Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Gillie, Benchorin"'
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-15 (2024)
Abstract Genome organization is thought to underlie cell type specific gene expression, yet how it is regulated in progenitors to produce cellular diversity is unknown. In Drosophila, a developmentally-timed genome reorganization in neural progenitor
Externí odkaz:
https://doaj.org/article/2fad957743af436282026f9d218b6c31
Publikováno v:
Bio-Protocol, Vol 7, Iss 7 (2017)
The electroretinogram (ERG) is a sensitive and noninvasive method for testing retinal function. In this protocol, we describe a method for performing ERGs in mice. Contact lenses on the mouse cornea measure the electrical response to a light stimulus
Externí odkaz:
https://doaj.org/article/26a376f19d8d443cbabd53fb91c0e8d7
Neural progenitors transit through multiple competence states that restrict production of each neural cell type. In Drosophila neuroblasts, a timed genome reorganization relocates the cell fate gene, hunchback, to the nuclear periphery, terminating c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae5a145407d66d4ae72610f5b527d5b7
https://doi.org/10.1101/2022.06.30.498164
https://doi.org/10.1101/2022.06.30.498164
Autor:
Douglas Vollrath, Douglas Yasumura, Gillie Benchorin, Michael T Matthes, Wei Feng, Natalie M Nguyen, Cecilia D Sedano, Melissa A Calton, Matthew M LaVail
Publikováno v:
PLoS Genetics, Vol 11, Iss 12, p e1005723 (2015)
Inherited photoreceptor degenerations (IPDs) are the most genetically heterogeneous of Mendelian diseases. Many IPDs exhibit substantial phenotypic variability, but the basis is usually unknown. Mutations in MERTK cause recessive IPD phenotypes assoc
Externí odkaz:
https://doaj.org/article/19a3a470e84d47019d54bf619c2aa96c
Autor:
Ming Chen, Stephen B. Montgomery, Dean Bok, Xin Li, Douglas Vollrath, Melissa A. Calton, Michael J. Gloudemans, Boxiang Liu, Brunilda Balliu, Nathan S. Abell, Gillie Benchorin, Jane Hu
The eye is an intricate organ with limited representation in large-scale functional genomics datasets. The retinal pigment epithelium (RPE) serves vital roles in ocular development and retinal homeostasis. We interrogated the genetics of gene express
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fba4d5eb91a12948d750276f971b7b9
https://doi.org/10.1101/446799
https://doi.org/10.1101/446799
Autor:
Ming Chen, Stephen B. Montgomery, Nathan S. Abell, Xin Li, Gillie Benchorin, Douglas Vollrath, Dean Bok, Jane Hu, Brunilda Balliu, Boxiang Liu, Melissa A. Calton, Michael J. Gloudemans
Publikováno v:
Communications Biology
Communications Biology, Vol 2, Iss 1, Pp 1-13 (2019)
Communications Biology, Vol 2, Iss 1, Pp 1-13 (2019)
The retinal pigment epithelium (RPE) serves vital roles in ocular development and retinal homeostasis but has limited representation in large-scale functional genomics datasets. Understanding how common human genetic variants affect RPE gene expressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f122c519272cd6866a406f3c43350b1
https://pubmed.ncbi.nlm.nih.gov/31123710
https://pubmed.ncbi.nlm.nih.gov/31123710
Publikováno v:
Molecular Vision
Purpose The Seahorse XFp platform is widely used for metabolic assessment of cultured cells. Current methods require replating of cells into specialized plates. This is problematic for certain cell types, such as primary human fetal RPE (hfRPE) cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22ae3a805e451c5a3c00643b29f91722
https://pubmed.ncbi.nlm.nih.gov/30034209
https://pubmed.ncbi.nlm.nih.gov/30034209
Publikováno v:
BIO-PROTOCOL. 7
The electroretinogram (ERG) is a sensitive and noninvasive method for testing retinal function. In this protocol, we describe a method for performing ERGs in mice. Contact lenses on the mouse cornea measure the electrical response to a light stimulus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe2240943bba96782670638048998e8a
https://doi.org/10.21769/bioprotoc.2218
https://doi.org/10.21769/bioprotoc.2218
Autor:
Melissa A. Calton, Gillie Benchorin, Wei Feng, Douglas Vollrath, Matthew M. LaVail, Michael T. Matthes, Douglas Yasumura, Natalie M. Nguyen, Cecilia D. Sedano
Publikováno v:
PLoS Genetics
PLoS genetics, vol 11, iss 12
PLoS Genetics, Vol 11, Iss 12, p e1005723 (2015)
PLoS genetics, vol 11, iss 12
PLoS Genetics, Vol 11, Iss 12, p e1005723 (2015)
Inherited photoreceptor degenerations (IPDs) are the most genetically heterogeneous of Mendelian diseases. Many IPDs exhibit substantial phenotypic variability, but the basis is usually unknown. Mutations in MERTK cause recessive IPD phenotypes assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b5ace712435b7bd239665004f8a44f4
http://europepmc.org/articles/PMC4687644
http://europepmc.org/articles/PMC4687644