The goal of the Molecular Biology and Next Generation Technologies (MBNGT) Core has been, and will continue to be, to provide essential molecular biology and genetic services in advanced technology areas, and to pioneer new areas of research that promote discovery, hypothesis-driven science and innovation to investigators in the Liver Research Center (LRC).
The specific aims of the MBNGT Core are predominantly two-fold. (1) To continue to provide basic services through the availability of dedicated space in the LRC with shared equipment unavailable in individual investigators laboratories. In addition, the Core Manager will continue to provide individualized teaching and service to facilitate the adaptation of molecular genetic assays and procedures to the wide spectrum of students, postdoctoral fellows, residents, fellows, physician-scientists and principle investigators incorporating these assays into their research. (2) To introduce new services primarily related to the dynamic technologies being rapidly employed in research based on massively parallel sequencing (aka. Next Generation Sequencing (NGS)) and advances in bioinformatics. The MBNGT Core will provide teaching and services allowing LRC scientists to access NGS through preparation of specialized libraries, isolation of exosomes and microRNA for deep sequencing and characterization of the microbiome. The close proximity of the MBNGT facility and the availability of staff to teach, advise experimental approaches, perform highly technical procedures and help interpret complex data sets will serve to enrich the research performed in the LRC.
It is estimated that over 30 million Americans have a liver disorder;further, liver disease is one of the ten leading causes of death in the United States. Although advances have been made in diagnosis and treatment of liver diseases, there is still much to be learned. The Liver Research Center at Einstein provides a multidisciplinary approach to the study of liver disease by integrating basic and clinical research efforts to foster development of new insights and paradigms.
|Liu, Zhongbo; Apontes, Pasha; Fomenko, Ekaterina V et al. (2018) Mangiferin Accelerates Glycolysis and Enhances Mitochondrial Bioenergetics. Int J Mol Sci 19:|
|Tekirdag, Kumsal; Cuervo, Ana Maria (2018) Chaperone-mediated autophagy and endosomal microautophagy: Joint by a chaperone. J Biol Chem 293:5414-5424|
|Zhao, Rongbao; Najmi, Mitra; Aluri, Srinivas et al. (2018) Concentrative Transport of Antifolates Mediated by the Proton-Coupled Folate Transporter (SLC46A1); Augmentation by a HEPES Buffer. Mol Pharmacol 93:208-215|
|Amengual, Jaume; Guo, Liang; Strong, Alanna et al. (2018) Autophagy Is Required for Sortilin-Mediated Degradation of Apolipoprotein B100. Circ Res 122:568-582|
|Schneider, Michael; Kumar, Vivek; Nordstrøm, Lars Ulrik et al. (2018) Inhibition of Delta-induced Notch signaling using fucose analogs. Nat Chem Biol 14:65-71|
|Iqbal, Niloy Jafar; Lu, Zhonglei; Liu, Shun Mei et al. (2018) Cyclin-dependent kinase 4 is a preclinical target for diet-induced obesity. JCI Insight 3:|
|Galsgaard, Katrine D; Winther-Sørensen, Marie; Ørskov, Cathrine et al. (2018) Disruption of glucagon receptor signaling causes hyperaminoacidemia exposing a possible liver-alpha-cell axis. Am J Physiol Endocrinol Metab 314:E93-E103|
|Shen, Ling; Liu, Yin; Tso, Patrick et al. (2018) Silencing steroid receptor coactivator-1 in the nucleus of the solitary tract reduces estrogenic effects on feeding and apolipoprotein A-IV expression. J Biol Chem 293:2091-2101|
|Dulyaninova, Natalya G; Ruiz, Penelope D; Gamble, Matthew J et al. (2018) S100A4 regulates macrophage invasion by distinct myosin-dependent and myosin-independent mechanisms. Mol Biol Cell 29:632-642|
|Kakabadze, Zurab; Kakabadze, Ann; Chakhunashvili, David et al. (2018) Decellularized human placenta supports hepatic tissue and allows rescue in acute liver failure. Hepatology 67:1956-1969|
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