Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Nathalie Kertesz"'
Autor:
Nathalie Kertesz, PhD
Publikováno v:
American Journal of Preventive Cardiology, Vol 19, Iss , Pp 100853- (2024)
Therapeutic Area: Pharmacologic Therapy Background: Individuals with severe hypertriglyceridemia have an increased acute pancreatitis (AP) risk. Current treatments fail to lower TGs below a threshold that exposes patients to the risk of AP. Plozasira
Externí odkaz:
https://doaj.org/article/a18f5010035349eca5241cf79d3559de
Autor:
John W. Day, Kelly Howell, Amy Place, Kimberly Long, Jose Rossello, Nathalie Kertesz, George Nomikos
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-15 (2022)
Abstract Spinal muscular atrophy (5q-SMA; SMA), a genetic neuromuscular condition affecting spinal motor neurons, is caused by defects in both copies of the SMN1 gene that produces survival motor neuron (SMN) protein. The highly homologous SMN2 gene
Externí odkaz:
https://doaj.org/article/23d4045b62054d5a94312babfd720376
Autor:
Robin Pokrzywinski, Katelyn Cutts, Hemal Shah, Nathalie Kertesz, Sabrina Lesh, Mara Sadanowicz, Guochen Song, Janet O’Neil, Doreen Barrett, Erin Barnobi, Scott Baver
Publikováno v:
Sunday, April 23.
Autor:
Hong Wu, Xin Liu, George Thomas, Nora Rozengurt, Hilda Martinez-Diaz, Matthias Groszer, Jing Gao, Gang Li, Shungyou Wang, Nathalie Kertesz, Ralf Lesche, Dan Freeman
Supplementary Figures 1-3 from Genetic Background Controls Tumor Development in Pten-Deficient Mice
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f15eca7ad65adeb8799c4a90a2acaac6
https://doi.org/10.1158/0008-5472.22365212.v1
https://doi.org/10.1158/0008-5472.22365212.v1
Autor:
John W. Day, Kelly Howell, Amy Place, Kimberly Long, Jose Rossello, Nathalie Kertesz, George Nomikos
Publikováno v:
BMC pediatrics. 22(1)
Spinal muscular atrophy (5q-SMA; SMA), a genetic neuromuscular condition affecting spinal motor neurons, is caused by defects in both copies of the SMN1 gene that produces survival motor neuron (SMN) protein. The highly homologous SMN2 gene primarily
Autor:
Janet O'Neil, Guochen Song, Shaun M. Cote, Ashish Kalra, Thomas Crawford, George Nomikos, Doreen Barrett, Yung Chyung, Nathalie Kertesz, Amy Place, Mara Sadanowicz, Sanela Bilic, Ryan Iarrobino
Publikováno v:
Journal of the Neurological Sciences. 429:118388
Autor:
Parkash S. Gill, Valery Krasnoperov, Ramachandra Reddy, Lucy Leshanski, Sergey Zozulya, S. Ram Kumar, Nathalie Kertesz
Publikováno v:
Blood. 107:2330-2338
The receptor tyrosine kinase EphB4 and its ligand EphrinB2 play a crucial role in vascular development during embryogenesis. The soluble monomeric derivative of the extracellular domain of EphB4 (sEphB4) was designed as an antagonist of EphB4/EphrinB
Publikováno v:
Developmental Biology. 276:101-110
Erythropoietin (EPO) is an essential growth factor that regulates erythrocyte production in mammals. In this study, we demonstrate a novel role of EPO in regulating angiogenesis in vivo. Epo and Epo receptor (EpoR) are expressed in the vasculature du
Autor:
Hilda Martinez-Diaz, Robert D. Cardiff, Nora Rozengurt, Hong Wu, Xuan Liu, Ralf Lesche, Heng-Hong Li, Gang Wei, Daniel J. Freeman, Nathalie Kertesz, Andrew G. Li, Andrew D. Whale
Publikováno v:
Cancer Cell. 3:117-130
We show in this study that PTEN regulates p53 protein levels and transcriptional activity through both phosphatase-dependent and -independent mechanisms. The onset of tumor development in p53+/−;Pten+/− mice is similar to p53−/− animals, and
Autor:
Shungyou Wang, Hong Wu, Nora Rozengurt, Jing Gao, Dan Freeman, Hilda Martinez-Diaz, Ralf Lesche, Xin Liu, Matthias Groszer, Gang Li, Nathalie Kertesz, George Thomas
Publikováno v:
Cancer research. 66(13)
PTEN is one of the most frequently mutated tumor suppressor genes in human cancers. Germ line mutations of PTEN have been detected in three rare autosomal-dominant disorders. However, identical mutations in the PTEN gene may lead to different symptom