Genetically engineered multicistronic allele of <i>Pmel</i> yielding highly specific <scp>CreERT2‐</scp> mediated recombination in the melanocyte lineage-Reference-Cited by-同舟云学术

Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2‐ mediated recombination in the melanocyte lineage

Published:2022-12-19 Issue:1 Volume:36 Page:71-77
ISSN:1755-1471
Container-title:Pigment Cell & Melanoma Research
language:en
Short-container-title:Pigment Cell Melanoma Res

Author:

Wilkinson Emma L.¹^ORCID,Brennan Louise C.¹^ORCID,Harrison Olivia J.²^ORCID,Crane‐Smith Zoe²^ORCID,Gautier Philippe²^ORCID,Keighren Margaret A.²^ORCID,Budd Peter²^ORCID,Swaminathan Karthic³^ORCID,Machesky Laura M.⁴^ORCID,Allinson Sarah L.¹^ORCID,Jackson Ian J.²⁵^ORCID,Mort Richard L.¹^ORCID

Affiliation:

1. Division of Biomedical and Life Sciences, Faculty of Health and Medicine Lancaster University Lancaster UK

2. MRC Human Genetics Unit, Institute of Genetics and Cancer, Western General Hospital University of Edinburgh Edinburgh UK

3. Centre for Skin Sciences, Faculty of Life Sciences University of Bradford Bradford UK

4. Cancer Research UK, Beatson Institute, and Institute of Cancer Sciences University of Glasgow Glasgow UK

5. Roslin Institute University of Edinburgh Roslin UK

Funder

Cancer Research UK

Medical Research Council Canada

National Centre for the Replacement Refinement and Reduction of Animals in Research

North West Cancer Research Fund

Medical Research Scotland

Publisher

Wiley

Subject

Dermatology,General Biochemistry, Genetics and Molecular Biology,Oncology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pcmr.13076

Reference19 articles.

1. Schwann Cell Precursors from Nerve Innervation Are a Cellular Origin of Melanocytes in Skin

2. A mart-1::Cre transgenic line induces recombination in melanocytes and retinal pigment epithelium

3. Pmel17 expression is Mitf-dependent and reveals cranial melanoblast migration during murine development

4. Characterization of melanocyte-specific inducible Cre recombinase transgenic mice