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プロフィール詳細
プロジェクトを作成
★★★★★
☆☆☆☆☆
Dr. Michaela D.に依頼
France

Market Analysis & Scientific Consulting | Stem Cell Expert | 10 years of experience in academia and industry

プロフィール概要
専門分野
サービス
Writing Technical Writing, Newswriting
Research Market Research, Technology Scouting, Fact Checking, Gap Analysis, Gray Literature Search, Scientific and Technical Research, Systematic Literature Review, Secondary Data Collection
Consulting Scientific and Technical Consulting
Data & AI Statistical Analysis
職務経験

Global Marketing Product Manager

Miltenyi Biotec

2月 2023 - 11月 2024

PhD candidate

INM Inserm U1051

10月 2017 - 4月 2021

International Relations Manager

Sci.Co.

1月 2017 - 7月 2017

Scientific Guest - Master research student

UC Davis

2月 2016 - 8月 2016

Masters Intern

VUMC Amsterdam

12月 2015 - 1月 2016

Master research intern

UMC Utrecht Hersencentrum Rudolf Magnus

3月 2015 - 10月 2015

Intern

Evangelismos Hospital Athens

12月 2013 - 4月 2014

Research Intern

NCSR Demokritos

11月 2012 - 12月 2013

Research Intern

LUMC Leiden University Medical Center

3月 2013 - 7月 2013

学歴

PhD in Gene Therapy

Université de Montpellier I

10月 2017 - 4月 2021

Masters in Regenerative Medicine & Technology

Utrecht University

2014 - 2016

Bachelor in Biology

University of Athens

9月 2008 - 12月 2013

認定資格
  • Diploma of Doctorate Degree

    University of Montpellier

    1月 2021 - 現在

出版物
JOURNAL ARTICLE
Carla Sanjurjo-Soriano, Nejla Erkilic, Krishna Damodar, Hassan Boukhaddaoui, Michalitsa Diakatou, Marcela Garita-Hernandez, Daria Mamaeva, Gregor Dubois, Zhour Jazouli, Carla Jimenez-Medina, et al. (2022). Retinoic acid delays initial photoreceptor differentiation and results in a highly structured mature retinal organoid . Stem Cell Research & Therapy.
Michalitsa Diakatou and Gregor Dubois and Nejla Erkilic and Carla Sanjurjo-Soriano and Isabelle Meunier and Vasiliki Kalatzis(2021). Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3 . International Journal of Molecular Sciences. 22. (5). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 2607. {MDPI} {AG}
Nejla Erkilic and Carla Sanjurjo-Soriano and Michalitsa Diakatou and Gaël Manes and Gregor Dubois and Christian P. Hamel and Isabelle Meunier and Vasiliki Kalatzis(2019). Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy . Stem Cell Research. 38. Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 101478. Elsevier {BV}
Michalitsa Diakatou and Gaël Manes and Beatrice Bocquet and Isabelle Meunier and Vasiliki Kalatzis(2019). Genome Editing as a Treatment for the Most Prevalent Causative Genes of Autosomal Dominant Retinitis Pigmentosa . International Journal of Molecular Sciences. 20. (10). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 2542. {MDPI} {AG}
Christian Siltanen and Michalitsa Diakatou and Jeremy Lowen and Amranul Haque and Ali Rahimian and Gulnaz Stybayeva and Alexander Revzin(2018). Corrigendum to “One step fabrication of hydrogel microcapsules with hollow core for assembly and cultivation of hepatocyte spheroids” [Acta Biomater. 50 (2017) 428–436] . Acta Biomaterialia. 71. Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 522. Elsevier {BV}
Dimitris Typas and Martijn S. Luijsterburg and Wouter W. Wiegant and Michaela Diakatou and Angela Helfricht and Peter E. Thijssen and Bram van~de~Broek and Leon H. Mullenders and Haico van~Attikum(2015). The de-ubiquitylating enzymes USP26 and USP37 regulate homologous recombination by counteracting RAP80 . Nucleic Acids Research. 43. (14). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 6919--6933. Oxford University Press ({OUP})