AMD干细胞视网膜模型染色体1风险解码博士职位

Fully Funded PhD Position: Decoding Chromosome 1 Risk in AMD Using Stem Cell–Derived Retinal Models

newcastle university · 英国 · Newcastle upon Tyne

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研究内容
利用干细胞衍生的视网膜模型和类器官,研究年龄相关性黄斑变性(AMD)中染色体1风险变异(如CFH Y402H)对感光细胞内在缺陷、细胞死亡及与视网膜色素上皮细胞(RPE)间串扰的影响。
申请条件
生物医学科学、干细胞生物学、眼科研究、神经科学、生物工程或相关领域的硕士学位(或同等学历);具备细胞培养、分子生物学经验或iPSC/类器官研究背景者优先;英语优秀。
待遇
提供年薪约42,000英镑的毛薪,并包含家庭津贴和流动津贴,享有世界一流的研究设施与跨国培训机会。
申请方式
通过电子邮件将CV(注明职位标题)、1页求职信以及1-2位学术推荐人的联系方式发送至Majlinda教授的邮箱。
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Majlinda Lako
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EURAXESS(欧洲科研人才门户,MSCA 官方导出) · 最近核对 2026-10-09
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  • is_phd
    Fully Funded PhD Position: Decoding Chromosome 1 Risk in AMD Using Stem Cell–Derived Retinal Models
  • english_ok
    Requirements / required languages / language: ENGLISH
  • bachelor_ok
    Requirements / required education level / degree: Master Degree or equivalent
官方导出原文

Fully Funded PhD Position: Decoding Chromosome 1 Risk in AMD Using Stem Cell–Derived Retinal Models Host: Newcastle University (UNEW), UK Consortium: MSCA Innovative Training Network Pandora Start date: 1.02.2027 | Application deadline: 30th October 2027 | Location: Newcastle upon Tyne, UK Are you passionate about tackling age-related macular degeneration (AMD) at the cellular and molecular level? Join the Pandora MSCA ITN consortium to investigate how Chromosome 1 (Chr1) AMD risk variants —including the complement factor H CFH Y402H polymorphism—drive intrinsic defects and cell death in photoreceptors , and how these cells crosstalk with retinal pigment epithelium (RPE) in health and disease.

The Challenge AMD risk factors disrupt the delicate choroid/Bruch’s membrane/RPE/retinal interface, leading to progressive dysfunction and loss of choroidal endothelial cells, RPEs cells, and Photoreceptors in advanced disease. While Chr1 risk is known to impair RPE (e.g., mitochondrial, and lysosomal damage in iPSC-RPE carrying CFH Y402H), it may also cause direct, cell-intrinsic pathology in Photoreceptors, potentially accelerating degeneration independently of RPE. This project will test that hypothesis and map the cell-type-specific pathomechanisms and intercellular crosstalk that underlie retinal vulnerability in AMD.

Your Project As DC1 (Doctoral Candidate 1) within Pandora, you will: • Differentiate iPSCs from controls and AMD patients carrying Chr1 risk variants (including CFH Y402H) into Retinal organoids enriched for photoreceptors. • Profile disease-relevant phenotypes using molecular, cellular, and ultrastructural assays to assess: • Oxidative stress and mitochondrial function • Lysosomal/autophagy flux and waste disposal • Inflammatory signalling and complement activation • Cell survival, death pathways, and barrier integrity

• Validate findings in human tissue via collaboration with the HEETR eye bank (P1-UT), accessing AMD donor eyes for histological and molecular correlation. • Model multicellular crosstalk by building RPE–Photoreceptor-choroid co-culture systems in perfusion platforms, enabling dynamic studies of nutrient/waste exchange, complement deposition, and stress propagation across the outer retina.

What You will Gain • World-class training in stem-cell differentiation, retinal organoid engineering, vascular biology, and advanced imaging/omics.nei.nih+1 • Transnational mobility and secondments across the Pandora consortium (academia, clinics, and industry). • Interdisciplinary skillset : from CRISPR/iPSC gene editing and single-cell transcriptomics to microfluidics, proteomics, and translational validation in human tissue. • Career development : scientific communication, project management, IP/translation, and outreach—core components of MSCA ITN training.

Who Should Apply We seek a highly motivated candidate with: • An MSc (or equivalent) in biomedical sciences, stem-cell biology, ophthalmic research, neuroscience, bioengineering, or related fields. • Experience (or strong interest) in cell culture, molecular biology, and ideally iPSC/organoid or endothelial/vascular models. • A drive to solve clinically meaningful problems and work in a collaborative, international team.

Familiarity with AMD biology, complement/immune pathways, or retinal imaging/assays is advantageous but not essential.

Requirements / required education level / degree: Master Degree or equivalent

Requirements / required education level / discipline: Neurosciences

Requirements / skills: • An MSc (or equivalent) in biomedical sciences, stem-cell biology, ophthalmic research, neuroscience, bioengineering, or related fields. • A drive to solve clinically meaningful problems and work in a collaborative, international team.

Requirements / specific requirements: Experience (or strong interest) in cell culture, molecular biology, and ideally iPSC/organoid or endothelial/vascular models. Familiarity with AMD biology, complement/immune pathways, or retinal imaging/assays is advantageous but not essential.

Requirements / required languages / language: ENGLISH

Requirements / required languages / language level: Excellent

Research experience / main research field: Neurosciences

Research experience / years of research experience: None

Research experience / main research field: Biological sciences

Research experience / years of research experience: None

Additional information / benefits: gross salary of about £42,000 /year, family support and mobility allowance

excellent research facilities comprising state of the art tissue culture facilities, access to multiple core facilities including genomics, bioimaging, flow cytometry and bioinformatics support.

Additional information / eligibility criteria: The applicant • shall not have resided or carried out his/her main activity (work, studies etc.) in UK for more than 12 months in the 36 months immediately before the recruitment date (unless as part of a compulsory national service or a procedure for obtaining refugee status under the Geneva Convention). • shall not already be in possession of a doctoral degree (*). • can be of any nationality.

*researchers who have successfully defended their doctoral thesis but who have not yet formally been awarded the doctoral degree will not be considered eligible

Additional information / selection process: Doctoral candidates will be selected based on scientific qualification and experience, research interest, additional knowledge/skills and their motivation to participate in an intersectoral research-training program.

Additional information / comment: Please send your CV, specifying the title of the position, a 1-page cover letter and the contact details of one or two academic referees to: Prof. Majlinda Lako at majlinda.lako@ncl.ac.uk If you have informal enquiries- please contact Prof. Majlinda Lako at majlinda.lako@ncl.ac.uk

Additional information / info website: https://www.retinalstemcellresearch.co.uk/

Work location / nr job positions: 1

Work location / job organisation institute: newcastle university

Work location / job country: United Kingdom

Work location / job city: Newcastle upon Tyne

Work location / job postal code: NE1 3BZ

Hiring contact / organisation institute: Newcastle University

Hiring contact / organisation institute type: Higher Education Institute

Hiring contact / division faculty: Biosciences institute

Hiring contact / country: United Kingdom

Hiring contact / city: newcastle

Hiring contact / state province: Tyne and Wear

Hiring contact / postal code: NE1 3BZ

Hiring contact / street: central parkway

Hiring contact / e mail: lindalako@gmail.com

Hiring contact / website: https://www.ncl.ac.uk

Hiring contact / phone: 07725325494

Application / how to apply: e-mail

Application / application email: Majlinda.Lako@ncl.ac.uk

EU funding / framework programme: Horizon Europe - MSCA

EU funding / cofund nr job position: 1

EU funding / cofund destination countries: United Kingdom

EU funding / sesam agreement number: 101312030

Research field / main research field: Neurosciences

Researcher profile: First Stage Researcher (R1)

Positions: PhD Positions

Contract: Temporary

Job status: Full-time

Application deadline (as exported; timezone unverified): 2026-10-30T15:00:44

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