{"id":6760,"date":"2020-10-22T16:13:36","date_gmt":"2020-10-22T14:13:36","guid":{"rendered":"https:\/\/sfbd.fr\/2020\/10\/22\/postdoctoral-position-in-developmental-neurobiology-at-institute-of-biology-valrose-ibv-nice-france\/"},"modified":"2021-06-16T18:42:17","modified_gmt":"2021-06-16T16:42:17","slug":"postdoctoral-position-in-developmental-neurobiology-at-institute-of-biology-valrose-ibv-nice-france","status":"publish","type":"post","link":"https:\/\/sfbd.fr\/en\/2020\/10\/22\/postdoctoral-position-in-developmental-neurobiology-at-institute-of-biology-valrose-ibv-nice-france\/","title":{"rendered":"Postdoctoral position in Developmental Neurobiology at Institute of Biology Valrose (iBV), Nice, France"},"content":{"rendered":"\n

<\/p>\n\n\n\n

A postdoctoral position is available from January 2021<\/u><\/strong> in the \u201cDevelopment and Function of Brain Circuits<\/em>\u201d team led by M. Studer. We aim to understand how rare genetic variants of key master genes of brain development and circuit assembly can cause neurodevelopmental diseases (NDDs). The project will determine the impact of missense variants identified in the NR2F1<\/em> gene on the heterogeneity of neurodevelopmental defects described in affected patients. The postdoc will study genotype\/phenotype correlations by using CRISPR\/Cas9 gene editing in vivo<\/em> and decipher the pathological contribution of representative variants in the mouse system. We expect that the results of this work using experimental systems as well as the identification of Nr2f1 direct targets and interacting partners will help in understanding the phenotypic heterogeneity of patients and unveil pathophysiological mechanisms common to multiple NDDs.<\/p>\n\n\n\n

Location<\/strong><\/p>\n\n\n\n

The team is located in the heart of Nice and is part of the the Institute of Biology Valrose (27 teams; 300 people; 25 nationalities), an international research centrethat brings together high-profile teams with complementary areas of expertise and with a common interest in translating basic research into knowledge for the clinic. The iBV provides state of the art core facilities, with a collaborative and lively atmosphere in a gorgeous city\/region. For more information, visit http:\/\/ibv.unice.fr\/EN\/institute\/presentation.php<\/a><\/p>\n\n\n\n

Qualification and experience<\/strong><\/p>\n\n\n\n

We are seeking highly motivated young candidates holding a PhD for less than 2 years. Preference will be given to applicants with a background in mouse genetics, cellular and molecular biology, confocal imaging and genome wide approaches. The position is opened for one year renewable up to 3 years (including medical benefits) starting as early as January 2021. Fluency in English is mandatory but ability to speak French is not required.<\/p>\n\n\n\n

Applications<\/strong><\/p>\n\n\n\n

Applications should contain a CV, a letter of motivation with a description of research accomplishments (2 pages max) and the contact information of two references able to recommend their research work directly to Michele.STUDER@unice.fr<\/a>.<\/p>\n\n\n\n

Selected related publications :<\/strong><\/p>\n\n\n\n

  1. Bertacchi M. et al., EMBO J. 2020 <\/em><\/strong>Jun 2. PMID: 32484994<\/strong><\/em><\/li>
  2. Bertacchi M. et al., EMBO Mol Med. 2019 <\/em><\/strong>Jul 18. PMID: 31318166<\/strong><\/em><\/li>
  3. Bertacchi M. et al., Review<\/em>, Brain Res. 2018,<\/em><\/strong> Apr 27. PMID: 29709504<\/strong>.<\/li>
  4. Bosch D.G.et al., Am J Hum Genet 2014,<\/em><\/strong> Feb 6.. PMID: 24462372<\/strong><\/li><\/ol>\n","protected":false},"excerpt":{"rendered":"

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