Colombian physician-scientist
Natalia Gomez-Ospina is a Colombian physician-scientist who studies genetic disorders and lysosomal storage disorders .[ 1] She was born in Medellín , Colombia .[ 2] She is an Assistant Professor of Pediatrics (Genetics) and of Pediatrics (Stem Cell Transplantation) at Stanford University and works at Lucile Packard Children's Hospital .[ 1] [ 2] She is a member of Stanford Bio-X .[ 3]
Education
Gomez-Ospina studied petroleum engineering at the National University of Colombia [ 4] before transferring to the University of Colorado Boulder , where she double-majored in Molecular , Cellular , and Developmental Biology and Biochemistry .[ 1] [ 2] [ 5] [ 6] She graduated summa cum laude .[ 5]
She joined the Medical Scientist Training Program at the Stanford University School of Medicine and earned her MD/PhD in 2011.[ 7] Her doctoral thesis was entitled, "The calcium channel CACNA1C gene: multiple proteins, diverse functions."
She spent a year in internal medicine at Santa Barbara Cottage hospital before pursuing a Dermatology residency at Johns Hopkins Hospital .[ 8] She completed her residency in Medical Genetics at Stanford Hospital .[ 9] Her post-doctoral work focused on hematopoietic stem cell transplantation in pediatrics.[ 3]
Research
Gomez-Ospina has published research in several academic journals , including The New England Journal of Medicine ,[ 10] Cell ,[ 11] Nature Communications ,[ 12] Nature Medicine ,[ 13] [ 14] and the American Journal of Medical Genetics .[ 2] [ 15]
Her professional work includes point-of-care testing for children with disorders in their ability to regulate ammonia levels. With her colleagues, Gomez-Ospina has developed a handheld device to measure levels of ammonia in serum .[ 16] [ 17] [ 18] [ 19]
References
^ a b c "Natalia Gomez-Ospina | Stanford Medicine Profiles" . med.stanford.edu . Retrieved 2021-01-23 .
^ a b c d "Natalia Gomez-Ospina's Profile | Stanford Profiles" . profiles.stanford.edu . Retrieved 2021-01-23 .
^ a b University, © Stanford; Stanford; California 94305 (2018-11-02). "Natalia Gomez-Ospina - Assistant Professor of Pediatrics (Genetics and Stem Cell Transplantation)" . Welcome to Bio-X . Retrieved 2021-01-23 . {{cite web }}
: CS1 maint: numeric names: authors list (link )
^ "Browsing by Author "Ospina Gómez, Natalia Andrea" " . repositorio.unal.edu.co . Retrieved 2021-01-23 .
^ a b "People" . Gomez-Ospina Lab . Retrieved 2021-01-23 .
^ Fromherz, S. (2004-01-15). "Mutations in -tubulin promote basal body maturation and flagellar assembly in the absence of -tubulin" . Journal of Cell Science . 117 (2): 303– 314. doi :10.1242/jcs.00859 . ISSN 0021-9533 . PMID 14676280 .
^ "MSTP Alumni (before 2015)" . MSTP MD-PhD Program . Retrieved 2021-01-23 .
^ "Dr. Natalia Gomez-Ospina, MD – Palo Alto, CA | Medical Genetics on Doximity" . Doximity . Retrieved 2021-01-23 .
^ University, © Stanford; Stanford; California 94305 (2020-01-31). "Natalia Gomez-Ospina" . Wu Tsai Neurosciences Institute . Retrieved 2021-01-23 . {{cite web }}
: CS1 maint: numeric names: authors list (link )
^ Gomez-Ospina, Natalia; Chang, Anne Lynn S.; Qu, Kun; Oro, Anthony E. (2012-06-07). "Translocation Affecting Sonic Hedgehog Genes in Basal-Cell Carcinoma" . New England Journal of Medicine . 366 (23): 2233– 2234. doi :10.1056/nejmc1115123 . ISSN 0028-4793 . PMC 3839666 . PMID 22670922 .
^ Gomez-Ospina, Natalia; Tsuruta, Fuminori; Barreto-Chang, Odmara; Hu, Linda; Dolmetsch, Ricardo (Nov 2006). "The C Terminus of the L-Type Voltage-Gated Calcium Channel CaV1.2 Encodes a Transcription Factor" . Cell . 127 (3): 591– 606. doi :10.1016/j.cell.2006.10.017 . PMC 1750862 . PMID 17081980 .
^ Gomez-Ospina, Natalia; Potter, Carol J.; Xiao, Rui; Manickam, Kandamurugu; Kim, Mi-Sun; Kim, Kang Ho; Shneider, Benjamin L.; Picarsic, Jennifer L.; Jacobson, Theodora A.; Zhang, Jing; He, Weimin (Apr 2014). "Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis" . Nature Communications . 7 (1): 10713. doi :10.1038/ncomms10713 . ISSN 2041-1723 . PMC 4759630 . PMID 26888176 .
^ Vakulskas, Christopher A.; Dever, Daniel P.; Rettig, Garrett R.; Turk, Rolf; Jacobi, Ashley M.; Collingwood, Michael A.; Bode, Nicole M.; McNeill, Matthew S.; Yan, Shuqi; Camarena, Joab; Lee, Ciaran M. (Aug 2018). "A high-fidelity Cas9 mutant delivered as a ribonucleoprotein complex enables efficient gene editing in human hematopoietic stem and progenitor cells" . Nature Medicine . 24 (8): 1216– 1224. doi :10.1038/s41591-018-0137-0 . ISSN 1078-8956 . PMC 6107069 . PMID 30082871 .
^ Charlesworth, Carsten T.; Deshpande, Priyanka S.; Dever, Daniel P.; Camarena, Joab; Lemgart, Viktor T.; Cromer, M. Kyle; Vakulskas, Christopher A.; Collingwood, Michael A.; Zhang, Liyang; Bode, Nicole M.; Behlke, Mark A. (Feb 2019). "Identification of preexisting adaptive immunity to Cas9 proteins in humans" . Nature Medicine . 25 (2): 249– 254. doi :10.1038/s41591-018-0326-x . ISSN 1078-8956 . PMC 7199589 . PMID 30692695 .
^ Weiss, Karin; Terhal, Paulien A.; Cohen, Lior; Bruccoleri, Michael; Irving, Melita; Martinez, Ariel F.; Rosenfeld, Jill A.; Machol, Keren; Yang, Yaping; Liu, Pengfei; Walkiewicz, Magdalena (Oct 2016). "De Novo Mutations in CHD4, an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive Dysmorphisms" . The American Journal of Human Genetics . 99 (4): 934– 941. doi :10.1016/j.ajhg.2016.08.001 . PMC 5065651 . PMID 27616479 .
^ "Researchers develop a portable blood ammonia detector" . EurekAlert! . Retrieved 2021-01-23 .
^ "Portable blood ammonia detector could be "life-changing" " . New Atlas . 2020-07-22. Retrieved 2021-01-23 .
^ "Portable blood ammonia detector" . ScienceDaily . Retrieved 2021-01-23 .
^ Kubota, Taylor (2020-07-24). "Device could help patients test blood ammonia levels at home" . Scope . Retrieved 2021-01-23 .
External links