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Elizabeth Yang

Showing results (31-40 of 58) with videos related to

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Ocular Immunology and Inflammation|May 29, 2014
Quality of Life in Patients with Noninfectious Uveitis Treated with or without Systemic Anti-inflammatory TherapyWei Gui, Matthew Dombrow, Inna Marcus, et al.
The Biochemical Journal|March 16, 2012
The B55α-containing PP2A holoenzyme dephosphorylates FOXO1 in islet β-cells under oxidative stressLing Yan, Shuangli Guo, Marie Brault, et al.
Ophthalmic Plastic and Reconstructive Surgery|March 12, 2026
Plug or Punctoplasty (POPPY) Study: Perforated Punctal Plug Versus Three-Snip Punctoplasty in the Treatment of Acquired Punctal StenosisJohn S Vekinis, Laura Ah-Kye, Jeremy J Hoffman, et al.
Journal of Pediatric Hematology/Oncology|October 27, 2010
A unique clinical presentation of X-linked lymphoproliferative syndrome with a novel mutation in SH2D1A and review of the literatureMichael J Eckrich, Elizabeth Yang, Jennifer Domm, et al.
Pediatric Blood & Cancer|February 23, 2018
Molecular characterization and multidisciplinary management of Gerbich hemolytic disease of the newbornRebecca N Levitt, Elise Gourri, Christoph Gassner, et al.
Orphanet Journal of Rare Diseases|March 13, 2021
Extending the phenotypic spectrum of PRPF8, PRPH2, RP1 and RPGR, and the genotypic spectrum of early-onset severe retinal dystrophyMichalis Georgiou, Naser Ali, Elizabeth Yang, et al.
BMC Cancer|April 18, 2019
Genome sequencing analysis of blood cells identifies germline haplotypes strongly associated with drug resistance in osteosarcoma patientsKrithika Bhuvaneshwar, Michael Harris, Yuriy Gusev, et al.
Molecular and Cellular Biology|August 29, 2003
Protein phosphatase 2A dephosphorylation of phosphoserine 112 plays the gatekeeper role for BAD-mediated apoptosisChi-Wu Chiang, Cindy Kanies, Kwang Woon Kim, et al.
Pediatric Hematology and Oncology|May 20, 2020
Gut microbial composition difference between pediatric ALL survivors and siblingsRonay Thomas, Wendy S W Wong, Reem Saadon, et al.
Blood Cells, Molecules & Diseases|March 5, 2013
Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type IIRoberta Russo, Concetta Langella, Maria Rosaria Esposito, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Ocular Immunology and Inflammation|May 29, 2014
Quality of Life in Patients with Noninfectious Uveitis Treated with or without Systemic Anti-inflammatory TherapyWei Gui, Matthew Dombrow, Inna Marcus, et al.
The Biochemical Journal|March 16, 2012
The B55α-containing PP2A holoenzyme dephosphorylates FOXO1 in islet β-cells under oxidative stressLing Yan, Shuangli Guo, Marie Brault, et al.
Ophthalmic Plastic and Reconstructive Surgery|March 12, 2026
Plug or Punctoplasty (POPPY) Study: Perforated Punctal Plug Versus Three-Snip Punctoplasty in the Treatment of Acquired Punctal StenosisJohn S Vekinis, Laura Ah-Kye, Jeremy J Hoffman, et al.
Journal of Pediatric Hematology/Oncology|October 27, 2010
A unique clinical presentation of X-linked lymphoproliferative syndrome with a novel mutation in SH2D1A and review of the literatureMichael J Eckrich, Elizabeth Yang, Jennifer Domm, et al.
Pediatric Blood & Cancer|February 23, 2018
Molecular characterization and multidisciplinary management of Gerbich hemolytic disease of the newbornRebecca N Levitt, Elise Gourri, Christoph Gassner, et al.
Orphanet Journal of Rare Diseases|March 13, 2021
Extending the phenotypic spectrum of PRPF8, PRPH2, RP1 and RPGR, and the genotypic spectrum of early-onset severe retinal dystrophyMichalis Georgiou, Naser Ali, Elizabeth Yang, et al.
BMC Cancer|April 18, 2019
Genome sequencing analysis of blood cells identifies germline haplotypes strongly associated with drug resistance in osteosarcoma patientsKrithika Bhuvaneshwar, Michael Harris, Yuriy Gusev, et al.
Molecular and Cellular Biology|August 29, 2003
Protein phosphatase 2A dephosphorylation of phosphoserine 112 plays the gatekeeper role for BAD-mediated apoptosisChi-Wu Chiang, Cindy Kanies, Kwang Woon Kim, et al.
Pediatric Hematology and Oncology|May 20, 2020
Gut microbial composition difference between pediatric ALL survivors and siblingsRonay Thomas, Wendy S W Wong, Reem Saadon, et al.
Blood Cells, Molecules & Diseases|March 5, 2013
Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type IIRoberta Russo, Concetta Langella, Maria Rosaria Esposito, et al.
Pageof 6