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美國(guó)國(guó)立衛(wèi)生研究院分子生物學(xué)方向博士后職位招聘

時(shí)間:2019-01-03來源:中國(guó)博士人才網(wǎng) 作者:佚名

  Postdoctoral position in lncRNAs and human diseases at NIH

  ·         The National Institutes of Health

  ·         Location: Bethesda, MD

  ·         Job Number: 7055030

  ·         Posting Date: Dec 30, 2018

  ·         Application Deadline: Open Until Filled

  Job Description

  Department of Health and Human Services

  National Institutes of Health

  National Heart, Lung, and Blood Institute

  Postdoctoral position in lncRNAs and human diseases at NIH

  A postdoctoral position is available in Haiming Cao’s laboratory in the Cardiovascular Branch of NIH, National Heart, Lung, and Blood Institute. The Cao lab is one of the first laboratories established through the NIH Earl Stadtman investigator recruitment, and is supported by mouse transgenic, human iPS, high-throughput sequencing, proteomics, advanced microscopy, animal surgery and bioinformatics core facilities. With an interdisciplinary research environment and strong intramural support, this position provides a unique opportunity for recent PhD awardees to deepen and broaden their research profile for advancing to an independent academic career.

  The Cao group studies the molecular and pathological basis of complex human diseases particularly diabetes, cardiovascular disorders and fatty liver disease with the goal of identifying novel therapeutic interventions. The lab has recently identified a large number of long noncoding RNAs (lncRNA) function as important metabolic regulators in mice and could constitute a new class of RNA therapeutic targets for diseases. However, lncRNA conservation among species is very low, and most human lncRNAs are human-specific, so insights into lncRNA functions derived from rodent-based studies might not be applicable to human physiology. To address this challenge and to establish a system for studying human lncRNAs in a physiological context, the Cao group has recently produced humanized mice in which the mouse liver is replaced by a human one. Using this powerful model, the lab has identified a significant number of human lncRNAs that overlap with disease-associated GWAS SNPs and at the same time regulate critical aspects of energy metabolism in humanized mice. The successful applicant is expected to further study the molecular mechanisms of these human lncRNAs and to target them for the development of novel therapeutics against human diseases. In general, researches in the Cao group emphasize bridging the gaps between exciting new findings in molecular biology and therapy development of human diseases. More information on the Cao group is available at http://www.nhlbi.nih.gov/research/intramural/researchers/pi/cao-haiming.

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