Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Lisa Glazewski"'
Autor:
Thomas H. Shaffer, Zubair H. Aghai, Suhita Gayen Nee'Betal, Yan Zhu, Diksha Shrestha, Deborah L. Stabley, George Xiangyun Ye, Lisa Glazewski, Jennifer Holbrook, Sankar Addya, Deepthi Alapati
Publikováno v:
Section on Neonatal-Perinatal Medicine Program.
Autor:
Salma Al Saai, Catherine Cheng, Emily Paglione, Shaili Patel, Deepti Anand, Salil A. Lachke, Shinichiro Chuma, Xiaolu Xu, Mona Batish, Lisa Glazewski, Robert W. Mason, Archana D. Siddam, Carrie E. Barnum, Velia M. Fowler, Shawn W. Polson, Soma Dash, Shuo Wei
Publikováno v:
Human Molecular Genetics
Mutations of the RNA granule component TDRD7 (OMIM: 611258) cause pediatric cataract. We applied an integrated approach to uncover the molecular pathology of cataract in Tdrd7−/− mice. Early postnatal Tdrd7−/− animals precipitously develop ca
Publikováno v:
J Proteomics
Neuroblastoma is the second most common pediatric cancer involving the peripheral nervous system in which stage IVS metastatic tumors regress due to spontaneous differentiation. 13-cis retinoic acid (13-cis RA) is currently used in the clinic for its
Publikováno v:
J Proteomics
Neuroblastoma, a cancer of the sympathetic nervous system, is the second most common pediatric cancer. A unique feature of neuroblastoma is remission in some patients due to spontaneous differentiation of metastatic tumors. 13-cis retinoic acid (13-c
Publikováno v:
Investigational New Drugs. 31:20-29
This study was designed to test the hypothesis that specific inhibition of cathepsins B and L will cause death of neuroblastoma cells. Five compounds that differ in mode and rate of inhibition of these two enzymes were all shown to cause neuroblastom
Autor:
Douglas A. Kerr, Dosh Whye, Robert W. Mason, Lisa Glazewski, Wenlan Wang, Kelvin H. Lee, Chia-Yen Wu, Leila Choe
Publikováno v:
BMC Neuroscience, Vol 12, Iss 1, p 25 (2011)
BMC Neuroscience
BMC Neuroscience
Background Deletion or mutation(s) of the survival motor neuron 1 (SMN1) gene causes spinal muscular atrophy (SMA), a neuromuscular disease characterized by spinal motor neuron death and muscle paralysis. Complete loss of the SMN protein is embryonic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f1ca0f33934d25ddd1f87f56ba44d75
Autor:
Matthew R. England, Lisa Glazewski, Anjan Matlapudi, Colin Craft, Bruce Korant, Rita Colella, Robert W. Mason, Guizhen Lu, Christopher N. Frantz
Publikováno v:
Cancer letters. 294(2)
A specific irreversible inhibitor of both cathepsins B and L, Fmoc-Tyr-Ala-CHN(2) (FYAD) induced apoptosis of neuroblastoma cells but not other tumor cells. Cysteine protease inhibitors that were not efficient inhibitors of both proteases did not cau
Publikováno v:
Investigative ophthalmologyvisual science. 46(6)
PURPOSE. This study is designed to provide a comprehensive expression profile of connexins in the human corneal epithelium (in vivo) and in cultured primary corneal epithelial cells (PCECs) (in vitro). It also evaluates the pathologic effects of a pa
Publikováno v:
Cancer Research. 70:666-666
Neuroblastoma is the most common extracranial solid tumor of childhood. Despite intensive combination therapies, the survival rate for children diagnosed with high-risk neuroblastoma remains below 40%, with surviving children suffering from severe si