulskas CA, Dever DP, Rettig GR, et al. (2018) A high-fidelity Cas9 mutant delivered as a ribonucleoprotein complex enables efficient gene editing in human hematopoietic stem and progenitor cells. Nature Medicine |
| Gomez-Ospina N, Scharenberg SG, Mantri S, et al. (2018) Engineering blood stem cells for autologous transplants for lysosomal diseases: Correction of mucopolysaccharidosis type I using genome-edited hematopoietic stem and progenitor cells Molecular Genetics and Metabolism. 123: S54-S55 |
| Crapster JA, Hudgins L, Chen JK, et al. (2017) A novel missense variant in the GLI3 zinc finger domain in a family with digital anomalies. American Journal of Medical Genetics. Part A |
| Weiss K, Terhal PA, Cohen L, et al. (2016) De Novo Mutations in CHD4, an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive Dysmorphisms. American Journal of Human Genetics |
| Yucel G, Altindag B, Gomez-Ospina N, et al. (2013) State-dependent signaling by Cav1.2 regulates hair follicle stem cell function. Genes & Development. 27: 1217-22 |