Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Nita Sachan"'
Autor:
Chaitali Misra, Nita Sachan, Caryn Rothrock McNally, Sara N Koenig, Haley A Nichols, Anuradha Guggilam, Pamela A Lucchesi, William T Pu, Deepak Srivastava, Vidu Garg
Publikováno v:
PLoS Genetics, Vol 8, Iss 5, p e1002690 (2012)
Defects of atrial and ventricular septation are the most frequent form of congenital heart disease, accounting for almost 50% of all cases. We previously reported that a heterozygous G296S missense mutation of GATA4 caused atrial and ventricular sept
Externí odkaz:
https://doaj.org/article/8e619ecf80d14f26a44be5766806ce46
Publikováno v:
Plant Cell Reports. 29:437-448
Plants produce an immense number of natural products and undifferentiated cells from various plant tissues have long been considered an ideal source for their synthesis. However, undifferentiated plant cells often either lose their biosynthetic capac
Autor:
Nita Sachan, Deane L. Falcone
Publikováno v:
Phytochemistry. 61:797-805
Putrescine N-methyltransferase (PMT) catalyzes the first committed step in the biosynthesis of pyrrolinium ring-containing alkaloids. Earlier studies have indicated that PMT gene expression is restricted to root tissue in Solanaceus plant species. Du
Autor:
Valentina Parra, D. Bennett Grinsfelder, Sarvjeet Singh, Zully Pedrozo, Beverly A. Rothermel, David Rotter, Nita Sachan
Publikováno v:
Journal of molecular and cellular cardiology. 74
Many important components of the cardiovascular system display circadian rhythmicity. In both humans and mice, cardiac damage from ischemia/reperfusion (I/R) is greatest at the transition from sleep to activity. The causes of this window of susceptib
Autor:
Sara N. Koenig, William T. Pu, Vidu Garg, Chaitali Misra, Caryn Rothrock McNally, Pamela A. Lucchesi, Nita Sachan, Deepak Srivastava, Haley A. Nichols, Anuradha Guggilam
Publikováno v:
Misra, C; Sachan, N; McNally, CR; Koenig, SN; Nichols, HA; Guggilam, A; et al.(2012). Congenital heart disease-causing Gata4 mutation displays functional deficits in vivo. PLoS Genetics, 8(5). doi: 10.1371/journal.pgen.1002690. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/2hw8b3rx
PLoS genetics, vol 8, iss 5
PLoS Genetics, Vol 8, Iss 5, p e1002690 (2012)
PLoS Genetics
PLoS genetics, vol 8, iss 5
PLoS Genetics, Vol 8, Iss 5, p e1002690 (2012)
PLoS Genetics
Defects of atrial and ventricular septation are the most frequent form of congenital heart disease, accounting for almost 50% of all cases. We previously reported that a heterozygous G296S missense mutation of GATA4 caused atrial and ventricular sept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a55935dbfd1491aa2f545302fad73bb
http://www.escholarship.org/uc/item/2hw8b3rx
http://www.escholarship.org/uc/item/2hw8b3rx
Publikováno v:
Circulation Research. 109
Many important components of the cardiovascular system display circadian rhythmicity. In humans, the incidence of myocardial infarction peaks in the morning. Furthermore, studies in mouse models have demonstrated that damage from ischemia/reperfusion
Autor:
James A. Bibb, David Rotter, John M. Shelton, Beverly A. Rothermel, Misook Oh, Joseph A. Hill, Victoria Copeland, Devanjan Sikder, Pavan K. Battiprolu, Erik Bush, D. Bennett Grinsfelder, Nita Sachan, Asim Dey
Publikováno v:
Circulation research. 108(4)
Rationale: Despite overwhelming evidence of the importance of circadian rhythms in cardiovascular health and disease, little is known regarding the circadian regulation of intracellular signaling pathways controlling cardiac function and remodeling.
Publikováno v:
Circulation. 118
Many important cardiovascular factors, including metabolism, heart rate, blood pressure, and hormone release, oscillate over a 24-hour period. In humans, the incidents of adverse cardiac events, such as myocardial infarction, and ventricular tachycar
Autor:
Joseph A. Hill, Na Wang, Nita Sachan, Makoto Kuro-o, Dian J. Cao, Beverly A. Rothermel, Robert D. Gerard, David J. Morris, Yan G. Ni
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 104(51)
Insulin resistance and metabolic syndrome are rapidly expanding public health problems. Acting through the PI3K/Akt pathway, insulin and insulin-like growth factor-1 (IGF-1) inactivate FoxO transcription factors, a class of highly conserved proteins
Autor:
Beverly A. Rothermel, Richard J. Patterson, Eric Klann, James A. Richardson, Asim Dey, Charles A. Hoeffer, John M. Shelton, Nita Sachan, Helen Wong
Regulator of calcineurin 1 (RCAN1/MCIP1/DSCR1) regulates the calmodulin-dependent phosphatase calcineurin. Because it is located on human chromosome 21,RCAN1has been postulated to contribute to mental retardation in Down syndrome and has been reporte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c1567885d9648d44e61027a62dbc05c
https://europepmc.org/articles/PMC6673398/
https://europepmc.org/articles/PMC6673398/